<?xml version="1.0" encoding="UTF-8" ?><xml><records><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>788</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">788</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Teppala, Dharma Teja</style></author><author><style face="normal" font="default" size="100%">Pejić, Milan</style></author><author><style face="normal" font="default" size="100%">Zagorac, Dejan</style></author><author><style face="normal" font="default" size="100%">Adabifiroozjaei, Esmaeil</style></author><author><style face="normal" font="default" size="100%">Goyal, Naina</style></author><author><style face="normal" font="default" size="100%">Molina-Luna, Leopoldo</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Matović, Branko</style></author><author><style face="normal" font="default" size="100%">Ionescu, Emanuel</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Single-source precursor synthesis of a compositionally complex early transitional metal nitride (V, Nb, Ta, Mo, W)Nx and its high temperature stability</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Applied Ceramic Technology</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">International Journal of Applied Ceramic Technology</style></full-title></periodical><pages><style face="normal" font="default" size="100%">e70120</style></pages><volume><style face="normal" font="default" size="100%">23</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">ammonolysis</style></keyword><keyword><style face="normal" font="default" size="100%">compositional complexity</style></keyword><keyword><style face="normal" font="default" size="100%">DFT</style></keyword><keyword><style face="normal" font="default" size="100%">modelling</style></keyword><keyword><style face="normal" font="default" size="100%">nitrides</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2026</style></year><pub-dates><date><style face="normal" font="default" size="100%">2026/02/01</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1546-542X</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract Compositionally complex transitional metal nitrides are an interesting class of ceramics with superior chemical, thermal, and mechanical stability, with a high potential in ultra-high temperature applications and catalysis. The exceptionality in the properties may partly be explained as a consequence of their high configuration entropy. Although promising candidates, the bulk synthesis of compositionally complex metal (carbo)nitrides remains challenging, often limited by purity and scalability due to significant oxygen contamination from gaseous reactants or nitrogen loss. To offset these disadvantages, the current manuscript proposes an alternative synthesis route for the synthesis of a compositionally complex nitride (V, Nb, Ta, Mo, W)Nx, which deviates from the typical solid-state and sputtering methods by employing an organometallic precursor route and a double ammonolysis process. This is a first attempt to synthesize such ceramics with low oxygen contamination in compositionally complex (carbo)nitrides with a scalable production. Using a multidisciplinary approach consisting of theoretical methods and experiments, the current study elucidates the evolution and stability of the precursor at high temperatures under carbon, and thereby obtained ceramics at different temperatures.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1111/ijac.70120</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1111/ijac.70120</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2026/01/26</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>778</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">778</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mattaparthi, Srinivas</style></author><author><style face="normal" font="default" size="100%">Srivastava, Ashutosh</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Ashish</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Tripathy, S. K.</style></author><author><style face="normal" font="default" size="100%">Karan, Himanshu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">High performance Rb2AgBiI6 perovskite solar cell with optimized charge transport layers for space applications</style></title><secondary-title><style face="normal" font="default" size="100%">Solar Energy Materials and Solar Cells</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Solar Energy Materials and Solar Cells</style></full-title></periodical><pages><style face="normal" font="default" size="100%">113995</style></pages><volume><style face="normal" font="default" size="100%">295</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Solar cell</style></keyword><keyword><style face="normal" font="default" size="100%">Double perovskite</style></keyword><keyword><style face="normal" font="default" size="100%">Radiation tolerance</style></keyword><keyword><style face="normal" font="default" size="100%">SRIM</style></keyword><keyword><style face="normal" font="default" size="100%">Space application</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2026</style></year><pub-dates><date><style face="normal" font="default" size="100%">2026/01/15/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0927-0248</style></isbn><abstract><style face="normal" font="default" size="100%">Perovskite solar cells (PSCs), both lead-based and lead-free, offer a promising energy solutions for space applications owing to their lightweight design and excellent radiation resistance. In this work, we have introduced Rb2AgBiI6 lead-free double perovskite material as absorber layer due to its significant properties such as favorable band gap, superior thermal stability, less toxic nature and studied the performance of Rb2AgBiI6 based PSCs under high radiation exposure. Here, WS2 and Cu2O have been used as an ETL and HTL material, respectively, due to their suitable band alignment and high carrier mobility. The absorber layer parameters such as thickness, doping, defect density, interfacial effects, and electron affinity, were optimized to enhance the device performance. Additionally, device reliability has been improved by optimizing shunt resistances, temperature stability, and incident light intensity. The proposed device has attained power conversion efficiency of 29.32 % with open circuit voltage (VOC) of 1.22 V, short-circuit current density (JSC) of 27.62 mA/cm2, and fill factor (FF) of 86.93 %. Furthermore, the impact of proton irradiation on proposed PSC was investigated, with a focus on ionization energy, recoil energy losses and vacancy production rates under different proton energies using SRIM simulator. Moreover, the proposed PSC demonstrates low ionization energy, reduced vacancy production rate and minimal recoil energy loss, highlighting its potential suitability for space applications. Additionally, the J–V characteristics of proposed PSC were analysed under AM0 and AM1.5G lighting conditions, both before and after proton irradiation, showcasing its robustness and efficiency in space-relevant environments.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0927024825005963</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.solmat.2025.113995</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>786</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">786</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lichtenberg, Andreas</style></author><author><style face="normal" font="default" size="100%">Chrubasik, Jan</style></author><author><style face="normal" font="default" size="100%">Rryci, Lukas</style></author><author><style face="normal" font="default" size="100%">Karimpour, Touraj</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Air-stable single-source CVD of ThO2 thin films</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Letters</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Materials Letters</style></full-title></periodical><pages><style face="normal" font="default" size="100%">140061</style></pages><volume><style face="normal" font="default" size="100%">407</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Thorium</style></keyword><keyword><style face="normal" font="default" size="100%">Thorium dioxide</style></keyword><keyword><style face="normal" font="default" size="100%">CVD</style></keyword><keyword><style face="normal" font="default" size="100%">Thin films</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2026</style></year><pub-dates><date><style face="normal" font="default" size="100%">2026/03/15/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0167-577X</style></isbn><abstract><style face="normal" font="default" size="100%">Thorium dioxide (ThO2) is gaining increasing technological relevance for next-generation nuclear and advanced functional material applications. These fields demand simple, safe and cost-effective methods for producing high-quality and compositionally uniform ThO2 coatings. In this work, we present a practical and user-friendly chemical vapor deposition (CVD) process that utilizes air-stable thorium acetylacetonate [Th(acac)4] as a single-source precursor. The resulting ThO2 films exhibit excellent phase purity and crystallinity, as well as uniform substrate coverage after calcination. This approach offers a safer and simplified alternative to previously reported routes, making a significant step toward scalable processing of actinide-based thin films.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0167577X26000194</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.matlet.2026.140061</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>777</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">777</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kumar, Anuj</style></author><author><style face="normal" font="default" size="100%">Goyal, Naina</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Bakhtiyarovich, Ibragimov Aziz</style></author><author><style face="normal" font="default" size="100%">Zhao, Yufeng</style></author><author><style face="normal" font="default" size="100%">Khalid, Mohammad</style></author><author><style face="normal" font="default" size="100%">Ubaidullah, Mohd</style></author><author><style face="normal" font="default" size="100%">Al-Enizi, Abdullah M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Advances in coordination engineering of M-N-C single atom catalysts for superior oxygen reduction performance</style></title><secondary-title><style face="normal" font="default" size="100%">Coordination Chemistry Reviews</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Coordination Chemistry Reviews</style></full-title></periodical><pages><style face="normal" font="default" size="100%">217244</style></pages><volume><style face="normal" font="default" size="100%">549</style></volume><keywords><keyword><style face="normal" font="default" size="100%">M-N-C materials</style></keyword><keyword><style face="normal" font="default" size="100%">ORR</style></keyword><keyword><style face="normal" font="default" size="100%">Coordination environments</style></keyword><keyword><style face="normal" font="default" size="100%">Doping</style></keyword><keyword><style face="normal" font="default" size="100%">Spin state</style></keyword><keyword><style face="normal" font="default" size="100%">Energy</style></keyword><keyword><style face="normal" font="default" size="100%">Coordination sphere</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2026</style></year><pub-dates><date><style face="normal" font="default" size="100%">2026/02/15/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0010-8545</style></isbn><abstract><style face="normal" font="default" size="100%">The oxygen reduction reaction (ORR) is a cornerstone of sustainable energy conversion technologies, such as fuel cells, metal–air batteries, and green synthesis of H2O2. However, the widespread adoption of ORR is hindered by persistent challenges in terms of catalytic activity, selectivity, and durability of the catalysts. A transformative approach to overcome these limitations is the chemical engineering of metal‑nitrogen‑carbon single-atom catalysts (M-N-C SACs), which allows precise tuning of electronic structures and coordination environments to mimic the efficiency of natural metalloenzymes. The electronic structure of M-N-C SACs can be modulated by incorporation of heteroatoms (e.g., S, B), which alter the d-band structure to enhance O2 adsorption and OO bond cleavage, consequently reducing the overpotential for ORR. Atomic-scale engineering of bond lengths, coordination numbers, and electronic states in metal‑nitrogen‑carbon single-atom catalysts (M-N-C SACs) significantly improves their ORR performance. Specifically, the engineering of the first and higher coordination spheres through ligand design or hetero-element doping enhances charge transfer dynamics and selectivity of 4e- process, which is a key step in ORR. This review systematically evaluates the influence of coordination engineering in M-N-C SACs on benchmark ORR metrics, while highlighting breakthroughs in operando techniques and advanced electron microscopy that resolve active-site dynamics under working conditions. This study highlights the integration of density functional theory (DFT) predictions with experimental validation to demonstrate the synergy between tailored coordination environments and catalytic activity. Finally, the existing challenges, such as the scalability of defect-engineered SACs and their long-term stability in acidic media, are discussed in the context of emerging catalytic materials. In addition, the opportunities in machine learning-guided design and plasma-enhanced synthesis of hierarchical N-doped carbons for electrode engineering are discussed.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0010854525008148</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.ccr.2025.217244</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>785</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">785</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kavraz, Pelin</style></author><author><style face="normal" font="default" size="100%">Bhardwaj, Aman</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Kuritka, Ivo</style></author><author><style face="normal" font="default" size="100%">Dmonte, David John</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Akcay, Namık</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hydrogen plasma treated iron vanadate nanoparticles for efficient ammonia sensing</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Surface Science</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Applied Surface Science</style></full-title></periodical><pages><style face="normal" font="default" size="100%">165537</style></pages><volume><style face="normal" font="default" size="100%">722</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Gas sensing</style></keyword><keyword><style face="normal" font="default" size="100%">Iron vanadate</style></keyword><keyword><style face="normal" font="default" size="100%">Hydrogen plasma</style></keyword><keyword><style face="normal" font="default" size="100%">Ammonia sensor</style></keyword><keyword><style face="normal" font="default" size="100%">Nanoparticles</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2026</style></year><pub-dates><date><style face="normal" font="default" size="100%">2026/03/15/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0169-4332</style></isbn><abstract><style face="normal" font="default" size="100%">In this study, we investigate the impact of hydrogen plasma treatment on the gas-sensing properties of iron vanadate (FeVO4) nanostructures. The FeVO4 nanoparticles were synthesized via a sol–gel method, followed by surface modification using hydrogen plasma. Both hydrogen plasma-treated (hp-FeVO4) and untreated (FeVO4) samples were systematically characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS) techniques. Gas sensing experiments revealed that hp-FeVO4 nanostructures exhibited a response to 50 ppm NH3 that was twice as high as that of untreated FeVO4 samples, highlighting the significant enhancement achieved through plasma surface engineering. Notably, the hp-FeVO4 sensor exhibited a response time of 72 s and a recovery time of 292 s, operating at a reduced temperature of 380 °C, possibly due to increased band bending on the plasma-treated surface. Moreover, the sensor exhibited promising repeatability, selectivity, and long-term stability without the need to incorporate noble metals. These findings highlight the strong potential of hydrogen plasma-modified iron vanadate for advanced gas sensing applications.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0169433225032544</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.apsusc.2025.165537</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>787</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">787</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Goyal, Naina</style></author><author><style face="normal" font="default" size="100%">Choudhary, Shweta</style></author><author><style face="normal" font="default" size="100%">Witulski, Benedict</style></author><author><style face="normal" font="default" size="100%">Yan, Shuai</style></author><author><style face="normal" font="default" size="100%">Singh, Bhupendra</style></author><author><style face="normal" font="default" size="100%">Kornienko, Nikolay</style></author><author><style face="normal" font="default" size="100%">Banerjee, Swastika</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Selective Dinitrogen Electroreduction to Ammonia on Zn2V2O7 Pyrochlore</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Catalysis</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Catalysis</style></full-title></periodical><dates><year><style face="normal" font="default" size="100%">2026</style></year><pub-dates><date><style face="normal" font="default" size="100%">2026/01/12</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><notes><style face="normal" font="default" size="100%">doi: 10.1021/acscatal.5c07714</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acscatal.5c07714</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acscatal.5c07714</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>779</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">779</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zhao, Si</style></author><author><style face="normal" font="default" size="100%">Wang, Haoheng</style></author><author><style face="normal" font="default" size="100%">Wang, Yan</style></author><author><style face="normal" font="default" size="100%">Li, Yuhang</style></author><author><style face="normal" font="default" size="100%">Zheng, Lituo</style></author><author><style face="normal" font="default" size="100%">Huang, Zhigao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hong, Zhensheng</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Inhibiting microdomain crystallinity of polymer-based electrolytes toward high-performance solid-state sodium batteries</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><pages><style face="normal" font="default" size="100%">111473</style></pages><volume><style face="normal" font="default" size="100%">145</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Solid-state battery</style></keyword><keyword><style face="normal" font="default" size="100%">PVDF-based polymer electrolyte</style></keyword><keyword><style face="normal" font="default" size="100%">Na metal</style></keyword><keyword><style face="normal" font="default" size="100%">Metal phthalocyanine</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/12/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><abstract><style face="normal" font="default" size="100%">Polyvinylidene fluoride (PVDF)-based solid electrolytes possess great potential to realize solid-state batteries, however, their low ionic conductivity from microdomain crystallinity and poor interfacial compatibility have hampered their applications Herein, we demonstrate a molecular regulation strategy by incorporating metal phthalocyanine with an extended π-conjugated structure to modify PVDF microdomain crystallinity toward high-performance solid-state sodium metal batteries. Two-dimensional wide-angle X-ray diffraction tests reveal the introduced zinc phthalocyanine (ZnPc) owning robust interaction with PVDF molecular chain effectively reduced the PVDF microdomain crystal orientation, leading to eighteen times larger ionic conductivity of 0.405 mS cm−1 than pristine PVDF electrolyte at room temperature and achieving high transference number of 0.63. The dielectric force microscopy further reveals the microdomain structure of PVDF-ZnPc polymer electrolyte with enhanced dielectric properties and homogeneous distribution. The evidence for inhibiting microdomain crystallinity has been revealed by In-situ XRD and FTIR spectra as well as theoretical calculations. Finally, composite PVDF-ZnPc polymer electrolyte with improved mechanical properties and well interface stability with Na metal anode enables the successful construction of Na//Na3V2(PO4)3 full battery, which displays high-rate capability, good cycling stability and impressive performance at wide temperature range of 60 to −20 °C. This Pc-in-polymer electrolyte offers a charming and general strategy for safe, low-cost and high-performance solid-state battery.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2211285525008328</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.nanoen.2025.111473</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>749</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">749</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zhao, Si</style></author><author><style face="normal" font="default" size="100%">Patrun, David</style></author><author><style face="normal" font="default" size="100%">Chen, Xudong</style></author><author><style face="normal" font="default" size="100%">Aytuna, Ziyaad</style></author><author><style face="normal" font="default" size="100%">Huang, Yiyin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hong, Zhensheng</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Tailoring single atom materials for regulating metal anode deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><pages><style face="normal" font="default" size="100%">110665</style></pages><volume><style face="normal" font="default" size="100%">135</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Single-atom materials</style></keyword><keyword><style face="normal" font="default" size="100%">Synthesis</style></keyword><keyword><style face="normal" font="default" size="100%">Characterization</style></keyword><keyword><style face="normal" font="default" size="100%">Metal anode</style></keyword><keyword><style face="normal" font="default" size="100%">Electrodeposition</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/03/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><abstract><style face="normal" font="default" size="100%">High-energy-density battery systems based on metal anodes have garnered tremendous research interests, holding promising applications in power grid systems, portable electronics, and electric mobility. However, the road to applications of various metal anodes is inhibited by the uneven electrodeposition and dendrites growth. The emerging single atom materials (SAMs) with tunable electronic structure provide a way to precisely adjust the electrochemical nucleation process at the atomic level, allowing the possibility of perfect homogeneous deposition of metal anode. This review article initially summarizes the various synthesis strategies and structural characterization of SAMs. Furthermore, it focuses on a comprehensive review of tailoring SAMs with unique advantages for regulating the metal (Li, Na, Zn, et al.) anode electrodeposition, offering fundamental view of designing SAMs for high-energy metal anode-based batteries. Finally, the article outlines the challenges and future research prospects of SAMs in advanced battery system applications.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2211285525000242</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.nanoen.2025.110665</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>770</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">770</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zhao, Si</style></author><author><style face="normal" font="default" size="100%">Chen, Xudong</style></author><author><style face="normal" font="default" size="100%">Patrun, David</style></author><author><style face="normal" font="default" size="100%">Zheng, Lituo</style></author><author><style face="normal" font="default" size="100%">Wang, Lili</style></author><author><style face="normal" font="default" size="100%">Wen, Zhenhai</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hong, Zhensheng</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Tailoring a High Loading Atomic Zinc with Weak Binding to Sodium Toward High-Energy Sodium Metal Batteries</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Small</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2410941</style></pages><volume><style face="normal" font="default" size="100%">21</style></volume><number><style face="normal" font="default" size="100%">9</style></number><keywords><keyword><style face="normal" font="default" size="100%">electrodeposition</style></keyword><keyword><style face="normal" font="default" size="100%">single-atom zinc</style></keyword><keyword><style face="normal" font="default" size="100%">sodium metal anode</style></keyword><keyword><style face="normal" font="default" size="100%">synthesis</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/03/01</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1613-6810</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract Single-atom materials provide a platform to precisely regulate the electrochemical redox behavior of electrode materials with atomic level. Here, a multifield-regulated sintering route is reported to rapidly prepare single-atom zinc with a very high loading mass of 24.7 wt.% by significantly improved diffusion kinetics and stronger charge transfer between zinc and nitrogen atoms. X-ray absorption near edge structure (XANES) spectra for Zn K-edges during the charge and discharge process verify the stable single-atom zinc structure and the reversible slight reduction and oxidation of Zn sites, which is much different from the previous report of the alloying reaction process. This result suggests atomic Zn acts as an active sites through weak binding with sodium to regulate the Na ion fluxes. Finally, Cu foil coated with a ≈2 µm layer of such material exhibits a high Coulombic efficiency of ≈99.99% up to 1700 cycles at 1 mA h cm?2. An ultra-low overpotential of 3 mV and an unprecedented life span of over 3200 h in a symmetrical cell is achieved. Due to the very thin coating layer, anode-free sodium battery fabricated by Na3V2(PO4)3 cathode displays a prominent energy density of 320 Wh Kg?1, demonstrating strong potential in practical application.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/smll.202410941</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/smll.202410941</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2025/08/05</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>773</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">773</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Youssef, Yomna A.</style></author><author><style face="normal" font="default" size="100%">Tammam, Salma N.</style></author><author><style face="normal" font="default" size="100%">Elshenawy, Basma M.</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Gad, Alaa A.</style></author><author><style face="normal" font="default" size="100%">Farag, Karin S.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Abdel-Kader, Reham M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Peptide-loaded chitosan nanoparticles improve mitochondrial and cognitive functions via inhibition of Aβ-ABAD interaction in Alzheimer’s disease</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Pharmaceutics and Biopharmaceutics</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">European Journal of Pharmaceutics and Biopharmaceutics</style></full-title></periodical><pages><style face="normal" font="default" size="100%">114778</style></pages><volume><style face="normal" font="default" size="100%">214</style></volume><keywords><keyword><style face="normal" font="default" size="100%">ABAD</style></keyword><keyword><style face="normal" font="default" size="100%">Alzheimer’s</style></keyword><keyword><style face="normal" font="default" size="100%">Amyloid-beta</style></keyword><keyword><style face="normal" font="default" size="100%">Chitosan</style></keyword><keyword><style face="normal" font="default" size="100%">Mitochondria</style></keyword><keyword><style face="normal" font="default" size="100%">Nanoparticles</style></keyword><keyword><style face="normal" font="default" size="100%">Peptide</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/09/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0939-6411</style></isbn><abstract><style face="normal" font="default" size="100%">Alzheimer’s disease (AD) is the most prevalent form of dementia. Mitochondrial dysfunction is recognized among the earliest pathological events in AD, and is closely-linked with the accumulation of amyloid-beta (Aβ) plaques which is a well-established hallmark of AD. The interplay between the two converges on the interaction of Aβ with the mitochondrial enzyme Aβ-binding alcohol dehydrogenase (ABAD), and the formation of Aβ-ABAD complex. This leads to the suppression of the normal function of ABAD, and elicits a number of detrimental events such as the excessive generation of reactive oxygen species (ROS) resulting in apoptosis of neuronal cells. To intercept the Aβ-ABAD interaction, a decoy peptide (DP) was employed, and was loaded into polymeric chitosan nanoparticles (CSNPs) for efficient delivery across the blood–brain barrier (BBB). In vivo studies on control and neuroinflammatory mouse models confirmed that NPs of the smaller size (SNPs; 59 ± 6 nm) accumulated in the brain with minimal off-target delivery. Unlike free DP, DP-loaded SNPs significantly improved cognitive functions as depicted by the modified Y-maze test. The DP also had protective effects on the mitochondria that were associated with a decrease in Aβ, an increase in ATP and a normalization in SOD activity. Additionally, the restoration of ABAD normal function was reflected by elevated estradiol levels. These findings indicate that the inhibition of Aβ-ABAD complex ameliorates Aβ-induced toxicity in AD, consequently enhancing both mitochondrial and cognitive functions.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0939641125001559</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.ejpb.2025.114778</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>760</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">760</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yadav, Jitendra</style></author><author><style face="normal" font="default" size="100%">Sharma, Anil K.</style></author><author><style face="normal" font="default" size="100%">Kumar, Manvendra</style></author><author><style face="normal" font="default" size="100%">Rajput, Parasmani</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Chaudhary, Dhirendra K.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Temperature-Mediated Dielectric Relaxation and Charge Transfer Mechanism in Cs3Bi2I9 Single Crystals</style></title><secondary-title><style face="normal" font="default" size="100%">physica status solidi (b)</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">physica status solidi (b)</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2400593</style></pages><volume><style face="normal" font="default" size="100%">262</style></volume><number><style face="normal" font="default" size="100%">6</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year></dates><isbn><style face="normal" font="default" size="100%">0370-1972</style></isbn><abstract><style face="normal" font="default" size="100%">Lead-free metal halide perovskite materials have received significant attention for optoelectronic devices due to their excellent properties and ecofriendly composition. Utilizing the inverse temperature crystallization technique, the Cs3Bi2I9 bismuth-based ternary halide perovskite single crystals measuring ≈5 mm are successfully grown. This study investigates dielectric relaxation and conduction mechanism using temperature-dependent impedance spectroscopy correlated with modulus spectroscopy across a frequency range (102–106 Hz) at temperatures ranging from 288 to 408 K. Negative temperature coefficient of resistance-type characteristics and temperature-dependent relaxation behavior in Cs3Bi2I9 lead-free single crystals with an estimated activation energy of 30 ± 1 meV is observed. Furthermore, significant temperature-dependent changes in dielectric properties, loss factor, electric modulus, and conductivity are observed and discussed. Notably, a pivotal transition of relaxation from non-Debye type to Debye type with increasing temperature is observed.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/abs/10.1002/pssb.202400593</style></url></related-urls><pdf-urls><url>internal-pdf://4116745534/S0010854525008148.ris</url></pdf-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/pssb.202400593</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>781</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">781</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wu, Zhiwei</style></author><author><style face="normal" font="default" size="100%">Tao, Jianming</style></author><author><style face="normal" font="default" size="100%">Lin, Lixin</style></author><author><style face="normal" font="default" size="100%">Wang, Jiangjie</style></author><author><style face="normal" font="default" size="100%">Li, Jiaxin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Lin, Yingbin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Towards High-Performance Lithium-Ion Batteries via Voltage Modulation of Silicon Anodes</style></title><secondary-title><style face="normal" font="default" size="100%">Carbon Neutralization</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Carbon Neutralization</style></full-title></periodical><pages><style face="normal" font="default" size="100%">e70052</style></pages><volume><style face="normal" font="default" size="100%">4</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">lithium-ion batteries</style></keyword><keyword><style face="normal" font="default" size="100%">silicon anode</style></keyword><keyword><style face="normal" font="default" size="100%">solid-state batteries</style></keyword><keyword><style face="normal" font="default" size="100%">voltage modulation</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/09/01</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">2769-3333</style></isbn><abstract><style face="normal" font="default" size="100%">ABSTRACT Silicon (Si) is a promising anode material for boosting the energy density of current lithium-ion batteries; however, Si anodes suffer from enormous volume modulations and unstable solid electrolyte interphases (SEI) associated with the voltage window. Nevertheless, the relationship between voltage changes and deterioration of electrochemical performance remains unclear. Through systematic investigation of Si anodes under various cut-off voltages, we reveal that an increased degree of delithiation generates high hoop stress around the particle surface, ultimately leading to SEI thickening, fragmentation, and reformation. Furthermore, residual Li retained within Si particles after delithiation facilitates bidirectional Li+ diffusion, from Si core to shell and from electrolyte to shell, during the subsequent lithiation process. This phenomenon reduces the internal Li+ concentration gradient, delays the formation of crystalline Li15Si4, and alters delithiation kinetics. In addition, we observed that maintaining the voltage window within a range that induces high hoop stress and prevents the formation of crystalline Li15Si4 enables the Si anode to achieve optimized cycling performance and capacity. This voltage modulation criterion is also applicable for nano-sized Si, graphite-Si composite anodes, and solid-state batteries. The practical effectiveness of this approach is demonstrated through the successful operation of 5?Ah LiCoO2/Si pouch cells, confirming that dynamic voltage control based on polarization can substantially enhance the cycle life of lithium-ion batteries.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/cnl2.70052</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/cnl2.70052</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2025/11/11</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>776</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">776</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Witulski, Benedict</style></author><author><style face="normal" font="default" size="100%">Goyal, Naina</style></author><author><style face="normal" font="default" size="100%">Patrun, David</style></author><author><style face="normal" font="default" size="100%">Pires, Fabio</style></author><author><style face="normal" font="default" size="100%">Aytuna, Ziyaad</style></author><author><style face="normal" font="default" size="100%">Alaei, Hamed</style></author><author><style face="normal" font="default" size="100%">Schiemann, Olav</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ag Cluster-Modified K0.5Na0.5NbO3 Piezocatalyst for Enhanced Electrochemical Dinitrogen Reduction Reaction</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2500764</style></pages><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">piezocatalysis</style></keyword><keyword><style face="normal" font="default" size="100%">piezo assisted electrochemical nitrogen reduction reaction</style></keyword><keyword><style face="normal" font="default" size="100%">piezo enhanced ammonia synthesis</style></keyword><keyword><style face="normal" font="default" size="100%">sol-gel</style></keyword><keyword><style face="normal" font="default" size="100%">metal alkoxide</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/07/04</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1438-1656</style></isbn><abstract><style face="normal" font="default" size="100%">Efforts in finding alternatives to Haber?Bosch process for chemical synthesis of ammonia still struggle with efficient N2 activation. Piezoelectric materials are promising cocatalysts to enhance the chemical kinetics of dinitrogen (N2) reduction through, built-in electric fields, upon mechanical activation, which can modulate the surface electrochemical potential. This work reports on the influence of piezoelectric potassium sodium niobate (K0.5Na0.5NbO3, KNN) as a lead-free cocatalyst for the electrochemical nitrogen reduction reaction to ammonia (NH3) under mild conditions, on a silver (Ag) catalyst. For piezoactivation, modified H-cell is engineered with the working electrode (Ag/KNN), enabling external mechanical actuating during electrochemical process. The results demonstrate that transient dipoles generated on the KNN surface through localized electric field improve threefold NH3 production (3.6??g h?1?cm?2) and a Faradaic efficiency up to 75%. Piezoinfluence is investigated through actuation-induced, linear sweep voltammetry, electrochemical impedance spectroscopy, chronoamperometry, and open-circuit potential measurements.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202500764</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202500764</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2025/08/23</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>759</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">759</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Florez, Alejandra</style></author><author><style face="normal" font="default" size="100%">Dodd-Clements, Keely</style></author><author><style face="normal" font="default" size="100%">Reb, Lennart Klaus</style></author><author><style face="normal" font="default" size="100%">Götte, Michael</style></author><author><style face="normal" font="default" size="100%">Grosch, Matthias</style></author><author><style face="normal" font="default" size="100%">Yang, Fengning</style></author><author><style face="normal" font="default" size="100%">Öz, Senol</style></author><author><style face="normal" font="default" size="100%">Mathies, Florian</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ramírez, Daniel</style></author><author><style face="normal" font="default" size="100%">Jaramillo, Franklin</style></author><author><style face="normal" font="default" size="100%">Unger, Eva</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Toward Green Processing of Perovskite Solar Cells: Protic Ionic Liquids Enable Water- and Alcohol-Based MAPbI3 Precursors Inks for Slot-Die Coating</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Energy Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Energy Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2403626</style></pages><volume><style face="normal" font="default" size="100%">15</style></volume><number><style face="normal" font="default" size="100%">16</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year></dates><isbn><style face="normal" font="default" size="100%">1614-6832</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract Halide perovskite solar cells are approaching commercialization, with solution processing emerging as a key method for large-scale production. This study introduces a significant advancement: using non-toxic solvents like water and alcohol in perovskite precursor inks facilitated by the protic ionic liquid methylammonium propionate (MAP). MAP effectively dissolves perovskite precursors such as lead acetate and methylammonium iodide, enabling the first stable water-based perovskite precursor ink suitable for one-step slot-die coating. This new ink formulation contrasts with conventional dimethylformamide (DMF) and dimethylsulfoxide (DMSO)-based inks, as evidenced by in-situ grazing incidence wide-angle X-ray scattering (GIWAXS), which revealed an intermediate-free liquid-to-solid transition. In-situ mass spectrometry also showed that organic molecules evaporate during annealing, resulting in a crystalline perovskite phase. Optimization of the solvent mixture to H2O/IPA/MAP enabled successful slot-die coating, yielding perovskite solar cells with an efficiency of up to 10%. This eco-friendly ink reduces toxicity and environmental impact compared to DMF-based inks, offering a longer shelf life and the possibility of using the ink in ambient conditions. This pioneering work represents the first report of a water-based green ink formulation for one-step thin film coating at room-temperature conditions by slot-die coating, highlighting its potential for sustainable commercial applications.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://advanced.onlinelibrary.wiley.com/doi/abs/10.1002/aenm.202403626</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/aenm.202403626</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>767</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">767</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tobechukwu Anthony, Eric</style></author><author><style face="normal" font="default" size="100%">Olthof, Selina</style></author><author><style face="normal" font="default" size="100%">Roitsch, Stefan</style></author><author><style face="normal" font="default" size="100%">Meerholz, Klaus</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Klein, Axel</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Bis-Thiosemicarbazone Pd(II) SiO2 Nanoparticle Conjugate for CC Coupling Catalysis</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2500245</style></pages><volume><style face="normal" font="default" size="100%">28</style></volume><number><style face="normal" font="default" size="100%">23</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year></dates><isbn><style face="normal" font="default" size="100%">1434-1948</style></isbn><abstract><style face="normal" font="default" size="100%">Pd(II) complexes of thiosemicarbazones (TSCs) have previously been used as homogenous precatalysts for constructing CC bonds. Herein, the first SiO2-supported homogeneous Pd(II)-TSC catalyst [PdL]–APTES–SiO2 (APTES = (3-aminopropyl)triethoxysilane) is reported for this purpose. This Pd complex–SiO2 nanoparticle (NP) conjugate is synthesized through covalent binding of the pentadentate bis(N4-(2-ethylphenyl)) 2,6-diacetyl-pyridine TSC onto monodispersed SiO2, followed by coordination of Pd(II). Characteristic shifts of resonances in the Fourier-transform infrared spectra allowed confirming the SiO2 functionalization and the Pd-binding. High-resolution X-ray photoelectron spectroscopy (XPS) analysis of N 1s, C 1s, and S 2p shows that the binding energies of the atoms in the CN, CS, CN, NH, pyridine-N, and imine-N groups shift to lower values upon Pd coordination. The absence of chloride in the XPS of the H2L–APTES–SiO2 conjugate strongly supports the successful covalent binding of the TSC onto the SiO2 NPs and is in line with the Sthiolate^Nimine^Npyridine^Namide coordination of Pd(II) in the conjugate that is also found in the model complex [Pd(L)]. The [PdL]–APTES–SiO2 NPs are used as precatalyst in Suzuki–Miyaura-type cross-coupling reactions with yields ranging from 70% to 83%.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/ejic.202500245</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/ejic.202500245</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>766</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">766</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Szymura, Annika</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Grohmann, Florian</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ionic liquid modified mesoporous silica nanocarriers for efficient drug delivery and hydrophobic surface engineering</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Advances</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Materials Advances</style></full-title></periodical><pages><style face="normal" font="default" size="100%">4220-4232</style></pages><volume><style face="normal" font="default" size="100%">6</style></volume><number><style face="normal" font="default" size="100%">13</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year></dates><publisher><style face="normal" font="default" size="100%">RSC</style></publisher><abstract><style face="normal" font="default" size="100%">Attaining covalent attachment of diverse molecules onto carrier surfaces without compromising their chemical identity and biological functionality remains a challenge. Here, a newly synthesized alkyne-functionalized ionic liquid, 1-hexadecyl-3-propargyl imidazolium bromide (HDPI), was chemically attached on the surface of azide-modified mesoporous silica nanocarriers (mSiO2, av. size 110 nm) based on the Menshutkin reaction and copper-catalyzed click chemistry. The HDPI-functionalized mSiO2 nanocarriers were loaded with tetracycline (TC) to develop a dual-action drug delivery system. Time-dependent drug release studies conducted at pH 7.4 and 37 °C over 48 h revealed controlled TC release. The long alkyl chain of the surface-bound ionic liquids (ILs) facilitated bacterial cell wall penetration, enhancing TC transport into both Gram-positive and Gram-negative bacteria. This dual-action mechanism was validated through antibacterial assays demonstrating that the surfactant-like IL disrupts bacterial cytoplasmic membranes, while the antibiotic induces cell death. Given the inherent antibacterial properties of ILs, we further investigated their ability to form stable, hydrophobic, and antimicrobial coatings on glass substrates under different environmental conditions. The results indicate that these IL-based coatings are uniform, durable, and hold significant potential for applications in healthcare and industry.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D4MA01267D</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D4MA01267D</style></url></related-urls><pdf-urls><url>internal-pdf://0675145322/S0010854525008148.ris</url></pdf-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D4MA01267D</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>765</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">765</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Singh, Bhupendra</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Field-enhanced chemical vapor deposition: new perspectives for thin film growth</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></full-title></periodical><pages><style face="normal" font="default" size="100%">20104-20142</style></pages><volume><style face="normal" font="default" size="100%">13</style></volume><number><style face="normal" font="default" size="100%">26</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><abstract><style face="normal" font="default" size="100%">Chemical vapor deposition (CVD) is a versatile technique for producing thin films and coatings of functional materials with diverse mechanical, electrochemical, electrical, tribological, and optical properties. The CVD process is governed by various experimental parameters including precursor chemistry, feed rate, growth temperature, pressure, and carrier or reactive gases. The growth kinetics depends on precursor decomposition that can be influenced by plasma-chemical or photo-dissociation processes to supplement thermal energy. More recently, the application of electric or magnetic fields during the CVD process has impacted the film growth beyond the conventional parametric space. This review highlights the influence of external field effects (plasma, photo-radiation, electric field, and magnetic field) on key steps of thin film processing, such as nucleation, grain growth, texture, density, phase formation, anisotropy, and kinetic stabilization. The emphasis is on recent technical, material, and phenomenological innovations in the CVD technique, with applied fields as extrinsic processing parameters offering new insights into future directions in the research and development of high-fidelity functional films and coatings.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D5TA01081K</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D5TA01081K</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D5TA01081K</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>772</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">772</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Silva, Cleiton P. M.</style></author><author><style face="normal" font="default" size="100%">Souza, Rafael A. C.</style></author><author><style face="normal" font="default" size="100%">Marrenjo, Gonçalves J.</style></author><author><style face="normal" font="default" size="100%">Patrun, David</style></author><author><style face="normal" font="default" size="100%">Poggere, Leticia</style></author><author><style face="normal" font="default" size="100%">Canobre, Sheila C.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Patrocinio, Antonio Otavio T.</style></author><author><style face="normal" font="default" size="100%">Lopes, Osmando F.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Boosting electrochemical CO2 to formate conversion via oxygen vacancy-rich 2D SnO2 gas diffusion electrodes</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Electroanalytical Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Journal of Electroanalytical Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">119239</style></pages><volume><style face="normal" font="default" size="100%">992</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Carbon dioxide</style></keyword><keyword><style face="normal" font="default" size="100%">Formate</style></keyword><keyword><style face="normal" font="default" size="100%">Tin oxide</style></keyword><keyword><style face="normal" font="default" size="100%">Two-dimensional materials</style></keyword><keyword><style face="normal" font="default" size="100%">Defect engineering</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/09/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1572-6657</style></isbn><abstract><style face="normal" font="default" size="100%">The development of efficient and earth-abundant catalysts for the electrochemical reduction of CO2 into value-added products is crucial for the circular economy and mitigation of the greenhouse effect. However, CO2 presents high stability and low solubility in aqueous electrolytes, and efficiency is often limited by CO2 diffusion through the liquid medium to the catalyst surface. This study investigates the combined influence of SnO2 morphology (nanospheres and nanosheets) and oxygen vacancies density in the synthesized oxides on the selective electrochemical reduction of CO2 to formate (HCOO−), employing a flow cell configuration and a gas diffusion electrode (GDE). Under optimized conditions, oxygen vacancy-rich SnO2 nanosheets exhibited the highest CO2-to-HCOO− efficiency, achieving selectivity above 90 %, a current density greater than −200 mA cm−2, and stable operation for 5 h. XPS analysis revealed the coexistence of Sn2+ and Sn4+ species on the surface directly related to the oxygen vacancies, suggesting a key role of the mixed oxidation states in decrease the charge transfer resistance and enhancing catalytic performance. The HCOO− selectivity of SnO2-based catalysts gradually decreased over time at high current densities due to salt deposition and flooding processes.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S1572665725003133</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.jelechem.2025.119239</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>790</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">790</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shlapakova, Lada E.</style></author><author><style face="normal" font="default" size="100%">Shvartsman, Vladimir V.</style></author><author><style face="normal" font="default" size="100%">Slautin, Boris N.</style></author><author><style face="normal" font="default" size="100%">Lupascu, Doru C.</style></author><author><style face="normal" font="default" size="100%">Grubova, Irina</style></author><author><style face="normal" font="default" size="100%">Sun, Yi-Yang</style></author><author><style face="normal" font="default" size="100%">Botvin, Vladimir V.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Surmeneva, Maria A.</style></author><author><style face="normal" font="default" size="100%">Surmenev, Roman A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Tailoring the topography, crystalline structure, and piezoelectric response of electrospun biodegradable poly(3-hydroxybutyrate) scaffolds by glycine loading</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Composites and Hybrid Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Composites and Hybrid Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">424</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">6</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/11/13</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2522-0136</style></isbn><abstract><style face="normal" font="default" size="100%">Tissue engineering (TE) represents an interdisciplinary field introduced for the recovery, preservation, and improvement of tissue function. Piezopolymers make it possible to generate exogenous potentials close to endogenous ones to promote tissue regeneration. Biodegradable poly(3-hydroxybutyrate) (PHB) has gained particular attention; however, the piezoelectric (PE) response of PHB is poor, and there is a need to improve it without compromising the biocompatibility of the scaffold. Herein, a drastic increase in the PE response of electrospun PHB scaffolds was achieved by incorporation of homogeneously distributed crystals of piezoactive β-glycine (Gly). We successfully optimized the electrospinning parameters to prepare composite PHB fibers with Gly content (5, 15, 20, and 30 wt%) and tailored topography, crystalline structure, and PE response. Gly incorporation creates a nanoporous textured surface of polymer fibers, which improves surface area, surface wettability, and the free surface energy of intrinsically hydrophobic scaffolds. In addition, Gly crystals act as nucleators for PHB crystallization, diminishing the polymer crystallite size and increasing its crystallinity degree from (39.9 ± 0.8) % for pure PHB to (45.8 ± 1.6) % for PHB-Gly-30. Using piezoelectric force microscopy, we obtained distributions of PE response along the fibers, uncovering a considerable increase in the lateral PE response for PHB scaffolds with 30 wt% Gly (from 0.28 ± 0.13 to 3.9 ± 1.0 pm/V) due to (i) the presence of PE β-Gly phase and (ii) higher PHB crystallinity. First-principles calculations revealed that the interaction of the Gly molecule with PHB surfaces occurred predominantly through hydrogen bonding and demonstrated a mechanism ranging from strong physisorption to weak chemisorption. This study opens new fundamental insights into straightforward one-stage engineering of biodegradable piezopolymer properties and offers a prospective scaffold for a wide range of TE applications.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1007/s42114-025-01487-8</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1007/s42114-025-01487-8</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>764</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">764</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Roy, Rajarshi</style></author><author><style face="normal" font="default" size="100%">Byranvand, Mahdi Malekshahi</style></author><author><style face="normal" font="default" size="100%">Zohdi, Mohamed Reza</style></author><author><style face="normal" font="default" size="100%">Magorian Friedlmeier, Theresa</style></author><author><style face="normal" font="default" size="100%">Das, Chittaranjan</style></author><author><style face="normal" font="default" size="100%">Hempel, Wolfram</style></author><author><style face="normal" font="default" size="100%">Zuo, Weiwei</style></author><author><style face="normal" font="default" size="100%">Kedia, Mayank</style></author><author><style face="normal" font="default" size="100%">Rendon, Jose Jeronimo</style></author><author><style face="normal" font="default" size="100%">Boehringer, Stephan</style></author><author><style face="normal" font="default" size="100%">Hailegnanw, Bekele</style></author><author><style face="normal" font="default" size="100%">Vorochta, Michael</style></author><author><style face="normal" font="default" size="100%">Mehl, Sascha</style></author><author><style face="normal" font="default" size="100%">Rai, Monika</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Ashish</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Saliba, Michael</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">All-inorganic CsPbI2Br perovskite solar cells with thermal stability at 250 °C and moisture-resilience via polymeric protection layers</style></title><secondary-title><style face="normal" font="default" size="100%">Energy &amp; Environmental Science</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Energy &amp; Environmental Science</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1920-1928</style></pages><volume><style face="normal" font="default" size="100%">18</style></volume><number><style face="normal" font="default" size="100%">4</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">1754-5692</style></isbn><abstract><style face="normal" font="default" size="100%">All-inorganic perovskites, such as CsPbI2Br, have emerged as promising compositions due to their enhanced thermal stability. However, they face significant challenges due to their susceptibility to humidity. In this work, CsPbI2Br perovskite is treated with poly(3-hexylthiophen-2,5-diyl) (P3HT) during the crystallization resulting in significant stability improvements against thermal, moisture and steady-state operation stressors. The perovskite solar cell retains ∼90% of the initial efficiency under relative humidity (RH) at ∼60% for 30 min, which is among the most stable all-inorganic perovskite devices to date under such harsh conditions. Furthermore, the P3HT treatment ensures high thermal stress tolerance at 250 °C for over 5 h. In addition to the stability enhancements, the champion P3HT-treated device shows a higher power conversion efficiency (PCE) of 13.5% compared to 12.7% (reference) with the stabilized power output (SPO) for 300 s. In addition, the P3HT-protected perovskite layer in ambient conditions shows ∼75% of the initial efficiency compared to the unprotected devices with ∼28% of their initial efficiency after 7 days of shelf life.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D4EE02385D</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D4EE02385D</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D4EE02385D</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>780</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">780</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pandian, Muthu Gomathy M.</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Ashish</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Subashchandran, Shanthi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Low-Temperature Solution-Processed SnO2 Electron Transport Layer for Stable, Lead-Free Cesium-Based Perovskite Solar Cells</style></title><secondary-title><style face="normal" font="default" size="100%">ECS Journal of Solid State Science and Technology</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ECS Journal of Solid State Science and Technology</style></full-title></periodical><pages><style face="normal" font="default" size="100%">095001</style></pages><volume><style face="normal" font="default" size="100%">14</style></volume><number><style face="normal" font="default" size="100%">9</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/09/05</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">IOP Publishing</style></publisher><isbn><style face="normal" font="default" size="100%">2162-8777&#xD;2162-8769</style></isbn><abstract><style face="normal" font="default" size="100%">The electron transport layer (ETL) plays a vital role in extracting and transporting photogenerated charge carriers in a halide-based perovskite solar cells (PSCs). Tin oxide (SnO2) is a promising alternative to titanium oxide (TiO2) as an ETL due to its better energy level alignment with the perovskite absorber layers, high mobility, stability, and ability to be deposited at lower temperature. However, despite these advantages and extensive research on lead-free perovskite thin film solar cells, the use of SnO2 as an ETL in all-inorganic lead-free PSCs has not been thoroughly investigated. This work presents the effect of SnO2 as an ETL interfaced with the Cs3Bi2I9 and CsBi3I10 lead-free perovskite thin films on their structural, morphological, and photoemission spectroscopic properties. Moreover, all inorganic perovskite solar cells have been fabricated for the first time to analyze the performance in the n-i-p planar architecture with device stacks comprising ITO/SnO2/(Cs3Bi2I9 or CsBi3I10)/Spiro-OMeTAD/Au. The CsBi3I10 device exhibited a photo conversion efficiency (PCE) of ∼1% with a fill factor of 59% while the Cs3Bi2I9 device showed a PCE of 0.15%. These findings mark significant progress in the eco-friendly development of lead-free Cs3Bi2I9 and CsBi3I10 perovskite-based solar cells. Low temperature SnO2 in lead-free perovskite solar cells, with device area 0.25 cm2. Photoemission properties of Cs3Bi2I9 and CsBi3I10 comparison is discussed. CsBi3I10 achieves ∼1% PCE, advancing eco-friendly lead-free solar cells.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1149/2162-8777/adfee7</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1149/2162-8777/adfee7</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>784</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">784</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Maschwitz, Timo</style></author><author><style face="normal" font="default" size="100%">Merten, Lena</style></author><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Majewski, Martin</style></author><author><style face="normal" font="default" size="100%">Haddadi Barzoki, Fatemeh</style></author><author><style face="normal" font="default" size="100%">Wu, Zijin</style></author><author><style face="normal" font="default" size="100%">Öz, Seren Dilara</style></author><author><style face="normal" font="default" size="100%">Kreusel, Cedric</style></author><author><style face="normal" font="default" size="100%">Theisen, Manuel</style></author><author><style face="normal" font="default" size="100%">Wang, Pang</style></author><author><style face="normal" font="default" size="100%">Schiffer, Maximilian</style></author><author><style face="normal" font="default" size="100%">Boccarella, Gianluca</style></author><author><style face="normal" font="default" size="100%">Marioth, Gregor</style></author><author><style face="normal" font="default" size="100%">Weidner, Henrik</style></author><author><style face="normal" font="default" size="100%">Schultheis, Sarah</style></author><author><style face="normal" font="default" size="100%">Schieferstein, Tim</style></author><author><style face="normal" font="default" size="100%">Gidaszewski, Dawid</style></author><author><style face="normal" font="default" size="100%">Julliev, Zavkiddin</style></author><author><style face="normal" font="default" size="100%">Kneschaurek, Ekaterina</style></author><author><style face="normal" font="default" size="100%">Munteanu, Valentin</style></author><author><style face="normal" font="default" size="100%">Zaluzhnyy, Ivan</style></author><author><style face="normal" font="default" size="100%">Bertram, Florian</style></author><author><style face="normal" font="default" size="100%">Jaffrès, Anaël</style></author><author><style face="normal" font="default" size="100%">He, Junjie</style></author><author><style face="normal" font="default" size="100%">Ashurov, Nigmat</style></author><author><style face="normal" font="default" size="100%">Stolterfoht, Martin</style></author><author><style face="normal" font="default" size="100%">Wolff, Christian M.</style></author><author><style face="normal" font="default" size="100%">Unger, Eva</style></author><author><style face="normal" font="default" size="100%">Olthof, Selina</style></author><author><style face="normal" font="default" size="100%">Brocks, Geert</style></author><author><style face="normal" font="default" size="100%">Tao, Shuxia</style></author><author><style face="normal" font="default" size="100%">Grüninger, Helen</style></author><author><style face="normal" font="default" size="100%">Ronsin, Olivier J. J.</style></author><author><style face="normal" font="default" size="100%">Harting, Jens</style></author><author><style face="normal" font="default" size="100%">Kotthaus, Andreas F.</style></author><author><style face="normal" font="default" size="100%">Kirsch, Stefan F.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hinderhofer, Alexander</style></author><author><style face="normal" font="default" size="100%">Schreiber, Frank</style></author><author><style face="normal" font="default" size="100%">Riedl, Thomas</style></author><author><style face="normal" font="default" size="100%">Brinkmann, Kai Oliver</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">How crystallization additives govern halide perovskite grain growth</style></title><secondary-title><style face="normal" font="default" size="100%">Nature Communications</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nature Communications</style></full-title></periodical><pages><style face="normal" font="default" size="100%">9894</style></pages><volume><style face="normal" font="default" size="100%">16</style></volume><number><style face="normal" font="default" size="100%">1</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/11/10</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2041-1723</style></isbn><abstract><style face="normal" font="default" size="100%">The preparation of perovskite solar cells from the liquid phase is a cornerstone of their immense potential. However, a clear relationship between the precursor ink and the formation of the resulting perovskite is missing. Established theories, such as heterogeneous nucleation and lead complex colloid formation, often prove unreliable, which has led to an overreliance on heuristics. Most high-performing perovskites use additives to control crystallization. Their role during crystallization is, however, elusive. Here, we provide evidence that typical crystallization additives do not predominantly impact the nucleation phase but rather facilitate coarsening grain growth by increasing ion mobility across grain boundaries. Drawing from the insights of our broad, interdisciplinary study that combines ex and in situ characterization methods, devices, simulations, and density function theory calculation, we propose a concept that proves valid for various additives and perovskite formulations. Moreover, we establish a direct link between additive engineering and perovskite post-processing, offering a unified framework for advancing material design and process engineering.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1038/s41467-025-65484-7</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1038/s41467-025-65484-7</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>755</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">755</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lichtenberg, Andreas</style></author><author><style face="normal" font="default" size="100%">Inderdühnen, Lidia</style></author><author><style face="normal" font="default" size="100%">Lichtenberg, Aida</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Heterobimetallic Uranium(V)-Alkali Metal Alkoxides: Expanding the Chemistry of f-Block Elements</style></title><secondary-title><style face="normal" font="default" size="100%">Molecules</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Molecules</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2361</style></pages><volume><style face="normal" font="default" size="100%">30</style></volume><number><style face="normal" font="default" size="100%">11</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year></dates><isbn><style face="normal" font="default" size="100%">1420-3049</style></isbn><accession-num><style face="normal" font="default" size="100%">doi:10.3390/molecules30112361</style></accession-num><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.mdpi.com/1420-3049/30/11/2361</style></url></related-urls><pdf-urls><url>internal-pdf://3083682174/S0939641125001559.ris</url><url>internal-pdf://3278097996/pericles_1613682921.ris</url></pdf-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>789</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">789</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kim, Miri</style></author><author><style face="normal" font="default" size="100%">Kim, Min-Ji</style></author><author><style face="normal" font="default" size="100%">Zhang, Yizhi</style></author><author><style face="normal" font="default" size="100%">Jang, Wonsik</style></author><author><style face="normal" font="default" size="100%">Yeom, Jiho</style></author><author><style face="normal" font="default" size="100%">Kim, Jongkyoung</style></author><author><style face="normal" font="default" size="100%">Kim, Hyoseok</style></author><author><style face="normal" font="default" size="100%">Lee, Seunghyun</style></author><author><style face="normal" font="default" size="100%">Lee, Jin Ho</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Wang, Haiyan</style></author><author><style face="normal" font="default" size="100%">Kim, Junghwan</style></author><author><style face="normal" font="default" size="100%">Lee, Sukbin</style></author><author><style face="normal" font="default" size="100%">Cho, Seungho</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Greenhouse-Gas-Driven Room-Temperature Synthesis of Compositionally Complex Nanomaterials via Anion–Cation Arrangement Control</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Letters</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Letters</style></full-title></periodical><pages><style face="normal" font="default" size="100%">17494-17502</style></pages><volume><style face="normal" font="default" size="100%">25</style></volume><number><style face="normal" font="default" size="100%">50</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/12/17</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">1530-6984</style></isbn><notes><style face="normal" font="default" size="100%">doi: 10.1021/acs.nanolett.5c05165</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.nanolett.5c05165</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.nanolett.5c05165</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>769</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">769</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Heshmati, Niusha</style></author><author><style face="normal" font="default" size="100%">Almandinger, Niklas</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Improving the ecological index in the solution processing of hybrid perovskites</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></full-title></periodical><dates><year><style face="normal" font="default" size="100%">2025</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><abstract><style face="normal" font="default" size="100%">Lead halide perovskites are taking center stage among photoactive materials due to their highly tunable properties and potential applications in photovoltaics and light-emitting devices. Hybrid perovskites have demonstrated exceptionally high solar cell efficiencies, which have quickly approached those of silicon photovoltaics. However, their technological readiness is hindered by limited environmental stability, the use of toxic solvents such as N,N-dimethylformamide (DMF), and concerns over lead (Pb) toxicity. This research presents a new green solvent system that combines biodegradable dihydrolevoglucosenone (Cyrene™) and 2-methyltetrahydrofuran (2-MeTHF) as a sustainable alternative to the hazardous DMF. This eco-friendly solvent system reduces reliance on conventional aprotic solvents in perovskite solar cell processing. Additionally, ethyl acetate was employed as a green antisolvent in the one-step spin coating process to enhance crystallization, selected for its lower toxicity compared to other common solvents. Investigation of solvent–solute interactions by various characterization techniques led to an optimized solvent blend of Cy-THF : DMSO (70 : 30 vol%) with an added 7.5 vol% acetonitrile that resulted in a desirable viscosity and a stable perovskite precursor solution. Additives, including methylammonium chloride (MACl, CH3NH3Cl) and thiourea (SC(NH2)2), were incorporated to improve the crystallinity and surface coverage of the perovskite films. The resulting thin films of cubic perovskite exhibited enhanced film quality and superior stability under ambient conditions, with optoelectronic properties comparable to those of DMF-based perovskites, achieving 95% of the DMF-reference device&apos;s efficiency. These results demonstrate the promise of green solvent systems, derived from recyclable carbon, for sustainable perovskite processing.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D5TA01277E</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D5TA01277E</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D5TA01277E</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>748</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">748</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Grödler, Dennis</style></author><author><style face="normal" font="default" size="100%">Kaden, Peter</style></author><author><style face="normal" font="default" size="100%">Sperling, Joseph M.</style></author><author><style face="normal" font="default" size="100%">Rotermund, Brian M.</style></author><author><style face="normal" font="default" size="100%">Scheibe, Benjamin</style></author><author><style face="normal" font="default" size="100%">Beck, Nicholas B.</style></author><author><style face="normal" font="default" size="100%">Lichtenberg, Andreas</style></author><author><style face="normal" font="default" size="100%">Albrecht, Thomas E.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Gericke, Robert</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and Characterization of Homo- and Heteroleptic Neptunium(IV) Heteroarylalkenolate Complexes</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2321-2328</style></pages><volume><style face="normal" font="default" size="100%">64</style></volume><number><style face="normal" font="default" size="100%">5</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/02/10</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><notes><style face="normal" font="default" size="100%">doi: 10.1021/acs.inorgchem.4c04521</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.inorgchem.4c04521</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.inorgchem.4c04521</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>782</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">782</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Goyal, Naina</style></author><author><style face="normal" font="default" size="100%">Dharmasigamani, Dhamotharan</style></author><author><style face="normal" font="default" size="100%">Pires, Fabio</style></author><author><style face="normal" font="default" size="100%">Kumar, Ravi</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">LiVO3/LiZnVO4 Nanocomposite: High Performance Electrocatalyst for Ambient Nitrogen Reduction to Ammonia</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">e202501627</style></pages><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">acid electrolyte</style></keyword><keyword><style face="normal" font="default" size="100%">electrochemical nitrogen reduction</style></keyword><keyword><style face="normal" font="default" size="100%">Li-based catalyst</style></keyword><keyword><style face="normal" font="default" size="100%">LiVO3</style></keyword><keyword><style face="normal" font="default" size="100%">LiZnVO4</style></keyword><keyword><style face="normal" font="default" size="100%">sol–gel reaction</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/10/10</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1438-1656</style></isbn><abstract><style face="normal" font="default" size="100%">The electrocatalytic nitrogen reduction reaction (e-NRR) has emerged as a sustainable alternative to the energy-intensive Haber?Bosch process for ammonia (NH3) synthesis. Lithium-based electrocatalysts are particularly promising due to the high thermodynamic affinity of lithium toward nitrogen, which facilitates spontaneous N2 adsorption to lower the activation energy required for dinitrogen dissociation. By promoting proton-coupled electron transfer and stabilizing NRR intermediates, the composite catalyst enhances reaction kinetics, enabling efficient NH3 production. While nonaqueous lithium-containing electrolytes suppress the hydrogen evolution reaction, lithium deposition from electrolyte decomposition inhibits e-NRR. This study addresses the challenge by structurally integrating lithium into a LiVO3/LiZnVO4 nanocomposite, which channels lithium into active catalytic sites rather than parasitic plating. The oxide-oxide nanocomposite electrocatalyst delivers an ammonia yield of 53.7??g?h?1?mgcat?1 and a Faradaic efficiency (FE) of 44.8% at ?0.5?V versus reversible hydrogen electrode in 0.1?M HCl electrolyte. To the best of the knowledge, this report presents a significant improvement in FE against other reported Li-mediated systems and rivalling transition metal-based catalysts.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202501627</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202501627</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2025/11/11</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>774</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">774</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Daniel, Miriam</style></author><author><style face="normal" font="default" size="100%">Rafi, Jithin</style></author><author><style face="normal" font="default" size="100%">Reza, Samim</style></author><author><style face="normal" font="default" size="100%">Thapa, Ranjit</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Neppolian, Bernaurdshaw</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhancing host-guest interactions through interfacial modulation of IRMOF-MXene hybrids: A detailed study on the significance of accessible functional groups in electrochemical detection</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Research Bulletin</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Materials Research Bulletin</style></full-title></periodical><pages><style face="normal" font="default" size="100%">113611</style></pages><volume><style face="normal" font="default" size="100%">192</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Electrochemical sensor</style></keyword><keyword><style face="normal" font="default" size="100%">Dopamine</style></keyword><keyword><style face="normal" font="default" size="100%">MXene</style></keyword><keyword><style face="normal" font="default" size="100%">IRMOF 3</style></keyword><keyword><style face="normal" font="default" size="100%">Amino functionalization</style></keyword><keyword><style face="normal" font="default" size="100%">Integration methods</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/12/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0025-5408</style></isbn><abstract><style face="normal" font="default" size="100%">Metal-organic frameworks (MOFs) offer excellent structural tuneability that enables selective host-guest interactions, but integrating them with conductive substrates like Ti3C2Tx MXene can reduce accessibility to functional groups. This work empirically analyzes the influence of synthesis strategy on the electrochemical performance of amino-functionalized IRMOF 3-MXene hybrids for dopamine (DA) sensing, restricting their availability for DA interaction and reducing sensing efficiency. In contrast, the post-synthetic hybrid retains free –NH₂ groups, enabling effective DA preconcentration, which allows subsequent electron transfer to the conductive Ti3C2Tx. This results in enhanced electrocatalytic response, with a synergistic index of 1.12, high sensitivity (263.8 µA mM−1 cm−2), and a low detection limit (56.4 nM) towards DA detection. The Schottky barrier formed at the MXene/IRMOF 3 interface modulates the charge transfer dynamics. Theoretical adsorption energy calculations further validate the experimental observations, highlighting the critical role of free and accessible functional groups in optimizing host-guest interactions for enhanced electrochemical performance.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0025540825003198</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.materresbull.2025.113611</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>757</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">757</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Cherasse, Marie</style></author><author><style face="normal" font="default" size="100%">Heshmati, Niusha</style></author><author><style face="normal" font="default" size="100%">Urban, Joanna M.</style></author><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Spencer, Michael S.</style></author><author><style face="normal" font="default" size="100%">Frenzel, Maximilian</style></author><author><style face="normal" font="default" size="100%">Perfetti, Luca</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Maehrlein, Sebastian F.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced Lattice Coherences and Improved Structural Stability in Quadruple A-Site Substituted Lead Bromide Perovskites</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Small</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2500977</style></pages><volume><style face="normal" font="default" size="100%">21</style></volume><number><style face="normal" font="default" size="100%">21</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year></dates><isbn><style face="normal" font="default" size="100%">1613-6810</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract Lead halide perovskites (LHPs) are promising materials for efficient photovoltaic devices; however, they often encounter limited structural stability and degradation problems that limit their technological potential. This study investigates a novel perovskite composition consisting of (Cs, MA, FA, GA)PbBr3, abbreviated as (4cat)PbBr3, to effectively enhance phase stability and optoelectronic characteristics. The spectroscopic data reveal improved structural order, electronic properties, and dynamic lattice response in a cubic phase, which is uniquely stabilized by the specific cation composition down to 80 K. Superior optoelectronic properties are verified by increased photoluminescence (PL) and 20-fold higher electron mobility, when compared to the single-cation composition, MAPbBr3. Notably, the ultrafast Terahertz-induced Kerr effect (TKE) reveals a dominating 1.1 THz octahedral twist mode, also observed in MAPbBr3, however with a doubled phonon coherence time in (4cat)PbBr3 at 80 K. The observation of higher structural order in the 4-cation composition is thus reflected by the prolonged lattice coherences, indicating enhanced dynamic screening effects that can explain the improved optoelectronic properties of (4cat)PbBr3. This study therefore sheds light on the influence of the A-site cation composition on the inorganic sublattice and its coherent dynamics, highly relevant to perovskite-based photovoltaic and optoelectronic technologies.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/abs/10.1002/smll.202500977</style></url></related-urls><pdf-urls><url>internal-pdf://3700669167/RSC_ (3).ris</url><url>internal-pdf://0548593685/RSC_ (1).bib</url></pdf-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/smll.202500977</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>771</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">771</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chen, Chenglong</style></author><author><style face="normal" font="default" size="100%">Lu, Keren</style></author><author><style face="normal" font="default" size="100%">Wang, Yicheng</style></author><author><style face="normal" font="default" size="100%">Cheng, Ru</style></author><author><style face="normal" font="default" size="100%">Xiang, Tingting</style></author><author><style face="normal" font="default" size="100%">Xia, Mingzhu</style></author><author><style face="normal" font="default" size="100%">Wang, Fengyun</style></author><author><style face="normal" font="default" size="100%">Lei, Wu</style></author><author><style face="normal" font="default" size="100%">Yang, Juan</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hao, Qingli</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">3D Printed Flexible Zinc-Ion Battery for Real-Time Health Monitoring Devices</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></full-title></periodical><pages><style face="normal" font="default" size="100%">23860-23871</style></pages><volume><style face="normal" font="default" size="100%">17</style></volume><number><style face="normal" font="default" size="100%">16</style></number><dates><year><style face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style face="normal" font="default" size="100%">2025/04/23</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><notes><style face="normal" font="default" size="100%">doi: 10.1021/acsami.4c22425</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsami.4c22425</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsami.4c22425</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>734</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">734</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ziegler, Richard</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Goya, Gerardo F</style></author><author><style face="normal" font="default" size="100%">Fuentes-García, Jesús Antonio</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Remote-Controlled Activation of the Release through Drug-Loaded Magnetic Electrospun Fibers</style></title><secondary-title><style face="normal" font="default" size="100%">Fibers</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Fibers</style></full-title></periodical><pages><style face="normal" font="default" size="100%">48</style></pages><volume><style face="normal" font="default" size="100%">12</style></volume><number><style face="normal" font="default" size="100%">6</style></number><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><isbn><style face="normal" font="default" size="100%">2079-6439</style></isbn><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>747</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">747</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Teppala, Dharma Teja</style></author><author><style face="normal" font="default" size="100%">Bernauer, Jan</style></author><author><style face="normal" font="default" size="100%">Drouillard, Esteve</style></author><author><style face="normal" font="default" size="100%">Kumar Geddam, Yaswanth</style></author><author><style face="normal" font="default" size="100%">Chen, Guoxing</style></author><author><style face="normal" font="default" size="100%">Widenmeyer, Marc</style></author><author><style face="normal" font="default" size="100%">Trapp, Maximilian</style></author><author><style face="normal" font="default" size="100%">Kleebe, Hans-Joachim</style></author><author><style face="normal" font="default" size="100%">Kumar, Ravi</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ionescu, Emanuel</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Facile Mechanochemical Synthesis of Compositionally Complex Spinel-type Oxides, (Co, Fe, Mn)3O4, (Co, Fe, Mn, Ni)3O4, and (Co, Cr, Fe, Mn, Ni)3O4</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></full-title></periodical><pages><style face="normal" font="default" size="100%">e202400134</style></pages><volume><style face="normal" font="default" size="100%">650</style></volume><number><style face="normal" font="default" size="100%">23</style></number><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><isbn><style face="normal" font="default" size="100%">0044-2313</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract In the current work, a simple mechanochemical route has been employed to preparatively access three spinel-type compositionally complex ceramics, i. e., (Co, Fe, Mn)3O4, (Co, Fe, Mn, Ni)3O4, and (Co, Cr, Fe, Mn, Ni)3O4. Hydrated nitrate salts of the respective transition metal elements were mechanically ground with ammonium hydrogen carbonate. The resulting paste-like mixture of metal hydroxides, oxyhydroxides, and carbonates was rinsed with water to remove the byproduct (NH4NO3) and converted into the respective single-phase spinel-type oxides via calcination. In situ X-ray diffraction (XRD) revealed the formation of the spinel-type structure (Fd 3‾ ${\bar{3}}$ m) already at temperatures as low as 150 °C. Typically, the calcination of the precursors at temperatures beyond 500 °C led to the formation of well-crystallized, single-phase spinel-type oxides with nearly equimolar composition and highly homogeneous distribution of the transition metals within the structure. The mechanochemical synthesis route in the present study is considered to be an easy, straightforward, and scalable access to compositionally complex oxides.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/abs/10.1002/zaac.202400134</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/zaac.202400134</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>754</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">754</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tabari, Taymaz</style></author><author><style face="normal" font="default" size="100%">Łabuz, Przemysław</style></author><author><style face="normal" font="default" size="100%">Singh, Dheerendra</style></author><author><style face="normal" font="default" size="100%">Maximenko, Alexey</style></author><author><style face="normal" font="default" size="100%">Gryboś, Joanna</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Sojka, Zbigniew</style></author><author><style face="normal" font="default" size="100%">Macyk, Wojciech</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">3DOM Fe/Co-containing perovskites as bifunctional ORR/OER electrocatalysts for a photo-rechargeable zinc battery</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Catalysis B: Environment and Energy</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Applied Catalysis B: Environment and Energy</style></full-title></periodical><pages><style face="normal" font="default" size="100%">124425</style></pages><volume><style face="normal" font="default" size="100%">358</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Zinc batteries</style></keyword><keyword><style face="normal" font="default" size="100%">Photo-battery</style></keyword><keyword><style face="normal" font="default" size="100%">Photo(electro)catalysis</style></keyword><keyword><style face="normal" font="default" size="100%">Materials design</style></keyword><keyword><style face="normal" font="default" size="100%">Electronic properties</style></keyword><keyword><style face="normal" font="default" size="100%">Overall efficiencies</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style face="normal" font="default" size="100%">2024/12/05/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0926-3373</style></isbn><abstract><style face="normal" font="default" size="100%">Three-dimensionally ordered mesoporous perovskites (La0.8Ba0.2Fe1–xCoxO3–δ (x = 0, 0.2, 0.4)), which are integrated with a silicon photovoltaic cell are prepared. Their overall solar energy conversion and storage efficiency in zinc-ion-based batteries was assessed. The electrocatalytic activities were measured in OER/ORR, while the galvanostatic charge/discharge processes were applied to study battery performance under 1 sun irradiation. The electronic properties of the electrocatalysts were determined by X-ray absorption and UV photoelectron spectroscopies. The importance of controlling the oxidation state of cobalt ions to increase the specific capacity and energy density of the batteries was shown. The ORR activity depends on oxygen vacancies, inferred from the XANES and EXAFS spectra analysis. Their presence is associated with the Co2+/Co3+ ratio which controls the beneficial eg orbitals occupancy via the high spin d7 electron configuration. Herein, we report an overall energy conversion efficiency of 12.6 % for the PV-integrated La0.8Ba0.2Fe0.8Co0.2O3–δ photo-rechargeable battery cell.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0926337324007392</style></url></related-urls><pdf-urls><url>internal-pdf://0413340349/S0025540825003198.ris</url><url>internal-pdf://2927267773/S1572665725003133 (2).ris</url><url>internal-pdf://4026266535/RSC_ (1).ris</url><url>internal-pdf://2302091380/pericles_10990682cAxA.enw</url><url>internal-pdf://0450507865/RSC_ (2).ris</url></pdf-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.apcatb.2024.124425</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>740</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">740</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sutorius, Anja</style></author><author><style face="normal" font="default" size="100%">Weißing, René</style></author><author><style face="normal" font="default" size="100%">Pèrez, Carina Rindtorff</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Hartl, Fabian</style></author><author><style face="normal" font="default" size="100%">Basu, Nilanjan</style></author><author><style face="normal" font="default" size="100%">Shin, Hyeon Suk</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Understanding vapor phase growth of hexagonal boron nitride</style></title><secondary-title><style face="normal" font="default" size="100%">Nanoscale</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nanoscale</style></full-title></periodical><pages><style face="normal" font="default" size="100%">15782-15792</style></pages><volume><style face="normal" font="default" size="100%">16</style></volume><number><style face="normal" font="default" size="100%">33</style></number><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>736</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">736</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Patrun, David</style></author><author><style face="normal" font="default" size="100%">Zhao, Si</style></author><author><style face="normal" font="default" size="100%">Aytuna, Ziyaad</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Miess, Michael</style></author><author><style face="normal" font="default" size="100%">Hong, Zhensheng</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Plasma-Enhanced SnOx Thin Films on Copper Current Collector for Safer Lithium Metal Batteries</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><pages><style face="normal" font="default" size="100%">109836</style></pages><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>744</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">744</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mukkavilli, Raghunath Sharma</style></author><author><style face="normal" font="default" size="100%">Moharana, Niraja</style></author><author><style face="normal" font="default" size="100%">Singh, Bhupendra</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Vollnhals, Florian</style></author><author><style face="normal" font="default" size="100%">Ichangi, Arun</style></author><author><style face="normal" font="default" size="100%">Kumar, KC Hari</style></author><author><style face="normal" font="default" size="100%">Christiansen, Silke</style></author><author><style face="normal" font="default" size="100%">Kim, Kwang-Ho</style></author><author><style face="normal" font="default" size="100%">Kwon, Sehun</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A review on electrocatalytic activities, phase stabilities, spectroscopic advancements, and photocorrosion in Ta-N phases</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><pages><style face="normal" font="default" size="100%">110046</style></pages><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><urls><pdf-urls><url>internal-pdf://1244844578/pericles_15213749650.enw</url></pdf-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>753</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">753</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Scheschkewitz, David</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Laudatio Prof. Dr. Dr. h.c. Michael Veith</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></full-title></periodical><pages><style face="normal" font="default" size="100%">e202400206</style></pages><volume><style face="normal" font="default" size="100%">650</style></volume><number><style face="normal" font="default" size="100%">24</style></number><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><isbn><style face="normal" font="default" size="100%">0044-2313</style></isbn><urls><related-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/abs/10.1002/zaac.202400206</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/zaac.202400206</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>731</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">731</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">M. Siribbal, Shifaa</style></author><author><style face="normal" font="default" size="100%">Jurewicz, Anna</style></author><author><style face="normal" font="default" size="100%">Hassan, Menna</style></author><author><style face="normal" font="default" size="100%">Iqbal, Sumiya</style></author><author><style face="normal" font="default" size="100%">Hu, Zhangjun</style></author><author><style face="normal" font="default" size="100%">Uvdal, Kajsa</style></author><author><style face="normal" font="default" size="100%">Hussain, Muhammad S</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Biocompatible Hollow Gadolinium Oxide Nanocarriers for the Transport of Bioactive Molecules to Cells</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Nano Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Nano Materials</style></full-title></periodical><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><isbn><style face="normal" font="default" size="100%">2574-0970</style></isbn><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>724</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">724</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lichtenberg, Andreas</style></author><author><style face="normal" font="default" size="100%">Lichtenberg, Aida</style></author><author><style face="normal" font="default" size="100%">Pieper, Melissa</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Mononuclear Uranium and Heterobimetallic Actinide (An=Th, U) Alkoxides with Divalent Group 14 Elements (MII=Ge, Sn, Pb)</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">e202300474</style></pages><volume><style face="normal" font="default" size="100%">27</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">Actinides</style></keyword><keyword><style face="normal" font="default" size="100%">Uranium</style></keyword><keyword><style face="normal" font="default" size="100%">Thorium</style></keyword><keyword><style face="normal" font="default" size="100%">Group 14 Elements</style></keyword><keyword><style face="normal" font="default" size="100%">Alkoxides</style></keyword><keyword><style face="normal" font="default" size="100%">tert-Butoxides</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style face="normal" font="default" size="100%">2024/01/12</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1434-1948</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract When compared to main group and lanthanide elements, the heterobimetallic alkoxides of actinide elements with metals other than alkali metals are elusive. We report here for the first time alkoxide derivatives containing early actinides and the divalent group 14 elements. For this purpose in this work, co-alcoholysis reactions of silyl amides of divalent group 14 elements (MII=Ge, Sn, Pb) and actinides (AnIV=Th, U) were studied that resulted in the formation of [AnM(OtBu)6] (1-AnM) (AnIV=Th, MII=Ge, Sn, Pb; AnIV=U, MII=Ge, Sn). A 2-electron redox reaction occurred in the UIV-PbII couple, which generated nearly quantitatively a UV alkoxide species and elemental lead. Precise adjustments of the stoichiometry in this reaction allowed to synthesize [U(OtBu)5Py] (3), amongst others in high yield. 3 and the UIV alkoxide [U(OtBu)4(Py)2] (4) described in this work represent first mononuclear UIV or UV containing alkoxides. First promising attempts to use [U(OtBu)5Py] (3) as a starting material in co-alcoholysis reactions with divalent group 14 silylamides resulted in the formation of heterobimetallic UV-MII alkoxides [UM(OtBu)7] (MII=Ge, Sn, Pb) amongst others. All compounds described in this study were thoroughly characterized by multi-nuclear NMR and IR spectroscopic investigations, single crystal X-ray diffraction data, and CHN- analysis.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/ejic.202300474</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/ejic.202300474</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2024/03/20</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>746</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">746</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lichtenberg, Andreas</style></author><author><style face="normal" font="default" size="100%">Altuntas, Kemal</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Karimpour, Touraj</style></author><author><style face="normal" font="default" size="100%">Diel, Simon</style></author><author><style face="normal" font="default" size="100%">Aytuna, Ziyaad</style></author><author><style face="normal" font="default" size="100%">Amadi, Chijioke Kingsley</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular Transformations for Direct Synthesis of Thorium Dioxide Films</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></full-title></periodical><pages><style face="normal" font="default" size="100%">e202400126</style></pages><volume><style face="normal" font="default" size="100%">650</style></volume><number><style face="normal" font="default" size="100%">23</style></number><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><isbn><style face="normal" font="default" size="100%">0044-2313</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract New Th(IV) complexes with high volatility were synthesized and applied as molecular single-source precursors for chemical vapor deposition (CVD) of ThO2 thin films. The change in the steric profile of alkoxide ligands and concomitant reduction in the molecular weight of [Th(L)2(OR)2] (1-OR, R=iso-propyl (1-OiPr) or tert-butyl (1-OtBu), L=N-(4,4,4-trifluorobut-1-ene-3-one)-methoxyethylamide)) had a profound effect on the vapor pressure (at 10−5 mbar) evident in the drop in sublimation temperature to 100 °C for the iso-propoxide derivative against 130 °C observed for the tert-(1-OtBu). Hirshfeld surface analysis of both complexes showed different degrees of intermolecular H⋅⋅⋅F interactions responsible for the observed differences in the volatilities of the two complexes. Both mixed-ligand compounds (1-OiPr, 1-OtBu) were applied in the CVD process to deposit thorium oxide thin films without any carrier or reactive gas that verified their suitability as single-source precursors to ThO2 coatings. Thin films of ThO2 were grown at 500 °C and 600 °C on Si/SiO2 substrates, which showed presence of C, N, and F presumably originating from the incorporation of ligand fragments in the growing CVD deposits. Subsequent calcination of CVD-grown ThO2 films at 800 °C in air led to phase pure ThO2 coatings with uniform morphology.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/abs/10.1002/zaac.202400126</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/zaac.202400126</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>745</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">745</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kazim, Samrana</style></author><author><style face="normal" font="default" size="100%">Huang, Chun</style></author><author><style face="normal" font="default" size="100%">Hemasiri, Naveen Harindu</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Ashish</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ahmad, Shahzada</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">MXene‐Based Energy Devices: From Progressive to Prospective</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Functional Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Functional Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2315694</style></pages><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><isbn><style face="normal" font="default" size="100%">1616-301X</style></isbn><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>726</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">726</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kazim, Samrana</style></author><author><style face="normal" font="default" size="100%">Huang, Chun</style></author><author><style face="normal" font="default" size="100%">Hemasiri, Naveen Harindu</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Ashish</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ahmad, Shahzada</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">MXene-Based Energy Devices: From Progressive to Prospective</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Functional Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Functional Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2315694</style></pages><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">additives</style></keyword><keyword><style face="normal" font="default" size="100%">energy storage</style></keyword><keyword><style face="normal" font="default" size="100%">interface engineering</style></keyword><keyword><style face="normal" font="default" size="100%">MXene</style></keyword><keyword><style face="normal" font="default" size="100%">perovskite solar cells</style></keyword><keyword><style face="normal" font="default" size="100%">secondary batteries</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style face="normal" font="default" size="100%">2024/02/26</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1616-301X</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract Every once in a while, a revolutionary technological development arises, which leads to a significant change in the way to approach research and push development efforts. The appetite for new technology compels society to look for game-changing materials, that can transform the industry and make advances. Sustainable energy production is paramount to addressing the climate crisis, and energy generation and storage play an important role in the development of self-powered microelectronic devices. The 2D materials, MXenes have emerged as promising candidates for energy and other applications owing to their inherent electrical merits, high specific surface area, and tunable properties. Particularly, in the context of additive and interfacial materials for perovskite solar cell fabrication and utilization as additives in secondary batteries, this review delves into the application of MXenes in such devices. The protocols of MXenes and their nanostructures tailoring toward such applications and, the underlying mechanism is uncovered. Further, the existing challenges and direction for future in MXene-based energy harvesters are discussed.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/adfm.202315694</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/adfm.202315694</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2024/03/20</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>729</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">729</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Iqbal, Sumiya</style></author><author><style face="normal" font="default" size="100%">Schneider, Tom-Jonas Klaus</style></author><author><style face="normal" font="default" size="100%">Truong, Thanh Tung</style></author><author><style face="normal" font="default" size="100%">Ulrich-Müller, Roman</style></author><author><style face="normal" font="default" size="100%">Nguyen, Phuong-Hien</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Carriers for hydrophobic drug molecules: lipid-coated hollow mesoporous silica particles, and the influence of shape and size on encapsulation efficiency</style></title><secondary-title><style face="normal" font="default" size="100%">Nanoscale</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nanoscale</style></full-title></periodical><pages><style face="normal" font="default" size="100%">11274-11289</style></pages><volume><style face="normal" font="default" size="100%">16</style></volume><number><style face="normal" font="default" size="100%">23</style></number><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>752</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">752</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Iqbal, S.</style></author><author><style face="normal" font="default" size="100%">Ilyas, S.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Vinković Vrček, Ivana</style></author><author><style face="normal" font="default" size="100%">de la Fuente, Jesus M.</style></author><author><style face="normal" font="default" size="100%">Apartsin, Evgeny K.</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Solid Nanocarriers and Bioconjugation Strategies for Efficient In Vivo Drug Transport</style></title><secondary-title><style face="normal" font="default" size="100%">Characterisation of Drug Nanocarriers</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">0</style></pages><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><publisher><style face="normal" font="default" size="100%">Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">978-1-83767-099-4</style></isbn><abstract><style face="normal" font="default" size="100%">This chapter provides the current state of research in the development of solid nanocarriers and discusses their physiochemical properties in relation to their interaction with the biological environment. Many material parameters such as morphology, surface charge, and hydrophobicity/hydrophilicity of nanomaterials are crucial factors in having a deterministic influence on their affinity towards specific cellular or molecular markers. By engineering these characteristics, nanomaterials can be customized for precision drug delivery to diseased cells, increasing therapeutic efficacy while minimizing off-target effects and more importantly reducing the systemic load. Moreover, the surface conjugation strategies, enabling the covalent attachment of various biomolecules (peptides, enzymes, proteins, small molecules, etc.), represent advancement against the conventional drug delivery and uptake models. Besides presenting an account of common bioconjugation strategies optimized for in vivo applications, the chapter also discusses stimuli-responsive nanocarriers, which are designed to respond to extrinsic triggers (pH fluctuations, temperature changes, etc.) in order to sense and respond to their target environment, enabling controlled and site-specific drug release crossing biological barriers and paving the way for precision in therapeutics.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1039/9781837672981-00034</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/9781837672981-00034</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2/20/2025</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>728</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">728</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ichangi, Arun</style></author><author><style face="normal" font="default" size="100%">Derichsweiler, Christina</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Clemens, Frank</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electrospun (K, Na) NbO3 Piezoceramic Fibers for Self‐Powered Tactile Sensing Application</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2301066</style></pages><volume><style face="normal" font="default" size="100%">26</style></volume><number><style face="normal" font="default" size="100%">1</style></number><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><isbn><style face="normal" font="default" size="100%">1438-1656</style></isbn><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>739</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">739</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gad, Alaa A.</style></author><author><style face="normal" font="default" size="100%">Tammam, Salma N.</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Mansour, Samar</style></author><author><style face="normal" font="default" size="100%">Youssef, Yomna A.</style></author><author><style face="normal" font="default" size="100%">Farag, Karin S.</style></author><author><style face="normal" font="default" size="100%">Abdel-Kader, Reham M.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhancing mitochondrial functions in neuroinflammatory mouse model using isoflavones-loaded nanoparticles: A potential approach for Alzheimer&apos;s disease treatment</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Drug Delivery Science and Technology</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Journal of Drug Delivery Science and Technology</style></full-title></periodical><pages><style face="normal" font="default" size="100%">106252</style></pages><volume><style face="normal" font="default" size="100%">101</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Alzheimer&apos;s disease</style></keyword><keyword><style face="normal" font="default" size="100%">Nanoparticles</style></keyword><keyword><style face="normal" font="default" size="100%">Mitochondrial biogenesis</style></keyword><keyword><style face="normal" font="default" size="100%">Daidzein</style></keyword><keyword><style face="normal" font="default" size="100%">PLGA</style></keyword><keyword><style face="normal" font="default" size="100%">Neuroinflammatory animal model</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style face="normal" font="default" size="100%">2024/11/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1773-2247</style></isbn><abstract><style face="normal" font="default" size="100%">A significant reduction in mitochondrial functions, coupled with increased oxidative stress, is believed to trigger the histological changes associated with the Alzheimer&apos;s disease (AD). Daidzein (DEZ) and Daidzin (DZ), natural isoflavones, exhibit anti-oxidant properties and enhance mitochondrial biogenesis. However, their low solubility presents challenges for drug circulation and adversely affecting their bioavailability. Novel drug-delivery modalities capable of overcoming these limitations and facilitating brain delivery could enhance therapeutic outcomes. In this work, Tween 80-coated PLGA-NPs and chitosan-coated PLGA-NPs (CS-PLGA-NPs) loaded with DEZ and DZ were evaluated for their ability to enhance cognition in a neuroinflammatory mouse model. The hydrodynamic diameter and zeta potential were measured to be 62 ± 13 nm and −16.8 ±1 mV for PLGA-NPs and to 159 ± 5 nm and +31 ± 5 mV for CS-PLGA-NPs. Biodistribution studies revealed accumulation of both PLGA-NPs and CS-PLGA-NPs in the brain following intravenous administration to animals with neuroinflammation induced by lipopolysaccharides (LPS). Administration of drug-loaded NPs improved cognitive functions compared to untreated animals, in contrast to unloaded NPs or free DEZ and DZ. Animals treated with DEZ-CS-PLGA-NPs and DZ-CS-PLGA-NPs showed significant reductions in superoxide dismutase levels compared to those receiving LPS, suggesting a role in mitigating oxidative stress. When compared to animals receiving LPS, concentrations of Amyloid-β were markedly reduced and complex I activity and ATP levels were significantly increased in animals receiving drug-loaded NPs, unloaded NPs and free drugs, indicating enhanced mitochondrial functions. For drug delivery, CS-PLGA-NPs outperformed PLGA-NPs due sustained drug-release resulting in higher drug concentrations in the brain.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S1773224724009213</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.jddst.2024.106252</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>723</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">723</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dmonte, David John</style></author><author><style face="normal" font="default" size="100%">Bhardwaj, Aman</style></author><author><style face="normal" font="default" size="100%">Kavraz, Pelin</style></author><author><style face="normal" font="default" size="100%">Slobodian, Rostislav</style></author><author><style face="normal" font="default" size="100%">Antos, Jan</style></author><author><style face="normal" font="default" size="100%">Sisman, Orhan</style></author><author><style face="normal" font="default" size="100%">Galusek, Dusan</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kuritka, Ivo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Detection of NH3 gas using CrVO4 nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">Sensors and Actuators B: Chemical</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">135380</style></pages><volume><style face="normal" font="default" size="100%">406</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Vanadate</style></keyword><keyword><style face="normal" font="default" size="100%">Chromium</style></keyword><keyword><style face="normal" font="default" size="100%">Nanoparticles</style></keyword><keyword><style face="normal" font="default" size="100%">Gas sensor</style></keyword><keyword><style face="normal" font="default" size="100%">Chemiresistivity</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style face="normal" font="default" size="100%">2024/05/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0925-4005</style></isbn><abstract><style face="normal" font="default" size="100%">Nanostructured chromium orthovanadate with an average particle size of 65 nm was prepared by the co-precipitation technique for the chemiresistive sensor. The morphology and particle size distribution of CrVO4 nanoparticles were examined by SEM and TEM. According to XRD, most of the prepared CrVO4 material (crystallites) has a monoclinic structure belonging to the space group C2/m. XPS and UV-Vis absorbance measurements provided additional information on the main phase and the surface. The material has shown reasonable selectivity towards the NH3 gas. The as-prepared CrVO4 nanostructures exhibit a maximum relative response of 32% to 50 ppm NH3. The identical dynamic response profiles during the sequential injections of 50 ppm NH3 evinced the repeatability of the sensor. The limit of detection (LOD) value of the sensor was estimated ca 0.7 ppm using relative response values towards a wide range of NH3 concentrations from 10 ppm to 100 ppm. The sensing mechanism was expressed in terms of the surface band bending phenomenon caused by the adsorption and desorption of the ammonia. The best sensor performance was achieved at 330 °C, where the effects of humidity and moisture can be neglected. The results confirmed that the CrVO4 nanomaterial has the potential to fabricate an affordable, easy-to-make, and reliable gas sensor for NH3 gas.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0925400524001096</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.snb.2024.135380</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>725</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">725</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Brune, Veronika</style></author><author><style face="normal" font="default" size="100%">Hartl, Fabian</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Aytuna, Ziyaad</style></author><author><style face="normal" font="default" size="100%">Patrun, David</style></author><author><style face="normal" font="default" size="100%">Hillebrand, David</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Single-crystalline WSe2 nanoflakes as efficient electrocatalysts</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Advances</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Materials Advances</style></full-title></periodical><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><publisher><style face="normal" font="default" size="100%">RSC</style></publisher><abstract><style face="normal" font="default" size="100%">This study presents a novel single molecular source with covalently bonded ligand systems, featuring pre-existing W–Se bonds, for direct synthesis of single crystalline flakes of 2D tungsten diselenide (WSe2). Synthesis and structural characterization of [W{(SeC2H4)2NMe}2] expand the class of single- source precursors for metal sulfides and selenides of general formula [MIV{(XC2H4)2NMe}2] (MIV = Ti, Zr, Hf, Mo, W, Sn; X = S, Se). Comprehensive analysis including NMR, elemental analysis, and single crystal X-ray diffraction, provide insights into structural characteristics of [W{(SeC2H4)2NMe}2] in solution and solid state. Microwave-assisted solvothermal decomposition at 300 °C for 15 minutes yielded highly crystalline WSe2 flakes, confirmed by XRD, SEM, EDS, and TEM analyses. Reduced reaction time under mild conditions enables reproducible generation of layered 2D WSe2 materials for large-scale applications. Electrochemical studies reveal increased electrocatalytic activity, attributed to enhanced electrochemical surface area (ECSA, 67.3 cm2) observed in the as-prepared WSe2 flower-like nanostructures.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D3MA01100C</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D3MA01100C</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D3MA01100C</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>732</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">732</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Brune, Veronika</style></author><author><style face="normal" font="default" size="100%">Hartl, Fabian</style></author><author><style face="normal" font="default" size="100%">Bhardwaj, Aman</style></author><author><style face="normal" font="default" size="100%">Halankar, Kruti</style></author><author><style face="normal" font="default" size="100%">Kwon, Se-Hun</style></author><author><style face="normal" font="default" size="100%">Kim, Kwang-Ho</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Main group metal chalcogenides for photoelectrochemical water splitting</style></title><secondary-title><style face="normal" font="default" size="100%">Photoelectrochemical Engineering for Solar Harvesting</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">271-309</style></pages><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><publisher><style face="normal" font="default" size="100%">Elsevier</style></publisher><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>738</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">738</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aytuna, Ziyaad</style></author><author><style face="normal" font="default" size="100%">Bhardwaj, Aman</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Patrun, David</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Sharma, Raghunath</style></author><author><style face="normal" font="default" size="100%">Papakollu, Kousik</style></author><author><style face="normal" font="default" size="100%">Kumar, Ravi</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular synthesis strategies for binary MO2 (M= V, Sn, Ti, Zr, Hf) high-entropy oxides as superior catalysts for enhanced oxygen evolution</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the European Ceramic Society</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Journal of the European Ceramic Society</style></full-title></periodical><pages><style face="normal" font="default" size="100%">7760-7768</style></pages><volume><style face="normal" font="default" size="100%">44</style></volume><number><style face="normal" font="default" size="100%">13</style></number><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><isbn><style face="normal" font="default" size="100%">0955-2219</style></isbn><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>730</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">730</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amadi, Chijioke Kingsley</style></author><author><style face="normal" font="default" size="100%">Karimpour, Touraj</style></author><author><style face="normal" font="default" size="100%">Jafari, Maziar</style></author><author><style face="normal" font="default" size="100%">Peng, Zhiyuan</style></author><author><style face="normal" font="default" size="100%">Van Gerven, David</style></author><author><style face="normal" font="default" size="100%">Brune, Veronika</style></author><author><style face="normal" font="default" size="100%">Hartl, Fabian</style></author><author><style face="normal" font="default" size="100%">Siaj, Mohamed</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and theoretical study of a mixed-ligand indium (iii) complex for fabrication of β-In 2 S 3 thin films via chemical vapor deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Dalton Transactions</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Dalton Transactions</style></full-title></periodical><pages><style face="normal" font="default" size="100%">9874-9886</style></pages><volume><style face="normal" font="default" size="100%">53</style></volume><number><style face="normal" font="default" size="100%">23</style></number><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>733</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">733</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Abie, Nahal</style></author><author><style face="normal" font="default" size="100%">Ünlü, Ceyda</style></author><author><style face="normal" font="default" size="100%">Pinho, Ana Rita</style></author><author><style face="normal" font="default" size="100%">Gomes, Maria C</style></author><author><style face="normal" font="default" size="100%">Remmler, Torsten</style></author><author><style face="normal" font="default" size="100%">Herb, Marc</style></author><author><style face="normal" font="default" size="100%">Grumme, Daniela</style></author><author><style face="normal" font="default" size="100%">Tabesh, Ehsan</style></author><author><style face="normal" font="default" size="100%">Shahbazi, Mohammad-Ali</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Designing of a Multifunctional 3D-Printed Biomimetic Theragenerative Aerogel Scaffold via Mussel-Inspired Chemistry: Bioactive Glass Nanofiber-Incorporated Self-Assembled Silk Fibroin with Antibacterial, Antiosteosarcoma, and Osteoinductive Properties</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></full-title></periodical><pages><style face="normal" font="default" size="100%">22809-22827</style></pages><volume><style face="normal" font="default" size="100%">16</style></volume><number><style face="normal" font="default" size="100%">18</style></number><dates><year><style face="normal" font="default" size="100%">2024</style></year></dates><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>717</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">717</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tutacz, Peter</style></author><author><style face="normal" font="default" size="100%">Stadler, Daniel</style></author><author><style face="normal" font="default" size="100%">Karimpour, Touraj</style></author><author><style face="normal" font="default" size="100%">Duchoň, Tomáš</style></author><author><style face="normal" font="default" size="100%">Cramm, Stefan</style></author><author><style face="normal" font="default" size="100%">Schneider, Claus Michael</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mueller, David N.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">External Magnetic Field Effects on Shape Anisotropy of TiO2 Nanostructures Grown from a Paramagnetic Ti(III) Precursor</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of Materials</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">8050-8056</style></pages><volume><style face="normal" font="default" size="100%">35</style></volume><number><style face="normal" font="default" size="100%">19</style></number><dates><year><style face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style face="normal" font="default" size="100%">2023/10/10</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><notes><style face="normal" font="default" size="100%">doi: 10.1021/acs.chemmater.3c01318</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.chemmater.3c01318</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.chemmater.3c01318</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>712</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">712</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sheng, Ruoyu</style></author><author><style face="normal" font="default" size="100%">Mu, Jing</style></author><author><style face="normal" font="default" size="100%">Chernozem, Roman V</style></author><author><style face="normal" font="default" size="100%">Mukhortova, Yulia R</style></author><author><style face="normal" font="default" size="100%">Surmeneva, Maria A</style></author><author><style face="normal" font="default" size="100%">Pariy, Igor O</style></author><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Xu, Changlu</style></author><author><style face="normal" font="default" size="100%">Surmenev, Roman A</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fabrication and Characterization of Piezoelectric Polymer Composites and Cytocompatibility with Mesenchymal Stem Cells</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></full-title></periodical><dates><year><style face="normal" font="default" size="100%">2023</style></year></dates><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>715</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">715</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Papakollu, Kousik</style></author><author><style face="normal" font="default" size="100%">Bhardwaj, Aman</style></author><author><style face="normal" font="default" size="100%">Ionescu, Emanuel</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kumar, Ravi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of Structural Changes at Various Length Scales in SiVOC Ceramic Nanocomposites on Electrocatalytic Performance for the Oxygen Reduction Reaction</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></full-title></periodical><pages><style face="normal" font="default" size="100%">34895-34908</style></pages><volume><style face="normal" font="default" size="100%">15</style></volume><number><style face="normal" font="default" size="100%">29</style></number><dates><year><style face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style face="normal" font="default" size="100%">2023/07/26</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><notes><style face="normal" font="default" size="100%">doi: 10.1021/acsami.3c05449</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsami.3c05449</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsami.3c05449</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>707</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">707</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lichtenberg, Andreas</style></author><author><style face="normal" font="default" size="100%">Zegke, Markus</style></author><author><style face="normal" font="default" size="100%">Nichol, Gary S</style></author><author><style face="normal" font="default" size="100%">Raauf, Aida</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of alkali metal cations on the formation of the heterobimetallic actinide tert-butoxides [AnM 3 (O t Bu) 7] and [AnM 2 (O t Bu) 6](An IV= Th, U; MI= Li, Na, K, Rb, Cs)</style></title><secondary-title><style face="normal" font="default" size="100%">Dalton Transactions</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Dalton Transactions</style></full-title></periodical><dates><year><style face="normal" font="default" size="100%">2023</style></year></dates><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>716</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">716</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lee, Hyeonkwon</style></author><author><style face="normal" font="default" size="100%">Aytuna, Ziyaad T.</style></author><author><style face="normal" font="default" size="100%">Bhardwaj, Aman</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">May, Benjamin</style></author><author><style face="normal" font="default" size="100%">Mueller, David N.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Controlling Degree of Inversion in MgFe2O4 Spinel Films Grown in External Magnetic Fields</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2300021</style></pages><volume><style face="normal" font="default" size="100%">25</style></volume><number><style face="normal" font="default" size="100%">18</style></number><keywords><keyword><style face="normal" font="default" size="100%">chemical vapor deposition</style></keyword><keyword><style face="normal" font="default" size="100%">heterometallic alkoxides</style></keyword><keyword><style face="normal" font="default" size="100%">magnesium ferrite</style></keyword><keyword><style face="normal" font="default" size="100%">magnetic field</style></keyword><keyword><style face="normal" font="default" size="100%">single-source precursor</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style face="normal" font="default" size="100%">2023/09/01</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1438-1656</style></isbn><abstract><style face="normal" font="default" size="100%">Single-phase magnesium ferrite spinel films (MgFe2O4) were grown by magnetic field-assisted chemical vapor deposition (mfCVD) of a mixed-metal precursor compound, [MgFe2(OtBu)8]. The formation of monophasic MgFe2O4 deposits as a function of the applied magnetic field strength (B?=?0.0, 0.5, and 1.0?T) was investigated and confirmed by X-ray diffraction and photoelectron spectroscopy analyses. Thin film cross-sectional electron microscopic analysis (FIB-SEM) exhibited higher grain growth and densification in MgFe2O4 films obtained under the magnetic field influence when compared to spinel samples grown under zero-field conditions. Application of an external magnetic field of varying strengths during the chemical vapor deposition process resulted in a change in the light absorption properties and crystal orientation in the MgFe2O4 films, evident in the decreased photoabsorbance analyzed by the UV-Vis spectra and the decrease of intensity of the (400) peak in MgFe2O4 films grown under magnetic field. A comprehensive analysis of X-ray diffraction and X-ray magnetic circular dichroism (XMCD) results indicated a higher degree of inversion in MgFe2O4 deposits grown in an external magnetic field corroborated by a larger contribution of ligand field transitions of tetrahedrally coordinated Fe(III) centers affecting the visible light absorption of MgFe2O4 films.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202300021</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202300021</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2023/11/03</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>727</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">727</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">von Toperczer, Florian</style></author><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Paramasivam, Gopinath</style></author><author><style face="normal" font="default" size="100%">Mathies, Florian</style></author><author><style face="normal" font="default" size="100%">Nandayapa, Edgar</style></author><author><style face="normal" font="default" size="100%">List-Kratochvil, Emil J. W.</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Lindfors, Klas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electrospun Electroluminescent CsPbBr3 Fibers as Flexible Perovskite Networks for Light-Emitting Application</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2201651</style></pages><volume><style face="normal" font="default" size="100%">25</style></volume><number><style face="normal" font="default" size="100%">10</style></number><keywords><keyword><style face="normal" font="default" size="100%">CsPbBr3</style></keyword><keyword><style face="normal" font="default" size="100%">electrospinning</style></keyword><keyword><style face="normal" font="default" size="100%">light-emitting diodes</style></keyword><keyword><style face="normal" font="default" size="100%">nanofibers</style></keyword><keyword><style face="normal" font="default" size="100%">perovskite</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style face="normal" font="default" size="100%">2023/05/01</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1438-1656</style></isbn><abstract><style face="normal" font="default" size="100%">Thin-film perovskite light-emitting diodes have gained increasing attention in the last 6?years. With the possibility to process the emitting layer from solution, the way for 1D morphology of the semiconductor for flexible devices is paved. Herein, for the first time single-step fabrication of CsPbBr3@PVP nanofibers in a customized electrospinning process performed under ambient conditions from a water-based precursor solution is reported. The water-based approach allows the incorporation of a conductive polymer into the compound fiber by blending the perovskite precursor ink with commercially available PEDOT:PSS dispersion. The results demonstrate electrospun fiber mats which are stable at ambient conditions for at least 5?months and can be utilized in electroluminescence devices. Photoluminescence studies on the perovskite fibers reveal a blueshift of the emission peak compared to thin films possibly due to the generation of nanocrystals of ≈12?nm by in?situ nanocrystal pinning as confirmed by transmission electron microscopy. A proof-of-concept electrically pumped light-emitting device is built with the obtained fiber mat. The perovskite nanofibers offer promising applications in flexible and stretchable optoelectronics.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202201651</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202201651</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2024/03/20</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>719</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">719</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">Heshmati, Niusha</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Potential and perspectives of halide perovskites in light emitting devices</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Convergence</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">47</style></pages><volume><style face="normal" font="default" size="100%">10</style></volume><number><style face="normal" font="default" size="100%">1</style></number><dates><year><style face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style face="normal" font="default" size="100%">2023/10/13</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2196-5404</style></isbn><abstract><style face="normal" font="default" size="100%">Light emitting diodes (LEDs) have become part of numerous electrical and electronic systems such as lighting, displays, status indicator lamps and wearable electronics. Owing to their excellent optoelectronic properties and deposition via simple solution process, metal halide perovskites possess unique potential for developing halide perovskite-based LEDs (PeLEDs) with superior photoluminescence efficiencies leading to external quantum efficiencies beyond 20% for PeLEDS. However, the limited durability, high operative voltages, and challenges of scale-up are persisting barriers in achieving required technology readiness levels. To build up the existing knowledge and raise the device performance this review provides a state-of-the-art study on the properties, film and device fabrication, efficiency, and stability of PeLEDs. In terms of commercialization, PeLEDs need to overcome materials and device challenges including stability, ion migration, phase segregation, and joule heating, which are discussed in this review. We hope, discussions about the strategies to overcome the stability issues and enhancement the materials intrinsic properties towards development more stable and efficient optoelectronic devices can pave the way for scalability and cost-effective production of PeLEDs.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1186/s40580-023-00395-1</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1186/s40580-023-00395-1</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>718</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">718</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">E. M. Sahnoun, Sabri</style></author><author><style face="normal" font="default" size="100%">Szymura, Annika</style></author><author><style face="normal" font="default" size="100%">Pes, Jonas</style></author><author><style face="normal" font="default" size="100%">Habib, Shahin</style></author><author><style face="normal" font="default" size="100%">Florea, Alexandru</style></author><author><style face="normal" font="default" size="100%">Schäfer, Laura</style></author><author><style face="normal" font="default" size="100%">Buhl, Eva Miriam</style></author><author><style face="normal" font="default" size="100%">Morgenroth, Agnieszka</style></author><author><style face="normal" font="default" size="100%">Habib, Pardes</style></author><author><style face="normal" font="default" size="100%">Mottaghy, Felix M.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Validation of Dual-Action Chemo-Radio-Labeled Nanocarriers with High Efficacy against Triple-Negative Breast Cancer</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></full-title></periodical><pages><style face="normal" font="default" size="100%">48963-48977</style></pages><volume><style face="normal" font="default" size="100%">15</style></volume><number><style face="normal" font="default" size="100%">42</style></number><dates><year><style face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style face="normal" font="default" size="100%">2023/10/25</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><notes><style face="normal" font="default" size="100%">doi: 10.1021/acsami.3c10579</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsami.3c10579</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsami.3c10579</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>720</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">720</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hartl, Fabian</style></author><author><style face="normal" font="default" size="100%">Brune, Veronika</style></author><author><style face="normal" font="default" size="100%">Lüggert, Sophie</style></author><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">van Gerven, David</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Ji, Seulgi</style></author><author><style face="normal" font="default" size="100%">Choi, Heechae</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Direct Synthesis of Two-Dimensional SnSe and SnSe2 through Molecular Scale Preorganization</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">6274-6287</style></pages><volume><style face="normal" font="default" size="100%">62</style></volume><number><style face="normal" font="default" size="100%">16</style></number><dates><year><style face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style face="normal" font="default" size="100%">2023/04/24</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><notes><style face="normal" font="default" size="100%">doi: 10.1021/acs.inorgchem.2c04083</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.inorgchem.2c04083</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.inorgchem.2c04083</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>709</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">709</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Grödler, Dennis</style></author><author><style face="normal" font="default" size="100%">Sperling, Joseph M</style></author><author><style face="normal" font="default" size="100%">Rotermund, Brian M</style></author><author><style face="normal" font="default" size="100%">Scheibe, Benjamin</style></author><author><style face="normal" font="default" size="100%">Beck, Nicholas B</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Albrecht-Schönzart, Thomas E</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Neptunium Alkoxide Chemistry: Expanding Alkoxides to the Transuranium Elements</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><dates><year><style face="normal" font="default" size="100%">2023</style></year></dates><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>710</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">710</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Drexelius, Marco</style></author><author><style face="normal" font="default" size="100%">Arnold, Rebekka</style></author><author><style face="normal" font="default" size="100%">Meinberger, Denise</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Neundorf, Ines</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Rational design of bifunctional chimeric peptides that combine antimicrobial and titanium binding activity</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Peptide Science</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">e3481</style></pages><dates><year><style face="normal" font="default" size="100%">2023</style></year></dates><isbn><style face="normal" font="default" size="100%">1075-2617</style></isbn><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>722</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">722</key></foreign-keys><ref-type name="Electronic Article">43</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dmonte, David J.</style></author><author><style face="normal" font="default" size="100%">Bhardwaj, Aman</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Kuřitka, Ivo</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sub PPM Detection of NO2 Using Strontium Doped Bismuth Ferrite Nanostructures</style></title><secondary-title><style face="normal" font="default" size="100%">Micromachines</style></secondary-title></titles><volume><style face="normal" font="default" size="100%">14</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">gas sensing</style></keyword><keyword><style face="normal" font="default" size="100%">bismuth ferrite</style></keyword><keyword><style face="normal" font="default" size="100%">ppb</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2023</style></year></dates><isbn><style face="normal" font="default" size="100%">2072-666X</style></isbn><abstract><style face="normal" font="default" size="100%">The present work investigates the NO2 sensing properties of acceptor-doped ferrite perovskite nanostructures. The Sr-doped BiFeO3 nanostructures were synthesized by a salt precursor-based modified pechini method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). The synthesized materials were drop coated to fabricate chemoresistive gas sensors, delivering a maximum sensitivity of 5.2 towards 2 ppm NO2 at 260 &amp;deg;C. The recorded values of response and recovery time are 95 s and 280 s, respectively. The sensor based on Bi0.8Sr0.2FeO3&amp;ndash;&amp;delta; (BSFO) that was operated was shown to have a LOD (limit of detection) as low as 200 ppb. The sensor proved to be promising for repeatability and selectivity measurements, indicating that the Sr doping Bismuth ferrite could be a potentially competitive material for sensing applications. A relevant gas-sensing mechanism is also proposed based on the surface adsorption and reaction behavior of the material.</style></abstract><urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.3390/mi14030644</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>721</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">721</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bhardwaj, Aman</style></author><author><style face="normal" font="default" size="100%">Bae, Hohan</style></author><author><style face="normal" font="default" size="100%">Mathur, Lakshya</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Song, Sun-Ju</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Efficient nitric oxide sensing on nanostructured La2MMnO6 (M: Co, Cu, Zn) electrodes</style></title><secondary-title><style face="normal" font="default" size="100%">Ceramics International</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">9607-9614</style></pages><volume><style face="normal" font="default" size="100%">49</style></volume><number><style face="normal" font="default" size="100%">6</style></number><keywords><keyword><style face="normal" font="default" size="100%">Mixed-potential</style></keyword><keyword><style face="normal" font="default" size="100%">Double perovskite oxide</style></keyword><keyword><style face="normal" font="default" size="100%">Nitric oxide</style></keyword><keyword><style face="normal" font="default" size="100%">Automotive sensor</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2023</style></year><pub-dates><date><style face="normal" font="default" size="100%">2023/03/15/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0272-8842</style></isbn><abstract><style face="normal" font="default" size="100%">Selective detection of nitric oxide (NO) is a challenge for automotive exhaust monitoring systems due to the instability of sensing architectures operating under extreme environments. Herein, yttria-stabilized zirconia (YSZ) solid-electrolyte-based electrochemical gas sensor was developed using double perovskite electrodes (DPO) for selective detection of NO. The La2MMnO6 (M: Co, Cu, Zn) phases were synthesized by sol-gel processing of constituent salts and characterized for physicochemical and sensing properties to investigate the impact of transition metal cations present in octahedral environments on charge transport properties. The La2ZnMnO6 with a predominant Zn2+–Mn4+ charge ordering excelled in the sensing characteristics with high sensitivity (33 mV/decade for 3–80 ppm NO concentration), fast response/recovery time (52/42 s) and significant NO selectivity at 500 °C. The sensing behavior of double perovskites was comprehensively explored and found to abide by the mixed-potential model. Moreover, stable sensing properties over a period of three weeks indicate the here-described sensors to be potentially competitive for onboard exhaust monitoring in automobiles.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0272884222041529</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.ceramint.2022.11.130</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>713</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">713</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amadi, Chijioke Kingsley</style></author><author><style face="normal" font="default" size="100%">Atamtürk, Ufuk</style></author><author><style face="normal" font="default" size="100%">Lichtenberg, Andreas</style></author><author><style face="normal" font="default" size="100%">Raauf, Aida</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Undirected C-H Bond Activation in Aluminium Hydrido Enaminonates</style></title><secondary-title><style face="normal" font="default" size="100%">Molecules</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Molecules</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2137</style></pages><volume><style face="normal" font="default" size="100%">28</style></volume><number><style face="normal" font="default" size="100%">5</style></number><dates><year><style face="normal" font="default" size="100%">2023</style></year></dates><isbn><style face="normal" font="default" size="100%">1420-3049</style></isbn><accession-num><style face="normal" font="default" size="100%">doi:10.3390/molecules28052137</style></accession-num><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.mdpi.com/1420-3049/28/5/2137</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>686</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">686</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zare, Mina</style></author><author><style face="normal" font="default" size="100%">Namratha, Keerthiraj</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Sultana, Afreen</style></author><author><style face="normal" font="default" size="100%">Hezam, Abdo</style></author><author><style face="normal" font="default" size="100%">L, Sunil</style></author><author><style face="normal" font="default" size="100%">Surmeneva, Maria A.</style></author><author><style face="normal" font="default" size="100%">Surmenev, Roman A.</style></author><author><style face="normal" font="default" size="100%">Nayan, M. B.</style></author><author><style face="normal" font="default" size="100%">Ramakrishna, Seeram</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Byrappa, Kullaiah</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Emerging Trends for ZnO Nanoparticles and Their Applications in Food Packaging</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Food Science &amp; Technology</style></secondary-title></titles><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/04/26</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><notes><style face="normal" font="default" size="100%">doi: 10.1021/acsfoodscitech.2c00043</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsfoodscitech.2c00043</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsfoodscitech.2c00043</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>691</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">691</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yang, Yang</style></author><author><style face="normal" font="default" size="100%">Hoang, Minh Tam</style></author><author><style face="normal" font="default" size="100%">Bhardwaj, Aman</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Wang, Hongxia</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Perovskite solar cells based self-charging power packs: Fundamentals, applications and challenges</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><pages><style face="normal" font="default" size="100%">106910</style></pages><volume><style face="normal" font="default" size="100%">94</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Self-charging power packs</style></keyword><keyword><style face="normal" font="default" size="100%">Perovskite solar cells</style></keyword><keyword><style face="normal" font="default" size="100%">Photocapacitors</style></keyword><keyword><style face="normal" font="default" size="100%">Photobatteries</style></keyword><keyword><style face="normal" font="default" size="100%">Overall efficiency</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/04/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><abstract><style face="normal" font="default" size="100%">Perovskite solar cells (PSCs) have advanced in leaps and bounds thanks to their significant merits of low processing cost, simple device structure and fabrication, and high photoelectric conversion efficiency, which make them strong contenders for next generation photovoltaic (PV) technology. Nevertheless, owing to the intermittent and fluctuant nature of solar radiation, PSCs are constrained in providing sustainable and reliable power output needed in practice. With the aid of energy storage systems, such as supercapacitors (SCs) and lithium-ion batteries (LIBs), integrated solar power packs comprised of a PSC unit and a SC or LIB unit can self-charge under illumination and deliver stable off-grid power supply for external loads whenever needed. Recently, this new concept based on synergistic integration of complementary energy conversion and storage has aroused intense research interest in the scientific community. Many efforts have been made to assemble multifunctional self-charging power packs (SCPPs). This review highlights the progress in the emerging field of both integrated PSC-SC photocapacitors and PSC-LIB photobatteries in detail, including new device concepts, operation mechanisms, and the performance for each part and the whole device. We further analyze the existing challenges and limitations of the SCPPs and propose strategies and perspectives for future development.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2211285521011599</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.nanoen.2021.106910</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>701</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">701</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Adam, Ruth</style></author><author><style face="normal" font="default" size="100%">Bhardwaj, Aman</style></author><author><style face="normal" font="default" size="100%">Neumann, Iuliia</style></author><author><style face="normal" font="default" size="100%">Cho, Sung Hun</style></author><author><style face="normal" font="default" size="100%">Yamada, Yuki</style></author><author><style face="normal" font="default" size="100%">Sekino, Tohru</style></author><author><style face="normal" font="default" size="100%">Tao, Jianming</style></author><author><style face="normal" font="default" size="100%">Hong, Zhensheng</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Carbon-coated electrospun V2O5 nanofibers as photoresponsive cathode for lithium-ion batteries</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">electrospinning</style></keyword><keyword><style face="normal" font="default" size="100%">light-rechargeable</style></keyword><keyword><style face="normal" font="default" size="100%">Li-ion battery</style></keyword><keyword><style face="normal" font="default" size="100%">PECVD</style></keyword><keyword><style face="normal" font="default" size="100%">vanadium pentoxide (V2O5)</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/08/18</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1438-1656</style></isbn><abstract><style face="normal" font="default" size="100%">Photo-rechargeable batteries represent a synergistic concept that integrates both energy harvesting and energy storage modalities based on dual-functional materials. We report here on electrospun vanadium oxide nanofibers (VNF) seamlessly coated with conductive carbon (VNF-C-120) as dual-action cathode materials for photo-rechargeable lithium-ion batteries. The materials delivered a high discharge capacity of 160 mAh g-1, which could be increased up to 184 mAh g-1 (C rate of 0.75) under light illumination that confirmed the photoresponsive behavior. Long-term stability tests (300 cycles at 0.75 C) and the postmortem analysis showed that besides being a conductive sheath, the carbon coating is also essential in retaining the structural and morphological stability of V2O5 fibers, which was manifested in a higher capacity retention upon cycling compared to the non-carbon-coated VNF (43.85% capacity retention VNF and 61.13% capacity retention for VNF-C-120 after 300 cycles). On the other hand, the pristine VNF electrode could not reach 400 cycles, due to the failure of the cell, which however was prevented in cells operating with carbon-coated electrodes. Further, the photo-rechargeability of the cell was demonstrated under a UV lamp that delivered an overall conversion efficiency of 4.24% for VNF and 5.07% for the VNF-C-120. This article is protected by copyright. All rights reserved.</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202200765</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202200765</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202200765</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202200765</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2022/08/25</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>696</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">696</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wang, Jinshan</style></author><author><style face="normal" font="default" size="100%">Lian, Ruqian</style></author><author><style face="normal" font="default" size="100%">Zhao, Si</style></author><author><style face="normal" font="default" size="100%">Zheng, Lituo</style></author><author><style face="normal" font="default" size="100%">Huang, Yiyin</style></author><author><style face="normal" font="default" size="100%">Wei, Mingdeng</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hong, Zhensheng</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ultrastable sodium metal plating/striping by engineering heterogeneous nucleation on TiO2 nanotube arrays</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Engineering Journal</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">134272</style></pages><volume><style face="normal" font="default" size="100%">431</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Sodium metal anode</style></keyword><keyword><style face="normal" font="default" size="100%">TiO nanotube arrays</style></keyword><keyword><style face="normal" font="default" size="100%">Electrochemical deposition</style></keyword><keyword><style face="normal" font="default" size="100%">Heterogeneous nucleation</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/03/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1385-8947</style></isbn><abstract><style face="normal" font="default" size="100%">Sodium metal is considered as an excellent anode material for sodium-based energy storage devices with both high energy density and low cost, but the uncontrollable growth of sodium metal seriously limits its application. Herein, we firstly propose 3D spaced TiO2 nanotube arrays (STNTs) uniformly coated with ultra-fine metal (Ag, Cu) nanocrystals as a substrate with absorption-diffusion regulation strategy to control the sodium metal deposition behavior. TiO2 has a higher sodiophilic activity with larger Na absorption energy than the traditional copper substrate. Moreover, it is found by ab initio molecular dynamics (AIMD) simulations that it is much easier for Na to spread upon the surface of silver compared to copper, and thus forming a mixed Na-Ag layer at the interface. As a result, sodium metal is inclined to deposit inside or along the nanotube in STNTs-Ag in nanoscale. Finally, STNTs-Ag||Na half-cell displays a high Coulombic efficiency ∼99.5% even after 500 cycles with 1 mAh cm−2. Symmetric cell of STNTs-Ag-Na exhibits an ultralow overpotential of 4 mV and a long-term cycling life over 1400 h. Moreover, STNTs-Ag-Na anode coupling with Na3V2(PO4)3 cathode exhibits a significantly reduced polarization voltage with 22 mV and improved rate performance with 110 mAhg−1 at 10 C.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S1385894721058459</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.cej.2021.134272</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>693</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">693</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Verma, Anjneya</style></author><author><style face="normal" font="default" size="100%">Kim, Kwang Ho</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Lee, Damin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Interdependence of the electrical performance of NiCuFeCoMn multi-structure carbonates as electrode material for supercapacitors</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Alloys and Compounds</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">166222</style></pages><volume><style face="normal" font="default" size="100%">922</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Multi-structure electrode</style></keyword><keyword><style face="normal" font="default" size="100%">Faradaic capacitor</style></keyword><keyword><style face="normal" font="default" size="100%">Carbonate hydroxide</style></keyword><keyword><style face="normal" font="default" size="100%">Hydrothermal method</style></keyword><keyword><style face="normal" font="default" size="100%">Supercapacitors</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/11/20/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0925-8388</style></isbn><abstract><style face="normal" font="default" size="100%">Mesoporous NiCuFeCoMn multi-structure compounds were grown as cathodes for supercapacitors using a hydrothermal method. A multi-structure electrode was constructed using a variety of nanostructures by varying the reaction time. These diverse nanostructures were highly beneficial in achieving a high electrical performance by increasing the electrode/electrolyte contact area and shortening the ion diffusion path. Optimized multi-structure arrays, which were heated for 12 h, had an excellent maximum specific capacitance of 1241 F g−1 at 3 A g−1, significantly greater than that of the other electrodes. Furthermore, the multi-structure electrode exhibited exceptional cycling stability, with 84.7% retention of the original capacitance after 5000 cycles. Moreover, an asymmetric supercapacitor with the optimized multi-structure compound as the positive electrode and graphene as the negative electrode demonstrated a high energy density of 61 W h kg−1 at a power density of 1017 W k g−1 and exceptional cycling stability by retaining 88.5% of the initial capacity after 5000 cycles. Additionally, the as-obtained asymmetric supercapacitor was capable of powering an LED light. Thus, in terms of electrical performance, the asymmetric supercapacitor fabricated with the NiCuFeCoMn multi-structure compounds outperformed the majority of previously reported transition-metal-based carbonate hydroxide asymmetric supercapacitors.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0925838822026135</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.jallcom.2022.166222</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>683</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">683</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Thiyagarajan, Ganesh Babu</style></author><author><style face="normal" font="default" size="100%">Mukkavilli, Raghunath Sharma</style></author><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Christiansen, Silke</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kumar, Ravi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Self-supported amorphous TaNx(Oy)/nickel foam thin film as an advanced electrocatalyst for hydrogen evolution reaction</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Communications</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">3310-3313</style></pages><volume><style face="normal" font="default" size="100%">58</style></volume><number><style face="normal" font="default" size="100%">20</style></number><dates><year><style face="normal" font="default" size="100%">2022</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">1359-7345</style></isbn><abstract><style face="normal" font="default" size="100%">Chemical vapor deposited (CVD) amorphous tantalum-oxy nitride film on porous three-dimensional (3D) nickel foam (TaNx(Oy)/NF) utilizing tantalum precursor, tris(diethylamino)(ethylimino)tantalum(V), ([Ta(NEt)(NEt2)3]) with preformed Ta–N bonds is reported as a potential self-supported electrocatalyst for hydrogen evolution reaction (HER). The morphological analyses revealed the formation of thin film of core–shell structured TaNx(Oy) coating (ca. 236 nm) on NF. In 0.5 M H2SO4, TaNx(Oy)/NF exhibited enhanced HER activity with a low onset potential as compared to the bare NF (−50 mV vs. −166 mV). The TaNx(Oy)/NF samples also displayed higher current density (−11.08 mA cm−2vs. −3.36 mA cm−2 at 400 mV), lower Tafel slope (151 mV dec−1vs. 179 mV dec−1) and lower charge transfer resistance exemplifying the advantage of TaNx(Oy) coating towards enhanced HER performance. The enhanced HER catalytic activity is attributed to the synergistic effect between the amorphous TaNx(Oy) film and the nickel foam.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D2CC00151A</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D2CC00151A</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D2CC00151A</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>692</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">692</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Surmenev, Roman A.</style></author><author><style face="normal" font="default" size="100%">Ivanov, Alexey N.</style></author><author><style face="normal" font="default" size="100%">Cecilia, Angelica</style></author><author><style face="normal" font="default" size="100%">Baumbach, Tilo</style></author><author><style face="normal" font="default" size="100%">Chernozem, Roman V.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Surmeneva, Maria A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electrospun composites of poly-3-hydroxybutyrate reinforced with conductive fillers for in vivo bone regeneration</style></title><secondary-title><style face="normal" font="default" size="100%">Open Ceramics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">100237</style></pages><volume><style face="normal" font="default" size="100%">9</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Biodegradable scaffolds</style></keyword><keyword><style face="normal" font="default" size="100%">Poly-3-hydroxybutyrate</style></keyword><keyword><style face="normal" font="default" size="100%">Osteoinductivity</style></keyword><keyword><style face="normal" font="default" size="100%">Electrospinning</style></keyword><keyword><style face="normal" font="default" size="100%">study</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/03/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2666-5395</style></isbn><abstract><style face="normal" font="default" size="100%">The aim of this study was to investigate the biocompatibility and osteoinductive properties of fibrous scaffolds implanted in the bone tissue of white rats in vivo. The effect of various concentrations of conductive PANi (2 and 3 wt%) and rGO (0.2 and 1 wt%) in the PHB scaffolds on the reparative processes of bone callus formation in white rats was studied. On the 28th day after implantation, a histomorphological study of the preparations of the transverse section of the diaphysis of the femur of the implantation area was performed. The results of implantation tests in the femur revealed that all the studied scaffolds are biocompatible and the most pronounced stimulating effect on bone formation was observed for hybrid PHB scaffolds doped with 3 wt% PANi and 0.2 wt% rGO compared with pure PHB scaffolds, thus determining further prospects to study the osteoinductive features of hybrid PHB scaffolds.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2666539522000207</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.oceram.2022.100237</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>703</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">703</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Siribbal, Shifaa M.</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Renner, Alexander M.</style></author><author><style face="normal" font="default" size="100%">Iqbal, Sumiya</style></author><author><style face="normal" font="default" size="100%">Muñoz Vázquez, Sergio</style></author><author><style face="normal" font="default" size="100%">Moawia, Abubakar</style></author><author><style face="normal" font="default" size="100%">Valldor, Martin</style></author><author><style face="normal" font="default" size="100%">Hussain, Muhammad S.</style></author><author><style face="normal" font="default" size="100%">Schomäcker, Klaus</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Click functionalized biocompatible gadolinium oxide core-shell nanocarriers for imaging of breast cancer cells</style></title><secondary-title><style face="normal" font="default" size="100%">RSC Advances</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">31830-31845</style></pages><volume><style face="normal" font="default" size="100%">12</style></volume><number><style face="normal" font="default" size="100%">49</style></number><dates><year><style face="normal" font="default" size="100%">2022</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><abstract><style face="normal" font="default" size="100%">Site-specific delivery using functionalized nanocarriers is in high demand in imaging applications of modern clinical research. To improve the imaging capabilities of conventionally used contrast agents and expand the targeting accuracy, functional gadolinium oxide based nanocarriers originated from homogeneous core shells structures (Gd2O3@SiO2@Fe3O4) were developed using a multilayer formation approach. The synthesis and chemical configuration for the covalent binding of macrocyclic chelating agents and estrogen targeting molecules on these nanocarriers were designed by a two-step chemical synthesis method. Initially, SiO2@Fe3O4 structures were prepared and encapsulated with a homogenous thin Gd2O3 overlayer. The exterior surface of the as-prepared carriers offered chemical binding with a breast cancer specific estrogen molecule, covalently grafted through a Click-Chemistry protocol. In the next step, to enhance the diagnostic imaging capabilities of these carriers, thiocyanate-linked chelator molecule, DOTA, was attached to the surface of estrogen bound Gd2O3@SiO2@Fe3O4 using basic reaction conditions. The active amino groups before and after conjugation of estrogen molecules on the surface were quantified using a fluorescamine based approach. Due to the covalent binding of the macrocyclic chelator to the Gd2O3@SiO2@Fe3O4 surface, core shell carriers showed potential radiolabeling efficiency using positron emitter radionuclide, gallium-68 (68Ga). Intracellular uptake of estrogen-conjugated carriers was evaluated with MCF7 breast cancer cell lines using confocal laser scanning microscopy and fluorescent flow cytometry. In addition, in vitro cytotoxicity studies of functional nanocarriers as compared to bare nanoparticles showed reduced toxicity to HEK-293 cells demonstrating the role of surface attached molecules in preventing direct exposure of the Gd2O3 surface to the cells. The as-developed gadolinium based nanocarriers presented excellent capabilities as biocompatible target-specific imaging probes which indicates great potential in the field of dual-mode contrast agents.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D2RA00347C</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D2RA00347C</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D2RA00347C</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>681</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">681</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Renner, Alexander M.</style></author><author><style face="normal" font="default" size="100%">Derichsweiler, Christina</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Fries, Jochen W. U.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">High efficiency capture of biomarker miRNA15a for noninvasive diagnosis of malignant kidney tumors</style></title><secondary-title><style face="normal" font="default" size="100%">Biomaterials Science</style></secondary-title></titles><dates><year><style face="normal" font="default" size="100%">2022</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">2047-4830</style></isbn><abstract><style face="normal" font="default" size="100%">To date, there are no preoperative and quantitative dynamics in clinical practice that can reliably differentiate between a benign and malignant renal cell carcinoma (RCC). For monitoring different analytes in body fluids, more than 40 different molecular biomarkers have been identified, however, they are associated with limited clinical sensitivity and/or non-optimal specificity due to their leaky nature. Previous work on RCC demonstrated the miRNA15a to be reliable and novel biomarker with 98.1% specificity and 100% sensitivity. Despite the high potential of miRNA15a biomarker, its clinical application is considerably hampered by the insensitive nature of the detection methods and low concentration of biomarker in samples that is aggravated by the high level of contamination due to other solutes present in body fluids. In this work, a non-invasive quantitative approach is demonstrated to overcome such diagnostics issues through biotin–streptavidin binding and fluorescence active magnetic nanocarriers that ensured prompt isolation, enrichment and purification of the biomarker miRNA15a from urine. The study demonstrates that detectable low levels of these miRNAs through miRNA capturing nanocarriers can potentially function as advanced diagnostic markers for the non-invasive investigation and early detection of renal cancer.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D1BM01737C</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D1BM01737C</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D1BM01737C</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>704</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">704</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rehermann, C</style></author><author><style face="normal" font="default" size="100%">Schröder, V</style></author><author><style face="normal" font="default" size="100%">Flatken, M</style></author><author><style face="normal" font="default" size="100%">Ünlü, F</style></author><author><style face="normal" font="default" size="100%">Shargaieva, O</style></author><author><style face="normal" font="default" size="100%">Hoell, A</style></author><author><style face="normal" font="default" size="100%">Merdasa, A</style></author><author><style face="normal" font="default" size="100%">Mathies, F</style></author><author><style face="normal" font="default" size="100%">Mathur, S</style></author><author><style face="normal" font="default" size="100%">Unger, EL</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Role of solution concentration in formation kinetics of bromide perovskite thin films during spin-coating monitored by optical in situ metrology</style></title><secondary-title><style face="normal" font="default" size="100%">RSC advances</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">32765-32774</style></pages><volume><style face="normal" font="default" size="100%">12</style></volume><number><style face="normal" font="default" size="100%">50</style></number><dates><year><style face="normal" font="default" size="100%">2022</style></year></dates><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>680</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">680</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Raauf, Aida</style></author><author><style face="normal" font="default" size="100%">Schläfer, Johannes</style></author><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Lichtenberg, Andreas</style></author><author><style face="normal" font="default" size="100%">Zegke, Markus</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Homo- and heteroleptic lanthanide-iron alkoxides as precursors in materials synthesis</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the Indian Chemical Society</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">100347</style></pages><keywords><keyword><style face="normal" font="default" size="100%">Heteroleptic</style></keyword><keyword><style face="normal" font="default" size="100%">Homoleptic</style></keyword><keyword><style face="normal" font="default" size="100%">Heterometallic</style></keyword><keyword><style face="normal" font="default" size="100%">Alkoxide</style></keyword><keyword><style face="normal" font="default" size="100%">Molecular structure</style></keyword><keyword><style face="normal" font="default" size="100%">Lanthanide</style></keyword><keyword><style face="normal" font="default" size="100%">Iron</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/01/13/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0019-4522</style></isbn><abstract><style face="normal" font="default" size="100%">Bimetallic iron-lanthanide alkoxides were synthesized by reacting [Ln{N(SiMe3)2}3] (Ln = Pr, Nd, Er) with [Fe2(OtBu)6] in excess tert-butly alcohol that triggered in-situ ligand exchange and Lewis acid-base interactions to form heterometallic compounds. Single crystal X-ray diffraction analyses of new compounds demonstrated that both Nd and Er containing compounds resulted in the formation of a hetero-bimetallic framework based on 1:1 Ln:Fe ratio, whereas higher Fe ratio (1:2) was observed when Pr was used as the rare earth metal, possibly due to its larger ionic radius (Pr(III): 0.99 Å). When the reaction was performed in the presence of chelating ligands (L: H-tfb-mea = N-(4,4,4-trifluorobut-1-en-3-on)-methoxyethyleneamine; H2-tfb-en = N–N′-bis-(4,4,4-trifluorobut-1-en-3-on)-ethylenediamine), heteroleptic Ln-Fe derivatives were formed that were used in a representative case ([NdFe(L)(OtBu)m(HOtBu)]) as efficient precursor to synthesize nanocrystalline NdFeO3 ceramic.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0019452222000097</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.jics.2022.100347</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>690</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">690</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pariy, Igor O.</style></author><author><style face="normal" font="default" size="100%">Chernozem, Roman V.</style></author><author><style face="normal" font="default" size="100%">Chernozem, Polina V.</style></author><author><style face="normal" font="default" size="100%">Mukhortova, Yulia R.</style></author><author><style face="normal" font="default" size="100%">Skirtach, Andre G.</style></author><author><style face="normal" font="default" size="100%">Shvartsman, Vladimir V.</style></author><author><style face="normal" font="default" size="100%">Lupascu, Doru C.</style></author><author><style face="normal" font="default" size="100%">Surmeneva, Maria A.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Surmenev, Roman A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hybrid biodegradable electrospun scaffolds based on poly(l-lactic acid) and reduced graphene oxide with improved piezoelectric response</style></title><secondary-title><style face="normal" font="default" size="100%">Polymer Journal</style></secondary-title></titles><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/07/13</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1349-0540</style></isbn><abstract><style face="normal" font="default" size="100%">Piezoelectric poly-L-lactide (PLLA) is a biodegradable polymer used in various biomedical applications. However, tailoring and controlling the structure of PLLA to enhance its piezoelectric response remains a challenge. In this work, extensive characterization was performed to reveal the effect of the reduced graphene oxide (rGO) content (0.2, 0.7, and 1.0 wt%) on the morphology, structure, thermal and piezoelectric behavior of PLLA scaffolds. Randomly oriented homogeneous fibers and a quasi-amorphous structure for pure PLLA and hybrid PLLA-rGO scaffolds were revealed. The addition of rGO affected the molecular structure of the PLLA scaffolds: for example, the number of polar C=O functional groups was increased. Increasing the content of rGO to 1 wt% resulted in decreased glass transition and melting temperatures and increased the degree of crystallinity of the scaffolds. The addition of 0.2 wt% rGO enhanced the effective local vertical and lateral piezoresponses by 2.3 and 15.4 times, respectively, in comparison with pure PLLA fibers. The presence of the shear piezoelectric α-phase (P212121) in uniaxially oriented PLLA fibers and C=O bond rotation in the polymer chains explained the observed piezoresponse. Thus, this study revealed routes to prepare hybrid biodegradable scaffolds with enhanced piezoresponse for tissue engineering applications.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1038/s41428-022-00669-1</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1038/s41428-022-00669-1</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>679</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">679</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ng, Philipp</style></author><author><style face="normal" font="default" size="100%">Pinho, Ana Rita</style></author><author><style face="normal" font="default" size="100%">Gomes, Maria C.</style></author><author><style face="normal" font="default" size="100%">Demidov, Yan</style></author><author><style face="normal" font="default" size="100%">Krakor, Eva</style></author><author><style face="normal" font="default" size="100%">Grume, Daniela</style></author><author><style face="normal" font="default" size="100%">Herb, Marc</style></author><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">Mano, João</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Maleki, Hajar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fabrication of Antibacterial, Osteo-inductor 3D Printed Aerogel-based Scaffolds by Incorporation of Drug Laden Hollow Mesoporous Silica Microparticles into the Self-assembled Silk Fibroin Biopolymer</style></title><secondary-title><style face="normal" font="default" size="100%">Macromolecular Bioscience</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">2100442</style></pages><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">3D printing</style></keyword><keyword><style face="normal" font="default" size="100%">Aerogels</style></keyword><keyword><style face="normal" font="default" size="100%">Bone tissue engineering</style></keyword><keyword><style face="normal" font="default" size="100%">Mesoporous silica nanoparticles</style></keyword><keyword><style face="normal" font="default" size="100%">Nanocomposites</style></keyword><keyword><style face="normal" font="default" size="100%">Photo-crosslinking</style></keyword><keyword><style face="normal" font="default" size="100%">Silk fibroin</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/01/14</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1616-5187</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract Thanks to the synergistic feature of individual components in hybrid porous (nano)biomaterials, their application in regenerative medicine has drawn significant attention. In this study, we have successfully designed the novel biomimetic aerogel-based composite scaffolds through a synergistic combination of wet chemical synthesis and advanced engineering approaches. To this aim, we initially synthesized the photo-crosslinkable methacrylated silk fibroin (SF-MA) biopolymer and methacrylated hollow mesoporous silica microcapsules (HMSC-MA) as the main constituents of our novel composite aerogels. Afterwards, by incorporation of drug-loaded HMSC-MA into the self-assembled SF-MA, printable gel-based composite inks were developed. By exploiting micro-extrusion-based three-dimensional (3D) printing, SF-MA-HMSC composite gels were printed by careful controlling their viscosity to provide a means to control the shape fidelity of the resulted printed gel constructs. The developed scaffold has shown a multitude of interesting biophysical and biological performances. Namely, thanks to the photo-crosslinking of the gel components during the 3D printing, the scaffolds became mechanically more stable than the pristine SF scaffolds. In addition, freeze-casting the printed constructs generated further interconnectivity in the printed pore struts resulting in the scaffolds with hierarchically organized porosities necessary for cell infiltration and growth. Also, due to the hollow and mesopore feature of the incorporated HMSC inside the aerogel constructs, the sustained release of antibacterial drug was observed, providing the scaffold with an excellent anti-infectivity toward both gram-negative and positive bacteria. Importantly, HMSC incorporated aerogel-based scaffolds promote cellular ingrowth and proliferation, promoting osteoblastic differentiation by inducing the expression of osteogenic markers and matrix mineralization. Finally, the osteoconductive, -inductive, and anti-infective composite aerogels of this study are expected to act as excellent bone implanting materials with an extra feature of local and sustained release of drug for efficient therapy of bone-related diseases. This article is protected by copyright. All rights reserved</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1002/mabi.202100442</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1002/mabi.202100442</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/mabi.202100442</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/mabi.202100442</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2022/01/17</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>687</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">687</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mukkavilli, Raghunath Sharma</style></author><author><style face="normal" font="default" size="100%">Ichangi, Arun</style></author><author><style face="normal" font="default" size="100%">Thiyagarajan, Ganesh Babu</style></author><author><style face="normal" font="default" size="100%">Vollnhals, Florian</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Bhardwaj, Aman</style></author><author><style face="normal" font="default" size="100%">Christiansen, Silke</style></author><author><style face="normal" font="default" size="100%">Neelakantan, Lakshman</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kumar, Ravi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electrospun 1D Ta3N5 -(O) nanofibers as advanced electrocatalysts for hydrogen evolution reaction in proton exchange membrane water electrolyser</style></title><secondary-title><style face="normal" font="default" size="100%">Open Ceramics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">100267</style></pages><volume><style face="normal" font="default" size="100%">10</style></volume><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/06/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2666-5395</style></isbn><abstract><style face="normal" font="default" size="100%">This study demonstrates the synthesis and characterisation of electrospun Ta3N5-(O) 1D-nanofibers for electrocatalytic hydrogen evolution reaction (HER) and its performance in a proton exchange membrane (PEM) water electrolyser. 1D nanofibers were synthesized by electrospinning of tantalum ethoxide/polyvinylpyrrolidone (PVP) sol followed by ammonolysis at varied temperatures (800–1000 °C). Elemental distribution of the nanofibers analysed through XPS, and bulk-EDS studies revealed an increase in surface oxygen concentration with an increase in nitridation temperature (from 900 °C to 1000 °C). The nanofibers were characterized to exhibit high electrocatalytic activity for hydrogen evolution reaction (HER) with a low overpotential of 320 mV to deliver 10 mA/cm2 in 0.5 M H2SO4 electrolyte. The Ta3N5-(O) 1D nanofibers were employed as novel electrocatalyst without any conducting supports in a PEM water electrolyser. A current density of 0.1 A/cm2 was achieved at an applied voltage of 2 V which is on par with earth-abundant electrocatalysts like MoS2. Furthermore, the electrospun nano fibers showed excellent stability with negligible losses over 6 h of prolonged operation. The study demonstrates the advantage of nanostructuring the electrocatalysts in enhancing the applicability of Ta3N5 and paves further a path for the development of high performance 1-D electrocatalysts for hydrogen evolution reactions (HER).</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2666539522000505</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.oceram.2022.100267</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>689</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">689</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Irfan, Muhammad</style></author><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Ullah, Hameed</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Prasad, Ram</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Electrospun Networks of ZnO-SnO&lt;sub&gt;2&lt;/sub&gt; Composite Nanowires as Electron Transport Materials for Perovskite Solar Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Nanomaterials</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">6043406</style></pages><volume><style face="normal" font="default" size="100%">2022</style></volume><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/08/02</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">Hindawi</style></publisher><isbn><style face="normal" font="default" size="100%">1687-4110</style></isbn><abstract><style face="normal" font="default" size="100%">Here, we report on the fabrication of one-dimensional (1D) zinc oxide-tin oxide (ZnO-SnO&lt;sub&gt;2&lt;/sub&gt;, ZTO) hollow nanostructures by coaxial electrospinning followed by investigations of their electron transport properties in regular perovskite solar cells (PSCs). The as-electrospun nanowires (NWs) were obtained as core-shell nanostructures comprised of polymeric core and metal oxide precursors-polymer shell. Thermal analysis studies of the as-electrospun NWs revealed the optimum calcination temperature for complete removal of the polymer and formation of phase pure ZTO. The obtained nanostructured ZTO materials revealed a porous morphology with tubular nanostructures, i.e., NTs. The porous structure of nanoparticles, i.e., NTs in this case, is of particular interest due to the following reasons: (a) structure, particularly 1D, has a profound influence on the electron transport properties, and (b) suitable porosity helps in effective infiltration of perovskite material and hence supports better charge transport at the ZTO-perovskite interface. The nanomaterials were characterized by Fourier transform infrared (FTIR), diffuse reflectance spectroscopy (DRS), and energy dispersive X-ray spectroscopy (EDX) to confirm the presence/absence of functional groups, establish band gap energies (&lt;inline-formula&gt;&lt;mml:math xmlns:mml=&quot;http://www.w3.org/1998/Math/MathML&quot; id=&quot;M1&quot;&gt;&lt;mml:msub&gt;&lt;mml:mrow&gt;&lt;mml:mi&gt;E&lt;/mml:mi&gt;&lt;/mml:mrow&gt;&lt;mml:mrow&gt;&lt;mml:mi&gt;g&lt;/mml:mi&gt;&lt;/mml:mrow&gt;&lt;/mml:msub&gt;&lt;/mml:math&gt;&lt;/inline-formula&gt;), and determine the elemental compositions, respectively. The ZTO NTs were used as electron transport media in the fabrication of perovskite solar cells (PSCs) and established the structure-property (electron transport) relationships. The highest solar to power conversion efficiency (PCE) of 13.0&amp;#x0025; (average: 11.90&amp;#x0025;) was measured for the PSCs based on ZTO NTs obtained by calcination of as-electrospun NWs at 800&amp;#x00B0;C. It indicates the fact that the calcination temperature influenced the structure which as a result influenced the electron transport property of the material used as ETL in PSCs.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1155/2022/6043406</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1155/2022/6043406</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>678</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">678</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Grödler, Dennis</style></author><author><style face="normal" font="default" size="100%">Weidemann, Martin L.</style></author><author><style face="normal" font="default" size="100%">Lichtenberg, Andreas</style></author><author><style face="normal" font="default" size="100%">Greven, Tobias</style></author><author><style face="normal" font="default" size="100%">Nickstadt, Robin</style></author><author><style face="normal" font="default" size="100%">Haydo, Malek</style></author><author><style face="normal" font="default" size="100%">Wickleder, Mathias</style></author><author><style face="normal" font="default" size="100%">Klein, Axel</style></author><author><style face="normal" font="default" size="100%">Johrendt, Dirk</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Zegke, Markus</style></author><author><style face="normal" font="default" size="100%">Raauf, Aida</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Heterobimetallic uranyl(vi) alkoxides of lanthanoids: formation through simple ligand exchange</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Communications</style></secondary-title></titles><dates><year><style face="normal" font="default" size="100%">2022</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">1359-7345</style></isbn><abstract><style face="normal" font="default" size="100%">Lanthanoid and actinoid silylamides are versatile starting materials. Herein we show how a simple ligand exchange with tert-butanol leads to the formation of the first trimeric heterobimetallic uranyl(vi)–lanthanoid(iii) alkoxide complexes. The μ3 coordination of the endogenous uranyl oxo atom results in a significant elongation of the bond length and a significant deviation from the linear uranyl arrangement.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D1CC05444A</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D1CC05444A</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D1CC05444A</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>682</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">682</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Deo, Meenal</style></author><author><style face="normal" font="default" size="100%">Möllmann, Alexander</style></author><author><style face="normal" font="default" size="100%">Haddad, Jinane</style></author><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Ashish</style></author><author><style face="normal" font="default" size="100%">Liu, Maning</style></author><author><style face="normal" font="default" size="100%">Tachibana, Yasuhiro</style></author><author><style face="normal" font="default" size="100%">Stadler, Daniel</style></author><author><style face="normal" font="default" size="100%">Bhardwaj, Aman</style></author><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Kirchartz, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Tantalum Oxide as an Efficient Alternative Electron Transporting Layer for Perovskite Solar Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Nanomaterials</style></secondary-title></titles><volume><style face="normal" font="default" size="100%">12</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">electron transport material</style></keyword><keyword><style face="normal" font="default" size="100%">amorphous Ta2O5</style></keyword><keyword><style face="normal" font="default" size="100%">n-type semiconductor</style></keyword><keyword><style face="normal" font="default" size="100%">perovskite solar cell</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2022</style></year></dates><isbn><style face="normal" font="default" size="100%">2079-4991</style></isbn><abstract><style face="normal" font="default" size="100%">Electron transporting layers facilitating electron extraction and suppressing hole recombination at the cathode are crucial components in any thin-film solar cell geometry, including that of metal&amp;ndash;halide perovskite solar cells. Amorphous tantalum oxide (Ta2O5) deposited by spin coating was explored as an electron transport material for perovskite solar cells, achieving power conversion efficiency (PCE) up to ~14%. Ultraviolet photoelectron spectroscopy (UPS) measurements revealed that the extraction of photogenerated electrons is facilitated due to proper alignment of bandgap energies. Steady-state photoluminescence spectroscopy (PL) verified efficient charge transport from perovskite absorber film to thin Ta2O5 layer. Our findings suggest that tantalum oxide as an n-type semiconductor with a calculated carrier density of ~7 &amp;times; 1018/cm3 in amorphous Ta2O5 films, is a potentially competitive candidate for an electron transport material in perovskite solar cells.</style></abstract><urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.3390/nano12050780</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>688</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">688</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Cuzzupè, Daniele T.</style></author><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">Bernhardt, Robin</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Grosch, Matthias</style></author><author><style face="normal" font="default" size="100%">Weißing, Rene</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">van Loosdrecht, Paul H. M.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thermally-induced drift of A-site cations at solid–solid interface in physically paired lead halide perovskites</style></title><secondary-title><style face="normal" font="default" size="100%">Scientific Reports</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">10241</style></pages><volume><style face="normal" font="default" size="100%">12</style></volume><number><style face="normal" font="default" size="100%">1</style></number><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/06/17</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2045-2322</style></isbn><abstract><style face="normal" font="default" size="100%">The promise of hybrid organic–inorganic halide perovskite solar cells rests on their exceptional power conversion efficiency routinely exceeding 25% in laboratory scale devices. While the migration of halide ions in perovskite thin films has been extensively investigated, the understanding of cation diffusion remains elusive. In this study, a thermal migration of A‑site cations at the solid–solid interface, formed by two physically paired MAPbI3 and FAPbI3 perovskite thin films casted on FTO, is demonstrated through continuous annealing at comparably low temperature (100 °C). Diffusion of methylammonium (CH3NH3+, MA+) cations into the low‑symmetry yellow δ‑FAPbI3 phase triggers a transition from the yellow (δ) to black (α) phase evident in the distinctive color change and verified by shifts in absorption bands and X‑ray diffraction patterns. Intermixing of the A‑site cations MA+ and FA+ (CH(NH2)2+) occurred for both systems, α‑MAPbI3/δ‑FAPbI3 and α‑MAPbI3/α‑FAPbI3. The structural and compositional changes in both cases support a thermally activated ion drift unambiguously demonstrated through changes in the absorption and X-ray photoelectron spectra. Moreover, the physical contact annealing (PCA) leads to healing of defects and pinholes in α‑MAPbI3 thin films, which was correlated to longer recombination lifetimes in mixed MAxFA1−xPbI3 thin films obtained after PCA and probed by ultrafast transient absorption spectroscopy.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1038/s41598-022-14452-y</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1038/s41598-022-14452-y</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>695</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">695</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Christoffels, Ronja</style></author><author><style face="normal" font="default" size="100%">Breitenbach, Carina</style></author><author><style face="normal" font="default" size="100%">Weber, Jean Patrick</style></author><author><style face="normal" font="default" size="100%">Körtgen, Lisa</style></author><author><style face="normal" font="default" size="100%">Tobeck, Christian</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Neudörfl, Jörg-Martin</style></author><author><style face="normal" font="default" size="100%">Farid, Majied Sadegh Zadeh</style></author><author><style face="normal" font="default" size="100%">Maslo, Melisa</style></author><author><style face="normal" font="default" size="100%">Strub, Erik</style></author><author><style face="normal" font="default" size="100%">Ruschewitz, Uwe</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">UoC-3: A Metal–Organic Framework with an Anionic Framework Based on Uranyl UO22+ Nodes and Partly Fluorinated Benzene-1,3,5-Tribenzoate Linkers</style></title><secondary-title><style face="normal" font="default" size="100%">Crystal Growth &amp; Design</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">681-692</style></pages><volume><style face="normal" font="default" size="100%">22</style></volume><number><style face="normal" font="default" size="100%">1</style></number><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/01/05</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">1528-7483</style></isbn><notes><style face="normal" font="default" size="100%">(née Stastny)&#xD;doi: 10.1021/acs.cgd.1c01199</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.cgd.1c01199</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.cgd.1c01199</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>700</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">700</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Choi, Heechae</style></author><author><style face="normal" font="default" size="100%">Han, HyukSu</style></author><author><style face="normal" font="default" size="100%">Moon, Seong- I.</style></author><author><style face="normal" font="default" size="100%">Je, Minyeong</style></author><author><style face="normal" font="default" size="100%">Lee, Seungwoo</style></author><author><style face="normal" font="default" size="100%">Kwon, Jiseok</style></author><author><style face="normal" font="default" size="100%">Kim, Seungchul</style></author><author><style face="normal" font="default" size="100%">Lee, Kwang-Ryeol</style></author><author><style face="normal" font="default" size="100%">Ali, Ghulam</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Paik, Ungyu</style></author><author><style face="normal" font="default" size="100%">Qiao, Shi-Zhang</style></author><author><style face="normal" font="default" size="100%">Song, Taeseup</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Strategy to utilize amorphous phase of semiconductor toward excellent and reliable photochemical water splitting performance: Roles of interface dipole moment and reaction parallelization</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Energy Research</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">3674-3685</style></pages><volume><style face="normal" font="default" size="100%">46</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">charge separation</style></keyword><keyword><style face="normal" font="default" size="100%">crystal-amorphous junction</style></keyword><keyword><style face="normal" font="default" size="100%">DFT</style></keyword><keyword><style face="normal" font="default" size="100%">photochemistry</style></keyword><keyword><style face="normal" font="default" size="100%">reaction parallelization</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/03/10</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">0363-907X</style></isbn><abstract><style face="normal" font="default" size="100%">Summary The roles of amorphous phases in photochemical water splitting of semiconductors are still in debate, as the effects of the amorphous phase are largely irregular even in a single material. We presumed that the photochemistry of crystal-amorphous mixed semiconductor systems would be governed by the interface characteristics, and conducted a systematic study to understand the origins of the largely varying photochemical reaction of semiconductors having an amorphous phase. First-principles calculations on crystalline anatase and amorphous TiO2 showed that the coexistence of crystalline and amorphous TiO2 and the exposure of the phase boundary are advantageous due to the accelerated charge separation by interface dipole moment and the parallelizable oxygen evolution reaction at the boundary. Our computation-based strategies were demonstrated in our experiments: only the TiO2 nanoparticle and nanotube having partial amorphization on surfaces have highly enhanced photocatalytic water splitting performances (approximately 700%) compared to the pristine and completely amorphized TiO2 systems.</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1002/er.7333</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1002/er.7333</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/er.7333</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/er.7333</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2022/08/10</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>706</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">706</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chernozem, Roman V</style></author><author><style face="normal" font="default" size="100%">Pariy, Igor</style></author><author><style face="normal" font="default" size="100%">Surmeneva, Maria A</style></author><author><style face="normal" font="default" size="100%">Shvartsman, Vladimir V</style></author><author><style face="normal" font="default" size="100%">Plankaert, Guillaume</style></author><author><style face="normal" font="default" size="100%">Verduijn, Joost</style></author><author><style face="normal" font="default" size="100%">Ghysels, Stef</style></author><author><style face="normal" font="default" size="100%">Abalymov, Anatolii</style></author><author><style face="normal" font="default" size="100%">Parakhonskiy, Bogdan V</style></author><author><style face="normal" font="default" size="100%">Gonçalves, Amanda</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Cell Behavior Changes and Enzymatic Biodegradation of Hybrid Electrospun Poly (3‐Hydroxybutyrate)‐Based Scaffolds with an Enhanced Piezoresponse after the Addition of Reduced Graphene Oxide</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Healthcare Materials</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">2201726</style></pages><dates><year><style face="normal" font="default" size="100%">2022</style></year></dates><isbn><style face="normal" font="default" size="100%">2192-2640</style></isbn><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>694</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">694</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chen, Yang</style></author><author><style face="normal" font="default" size="100%">Zhao, Si</style></author><author><style face="normal" font="default" size="100%">Yu, Yueyue</style></author><author><style face="normal" font="default" size="100%">Wei, Mingdeng</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hong, Zhensheng</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A General Synthesis of Mesoporous Hollow Carbon Spheres with Extraordinary Sodium Storage Kinetics by Engineering Solvation Structure</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Small</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2106513</style></pages><volume><style face="normal" font="default" size="100%">18</style></volume><number><style face="normal" font="default" size="100%">10</style></number><keywords><keyword><style face="normal" font="default" size="100%">anodes</style></keyword><keyword><style face="normal" font="default" size="100%">general synthesis</style></keyword><keyword><style face="normal" font="default" size="100%">hollow carbon spheres</style></keyword><keyword><style face="normal" font="default" size="100%">sodium-ion capacitors</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/03/01</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1613-6810</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract Porous and hollow carbon materials have great superiority and prospects in electrochemical energy applications, especially for surface charge storage due to the high active surface. Herein, a general strategy is developed to synthesize mesoporous hollow carbon spheres (MHCS) with controllable texture and compositions by the synergistic effect of dopamine polymerization and metal catalysis (Cu, Bi, Zn). Mesoporous MHCS?Cu and MHCS?Bi are regular spheres, while mesoporous MHCS?Zn possesses an inward concave texture, and simultaneously has a very high surface area of 1675.5 m2 g-1 and lower oxygen content through the catalytic deoxygenation effect. MHCS?Zn displays an exceptional sodium storage kinetics and excellent long cycling life with 171.9 mAh g-1 after 2500 cycles at 5 A g-1 in compatible ether-based electrolytes. Such electrolyte enables enhanced solvated Na+ transport kinetics with appropriate electrostatic interactions at the surface of carbon anode as revealed by molecular dynamics simulations and molecular surface electrostatic potential calculations. Such an anode also displays basically constant capacity working at 0 °C, and still delivers 140 mAh g-1 at 3 A g-1 under -20 °C. Moreover, MHCS?Zn anode is coupled with Na3V2(PO4)3 cathode to construct a hybrid capacitor, which exhibits a high energy density of 145 Wh Kg-1 at a very high power of 8009 W kg-1.</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1002/smll.202106513</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1002/smll.202106513</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/smll.202106513</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/smll.202106513</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2022/08/10</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>685</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">685</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Brune, Veronika</style></author><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Ates, Nursima</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular Precursors to Group IV Dichalcogenides MS2 (M = Ti, Zr, Hf)</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></full-title></periodical><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">Single molecular source2D materialTDMCCVDS ligands</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/04/11</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">0044-2313</style></isbn><abstract><style face="normal" font="default" size="100%">New chemical routes to synthesize layered 2D transition metal dichalcogenides (TMDCs) are highly desired. We report here a new class of molecular precursors of general formula [MIV(SC2H4N(Me)C2H4S)2] (MIV=Ti, Zr, Hf) that offers a reliable synthetic access to 2D TMDC materials as demonstrated in the representative case of TiS2 synthesis. The complexation of the TM centers by the chelating tridentate ligand (HSC2H4)2NMe produced stable monomeric complexes, [Ti(SC2H4N(Me)C2H4S)2], [Zr(SC2H4N(Me)C2H4S)2] and [Hf(SC2H4N(Me)C2H4S)2], displaying a distorted octahedral environment around metal centers formed by four S and two N donor atoms of the ligand moiety. The characterization of molecular precursors by NMR, single-crystal diffraction analysis, IR spectroscopy and elemental analysis confirmed the presence of metal-sulfur bonds that are crucial in facilitating the formation of MS2 phases. Thermal decomposition behaviour of the three molecular compounds was investigated by TG-DCS measurements that confirmed their decomposition into solid phases. Interestingly, the preorganized M-S bonds in the precursor molecules also influenced the formation of titanium disulfide thin films by chemical vapor phase deposition. The solid thin films of TiS2 were characterized by X-ray spectroscopy analysis and atomic scale imaging. The complexes presented in this work represent a promising chemistry driven approach towards reproducible and scalable synthesis of van der Waals 2D heterostructures.</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1002/zaac.202200049</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1002/zaac.202200049</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/zaac.202200049</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/zaac.202200049</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2022/04/13</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>684</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">684</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Brune, Veronika</style></author><author><style face="normal" font="default" size="100%">Bohr, Christoph</style></author><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Hirt, Sebastian Daniel</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Wennig, Sebastian</style></author><author><style face="normal" font="default" size="100%">Oberschachtsiek, Bernd</style></author><author><style face="normal" font="default" size="100%">Ichangi, Arun</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A novel molecular synthesis route to Li2S loaded carbon fibers for lithium–sulfur batteries</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></full-title></periodical><dates><year><style face="normal" font="default" size="100%">2022</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><abstract><style face="normal" font="default" size="100%">The synthesis of a novel air-stable molecular precursor (LiSC2H4)2NMe enables the formation of the desired 1D lithium sulfide (Li2S) via the electrospinning method under ambient conditions. The solubility of the precursor in polar solvents combined with a common polymer (PVP) allowed a suitable spinning solution to obtain ideal green Li2S loaded fibers. 3D fiber mats of the calcined homogeneous 1D electrospun Li2S/C fibers were characterized by electron microscopy and X-ray powder diffraction analysis. Direct integration of Li2S in an electronically conductive carbon matrix as the cathode obviates the need of elemental lithium as the anode, which is a great advantage against the reported lithium–sulfur batteries. An initial capacity of about 870 mA h g−1 at C/20, a capacity retention of 73% after 100 cycles at C/10 and a capacity of about 400 mA h g−1 at 1C were observed for the presented system.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D2TA00369D</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D2TA00369D</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D2TA00369D</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>705</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">705</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bhardwaj, Aman</style></author><author><style face="normal" font="default" size="100%">Bae, Hohan</style></author><author><style face="normal" font="default" size="100%">Mathur, Lakshya</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Song, Sun-Ju</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Cubic Bi2O3-Based Electrochemical Nitric Oxide Sensor Using Double Perovskite Oxide Electrodes</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of The Electrochemical Society</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">117510</style></pages><volume><style face="normal" font="default" size="100%">169</style></volume><number><style face="normal" font="default" size="100%">11</style></number><dates><year><style face="normal" font="default" size="100%">2022</style></year></dates><isbn><style face="normal" font="default" size="100%">1945-7111</style></isbn><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>702</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">702</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Atamtürk, Ufuk</style></author><author><style face="normal" font="default" size="100%">Jung, Eunhwan</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Tale of Two Bismuth Alkylthiolate Precursors’ Bifurcating Paths in Chemical Vapor Deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of Materials</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">7344-7356</style></pages><volume><style face="normal" font="default" size="100%">34</style></volume><number><style face="normal" font="default" size="100%">16</style></number><dates><year><style face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style face="normal" font="default" size="100%">2022/08/23</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><notes><style face="normal" font="default" size="100%">doi: 10.1021/acs.chemmater.2c01351</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.chemmater.2c01351</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.chemmater.2c01351</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>656</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">656</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wilk, Barbara</style></author><author><style face="normal" font="default" size="100%">Öz, Senol</style></author><author><style face="normal" font="default" size="100%">Radicchi, Eros</style></author><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Ahmad, Taimoor</style></author><author><style face="normal" font="default" size="100%">Herman, Artur P.</style></author><author><style face="normal" font="default" size="100%">Nunzi, Francesca</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kudrawiec, Robert</style></author><author><style face="normal" font="default" size="100%">Wojciechowski, Konrad</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Green Solvent-Based Perovskite Precursor Development for Ink-Jet Printed Flexible Solar Cells</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Sustainable Chemistry &amp; Engineering</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">3920-3930</style></pages><volume><style face="normal" font="default" size="100%">9</style></volume><number><style face="normal" font="default" size="100%">10</style></number><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/03/15</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acssuschemeng.0c09208</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acssuschemeng.0c09208</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>667</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">667</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Yu, Wenhua</style></author><author><style face="normal" font="default" size="100%">Singh, Dileep</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Functionalized few-layered graphene nanoplatelets for superior thermal management in heat transfer nanofluids</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Applied Ceramic Technology</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">International Journal of Applied Ceramic Technology</style></full-title></periodical><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/09/02</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1546-542X</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract The superior thermal conductivity and lightweight of graphene flakes make them materials of choice for advanced heat transfer applications, especially for transport of electricity from sustainable power stations such as concentrating solar power plants. In view of the excellent thermal conductivity of graphene or graphene-like nanomaterials (3,000-5,000 W m?1 K?1), their dispersion into conventional host fluids such as water (0.613 W m?1 K?1) or ethylene glycol (0.25 W m?1 K?1) can significantly improve fluid heat transfer characteristics. The two-dimensional structure and high surface area as well as cost-efficiency carbon-based material makes graphene nanoplatelets (GNPs) suitable for large-scale applications in colloidal thermal conductive fluids. For an efficient dispersion of GNPs in base fluids, intrinsically hydrophobic GNPs were acid-treated to obtain highly concentrated (4 wt.%) graphene-based nanofluids. Investigations on various GNP sizes and reaction parameters showed significant influences on the resulting thermal conductivity values of the nanofluid. After 14-h measurements in a dormant system, the most efficient nanofluid reached a thermal conductivity of 0.586 W m?1 K?1 (the base fluid of 0.391 W m?1 K?1) and a low viscosity of 6.39 cP resulting in an overall efficiency improvement of 77 %, when compared to the base fluid without particles. This article is protected by copyright. All rights reserved</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1111/ijac.13875</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1111/ijac.13875</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1111/ijac.13875</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1111/ijac.13875</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2021/09/06</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>659</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">659</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Ashish</style></author><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">Bohr, Christoph</style></author><author><style face="normal" font="default" size="100%">Bliesener, Andrea</style></author><author><style face="normal" font="default" size="100%">Öz, Seren Dilara</style></author><author><style face="normal" font="default" size="100%">Jena, Ajay Kumar</style></author><author><style face="normal" font="default" size="100%">Ando, Yoichi</style></author><author><style face="normal" font="default" size="100%">Miyasaka, Tsutomu</style></author><author><style face="normal" font="default" size="100%">Kirchartz, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Single- or double A-site cations in A3Bi2I9 bismuth perovskites: What is the suitable choice?</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Research</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1794-1804</style></pages><volume><style face="normal" font="default" size="100%">36</style></volume><number><style face="normal" font="default" size="100%">9</style></number><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/05/01</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2044-5326</style></isbn><abstract><style face="normal" font="default" size="100%">Investigations on the effect of single or double A-site cation engineering on the photovoltaic performance of bismuth perovskite-inspired materials (A3Bi2I9) are rare. Herein, we report novel single- and double-cation based bismuth perovskite-inspired materials developed by (1) completely replacing CH3NH3+ (methylammonium, MA+) in MA3Bi2I9 with various organic cations such as CH(NH2)2+ (formamidinium, FA+), (CH3)2NH2+ (dimethylammonium, DMA+), C(NH2)3+ (guanidinium, GA+) and inorganic cations such as cesium (Cs+), rubidium (Rb+), potassium (K+), sodium (Na+) and lithium (Li+) and (2) partially replacing MA+ with Cs+ in different stoichiometric ratios. Compared to single-cation based bismuth perovskite devices, the double-cation bismuth perovskite device showed an increment in the device power conversion efficiency (PCE) up to 1.5% crediting to the reduction in the bandgap. This is the first study demonstrating double-cation based bismuth perovskite showing bandgap reduction and increment in device efficiency and opens up the possibilities towards compositional engineering for improved device performance.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1557/s43578-021-00155-z</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1557/s43578-021-00155-z</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>674</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">674</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Jung, Eunhwan</style></author><author><style face="normal" font="default" size="100%">Oez, Senol</style></author><author><style face="normal" font="default" size="100%">Choi, Heechae</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chemical Processing of Mixed-Cation Hybrid Perovskites: Stabilizing Effects of Configurational Entropy</style></title></titles><pages><style face="normal" font="default" size="100%">1-24</style></pages><dates><year><style face="normal" font="default" size="100%">2021</style></year></dates><isbn><style face="normal" font="default" size="100%">ISBN: 978-3-527-34715-5</style></isbn><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>675</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">675</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Deo, Meenal</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kirchartz, Thomas</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Ashish</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Bismuth-based halide perovskite and perovskite-inspired light absorbing materials for photovoltaics</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Physics D: Applied Physics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">113002</style></pages><volume><style face="normal" font="default" size="100%">55</style></volume><number><style face="normal" font="default" size="100%">11</style></number><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/11/10</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">IOP Publishing</style></publisher><isbn><style face="normal" font="default" size="100%">0022-3727&#xD;1361-6463</style></isbn><abstract><style face="normal" font="default" size="100%">The efficiency of organic-inorganic hybrid lead halide perovskite solar cells (PSCs) has increased over 25% within a frame of ten years, which is phenomenal and indicative of the promising potential of perovskite materials in impacting the next generation solar cells. Despite high technology readiness of PSCs, the presence of lead has raised concerns about the adverse effect of lead on human health and the environment that may slow down or inhibit the commercialization of PSCs. Thus, there is a dire need to identify materials with lower toxicity profile and comparable optoelectronic properties in regard to lead-halide perovskites. In comparison to tin-, germanium-, and copper-based PSCs, which suffer from stability issues under ambient operation, bismuth-based perovskite and perovskite-inspired materials have gained attention because of their enhanced stability in ambient atmospheric conditions. In this topical review, we initially discuss the background of lead and various lead-free perovskite materials and further discuss the fundamental aspects of various bismuth-based perovskite and perovskite-inspired materials having a chemical formula of A3Bi2X9, A2B′BiX6, B′aBibXa+3b (A = Cs+, MA+ and bulky organic ligands; B′ = Ag+, Cu+; X = I−, Cl−, Br−) and bismuth triiodide (BiI3) semiconducting material particularly focusing on their structure, optoelectronic properties and the influence of compositional variation on the photovoltaic device performance and stability</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1088/1361-6463/ac3033</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1088/1361-6463/ac3033</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>657</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">657</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Thiyagarajan, Ganesh Babu</style></author><author><style face="normal" font="default" size="100%">Shanmugam, Vasu</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Moodakare, Sahana B.</style></author><author><style face="normal" font="default" size="100%">Kumar, Ravi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">TiNb2O7-Keratin derived carbon nanocomposites as novel anode materials for high-capacity lithium-ion batteries</style></title><secondary-title><style face="normal" font="default" size="100%">Open Ceramics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">100131</style></pages><volume><style face="normal" font="default" size="100%">6</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Precursor derived ceramics</style></keyword><keyword><style face="normal" font="default" size="100%">Lithium-ion batteries</style></keyword><keyword><style face="normal" font="default" size="100%">Titanium niobate</style></keyword><keyword><style face="normal" font="default" size="100%">Keratin derived carbon</style></keyword><keyword><style face="normal" font="default" size="100%">Nanocomposites</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/06/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2666-5395</style></isbn><abstract><style face="normal" font="default" size="100%">TiNb2O7/carbon nanocomposites synthesized through a simple, surfactant assisted precursor route is reported as a promising alternative anode material for lithium-ion batteries (LIBs). The carbon component of the nanocomposites is derived from an inexpensive and sustainable keratin rich biological source. The reinforcement of carbon in TiNb2O7 facilitated the formation of non-stoichiometric (Ti0.712Nb0.288)O2 crystalline phase, in addition to the stoichiometric TiNb2O7 phase. It also yielded a high specific surface area (~90 ​m2 ​g−1) and reduced crystallite size (~4 ​nm). Electrochemical results exemplified high reversible capacity of 356 mAh g−1 at 0.1 ​C and remarkable rate capability of ~26 mAh g−1 at ultra-high current rate of 32C. TiNb2O7/carbon nanocomposites also demonstrated remarkable cyclic stability with large capacity retention of 85% even after 50 cycles at 1 ​C. The experimental data attests the potential of TiNb2O7/keratin derived carbon nanocomposites as economically and environmentally viable promising anode material for LIBs.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2666539521000778</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.oceram.2021.100131</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>655</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">655</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Schütz, Markus B.</style></author><author><style face="normal" font="default" size="100%">Renner, Alexander M.</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">Guliyev, Mehrab</style></author><author><style face="normal" font="default" size="100%">Krapf, Philipp</style></author><author><style face="normal" font="default" size="100%">Neumaier, Bernd</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">18F-Labeled magnetic nanovectors for bimodal cellular imaging</style></title><secondary-title><style face="normal" font="default" size="100%">Biomaterials Science</style></secondary-title></titles><dates><year><style face="normal" font="default" size="100%">2021</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">2047-4830</style></isbn><abstract><style face="normal" font="default" size="100%">Surface modification of nanocarriers enables selective attachment to specific molecular targets within a complex biological environment. Besides the enhanced uptake due to specific interactions, the surface ligands can be utilized for radiolabeling applications for bimodal imaging ensured by positron emission topography (PET) and magnetic resonance imaging (MRI) functions in one source. Herein, we describe the surface functionalization of magnetite (Fe3O4) with folic acid as a target vector. Additionally, the magnetic nanocarriers were conjugated with appropriate ligands for subsequent copper-catalyzed azide–alkyne cycloaddition or carbodiimide coupling reactions to successfully achieve radiolabeling with the PET-emitter 18F. The phase composition (XRD) and size analysis (TEM) confirmed the formation of Fe3O4 nanoparticles (6.82 nm ± 0.52 nm). The quantification of various surface functionalities was performed by Fourier-transform infrared spectroscopy (FT-IR) and ultraviolet-visible microscopy (UV-Vis). An innovative magnetic-HPLC method was developed in this work for the determination of the radiochemical yield of the 18F-labeled NPs. The as-prepared Fe3O4 particles demonstrated high radiochemical yields and showed high cellular uptake in a folate receptor overexpressing MCF-7 cell line, validating bimodal imaging chemical design and a magnetic HPLC system. This novel approach, combining folic acid-capped Fe3O4 nanocarriers as a targeting vector with 18F labeling, is promising to apply this probe for bimodal PET/MR-studies.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D1BM00616A</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D1BM00616A</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D1BM00616A</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>673</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">673</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Schmidt-Mende, Lukas</style></author><author><style face="normal" font="default" size="100%">Dyakonov, Vladimir</style></author><author><style face="normal" font="default" size="100%">Olthof, Selina</style></author><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Lê, Khan Moritz Trong</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Karabanov, Andrei D.</style></author><author><style face="normal" font="default" size="100%">Lupascu, Doru C.</style></author><author><style face="normal" font="default" size="100%">Herz, Laura M.</style></author><author><style face="normal" font="default" size="100%">Hinderhofer, Alexander</style></author><author><style face="normal" font="default" size="100%">Schreiber, Frank</style></author><author><style face="normal" font="default" size="100%">Chernikov, Alexey</style></author><author><style face="normal" font="default" size="100%">Egger, David A.</style></author><author><style face="normal" font="default" size="100%">Shargaieva, Oleksandra</style></author><author><style face="normal" font="default" size="100%">Cocchi, Caterina</style></author><author><style face="normal" font="default" size="100%">Unger, Eva</style></author><author><style face="normal" font="default" size="100%">Saliba, Michael</style></author><author><style face="normal" font="default" size="100%">Byranvand, Mahdi Malekshahi</style></author><author><style face="normal" font="default" size="100%">Kroll, Martin</style></author><author><style face="normal" font="default" size="100%">Nehm, Frederik</style></author><author><style face="normal" font="default" size="100%">Leo, Karl</style></author><author><style face="normal" font="default" size="100%">Redinger, Alex</style></author><author><style face="normal" font="default" size="100%">Höcker, Julian</style></author><author><style face="normal" font="default" size="100%">Kirchartz, Thomas</style></author><author><style face="normal" font="default" size="100%">Warby, Jonathan</style></author><author><style face="normal" font="default" size="100%">Gutierrez-Partida, Emilio</style></author><author><style face="normal" font="default" size="100%">Neher, Dieter</style></author><author><style face="normal" font="default" size="100%">Stolterfoht, Martin</style></author><author><style face="normal" font="default" size="100%">Würfel, Uli</style></author><author><style face="normal" font="default" size="100%">Unmüssig, Moritz</style></author><author><style face="normal" font="default" size="100%">Herterich, Jan</style></author><author><style face="normal" font="default" size="100%">Baretzky, Clemens</style></author><author><style face="normal" font="default" size="100%">Mohanraj, John</style></author><author><style face="normal" font="default" size="100%">Thelakkat, Mukundan</style></author><author><style face="normal" font="default" size="100%">Maheu, Clément</style></author><author><style face="normal" font="default" size="100%">Jaegermann, Wolfram</style></author><author><style face="normal" font="default" size="100%">Mayer, Thomas</style></author><author><style face="normal" font="default" size="100%">Rieger, Janek</style></author><author><style face="normal" font="default" size="100%">Fauster, Thomas</style></author><author><style face="normal" font="default" size="100%">Niesner, Daniel</style></author><author><style face="normal" font="default" size="100%">Yang, Fengjiu</style></author><author><style face="normal" font="default" size="100%">Albrecht, Steve</style></author><author><style face="normal" font="default" size="100%">Riedl, Thomas</style></author><author><style face="normal" font="default" size="100%">Fakharuddin, Azhar</style></author><author><style face="normal" font="default" size="100%">Vasilopoulou, Maria</style></author><author><style face="normal" font="default" size="100%">Vaynzof, Yana</style></author><author><style face="normal" font="default" size="100%">Moia, Davide</style></author><author><style face="normal" font="default" size="100%">Maier, Joachim</style></author><author><style face="normal" font="default" size="100%">Franckevičius, Marius</style></author><author><style face="normal" font="default" size="100%">Gulbinas, Vidmantas</style></author><author><style face="normal" font="default" size="100%">Kerner, Ross A.</style></author><author><style face="normal" font="default" size="100%">Zhao, Lianfeng</style></author><author><style face="normal" font="default" size="100%">Rand, Barry P.</style></author><author><style face="normal" font="default" size="100%">Glück, Nadja</style></author><author><style face="normal" font="default" size="100%">Bein, Thomas</style></author><author><style face="normal" font="default" size="100%">Matteocci, Fabio</style></author><author><style face="normal" font="default" size="100%">Castriotta, Luigi Angelo</style></author><author><style face="normal" font="default" size="100%">Di Carlo, Aldo</style></author><author><style face="normal" font="default" size="100%">Scheffler, Matthias</style></author><author><style face="normal" font="default" size="100%">Draxl, Claudia</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Roadmap on organic–inorganic hybrid perovskite semiconductors and devices</style></title><secondary-title><style face="normal" font="default" size="100%">APL Materials</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">109202</style></pages><volume><style face="normal" font="default" size="100%">9</style></volume><number><style face="normal" font="default" size="100%">10</style></number><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/10/01</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Institute of Physics</style></publisher><urls><related-urls><url><style face="normal" font="default" size="100%">https://aip.scitation.org/doi/abs/10.1063/5.0047616</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1063/5.0047616</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2021/10/26</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>617</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">617</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Raauf, Aida</style></author><author><style face="normal" font="default" size="100%">Leduc, Jennifer</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Stadler, Daniel</style></author><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Grosch, Matthias</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Magnetic Field-Assisted Chemical Vapor Deposition of UO2 Thin Films</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1915-1921</style></pages><volume><style face="normal" font="default" size="100%">60</style></volume><number><style face="normal" font="default" size="100%">3</style></number><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/02/01</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.inorgchem.0c03387</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.inorgchem.0c03387</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>651</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">651</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Raauf, Aida</style></author><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Sekhar, Praveen K.</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synergistic Acceptor-Donor Interplay of Nd2Sn2O7 Pyrochlore based Sensor in Selective Detection of Hydrogen</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of The Electrochemical Society</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">047501</style></pages><volume><style face="normal" font="default" size="100%">168</style></volume><number><style face="normal" font="default" size="100%">4</style></number><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/04/01</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">The Electrochemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">0013-4651&#xD;1945-7111</style></isbn><abstract><style face="normal" font="default" size="100%">Nanostructured thin film of Nd2Sn2O7 pyrochlore obtained by solution processing of a single molecular precursor with Nd-Sn ratio of 1:1 was found to show unprecedently high selectivity towards hydrogen sensing in the temperature range 200 °C–450 °C. Formation of crystalline Nd2Sn2O7 upon annealing the xerogel in air at 800 °C was confirmed by powder X-ray diffraction analysis. The heat-treated pyrochlore films exhibited a porous structure with interconnected grains confirmed by scanning electron microscope images. The gas sensing behavior of the device towards various analyte gases (H2, CO, CH4, NO2, NH3) showed remarkably high selectivity towards H2, while no sensor response against other reducing and oxidizing gases was monitored. The highest sensitivity towards H2 was detected at 300 °C with a linear trend observed in the sensitivity values and H2 concentration (5%–30%). Intercorrelated analysis of sensor characteristics, surface spectroscopy before and after hydrogen treatment and implications of unique crystallographic features of the pyrochlore lattice demonstrated a novel defined subsequent detection mechanism, which strongly differs from conventional binary oxides like SnO2. The significant increase in operating temperature upon H2 exposure is apparently caused by the exothermic reaction between pyrochlore and molecular hydrogen to generate highly reactive hydride species during the detection mechanism. The high efficiency and reproducibility of the investigated sensor devices indicates the potential of Nd2Sn2O7 based sensors for hydrogen safety applications.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1149/1945-7111/abf013</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1149/1945-7111/abf013</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>645</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">645</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pandit, Bidhan</style></author><author><style face="normal" font="default" size="100%">Rondiya, Sachin R.</style></author><author><style face="normal" font="default" size="100%">Dzade, Nelson Y.</style></author><author><style face="normal" font="default" size="100%">Shaikh, Shoyebmohamad F.</style></author><author><style face="normal" font="default" size="100%">Kumar, Nitish</style></author><author><style face="normal" font="default" size="100%">Goda, Emad S.</style></author><author><style face="normal" font="default" size="100%">Al-Kahtani, Abdullah A.</style></author><author><style face="normal" font="default" size="100%">Mane, Rajaram S.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Salunkhe, Rahul R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">High Stability and Long Cycle Life of Rechargeable Sodium-Ion Battery Using Manganese Oxide Cathode: A Combined Density Functional Theory (DFT) and Experimental Study</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></full-title></periodical><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/02/25</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsami.0c21081</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsami.0c21081</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>642</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">642</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nahrstedt, Vanessa</style></author><author><style face="normal" font="default" size="100%">Stadler, Daniel</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Duchoň, Tomáš</style></author><author><style face="normal" font="default" size="100%">Mueller, David N.</style></author><author><style face="normal" font="default" size="100%">Schneider, Claus M.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular Level Synthesis of InFeO3 and InFeO3/Fe2O3 Nanocomposites</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/02/23</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.inorgchem.0c03425</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.inorgchem.0c03425</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>646</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">646</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nahrstedt, Vanessa</style></author><author><style face="normal" font="default" size="100%">Raauf, Aida</style></author><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Brune, Veronika</style></author><author><style face="normal" font="default" size="100%">Schläfer, Johannes</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Unusual Reactivity of Silicon Grease Towards Metal Alkoxides: Serendipity for Structural Chemistry</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></full-title></periodical><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">heterometallic alkoxides</style></keyword><keyword><style face="normal" font="default" size="100%">cerium tert butoxide</style></keyword><keyword><style face="normal" font="default" size="100%">zirconium iso propoxide</style></keyword><keyword><style face="normal" font="default" size="100%">indium iso propoxide</style></keyword><keyword><style face="normal" font="default" size="100%">siloxanes</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/03/19</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">0044-2313</style></isbn><abstract><style face="normal" font="default" size="100%">Controlled synthesis of moisture sensitive metal alkoxides demands the use of silicon grease for the inert synthetic manipulation of starting materials using glass apparatus to avoid adventitious hydrolysis.  Spontaneous reaction of the siloxane units (-OSi(Me3)2)n) with the synthesized alkoxides often leads to molecular metal alkoxides based siloxane frameworks.  These spontaneous incorporation of siloxane units into homo- and heterometallic alkoxide building blocks lead to the new multinuclear homo- and heterometallic alkoxide-siloxide compounds [Ce2(OtBu)4{Me2Si(OtBu)O}2(NO3)2] (1), [Zr{(OiPr)2{Me2SiO2}Sr{Zr2(OiPr)8}}2] (2) and [Sn2In2O2{Me2Si(OiPr)O}(OiPr)5]2 (3). Multifunctional coordination properties of these siloxane units enable the molecular approach to synthetically demanding polymetallic complexes for potential MOx-SiOx nanocomposites fabrication.</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1002/zaac.202000474</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1002/zaac.202000474</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/zaac.202000474</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/zaac.202000474</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2021/03/19</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>699</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">699</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mahmoudi, Tahmineh</style></author><author><style face="normal" font="default" size="100%">Rho, Won-Yeop</style></author><author><style face="normal" font="default" size="100%">Kohan, Mohammadhosein</style></author><author><style face="normal" font="default" size="100%">Im, Yeon Ho</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hahn, Yoon-Bong</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Suppression of Sn2+/Sn4+ oxidation in tin-based perovskite solar cells with graphene-tin quantum dots composites in active layer</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><pages><style face="normal" font="default" size="100%">106495</style></pages><volume><style face="normal" font="default" size="100%">90</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Tin-based perovskite solar cells</style></keyword><keyword><style face="normal" font="default" size="100%">Suppression of Sn/Sn oxidation</style></keyword><keyword><style face="normal" font="default" size="100%">Graphene-tin quantum dots composite</style></keyword><keyword><style face="normal" font="default" size="100%">Efficiency and stability</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/12/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><abstract><style face="normal" font="default" size="100%">Tin (Sn) halide perovskite has been a promising candidate in lead-free perovskite solar cells (PSCs), but its chemical instability attributed to Sn2+/Sn4+ oxidation reduces device performance and stability. To address this problem, we propose a new approach, i.e. fabrication of mesoporous n-i-p Sn-based PSCs with the photoactive composite made of mixed-organic-cation Sn halide perovskite and reduced graphene oxide (rGO) sheets anchored with Sn quantum dots (i.e., FA0.8MA0.2SnI3/rGO-Sn QDs). The rGO-Sn QDs in active layer not only suppress the destructive Sn2+/Sn4+oxidation and recombination but also accelerate charge transport, improve charge-carrier lifetime and reduce trap state density. Compared to the power conversion efficiency (PCE) of Sn-PSC without Sn QDs, the composite-basted champion device showed 55% increase in efficiency, attributed to strong suppression of Sn2+/Sn4+oxidation and recombination. Furthermore, the champion device showed remarkable reproducibility and stability improvement, representing an essential step for the practical use of low-cost and lead-free PSCs.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2211285521007485</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.nanoen.2021.106495</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>648</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">648</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lontio Fomekong, Roussin</style></author><author><style face="normal" font="default" size="100%">You, Shujie</style></author><author><style face="normal" font="default" size="100%">Frohnhoven, Robert</style></author><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Saruhan, Bilge</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Self-decoration of Barium Titanate with Rhodium-NP via a facile co-precipitation route for NO sensing in hot gas environment</style></title><secondary-title><style face="normal" font="default" size="100%">Sensors and Actuators B: Chemical</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">129848</style></pages><volume><style face="normal" font="default" size="100%">338</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Rh-loaded BaTiO</style></keyword><keyword><style face="normal" font="default" size="100%">Co-precipitation</style></keyword><keyword><style face="normal" font="default" size="100%">High-temperature sensor</style></keyword><keyword><style face="normal" font="default" size="100%">Nitrogen oxide</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/07/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0925-4005</style></isbn><abstract><style face="normal" font="default" size="100%">There is an urgent need to develop real-time gas sensors capable of detection under hot-gas (&gt;400 °C) flow, for applications such as exhaust emission control. In this context, Rh-doped BaTiO3 has been prepared by a co-precipitation route and heat-treated at 900 °C under 2 % hydrogen to obtain in-situ Rh-nanoparticle decoration of submicron BaTiO3 particles. X-ray diffraction, Raman, and X-Ray photoelectron spectrometry analysis confirm the presence of Barium Titanate phases and the substitution of Ti4+ by Rh3+. According to the analytic evidence, thermal hydrogen treatment leads probably to Rhodium diffusion out of titanate lattice, yielding a self-decoration of the nano-sized Barium Titanate particles. Further NO-sensing tests revealed that the sensors produced by deposition of this in-situ Rh-loaded BaTiO3 on the interdigitated electrodes (IDE) yield a significant increase of selectivity and response (∼18 % for 200 ppm NO) towards NO, for the first time, under a hot-gas environment reaching up to 900 °C as synthetic humid air being the carrier gas. The calculated response and recovery times are reasonable, and observed reproducibility confirms suitability to practical applications. Relying on the carried investigations, this good sensing performance can be explained by the creation of excessive oxygen vacancies resulting from Rhodium&apos;s surface diffusion. Moreover, it is to claim that excellent catalytic activity of Rhodium plays a key role in enhancing NO-sensing performance.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0925400521004172</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.snb.2021.129848</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>672</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">672</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lee, Damin</style></author><author><style face="normal" font="default" size="100%">Verma, Anjneya</style></author><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Kim, Kwang Ho</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hybrid nanostructured PAN@NiCu(CO3)(OH)2 composite for flexible high-performance supercapacitors</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Research</style></secondary-title></titles><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/10/22</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2044-5326</style></isbn><abstract><style face="normal" font="default" size="100%">A binder-free porous NiCu(CO3)(OH)2 composite was grown on a polyacrylonitrile (PAN) nanofiber substrate using a hydrothermal method. PAN nanofibers were fabricated by the electrospinning method, thus producing a substrate with a nano-sized diameter and high specific surface area. The composite NiCu(CO3)(OH)2 nanowires on PAN nanofibers provided the large specific surface area required for the redox reaction. Transition metal-based nanowires and nano-sized PAN substrates indicate a synergistic effect in electrochemical performance. The NiCu(CO3)(OH)2 on PAN composite showed a remarkable maximum specific capacity of 870 mAh g−1 at a current density of 3 A g−1, which indicates that it can be a suitable electrode material. In addition, an asymmetric supercapacitor with NiCu(CO3)(OH)2 on PAN composite as the cathode and graphene as the anode showed an ultra-high energy density of 89.2 W h kg−1 at a power density of 835 W kg−1 and a capacitance retention of 90.1% after 5000 cycles.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1557/s43578-021-00349-5</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1557/s43578-021-00349-5</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>620</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">620</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lee, Damin</style></author><author><style face="normal" font="default" size="100%">Lee, Hyun Woo</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kim, Kwang Ho</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of Cycling Stability on Structure and Properties of MnCo2S4 Nanocomposite for High-Performance Supercapacitors</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Alloys and Compounds</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">158850</style></pages><keywords><keyword><style face="normal" font="default" size="100%">hydrothermal method</style></keyword><keyword><style face="normal" font="default" size="100%">nanostructure</style></keyword><keyword><style face="normal" font="default" size="100%">manganese-cobalt</style></keyword><keyword><style face="normal" font="default" size="100%">metal sulfides composite</style></keyword><keyword><style face="normal" font="default" size="100%">supercapacitors</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/02/02/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0925-8388</style></isbn><abstract><style face="normal" font="default" size="100%">Mesoporous MnCo2S4 composites directly grown on porous Ni foam were prepared by a facile hydrothermal method for high-performance supercapacitors. The nanostructure of MnCo2S4 composite electrodes plays an important role in achieving desirable electrical properties by providing a large surface area that greatly improves the electrode/electrolyte contact area and shortens the ion diffusion paths. As a result, the MnCo2S4 electrode exhibits the advantages of high conductivity and a fast-redox reaction rate. Moreover, metal sulfides are receiving more attention for use in supercapacitors owing to their higher electrical conductivity than those of metal oxides/hydroxides. However, these sulfides are difficult to apply in practice owing to a low potential window. In this study, to compensate for these shortcomings, we experimented with adding glycerol and ethylene glycol to the MnCo2S4 composite. Among the obtained composites, the glycerol-MnCo2S4 electrodes showed high-capacity retention after many cycles and a remarkable maximum specific capacitance of 1218.7Fg-1 at 3Ag-1, which was significantly higher than that of other electrodes. The cycling stability of the glycerol-MnCo2S4 composite electrode was also measured to be the highest at 92.4% after 5000 cycles. In addition, the glycerol-MnCo2S4 composite was confirmed to have the highest specific capacitance, after 5000 cycles (484.2Fg-1 at 3Ag-1). In addition, we fabricated an asymmetric supercapacitor employing the glycerol-MnCo2S4 composite as the positive electrode and graphene as the negative electrode, which exhibited a high energy density of 32.9Wh kg-1 at a power density of 295.2Wkg-1 and a remarkable cycling stability, with 87.7% capacitance retention after 5,000 cycles. These advantages show that the glycerol-MnCo2S4 electrodes prepared by the hydrothermal method could be a promising positive electrode material for high-performance asymmetric supercapacitors.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0925838821002577</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.jallcom.2021.158850</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>661</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">661</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kulkarni, Ashish</style></author><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Pant, Namrata</style></author><author><style face="normal" font="default" size="100%">Kaur, Jagjit</style></author><author><style face="normal" font="default" size="100%">Bohr, Christoph</style></author><author><style face="normal" font="default" size="100%">Jena, Ajay Kumar</style></author><author><style face="normal" font="default" size="100%">Öz, Senol</style></author><author><style face="normal" font="default" size="100%">Yanagida, Masatoshi</style></author><author><style face="normal" font="default" size="100%">Shirai, Yasuhiro</style></author><author><style face="normal" font="default" size="100%">Ikegami, Masashi</style></author><author><style face="normal" font="default" size="100%">Miyano, Kenjiro</style></author><author><style face="normal" font="default" size="100%">Tachibana, Yasuhiro</style></author><author><style face="normal" font="default" size="100%">Chakraborty, Sudip</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Miyasaka, Tsutomu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Concerted Ion-Migration and Diffusion Induced Degradation in Lead-Free Ag3BiI6 Rudorffite Solar Cells under Ambient Conditions</style></title><secondary-title><style face="normal" font="default" size="100%">Solar RRL</style></secondary-title></titles><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">degradation</style></keyword><keyword><style face="normal" font="default" size="100%">gold electrode</style></keyword><keyword><style face="normal" font="default" size="100%">ion-migration</style></keyword><keyword><style face="normal" font="default" size="100%">lead-free</style></keyword><keyword><style face="normal" font="default" size="100%">silver bismuth iodide</style></keyword><keyword><style face="normal" font="default" size="100%">solar cell</style></keyword><keyword><style face="normal" font="default" size="100%">stability.</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/06/29</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">2367-198X</style></isbn><abstract><style face="normal" font="default" size="100%">Silver bismuth iodide (SBI) materials have recently gained attention as non-toxic alternatives to lead perovskites. Although most of the studies have been focusing on photovoltaic performance, the inherent ionic nature of SBI materials, their diffusive behaviour, and influence on material/device stability is underexplored. Herein, AgBi2I7, Ag2BiI5, and Ag3BiI6 thin-films are developed in controlled ambient humidity conditions with a decent efficiency up to 2.32%. While exploring the device stability, it is found that Ag3BiI6 exhibits a unique ion-migration behaviour where Ag+, Bi3+, and I? ions migrate and diffuse through the dopant-free hole-transport layer (HTL) leading to degradation. Interestingly, this ion-migration behaviour is relatively fast for the case of anti-solvent processed Ag3BiI6 thin-film-based devices contrasting the case of without anti-solvent and is not observed for other SBI materials-based devices. Theoretical calculations suggest that low decomposition enthalpy favours the decomposition of Ag3BiI6 to AgI and BiI3 causing migration of ions to the electrode which is protected by employing thick HTL. The new mechanism reported herein underlines the importance of SBI material composition and fundamental mechanism understanding on the stability of Ag3BiI6 material for better solar cell design and also in extending the applications of unique ion-migration behaviour in various optoelectronics. This article is protected by copyright. All rights reserved.</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1002/solr.202100077</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1002/solr.202100077</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/solr.202100077</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/solr.202100077</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2021/07/05</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>660</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">660</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Krakor, Eva</style></author><author><style face="normal" font="default" size="100%">Saniternik, Sven</style></author><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Frohnhoven, Robert</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Drexelius, Marco</style></author><author><style face="normal" font="default" size="100%">Tosun, Nurgül</style></author><author><style face="normal" font="default" size="100%">Neundorf, Ines</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hollow mesoporous silica capsules loaded with copper, silver and zinc oxide nanoclusters for sustained antibacterial efficacy</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the American Ceramic Society</style></secondary-title></titles><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/06/30</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">0002-7820</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract Intensive and overuse of antibiotics during the last years has triggered a distinct rise in antibiotic resistance worldwide. In addition to the newly developed antimicrobials, there is a high demand for alternative treatment options against persistent bacterial infections. The biocidal impact of transition metal ions like copper (Cu2+), silver (Ag+), and zinc (Zn2+) also known as oligodynamic effect has been used through ages to kill or inhibit the growth of microorganisms and to employ long-term prevention strategies against their biological antagonists. Herein, we report on the synthesis of Cu, Ag and Zn metal and corresponding oxide nanoparticles immobilized on hollow mesoporous silica capsules (HMSCs) obtained by a hard-template assisted sol-gel synthesis followed by reduction of appropriate metal salts in the presence of HMSCs. Compartmentalization of nanosized metal and oxide clusters in Ag@HMSCs, Cu@HMSCs and ZnO@HMSCs particles prevented their agglomeration and offered a high release kinetics of metal ions between 2.0-3.7 mM during 24 hours, as monitored by UV-vis analyses. The distribution and morphology of pristine and metal functionalized HMSCs was evaluated by transmission electron microscopy (TEM) analysis revealing the successful synthesis of Ag, Cu and ZnO nanoparticles supported on HMSCs. X-ray photoelectron spectroscopy (XPS) revealed that mainly Cu(II), Ag(0) and Zn(II) species were present in the modified HMSCs. In addition to the surface attachment of preformed metal (Ag and Cu) and metal oxide (ZnO) cluster, nucleation of metal nanoparticles inside the void of HMSCs provided an internal reservoir which allowed for a time-dependent release of metal ions through slower dissolution rates leading to a long-term and sustained bacterial inhibition over several hours. The high antimicrobial efficiency of Ag@HMSCs, Cu@HMSCs, and ZnO@HMSCs particles was investigated towards both Gram-positive (B. subtilis) and Gram-negative (E. coli) bacteria by INT assays showing a complete growth inhibition for both bacteria types after 24 hours. While Ag@HMSCs and Cu@HMSCs showed a higher susceptibility against Gram-negative bacteria, ZnO@HMSCs showed a higher susceptibility against Gram-positive bacteria. This demonstrates the promise of metal-loaded capsules as antibacterial delivery vehicles with dual-mode time release profiles being potential alternatives for antibiotic drugs.</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1111/jace.18002</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1111/jace.18002</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1111/jace.18002</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1111/jace.18002</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2021/07/05</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>650</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">650</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Krakor, Eva</style></author><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Brune, Veronika</style></author><author><style face="normal" font="default" size="100%">Hohnsen, Johannes</style></author><author><style face="normal" font="default" size="100%">Frenzen, Lars</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Selective degradation of synthetic polymers through enzymes immobilized on nanocarriers</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Communications</style></secondary-title></titles><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/04/26</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2159-6867</style></isbn><abstract><style face="normal" font="default" size="100%">In order to develop new sustainable and reusable concepts for the degradation of omnipresent industrial plastics, immobilization of (bio)catalysts on nanocarriers offers unique opportunities for selective depolymerization and catalyst recovery. In this study, enzymes (lipase and cutinase) were covalently immobilized on carrier nanoparticles (SiO2 and Fe3O4@SiO2) through 3-(aminopropyl)trimethoxysilane and glutaraldehyde linkers forming a stable bond to enzyme molecules. The presence of enzymes on the surface was confirmed by zeta potential and XPS measurements, while their degradation activity and long-term stability of up to 144 h was demonstrated by the conversion of 4-nitrophenyl acetate to 4-nitrophenol. Furthermore, enzymatic decomposition (hydrolysis/oxidation) of electrospun polycaprolactone fiber mats was verified through morphological (SEM) and weight loss studies, which evidently showed a change in the fiber morphology due to enzymatic degradation and accordingly a weight loss.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1557/s43579-021-00039-7</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1557/s43579-021-00039-7</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>697</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">697</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kaur, Jasleen</style></author><author><style face="normal" font="default" size="100%">Arroub, Karim</style></author><author><style face="normal" font="default" size="100%">Drzezga, Alexander</style></author><author><style face="normal" font="default" size="100%">Schomäcker, Klaus</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis, proteolytic stability, and in vitro evaluation of DOTA conjugated p160 peptide based radioconjugates: [177Lu]Lu–DOTA–p160</style></title><secondary-title><style face="normal" font="default" size="100%">Organic &amp; Biomolecular Chemistry</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">9849-9854</style></pages><volume><style face="normal" font="default" size="100%">19</style></volume><number><style face="normal" font="default" size="100%">45</style></number><dates><year><style face="normal" font="default" size="100%">2021</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">1477-0520</style></isbn><abstract><style face="normal" font="default" size="100%">In this work, we describe the synthesis, in vitro stability, and preliminary biological evaluation of [177Lu]Lu–DOTA–p160 peptide-based radiopharmaceuticals. Our findings highlight that all DOTA–p160–peptide radioconjugates exhibit favorable proteolytic and enzymatic stability with a prolonged half-life in human plasma and serum. Cell uptake studies carried out on MCF-7 cell line revealed saturable binding of the radioconjugates in the nanomolar range, thereby demonstrating their promising potential in the imaging and therapy of breast tumors.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D1OB01812D</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D1OB01812D</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D1OB01812D</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>665</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">665</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ichangi, Arun</style></author><author><style face="normal" font="default" size="100%">Shvartsman, Vladmir V.</style></author><author><style face="normal" font="default" size="100%">Lupascu, Doru C.</style></author><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">Grosch, Matthias</style></author><author><style face="normal" font="default" size="100%">Kathrin Schmidt-Verma, Anna</style></author><author><style face="normal" font="default" size="100%">Bohr, Christoph</style></author><author><style face="normal" font="default" size="100%">Verma, Anjneya</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Li and Ta-modified KNN piezoceramic fibers for vibrational energy harvesters</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the European Ceramic Society</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Journal of the European Ceramic Society</style></full-title></periodical><keywords><keyword><style face="normal" font="default" size="100%">KNN</style></keyword><keyword><style face="normal" font="default" size="100%">Lead-free</style></keyword><keyword><style face="normal" font="default" size="100%">Nanofibers</style></keyword><keyword><style face="normal" font="default" size="100%">Piezoelectric nanogenerator</style></keyword><keyword><style face="normal" font="default" size="100%">Energy harvesting</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/08/10/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0955-2219</style></isbn><abstract><style face="normal" font="default" size="100%">Piezoelectric energy harvesters (PEH) hold enormous potential for converting mechanical energy from our surrounding environment into electrical energy that can be used for powering portable electronics. Potassium sodium niobate (KNN) is one of the promising alternatives to replace lead-based piezoelectric materials. This work presents a cutting-edge demonstration of synthesis-function-device integration of piezoelectric nanofibers, where the morphology and the composition are engineered towards achieving high device output. We report a flexible nanogenerator based on electrospun Li and Ta-modified lead-free KNN nanofibers yielding a high voltage output of 5.6 V, which is around 9-fold higher than for the Mn-doped KNN nanofibers reported previously. The influence of Li and Ta-incorporation into the KNN lattice on the electromechanical coupling and the effect of a nanofiber morphology are investigated. The net-shaped KNN and Li and Ta-modified KNN nanofibers, synthesized by electrospinning of appropriate sols, maintain their structural integrity upon calcination and firing steps. The phase analysis (XRD) confirms the formation of single-phase (KNN) material. Li and Ta are found to be incorporated on the A and B-sites of the perovskite lattice, respectively. Piezo force microscopy data show the heat-treated nanofibers to exhibit multi-domain ferroelectric properties.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0955221921005689</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.jeurceramsoc.2021.08.010</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>677</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">677</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ichangi, Arun</style></author><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">Queralto, Albert</style></author><author><style face="normal" font="default" size="100%">Grosch, Matthias</style></author><author><style face="normal" font="default" size="100%">Weissing, Rene</style></author><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Chijioke, Amadi Kingsley</style></author><author><style face="normal" font="default" size="100%">Verma, Anjneya</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Surmenev, Roman</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electrospun BiFeO3 nanofibers for vibrational energy harvesting application</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">BFO</style></keyword><keyword><style face="normal" font="default" size="100%">electrospinning</style></keyword><keyword><style face="normal" font="default" size="100%">energy harvesting</style></keyword><keyword><style face="normal" font="default" size="100%">lead-free</style></keyword><keyword><style face="normal" font="default" size="100%">perovskite oxide</style></keyword><keyword><style face="normal" font="default" size="100%">piezoelectric nanogenerator</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/12/06</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1438-1656</style></isbn><abstract><style face="normal" font="default" size="100%">Bismuth ferrite (BiFeO3, BFO) has found application in a wide range of fields owing to its fascinating multiferroic properties. In this study, the interplay between the piezoelectric property and morphology of BFO nanostructures was exploited for vibrational energy harvesting application by tailoring BFO to a high aspect ratio and high surface area nanofiber morphology. This work demonstrates a facile pathway for the fabrication of high-performance flexible nanogenerators, based on BFO nanofibers, from a cost-effective and energy-efficient electrospinning technique. The X-ray diffraction data of calcined fibers confirmed the formation of non-centrosymmetric crystalline perovskite phase. The morphological characterization by scanning electron microscopy showed a compact anisotropic nanofibrous morphology. For the fabrication of nanogenerators, BFO nanofibers were embedded in a piezoactive polymer matrix (polyvinylidenfluorid, PVDF). As fabricated BFO/PVDF composite nanogenerators produced a high peak-to-peak voltage output of 7.6 V, with an average output power density of 185±106 nW/cm2 upon periodic application of force through finger knocking. This article is protected by copyright. All rights reserved.</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202101394</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202101394</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202101394</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202101394</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2021/12/09</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>653</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">653</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hong, Zhensheng</style></author><author><style face="normal" font="default" size="100%">Maleki, Hajar</style></author><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Zhen, Yichao</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Lee, Damin</style></author><author><style face="normal" font="default" size="100%">Kim, Kwang-Ho</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">New insights into carbon-based and MXene anodes for Na and K-ion storage: A review</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Energy Chemistry</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">660-691</style></pages><volume><style face="normal" font="default" size="100%">62</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Na-ion batteries</style></keyword><keyword><style face="normal" font="default" size="100%">K-ion batteries</style></keyword><keyword><style face="normal" font="default" size="100%">Anode</style></keyword><keyword><style face="normal" font="default" size="100%">Carbon materials</style></keyword><keyword><style face="normal" font="default" size="100%">Structure design</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/11/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2095-4956</style></isbn><abstract><style face="normal" font="default" size="100%">Na-ion batteries and K-ion batteries are promising alternatives to vastly used lithium-ion batteries mainly due to the larger natural abundance of sodium and potassium resources. Carbon-based and MXene materials have received increasing attention due to their unique layered structure to accommodate the larger sodium and potassium ions. It’s proposed that ionic size disparity (K+: 1.38 Å; Na+: 0.97 Å; Li+: 0.76 Å) leads to sluggish intercalation and extraction kinetics in larger alkali metal ions (AMIs). Nevertheless, the electrochemical inactivity of sodium intercalation in graphite suggests that different chemical properties of AMs and their interactions with carbon host and electrolytes is crucial for interfacial instability and irreversible capacity loss. Structural modifications by expanding interlayer spacing and defect engineering enable reduced diffusion barriers and enhanced insertion of sodium or potassium, but it blurs the electrochemical performance between battery and capacitor. This review provides insight into 2D carbon materials and their architectures for Na and K-ion batteries through an in-depth analysis of structure–property interdependence and different electrochemical mechanisms supported by both experimental and theoretical data to discuss the promises and challenges of post-lithium batteries. Finally, the perspectives and potential directions regarding material design concepts for 2D carbon-based nanomaterials and MXene phases for metal-ion storage are proposed.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2095495621002436</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.jechem.2021.04.031</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>670</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">670</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hoang, Minh Tam</style></author><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Martens, Wayde</style></author><author><style face="normal" font="default" size="100%">Bell, John</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Wang, Hongxia</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Towards the environmentally friendly solution processing of metal halide perovskite technology</style></title><secondary-title><style face="normal" font="default" size="100%">Green Chemistry</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">5302-5336</style></pages><volume><style face="normal" font="default" size="100%">23</style></volume><number><style face="normal" font="default" size="100%">15</style></number><dates><year><style face="normal" font="default" size="100%">2021</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">1463-9262</style></isbn><abstract><style face="normal" font="default" size="100%">Metal halide perovskite materials have demonstrated unique properties for applications in optoelectrical devices such as solar cells, light-emitting diodes and photodetectors. The unprecedented world-record energy conversion efficiency of over 25% achieved with solution-processed perovskite solar cells is escalating research towards the commercialisation of the perovskite materials. Nevertheless, the use of large amounts of hazardous and carcinogenic solvents such as N,N-dimethylformamide (DMF), N-methyl-2-pyrrolidone (NMP), and skin-penetrating dimethyl sulfoxide (DMSO) in the current perovskite synthesis protocols are limited for the commercial uptake of perovskite technology as these detrimental solvents can cause environmental, health and safety issues. Therefore, the development of alternative environmentally-friendly, green solvents for the synthesis of perovskite materials including thin films, nanocrystals or single-crystals with desirable properties is critical for the commercialisation of perovskite technologies. In this review, we summarize the research progress of solution-processable perovskite material using low-toxic and green solvent alternatives. We discuss the fundamental properties that need to be considered in screening solvents for the solution processing of metal halide perovskites. By carefully analysing the common features of solvents and anti-solvent systems that have been reported for making perovskite precursor inks for applications in solar cells and light-emitting diodes, we provide insight into the relationship between the solvent molecular ligand – properties of perovskite materials – device performance. We discuss the advantages and challenges of each type of green solvent based on their performance in metal halide perovskite technology, effects on the environment, human health and safety, aiming to provide guidelines towards green metal halide perovskite technology.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D1GC01756J</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D1GC01756J</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D1GC01756J</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>643</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">643</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Grödler, Dennis</style></author><author><style face="normal" font="default" size="100%">Haseloer, Alexander</style></author><author><style face="normal" font="default" size="100%">Tobeck, Christian</style></author><author><style face="normal" font="default" size="100%">Bulut, Yusuf</style></author><author><style face="normal" font="default" size="100%">Neudörfl, Jörg M.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ruschewitz, Uwe</style></author><author><style face="normal" font="default" size="100%">Klein, Axel</style></author><author><style face="normal" font="default" size="100%">Wickleder, Mathias S.</style></author><author><style face="normal" font="default" size="100%">Zegke, Markus</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thiosemicarbazone Complexes of Uranium(IV)</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></full-title></periodical><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">Actinides</style></keyword><keyword><style face="normal" font="default" size="100%">Uranium</style></keyword><keyword><style face="normal" font="default" size="100%">Thiosemicarbazones</style></keyword><keyword><style face="normal" font="default" size="100%">Homoleptic complexes</style></keyword><keyword><style face="normal" font="default" size="100%">Electrochemistry</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/02/01</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1434-1948</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract The first homoleptic thiosemicarbazone complexes of uranium were isolated by reacting uranium tetrachloride in a salt metathesis or acid-base reaction with four equivalents of Na(BzTSC) or H(BzTSC) (BzTSC=benzylthiosemicarbazone), carrying a non-methylated (L1), monomethylated (L2) or dimethylated (L3) terminal amino group, in moderate yields. [U(BzTSCNH2)4] (1), [U(BzTSCNH(CH3))4] (2) and [U(BzTSCN(CH3)2)4] (3) show a remarkable stability towards air, with oxidation potentials in THF between +0.43 and +0.53?V and reduction potentials between ?2.53 and ?2.67?V vs. ferrocene/ferrocenium. The simple methylation of the terminal amino group of the ligand allows for controlled changes in the coordination environments of the complexes. Thermogravimetric analyses indicate that the complexes are stable up to 155?°C.</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1002/ejic.202001118</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1002/ejic.202001118</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/ejic.202001118</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/ejic.202001118</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2021/03/02</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>662</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">662</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Fries, Jochen W. U.</style></author><author><style face="normal" font="default" size="100%">Brune, Veronika</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Magnetic nanoparticle-based amplification of microRNA detection in body fluids for early disease diagnosis</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry B</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">9-22</style></pages><volume><style face="normal" font="default" size="100%">9</style></volume><number><style face="normal" font="default" size="100%">1</style></number><dates><year><style face="normal" font="default" size="100%">2021</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">2050-750X</style></isbn><abstract><style face="normal" font="default" size="100%">Circulating biomarkers such as microRNAs (miRNAs), short noncoding RNA strands, represent prognostic and diagnostic indicators for a variety of physiological disorders making their detection and quantification an attractive approach for minimally invasive early disease diagnosis. However, highly sensitive and selective detection methods are required given the generally low abundance of miRNAs in body fluids together with the presence of large amounts of other potentially interfering biomolecules. Although a variety of miRNA isolation and detection methods have been established in clinics, they usually require trained personnel and often constitute labor-, time- and cost-intensive approaches. During the last years, nanoparticle-based biosensors have received increasing attention due to their superior detection efficiency even in very low concentration regimes. This is based on their unique physicochemical properties in combination with their high surface area that allows for the immobilization of multiple recognition sites resulting in fast and effective recognition of analytes. Among various materials, magnetic nanoparticles have been identified as useful tools for the separation, concentration, and detection of miRNAs. Here, we review state-of-the-art technology with regard to magnetic particle-based miRNA detection from body fluids, critically discussing challenges and future perspective of such biosensors while comparing their handling, sensitivity as well as selectivity against the established miRNA isolation and detection methods.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D0TB02165B</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D0TB02165B</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D0TB02165B</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>664</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">664</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Bulut, Yusuf</style></author><author><style face="normal" font="default" size="100%">Czympiel, Lisa</style></author><author><style face="normal" font="default" size="100%">Weißing, René</style></author><author><style face="normal" font="default" size="100%">Nahrstedt, Vanessa</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Grosch, Matthias</style></author><author><style face="normal" font="default" size="100%">Raauf, Aida</style></author><author><style face="normal" font="default" size="100%">Verma, Anjneya</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Piezo-enhanced Activation of Dinitrogen for Room Temperature Production of Ammonia</style></title><secondary-title><style face="normal" font="default" size="100%">Nanotechnology</style></secondary-title></titles><dates><year><style face="normal" font="default" size="100%">2021</style></year></dates><isbn><style face="normal" font="default" size="100%">0957-4484</style></isbn><abstract><style face="normal" font="default" size="100%">The catalytic conversion of nitrogen to ammonia remains an energy-intensive process, demanding advanced concepts for nitrogen fixation. The major obstacle of nitrogen fixation lies in the intrinsically high bond energy (941 kJ/mol) and the absence of a permanent dipole in N≡N molecule. This kinetic barrier is addressed in this study by an efficient piezo-enhanced gold catalysis as demonstrated by the room temperature reduction of dinitrogen into ammonia. Nanoscopic gold clusters were immobilized on thin film piezoelectric support potassium sodium niobate (K0.5Na0.5NbO3, KNN) by chemical vapor deposition of a new Au(III) precursor [Me2Au(PyTFP)(H2O)] 1 (PyTFP = (Z)-3,3,3-trifluoro-1-(pyridin-2-yl)-prop-1-en-2-olate) that exhibited high volatility (60 °C, 10-3 mbar) and clean decomposition mechanism to deliver pure elemental gold. The gold-functionalized KNN films served as an efficient catalytic system for ammonia production with a Faradaic efficiency of 18.9% driven by ultrasonic actuation. Our results show that the spontaneous polarization of piezoelectric materials under external electrical fields augments the sluggish electron transfer kinetics by creating instant dipoles in adsorbed N2 molecules to deliver a piezo-enhanced catalytic system for sustained activation of dinitrogen molecules.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">http://iopscience.iop.org/article/10.1088/1361-6528/ac1a96</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>644</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">644</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dilamian, Mandana</style></author><author><style face="normal" font="default" size="100%">Joghataei, Majid</style></author><author><style face="normal" font="default" size="100%">Ashrafi, Zahra</style></author><author><style face="normal" font="default" size="100%">Bohr, Christoph</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Maleki, Hajar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">From 1D electrospun nanofibers to advanced multifunctional fibrous 3D aerogels</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Materials Today</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">100964</style></pages><volume><style face="normal" font="default" size="100%">22</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Fibrous aerogel</style></keyword><keyword><style face="normal" font="default" size="100%">Nanofiber</style></keyword><keyword><style face="normal" font="default" size="100%">Fibrous mat</style></keyword><keyword><style face="normal" font="default" size="100%">Electrospinning</style></keyword><keyword><style face="normal" font="default" size="100%">3D structure</style></keyword><keyword><style face="normal" font="default" size="100%">Freeze-casting</style></keyword><keyword><style face="normal" font="default" size="100%">Ice-templating</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/03/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2352-9407</style></isbn><abstract><style face="normal" font="default" size="100%">A new class of aerogels based on advanced 1D nanofibers have emerged recently. What makes this class of aerogel, known as “fibrous aerogels,” to stand out from those obtained from traditional sol-gel processed and supercritical drying method is its ease of processability, versatility, and multifunctionality. The fibrous aerogels not only hold intrinsic aerogels properties such as porosity, low density, and high specific surface area but also benefit from the inherent features of electrospun nanofibers, dual micro-/nanoporous structures, and fragmented fibrillar entanglement in the nano-/microscale. Besides, the versatility in the electrospinning and freeze-casting techniques render the process with the possibility of selecting a wide range of materials as the building blocks as well as tunable porosity and different geometrical shapes, which lead to superior mechanical properties and additional functionalities. This review has highlighted the historical developments, design principles, recent breakthroughs in emerging applications, and a fresh perspective for upcoming research in the field of fibrous aerogels.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S2352940721000299</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.apmt.2021.100964</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>668</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">668</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chernozem, Roman V.</style></author><author><style face="normal" font="default" size="100%">Romanyuk, Konstantin N.</style></author><author><style face="normal" font="default" size="100%">Grubova, Irina</style></author><author><style face="normal" font="default" size="100%">Chernozem, Polina V.</style></author><author><style face="normal" font="default" size="100%">Surmeneva, Maria A.</style></author><author><style face="normal" font="default" size="100%">Mukhortova, Yulia R.</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kholkin, Andrei L.</style></author><author><style face="normal" font="default" size="100%">Neyts, Erik</style></author><author><style face="normal" font="default" size="100%">Parakhonskiy, Bogdan</style></author><author><style face="normal" font="default" size="100%">Skirtach, Andre G.</style></author><author><style face="normal" font="default" size="100%">Surmenev, Roman A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced piezoresponse and surface electric potential of hybrid biodegradable polyhydroxybutyrate scaffolds functionalized with reduced graphene oxide for tissue engineering</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><pages><style face="normal" font="default" size="100%">106473</style></pages><keywords><keyword><style face="normal" font="default" size="100%">polyhydroxybutyrate</style></keyword><keyword><style face="normal" font="default" size="100%">reduced graphene oxide</style></keyword><keyword><style face="normal" font="default" size="100%">scaffolds</style></keyword><keyword><style face="normal" font="default" size="100%">surface potential</style></keyword><keyword><style face="normal" font="default" size="100%">piezoelectric response</style></keyword><keyword><style face="normal" font="default" size="100%">modelling</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/08/31/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><abstract><style face="normal" font="default" size="100%">Piezoelectricity is considered one of the key functionalities in biomaterials to boost bone tissue regeneration, however, integrating biocompatibility, biodegradability and 3D structure with pronounced piezoresponse remains a material challenge. Herein, novel hybrid biocompatible 3D scaffolds based on biodegradable poly(3-hydroxybutyrate) (PHB) and reduced graphene oxide (rGO) flakes have been developed. Nanoscale insights revealed a more homogenous distribution and superior surface potential values of PHB fibers (33 ± 29mV) with increasing rGO content up to 1.0wt.% (314 ± 31mV). The maximum effective piezoresponse was detected at 0.7wt.% rGO content, demonstrating 2.5 and 1.7 times higher out-of-plane and in-plane values, respectively, than that for pure PHB fibers. The rGO addition led to enhanced zigzag chain formation between paired lamellae in PHB fibers. In contrast, a further increase in rGO content reduced the α-crystal size and prevented zigzag chain conformation. A corresponding model explaining structural and molecular changes caused by rGO addition in electrospun PHB fibers is proposed. In addition, finite element analysis revealed a negligible vertical piezoresponse compared to lateral piezoresponse in uniaxially oriented PHB fibers based on α-phase (P212121 space group). Thus, the present study demonstrates promising results for the development of biodegradable hybrid 3D scaffolds with an enhanced piezoresponse for various tissue engineering applications.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S221128552100728X</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.nanoen.2021.106473</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>676</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">676</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Brune, Veronika</style></author><author><style face="normal" font="default" size="100%">Raydan, Nidal</style></author><author><style face="normal" font="default" size="100%">Sutorius, Anja</style></author><author><style face="normal" font="default" size="100%">Hartl, Fabian</style></author><author><style face="normal" font="default" size="100%">Purohit, Bhagyesh</style></author><author><style face="normal" font="default" size="100%">Gahlot, Sweta</style></author><author><style face="normal" font="default" size="100%">Bargiela, Pascal</style></author><author><style face="normal" font="default" size="100%">Burel, Laurence</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Atamtürk, Ufuk</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Mishra, Shashank</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Single source precursor route to nanometric tin chalcogenides</style></title><secondary-title><style face="normal" font="default" size="100%">Dalton Transactions</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Dalton Transactions</style></full-title></periodical><dates><year><style face="normal" font="default" size="100%">2021</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">1477-9226</style></isbn><abstract><style face="normal" font="default" size="100%">Low-temperature solution phase synthesis of nanomaterials using designed molecular precursors enjoys tremendous advantages over traditional high-temperature solid-state synthesis. These include atomic-level control over stoichiometry, homogeneous elemental dispersion and uniformly distributed nanoparticles. For exploiting these advantages, however, rationally designed molecular complexes having certain properties are usually required. We report here the synthesis and complete characterization of new molecular precursors containing direct Sn–E bonds (E = S or Se), which undergo facile decomposition under different conditions (solid/solution phase, thermal/microwave heating, single/mixed solvents, varying temperatures, etc.) to afford phase-pure or mixed-phase tin chalcogenide nanoflakes with defined ratios.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D1DT02964A</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D1DT02964A</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D1DT02964A</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>663</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">663</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Brune, Veronika</style></author><author><style face="normal" font="default" size="100%">Grosch, Matthias</style></author><author><style face="normal" font="default" size="100%">Weißing, René</style></author><author><style face="normal" font="default" size="100%">Hartl, Fabian</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Mishra, Shashank</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of the choice of precursors on the synthesis of two-dimensional transition metal dichalcogenides</style></title><secondary-title><style face="normal" font="default" size="100%">Dalton Transactions</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Dalton Transactions</style></full-title></periodical><dates><year><style face="normal" font="default" size="100%">2021</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">1477-9226</style></isbn><abstract><style face="normal" font="default" size="100%">The interest in transition metal dichalcogenides (TMDCs; MEy/2; M = transition metal; E = chalcogenide, y = valence of the metal) has grown exponentially across various science and engineering disciplines due to their unique structural chemistry manifested in a two-dimensional lattice that results in extraordinary electronic and transport properties desired for applications in sensors, energy storage and optoelectronic devices. Since the properties of TMDCs can be tailored by changing the stacking sequence of 2D monolayers with similar or dis-similar materials, a number of synthetic routes essentially based on the disintegration of bulk (e.g., chemical exfoliation) or the integration of atomic constituents (e.g., vapor phase growth) have been explored. Despite a large body of data available on the chemical synthesis of TMDCs, experimental strategies with high repeatability of control over film thickness, phase and compositional purity remain elusive, which calls for innovative synthetic concepts offering, for instance, self-limited growth in the z-direction and homogeneous lateral topography. This review summarizes the recent conceptual advancements in the growth of layered van der Waals TMDCs from both mixtures of metal and chalcogen sources (multi-source precursors; MSPs) and from molecular compounds containing metals and chalcogens in one starting material (single-source precursor; SSPs). The critical evaluation of the strengths, limitations and opportunities of MSP and SSP approaches is provided as a guideline for the fabrication of TMDCs from commercial and customized molecular precursors. For example, alternative synthetic pathways using tailored molecular precursors circumvent the challenges of differential nucleation and crystal growth kinetics that are invariably associated with conventional gas phase chemical vapor transport (CVT) and chemical vapor deposition (CVD) of a mixture of components. The aspects of achieving high compositional purity and alternatives to minimize competing reactions or side products are discussed in the context of efficient chemical synthesis of TMDCs. Moreover, a critical analysis of the potential opportunities and existing bottlenecks in the synthesis of TMDCs and their intrinsic properties is provided.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/D1DT01397A</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D1DT01397A</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/D1DT01397A</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>671</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">671</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bohr, Christoph</style></author><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Triaxial Perovskite Composite Fibers – Spinning the Way to Flexible Solar Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">core-shell</style></keyword><keyword><style face="normal" font="default" size="100%">electrospinning</style></keyword><keyword><style face="normal" font="default" size="100%">halide perovskites</style></keyword><keyword><style face="normal" font="default" size="100%">triaxial fibers</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/09/12</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1438-1656</style></isbn><abstract><style face="normal" font="default" size="100%">Hybrid halide perovskites have made significant progress in achievably high photoconversion efficiencies (&gt; 25%) and stability as a function of their chemical engineering realized by isomorphous substitution at all three sites in AMX3 composition. Whereas the focus of current research lies on planar (2D) devices, this work brings forth an innovative structural engineering concept based on direct electrospinning of the three major perovskite solar cell components namely photoabsorber, hole- and electron- transport materials as continuous single triaxial fibers of µm radial dimensions (&lt; 5 µm). These perovskite fibers lay the foundation of materials engineering for fabricating tiny solar cells, which can either be woven into fabrics or incorporated as single fibers to power wearables and a variety of devices or sensors, forming the internet of things. The structures of the here presented coaxial CuSCN/MAPbI3 (MA=CH3NH3 +) and triaxial CuSCN/MAPbI3/ZnO-Zn(OAc)2 composite fibers were verified by X-ray diffraction data and electron microscopy coupled with energy dispersive spectroscopy and cross-sectional analysis with focussed ion beam. This work demonstrates the first report where the entire PV device and material configuration is achieved as concentric axial cables fabricated via single-step electrospinning process. This article is protected by copyright. All rights reserved.</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202100773</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202100773</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202100773</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202100773</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2021/09/15</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>669</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">669</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bandar Abadi, Mohsen</style></author><author><style face="normal" font="default" size="100%">Weissing, Rene</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Demidov, Yan</style></author><author><style face="normal" font="default" size="100%">Auer, Jaqueline</style></author><author><style face="normal" font="default" size="100%">Ghazanfari, Samaneh</style></author><author><style face="normal" font="default" size="100%">Anasori, Babak</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Maleki, Hajar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nacre-Mimetic, Mechanically Flexible, and Electrically Conductive Silk Fibroin-MXene Composite Foams as Piezoresistive Pressure Sensors</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></full-title></periodical><pages><style face="normal" font="default" size="100%">34996-35007</style></pages><volume><style face="normal" font="default" size="100%">13</style></volume><number><style face="normal" font="default" size="100%">29</style></number><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/07/28</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsami.1c09675</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsami.1c09675</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>666</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">666</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Atamtürk, Ufuk</style></author><author><style face="normal" font="default" size="100%">Brune, Veronika</style></author><author><style face="normal" font="default" size="100%">Mishra, Shashank</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Vapor Phase Synthesis of SnS Facilitated by Ligand-Driven “Launch Vehicle” Effect in Tin Precursors</style></title><secondary-title><style face="normal" font="default" size="100%">Molecules</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Molecules</style></full-title></periodical><volume><style face="normal" font="default" size="100%">26</style></volume><number><style face="normal" font="default" size="100%">17</style></number><keywords><keyword><style face="normal" font="default" size="100%">single-source precursor</style></keyword><keyword><style face="normal" font="default" size="100%">chemical vapor deposition</style></keyword><keyword><style face="normal" font="default" size="100%">tin sulfide</style></keyword><keyword><style face="normal" font="default" size="100%">tertiary butyl sulfide</style></keyword><keyword><style face="normal" font="default" size="100%">single-crystal structure</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year></dates><isbn><style face="normal" font="default" size="100%">1420-3049</style></isbn><abstract><style face="normal" font="default" size="100%">Extraordinary low-temperature vapor-phase synthesis of SnS thin films from single molecular precursors is attractive over conventional high-temperature solid-state methods. Molecular-level processing of functional materials is accompanied by several intrinsic advantages such as precise control over stoichiometry, phase selective synthesis, and uniform substrate coverage. We report here on the synthesis of a new heteroleptic molecular precursor containing (i) a thiolate ligand forming a direct Sn-S bond, and (ii) a chelating O^N^N-donor ligand introducing a “launch vehicle”-effect into the synthesized compound, thus remarkably increasing its volatility. The newly synthesized tin compound [Sn(SBut)(tfb-dmeda)] 1 was characterized by single-crystal X-ray diffraction analysis that verified the desired Sn:S ratio in the molecule, which was demonstrated in the direct conversion of the molecular complex into SnS thin films. The multi-nuclei (1H, 13C, 19F, and 119Sn) and variable-temperature 1D and 2D NMR studies indicate retention of the overall solid-state structure of 1 in the solution and suggest the presence of a dynamic conformational equilibrium. The fragmentation behavior of 1 was analyzed by mass spectrometry and compared with those of homoleptic tin tertiary butyl thiolates [Sn(SBut)2] and [Sn(SBut)4]. The precursor 1 was then used to deposit SnS thin films on different substrates (FTO, Mo-coated soda-lime glass) by CVD and film growth rates at different temperatures (300–450 °C) and times (15–60 min), film thickness, crystalline quality, and surface morphology were investigated.</style></abstract><urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.3390/molecules26175367</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>658</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">658</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Arroub, Karim</style></author><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thermoresponsive Poly (N-Isopropylacrylamide)/Polycaprolacton Nanofibrous Scaffolds for Controlled Release of Antibiotics</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2100221</style></pages><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">antibiotics</style></keyword><keyword><style face="normal" font="default" size="100%">controlled release</style></keyword><keyword><style face="normal" font="default" size="100%">nanofibers</style></keyword><keyword><style face="normal" font="default" size="100%">thermoresponsive polymers</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style face="normal" font="default" size="100%">2021/04/08</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1438-1656</style></isbn><abstract><style face="normal" font="default" size="100%">Smart antibacterial materials capable of releasing antibiotic drugs upon exposure to external triggers are highly desired for various medical applications. Herein, the fabrication of thermosensitive drug-loaded core?shell nanofibers using the electrospinning technique combined with in?situ UV photopolymerization is reported on. The electrospinning method is used for shaping the core structure comprising biodegradable polymer polycaprolactone (PCL). The PCL fibers are coated with the temperature-responsive poly-N-isopropylacrylamide (PNIPAM) via a UV photopolymerization process that allows to precisely control the shell thickness as verified by transmission electron microscope (TEM) analysis. The temperature-dependent switchable wettability of prepared core?shell fibers is investigated and visualized though water contact angle measurements below and above the lower critical solution temperature. Loading of the antibiotic drug doxycycline hyclate (Doxy) in the PCL core nanofibers results in drug-encapsulating fiber meshes that allow diffusion of drug molecules through the PNIPAM shell in a temperature-dependent manner. The antibacterial activity is examined using Gram-negative Escherichia coli (E. coli) as well as Gram-positive Staphylococcus aureus (S. aureus) bacteria. The results demonstrate the high suitability of prepared biocompatible electrospun core?shell PCL/PNIPAM nanofibers as carriers for antibiotic drugs with temperature-sensitive release behavior.</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202100221</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202100221</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202100221</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202100221</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2021/06/24</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>589</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">589</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zhen, Yichao</style></author><author><style face="normal" font="default" size="100%">Sa, Rongjian</style></author><author><style face="normal" font="default" size="100%">Zhou, Kaiqiang</style></author><author><style face="normal" font="default" size="100%">Ding, Lingyi</style></author><author><style face="normal" font="default" size="100%">Chen, Yang</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hong, Zhensheng</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Fujian Normal Univ, Coll Phys &amp; Energy, Fujian Prov Key Lab Quantum Manipulat &amp; New Energ, Fuzhou 350117, Fujian, Peoples R China&#xD;Minjiang Univ, Inst Oceanog, Fuzhou 350108, Fujian, Peoples R China&#xD;Fujian Prov Collaborat Innovat Ctr Adv High Field, Fuzhou 350117, Peoples R China&#xD;Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Breaking the limitation of sodium-ion storage for nanostructured carbon anode by engineering desolvation barrier with neat electrolytes</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nano Energy</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><alt-periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></alt-periodical><pages><style face="normal" font="default" size="100%">104895</style></pages><volume><style face="normal" font="default" size="100%">74</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Sodium ion battery, Nanocarbon, Ether electrolytes, Desolvation barrier</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/08/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000547341500005</style></accession-num><abstract><style face="normal" font="default" size="100%">The innate limitation of sodium-ion storage for nanostrutured carbon anode can be breaken by neat ether electrolytes. The strong adsorption and decomposition of electrolytes on graphene planes is remarkably reduced in ether solvents due to the small Na+ desolvation barrier and decreased Gibbs free energies of adsorption. Download : Download high-res image (322KB)Download : Download full-size image</style></abstract><notes><style face="normal" font="default" size="100%">Mi3wj&#xD;Times Cited:2&#xD;Cited References Count:66</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S2211285520304523</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.nanoen.2020.104895</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>612</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">612</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Verma, Anjneya</style></author><author><style face="normal" font="default" size="100%">Panayanthatta, Namanu</style></author><author><style face="normal" font="default" size="100%">Ichangi, Arun</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Montes, Laurent</style></author><author><style face="normal" font="default" size="100%">Bano, Edwige</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Interdependence of Piezoelectric Coefficient and Film Thickness in LiTaO3 Cantilevers</style></title><secondary-title><style face="normal" font="default" size="100%">J. Am. Ceram. Soc.</style></secondary-title></titles><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">LiTaO3, perovskite, piezoceramics, thick films, vibrational energy harvesters</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/12/02/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0002-7820</style></isbn><abstract><style face="normal" font="default" size="100%">Electromechanical energy demands homogenous thick films of piezoceramics with sufficiently large piezoelectric constant and reproducible performance. Single‐phase LiTaO3 films deposited by sol‐gel processing have been fabricated as cantilevers to investigate the interdependence of dielectric and piezoelectric properties as a function of film thickness. Phase pure LiTaO3 films with varying thickness in the range of 2.07‐4.37 µm on stainless steel substrates were obtained after calcination of samples at 650 °C. The relative permittivity of optimized spin‐coated films peaked at 479.73 (1 kHz), whereas the piezoelectric coefficient (d33 mode) determined by piezo force microscopy was in the range of 21‐24 pm/V. The effect of poling was studied through the butterfly and phase curves. A figure of merit up to 3.29 (10‐18 m2/V2) was determined for cantilever devices, which were able to generate a peak‐to‐peak voltage of 0.046‐0.15 V using a 1 MΩ resistor as an impedance load at a fixed acceleration of 1.5 m/s2. While the power density was in the range of ~ 4‐20x10‐9 W/m3, increased with the increasing film thickness. The leakage current density decreased in the range of 4x10‐5‐6x10‐7 A/m2 in the same direction. As both ferroelectric and piezoelectric properties of LiTaO3 films are dependent on film thickness, an optimal energy conversion efficiency was obtained for a thickness of ~3 µm. Furthermore, these devices were tested up to a temperature of 150 °C for voltage generation. Given the need for lead‐free piezoelectric materials for environmental applications, these LiTaO3 cantilevers are very promising for vibrational energy harvester applications especially due to their cost effectiveness, small size, stability at higher temperatures, and repeatable properties which makes them suitable for MEMS devices for industrial applications.</style></abstract><label><style face="normal" font="default" size="100%">Verma2020Dec</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1111/jace.17606</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1111/jace.17606</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>596</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">596</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Jung, Eunhwan</style></author><author><style face="normal" font="default" size="100%">Haddad, Jinane</style></author><author><style face="normal" font="default" size="100%">Kulkarni, Ashish</style></author><author><style face="normal" font="default" size="100%">Öz, Senol</style></author><author><style face="normal" font="default" size="100%">Choi, Heechae</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Chakraborty, Sudip</style></author><author><style face="normal" font="default" size="100%">Kirchartz, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Understanding the interplay of stability and efficiency in A-site engineered lead halide perovskites</style></title><secondary-title><style face="normal" font="default" size="100%">APL Mater.</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">070901</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">7</style></number><section><style face="normal" font="default" size="100%">070901</style></section><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/07/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2166-532X</style></isbn><abstract><style face="normal" font="default" size="100%">Organic–inorganic hybrid lead halide perovskites have gained significant attention as light-harvesting materials in thin-film photovoltaics due to their exceptional optoelectronic properties and simple fabrication process. The power conversion efficiency of perovskite solar cells (PSCs) has surged beyond 25% in a short time span. Their transition to commercial market is a “work in progress” due to limited long-term operational stability and the persisting environmental concern due to the presence of lead. Comprehensive investigations on the interplay of material composition and interfacial effects on the device performance of PSCs based on methylammonium lead iodide have shown the crucial role of an A-site cation in incipient deterioration of the material through external stimuli (moisture, light, oxygen, or heat). Consequently, a partial or complete replacement of A-site cations by up to four isoelectronic substituents has resulted in many new perovskite compositions. The correlations between the chemical composition and the optoelectronic properties are, however, not always easy to determine. A-site cation management is governed by stability and charge neutrality of the lattice, and the choices include Cs+-cations and organic cations such as CH3NH3+ or CH(NH2)2+ and combinations thereof. Since the size of the cations is an important structural parameter, an adequate compositional engineering of the A-site could effectively optimize the stability by reducing non-radiative defect sites and enhancing carrier lifetimes. This Perspective reflects on the experimental strategies for A-site cation management and their direct impact on the stability and device performance. It also highlights the opportunities and challenges for further research and industrial commercialization of PSCs.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1063/5.0011851</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1063/5.0011851</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>602</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">602</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Szymura, Annika</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Horn, Mareike</style></author><author><style face="normal" font="default" size="100%">Neundorf, Ines</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;Univ Cologne, Inst Biochem, Zulpicherstr 47a, D-50674 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Multivalent magnetic nanoaggregates with unified antibacterial activity and selective uptake of heavy metals and organic pollutants</style></title><secondary-title><style face="normal" font="default" size="100%">J. Mol. Liq.</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Mol Liq</style></alt-title></titles><pages><style face="normal" font="default" size="100%">114002</style></pages><volume><style face="normal" font="default" size="100%">317</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Magnetic nanoaggregates, Polyacrylic acid, L-Cysteine, 1-Hexadecyl-3-vinyl imidazolium bromide, Ni(II) ions, Methylene blue, Antibacterial activity</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/11/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0167-7322</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000580655700068</style></accession-num><abstract><style face="normal" font="default" size="100%">Covalently functionalized magnetite (Fe3O4) nanoaggregates carrying an imidazolium-derivative (1-hexadecyl-3-vinyl imidazolium bromide, HDVI) and L-cysteine (L-Cys) as surface ligands act as bimodal water-treatment particulate agents (HDVI@L-Cys@PAA@Fe3O4) with high antibacterial efficacy and specific surface adsorption properties. For covalent conjugation of HDVI the polyacrylic acid (PAA)-coated magnetite nanocrystals (PAA@Fe3O4) were functionalized with L-cysteine via carbodiimide coupling (L-Cys@PAA@Fe3O4) having terminal -SH groups that were used for thiol-ene click chemistry. The carefully performed series of water-remediation tests with magnetically separable HDVI@L-Cys@PAA@Fe3O4 nanoaggregates demonstrated their high efficiency in the concomitant removal transition metal ions and organic pollutant without losing the antibacterial effect. Time-dependent adsorption experiments showed high degree (&gt;90%) of trapping and removal activity. Antibacterial action of the HDVI@L-Cys@PAA@Fe3O4 nanoaggregates originates from the amphiphilic structure of HDVI groups capable of penetrating the bacterial cell walls. The presence of surface-bound ligands and conversion efficiency of carbodiimide and click chemistry protocol was verified by FT-IR, elemental and thermogravimetric analysis. The phase, composition morphology and surface charge of nanoaggregates were examined by XRD, SEM/TEM and zeta potential studies, respectively. The experimental findings reported here represent a conceptual advancement in the state-of-the-art magnetic beads developed for water purification or remediation purposes. Our results evidently demonstrate that nanoaggregates are highly effective in unifying bactericidal activity against different microorganism with heavy metal and organic pollutant removal properties. Graphical abstract Download : Download high-res image (372KB)Download : Download full-size image</style></abstract><label><style face="normal" font="default" size="100%">Szymura2020Nov</style></label><notes><style face="normal" font="default" size="100%">Oe6rm&#xD;Times Cited:0&#xD;Cited References Count:64</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0167732220332864</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.molliq.2020.114002</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>610</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">610</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Surmenev, R. A.</style></author><author><style face="normal" font="default" size="100%">Chernozem, R. V.</style></author><author><style face="normal" font="default" size="100%">Skirtach, A. G.</style></author><author><style face="normal" font="default" size="100%">Bekareva, A. S.</style></author><author><style face="normal" font="default" size="100%">Leonova, L. A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Ivanov, Yu. F.</style></author><author><style face="normal" font="default" size="100%">Surmeneva, M. A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hydrothermal synthesis of barium titanate nano/microrods and particle agglomerates using a sodium titanate precursor</style></title><secondary-title><style face="normal" font="default" size="100%">Ceram. Int.</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">hydrothermal synthesis, barium titanate, precursor, microrods, nanowires, alkalinity</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/12/05/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0272-8842</style></isbn><abstract><style face="normal" font="default" size="100%">The ion exchange processes and phase formation were studied by varying the properties of 1D barium titanate nanostructures. Temperature-, time- and alkalinity-dependent experiments were performed to study the BaTiO3 formation mechanism involving the generation of chemical sites which induced in situ transformation and dissolution-precipitation reactions occurring in a hydrothermal treatment procedure. As a result of the hydrothermal synthesis, BaTiO3 nano- and microrods with surface nanomaces and nanoparticle aggregates were formed in the temperature range of 160 to 210°C, alkalinity range of 0.025 to 0.15 M and time range of 45 to 90 min. X-ray diffraction analysis revealed a significant increase in BaTiO3 material purity with increasing alkalinity from 0.025 to 0.15 M, even after a synthesis time of 45 min. In turn, Raman spectroscopy results showed that an increase in the synthesis time allowed not only BaTiO3 purity improvement, but also its phase composition control. The tetragonal phase of BaTiO3 was clearly observed after 6 h of hydrothermal synthesis at 210°C and various alkalinities (from 0.025 to 0.15 M), while 45 and 90 min resulted in a mixture of cubic or tetragonal phases. Transmission electron microscopy demonstrated that BaTiO3 nanoparticles consisted of mainly tetragonal phases or a mixture of cubic and tetragonal phases, while BaTiO3 nano-/microrods preferably had cubic phases. Thus, variation of the temperature, time and alkalinity upon hydrothermal synthesis allowed the formation of BaTiO3 nano- and microstructures with different morphologies and phase compositions for diverse applications from biomedicine to microelectronics.</style></abstract><label><style face="normal" font="default" size="100%">Surmenev2020Dec</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0272884220336087</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.ceramint.2020.12.011</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>569</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">569</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Stadler, Daniel</style></author><author><style face="normal" font="default" size="100%">Hemmer, Eva</style></author><author><style face="normal" font="default" size="100%">Anasori, Babak</style></author><author><style face="normal" font="default" size="100%">Hood, Zachary D.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Mat Res Soc, Acad Affairs Comm, Warrendale, PA 15086 USA</style></auth-address><titles><title><style face="normal" font="default" size="100%">Career progression through professional engagement: The impact of MRS student-led activities</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Bulletin</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Mrs Bull</style></alt-title></titles><pages><style face="normal" font="default" size="100%">306-307</style></pages><volume><style face="normal" font="default" size="100%">45</style></volume><number><style face="normal" font="default" size="100%">4</style></number><section><style face="normal" font="default" size="100%">306</style></section><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">Apr</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0883-7694&#xD;1938-1425</style></isbn><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1557/mrs.2020.99</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1557/mrs.2020.99</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>579</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">579</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sekhar, Praveen K.</style></author><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Ojelere, Olusola</style></author><author><style face="normal" font="default" size="100%">Saha, Tonmoy Kumar</style></author><author><style face="normal" font="default" size="100%">Riheen, Manjurul Ahsan</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Washington State Univ Vancouver, Sch Engn &amp; Comp Sci, Nanomat &amp; Sensors Lab, Vancouver, WA 98686 USA&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Electrochemical Gas Sensor Integrated with Vanadium Monoxide Nanowires for Monitoring Low Concentrations of Ammonia Emission</style></title><secondary-title><style face="normal" font="default" size="100%">J. Electrochem. Soc.</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Electrochem Soc</style></alt-title></titles><pages><style face="normal" font="default" size="100%">027548</style></pages><volume><style face="normal" font="default" size="100%">167</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">animal feeding operations</style></keyword><keyword><style face="normal" font="default" size="100%">paper</style></keyword><keyword><style face="normal" font="default" size="100%">deposition</style></keyword><keyword><style face="normal" font="default" size="100%">feedlot</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/02/05/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1945-7111</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000517917200002</style></accession-num><abstract><style face="normal" font="default" size="100%">An electrochemical sensor for the detection of extremely low concentration of ammonia (1 part per billion, ppb) was fabricated by integrating vanadium monoxide (VOx; x = 0.8–1.2) nanowires on the platinum electrodes. The nanowire-based sensor responds at room temperature non-linearly to a staircase sequence of ammonia from 1 ppb to 100 ppb. The rise and fall time of the nanowire sensor was found to be 10 s and 9 s, respectively. While the immobilization of VO nanowires increased the electrochemical surface area, the defect rich and ionic nature of the VO surface (V2+O2−) facilitated the chemical interaction and adsorption of polar ammonia molecules as evident in the room temperature response of the VO@Pt amperometric electrochemical sensor. The availability of metal centered d-electrons and the semiconductor nature of vanadium monoxide lowered the interfacial resistance of the nanowire-modified sensor enabling the lower detection limit of ammonia. The sensor seems to respond to CH4, H2S and C3H6 as well although the NH3 response is nearly six-fold compared to these common interfering compounds. The results pave the way for a low-cost alternative paper-based sensor to monitor ammonia emissions primarily from confined animal feeding operations (CAFOs).</style></abstract><notes><style face="normal" font="default" size="100%">Kr9eu&#xD;Times Cited:2&#xD;Cited References Count:25</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1149/1945-7111/ab7114</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1149/1945-7111/ab7114</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>618</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">618</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Schütz, Markus B.</style></author><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Reversible Covalent Assembly of Nanoparticles through On-Surface Diels–Alder Reaction</style></title><secondary-title><style face="normal" font="default" size="100%">Langmuir</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1552-1558</style></pages><volume><style face="normal" font="default" size="100%">36</style></volume><number><style face="normal" font="default" size="100%">6</style></number><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/02/18</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">0743-7463</style></isbn><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.langmuir.9b02261</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.langmuir.9b02261</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>583</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">583</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Schütz, Markus B.</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Lê, Khan</style></author><author><style face="normal" font="default" size="100%">Valldor, Martin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanoparticle Arrays Having Directed Hybrid Topology via Covalent Self-Assembly of Iron Oxide and Silica Nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Appl. Nano Mater.</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">5936-5943</style></pages><volume><style face="normal" font="default" size="100%">2020</style></volume><number><style face="normal" font="default" size="100%">6</style></number><section><style face="normal" font="default" size="100%">5936</style></section><keywords><keyword><style face="normal" font="default" size="100%">iron oxide, click chemistry, silica nanoparticles, magnetic properties, imaging</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/05/28/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2574-0970&#xD;2574-0970</style></isbn><abstract><style face="normal" font="default" size="100%">Combining individual nanoparticles (NPs) of different chemical composition and surface chemistry offers an unexplored synthetic avenue for unifying different functionalities into a topologically defined hybrid structure. In this study, multiparticle architectures (α-Fe2O3@SiO2, α-Fe2O3@γ-Fe2O3) were fabricated by a directed self-assembly of nanoparticles carrying complementary surface ligands suitable for click chemistry. For this purpose, the surface-rooted hydroxyl groups of freshly prepared α-Fe2O, γ-Fe2O3, and SiO2 nanoparticles were utilized for facile conjugation of organic ligands, 4-(azidoacetyl)-catechol, and 10-undecynoic acid to subsequently perform copper catalyzed reactions. This work explores specific chemical interactions among functionalized nanoparticles of different sizes and compositions to create nanoparticle assemblies with hybrid topologies. Here, developed on-surface chemistry protocols demonstrate that chemical specificity known for click-chemistry protocols among molecular species is equally effective between the ligands grafted on the surface of nanoparticles. Owing to the presence of active ligands and their mutual binding affinities, architectures of nanoparticles with a high degree of symmetry and notable magnetic properties were obtained. The exterior of the nanoassembly presents active surface groups for further functionalization and attachment of modality such as the dual-mode magnetic resonance imaging. The morphology and crystalline nature of the NPs were investigated by transmission electron microscopy and X-ray diffraction analysis, whereas the active nature of the surface attached groups was determined by NMR, Fourier transform infrared, UV–vis, and ζ-potential measurements.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsanm.0c01097</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsanm.0c01097</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>605</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">605</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Schmidt-Verma, Anna K.</style></author><author><style face="normal" font="default" size="100%">Renner, Alexander M.</style></author><author><style face="normal" font="default" size="100%">Wilhelm, Michael</style></author><author><style face="normal" font="default" size="100%">Bohr, Christoph</style></author><author><style face="normal" font="default" size="100%">Goenuellue, Yakup</style></author><author><style face="normal" font="default" size="100%">Rudigier-Voigt, Eveline</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">High-Temperature Ultrahydrophobic Ceramic Coatings from Surface-Functionalized MgAl2O4 Nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">Adv. Eng. Mater.</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">2000738</style></pages><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><section><style face="normal" font="default" size="100%">2000738</style></section><keywords><keyword><style face="normal" font="default" size="100%">high-temperature stable, magnesium aluminum spinels, nanoparticles, superhydrophobic surfaces, titanium dioxide</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/08/17/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1438-1656</style></isbn><abstract><style face="normal" font="default" size="100%">Innovative coatings that can shield functional surfaces from environmental and temperature impact are essential to increase the life time of devices and reduce the maintenance costs. Superhydrophobic ceramic coatings with self‐cleaning properties and stability at high‐temperatures (up to 300 °C) are eco‐friendly alternative to aggressive surface‐cleaning agents. Despite the wide range of possible applications for hydrophobic surfaces, the practical implementation of currently used polymeric fluoro‐silanes is restricted by their low thermal stability, which is an essential figure of merit. Herein, a nonadhesive coating with an exceptionally low surface‐energy (contact angle ≈180°) is developed by chemical conjugation of MgAl2O4 spinel nanoparticles (NPs) with perfluorodecyltrichlorosilane (FDTS). The cross‐conjugation of FDTS and MgAl2O4 is substantiated by condensation reactions between the surface‐rooted hydroxyl groups and chloride ligands of fluorosilane. Compared with the coatings based on pure fluorosilanes, the FDTS@MgAl2O4 core‐shell particles unify optical transparency and high‐temperature stability imparted by spinel reinforcement with the superhydrophobicity induced by FDTS periphery. Addition of TiO2 NPs to MgAl2O4 sol unifies the ultrahydrophobicity of FDTS@MgAl2O4 with UV‐absorption properties of TiO2 to produce a new UV‐ and temperature‐resistant ultrahydrophobic coating system.</style></abstract><label><style face="normal" font="default" size="100%">Schmidt-Verma2020Aug</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/adem.202000738</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/adem.202000738</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>609</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">609</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Renner, Alexander M.</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Schlößer, Hans A.</style></author><author><style face="normal" font="default" size="100%">Szymura, Annika</style></author><author><style face="normal" font="default" size="100%">Roitsch, Stefan</style></author><author><style face="normal" font="default" size="100%">Wennhold, Kerstin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Institute of Inorganic Chemistry, University of Cologne, Greinstr. 6, 50939 Cologne, Germany.&#xD;Center for Molecular Medicine Cologne, University of Cologne, Robert-Koch-Str. 21, 50931 Cologne, Germany.&#xD;Institute of Physical Chemistry, University of Cologne, Greinstr. 6, 50939 Cologne, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Receptor-Mediated In Vivo Targeting of Breast Cancer Cells with 17α-Ethynylestradiol-Conjugated Silica-Coated Gold Nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">Langmuir</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">14819-14828</style></pages><volume><style face="normal" font="default" size="100%">2020</style></volume><number><style face="normal" font="default" size="100%">48</style></number><edition><style face="normal" font="default" size="100%">2020/11/20</style></edition><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/11/19/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0743-7463</style></isbn><accession-num><style face="normal" font="default" size="100%">33210924</style></accession-num><abstract><style face="normal" font="default" size="100%">Efficient therapies for breast cancer remain elusive because of the lack of strategies for targeted transport and receptor-mediated uptake of synthetic drug molecules by cancer cells. Conjugation of nanoparticles (NPs) with active targeting ligands enabling selective molecular recognition of antigens expressed on the surface of cancer cells is promising for localization and treatment of malignant cells. In this study, covalent attachment of synthetic estrogen 17α-ethynylestradiol on the silica (SiO2) shell of silica-gold NPs (SiO2@Au) was undertaken to improve the cancer-targeting ability of the nano-biotags. Chemical and structural analysis of the bioconjugates examined in solution (UV–vis and ξ-potential) and solid state (Fourier transform infrared spectroscopy, X-ray diffractometry, and transmission electron microscopy) confirmed the identity of the carrier particles and surface-bound ligands. The mesoporous silica shell served as a reservoir for anticancer drugs (doxorubicin and quercetin) and to facilitate covalent attachment of receptor molecules by click chemistry protocols. The chemoselective recognition between the nanoconjugates and cell membranes was successfully demonstrated by the accumulation of nanoprobes in the tumor tissue of mice with subcutaneous breast cancer, whereas healthy cells were unaffected. The drug release studies showed sustained release kinetics over several weeks. These findings elaborate the exceptional selectivity and potential of estrogen-coated nano-biolabels in efficient diagnosis and detection of breast cancer cells.</style></abstract><label><style face="normal" font="default" size="100%">Renner2020Nov</style></label><notes><style face="normal" font="default" size="100%">Renner, Alexander M&#xD;Ilyas, Shaista&#xD;Schlosser, Hans A&#xD;Szymura, Annika&#xD;Roitsch, Stefan&#xD;Wennhold, Kerstin&#xD;Mathur, Sanjay&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;Langmuir. 2020 Dec 8;36(48):14819-14828. doi: 10.1021/acs.langmuir.0c02820. Epub 2020 Nov 19.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acs.langmuir.0c02820</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.langmuir.0c02820</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>588</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">588</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Queraltó, Albert</style></author><author><style face="normal" font="default" size="100%">György, Enikö</style></author><author><style face="normal" font="default" size="100%">Ivan, Raluca</style></author><author><style face="normal" font="default" size="100%">Pérez del Pino, Ángel</style></author><author><style face="normal" font="default" size="100%">Frohnhoven, Robert</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Enhanced UV-Vis Photodegradation of Nanocomposite Reduced Graphene Oxide/Ferrite Nanofiber Films Prepared by Laser-Assisted Evaporation</style></title><secondary-title><style face="normal" font="default" size="100%">Crystals</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">271</style></pages><volume><style face="normal" font="default" size="100%">10</style></volume><number><style face="normal" font="default" size="100%">4</style></number><section><style face="normal" font="default" size="100%">271</style></section><keywords><keyword><style face="normal" font="default" size="100%">electrospinning, MAPLE, nanofibers, photodegradation, graphene oxide</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/04//</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2073-4352</style></isbn><abstract><style face="normal" font="default" size="100%">Nanocomposite films of rGO/MFeO3 (M = Bi, La) nanofibers were grown by matrix-assisted pulsed laser evaporation of frozen target dispersions containing GO platelets and MFeO3 nanofibers. Electron microscopy investigations confirmed the successful fabrication of MFeO3 nanofibers by electrospinning Part of nanofibers were broken into shorter units, and spherical nanoparticles were formed during laser processing. Numerical simulations were performed in order to estimate the maximum temperature values reached by the nanofibers during laser irradiation. X-ray diffraction analyses revealed the formation of perovskite MFeO3 phase, whereas secondary phases of BiFeO3 could not be completely avoided, due to the high volatility of bismuth. XPS measurements disclosed the presence of metallic bismuth and Fe2+ for BiFeO3, whereas La2(CO3)3 and Fe2+ were observed in case of LaFeO3 nanofibers. High photocatalytic efficiencies for the degradation of methyl orange were achieved for nanocomposite films, both under UV and visible light irradiation conditions. Degradation values of up to 70% after 400 min irradiation were obtained for rGO/LaFeO3 nanocomposite thin layers, with weights below 10 µg, rGO platelets acting as reservoirs for photoelectrons generated at the surface of MFeO3.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.mdpi.com/2073-4352/10/4/271</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.3390/cryst10040271</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>611</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">611</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Podhorsky, Jan</style></author><author><style face="normal" font="default" size="100%">Babiak, Michal</style></author><author><style face="normal" font="default" size="100%">Pinkas, Jiri</style></author><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Moravec, Zdenek</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">New mixed-ligand organoaluminum heteroarylalkenolates</style></title><secondary-title><style face="normal" font="default" size="100%">Polyhedron</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">114953</style></pages><volume><style face="normal" font="default" size="100%">194</style></volume><section><style face="normal" font="default" size="100%">114953</style></section><keywords><keyword><style face="normal" font="default" size="100%">aluminum, heteroarylalkenolate, alanes, metal organic, crystallography</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/12/03/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0277-5387</style></isbn><abstract><style face="normal" font="default" size="100%">We have successfully synthesized and structurally characterized eight novel aluminum compounds with N,O-β-heteroarylalkenolate ligands (L) containing a CF3 group. The reactions of 3,3,3-trifluoro(dimethyl-1,3-oxazol-2-yl)propen-2-ol (H-DMOTFP), 3,3,3-trifluoro(pyridin-2-yl)propen-2-ol (H-PyTFP), and 3,3,3-trifluoro(1,3-benzthiazol-2-yl)propen-2-ol (H-BTTFP) with chloroalanes R2AlCl and RAlCl2 (R = Et, iBu) in dry aprotic solvents provided complexes displaying several types of molecular structures. Effects of ligand, solvent, and crystallization conditions were investigated. The most common and stable products were chloride complexes [AlCl(L)2] with five-coordinated aluminum centers represented by [AlCl(DMOTFP)2] (1) and [AlCl(PyTFP)2] (2). A six-coordinated aluminum complex with a coordinated THF was obtained as [AlCl(THF)(PyTFP)2] (2⋅THF). Complexes with preserved alkyl groups [AlR(L)2] were isolated as [AlEt(BTTFP)2] (3) and [AliBu(DMOTFP)2] (4). An intermolecular rearrangement led to an ionic complex [Al(PyTFP)2(THF)2][iBuAlCl3] (5). In the reactions of H-BTTFP, the complex 3 with two ligands, as well as molecules [AlRCl(L)] with only one ligand attached were characterized as [AlEtCl(BTTFP)] (6) and [AliBuCl(BTTFP)] (7). The thermal properties of obtained complexes were investigated by TG/DSC and HT/XRD analyses. Graphical abstract A series of reactions between alkylaluminium chlorides and trifluoroacetonylazine-based N,O-β-heteroarylalkenolates, depending on the reaction conditions, provided eight new complexes. Aluminium centers have different coordination numbers and form various polyhedra. Thermal processing of obtained compounds leads to alumina. Download : Download high-res image (49KB)Download : Download full-size image</style></abstract><label><style face="normal" font="default" size="100%">Podhorsky2020Dec</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0277538720306100</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.poly.2020.114953</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>581</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">581</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pal, Shaili</style></author><author><style face="normal" font="default" size="100%">Kumar, Sunil</style></author><author><style face="normal" font="default" size="100%">Verma, Alkadevi</style></author><author><style face="normal" font="default" size="100%">Kumar, Ajay</style></author><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Prakash, Rajiv</style></author><author><style face="normal" font="default" size="100%">Sinha, Indrajit</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Banaras Hindu Univ, Dept Chem, Indian Inst Technol, Varanasi 221005, Uttar Pradesh, India&#xD;Rewa Engn Coll, Dept Chem, Rewa 486002, India&#xD;Banaras Hindu Univ, Sch Mat Sci &amp; Technol, Indian Inst Technol, Varanasi 221005, Uttar Pradesh, India&#xD;Univ Cologne, Inst Inorgan Chem, Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Development of magnetically recyclable visible light photocatalysts for hydrogen peroxide production</style></title><secondary-title><style face="normal" font="default" size="100%">Mater. Sci. Semicond. Process.</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Mat Sci Semicon Proc</style></alt-title></titles><pages><style face="normal" font="default" size="100%">105024</style></pages><volume><style face="normal" font="default" size="100%">112</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Visible light photocatalyst, superparamagnetic starch functionalized magnetite, Ag/Ag2O nanostructures, H2O2 production</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/06/15/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1369-8001</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000520894200006</style></accession-num><abstract><style face="normal" font="default" size="100%">The development of magnetically recyclable photocatalysts for economic and green H2O2 synthesis from water and oxygen only is virtually unexplored. Magnetic recyclability makes possible cost-effective laboratory or industrial reuse of the catalyst. The present research shows that magnetically recyclable starch functionalized Fe3O4/Ag/Ag2O superparamagnetic nanocomposites are very good visible light photocatalysts for H2O2 formation. These nanocomposites were prepared by precipitating Ag/Ag2O fine-sized nanostructures on starch functionalized magnetite nanoparticles (SMNPs). HR-TEM, XRD, and XPS analysis results showed the formation of SMNPs dotted with fine-sized Ag/Ag2O nanostructures smaller than their quantum confinement regimes. A p-n heterojunction is formed between (n-type) starch functionalized magnetite and (p-type) Ag2O components. Enhanced charge separation and the presence of plasmonic Ag nanostructures on the SM component cause efficient oxygen reduction with high H2O2 formation rates.</style></abstract><notes><style face="normal" font="default" size="100%">Kw0wp&#xD;Times Cited:0&#xD;Cited References Count:53</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S1369800119318542</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.mssp.2020.105024</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>585</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">585</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Oz, S.</style></author><author><style face="normal" font="default" size="100%">Jena, A. K.</style></author><author><style face="normal" font="default" size="100%">Kulkarni, A.</style></author><author><style face="normal" font="default" size="100%">Mouri, K.</style></author><author><style face="normal" font="default" size="100%">Yokoyama, T.</style></author><author><style face="normal" font="default" size="100%">Takei, I.</style></author><author><style face="normal" font="default" size="100%">Ünlü, F.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Miyasaka, T.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Toin Univ Yokohama, Aoba Ku, Yokohama, Kanagawa 2258503, Japan&#xD;Mitsubishi Chem Corp, Sci &amp; Innovat Ctr, Aoba Ku, Yokohama, Kanagawa 2278502, Japan&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Lead(II) Propionate Additive and a Dopant-Free Polymer Hole Transport Material for CsPbI2Br Perovskite Solar Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Acs Energy Letters</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Acs Energy Lett</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1292-1299</style></pages><volume><style face="normal" font="default" size="100%">5</style></volume><number><style face="normal" font="default" size="100%">4</style></number><keywords><keyword><style face="normal" font="default" size="100%">highly efficient</style></keyword><keyword><style face="normal" font="default" size="100%">halide perovskites</style></keyword><keyword><style face="normal" font="default" size="100%">alpha-cspbi3</style></keyword><keyword><style face="normal" font="default" size="100%">phase</style></keyword><keyword><style face="normal" font="default" size="100%">stabilization</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">Apr 10</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2380-8195</style></isbn><abstract><style face="normal" font="default" size="100%">All-inorganic perovskites (CsPbI3 and CsPbI2Br), owing to their greater thermal stability compared to organic-inorganic hybrid perovskites, are becoming popular in perovskite photovoltaics, but the problem that remains with CsPbI2Br (or CsPbI3) is the humidity-assisted phase transformation. Herein, we report on the formation of CsPbI2Br alpha-phase and improvement of its phase stability under ambient atmosphere (20-30% relative humidity) by Pb(II) propionate additive in the CsPbI2Br precursor. Solar cells employing a CsPbI2Br film with an optimum concentration of the additive (1 mol %) and a donor-acceptor type polymer (synthesized by us) as dopant-free hole transport material that has a better energy level matching with CsPbI2Br (compared to other polymers like P3HT, PTAA, and asy-PBTBDT) work with a champion power conversion cell efficiency of 14.58%. A continuous increase in the open-circuit voltage, reaching 1.36 V for 5 mol % Pb(II) propionate, indicates a remarkable defect-passivation effect by the additive.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsenergylett.0c00244</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsenergylett.0c00244</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>608</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">608</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Onwudiwe, Damian C.</style></author><author><style face="normal" font="default" size="100%">Olatunde, Olalekan C.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Structural studies and morphological properties of antimony sulphide nanorods obtained by solvothermal synthesis</style></title><secondary-title><style face="normal" font="default" size="100%">Physica B</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">412691</style></pages><section><style face="normal" font="default" size="100%">412691</style></section><keywords><keyword><style face="normal" font="default" size="100%">Antimony sulphide, Nanorods, Structural studies, Morphology, Optical properties</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/11/10/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0921-4526</style></isbn><abstract><style face="normal" font="default" size="100%">Antimony sulphide (Sb2S3) is an interesting material for numerous optoelectronic applications due to its unique structural, morphological and optical properties, which are highly tuneable by different process parameters. By using a heat-up approach, antimony(III) tris(N-ethyl-N-phenyldithiocarbamate) has been utilised as single source precursor to prepare Sb2S3 in oleylamine (OLA). The effect of the reaction time on the structural, morphological and optical properties of the as-synthesized Sb2S3 was evaluated. The structural properties were explored using the Rietveld analysis to model the crystal structure of the antimony sulphide produced, and Willamson-Hall analysis was used to study the strain in the prepared materials. A good control of shape, with uniform nanorods, were obtained without any secondary morphology throughout the reaction time considered, with aspect ratio that varied from 6.1 to 10.7. The band gap energies estimated from the absorption spectra of the nanorods were in the range of 1.5–1.7 eV.</style></abstract><label><style face="normal" font="default" size="100%">Onwudiwe2020Nov</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S092145262030675X</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.physb.2020.412691</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>160</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">160</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Möllmann, Alexander</style></author><author><style face="normal" font="default" size="100%">Bialuschewski, Danny</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Tachibana, Yasuhiro</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Guillon, Olivier</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Functional metal oxide ceramics as electron transport medium in photovoltaics and photo-electrocatalysis</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced ceramics for energy conversion and storage</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">207 -- 273</style></pages><section><style face="normal" font="default" size="100%">6</style></section><keywords><keyword><style face="normal" font="default" size="100%">2020, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year></dates><pub-location><style face="normal" font="default" size="100%">Amsterdam</style></pub-location><publisher><style face="normal" font="default" size="100%">Elsevier Ltd.</style></publisher><isbn><style face="normal" font="default" size="100%">978-0-08-102726-4</style></isbn><label><style face="normal" font="default" size="100%">Mollmann2020</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>591</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">591</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Maleki, H.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Klein, A.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Birjand, Dept Carpet, Univ Blvd, Birjand 9717434765, Iran&#xD;Univ Cologne, Inst Inorgan Chem, Dept Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Antibacterial Ag containing core-shell polyvinyl alcohol-poly (lactic acid) nanofibers for biomedical applications</style></title><secondary-title><style face="normal" font="default" size="100%">Polymer Engineering and Science</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Polym Eng Sci</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1221-1230</style></pages><volume><style face="normal" font="default" size="100%">60</style></volume><number><style face="normal" font="default" size="100%">6</style></number><keywords><keyword><style face="normal" font="default" size="100%">antibacterial</style></keyword><keyword><style face="normal" font="default" size="100%">coaxial electrospinning</style></keyword><keyword><style face="normal" font="default" size="100%">core-shell fibers</style></keyword><keyword><style face="normal" font="default" size="100%">poly (lactic acid)</style></keyword><keyword><style face="normal" font="default" size="100%">polyvinyl alcohol</style></keyword><keyword><style face="normal" font="default" size="100%">silver nanoparticles</style></keyword><keyword><style face="normal" font="default" size="100%">in-situ synthesis</style></keyword><keyword><style face="normal" font="default" size="100%">silver nanoparticles</style></keyword><keyword><style face="normal" font="default" size="100%">hybrid nanocomposite</style></keyword><keyword><style face="normal" font="default" size="100%">wound dressings</style></keyword><keyword><style face="normal" font="default" size="100%">drug-delivery</style></keyword><keyword><style face="normal" font="default" size="100%">mats</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">Mar 25</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0032-3888</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000521460100001</style></accession-num><abstract><style face="normal" font="default" size="100%">Core-shell-structured polyvinyl alcohol (PVA)-poly (lactic acid) (PLA) nanofibers combining the hydrophilic trait of PVA and the biocompatibility of PLA were produced using coaxial electrospinning. This allowed the incorporation of AgNO3 in the PVA core of the distinct fibers as shown through transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy (FTIR). Scanning electron microscopy (SEM) showed relatively uniform and bead-free fibers with smooth surfaces. Ag-containing fibers show significantly decreased diameters compared with Ag-free samples as a result of the increased conductivity of the spinning solutions with increasing amounts of AgNO3. In a postsynthetic treatment, the AgNO3 was reduced forming silver nanoparticles (Ag NPs). Ag NPs of 45 to 90 nm size were located in the PVA core but also on the surface of the core-shell fibers and as individual, agglomerated, and polymer-coated particles of 100-200 nm. Powder X-ray diffraction (PXRD), energy dispersive X-ray spectroscopy (EDX), and UV-vis absorption spectroscopy confirmed the increasing amounts of Ag in the core-shell fibers when using increasing amounts of AgNO3 in the spinning solutions. The antibacterial activity of the nanofiber mats against two prokaryotes Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) increased with increasing amounts of Ag, as expected and produces inhibition zones of 1 to 2 mm.</style></abstract><notes><style face="normal" font="default" size="100%">Kw8vb&#xD;Times Cited:1&#xD;Cited References Count:49</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/pen.25375</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/pen.25375</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>567</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">567</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Luo, Lan</style></author><author><style face="normal" font="default" size="100%">Zhou, Kaiqiang</style></author><author><style face="normal" font="default" size="100%">Lian, Ruqian</style></author><author><style face="normal" font="default" size="100%">Lu, Yanzhong</style></author><author><style face="normal" font="default" size="100%">Zhen, Yichao</style></author><author><style face="normal" font="default" size="100%">Wang, Jinshan</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hong, Zhensheng</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Cation-Deficient TiO2(B) Nanowires with Protons Charge Compensation for Regulating Reversible Magnesium Storage</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><pages><style face="normal" font="default" size="100%">104716</style></pages><volume><style face="normal" font="default" size="100%">72</style></volume><section><style face="normal" font="default" size="100%">104716</style></section><dates><year><style face="normal" font="default" size="100%">2020</style></year></dates><isbn><style face="normal" font="default" size="100%">22112855</style></isbn><urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.nanoen.2020.104716</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>577</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">577</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Luo, Lan</style></author><author><style face="normal" font="default" size="100%">Zhen, Yichao</style></author><author><style face="normal" font="default" size="100%">Lu, Yanzhong</style></author><author><style face="normal" font="default" size="100%">Zhou, Kaiqiang</style></author><author><style face="normal" font="default" size="100%">Huang, Jinxian</style></author><author><style face="normal" font="default" size="100%">Huang, Zhigao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hong, Zhensheng</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Fujian Provincial Key Laboratory of Quantum Manipulation and New Energy Materials, College of Physics and Energy, Fujian Normal University, Fuzhou, Fujian 350117, China and Fujian Provincial Collaborative Innovation Center for Optoelectronic Semiconductors and Efficient Devices, Xiamen, 361005, China.&#xD;Fujian Provincial Key Laboratory of Quantum Manipulation and New Energy Materials, College of Physics and Energy, Fujian Normal University, Fuzhou, Fujian 350117, China.&#xD;Institute of Inorganic Chemistry, University of Cologne, Greinstr. 6, 50939 Cologne, Germany. winter0514@163.com.&#xD;Fujian Provincial Key Laboratory of Quantum Manipulation and New Energy Materials, College of Physics and Energy, Fujian Normal University, Fuzhou, Fujian 350117, China and Institute of Inorganic Chemistry, University of Cologne, Greinstr. 6, 50939 Cologne, Germany. winter0514@163.com.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Structural evolution from layered Na 2 Ti 3 O 7 to Na 2 Ti 6 O 13 nanowires enabling a highly reversible anode for Mg-ion batteries</style></title><secondary-title><style face="normal" font="default" size="100%">Nanoscale</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nanoscale</style></full-title></periodical><pages><style face="normal" font="default" size="100%">230–238</style></pages><volume><style face="normal" font="default" size="100%">12</style></volume><number><style face="normal" font="default" size="100%">1</style></number><edition><style face="normal" font="default" size="100%">2019/12/10</style></edition><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020///</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2040-3372 (Electronic)&#xD;2040-3364 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">31815995</style></accession-num><abstract><style face="normal" font="default" size="100%">The development of suitable host materials for the reversible storage of divalent ions such as Mg(2+) is still a big challenge and its progress to date has been slow compared to that of monovalent Li(+) or Na(+). Herein, we present the study of layered sodium trititanate (Na2Ti3O7) and sodium hexatitanate (Na2Ti6O13) nanowires as anode materials for rechargeable Mg-ion batteries. It is found for the first time that the structural evolution from layered Na2Ti3O7 to Na2Ti6O13 with a more condensate three-dimensional microporous structure enables remarkably enhanced Mg-ion storage performance. The Na2Ti6O13 electrode can achieve a large initial discharge and charge capacity of 165.8 and 147.7 mA h g(-1) at 10 mA g(-1) with a record high initial coulombic efficiency up to 89.1%. Ex situ XRD, Raman measurements and EDX mapping were used to investigate the electrochemical reaction mechanism. It is suggested that the irreversible structure change and the formation of insoluble NaCl with high yield and large particles when Na(+) is replaced by inserted Mg(2+) for the Na2Ti3O7 electrode could be ascribed to the rapid decline in capacity. By contrast, the Na2Ti6O13 electrode exhibits good structure stability during the Mg-ion insertion/extraction process, leading to good rate performance and cycling stability.</style></abstract><notes><style face="normal" font="default" size="100%">Luo, Lan&#xD;Zhen, Yichao&#xD;Lu, Yanzhong&#xD;Zhou, Kaiqiang&#xD;Huang, Jinxian&#xD;Huang, Zhigao&#xD;Mathur, Sanjay&#xD;Hong, Zhensheng&#xD;eng&#xD;England&#xD;Nanoscale. 2020 Jan 7;12(1):230-238. doi: 10.1039/c9nr08003a. Epub 2019 Dec 9.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://pubs.rsc.org/en/content/articlehtml/2020/nr/c9nr08003a</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c9nr08003a</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>598</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">598</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Je, Minyeong</style></author><author><style face="normal" font="default" size="100%">Choi, Heechae</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Roitsch, Stefan</style></author><author><style face="normal" font="default" size="100%">Müller, Ralf</style></author><author><style face="normal" font="default" size="100%">Mane, Rajaram S.</style></author><author><style face="normal" font="default" size="100%">Kim, Kwang Ho</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Dept Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;SRTM Univ, Sch Phys Sci, Nanded, India&#xD;Pusan Natl Univ, Global Frontier R&amp;D Ctr Hybrid Interface Mat, 30 Jangjeon Dong, Busan 609735, South Korea</style></auth-address><titles><title><style face="normal" font="default" size="100%">Boosting nitrogen-doping and controlling interlayer spacing in pre-reduced graphene oxides</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nano Energy</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><alt-periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></alt-periodical><pages><style face="normal" font="default" size="100%">105286</style></pages><volume><style face="normal" font="default" size="100%">78</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Reduced graphene oxide, Freestanding and flexible films, Pre-reduction, N-doping, Li-ion batteries, Binder-free anode material</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/08/14/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2211-2855</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000596605600004</style></accession-num><abstract><style face="normal" font="default" size="100%">Controlling interlayer spacing in graphene oxide materials is an effective strategy to unify high conductivity with high intercalation and storage properties. Free-standing films of reduced graphene oxide (rGO) match these characteristics and are capable of replacing metal-based anodes in lithium-ion batteries (LIBs) crucially essential for enhanced flexibility and gravimetric energy density of devices currently sought for wearable and stretchable electronics. Restoring high electrical conductivity through chemical reduction of graphene oxide (GO) remains elusive due to interplay of desired in-plane conductivity and interlayer ion transport. A chemical pre-reduction step introduced in this work alleviated the defect density in graphene oxides to enable the incorporation of nitrogen by annealing in NH3 atmosphere. Decreased oxygen contents were observed upon pre-reduction through a deoxygenation process (C:O ratio GO: 1.7, rGO: 11.4, pre-reduced rGO: 34.8) to effectively restore the aromatic character in rGO films. The pre-reduction altered the chemical topography and reinforced the interlayer interactions of the resulting N:rGO films to boost the electrical conductivity (pre-reduced rGO: 11759 S m−1, pre-reduced N:rGO: 25253 S m−1) and produce more densely packed structures. DFT calculations confirmed a gradual decrease in interlayer spacing values in GO (4.85Å Å ), N:rGO (3.83Å Å ) and pre-reduced N:rGO* (3.61Å Å ) samples, which validated the critical role of chemical pre-reduction. The DFT calculations also explained the differential behavior of N-doped and pre-reduced rGO films on significantly enhanced electrical conductivity and lithium storage capacity (rGO: 1208 S m−1, 261 mAh g−1; N:rGO: 10574 S m−1, 529 mAh g−1). This work presents a facile pathway to overcome the persisting limitation of 2D carbon nanostructures prepared by aqueous processing to produce chemically engineered graphitic carbons as anodes for lithium ion batteries. Graphical abstract Download : Download high-res image (342KB)Download : Download full-size image</style></abstract><label><style face="normal" font="default" size="100%">Ludwig2020Aug</style></label><notes><style face="normal" font="default" size="100%">Pb9ar&#xD;Times Cited:0&#xD;Cited References Count:82</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S2211285520308636</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.nanoen.2020.105286</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>614</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">614</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lu, Y. Z.</style></author><author><style face="normal" font="default" size="100%">Wang, J. S.</style></author><author><style face="normal" font="default" size="100%">Chen, Y.</style></author><author><style face="normal" font="default" size="100%">Zheng, X. Y.</style></author><author><style face="normal" font="default" size="100%">Yao, H. R.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Hong, Z. S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Fujian Normal Univ, Coll Phys &amp; Energy, Fujian Prov Key Lab Quantum Manipulat &amp; New Energ, Fuzhou 350117, Peoples R China&#xD;Fujian Prov Collaborat Innovat Ctr Adv High Field, Fuzhou 350117, Peoples R China&#xD;Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Spatially Controlled Lithium Deposition on Silver-Nanocrystals-Decorated TiO2 Nanotube Arrays Enabling Ultrastable Lithium Metal Anode</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Functional Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Adv Funct Mater</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Functional Materials</style></full-title></periodical><keywords><keyword><style face="normal" font="default" size="100%">host</style></keyword><keyword><style face="normal" font="default" size="100%">lithium metal anodes</style></keyword><keyword><style face="normal" font="default" size="100%">silver nanocrystals decoration</style></keyword><keyword><style face="normal" font="default" size="100%">tio2 nanotubes</style></keyword><keyword><style face="normal" font="default" size="100%">electrolytes</style></keyword><keyword><style face="normal" font="default" size="100%">growth</style></keyword><keyword><style face="normal" font="default" size="100%">ion</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">Dec 18</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1616-301x</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000599600200001</style></accession-num><abstract><style face="normal" font="default" size="100%">3D scaffolds and heterogeneous seeds are two effective ways to guide Li deposition and suppress Li dendrite growth. Herein, 3D TiO2 nanotube (TNT) arrays decorated using ultrafine silver nanocrystals (7-10 nm) through cathodic reduction deposition are first demonstrated as a confined space host for lithium metal deposition. First, TiO2 possesses intrinsic lithium affinity with large Li absorption energy, which facilitates Li capture. Then, ultrafine silver nanocrystals decoration allows the uniform and selective nucleation in nanoscale without a nucleation barrier, leading to the extraordinary formation of lithium metal importing into 3D nanotube arrays. As a result, Li metal anode deposited on such a binary architecture (TNT-Ag-Li) delivers a high Coulomb efficiency at around 99.4% even after 300 cycles with a capacity of 2 mA h cm(-2). Remarkably, TNT-Ag-Li exhibits ultralow overpotential of 4 mV and long-term cycling life over 2500 h with a capacity of 2 mAh cm(-2) in Li symmetric cells. Moreover, the full battery with 3D spaced Li nanotubes anode and LiFeO4 cathode exhibits a stable and high capacity of 115 mA h g(-1) at 5 C and an excellent Coulombic efficiency of approximate to 100% over 500 cycles.</style></abstract><notes><style face="normal" font="default" size="100%">Pg2wb&#xD;Times Cited:0&#xD;Cited References Count:43</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000599600200001</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">ARTN 2009605&#xD;10.1002/adfm.202009605</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>603</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">603</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lee, Damin</style></author><author><style face="normal" font="default" size="100%">Lee, Hyun Woo</style></author><author><style face="normal" font="default" size="100%">Shinde, Nanasaheb M.</style></author><author><style face="normal" font="default" size="100%">Yun, Je Moon</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kim, Kwang Ho</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">School of Materials Science and Engineering, Pusan National University, San 30 Jangjeon-dong, Geumjeong-gu, Busan 609-735, Republic of Korea. kwhokim@pusan.ac.kr.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Synthesis of nickel–copper composite with controllable nanostructure through facile solvent control as positive electrode for high-performance supercapacitors</style></title><secondary-title><style face="normal" font="default" size="100%">Dalton Trans.</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">13123-13133</style></pages><volume><style face="normal" font="default" size="100%">49</style></volume><number><style face="normal" font="default" size="100%">37</style></number><edition><style face="normal" font="default" size="100%">2020/09/16</style></edition><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/09/15/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1477-9226</style></isbn><accession-num><style face="normal" font="default" size="100%">32930269</style></accession-num><abstract><style face="normal" font="default" size="100%">The surface characteristics of electrodes vary depending on the solvent used. Furthermore, electrochemical performance varies depending on the surface morphology of the electrode. In this study, we grew 3D binary NiCu-based composites on Ni foam, via a binder-free hydrothermal method, for use as a cathode in high-performance supercapacitors. We employed different solvents to prepare the electrodes by adjusting the ratio of deionized water (DI water) to methanol. The electrode prepared using DI water as the solvent had the largest surface area with a nanowire structure. This morphology allowed for good electrical performance by greatly improving the electrode and electrolyte contact area and shortening the ion diffusion path. The optimized deposition of NiCu(CO3)(OH)2 nanowires (50 mL of DI water as solvent) showed an excellent maximum specific capacity of 758.9 mA h g−1 at a current density of 3 A g−1, as well as outstanding cycling performance with 87.2% retention after 5000 cycles. In this work, we focused on the large specific surface area and suitable electrochemical properties of NiCu(CO3)(OH)2 electrodes with various solvents. As a result, the asymmetric supercapacitor (ASC) using the NiCu(CO3)(OH)2 electrode prepared with 50 ml of DI water as the solvent as the positive electrode and graphene as the negative electrode, exhibited an energy density of 26.7 W h kg−1 at a power density of 2534 W kg−1, and excellent cycling stability with 91.3% retention after 5000 cycles. The NiCu(CO3)(OH)2//graphene ASC could turn on an LED light and demonstrated better electrical performance than most previously reported nickel- and copper-based carbonate hydroxide ASCs. In addition, in the present scenario where many nanoscale studies are conducted, a method of controlling the nanostructure of a material through facile solvent control will be of great help to many researchers.</style></abstract><label><style face="normal" font="default" size="100%">Lee2020Sep</style></label><notes><style face="normal" font="default" size="100%">Lee, Damin&#xD;Lee, Hyun Woo&#xD;Shinde, Nanasaheb M&#xD;Yun, Je Moon&#xD;Mathur, Sanjay&#xD;Kim, Kwang Ho&#xD;eng&#xD;England&#xD;Dalton Trans. 2020 Oct 7;49(37):13123-13133. doi: 10.1039/d0dt02427a. Epub 2020 Sep 15.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/D0DT02427A</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/d0dt02427a</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>606</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">606</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jürgensen, Lasse</style></author><author><style face="normal" font="default" size="100%">Höll, David</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Schmidt-Verma, Anna Kathrin</style></author><author><style face="normal" font="default" size="100%">Raauf, Aida</style></author><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Institute of Inorganic Chemistry, University of Cologne, Greinstrasse 6, D-50939 Cologne, Germany. sanjay.mathur@uni-koeln.de.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Controlled Growth of Cu and CuOx Thin Films from Subvalent Copper Precursors</style></title><secondary-title><style face="normal" font="default" size="100%">Dalton Trans.</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">13317-13325</style></pages><volume><style face="normal" font="default" size="100%">49</style></volume><number><style face="normal" font="default" size="100%">38</style></number><edition><style face="normal" font="default" size="100%">2020/09/18</style></edition><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020///</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1477-9234 (Electronic)&#xD;1477-9226 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">32940296</style></accession-num><abstract><style face="normal" font="default" size="100%">A new Cu(i) precursor, [(COD)Cu(TFB-TFEA)] (COD = 1,5-cyclooctadiene and TFB-TFEA = N-(4,4,4-trifluorobut-1-en-3-on)-6,6,6-trifluoroethylamine) with high volatility and a clean thermal decomposition pattern was tested for thermal and plasma-assisted chemical vapor deposition (CVD). The heteroleptic configuration based on an anionic and a chelating neutral ligand unified both reactivity and sufficient stability resulting in an intrinsic molecular control over the composition of the resulting CVD deposits. The electronic influence of the ligand on the metal site was studied by 1D and 2D NMR spectroscopy, while EI mass spectrometry revealed the ligand elimination cascade. Thermal and plasma CVD experiments demonstrated the suitability of the copper compound for an atom-efficient (high molecule-to-material yield) deposition of copper(0) and copper(i) oxide films that could be converted into crystalline copper(ii) oxide upon heat treatment at 500 degrees C.</style></abstract><label><style face="normal" font="default" size="100%">Jurgensen2020</style></label><notes><style face="normal" font="default" size="100%">Jurgensen, Lasse&#xD;Holl, David&#xD;Frank, Michael&#xD;Ludwig, Tim&#xD;Graf, David&#xD;Schmidt-Verma, Anna Katrin&#xD;Raauf, Aida&#xD;Gessner, Isabel&#xD;Mathur, Sanjay&#xD;eng&#xD;England&#xD;Dalton Trans. 2020 Oct 6;49(38):13317-13325. doi: 10.1039/d0dt02570d.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://pubs.rsc.org/en/content/articlehtml/2020/dt/d0dt02570d</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/d0dt02570d</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>619</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">619</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jürgensen, Lasse</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Welter, Katharina</style></author><author><style face="normal" font="default" size="100%">Jägermann, Wolfram</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanostructured IrOx Coatings for Efficient Oxygen Evolution Reactions in PV-EC Setup</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für Physikalische Chemie</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">911-924</style></pages><volume><style face="normal" font="default" size="100%">234</style></volume><number><style face="normal" font="default" size="100%">5</style></number><dates><year><style face="normal" font="default" size="100%">2020</style></year></dates><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1515/zpch-2019-1450</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">doi:10.1515/zpch-2019-1450</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>564</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">564</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jurewicz, Anna</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Uppal, Jasleen</style></author><author><style face="normal" font="default" size="100%">Ivandic, Ivan</style></author><author><style face="normal" font="default" size="100%">Korsching, Sigrun</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Univ Cologne, Inst Genet, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Evaluation of Magnetite Nanoparticle-based Toxicity on Embryo-Larvae Stages of Zebrafish (Danio rerio)</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Nano Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Acs Appl Nano Mater</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Nano Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1621-1629</style></pages><volume><style face="normal" font="default" size="100%">3</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">zebrafish (zf)</style></keyword><keyword><style face="normal" font="default" size="100%">iron oxide</style></keyword><keyword><style face="normal" font="default" size="100%">toxicity</style></keyword><keyword><style face="normal" font="default" size="100%">embryo</style></keyword><keyword><style face="normal" font="default" size="100%">larvae</style></keyword><keyword><style face="normal" font="default" size="100%">fluorescence</style></keyword><keyword><style face="normal" font="default" size="100%">iron-oxide nanoparticles</style></keyword><keyword><style face="normal" font="default" size="100%">silver nanoparticles</style></keyword><keyword><style face="normal" font="default" size="100%">nanomaterials</style></keyword><keyword><style face="normal" font="default" size="100%">functionalization</style></keyword><keyword><style face="normal" font="default" size="100%">delivery</style></keyword><keyword><style face="normal" font="default" size="100%">model</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">Feb</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2574-0970</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000517856800074</style></accession-num><abstract><style face="normal" font="default" size="100%">Iron oxide nanoparticles (NPs) are extensively used in various biomedical applications due to their suitability as carriers of diagnostic and therapeutic agents. Herein, we report on the evaluation of concentration-dependent toxicity studies of iron oxide (magnetite) NPs in zebrafish (Danio rerio). To follow the update of iron oxide NPs in the animal model, particles were functionalized by conjugating a fluorescent dye (Congo red) that serves as an efficient probe to track the uptake and accumulations of nanoparticles from the early life stages of zebrafish. As in vivo model organism to study the diffusion an in vivo toxicity, zebrafish embryos and larvae were treated with different concentrations of CR@Fe3O4 conjugates (100-800 mu g/mL) for 4-96 h postfertilization (hpf). Monitoring of mortality, hatching rate, and whole-embryo cellular death showed that incubation of low concentrations of the NPs did not exhibit adverse developmental toxicity during embryonic and larval stages of zebrafish. Minimal toxic effects were observed at high concentration (800 mu g/mL) of CR@Fe3O4, causing mortality and delay in hatching cycles. However, CR@Fe3O4 exhibited higher toxic effect on zebrafish larvae, suggesting higher bioavailability of the NPs on the tested animal stage. This study provides an investigation on developmental toxicity in zebrafish caused by Fe3O4 NPs and provides innovative insight into CR@Fe3O4 NPs serving as an optical probe to study the potential nanotoxicological effects of NPs in in vivo systems.</style></abstract><notes><style face="normal" font="default" size="100%">Kr8ho&#xD;Times Cited:0&#xD;Cited References Count:40</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000517856800074</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsanm.9b02330</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>587</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">587</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jung, E.</style></author><author><style face="normal" font="default" size="100%">Budzinauskas, K.</style></author><author><style face="normal" font="default" size="100%">Oz, S.</style></author><author><style face="normal" font="default" size="100%">Ünlü, F.</style></author><author><style face="normal" font="default" size="100%">Kuhn, H.</style></author><author><style face="normal" font="default" size="100%">Wagner, J.</style></author><author><style face="normal" font="default" size="100%">Grabowski, D.</style></author><author><style face="normal" font="default" size="100%">Klingebiel, B.</style></author><author><style face="normal" font="default" size="100%">Cherasse, M.</style></author><author><style face="normal" font="default" size="100%">Dong, J. W.</style></author><author><style face="normal" font="default" size="100%">Aversa, P.</style></author><author><style face="normal" font="default" size="100%">Vivo, P.</style></author><author><style face="normal" font="default" size="100%">Kirchartz, T.</style></author><author><style face="normal" font="default" size="100%">Miyasaka, T.</style></author><author><style face="normal" font="default" size="100%">van Loosdrecht, P. H. M.</style></author><author><style face="normal" font="default" size="100%">Perfetti, L.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Phys 2, Cologne, Germany&#xD;Inst Polytech Paris, Lab Solides Irradies, Ecole Polytech, CNRS,CEA,DRF,IRAMIS, F-91128 Palaiseau, France&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Toin Univ Yokohama, Grad Sch Engn, Yokohama, Kanagawa 2258503, Japan&#xD;Forschungszentrum Julich, IEK 5 Photovolta, D-52425 Julich, Germany&#xD;Tampere Univ, Fac Engn &amp; Nat Sci, FI-33101 Tampere, Finland&#xD;Univ Duisburg Essen, Fac Engn, D-47057 Duisburg, Germany&#xD;Univ Duisburg Essen, CENIDE, D-47057 Duisburg, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Femto- to Microsecond Dynamics of Excited Electrons in a Quadruple Cation Perovskite</style></title><secondary-title><style face="normal" font="default" size="100%">Acs Energy Letters</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Acs Energy Lett</style></alt-title></titles><pages><style face="normal" font="default" size="100%">785-792</style></pages><volume><style face="normal" font="default" size="100%">5</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">enhanced carrier lifetime</style></keyword><keyword><style face="normal" font="default" size="100%">solar-cells</style></keyword><keyword><style face="normal" font="default" size="100%">radiative recombination</style></keyword><keyword><style face="normal" font="default" size="100%">halide perovskites</style></keyword><keyword><style face="normal" font="default" size="100%">guanidinium</style></keyword><keyword><style face="normal" font="default" size="100%">methylammonium</style></keyword><keyword><style face="normal" font="default" size="100%">efficient</style></keyword><keyword><style face="normal" font="default" size="100%">trihalide</style></keyword><keyword><style face="normal" font="default" size="100%">films</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">Mar 13</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2380-8195</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000526311000012</style></accession-num><abstract><style face="normal" font="default" size="100%">Quadruple cation mixed halide perovskite, GA(0.015)Cs(0.046)MA(0.152)FA(0.787)Pb(I0.815Br0.185)(3), single crystals were grown for the first time using an inverse temperature crystallization process. Solar cell devices in n-i-p stack configuration using thin films of the same materials showed power conversion efficiency above 20%. Complementary time-resolved spectroscopy confirmed that polycrystal-line thin films and single crystals identically composed exhibit similar carrier dynamics in the picosecond range. Cooling of excited carriers and bandgap renormalization occur on the same time scale of 200-300 fs. The radiative recombination coefficient (1.2 x 10(-9) cm(3)/s) is comparable to values reported for a GaAs semiconductor. At low excitation density, a long carrier lifetime of 3.2 mu s was recorded possibly due to the passivation of recombination centers. This study clarifies discrepancies about the lifetime of hot carriers, the impact of radiative recombination, and the role of recombination centers on solar cell performance. The quadruple cation perovskites displayed short time dynamics with slow recombination of charge carriers.</style></abstract><notes><style face="normal" font="default" size="100%">Ld8xr&#xD;Times Cited:0&#xD;Cited References Count:48</style></notes><urls><related-urls><url><style face="underline" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000526311000012</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsenergylett.9b02684</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>607</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">607</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Ullah, Nighat K.</style></author><author><style face="normal" font="default" size="100%">Ilyas, Muhammad</style></author><author><style face="normal" font="default" size="100%">Wennhold, Kerstin</style></author><author><style face="normal" font="default" size="100%">Iqbal, Maria</style></author><author><style face="normal" font="default" size="100%">Schlößer, Hans A.</style></author><author><style face="normal" font="default" size="100%">Hussain, Muhammad S.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Institute of Inorganic Chemistry, University of Cologne, Greinstrasse 6, 50939 Cologne, Germany.&#xD;Professorship for Population Genetics, Department of Life Science Systems, Technical University of Munich, Liesel-Beckmann Strasse 2, 85354 Freising, Germany.&#xD;Center for Molecular Medicine Cologne and Translational Immunology, University Hospital Cologne, 50931 Cologne, Germany.&#xD;Medical Microbiology, Immunology and Hygiene, University Hospital Cologne, Goldenfelsstrasse 19-21, 50935 Cologne, Germany.&#xD;Institute of Biochemistry I, Center for Molecular Medicine, University of Cologne, Joseph-Stelzmann-Strasse 52, 50931 Cologne, Germany.&#xD;Cologne Center for Genomics (CCG), University of Cologne, Weyertal 115b, 50931 Cologne, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Mediating the Fate of Cancer Cell Uptake: Dual-Targeted Magnetic Nanovectors with Biotin and Folate Surface Ligands</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Biomater. Sci. Eng.</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">6138-6147</style></pages><volume><style face="normal" font="default" size="100%">2020</style></volume><number><style face="normal" font="default" size="100%">11</style></number><edition><style face="normal" font="default" size="100%">2021/01/16</style></edition><keywords><keyword><style face="normal" font="default" size="100%">iron oxide, biotin, folic acid, carbodiimide coupling, click chemistry, receptor-mediated uptake</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/10/22/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2373-9878 (Electronic)&#xD;2373-9878 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">33449668</style></accession-num><abstract><style face="normal" font="default" size="100%">Recognition of folate and biotin surface receptors by dual-functionalized nanoparticles (NPs) is key for site-selective receptor-mediated transport of anticancer drugs to cancer cells. We present here dopamine-capped iron oxide nanoprobes (Fe3O4, 10 ± 2 nm) containing two surface-grafted biologically relevant ligands, namely, folic acid (FA) and biotin (BT). The covalent attachment of both FA and BT on Fe3O4 nanoparticles was achieved by following carbodiimide coupling and click-chemistry protocols. The dual-function Fe3O4 probes were delivered into E-G7 and human HeLa cancer cell lines and tested toward their cellular uptake by immunofluorescence and flow cytometry analysis. Owing to receptor-mediated endocytosis, enhanced accumulation of nanoprobes in cancer cells was successfully monitored by confocal laser microscopy. When compared to dual-function probes, single-functionalized nanoparticles possessing either FA or BT ligands showed significantly reduced uptake in the tested cell lines, underlining the superior interaction potential of dual-purpose probes. A time-dependent receptor-mediated endocytosis of FA–Fe3O4–BT nanovectors was demonstrated by flow cytometry analysis, whereas the unfunctionalized NPs did not show any specificity in terms of uptake. Besides their specific uptake, the surface-functionalized nanoparticles exhibited promising cytotoxicity profiles by demonstrating good viability of more than 95% with analogous cancer cell lines. Our results demonstrate that dual and/or multivariate conjugation of receptor-specific ligands on NPs is highly effective in molecular recognition of surface biomarkers that enhances their potential in anticancer treatment for pretargeting-radio strategies based on biotin/avidin interactions.</style></abstract><label><style face="normal" font="default" size="100%">Ilyas2020Oct</style></label><notes><style face="normal" font="default" size="100%">Ilyas, Shaista&#xD;Ullah, Nighat K&#xD;Ilyas, Muhammad&#xD;Wennhold, Kerstin&#xD;Iqbal, Maria&#xD;Schlosser, Hans A&#xD;Hussain, Muhammad S&#xD;Mathur, Sanjay&#xD;eng&#xD;ACS Biomater Sci Eng. 2020 Nov 9;6(11):6138-6147. doi: 10.1021/acsbiomaterials.0c00771. Epub 2020 Oct 22.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acsbiomaterials.0c00771</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsbiomaterials.0c00771</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>595</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">595</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Haddad, Jinane</style></author><author><style face="normal" font="default" size="100%">Krogmeier, Benedikt</style></author><author><style face="normal" font="default" size="100%">Klingebiel, Benjamin</style></author><author><style face="normal" font="default" size="100%">Krückemeier, Lisa</style></author><author><style face="normal" font="default" size="100%">Melhem, Stephanie</style></author><author><style face="normal" font="default" size="100%">Liu, Zhifa</style></author><author><style face="normal" font="default" size="100%">Hüpkes, Jürgen</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kirchartz, Thomas</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Forschungszentrum Julich, IEK5 Photovolta, D-52425 Julich, Germany&#xD;Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;Univ Duisburg Essen, Fac Engn, Carl Benz Str 199, D-47057 Duisburg, Germany&#xD;Univ Duisburg Essen, CENIDE, Carl Benz Str 199, D-47057 Duisburg, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Analyzing Interface Recombination in Lead-Halide Perovskite Solar Cells with Organic and Inorganic Hole-Transport Layers</style></title><secondary-title><style face="normal" font="default" size="100%">Adv. Mater. Interfaces</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Adv Mater Interfaces</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2000366</style></pages><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">angle-resolved XPS, CuOx, hole-transport layers, nonradiative voltage losses, perovskite solar cells, photovoltaics, ultraviolet photoelectron spectroscopy</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/06/28/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2196-7350</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000543730100001</style></accession-num><abstract><style face="normal" font="default" size="100%">The interfaces between absorber and transport layers are shown to be critical for perovskite device performance. However, quantitative characterization of interface recombination has so far proven to be highly challenging in working perovskite solar cells. Here, methylammonium lead halide (CH3NH3PbI3) perovskite solar cells are studied based on a range of different hole‐transport layers, namely, an inorganic hole‐transport layer CuOx, an organic hole‐transport layer poly(triarylamine) (PTAA), and a bilayer of CuOx/PTAA. The cells are completed by a [6,6]‐phenyl‐C61‐butyric acid methyl ester (PCBM)/bathocuproine/Ag electron contact. Energy levels are characterized using photoelectron spectroscopy and recombination dynamics by combining steady‐state photoluminescence and transient photoluminescence with numerical simulations. While the PTAA‐based devices hardly show any interface recombination losses and open‐circuit voltages &gt;1.2 V, substantial losses are observed for the samples with a direct CuOx/perovskite interface. These losses are assigned to a combination of energetic misalignment at the CuOx/perovskite interface coupled with increased interface recombination velocities at the perovskite/PCBM interface.</style></abstract><notes><style face="normal" font="default" size="100%">Ng4pr&#xD;Times Cited:2&#xD;Cited References Count:72</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/admi.202000366</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/admi.202000366</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>566</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">566</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Queraltó, Albert</style></author><author><style face="normal" font="default" size="100%">Lepcha, Ashish</style></author><author><style face="normal" font="default" size="100%">Appel, Linus</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Electrospun SrNb2O6 photoanodes from single-source precursors for photoelectrochemical water splitting</style></title><secondary-title><style face="normal" font="default" size="100%">Solar Energy Materials and Solar Cells</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Sol Energ Mat Sol C</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Solar Energy Materials and Solar Cells</style></full-title></periodical><pages><style face="normal" font="default" size="100%">110485</style></pages><volume><style face="normal" font="default" size="100%">210</style></volume><keywords><keyword><style face="normal" font="default" size="100%">single-source precursors</style></keyword><keyword><style face="normal" font="default" size="100%">nanofibers</style></keyword><keyword><style face="normal" font="default" size="100%">electrospinning</style></keyword><keyword><style face="normal" font="default" size="100%">water splitting</style></keyword><keyword><style face="normal" font="default" size="100%">photoelectrochemical water splitting</style></keyword><keyword><style face="normal" font="default" size="100%">photocatalytic activity</style></keyword><keyword><style face="normal" font="default" size="100%">optical-properties</style></keyword><keyword><style face="normal" font="default" size="100%">thin-films</style></keyword><keyword><style face="normal" font="default" size="100%">niobium</style></keyword><keyword><style face="normal" font="default" size="100%">strontium</style></keyword><keyword><style face="normal" font="default" size="100%">nanofibers</style></keyword><keyword><style face="normal" font="default" size="100%">tantalum</style></keyword><keyword><style face="normal" font="default" size="100%">hydrogen</style></keyword><keyword><style face="normal" font="default" size="100%">crystal</style></keyword><keyword><style face="normal" font="default" size="100%">barium</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun 15</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0927-0248</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000528198800012</style></accession-num><abstract><style face="normal" font="default" size="100%">Electrospinning of SrNb2O6 nanofibers from a single bimetallic alkoxide precursor [SrNb2((OPr)-Pr-i)(12)((HOPr)-Pr-i)] and the application of resulting oxide nanofiber meshes as potential photoanode material for solar water splitting is reported. Direct formation of single phase SrNb2O6 nanofibers from the precursor gel was favored by the tailored Sr:Nb ratio (1:2) and preordering of cations through Sr-O(R)-Nb units present in the molecular precursor. X-ray diffraction and photoelectron spectroscopy confirmed the chemical composition and formation of SrNb2O6 phase. A minor amount of orthorhombic SrNb6O16 phase was observed, when small excess of alkali metal was present during the precursor synthesis. The optical bandgap of photoelectrodes, produced by doctor blading and spin coating of the nanofibers, revealed bandgap energies between 3.25 and 3.43 eV, owing to different microstructure of the photoelectrodes. The measurement of photoelectrochemical properties in basic conditions showed photocurrent density values at 1.23 eV ranging from 0.06 mA/cm(2) to 0.16 mA/cm(2). A maximum value of 0.6 mA/cm(2) was obtained for spin-coated nanofiber photoelectrodes.</style></abstract><notes><style face="normal" font="default" size="100%">Lg6hd&#xD;Times Cited:2&#xD;Cited References Count:56</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000528198800012</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">ARTN 110485&#xD;10.1016/j.solmat.2020.110485</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>580</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">580</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Ojelere, Olusola</style></author><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Juergensen, Lasse</style></author><author><style face="normal" font="default" size="100%">Grosch, Mathias</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Structure-Decomposition relationships of homoleptic and heteroleptic vanadium(IV) alkoxides for defined gas phase depositions of VO2 and V2O3 thin films</style></title><secondary-title><style face="normal" font="default" size="100%">Mater. Today:. Proc.</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">2445-2450</style></pages><volume><style face="normal" font="default" size="100%">33</style></volume><section><style face="normal" font="default" size="100%">2445</style></section><keywords><keyword><style face="normal" font="default" size="100%">Precursor chemistry, Gas phase deposition, Vanadium dioxide, Reaction mechanism, Thermochromic windows</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/02/07/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2214-7853</style></isbn><abstract><style face="normal" font="default" size="100%">A facile high yield synthesis of a novel non-oxo heteroleptic vanadium(IV) alkoxide with chelating asymmetric fluorinated ß-heteroarylacetamides (2,2,2-trifluoro-N-(pyridine-2-yl)acetamide (H-PyTFA) (1)) with the general formula [V(OtBu)2(PyTFA)2] (4) as precursor for nanostructured vanadium oxides films deposited by chemical vapor deposition (CVD) is presented here. Single crystal X-ray analysis, electron paramagnetic resonance (EPR) spectroscopy and mass spectrometry (EI-MS) revealed the unambiguous structural and electronic features of the monomeric octahedral complex 4. Comparative thermogravimetric studies with homoleptic monomeric vanadium(IV) tert–butoxide [V(OtBu)4] (2) and trimeric [V3(μ-OEt)4(OEt)8] (3) displayed the strong influence of the alkyl function in vanadium(IV) alkoxides and chelating ligands on volatility, stability and thermal decomposition pathways to different oxide phases and morphologies. We demonstrated a controlled two-step thermal decomposition of heteroleptic vanadium(IV) alkoxide (4) which offer new opportunities for a versatile growth by the enlarged ‘CVD window’ between sublimation temperature and decomposition temperature and selective self-limited growth originated from the ‘Energy trap’ between the first and second decomposition steps. Preliminary CVD experiments proofed the successful conversion of the heteroleptic precursor 4 into vanadium dioxide with ribbon-like morphology on silicon, which revealed the impact of molecular precursor engineering on crystal growth kinetics.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S2214785320304338</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.matpr.2020.01.334</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>570</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">570</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gessner, I.</style></author><author><style face="normal" font="default" size="100%">Klimpel, A.</style></author><author><style face="normal" font="default" size="100%">Klussmann, M.</style></author><author><style face="normal" font="default" size="100%">Neundorf, I.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;Univ Cologne, Inst Biochem, Zuelpicher Str 47, D-50674 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Interdependence of charge and secondary structure on cellular uptake of cell penetrating peptide functionalized silica nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">Nanoscale Advances</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nanoscale Adv</style></alt-title></titles><pages><style face="normal" font="default" size="100%">453-462</style></pages><volume><style face="normal" font="default" size="100%">2</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">circular-dichroism spectra</style></keyword><keyword><style face="normal" font="default" size="100%">delivery</style></keyword><keyword><style face="normal" font="default" size="100%">size</style></keyword><keyword><style face="normal" font="default" size="100%">biodistribution</style></keyword><keyword><style face="normal" font="default" size="100%">adsorption</style></keyword><keyword><style face="normal" font="default" size="100%">vectors</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan 1</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2516-0230</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000508943100037</style></accession-num><abstract><style face="normal" font="default" size="100%">The capability of cell-penetrating peptides (CPPs) to enable translocation of cargos across biological barriers shows promising pharmaceutical potential for the transport of drug molecules, as well as nanomaterials, into cells. Herein, we report on the optimization of a CPP, namely sC18, in terms of its translocation efficiency and investigate new CPPs regarding their interaction with silica nanoparticles (NPs). First, alanine scanning of sC18 yielded 16 cationic peptides from which two were selected for further studies. Whereas in the first case, a higher positive net charge and enhanced amphipathicity resulted in significantly higher internalization rates than sC18, the second one demonstrated reduced cellular uptake efficiencies and served as a control. We then attached these CPPs to silica nanoparticles of different sizes (50, 150 and 300 nm) via electrostatic interactions and could demonstrate that the secondary alpha-helical structure of the peptides was preserved. Following this, cellular uptake studies using HeLa cells showed that the tested CPP-NPs were successfully translocated into HeLa cells in a size-dependent manner. Moreover, depending on the CPP used, we realized differences in translocation efficiency, which were similar to what we had observed for the free peptides. All in all, we highlight the high potential of sequential fine-tuning of CPPs and provide novel insights into their interplay with inorganic biologically benign nanoparticles. Given the high cellular permeability of CPPs and their ability to translocate into a wide spectrum of cell types, our studies may stimulate future research of CPPs with inorganic nanocarrier surfaces.</style></abstract><notes><style face="normal" font="default" size="100%">Kf0ls&#xD;Times Cited:0&#xD;Cited References Count:37</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000508943100037</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c9na00693a</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>604</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">604</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gangl, Maurice</style></author><author><style face="normal" font="default" size="100%">Ünlü, Feray</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Banerji, Amitabh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Solarzellen mit Bismut statt Blei</style></title><secondary-title><style face="normal" font="default" size="100%">Nachr. Chem.</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">20–23</style></pages><volume><style face="normal" font="default" size="100%">68</style></volume><number><style face="normal" font="default" size="100%">7-8</style></number><section><style face="normal" font="default" size="100%">20</style></section><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/07/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1439-9598</style></isbn><abstract><style face="normal" font="default" size="100%">Organisch‐anorganische Hybrid‐Perowskite gelten als Wundermaterial für die Photovoltaik und werden weltweit erforscht. Allerdings können die Materialien Blei freisetzen und eignen sich daher nicht für Experimente in der Schule. Eine Alternative ist eine perowskitähnliche Solarzelle auf Rudorffit‐Basis, die verhältnismäßig preiswert und einfach selbst zu bauen ist.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/nadc.20204090159</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/nadc.20204090159</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>582</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">582</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ding, Li</style></author><author><style face="normal" font="default" size="100%">Leduc, Jennifer</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Li, Yan</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Peking Univ, Beijing Natl Lab Mol Sci, State Key Lab Rare Earth Mat Chem &amp; Applicat, Key Lab Phys &amp; Chem Nanodevices,Coll Chem &amp; Mol E, Beijing 100871, Peoples R China&#xD;Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Gelation of uranyl ions and gel-derived uranium oxide nanoparticles for gas sensing</style></title><secondary-title><style face="normal" font="default" size="100%">Nanoscale Adv.</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nanoscale Adv</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2478-2484</style></pages><volume><style face="normal" font="default" size="100%">2</style></volume><number><style face="normal" font="default" size="100%">6</style></number><keywords><keyword><style face="normal" font="default" size="100%">in-situ</style></keyword><keyword><style face="normal" font="default" size="100%">catalysts</style></keyword><keyword><style face="normal" font="default" size="100%">coordination</style></keyword><keyword><style face="normal" font="default" size="100%">nanocrystals</style></keyword><keyword><style face="normal" font="default" size="100%">temperatures</style></keyword><keyword><style face="normal" font="default" size="100%">performance</style></keyword><keyword><style face="normal" font="default" size="100%">hydrolysis</style></keyword><keyword><style face="normal" font="default" size="100%">alcohols</style></keyword><keyword><style face="normal" font="default" size="100%">elements</style></keyword><keyword><style face="normal" font="default" size="100%">uv</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/05/06/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2516-0230</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000543283200027</style></accession-num><abstract><style face="normal" font="default" size="100%">We developed a sol-gel method to synthesize uranium oxide nanoparticles with a clean surface and mixed valences of uranium at the surface. Uranyl gel was formed in ethylene glycol without incorporating any organic gelator and was readily converted to uranium dioxide nanoparticles with uniform sizeviamicrowave treatment. The as-prepared uranyl gel showed a high storage modulus of 0.48 kPa. The formation of the gel skeleton benefits from interlinkage of uranyl ions, which was revealed by UV-Vis spectroscopy and X-ray absorption. The U=O-ax bond was elongated by 0.1 angstrom and the U-O-eq bond was shortened by 0.25 angstrom by the gelation. The gel showed thixotropic and self-healing properties owing to the soft connection in the gel skeleton and photo-response attributed to the photo-reduction reaction between uranyl ions and matrix solvent. With the great inclusion properties, the uranyl gel was decomposed by microwave treatment into uranium dioxide nanoparticles with a size of similar to 4 nm. The resultant UO2 nanoparticles were easily oxidized in air, and thus presented an n-type semiconductor behaviour and sensitivity to both oxidative and reductive gases such as NO2, EtOH, CO, and NH3.</style></abstract><notes><style face="normal" font="default" size="100%">Mc4uf&#xD;Times Cited:0&#xD;Cited References Count:63</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://pubs.rsc.org/en/content/articlelanding/2020/NA/D0NA00224K#!divAbstract</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/d0na00224k</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>565</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">565</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bohr, Christoph</style></author><author><style face="normal" font="default" size="100%">Yu, Pengmei</style></author><author><style face="normal" font="default" size="100%">Scigaj, Mateusz</style></author><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Coll, Mariona</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;ICMAB CSIC, Inst Ciencia Mat Barcelona, Campus UAB, Barcelona 08193, Spain</style></auth-address><titles><title><style face="normal" font="default" size="100%">Atomic scale growth of GdFeO3 perovskite thin films</style></title><secondary-title><style face="normal" font="default" size="100%">Thin Solid Films</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Thin Solid Films</style></alt-title></titles><pages><style face="normal" font="default" size="100%">137848</style></pages><volume><style face="normal" font="default" size="100%">698</style></volume><keywords><keyword><style face="normal" font="default" size="100%">gadolinium orthoferrite</style></keyword><keyword><style face="normal" font="default" size="100%">single source precursor</style></keyword><keyword><style face="normal" font="default" size="100%">atomic layer deposition</style></keyword><keyword><style face="normal" font="default" size="100%">thin films</style></keyword><keyword><style face="normal" font="default" size="100%">nanomaterials</style></keyword><keyword><style face="normal" font="default" size="100%">alkoxides</style></keyword><keyword><style face="normal" font="default" size="100%">iron-oxide films</style></keyword><keyword><style face="normal" font="default" size="100%">layer deposition</style></keyword><keyword><style face="normal" font="default" size="100%">gadolinium orthoferrite</style></keyword><keyword><style face="normal" font="default" size="100%">aluminum-oxide</style></keyword><keyword><style face="normal" font="default" size="100%">refeo3 re</style></keyword><keyword><style face="normal" font="default" size="100%">mocvd</style></keyword><keyword><style face="normal" font="default" size="100%">ald</style></keyword><keyword><style face="normal" font="default" size="100%">precursors</style></keyword><keyword><style face="normal" font="default" size="100%">systems</style></keyword><keyword><style face="normal" font="default" size="100%">eu</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">Mar 31</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0040-6090</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000521128800003</style></accession-num><abstract><style face="normal" font="default" size="100%">Thin films of multiferroic gadolinium orthoferrite (GdFeO3) are of significant interest due to intrinsic coupling of magnetic and ferroelectric order in their monolithic bimetallic structures relevant for potential applications in magneto-optical data storage devices. Formation of this composition in stoichiometric pure form is challenging due to facile formation of the thermodynamically preferred garnet phase (Gd3Fe5O12) that mostly coexists as a minor phase in gadolinium orthoferrite films. We report herein the selective epitaxial growth of GdFeO3 films by atomic layer deposition of a single bimetallic precursor [GdFe((OBu)-Bu-t)(6)(C5H5N)(2)] containing Gd:Fe in the required stoichiometric ratio, and using ozone as co-reactant. Intact vaporisation of [GdFe((OBu)-Bu-t)(6)(C5H5N)(2)] in the gas phase and its clean conversion into the complex oxide phase as validated by mass spectral studies and thermogravimetry demonstrate the potential of the Gd-Fe compound as an efficient single-source precursor. Epitaxial growth of GdFeO3 on SrTiO3 substrates was confirmed by X-ray diffraction analysis, whereas the presence of Fe3+ and Gd3+ without any traces of N species from the ligands was verified by X- ray photoelectron spectroscopy. Magnetic properties of the resulting perovskite films studied by superconducting quantum interference device measurements revealed the superposition of two independent magnetic contributions due to paramagnetic (Gd3+) and ferromagnetic (Fe3+) sublattices in GdFeO3.</style></abstract><notes><style face="normal" font="default" size="100%">Kw4if&#xD;Times Cited:1&#xD;Cited References Count:56</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000521128800003</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">ARTN 137848&#xD;10.1016/j.tsf.2020.137848</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>597</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">597</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Barani, Hossein</style></author><author><style face="normal" font="default" size="100%">Haseloer, Alexander</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Klein, Axel</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Birjand, Dept Carpet, Birjand, Iran&#xD;Univ Cologne, Inst Inorgan Chem, Dept Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Sustained release of a thiosemicarbazone from antibacterial electrospun poly(lactic-co-glycolic acid) fiber mats</style></title><secondary-title><style face="normal" font="default" size="100%">Polym. Adv. Technol.</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Polym Advan Technol</style></alt-title></titles><pages><style face="normal" font="default" size="100%">3182-3193</style></pages><volume><style face="normal" font="default" size="100%">n/a</style></volume><number><style face="normal" font="default" size="100%">n/a</style></number><keywords><keyword><style face="normal" font="default" size="100%">bacteriostatic properties, controlled drug release, nano fiber mats, PLGA, thiosemicarbazone</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style face="normal" font="default" size="100%">2020/07/28/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1042-7147</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000563841800001</style></accession-num><abstract><style face="normal" font="default" size="100%">Antibacterial fiber mats of poly(lactic‐co‐glycolic acid) (PLGA) were produced in the presence of different amounts of the thiosemicarbazone (TSC) N 4‐(S )‐(1‐phenylethyl)‐2‐(pyridin‐2‐ylmethylene)hydrazine‐1‐carbothioamide (HfpyTSCmB) through electrospinning. Increasing amounts (0, 2.5, 5, and 10 wt%) of TSC in the PLGA spinning solution in 2,2,2‐trifluoroethanol (TFE) caused an increase up to 230% in conductivity and up to 27% in viscosity. The morphology of the electrospun fibers was studied using scanning electron microscope (SEM) and showed the formation of uniform, bead free, cylindrical, and smooth fiber mats. Increasing amounts of HfpyTSCmB in the polymer solution resulted also in significant shrinking of the diameter and narrowing of the size distribution of the fibers in line with the increased conductivity of the spinning solutions. Nuclear magnetic resonance (NMR) spectroscopy and thermal methods (DSC and TG/DTA) gave proof for the chemical integrity of HfpyTSCmB in the fiber mats after the electrospinning process. The release profile of HfpyTSCmB from the fibers was examined using UV‐vis absorption spectroscopy. The observed release data during 21 days was fitted to different mathematical models with the best results obtained from the Higuchi release model. The fiber mat samples showed effective antibacterial properties with inhibition zones of 0.5 to 1.5 mm against the Gram‐positive Staphylococcus aureus and the Gram‐negative Escherichia coli .</style></abstract><label><style face="normal" font="default" size="100%">Barani2020Jul</style></label><notes><style face="normal" font="default" size="100%">Ok4lc&#xD;Times Cited:0&#xD;Cited References Count:63</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/pat.5043</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/pat.5043</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>562</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">562</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zare, Mina</style></author><author><style face="normal" font="default" size="100%">Namratha, Keerthiraj</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Hezam, Abdo</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Byrappa, Kullaiah</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Institute of Inorganic Chemistry , University of Cologne , D-50939 Cologne , Germany.&#xD;Adichunchanagiri University , B.G. Nagara 571448 , Mandya District, India.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Smart Fortified PHBV-CS Biopolymer with ZnO–Ag Nanocomposites for Enhanced Shelf Life of Food Packaging</style></title><secondary-title><style face="normal" font="default" size="100%">ACS applied materials &amp; interfaces</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></full-title></periodical><pages><style face="normal" font="default" size="100%">48309-48320</style></pages><volume><style face="normal" font="default" size="100%">11</style></volume><number><style face="normal" font="default" size="100%">51</style></number><edition><style face="normal" font="default" size="100%">2019/11/28</style></edition><keywords><keyword><style face="normal" font="default" size="100%">Anti-Bacterial Agents/*chemistry</style></keyword><keyword><style face="normal" font="default" size="100%">Biopolymers/*chemistry</style></keyword><keyword><style face="normal" font="default" size="100%">Chitosan/*chemistry</style></keyword><keyword><style face="normal" font="default" size="100%">Food Packaging</style></keyword><keyword><style face="normal" font="default" size="100%">Nanocomposites/*chemistry</style></keyword><keyword><style face="normal" font="default" size="100%">Time Factors</style></keyword><keyword><style face="normal" font="default" size="100%">Zinc Oxide/*chemistry</style></keyword><keyword><style face="normal" font="default" size="100%">Phbv</style></keyword><keyword><style face="normal" font="default" size="100%">ZnO-Ag nanocomposite</style></keyword><keyword><style face="normal" font="default" size="100%">chitosan</style></keyword><keyword><style face="normal" font="default" size="100%">degradable biopolymer</style></keyword><keyword><style face="normal" font="default" size="100%">hydrothermal</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Dec 26</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><accession-num><style face="normal" font="default" size="100%">31774258</style></accession-num><abstract><style face="normal" font="default" size="100%">Thymus vulgaris leaf extract was used as a stabilizer and reducing agent in the green, facile, and biomimetic hydrothermal decomposition reaction for the fabrication of zinc oxide-silver nanocomposites (ZnO-Ag NCs). The nanocomposite (NC) as an active agent was integrated into poly(3-hydroxybutyrate-co-3-hydroxyvalerate)-chitosan (PHBV-CS) in a highly precise ratio of solvent mixture by ultrasonication without the aid of any coupling agent to fabricate the novel degradable biopolymer (BP) nanocomposite via solvent casting method to enhance the mechanical properties and antimicrobial activity and with the lowest immigration rate to improve the shelf life of poultry items. The ZnO-Ag NCs as a nanoactive agent in the food packaging preserved food safety by controlling its spoilage. The morphology, physical, mechanical, barrier, antibacterial, and migration properties of the nanocrystals were assessed via several characterization methods to show the enhancement of the prepared polymer in various aspects of properties. The NCs BP were used for potential sensory evaluation of chicken breast refrigerated over a period of 15 days. The data demonstrated that these bio-based nanocomposites show great antimicrobial activity that offers perspectives for the replacement of traditional petrochemical-based polymers currently used for food packaging of poultry items.</style></abstract><notes><style face="normal" font="default" size="100%">Zare, Mina&#xD;Namratha, Keerthiraj&#xD;Ilyas, Shaista&#xD;Hezam, Abdo&#xD;Mathur, Sanjay&#xD;Byrappa, Kullaiah&#xD;eng&#xD;ACS Appl Mater Interfaces. 2019 Dec 26;11(51):48309-48320. doi: 10.1021/acsami.9b15724. Epub 2019 Dec 11.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.ncbi.nlm.nih.gov/pubmed/31774258</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsami.9b15724</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>185</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">185</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Surmenev, Roman A.</style></author><author><style face="normal" font="default" size="100%">Orlova, Tetiana N.</style></author><author><style face="normal" font="default" size="100%">Chernozem, Roman V.</style></author><author><style face="normal" font="default" size="100%">Ivanova, Anna A.</style></author><author><style face="normal" font="default" size="100%">Bartasyte, Ausrine</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Surmeneva, Maria A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hybrid lead-free polymer-based scaffolds with improved piezoelectric response for biomedical energy-harvesting applications: A review</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><keywords><keyword><style face="normal" font="default" size="100%">2019, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year></dates><isbn><style face="normal" font="default" size="100%">22112855</style></isbn><label><style face="normal" font="default" size="100%">Surmenev2019</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://linkinghub.elsevier.com/retrieve/pii/S221128551930391X</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>184</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">184</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Surmenev, Roman</style></author><author><style face="normal" font="default" size="100%">Zviagin, Andrei</style></author><author><style face="normal" font="default" size="100%">Surmeneva, Maria</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Pyeon, Myeongwhun</style></author><author><style face="normal" font="default" size="100%">Tutacz, Peter</style></author><author><style face="normal" font="default" size="100%">Chernozem, Roman</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Ivanov, Yurii</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Natl Res Tomsk Polytech Univ, Phys Mat Sci &amp; Composite Mat Ctr, Tomsk 634050, Russia&#xD;Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;IHCE, 2-3 Akad Chesky Ave, Tomsk 634055, Russia</style></auth-address><titles><title><style face="normal" font="default" size="100%">Enhanced piezoelectric response of hybrid biodegradable 3D poly(3-hydroxybutyrate) scaffolds coated with hydrothermally deposited ZnO for biomedical applications</style></title><secondary-title><style face="normal" font="default" size="100%">European Polymer Journal</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Eur Polym J</style></alt-title></titles><pages><style face="normal" font="default" size="100%">272-279</style></pages><volume><style face="normal" font="default" size="100%">117</style></volume><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Aug</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0014-3057</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000473842300026</style></accession-num><abstract><style face="normal" font="default" size="100%">Fibrous scaffolds based on biodegradable piezoelectric poly(3-hydroxybutyrate) (PHB) polymers were fabricated via electrospinning. Hydrothermal deposition of zinc oxide (ZnO) on the surfaces of fibrous PHB scaffolds resulted in a homogeneous ZnO layer that grew conformally on the porous polymeric scaffold. X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) results confirmed the formation of a hexagonal wurtzite crystal structure of ZnO on the PHB fibres. XRD patterns, TEM and EDS analysis revealed a bimodal morphology with rod-like nanostructures that grew preferentially along the c-axis as well as nanoparticles that grew randomly. The piezoelectric charge coefficient d(33) for pristine PHB scaffolds was 2.9 +/- 0.1 pC.N-1, whereas after ZnO deposition, it substantially increased to 13.7 +/- 1.6 pC.N-1. Moreover, the output surface electrical potential of PHB scaffolds after ZnO deposition also substantially increased from 0.58 +/- 0.02 to 0.88 +/- 0.04 V, showing enhanced electromechanical coupling in the piezoelectric nanocomposites. The output surface electric potential for ZnO-coated PHB scaffolds was stable within 1200 loading cycles. In addition, the ZnO rod-like nanostructured surface improved the wettability of PHB fibrous scaffolds, demonstrating synergy between the ceramic and polymeric phases in PHB/ZnO composites. Therefore, the hybrid biodegradable piezoelectric scaffolds reported in the present study are potentially useful for biomedical applications, where both improved piezoelectric response and surface wettability are required.</style></abstract><label><style face="normal" font="default" size="100%">Surmenev2019</style></label><notes><style face="normal" font="default" size="100%">Ig5kp&#xD;Times Cited:8&#xD;Cited References Count:45</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000473842300026</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.eurpolymj.2019.05.016</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>183</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">183</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Straub, Mark</style></author><author><style face="normal" font="default" size="100%">Leduc, Jennifer</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Raauf, Aida</style></author><author><style face="normal" font="default" size="100%">Lohrey, Trevor</style></author><author><style face="normal" font="default" size="100%">Minasian, Stefan</style></author><author><style face="normal" font="default" size="100%">Arnold, John</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Department of Chemistry, University of California, Berkeley, Berkeley, CA, 94720, USA.&#xD;Heavy Element Chemistry Group, Chemical Sciences Division, Lawrence Berkeley National Lab, Berkeley, CA, 94720, USA.&#xD;Institute of Inorganic Chemistry, University of Cologne, 50939, Cologne, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Chemical Vapor Deposition of Phase-Pure Uranium Dioxide Thin Films from Uranium(IV) Amidate Precursors</style></title><secondary-title><style face="normal" font="default" size="100%">Angewandte Chemie International Edition</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">5805--5809</style></pages><volume><style face="normal" font="default" size="100%">58</style></volume><number><style face="normal" font="default" size="100%">17</style></number><edition><style face="normal" font="default" size="100%">2019/03/02</style></edition><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Apr 16</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1521-3773 (Electronic)&#xD;1433-7851 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">30821048</style></accession-num><abstract><style face="normal" font="default" size="100%">Homoleptic uranium(IV) amidate complexes have been synthesized and applied as single-source molecular precursors for chemical vapor deposition of UO2 thin films. These precursors decompose by alkene elimination to give highly crystalline, phasepure UO2 films with an unusual branched heterostructure.</style></abstract><label><style face="normal" font="default" size="100%">Straub2019</style></label><notes><style face="normal" font="default" size="100%">Straub, Mark D&#xD;Leduc, Jennifer&#xD;Frank, Michael&#xD;Raauf, Aida&#xD;Lohrey, Trevor D&#xD;Minasian, Stefan G&#xD;Mathur, Sanjay&#xD;Arnold, John&#xD;eng&#xD;DE-AC02-05CH11231/U.S. Department of Energy&#xD;Deutscher Akademischer Austauschdienst&#xD;SPP 1613/Deutsche Forschungsgemeinschaft&#xD;SPP 1959/Deutsche Forschungsgemeinschaft&#xD;Universitat zu Koln&#xD;Germany&#xD;Angew Chem Int Ed Engl. 2019 Apr 16;58(17):5749-5753. doi: 10.1002/anie.201901924. Epub 2019 Mar 20.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.ncbi.nlm.nih.gov/pubmed/30821048</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/anie.201901924</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>182</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">182</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Stadler, Daniel</style></author><author><style face="normal" font="default" size="100%">Mueller, David N.</style></author><author><style face="normal" font="default" size="100%">Brede, Thomas</style></author><author><style face="normal" font="default" size="100%">Duchoň, Tomáš,</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Sarkar, Anirban</style></author><author><style face="normal" font="default" size="100%">Giesen, Margret</style></author><author><style face="normal" font="default" size="100%">Schneider, Claus M.</style></author><author><style face="normal" font="default" size="100%">Volkert, Cynthia A.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Institute of Inorganic Chemistry , University of Cologne , Greinstrasse 6 , D-50939 Cologne , Germany.&#xD;Forschungszentrum Julich GmbH , Peter Grunberg Institute (PGI-6) , D-52425 Julich , Germany.&#xD;Institute of Materials Physics , Georg-August-University Goettingen , Friedrich-Hund-Platz 1 , D-37077 Goettingen , Germany.&#xD;Center for Neutron Science (JCNS-2) and Peter Grunberg Institute (PGI-4), JARA-FIT , Forschungszentrum Julich , D-52425 Julich , Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Magnetic Field-Assisted Chemical Vapor Deposition of Iron Oxide Thin Films: Influence of Field-Matter Interactions on Phase Composition and Morphology</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry Letters</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">6253-6259</style></pages><volume><style face="normal" font="default" size="100%">10</style></volume><number><style face="normal" font="default" size="100%">20</style></number><edition><style face="normal" font="default" size="100%">2019/09/11</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2019, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Oct 17</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1948-7185</style></isbn><accession-num><style face="normal" font="default" size="100%">31500420</style></accession-num><abstract><style face="normal" font="default" size="100%">Magnetic field-assisted CVD offers a direct pathway to manipulate the evolution of microstructure, phase composition, and magnetic properties of the as-prepared film. We report on the role of applied magnetic fields (0.5 T) during a cold-wall CVD deposition of iron oxide from [Fe(III)(O(t)Bu)3]2 leading to higher crystallinity, larger particulates, and better out-of-plane magnetic anisotropy, if compared with zero-field depositions. Whereas selective formation of homogeneous magnetite films was observed for the field-assisted process, coexistence of hematite and amorphous iron(III) oxide was confirmed under zero-field conditions. Comparison of the coercive field (11 vs 60 mT) indicated lower defect concentration for the field-assisted process with nearly superparamagnetic behavior. X-ray photoemission electron microscopy (X-PEEM) in absorption mode at the O-K and Fe-L3,2 edges confirmed the selective formation of magnetite (field-assisted) and hematite (zero-field) with coexisting amorphous phases, respectively, emphasizing the importance of field-matter interactions in the phase-selective synthesis of magnetic thin films.</style></abstract><label><style face="normal" font="default" size="100%">Stadler2019</style></label><notes><style face="normal" font="default" size="100%">Stadler, Daniel&#xD;Mueller, David N&#xD;Brede, Thomas&#xD;Duchon, Tomas&#xD;Fischer, Thomas&#xD;Sarkar, Anirban&#xD;Giesen, Margret&#xD;Schneider, Claus M&#xD;Volkert, Cynthia A&#xD;Mathur, Sanjay&#xD;eng&#xD;J Phys Chem Lett. 2019 Oct 17;10(20):6253-6259. doi: 10.1021/acs.jpclett.9b02381. Epub 2019 Oct 3.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.ncbi.nlm.nih.gov/pubmed/31500420</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.jpclett.9b02381</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>181</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">181</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Stadler, Daniel</style></author><author><style face="normal" font="default" size="100%">Brede, Thomas</style></author><author><style face="normal" font="default" size="100%">Schwarzbach, Danny</style></author><author><style face="normal" font="default" size="100%">Maccari, Fernando</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Gutfleisch, Oliver</style></author><author><style face="normal" font="default" size="100%">Volkert, Cynthia A.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Dept Chem, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;Univ Goettingen, Inst Mat Phys, Friedrich Hund Pl 1, D-37077 Gottingen, Germany&#xD;Tech Univ Darmstadt, Mat Sci, Alarich Weiss Str 16, D-64287 Darmstadt, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Anisotropy control in magnetic nanostructures through field-assisted chemical vapor deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Nanoscale Advances</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nanoscale Adv</style></alt-title></titles><pages><style face="normal" font="default" size="100%">4290-4295</style></pages><volume><style face="normal" font="default" size="100%">1</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">2019, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Nov 1</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2516-0230</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000496186600006</style></accession-num><abstract><style face="normal" font="default" size="100%">Chemical vapor deposition of iron pentacarbonyl (Fe(CO)5) in an external magnetic field (B = 1.00 T) was found to significantly affect the microstructure and anisotropy of as-deposited iron crystallites that could be transformed into anisotropic hematite (α-Fe2O3) nanorods by aerobic oxidation. The deterministic influence of external magnetic fields on CVD deposits was found to be substrate-independent as demonstrated by the growth of anisotropic α-Fe columns on FTO (F:SnO2) and Si (100), whereas the films deposited in the absence of the magnetic field were constituted by isotropic grains. TEM images revealed gradual increase in average crystallite size in correlation to the increasing field strength and orientation, which indicates the potential of magnetic field-assisted chemical vapor deposition (mfCVD) in controlling the texture of the CVD grown thin films. Given the facet-dependent activity of hematite in forming surface-oxygenated intermediates, exposure of crystalline facets and planes with high atomic density and electron mobilities is crucial for oxygen evolution reactions. The field-induced anisotropy in iron nanocolumns acting as templates for growing textured hematite pillars resulted in two-fold higher photoelectrochemical efficiency for hematite films grown under external magnetic fields (J = 0.050 mA cm−2), when compared to films grown in zero field (J = 0.027 mA cm−2). The dark current measurements indicated faster surface kinetics as the origin of the increased catalytic activity.</style></abstract><label><style face="normal" font="default" size="100%">Stadler2019</style></label><notes><style face="normal" font="default" size="100%">Jm4kz&#xD;Times Cited:0&#xD;Cited References Count:30</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000496186600006</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c9na00467j</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>180</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">180</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sinusaite, Lauryna</style></author><author><style face="normal" font="default" size="100%">Renner, Alexander M.</style></author><author><style face="normal" font="default" size="100%">Schütz, Markus B.</style></author><author><style face="normal" font="default" size="100%">Antuzevics, Andris</style></author><author><style face="normal" font="default" size="100%">Rogulis, Uldis</style></author><author><style face="normal" font="default" size="100%">Grigoraviciute-Puroniene, Inga</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Zarkov, Aleksej</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Vilnius Univ, Inst Chem, Naugarduko 24, LT-03225 Vilnius, Lithuania&#xD;Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;Univ Latvia, Inst Solid State Phys, Kengaraga 8, LV-1063 Riga, Latvia</style></auth-address><titles><title><style face="normal" font="default" size="100%">Effect of Mn doping on the low-temperature synthesis of tricalcium phosphate (TCP) polymorphs</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the European Ceramic Society</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Eur Ceram Soc</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Journal of the European Ceramic Society</style></full-title></periodical><pages><style face="normal" font="default" size="100%">3257-3263</style></pages><volume><style face="normal" font="default" size="100%">39</style></volume><number><style face="normal" font="default" size="100%">10</style></number><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Aug</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09552219</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000468715700034</style></accession-num><abstract><style face="normal" font="default" size="100%">Effect of Mn doping on the low - temperature synthesis of tricalcium phosphate (TCP) polymorphs was demonstrated in α - and β - TCP po lymorphs prepared by wet precipitation method under identical conditions and anneal ed at 700 °C . Calcium phosphates with Mn doping level in the range from 1 to 5 mol% were studied and the f ormation of desired polymorph was controlled by varying Mn content in as - prepared precipitates. It was found that increas ing Mn content resulted in the formation of β - TCP, while α - TCP was obtained with low Mn doping level , whereas a mixture of two polymorphs was obtained for intermediate Mn concentrations. Moreove r, doping with Mn ions allow ed the synthesis of β - TCP at relatively low temperature ( 700 °C ) . S ynthesized compounds were characterized by X - ray diffraction (XRD) analysis , electr on paramagnetic resonance (EPR), Fourier - transform infrared spectroscopy (FTIR) , s canning electron microscopy (SEM) , inductively coupled plasma optical emission spectrometry (ICP - OES) and colorimetric MTT assay.</style></abstract><label><style face="normal" font="default" size="100%">Sinusaite2019</style></label><notes><style face="normal" font="default" size="100%">Hz2yw&#xD;Times Cited:8&#xD;Cited References Count:53</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://linkinghub.elsevier.com/retrieve/pii/S0955221919302249</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.jeurceramsoc.2019.03.057</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>593</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">593</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sekhar, P. K.</style></author><author><style face="normal" font="default" size="100%">Ludwig, T.</style></author><author><style face="normal" font="default" size="100%">Wilhelm, M.</style></author><author><style face="normal" font="default" size="100%">Graf, D.</style></author><author><style face="normal" font="default" size="100%">Riheen, M. A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Washington State Univ Vancouver, Sch Engn &amp; Comp Sci, Nanomat &amp; Sensors Lab, Vancouver, WA 98686 USA&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Potentiometric Ethene Sensor for Postharvest Detection Applications</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the Electrochemical Society</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Electrochem Soc</style></alt-title></titles><pages><style face="normal" font="default" size="100%">B1477-B1482</style></pages><volume><style face="normal" font="default" size="100%">166</style></volume><number><style face="normal" font="default" size="100%">15</style></number><keywords><keyword><style face="normal" font="default" size="100%">gas sensors</style></keyword><keyword><style face="normal" font="default" size="100%">ethylene</style></keyword><keyword><style face="normal" font="default" size="100%">nanoparticles</style></keyword><keyword><style face="normal" font="default" size="100%">liquid</style></keyword><keyword><style face="normal" font="default" size="100%">growth</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Oct 30</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0013-4651</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000493563400002</style></accession-num><abstract><style face="normal" font="default" size="100%">A sensitive and selective electrochemical sensor for the detection of ethene is reported. Reduced Graphene Oxide (rGO)-Copper (Cu) nanocomposite modified Lanthanum Strontium Chromite (LSC) and Pt are used as electrodes. Yttria-Stabilized Zirconia (YSZ) is used as the solid electrolyte. This bilayer electrochemical sensor was suitable for the detection of up to 10 parts per billion (ppb) of ethene that is of significant interest for post-harvest monitoring applications. The mixed potential sensor responded non-linearly to varying concentrations of Ethene (0 to 100 ppb). A 30% reduction in ethene sensor response was observed when the relative humidity was increased to 80% (from 10%). The optimal operating temperature of the sensor was found to be 500 degrees C considering the sensitivity-response time trade-off. The device exhibited a strong interference rejection potential to NH3 and CO. The next generation of such a mixed potential sensor with integrated heaters and miniaturized implementation will enable the possibility of ethene sensor commercialization similar to the automotive oxygen sensor. (C) 2019 The Electrochemical Society.</style></abstract><notes><style face="normal" font="default" size="100%">Ji6fo&#xD;Times Cited:4&#xD;Cited References Count:34</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000493563400002</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1149/2.0501915jes</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>179</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">179</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Renner, Alexander M.</style></author><author><style face="normal" font="default" size="100%">Schütz, Markus B.</style></author><author><style face="normal" font="default" size="100%">Moog, Daniel</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electroacoustic quantification of surface bound ligands in functional nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry Select</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">11959-11964</style></pages><volume><style face="normal" font="default" size="100%">4</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2019, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year></dates><abstract><style face="normal" font="default" size="100%">The electrokinetic sonic amplitude (ESA) is one of the most versatile techniques for deriving the zeta potential of nanoparticles before, during and after surface functionalization with different ligands, thus overcoming current limitations of well‐established electrophoretic measurement principles. We present a novel method for direct quantification of accessible hydroxide groups available on the surface of silica nanoparticles by the ESA effect, supported by simultaneous electrical conductivity measurements. Moreover, the in‐operando determination of varying zeta potential during addition of carboxylic acids demonstrate a profound way to quantify surface‐bound ligands, which still poses a challenge in following the surface modification of nanoparticles. In this study, phase pure cuboidal hematite particles were chosen as a model system with an initial zeta potential between +50 and +55 mV in ethanol. Using both citric acid and 10‐undecynoic acid as surface‐modifiers, the correlation between the degree of surface functionalization and zeta potential was investigated. The decrease of zeta potential of hematite particles during the titration of 10‐undecynoic acid or citric acid could be directly correlated to a successful surface functionalization in contrast to a surface protonation, which would be expected in case of both carboxylic acids. Furthermore, the addition of 10‐undecynoic acid led to a stabilization effect on the zeta potential of cuboidal hematite particles. These results highlight the hitherto unexplored potential of ESA techniques as a quantification method in nanoparticle surface modification.</style></abstract><label><style face="normal" font="default" size="100%">Renner2019</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/slct.201902710</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>634</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">634</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Queraltó, Albert</style></author><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Frohnhoven, Robert</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Vanrompay, Hans</style></author><author><style face="normal" font="default" size="100%">Bals, Sara</style></author><author><style face="normal" font="default" size="100%">Bartasyte, Ausrine</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">LaFeO3 Nanofibers for High Detection of Sulfur-Containing Gases</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Sustainable Chemistry &amp; Engineering</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">6023-6032</style></pages><volume><style face="normal" font="default" size="100%">7</style></volume><number><style face="normal" font="default" size="100%">6</style></number><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">2019/03/18</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acssuschemeng.8b06132</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acssuschemeng.8b06132</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>177</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">177</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Queraltó, Albert</style></author><author><style face="normal" font="default" size="100%">Frohnhoven, Robert</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Gómez, Andrés</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Intrinsic piezoelectric characterization of BiFeO 3 nanofibers and its implications for energy harvesting</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Surface Science</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Applied Surface Science</style></full-title></periodical><pages><style face="normal" font="default" size="100%">144760</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2019, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year></dates><isbn><style face="normal" font="default" size="100%">0169-4332</style></isbn><abstract><style face="normal" font="default" size="100%">Perovskite oxide-based ferroelectrics are interesting in energy applications due to their electrical and optical properties. Nanostructuring opens new paths to increase the surface-to-volume ratio, porosity, and mechanical flexibility as compared with bulk materials, improving and tuning properties associated with piezoelectricity, ferroelectricity, piezoelectrochemistry, electrical conductivity, and catalysis. To elucidate the impact of nanostructuration, in piezoelectricity, we characterized one of the most promising perovskite materials, bismuth ferrite (BiFeO3), in the form of 1D nanostructures, namely nanofibers. A set of BiFeOx precursor nanofibers were electrospun from a chemical sol and calcined at 600 °C to obtain the final BiFeO3 nanofiber structure. By scanning the nanofiber sample, the piezo-generated charge at the nanoscale level was studied by Direct Piezoelectric Force Microscopy (DPFM). Our results report that the direct piezoelectric coefficient of the polycrystalline nanofibers is d33=11 pC/N, which corresponds to a smaller value as compared with epitaxial films, 22 pC/N for 60 nm films and 43 pC/N for 400 nm films. The diminishing of piezoelectric property characteristics is mainly attributed to the impact of nanostructuration. The nanofibers impose another clamping factor that decreases the BiFeO3 piezoelectric property, reducing their use as energy harvesters in favor of catalytic applications, water splitting, or photovoltaic applications.</style></abstract><label><style face="normal" font="default" size="100%">Queralto2019</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.apsusc.2019.144760</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>176</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">176</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pyeon, Myeongwhun</style></author><author><style face="normal" font="default" size="100%">Rauch, Vanessa</style></author><author><style face="normal" font="default" size="100%">Stadler, Daniel</style></author><author><style face="normal" font="default" size="100%">Gürsoy, Mehmet</style></author><author><style face="normal" font="default" size="100%">Deo, Meenal</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Hwang, Taejin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Selcuk Univ, Chem Engn Dept, TR-42075 Selcuklu, Konya, Turkey&#xD;Korea Inst Ind Technol KITECH, Heat Treatment R&amp;D Grp, Siheung Si 11358, Gyeonggi Do, South Korea</style></auth-address><titles><title><style face="normal" font="default" size="100%">Magnetic Field‐Assisted Control of Phase Composition and Texture in Photocatalytic Hematite Films</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Adv Eng Mater</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1900195</style></pages><volume><style face="normal" font="default" size="100%">21</style></volume><number><style face="normal" font="default" size="100%">8</style></number><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Aug</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1438-1656</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000481868900025</style></accession-num><abstract><style face="normal" font="default" size="100%">We report the influence of external magnetic fields applied parallel or perpendicular to the substrate during plasma chemical vapor deposition (PECVD) of hematite (α‐Fe2O3) nanostructures. Hematite films grown from iron precursors show pronounced changes in phase composition (pure hematite vs. coexistence of hematite and magnetite) and crystallographic textures depending upon whether PECVD is performed with or without the influence of external magnetic field. Static magnetic fields created by rod‐type (RTMs) or disk‐type magnets (DTMs) results in hematite films with anisotropic or equiaxed grains, respectively. Using RTMs, a superior photoelectrochemical (PEC) performance is obtained for hematite photoanodes synthesized under perpendicularly applied magnetic field (with respect to substrate), whereas parallel magnetic field results in the most efficient hematite photoanode in the case of DTM. The experimental data on microstructure and functional properties of hematite films show that application of magnetic fields has a significant effect on the crystallite size and texture with preferred growth and/or suppression of grains with specific texture in Fe2O3 films. Investigations on the water splitting properties of the hematite films in a photoelectrochemical reactor reveal that photocurrent values of hematite photoanodes are remarkably different for films deposited with (0.659 mA cm−2) or without (0.484 mA cm−2) external magnetic field.</style></abstract><label><style face="normal" font="default" size="100%">Pyeon2019</style></label><notes><style face="normal" font="default" size="100%">Is0uv&#xD;Times Cited:1&#xD;Cited References Count:37</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/abs/10.1002/adem.201900195</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">ARTN 1900195&#xD;10.1002/adem.201900195</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>635</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">635</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pariy, I. O.</style></author><author><style face="normal" font="default" size="100%">Ivanova, A. A.</style></author><author><style face="normal" font="default" size="100%">Shvartsman, V. V.</style></author><author><style face="normal" font="default" size="100%">Lupascu, D. C.</style></author><author><style face="normal" font="default" size="100%">Sukhorukov, G. B.</style></author><author><style face="normal" font="default" size="100%">Ludwig, T.</style></author><author><style face="normal" font="default" size="100%">Bartasyte, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Surmeneva, M. A.</style></author><author><style face="normal" font="default" size="100%">Surmenev, R. A.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Physical Materials Science and Composite Materials Centre, National Research Tomsk Polytechnic University, 634050 Tomsk, Russia. igor-parij1995@mail.ru.&#xD;Physical Materials Science and Composite Materials Centre, National Research Tomsk Polytechnic University, 634050 Tomsk, Russia. metallurg_annet@mail.ru.&#xD;Institute for Materials Science and Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, 45141 Essen, Germany. vladimir.shvartsman@uni-due.de.&#xD;Institute for Materials Science and Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, 45141 Essen, Germany. doru.lupascu@uni-due.de.&#xD;School of Engineering and Materials Science, Queen Mary University of London, London E1 4NS, UK. g.sukhorukov@qmul.ac.uk.&#xD;University of Cologne, 50923 Cologne, Germany. tim.ludwig@uni-koeln.de.&#xD;FEMTO-ST Institute, 25000 Besançon, France. ausrine.bartasyte@femto-st.fr.&#xD;University of Cologne, 50923 Cologne, Germany. sanjay.mathur@uni-koeln.de.&#xD;Physical Materials Science and Composite Materials Centre, National Research Tomsk Polytechnic University, 634050 Tomsk, Russia. surmenevamaria@mail.ru.&#xD;Physical Materials Science and Composite Materials Centre, National Research Tomsk Polytechnic University, 634050 Tomsk, Russia. rsurmenev@mail.ru.&#xD;University of Cologne, 50923 Cologne, Germany. rsurmenev@mail.ru.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Piezoelectric Response in Hybrid Micropillar Arrays of Poly(Vinylidene Fluoride) and Reduced Graphene Oxide</style></title><secondary-title><style face="normal" font="default" size="100%">Polymers (Basel)</style></secondary-title></titles><volume><style face="normal" font="default" size="100%">11</style></volume><number><style face="normal" font="default" size="100%">6</style></number><edition><style face="normal" font="default" size="100%">2019/06/23</style></edition><keywords><keyword><style face="normal" font="default" size="100%">hybrid film</style></keyword><keyword><style face="normal" font="default" size="100%">piezoelectric response</style></keyword><keyword><style face="normal" font="default" size="100%">poly(vinylidene fluoride)</style></keyword><keyword><style face="normal" font="default" size="100%">reduced graphene oxide</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun 20</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2073-4360</style></isbn><accession-num><style face="normal" font="default" size="100%">31226755</style></accession-num><abstract><style face="normal" font="default" size="100%">This study was dedicated to the investigation of poly(vinylidene fluoride) (PVDF) micropillar arrays obtained by soft lithography followed by phase inversion at a low temperature. Reduced graphene oxide (rGO) was incorporated into the PVDF as a nucleating filler. The piezoelectric properties of the PVDF-rGO composite micropillars were explored via piezo-response force microscopy (PFM). Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) showed that α, β, and γ phases co-existed in all studied samples, with a predominance of the γ phase. The piezoresponse force microscopy (PFM) data provided the local piezoelectric response of the PVDF micropillars, which exhibited a temperature-induced downward dipole orientation in the pristine PVDF micropillars. The addition of rGO into the PVDF matrix resulted in a change in the preferred polarization direction, and the piezo-response phase angle changed from -120° to 20°-40°. The pristine PVDF and PVDF loaded with 0.1 wt % of rGO after low-temperature quenching were found to possess a piezoelectric response of 86 and 87 pm/V respectively, which are significantly higher than the |d(33)(eff)| in the case of imprinted PVDF 64 pm/V. Thus, the addition of rGO significantly affected the domain orientation (polarization) while quenching increased the piezoelectric response.</style></abstract><notes><style face="normal" font="default" size="100%">2073-4360&#xD;Pariy, Igor O&#xD;Ivanova, Anna A&#xD;Shvartsman, Vladimir V&#xD;Orcid: 0000-0002-7155-2473&#xD;Lupascu, Doru C&#xD;Sukhorukov, Gleb B&#xD;Ludwig, Tim&#xD;Bartasyte, Ausrine&#xD;Orcid: 0000-0002-8862-2669&#xD;Mathur, Sanjay&#xD;Surmeneva, Maria A&#xD;Surmenev, Roman A&#xD;Orcid: 0000-0002-8061-3047&#xD;73/2019/Tomsk Polytechnic University/&#xD;Journal Article&#xD;Polymers (Basel). 2019 Jun 20;11(6):1065. doi: 10.3390/polym11061065.</style></notes><urls></urls><custom2><style face="normal" font="default" size="100%">PMC6632062</style></custom2><electronic-resource-num><style face="normal" font="default" size="100%">10.3390/polym11061065</style></electronic-resource-num><remote-database-provider><style face="normal" font="default" size="100%">NLM</style></remote-database-provider><language><style face="normal" font="default" size="100%">eng</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>175</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">175</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ojelere, Olusola</style></author><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Fac Math &amp; Nat Sci, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Molecularly Engineered Lithium–Chromium Alkoxide for Selective Synthesis of LiCrO2 and Li2CrO4 Nanomaterials</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganics</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Inorganics</style></alt-title></titles><pages><style face="normal" font="default" size="100%">22</style></pages><volume><style face="normal" font="default" size="100%">7</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2019, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Feb</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2304-6740</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000460321800003</style></accession-num><abstract><style face="normal" font="default" size="100%">Achieving control over the phase-selective synthesis of mixed metal oxide materials remains a challenge to the synthetic chemist due to diffusion-driven growth, which necessitates the search for new compounds with pre-existent chemical bonds between the phase-forming elements. We report here a simple solvothermal process to fabricate LiCrO2 and Li2CrO4 nanoparticles from bimetallic single-source precursors, demonstrating the distinctive influence of molecular design and calcination conditions on the resulting nanomaterials. The chemical identity of [Li2Cr(OtBu)4Cl(THF)2] (1) and [LiCr(OtBu)2(PyCH=COCF3)2(THF)2] (2) was unambiguously established in the solid state by single-crystal X-ray diffraction, revealing the formation of a coordination polymeric chain in compound 1, whereas electron paramagnetic resonance spectroscopy (EPR) studies revealed a monomeric structure in solution. TEM analysis of synthesized LiCrO2 nanoparticles showed nearly uniform particles size of approximately 20 nm. The sensitivity of the LiCrO2 phase towards oxidation was investigated by X-ray diffraction, revealing the formation of the stable Li2CrO4 after calcination in air.</style></abstract><label><style face="normal" font="default" size="100%">Ojelere2019</style></label><notes><style face="normal" font="default" size="100%">Hn6up&#xD;Times Cited:2&#xD;Cited References Count:36</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.mdpi.com/2304-6740/7/2/22</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">ARTN 22&#xD;10.3390/inorganics7020022</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>174</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">174</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Möllmann, Alexander</style></author><author><style face="normal" font="default" size="100%">Gedamu, Dawit</style></author><author><style face="normal" font="default" size="100%">Vivo, Paola</style></author><author><style face="normal" font="default" size="100%">Frohnhoven, Robert</style></author><author><style face="normal" font="default" size="100%">Stadler, Daniel</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Ka, Ibrahim</style></author><author><style face="normal" font="default" size="100%">Steinhorst, Maximilian</style></author><author><style face="normal" font="default" size="100%">Nechache, Riad</style></author><author><style face="normal" font="default" size="100%">Rosei, Federico</style></author><author><style face="normal" font="default" size="100%">Cloutier, Sylvain G.</style></author><author><style face="normal" font="default" size="100%">Kirchartz, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Highly Compact TiO2 Films by Spray Pyrolysis and Application in Perovskite Solar Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1801196</style></pages><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year></dates><abstract><style face="normal" font="default" size="100%">Transparent and pinhole free hole‐blocking layers such as TiO2 grown at low temperatures and by scalable processes are necessary to reduce production costs and thus enabling commercialization of perovskite solar cells. Here, the authors compare the transport properties of TiO2 compact layers grown by spray pyrolysis from commonly used titanium diisopropoxide bisacetylacetonate ([Ti(OPri)2(acac)2]) precursor to films grown by spray pyrolysis of TiCl4. Spray pyrolysis provides insights into the interdependence of precursor chemistry and electron transport properties of TiO2 films and their influence on the performance of the perovskite solar cells. X‐ray diffraction and X‐ray photoelectron spectroscopy data confirm the chemical and structural composition of the obtained films. Thin film deposition at lower temperature (150 °C) are conducted using TiCl4 to evaluate the influence of crystal growth and topography by scanning electron microscopy and atomic force microscopy as well as thickness (profilometry) and transmittance (UV/Vis spectroscopy) on the power conversion efficiency of perovskite solar cells. TiO2 compact layers grown from TiCl4 enhance the power conversion efficiency by acting as superior electron transfer medium and by reducing hysteresis behavior, when compared to films grown using titanium diisopropoxide bisacetylacetonate. UV/Vis spectroscopy and external quantum efficiency studies reveal the correlation of transmittance on the power conversion efficiency.</style></abstract><label><style face="normal" font="default" size="100%">Mollmann2019</style></label><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>173</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">173</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Marandi, Afsaneh</style></author><author><style face="normal" font="default" size="100%">Bahadori, Mehrnaz</style></author><author><style face="normal" font="default" size="100%">Tangestaninejad, Shahram</style></author><author><style face="normal" font="default" size="100%">Moghadam, Majid</style></author><author><style face="normal" font="default" size="100%">Mirkhani, Valiollah</style></author><author><style face="normal" font="default" size="100%">Mohammadpoor-Baltork, Iraj</style></author><author><style face="normal" font="default" size="100%">Frohnhoven, Robert</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Sandleben, Aaron</style></author><author><style face="normal" font="default" size="100%">Klein, Axel</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Isfahan, Dept Chem, Catalysis Div, Esfahan 8174673441, Iran&#xD;Univ Cologne, Dept Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Cycloaddition of CO2 with epoxides and esterification reactions using the porous redox catalyst Co-POM@MIL-101(Cr)</style></title><secondary-title><style face="normal" font="default" size="100%">New Journal of Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">New J Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">15585--15595</style></pages><volume><style face="normal" font="default" size="100%">43</style></volume><number><style face="normal" font="default" size="100%">39</style></number><keywords><keyword><style face="normal" font="default" size="100%">2019, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Oct 21</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1144-0546</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000489157400008</style></accession-num><abstract><style face="normal" font="default" size="100%">The catalytic activity of the recently reported Co-POM@MIL-101(Cr) composite, synthesized from K5[CoW12O40] (Co‐POM) and chromium(III) terephthalate (MIL‐101), was studied in the solvent-free cycloaddition of CO2 with epoxides and esterification of...The catalytic activity of the recently reported Co-POM@MIL-101(Cr) composite, synthesized from K5[CoW12O40] (Co‐POM) and chromium(III) terephthalate (MIL‐101), was studied in the solvent-free cycloaddition of CO2 with epoxides and esterification of acetic acid with various alcohols. The Co-POM@MIL-101(Cr) composite was synthesized using a one-pot HF-free method in a “bottle around ship” strategy. The material was thoroughly characterized using several methods such as (powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance spectroscopy (EPR). Temperature programmed desorption (TPD) of NH3 and CO2, and the CO2 adsorption capacity (adsorption isotherms) were used to study the acid-base properties of the materials. The combination of the electron-transfer character of Co(III)-POM and ordered mesopores in MIL-101(Cr) creates an efficient catalytic system with mild conditions (90 °C and 20 bar CO2 pressure) for solvent-free cycloaddition of CO2 to various epoxides. Esterification of acetic acid with alcohols was also carried out using the Co-POM@MIL-101 catalysts and high yields were achieved for different alcohols. The catalysis experiments also clearly show that the active site in this heterogeneous catalyst is the Co(III) center in the Keggin anion structure. It presumably conducts both the cycloaddition of CO2 to epoxides and the esterification reaction via an outer-sphere electron transfer mechanism using the Co(III)/Co(II) redox pair. The heterogeneous Co‐POM@MIL‐101 catalysts were separated by simple filtration and reused five times in the cycloaddition of CO2 with styrene epoxide and seven times for the esterification of acetic acid with benzyl alcohol with negligible leaching of Co‐POM and no considerable loss of activity.</style></abstract><label><style face="normal" font="default" size="100%">Marandi2019</style></label><notes><style face="normal" font="default" size="100%">Jc3dg&#xD;Times Cited:3&#xD;Cited References Count:76</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000489157400008</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c9nj02607j</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>172</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">172</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lee, Damin</style></author><author><style face="normal" font="default" size="100%">Kim, Kyung Su</style></author><author><style face="normal" font="default" size="100%">Yun, Je Moon</style></author><author><style face="normal" font="default" size="100%">Yoon, Seog-Young</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shin, Heon-Cheol</style></author><author><style face="normal" font="default" size="100%">Kim, Kwang Ho</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Pusan Natl Univ, Sch Mat Sci &amp; Engn, San 30 Jangjeon Dong, Busan 609735, South Korea&#xD;Pusan Natl Univ, Global Frontier R&amp;D Ctr Hybrid Interface Mat, San 30 Jangjeon Dong, Busan 609735, South Korea&#xD;Cologne Univ, Dept Chem, Chair Inorgan &amp; Mat Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Synergistic effects of dual nano-type electrode of NiCo-nanowire/NiMn-nanosheet for high-energy supercapacitors</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Alloys and Compounds</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Alloy Compd</style></alt-title></titles><pages><style face="normal" font="default" size="100%">119-128</style></pages><volume><style face="normal" font="default" size="100%">789</style></volume><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun 15</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09258388</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000464542700015</style></accession-num><abstract><style face="normal" font="default" size="100%">A unique three-dimensional hybrid NiCo(CO3)(OH)2 nanowire/NiMn(CO3)(OH)2 nanosheet composite was fabricated using a facile hydrothermal method as a binder-free electrode directly grown on Ni foam for supercapacitors. We examined the synergistic effect by fabricating Ni-Co-Mn ternary electrodes that used Ni-Co with a large specific surface area and Mn with a very high theoretical capacity. The new hybrid electrode had good electrochemical characteristics, exhibiting remarkably high specific capacitances of 1673.3 and 453.0 F g−1 at 3 and 15 A g−1, respectively. Compared with other samples, the capacitance showed less reduction as the current density increased. This result indicates stable electrode properties with increasing voltage. The cycling stability of the hybrid NiCo(CO3)(OH)2/NiMn(CO3)(OH)2 composite was measured as 82.1% after 5000 cycles. Additionally, we fabricated an asymmetric supercapacitor employing the NiCo(CO3)(OH)2/NiMn(CO3)(OH)2 composite as the positive electrode and graphene as the negative electrode, which exhibited a high energy density of 27.2 W h kg−1 at a power density of 702.7 W kg−1 and a remarkable cycling stability, with 89.4% capacitance retention after 5000 cycles. Thus, for the first time, we investigated the dual nano-type structure of an NiCo(CO3)(OH)2 nanowire/NiMn(CO3)(OH)2 nanosheet electrode for supercapacitors and obtained satisfactory results.</style></abstract><label><style face="normal" font="default" size="100%">Lee2019</style></label><notes><style face="normal" font="default" size="100%">Ht4ok&#xD;Times Cited:10&#xD;Cited References Count:42</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">https://linkinghub.elsevier.com/retrieve/pii/S0925838819307339</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.jallcom.2019.02.267</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>170</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">170</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Leduc, Jennifer</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Ruoko, Teropetri</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mayrhofer, Leonhard</style></author><author><style face="normal" font="default" size="100%">Tkachenko, Nikolai V</style></author><author><style face="normal" font="default" size="100%">Dong, Chungli</style></author><author><style face="normal" font="default" size="100%">Held, Alexander</style></author><author><style face="normal" font="default" size="100%">Moseler, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Tampere Univ Technol, Lab Chem &amp; Bioengn, FI-33720 Tampere, Finland&#xD;Fraunhofer Inst Mech Mat IWM, Freiburg, Germany&#xD;Tamkang Univ, Dept Phys, Tamsui, Taiwan</style></auth-address><titles><title><style face="normal" font="default" size="100%">Electronically Coupled Uranium and Iron Oxide Heterojunctions as Efficient Water Oxidation Catalysts</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Functional Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Adv Funct Mater</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Functional Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1905005</style></pages><volume><style face="normal" font="default" size="100%">29</style></volume><number><style face="normal" font="default" size="100%">50</style></number><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">October</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1616-301X</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000491124400001</style></accession-num><abstract><style face="normal" font="default" size="100%">The most critical challenge faced in realizing a high efficiency photoelectrochemical water splitting process is the lack of suitable photoanodes enabling the transfer of four electrons involved in the complex oxygen evolution reaction (OER). Uranium oxides are efficient catalysts due to their wide range optical absorption (E-g approximate to 1.8-3.2 eV), high photoconductivity, and multiple valence switching among uranium centers that improves the charge propagation kinetics. Herein, thin films of depleted uranium oxide (U3O8) are demonstrated grown via chemical vapor deposition effectively accelerate the OER in conjunction with hematite (alpha-Fe2O3) overlayers through a built-in potential at the interface. Density functional theory simulations demonstrate that the multivalence of U and Fe ions induce the adjustment of the band alignment subject to the concentration of interfacial Fe ions. In general, the equilibrium state depicts a type II band edge as the favored alignment, which improves charge-transfer processes as observed in transient and X-ray absorption (TAS and XAS) spectroscopy. The enhanced water splitting photocurrent density of the heterostructures (J = 2.42 mA cm(-2)) demonstrates the unexplored potential of uranium oxide in artificial photosynthesis.</style></abstract><label><style face="normal" font="default" size="100%">Leduc2019</style></label><notes><style face="normal" font="default" size="100%">Kp9rj&#xD;Times Cited:1&#xD;Cited References Count:54</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/10.1021/acscatal.8b04924</style></url><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/abs/10.1002/adfm.201905005</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">ARTN 1905005&#xD;10.1002/adfm.201905005</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>171</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">171</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Leduc, Jennifer</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Ghamgosar, Pedram</style></author><author><style face="normal" font="default" size="100%">You, Shujie</style></author><author><style face="normal" font="default" size="100%">Mouzon, Johanne</style></author><author><style face="normal" font="default" size="100%">Choi, Heechae</style></author><author><style face="normal" font="default" size="100%">Vomiero, Alberto</style></author><author><style face="normal" font="default" size="100%">Grosch, Matthias</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Lulea Univ Technol, Dept Engn Sci &amp; Math, Div Mat Sci, S-97187 Lulea, Sweden</style></auth-address><titles><title><style face="normal" font="default" size="100%">Electronically-Coupled Phase Boundaries in alpha-Fe2O3/Fe3O4 Nanocomposite Photoanodes for Enhanced Water Oxidation</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Nano Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Acs Appl Nano Mater</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Nano Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">334-342</style></pages><volume><style face="normal" font="default" size="100%">2</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2574-0970</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000464491500036</style></accession-num><abstract><style face="normal" font="default" size="100%">Photoelectrochemical (PEC) water splitting reactions are promising for sustainable hydrogen production from renewable sources. We report here, the preparation of α-Fe2O3/Fe3O4 composite films via a single-step chemical vapor deposition of [Fe(OtBu)3]2 and their use as efficient photoanode materials in PEC setups. Film thickness and phase segregation was controlled by varying the deposition time and corroborated through cross-section Raman spectroscopy and scanning electron microscopy. The highest water oxidation activity (0.48 mA/cm2 at 1.23 V vs RHE) using intermittent AM 1.5 G (100 mW/cm2) standard illumination was found for hybrid films with a thickness of 11 µm. This phenomenon is attributed to an improved electron transport resulting from a higher magnetite content towards the substrate interface and an increased light absorption due to the hematite layer mainly located at the top surface of the film. The observed high efficiency of α-Fe2O3/Fe3O4 nanocomposite photoanodes is attributed to the close proximity and establishment of 3D interfaces between the weakly ferro- (Fe2O3) and ferrimagnetic (Fe3O4) oxides, which in view of their differential chemical constitution and valence states of Fe ions (Fe2+/Fe3+) can enhance the charge separation and thus the overall electrical conductivity of the layer.</style></abstract><label><style face="normal" font="default" size="100%">Leduc2019</style></label><notes><style face="normal" font="default" size="100%">Ht3vo&#xD;Times Cited:7&#xD;Cited References Count:54</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/10.1021/acsanm.8b01936</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsanm.8b01936</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>169</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">169</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Leduc, Jennifer</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Jürgensen, Lasse</style></author><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Raauf, Aida</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Chemistry of actinide centers in heterogeneous catalytic transformations of small molecules</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Catalysis</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Acs Catal</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Catalysis</style></full-title></periodical><pages><style face="normal" font="default" size="100%">acscatal.8b04924</style></pages><volume><style face="normal" font="default" size="100%">9</style></volume><number><style face="normal" font="default" size="100%">6</style></number><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2155-5435</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000471212600002</style></accession-num><abstract><style face="normal" font="default" size="100%">The chemistry of actinide molecules and materials has shown remarkable conceptual advancements in the past decade illustrating their unique reactivity profiles, when compared with lanthanides and transition elements, but there are still some challenging questions on the intriguing stability of low valent states and the significant role of 5f orbitals in bonding and reactivity of actinides. The distinctive electronic flexibility of actinide centers makes them potential catalysts for heterogeneous molecular transformations because of the kinetic lability of their coordination states and facile switching among oxidaton states. Actinide-enabled chemical transformations such as the six-electron reduction of dinitrogen into two reactive ammonia molecules or four-electron oxidation of water into oxygen under mild conditions are promising pathways in the quest of highefficiency heterogeneous catalysts. This Review provides a comprehensive account on actinide-mediated catalytic transformation of small molecules such as CO, CO2, N2, O2, H2O, CH4, HCl, and NH3. The emphasis is placed on the emerging phenomena in actinide-based solid catalysts and controlled synthesis of nanostructured actinide materials as pristine and substrate-grown phases. The mechanistic investigations highlight the influence of the 5f electrons in multielectron transfer reactions and the propensity of actinide centers to achieve higher oxidation states that defines the surface termination in actinide oxides. Finally, the status and perspectives of actinide-containing materials beyond the nuclear fuel applications is discussed, underlining their exciting chemistry and unexplored potential toward alternative catalytic energy production processes.</style></abstract><label><style face="normal" font="default" size="100%">Leduc2019</style></label><notes><style face="normal" font="default" size="100%">Ic8ft&#xD;Times Cited:9&#xD;Cited References Count:222</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000471212600002</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acscatal.8b04924</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>167</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">167</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jawad, Muhammad</style></author><author><style face="normal" font="default" size="100%">Khan, Abdul Faheem</style></author><author><style face="normal" font="default" size="100%">Waseem, Amir</style></author><author><style face="normal" font="default" size="100%">Kamboh, Afzal Hussain</style></author><author><style face="normal" font="default" size="100%">Mohsin, Muhammad</style></author><author><style face="normal" font="default" size="100%">Shahzad, Sohail Anjum</style></author><author><style face="normal" font="default" size="100%">Shah, Sajid Hussain</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shaikh, Ahson Jabbar</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Effect of gold nanoparticles on transmittance and conductance of graphene oxide thin films and efficiency of perovskite solar cells</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Nanoscience</style></secondary-title></titles><number><style face="normal" font="default" size="100%">0123456789</style></number><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year></dates><isbn><style face="normal" font="default" size="100%">2190-5509</style></isbn><label><style face="normal" font="default" size="100%">Jawad2019</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://link.springer.com/10.1007/s13204-019-01134-x</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>166</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">166</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jang, Soo‐Young</style></author><author><style face="normal" font="default" size="100%">Kim, In‐Bok</style></author><author><style face="normal" font="default" size="100%">Kang, Minji</style></author><author><style face="normal" font="default" size="100%">Fei, Zuping</style></author><author><style face="normal" font="default" size="100%">Jung, Eunhwan</style></author><author><style face="normal" font="default" size="100%">McCarthy‐Ward, Thomas</style></author><author><style face="normal" font="default" size="100%">Shaw, Jessica</style></author><author><style face="normal" font="default" size="100%">Lim, Dae‐Hee</style></author><author><style face="normal" font="default" size="100%">Kim, Yeon‐Ju</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Heeney, Martin</style></author><author><style face="normal" font="default" size="100%">Kim, Dong‐Yu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Diseleno[3,2‐b:2′,3′‐d]selenophene‐Containing High‐Mobility Conjugated Polymer for Organic Field‐Effect Transistors</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Science</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1900245</style></pages><volume><style face="normal" font="default" size="100%">6</style></volume><number><style face="normal" font="default" size="100%">13</style></number><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">April</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2198-3844</style></isbn><label><style face="normal" font="default" size="100%">Jang2019</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.nature.com/articles/s41598-019-39575-7</style></url><url><style face="normal" font="default" size="100%">https://onlinelibrary.wiley.com/doi/abs/10.1002/advs.201900245</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>573</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">573</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gessner, I.</style></author><author><style face="normal" font="default" size="100%">Yu, X. J.</style></author><author><style face="normal" font="default" size="100%">Jungst, C.</style></author><author><style face="normal" font="default" size="100%">Klimpel, A.</style></author><author><style face="normal" font="default" size="100%">Wang, L. Y.</style></author><author><style face="normal" font="default" size="100%">Fischer, T.</style></author><author><style face="normal" font="default" size="100%">Neundorf, I.</style></author><author><style face="normal" font="default" size="100%">Schauss, A. C.</style></author><author><style face="normal" font="default" size="100%">Odenthal, M.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Geinstr 6, D-50939 Cologne, Germany&#xD;Univ Hosp Cologne, Inst Pathol, Kerpener Str 62, D-50924 Cologne, Germany&#xD;Univ Cologne, Ctr Mol Med CMMC, Robert Koch Str 21, D-50931 Cologne, Germany&#xD;Univ Cologne, Imaging Facil, Cluster Excellence Cellular Stress Responses Agin, Joseph Stelzmann Str 26, D-50931 Cologne, Germany&#xD;Univ Cologne, Inst Biochem, Zuelpicher Str 47, D-50674 Cologne, Germany&#xD;Univ Clin Cologne &amp; Bonn, Ctr Integrat Oncol, Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Selective Capture and Purification of MicroRNAs and Intracellular Proteins through Antisense-vectorized Magnetic Nanobeads</style></title><secondary-title><style face="normal" font="default" size="100%">Scientific Reports</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Sci Rep-Uk</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2069</style></pages><volume><style face="normal" font="default" size="100%">9</style></volume><number><style face="normal" font="default" size="100%">1</style></number><edition><style face="normal" font="default" size="100%">2019/02/16</style></edition><keywords><keyword><style face="normal" font="default" size="100%">nanocarriers</style></keyword><keyword><style face="normal" font="default" size="100%">separation</style></keyword><keyword><style face="normal" font="default" size="100%">particles</style></keyword><keyword><style face="normal" font="default" size="100%">delivery</style></keyword><keyword><style face="normal" font="default" size="100%">therapy</style></keyword><keyword><style face="normal" font="default" size="100%">disease</style></keyword><keyword><style face="normal" font="default" size="100%">sirna</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Feb 14</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2045-2322</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000458619600069</style></accession-num><abstract><style face="normal" font="default" size="100%">MicroRNAs (miRNAs) are small non-coding nucleotides playing a crucial role in posttranscriptional expression and regulation of target genes in nearly all kinds of cells. In this study, we demonstrate a reliable and efficient capture and purification of miRNAs and intracellular proteins using magnetic nanoparticles functionalized with antisense oligonucleotides. For this purpose, a tumor suppressor miRNA (miR-198), deregulated in several human cancer types, was chosen as the model oligonucleotide. Magnetite nanoparticles carrying the complementary sequence of miR-198 (miR-198 antisense) on their surface were delivered into cells and subsequently used for the extracellular transport of miRNA and proteins. The successful capture of miR-198 was demonstrated by isolating RNA from magnetic nanoparticles followed by real-time PCR quantification. Our experimental data showed that antisense-coated particles captured 5-fold higher amounts of miR-198 when compared to the control nanoparticles. Moreover, several proteins that could play a significant role in miR-198 biogenesis were found attached to miR-198 conjugated nanoparticles and analyzed by mass spectrometry. Our findings demonstrate that a purpose-driven vectorization of magnetic nanobeads with target-specific recognition ligands is highly efficient in selectively transporting miRNA and disease-relevant proteins out of cells and could become a reliable and useful tool for future diagnostic, therapeutic and analytical applications.</style></abstract><notes><style face="normal" font="default" size="100%">Hl3ml&#xD;Times Cited:4&#xD;Cited References Count:24</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000458619600069</style></url></related-urls></urls><custom2><style face="normal" font="default" size="100%">PMC6375918</style></custom2><electronic-resource-num><style face="normal" font="default" size="100%">ARTN 2069&#xD;10.1038/s41598-019-39575-7</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>572</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">572</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gessner, I.</style></author><author><style face="normal" font="default" size="100%">Krakor, E.</style></author><author><style face="normal" font="default" size="100%">Styrnol, S.</style></author><author><style face="normal" font="default" size="100%">Klimpel, A.</style></author><author><style face="normal" font="default" size="100%">Neundorf, I.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;Univ Cologne, Inst Biochem, Zuelpicher Str 47, D-50674 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Copper-free click functionalization of glucose-derived carbon spheres for tumor targeting</style></title><secondary-title><style face="normal" font="default" size="100%">Mrs Advances</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Mrs Adv</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2881-2887</style></pages><volume><style face="normal" font="default" size="100%">4</style></volume><number><style face="normal" font="default" size="100%">53</style></number><keywords><keyword><style face="normal" font="default" size="100%">biomedical</style></keyword><keyword><style face="normal" font="default" size="100%">biomaterial</style></keyword><keyword><style face="normal" font="default" size="100%">hydrothermal</style></keyword><keyword><style face="normal" font="default" size="100%">surface chemistry</style></keyword><keyword><style face="normal" font="default" size="100%">tissue</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year></dates><isbn><style face="normal" font="default" size="100%">2059-8521</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000511400200003</style></accession-num><abstract><style face="normal" font="default" size="100%">The dysfunctional metabolism of glucose in cancer cells represents a new avenue for cancer targeting based on sugar-derived carriers. Here, glucose-derived carbon spheres (CS) were prepared through a simple hydrothermal method, yielding highly homogenous spherical particles that exhibited excellent stability in aqueous solution. The abundant presence of surface hydroxyl functionalities was used for a subsequent condensation of an amino silane that was the basis for further covalent coupling strategies. CS were modified with a cyclooctyne derivative providing a highly selective binding site for copper-free click reactions. Moreover, the surface modification of CS with a dye-label allowed for their intracellular detection revealing a preferential uptake of CS, compared to silica particles, in tumor cells. These results thus demonstrate the highly promising potential of glucose-derived particles for tumor targeting applications and their efficient surface modification.</style></abstract><notes><style face="normal" font="default" size="100%">Sp. Iss. SI&#xD;Ki5ov&#xD;Times Cited:0&#xD;Cited References Count:12</style></notes><urls><related-urls><url><style face="underline" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000511400200003</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1557/adv.2019.488</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>164</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">164</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Klimpel, Annika</style></author><author><style face="normal" font="default" size="100%">Klußmann, Merlin</style></author><author><style face="normal" font="default" size="100%">Neundorf, Ines</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Interdependence of charge and secondary structure on cellular uptake of cell penetrating peptide functionalized silica nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">Nanoscale Advances</style></secondary-title></titles><volume><style face="normal" font="default" size="100%">Accepted</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2019, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year></dates><abstract><style face="normal" font="default" size="100%">The capability of cell-penetrating peptides (CPPs) to enable translocation of cargos across biological barriers carries promising pharmaceutical potential for the transport of drug molecules, as well as nanomaterials, into cells. Herein, we report on optimization of a CPP, namely sC18, in terms of its translocation efficiency, and on investigating those new CPPs regarding their interaction with silica nanoparticles (NPs). First, alanine scanning of sC18 yielded 16 cationic peptides from which two were selected for further studies. Whereas in the first case, a higher positive net charge and enhanced amphipathicity resulted in significantly higher internalization rates than sC18, the second one demonstrated reduced cellular uptake efficiencies, and served as a control. We then attached these CPPs to silica nanoparticles of different sizes (50, 150 and 300 nm) via electrostatic interactions and could demonstrate that the secondary alpha-helical structure of the peptides was preserved. Following, cellular uptake studies using HeLa cells showed that the tested CPP-NPs were successfully translocated into HeLa cells in a size-dependent manner. Moreover, dependent on the CPP used, we realized differences in translocation efficiency, which was similar to what we had observed for the free peptides. All in all, we highlight the high potential of sequential fine-tuning of CPPs and provide novel insights into their interplay with biologically inorganic benign nanoparticles. Given the high cellular permeability of CPPs and their ability to translocate into a wide spectrum of cell types, our studies may stimulate future research of CPPs with inorganic nanocarrier surfaces.</style></abstract><label><style face="normal" font="default" size="100%">Gessner2019</style></label><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>574</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">574</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Frank, M.</style></author><author><style face="normal" font="default" size="100%">Jurgensen, L.</style></author><author><style face="normal" font="default" size="100%">Leduc, J.</style></author><author><style face="normal" font="default" size="100%">Stadler, D.</style></author><author><style face="normal" font="default" size="100%">Graf, D.</style></author><author><style face="normal" font="default" size="100%">Gessner, I.</style></author><author><style face="normal" font="default" size="100%">Zajusch, F.</style></author><author><style face="normal" font="default" size="100%">Fischer, T.</style></author><author><style face="normal" font="default" size="100%">Rose, M. A.</style></author><author><style face="normal" font="default" size="100%">Mueller, D. N.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Dept Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;Rhein Westfal TH Aachen, Inst Elect Mat IWE2, Sommerfeldstr 18-24, D-52074 Aachen, Germany&#xD;Forschungszentrum Juelich, Peter Gruenberg Inst, Wilhelm Johnen Str, D-52425 Julich, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Volatile Rhenium(I) Compounds with Re-N Bonds and Their Conversion into Oriented Rhenium Nitride Films by Magnetic Field-Assisted Vapor Phase Deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Inorg Chem</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">10408-10416</style></pages><volume><style face="normal" font="default" size="100%">58</style></volume><number><style face="normal" font="default" size="100%">15</style></number><edition><style face="normal" font="default" size="100%">2019/07/11</style></edition><keywords><keyword><style face="normal" font="default" size="100%">mechanical-properties</style></keyword><keyword><style face="normal" font="default" size="100%">hydrogen</style></keyword><keyword><style face="normal" font="default" size="100%">complexes</style></keyword><keyword><style face="normal" font="default" size="100%">catalyst</style></keyword><keyword><style face="normal" font="default" size="100%">carbon</style></keyword><keyword><style face="normal" font="default" size="100%">deoxydehydration</style></keyword><keyword><style face="normal" font="default" size="100%">precursors</style></keyword><keyword><style face="normal" font="default" size="100%">uranium(iv)</style></keyword><keyword><style face="normal" font="default" size="100%">morphology</style></keyword><keyword><style face="normal" font="default" size="100%">diboride</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Aug 5</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000480371400097</style></accession-num><abstract><style face="normal" font="default" size="100%">New heteroleptic rhenium(I) compounds, [fac-Re(I)-(CO)(3)(L)] (e.g., L= tfb-dmpda, (N,N-(4,4,4-trifluorobut-1-en-3-on)-dimethyl propylene diamine)), containing anionic and neutral ligands act as efficient precursors to grow polycrystalline rhenium nitride (ReN) films by their vapor phase deposition at 600 degrees C. Deposition of ReN films under an external magnetic field showed an orientation effect with preferred growth of crystallites along &lt; 100 &gt; direction. Rhenium complexes reported here unify high stability and reactivity in a single molecule through a Janus-type coordination around a Re center, constituted by a chelating tridentate ligand and three carbonyl groups imparting a facial geometry. Single-crystal diffraction analysis confirmed the structural integrity of the new rhenium compounds. The rigidity of molecular framework was validated in solution via 1D and 2D NMR spectroscopy, in the gas phase via mass spectrometry, and in the solid-state by thermogravimetric analysis and differential scanning calorimetry studies. The analytical data showed that pre-existent Re-N bonds in [fac-Re(I)(CO)(3)(L)] facilitated low-temperature formation of crystalline ReN deposits confirmed by grazing angle X-ray diffraction analysis. The surface chemical composition and the uniformity of microstructure were provided by X-ray photoelectron spectroscopy (XPS) and scanning and transmission electron microscopy (SEM/TEM), respectively.</style></abstract><notes><style face="normal" font="default" size="100%">Ip9lk&#xD;Times Cited:1&#xD;Cited References Count:81</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000480371400097</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.inorgchem.9b01656</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>162</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">162</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Brune, Veronika</style></author><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular Routes to Two-Dimensional Metal Dichalcogenides MX 2 (M = Mo, W; X = S, Se)</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">9922--9934</style></pages><volume><style face="normal" font="default" size="100%">58</style></volume><number><style face="normal" font="default" size="100%">15</style></number><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year></dates><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><label><style face="normal" font="default" size="100%">Brune2019</style></label><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>161</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">161</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bohr, Christoph</style></author><author><style face="normal" font="default" size="100%">Pfeiffer, Markus</style></author><author><style face="normal" font="default" size="100%">Öz, Senol</style></author><author><style face="normal" font="default" size="100%">von Toperczer, Florian</style></author><author><style face="normal" font="default" size="100%">Lepcha, Ashish</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Schütz, Markus</style></author><author><style face="normal" font="default" size="100%">Lindfors, Klas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Institute of Inorganic Chemistry , University of Cologne , Greinstr. 6 , 50939 Cologne , Germany.&#xD;Institute of Physical Chemistry , University of Cologne , Luxemburger Str. 116 , 50939 Cologne , Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Electrospun Hybrid Perovskite Fibers—Flexible Networks of One-Dimensional Semiconductors for Light-Harvesting Applications</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></full-title></periodical><pages><style face="normal" font="default" size="100%">acsami.9b05700</style></pages><volume><style face="normal" font="default" size="100%">11</style></volume><number><style face="normal" font="default" size="100%">28</style></number><edition><style face="normal" font="default" size="100%">2019/07/03</style></edition><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jul 17</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><accession-num><style face="normal" font="default" size="100%">31265229</style></accession-num><abstract><style face="normal" font="default" size="100%">Thin-film organic-inorganic hybrid perovskite (MeNH3PbI3) solar cells have displayed remarkably high photoconversion efficiencies, making their net-shaping as flexible device elements desirable for a number of applications. Simulations show greatly enhanced light absorption in perovskite fibers in comparison to their thin-film counterparts, which demand the processing of hybrid perovskites in the one-dimensional morphology. We report here on the single-step fabrication of MeNH3PbI3 nanofibers on a customized electrospinning process performed under inert conditions. Our results demonstrate reproducible synthesis of electrospun fiber mats in which the fiber dimensions were tailored by adjusting the polymer (PVP) content. Photoluminescence studies on the perovskite fibers revealed a blue shift of the emission peak possibly due to strain or charge confinement effects. The hybrid perovskite nanofibers offer promising applications in flexible and stretchable optoelectronics.</style></abstract><label><style face="normal" font="default" size="100%">Bohr2019</style></label><notes><style face="normal" font="default" size="100%">Bohr, Christoph&#xD;Pfeiffer, Markus&#xD;Oz, Senol&#xD;von Toperczer, Florian&#xD;Lepcha, Ashish&#xD;Fischer, Thomas&#xD;Schutz, Markus&#xD;Lindfors, Klas&#xD;Mathur, Sanjay&#xD;eng&#xD;ACS Appl Mater Interfaces. 2019 Jul 17;11(28):25163-25169. doi: 10.1021/acsami.9b05700. Epub 2019 Jul 2.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/10.1021/acsami.9b05700</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsami.9b05700</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>621</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">621</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Xia, Qi Xun</style></author><author><style face="normal" font="default" size="100%">Shinde, Nanasaheb M.</style></author><author><style face="normal" font="default" size="100%">Yun, Je Moon</style></author><author><style face="normal" font="default" size="100%">Zhang, Tengfei</style></author><author><style face="normal" font="default" size="100%">Mane, Rajaram S.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kim, Kwang Ho</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Bismuth Oxychloride/MXene symmetric supercapacitor with high volumetric energy density</style></title><secondary-title><style face="normal" font="default" size="100%">Electrochimica Acta</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">351-360</style></pages><volume><style face="normal" font="default" size="100%">271</style></volume><keywords><keyword><style face="normal" font="default" size="100%">BiOCl</style></keyword><keyword><style face="normal" font="default" size="100%">TiCT</style></keyword><keyword><style face="normal" font="default" size="100%">MXene</style></keyword><keyword><style face="normal" font="default" size="100%">Symmetric supercapacitors</style></keyword><keyword><style face="normal" font="default" size="100%">Volumetric energy density</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">2018/05/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0013-4686</style></isbn><abstract><style face="normal" font="default" size="100%">Since the discovery of two-dimensional (2D) graphene, a new class of 2D materials with excellent electrical conductivity has recently been attracting attention in studying promising electrode materials in energy storage applications. Herein, bismuth oxychloride nanosheets-immobilised Ti3C2Tx MXene material (TCBOC) is synthesised by a facile and cost-effective chemical bath deposition (CBD) route. The bismuth oxychloride (BiOCl) nanosheets are grown and immobilised on surfaces of Ti3C2Tx-MXene flakes. An electrode based on the TCBOC nanocomposite exhibited a remarkably volumetric specific capacitance of 396.5 F cm-3 at 1 A g−1 and 228.0 F cm-3 at 15 A g−1. Furthermore, a symmetric supercapacitor (SSC) assembled using TCBOC material proves to have a high energy density of 15.2 Wh kg−1 at a power density of 567.4 W kg−1 compared to SSCs using previously reported Ti3C2Tx MXene materials. The SSC shows cycle life retention of 85.0% after 5000 cycles (at 5 A g−1). The enhanced capacitive performance is attributed to the increased surface area due to BiOCl nanosheets anchored on a 2D MXene surface, the activities of BiOCl sheets, and the excellent conductivity of a Ti3C2Tx MXene material.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0013468618306856</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.electacta.2018.03.168</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>206</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">206</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wang, Meng</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Pyeon, Myeongwhun</style></author><author><style face="normal" font="default" size="100%">Diao, Zhidan</style></author><author><style face="normal" font="default" size="100%">Czympiel, Lisa</style></author><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author><author><style face="normal" font="default" size="100%">Shen, Shaohua</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Xi An Jiao Tong Univ, Int Res Ctr Renewable Energy, State Key Lab Multiphase Flow Power Engn, Xian 710049, Shaanxi, Peoples R China&#xD;Univ Cologne, Dept Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;NASA, Ohio Aerosp Inst, Glenn Res Ctr, Cleveland, OH 44135 USA</style></auth-address><titles><title><style face="normal" font="default" size="100%">Trace Amount of Platinum Supported on Carbonized Biomorphic Wood for Efficient Electrochemical Hydrogen Evolution in Alkaline Condition</style></title><secondary-title><style face="normal" font="default" size="100%">ChemistrySelect</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chemistryselect</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2140--2143</style></pages><volume><style face="normal" font="default" size="100%">3</style></volume><number><style face="normal" font="default" size="100%">7</style></number><keywords><keyword><style face="normal" font="default" size="100%">2018, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">February</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">23656549</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000425627700029</style></accession-num><abstract><style face="normal" font="default" size="100%">Carbonized biomorphic wood (Bio-C), which features unique properties such as highly ordered microtexture, well-developed porous structure, and low charge transfer resistance, was prepared as a promising scaffold with trace amount of platinum (Pt) supported to efficiently electrocatalyze hydrogen evolution reaction (HER). Pt/Bio-C nanocomposites demonstrated superior HER activity with a current density reaching as high as similar to 58 mA cm(-2) at -0.2 V vs. reversible hydrogen electrode (RHE) in strongly alkaline condition.</style></abstract><label><style face="normal" font="default" size="100%">Wang2018</style></label><notes><style face="normal" font="default" size="100%">Fw9ai&#xD;Times Cited:0&#xD;Cited References Count:23</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/slct.201702959</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/slct.201702959</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>205</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">205</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Stadler, Daniel</style></author><author><style face="normal" font="default" size="100%">Siribbal, Shifaa Mohammed</style></author><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Öz, Senol</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Dept Chem, Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Asymmetric attachment and functionalization of plasmonic nanoparticles on ceramic interfaces</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Nanostructure in Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Nanostructure Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">33-44</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2018, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">February</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2008-9244</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000429488000004</style></accession-num><abstract><style face="normal" font="default" size="100%">The demands for materials that integrate more than one functional imaging or therapeutic unit are of increasing interest for biomedical applications. Here, we present the step-by-step preparation of asymmetric and optically active particles, namely, Gd2O3@Ag, Gd2O3@Au, SiO2-N-3@Au, and SiO2-SH@Au . Successful attachment of plasmonic nanoparticles to the surface of metal-oxide spheres without necessity of a potentially toxic inter-adhesive layer was proven by optical methods as well as X-ray photoelectron spectroscopy. The combination of optical and magnetic properties as present in Gd2O3@Ag and Gd2O3@Au Janus-type particles leads to dual-imaging probes for optical and magnetic resonance imaging. In addition, functional groups, such as azide groups, were linked to the surface of silica particles previous to Au nanoparticle attachment. Subsequent site-selective click reactions with 5-FAM were successfully performed as demonstrated by UV-Vis measurements. All described systems exhibited excellent long-term stability and can, therefore, be considered as promising candidates for theranostic applications.&#xD;[GRAPHICS]&#xD;.</style></abstract><label><style face="normal" font="default" size="100%">Stadler2018</style></label><notes><style face="normal" font="default" size="100%">Gc0sl&#xD;Times Cited:1&#xD;Cited References Count:52</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://link.springer.com/10.1007/s40097-018-0252-y</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1007/s40097-018-0252-y</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>204</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">204</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Siribbal, Shifaa M.</style></author><author><style face="normal" font="default" size="100%">Schläfer, Johannes</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Hu, Zhangjun</style></author><author><style face="normal" font="default" size="100%">Uvdal, Kajsa</style></author><author><style face="normal" font="default" size="100%">Valldor, Martin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;Max Planck Inst Chem Phys Solids, Nothnitzer Str 40, D-01187 Dresden, Germany&#xD;Linkoping Univ, Dept Phys Chem &amp; Biol IFM, Div Mol Surface Phys &amp; Nanosci, S-58183 Linkoping, Sweden</style></auth-address><titles><title><style face="normal" font="default" size="100%">Air-Stable Gadolinium Precursors for the Facile Microwave-Assisted Synthesis of Gd2O3 Nanocontrast Agents for Magnetic Resonance Imaging</style></title><secondary-title><style face="normal" font="default" size="100%">Crystal Growth &amp; Design</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Cryst Growth Des</style></alt-title></titles><pages><style face="normal" font="default" size="100%">633-641</style></pages><volume><style face="normal" font="default" size="100%">18</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2018, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">January</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1528-7483</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000424851400013</style></accession-num><abstract><style face="normal" font="default" size="100%">Using metal organic precursors in materials synthesis remains a challenge due to their high moisture susceptibility. In this work, we describe a facile methodology for the synthesis of Gd2O3-based contrast agents from two new gadolinium-based complexes. [Gd(PyTFP)(4)] (PyH) 1 (PyTFP = C8H5NOF3, Py = C5H5N) and [Gd(DMOTFP)(3)Py] 2 (DMOTFP = C8H7NO2F3) were synthesized via a classical ligand exchange reaction of [Gd{N(SiMe3)(2)}(3)] under inert conditions. As a result, X-ray diffraction analysis revealed a distorted square antiprismatic coordination and an augmented triangular prismatic arrangement of ligands around gadolinium atoms in 1 and 2, respectively. It also showed that 1 is an anionic complex of formula [Gd(PyTFP)(4)](PyH), while a neutral tris-compound, [Gd(DMOTFP)(3)Py], was obtained as a pyridine adduct in 2. Fast and reproducible microwave-assisted decomposition of 1 and 2 provided homogeneous Gd(OH)(3) nanorods at mild temperature without using any surfactant or capping reagent. As-synthesized nanorods were easily transformed into a cubic phase of Gd2O3 nanoparticles by thermal treatment under ambient conditions. The magnetic measurement showed the typical paramagnetic behavior of the Gd2O3 nanoparticles (NPs). The cytotoxicity profile demonstrates the biocompatibility and negligible toxicity of the as-synthesized nanoprobes. The suggested approach provides a new class of gadolinium-based precursors which allows facile synthesis of highly crystalline Gd2O3 NPs.</style></abstract><label><style face="normal" font="default" size="100%">Siribbal2018</style></label><notes><style face="normal" font="default" size="100%">Fv8qm&#xD;Times Cited:3&#xD;Cited References Count:55</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/10.1021/acs.cgd.7b00787</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.cgd.7b00787</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>203</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">203</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Singh, Trilok</style></author><author><style face="normal" font="default" size="100%">Öz, Senol</style></author><author><style face="normal" font="default" size="100%">Sasinska, Alexander</style></author><author><style face="normal" font="default" size="100%">Frohnhoven, Robert</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Miyasaka, Tsutomu</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sulfate-Assisted Interfacial Engineering for High Yield and Efficiency of Triple Cation Perovskite Solar Cells with Alkali-Doped TiO 2 Electron-Transporting Layers</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Functional Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Functional Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1706287</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2018, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">January</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1616301X</style></isbn><label><style face="normal" font="default" size="100%">Singh2018</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/adfm.201706287</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>623</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">623</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Simsir, Hamza</style></author><author><style face="normal" font="default" size="100%">Eltugral, Nurettin</style></author><author><style face="normal" font="default" size="100%">Frohnhoven, Robert</style></author><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Karagoz, Selhan</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Anode performance of hydrothermally grown carbon nanostructures and their molybdenum chalcogenides for Li-ion batteries</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Communications</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">610-616</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">2</style></number><edition><style face="normal" font="default" size="100%">2018/05/03</style></edition><dates><year><style face="normal" font="default" size="100%">2018</style></year></dates><publisher><style face="normal" font="default" size="100%">Cambridge University Press</style></publisher><isbn><style face="normal" font="default" size="100%">2159-6859</style></isbn><abstract><style face="normal" font="default" size="100%">Three different hydrothermally grown carbonaceous materials and their molybdenum chalcogenides derived from glucose (HTC, HTC–MoO2, HTC–MoS2) were investigated to evaluate their potential as Li-ion battery anodes. All tested materials exhibited good cycling performance at a current density of 100 mA/g and showed high coulombic efficiency, &amp;gt;98%, after the 50th cycle. Reversible charge capacities of HTC, HTC–MoO2, and HTC–MoS2 were 296, 266, and 484 mAh/g, respectively, after 50 successive cycles. This study demonstrated that the HTC–MoS2 showed the highest reversible charge capacity which promises to be a good candidate for an environmentally friendly anode material for Li-ion batteries.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.cambridge.org/core/article/anode-performance-of-hydrothermally-grown-carbon-nanostructures-and-their-molybdenum-chalcogenides-for-liion-batteries/475D26C3F980D7CE90DCF1D68A81CFA9</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1557/mrc.2018.71</style></electronic-resource-num><remote-database-name><style face="normal" font="default" size="100%">Cambridge Core</style></remote-database-name><remote-database-provider><style face="normal" font="default" size="100%">Cambridge University Press</style></remote-database-provider></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>622</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">622</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sasinska, Alexander</style></author><author><style face="normal" font="default" size="100%">Leduc, Jennifer</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Czympiel, Lisa</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Christiansen, Silke H.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Competitive interplay of deposition and etching processes in atomic layer growth of cobalt and nickel metal films</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Research</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">4241-4250</style></pages><volume><style face="normal" font="default" size="100%">33</style></volume><number><style face="normal" font="default" size="100%">24</style></number><edition><style face="normal" font="default" size="100%">2018/11/05</style></edition><keywords><keyword><style face="normal" font="default" size="100%">atomic layer deposition</style></keyword><keyword><style face="normal" font="default" size="100%">X-ray photoelectron spectroscopy (XPS)</style></keyword><keyword><style face="normal" font="default" size="100%">surface reaction</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year></dates><publisher><style face="normal" font="default" size="100%">Cambridge University Press</style></publisher><isbn><style face="normal" font="default" size="100%">0884-2914</style></isbn><abstract><style face="normal" font="default" size="100%">Atomic layer deposition (ALD) of air stable cobalt and nickel complexes based on tridentate enaminones N,N-(4,4,4-trifluorobut-1-en-3-on)-dimethylethyldiamine (Htfb-dmeda) and N,N-(4,4,4-trifluorobut-1-en-3-on)-dimethylpropyldiamine (Htfb-dmpda) successfully produced metallic cobalt and nickel thin films. Detailed X-ray photoelectron spectroscopy (XPS) studies on the binding interaction of the first precursor monolayer with the surface functional groups elucidated the chemisorption behavior of the new precursor systems. A reactive remote hydrogen plasma was used as the co-reactant to activate the precursor decomposition yielding metal hydroxide intermediates. Subsequent hydrogen plasma etching of as-deposited films resulted in phase-pure metallic films through a recrystallization process, verified by surface and sub-surface XPS. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) analyses revealed pinhole-free films, with low surface roughness (0.2 ± 0.06 nm root mean square, RMS) for both, cobalt and nickel thin films. Herein, the competitive role of hydrogen as etchant and reactant was demonstrated as prolonged plasma exposure time periods resulted in the formation of metal hydrides. This is mostly due to the catalytic dissociation of molecular hydrogen on transition metal surfaces, which already occurs upon low energy input.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.cambridge.org/core/article/competitive-interplay-of-deposition-and-etching-processes-in-atomic-layer-growth-of-cobalt-and-nickel-metal-films/5CB5ED52E21366EAAA83BA538D94701B</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1557/jmr.2018.379</style></electronic-resource-num><remote-database-name><style face="normal" font="default" size="100%">Cambridge Core</style></remote-database-name><remote-database-provider><style face="normal" font="default" size="100%">Cambridge University Press</style></remote-database-provider></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>200</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">200</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Rumyantseva, M.N.</style></author><author><style face="normal" font="default" size="100%">Vladimirova, S.A.</style></author><author><style face="normal" font="default" size="100%">Vorobyeva, N.A.</style></author><author><style face="normal" font="default" size="100%">Giebelhaus, I.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Chizhov, A.S.</style></author><author><style face="normal" font="default" size="100%">Khmelevsky, N.O.</style></author><author><style face="normal" font="default" size="100%">Aksenenko, A. Yu.</style></author><author><style face="normal" font="default" size="100%">Kozlovsky, V.F.</style></author><author><style face="normal" font="default" size="100%">Karakulina, O.M.</style></author><author><style face="normal" font="default" size="100%">Hadermann, J.</style></author><author><style face="normal" font="default" size="100%">Abakumov, A.M.</style></author><author><style face="normal" font="default" size="100%">Gaskov, A.M.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Moscow MV Lomonosov State Univ, Chem Dept, Moscow 119991, Russia&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Moscow State Technol Univ, LISM, Moscow 127055, Russia&#xD;Univ Antwerp, EMAT, B-2020 Antwerp, Belgium&#xD;Skolkovo Inst Sci &amp; Technol, Moscow 143026, Russia</style></auth-address><titles><title><style face="normal" font="default" size="100%">p -CoOx/n-SnO2 nanostructures: New highly selective materials for H2S detection</style></title><secondary-title><style face="normal" font="default" size="100%">Sensors and Actuators B: Chemical</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Sensor Actuat B-Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">564--571</style></pages><volume><style face="normal" font="default" size="100%">255</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2018, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">February</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09254005</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000414151800068</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanostructures p-CoOx/n-SnO2 based on tin oxide nanowires have been prepared by two step CVD technique and characterized in detail by XRD, XRF, XPS, HAADF-STEM imaging and EDX-STEM mapping. Depending on the temperature of decomposition of cobalt complex during the second step of CVD synthesis of nanostructures cobalt oxide forms a coating and/or isolated nanoparticles on SnO2 nanowire surface. It was found that cobalt presents in +2 and +3 oxidation states. The measurements of gas sensor properties have been carried out during exposure to CO (14 ppm), NH3 (21 ppm), and H2S (2 ppm) in dry air. The opposite trends were observed in the effect of cobalt oxide on the SnO2 gas sensitivity when detecting CO or NH3 in comparison to H2S. The decrease of sensor signal toward CO and NH3 was attributed to high catalytic activity of Co3O4 in oxidation of these gases. Contrary, the significant increase of sensor signal in the presence of H2S was attributed to the formation of metallic cobalt sulfide and removal of the barrier between p-CoOx and n-SnO2. This effect provides an excellent selectivity of p-CoOx/n-SnO2 nanostructures in H2S detection. (C) 2017 Elsevier B.V. All rights reserved.</style></abstract><label><style face="normal" font="default" size="100%">Rumyantseva2018</style></label><notes><style face="normal" font="default" size="100%">1&#xD;Fl3uy&#xD;Times Cited:14&#xD;Cited References Count:43</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0925400517315204</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.snb.2017.08.096</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>624</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">624</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Queraltó, Albert</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Photoelectrochemical response of Fe2O3 films reinforced with BiFeO3 nanofibers</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Communications</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1211-1215</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">3</style></number><edition><style face="normal" font="default" size="100%">2018/06/05</style></edition><dates><year><style face="normal" font="default" size="100%">2018</style></year></dates><publisher><style face="normal" font="default" size="100%">Cambridge University Press</style></publisher><isbn><style face="normal" font="default" size="100%">2159-6859</style></isbn><abstract><style face="normal" font="default" size="100%">BiFeO3 (BFO) p-type semiconducting nanofibers were deposited on fluorine-doped SnO2 substrates by a combination of electrospinning (BiFeO3) and spin-coating (Fe2O3) procedures. Photocurrent density values of BFO nanofibers which increased with the annealing temperature to values six times larger were obtained. Different amounts of BFO nanofibers (5, 10, and 25 wt%) were also integrated into α-Fe2O3 films. The photocurrent density of the α-Fe2O3/BFO nanofiber films had the highest value for a 10 wt% BFO nanofibers. The anisotropy in charge transport due to the underlying nanofibrous pathways which prevented the charge carrier recombination was the main cause for the enhancement of the photocurrent density.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.cambridge.org/core/article/photoelectrochemical-response-of-fe2o3-films-reinforced-with-bifeo3-nanofibers/D4C57F2DEE6DBFDBEB9478573CA9F444</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1557/mrc.2018.101</style></electronic-resource-num><remote-database-name><style face="normal" font="default" size="100%">Cambridge Core</style></remote-database-name><remote-database-provider><style face="normal" font="default" size="100%">Cambridge University Press</style></remote-database-provider></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>626</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">626</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pyeon, Myeongwhun</style></author><author><style face="normal" font="default" size="100%">Ruoko, Tero-Petri</style></author><author><style face="normal" font="default" size="100%">Leduc, Jennifer</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Deo, Meenal</style></author><author><style face="normal" font="default" size="100%">Tkachenko, Nikolai V.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Critical role and modification of surface states in hematite films for enhancing oxygen evolution activity</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Research</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">455-466</style></pages><volume><style face="normal" font="default" size="100%">33</style></volume><number><style face="normal" font="default" size="100%">4</style></number><edition><style face="normal" font="default" size="100%">2018/01/11</style></edition><keywords><keyword><style face="normal" font="default" size="100%">plasma-enhanced CVD (PECVD) (deposition)</style></keyword><keyword><style face="normal" font="default" size="100%">thin film</style></keyword><keyword><style face="normal" font="default" size="100%">surface chemistry</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year></dates><publisher><style face="normal" font="default" size="100%">Cambridge University Press</style></publisher><isbn><style face="normal" font="default" size="100%">0884-2914</style></isbn><abstract><style face="normal" font="default" size="100%">Hematite films deposited by plasma-enhanced chemical vapor deposition of iron pentacarbonyl [Fe(CO)5] in an oxygen plasma were modified by postdeposition (i) oxygen plasma treatment and (ii) short annealing treatments to reduce the defects and to modify the (sub)surface states and consequently the photoelectrochemical properties. The oxygen plasma treatment resulted in the increase of particle size and augmented surface roughening by densification of grains. Moreover, it induced saturated surface states with reactive oxygen species (O−, OH−), evident in the X-ray photoelectron spectroscopy (XPS). Under standard illumination (1.5 AM; 100 mW/cm2; 150 W xenon lamp), when compared to the pristine hematite coating (0.696 mA/cm2 at 1.23 V versus RHE and 0.74 V onset) the oxygen plasma-treated films showed severe deterioration in photocurrent density of 0.035 mA/cm2 and an anodic shift in the onset potential (1.10 V onset) due to oxygen rich surface. In a second set of experiments, the oxygen plasma-treated hematite films were briefly annealed (10 min at 750 °C) and the signals of Fe 2p and O 1s recovered to higher binding energies, indicating the formation of oxygen vacancies. In addition, a superior photocurrent density value of max. 1.306 mA/cm2 at 1.23 V versus RHE to that of the pristine hematite photoanode with 0.74 V onset was obtained. Transient absorption spectroscopy further elucidated that the oxygen plasma-induced electron trap states acting as recombination centers that are unfavorable for photoelectrochemical activity. The alteration in Fe:O stoichiometry and thus photocurrent density are corroborated by determination of water oxidation rates in annealed (7.1 s−1) and oxygen plasma treated (2.5 s−1) samples.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.cambridge.org/core/article/critical-role-and-modification-of-surface-states-in-hematite-films-for-enhancing-oxygen-evolution-activity/3B478A2D9DC5C8BDC3AA6327E59DAB10</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1557/jmr.2017.465</style></electronic-resource-num><remote-database-name><style face="normal" font="default" size="100%">Cambridge Core</style></remote-database-name><remote-database-provider><style face="normal" font="default" size="100%">Cambridge University Press</style></remote-database-provider></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>625</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">625</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Podhorsky, Jan</style></author><author><style face="normal" font="default" size="100%">Murauskas, Tomas</style></author><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Babiak, Michal</style></author><author><style face="normal" font="default" size="100%">Pinkas, Jiri</style></author><author><style face="normal" font="default" size="100%">Plausinaitiene, Valentina</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Abrutis, Adulfas</style></author><author><style face="normal" font="default" size="100%">Moravec, Zdenek</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Preparation of Heteroleptic Tin(IV) N,O-β-Heteroarylalkenolate Complexes and Their Properties as PI-MOCVD Precursors for SnO2 Deposition</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">5027-5035</style></pages><volume><style face="normal" font="default" size="100%">2018</style></volume><number><style face="normal" font="default" size="100%">46</style></number><keywords><keyword><style face="normal" font="default" size="100%">Chemical vapor deposition</style></keyword><keyword><style face="normal" font="default" size="100%">Fluorinated ligands</style></keyword><keyword><style face="normal" font="default" size="100%">Sensors</style></keyword><keyword><style face="normal" font="default" size="100%">Thin films</style></keyword><keyword><style face="normal" font="default" size="100%">Tin dioxide</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">2018/12/13</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">1434-1948</style></isbn><abstract><style face="normal" font="default" size="100%">We have successfully prepared and structurally characterized five novel tin(IV) heteroleptic N,O-?-heteroarylalkenolates containing ?CF3 groups. The synthetic route used reactions of Sn(OtBu)4 with 3,3,3-trifluoro(pyridin-2-yl)propen-2-ol (PyTFPH), 3,3,3-trifluoro(dimethyl-1,3-oxazol-2-yl)propen-2-ol (DMOTFPH), and 3,3,3-trifluoro(1,3-benzthiazol-2-yl)propen-2-ol (BTTFPH) in dry aprotic solvents leading to elimination of tert-butanol and formation of Sn(OtBu)2(PyTFP)2 (1), Sn(OtBu)2(DMOTFP)2 (2), and Sn(OtBu)2(BTTFP)2 (3). The chelating ligands employed a bidentate N∩O donor set. The reactivity of OtBu groups in the obtained Sn(OtBu)2(N∩O)2 complexes was further investigated in reactions with fluorinated alcohols, 2,2,2-trifluoroethanol (TFEH) and 1,1,1,3,3,3-hexafluoro-2-propanol (HFPH). Two complexes Sn(TFE)2(DMOTFP)2 (4) and Sn(HFP)2(PyTFP)2 (5) were obtained and structurally characterized. Thermal behavior of complexes 1?5 was studied by thermogravimetry and differential scanning calorimetry (TG/DSC). The most volatile compounds Sn(OtBu)2(PyTFP)2 (1) and Sn(OtBu)2(DMOTFP)2 (2) were chosen and tested in a PI-MOCVD process for the SnO2 growth on sapphire-C substrates. Film growth rates at different temperatures (500?900 °C), crystalline quality, surface roughness, transparency in UV/Vis-mid-IR spectral ranges have been investigated. The results showed that these two compounds are suitable precursors for MOCVD deposition of high quality SnO2 films. Fabricated films displayed good response to CO and NO2 in chemo-resistive gas sensing measurements.</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1002/ejic.201800913</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1002/ejic.201800913</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/ejic.201800913</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/ejic.201800913</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2021/02/03</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>627</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">627</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ojelere, Olusola</style></author><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Vogt, Nicholas</style></author><author><style face="normal" font="default" size="100%">Klein, Axel</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Reductive transformation of V(iii) precursors into vanadium(ii) oxide nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Dalton Transactions</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Dalton Transactions</style></full-title></periodical><pages><style face="normal" font="default" size="100%">6842-6849</style></pages><volume><style face="normal" font="default" size="100%">47</style></volume><number><style face="normal" font="default" size="100%">19</style></number><dates><year><style face="normal" font="default" size="100%">2018</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">1477-9226</style></isbn><abstract><style face="normal" font="default" size="100%">Vanadium(ii) oxide nanostructures are promising materials for supercapacitors and electrocatalysis because of their excellent electrochemical properties and high surface area. In this study, new homoleptic vanadium(iii) complexes with bi-dentate O,N-chelating heteroarylalkenol ligands (DmoxCHCOCF3, PyCHCOCF3 and PyNCOCF3) were synthesized and successfully transformed by reductive conversion into VO nanowires. The chemical identity of V(iii) complexes and their redox behaviour were unambiguously established by single crystal X-ray diffraction studies, cyclic voltammetry, spectrometric studies and DFT calculations. Transformation into the metastable VO phase was verified by powder X-ray diffraction and thermo-gravimetry. Transmission electron microscopy and X-ray photoelectron spectroscopy data confirmed the morphology and chemical composition of VO nanostructures, respectively.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/C8DT00848E</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C8DT00848E</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/C8DT00848E</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>195</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">195</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mukherjee, Sourav P.</style></author><author><style face="normal" font="default" size="100%">Bondarenko, Olesja</style></author><author><style face="normal" font="default" size="100%">Kohonen, Pekka</style></author><author><style face="normal" font="default" size="100%">Andón, Fernando T.</style></author><author><style face="normal" font="default" size="100%">Brzicová, Táňa</style></author><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Bottini, Massimo</style></author><author><style face="normal" font="default" size="100%">Calligari, Paolo</style></author><author><style face="normal" font="default" size="100%">Stella, Lorenzo</style></author><author><style face="normal" font="default" size="100%">Kisin, Elena</style></author><author><style face="normal" font="default" size="100%">Shvedova, Anna</style></author><author><style face="normal" font="default" size="100%">Autio, Reija</style></author><author><style face="normal" font="default" size="100%">Salminen-Mankonen, Heli</style></author><author><style face="normal" font="default" size="100%">Lahesmaa, Riitta</style></author><author><style face="normal" font="default" size="100%">Fadeel, Bengt</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Nanosafety &amp; Nanomedicine Laboratory, Division of Molecular Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17177, Stockholm, Sweden.&#xD;Laboratory of Environmental Toxicology, National Institute of Chemical Physics and Biophysics, Tallinn, 12618, Estonia.&#xD;Laboratory of Cellular Immunology, Humanitas Clinical and Research Institute, 20089, Rozzano-Milano, Italy.&#xD;Department of Genetic Toxicology and Nanotoxicology, Institute of Experimental Medicine AS CR, 14220, Prague, Czech Republic.&#xD;Inorganic and Materials Chemistry, University of Cologne, 50939, Cologne, Germany.&#xD;Department of Experimental Medicine and Surgery, University of Rome Tor Vergata, Rome, 00173, Italy.&#xD;Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, 92037, USA.&#xD;Department of Chemical Sciences and Technologies, University of Rome Tor Vergata, Rome, 00133, Italy.&#xD;Exposure Assessment Branch, National Institute for Occupational Safety and Health, Morgantown, WV, 26505, USA.&#xD;Department Pharmacology &amp; Physiology, West Virginia University, Morgantown, WV, 26505, USA.&#xD;Faculty of Social Sciences, University of Tampere, 33014, Tampere, Finland.&#xD;Turku Centre for Biotechnology, University of Turku, 20520 Turku, and Abo Akademi University, 20500, Turku, Finland.&#xD;Nanosafety &amp; Nanomedicine Laboratory, Division of Molecular Toxicology, Institute of Environmental Medicine, Karolinska Institutet, 17177, Stockholm, Sweden. Bengt.Fadeel@ki.se.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Macrophage sensing of single-walled carbon nanotubes via Toll-like receptors</style></title><secondary-title><style face="normal" font="default" size="100%">Scientific Reports</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1115</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">1</style></number><edition><style face="normal" font="default" size="100%">2018/01/20</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2018, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">December</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2045-2322</style></isbn><accession-num><style face="normal" font="default" size="100%">29348435</style></accession-num><abstract><style face="normal" font="default" size="100%">Carbon-based nanomaterials including carbon nanotubes (CNTs) have been shown to trigger inflammation. However, how these materials are &apos;sensed&apos; by immune cells is not known. Here we compared the effects of two carbon-based nanomaterials, single-walled CNTs (SWCNTs) and graphene oxide (GO), on primary human monocyte-derived macrophages. Genome-wide transcriptomics assessment was performed at sub-cytotoxic doses. Pathway analysis of the microarray data revealed pronounced effects on chemokine-encoding genes in macrophages exposed to SWCNTs, but not in response to GO, and these results were validated by multiplex array-based cytokine and chemokine profiling. Conditioned medium from SWCNT-exposed cells acted as a chemoattractant for dendritic cells. Chemokine secretion was reduced upon inhibition of NF-kappaB, as predicted by upstream regulator analysis of the transcriptomics data, and Toll-like receptors (TLRs) and their adaptor molecule, MyD88 were shown to be important for CCL5 secretion. Moreover, a specific role for TLR2/4 was confirmed by using reporter cell lines. Computational studies to elucidate how SWCNTs may interact with TLR4 in the absence of a protein corona suggested that binding is guided mainly by hydrophobic interactions. Taken together, these results imply that CNTs may be &apos;sensed&apos; as pathogens by immune cells.</style></abstract><label><style face="normal" font="default" size="100%">Mukherjee2018</style></label><notes><style face="normal" font="default" size="100%">Mukherjee, Sourav P&#xD;Bondarenko, Olesja&#xD;Kohonen, Pekka&#xD;Andon, Fernando T&#xD;Brzicova, Tana&#xD;Gessner, Isabel&#xD;Mathur, Sanjay&#xD;Bottini, Massimo&#xD;Calligari, Paolo&#xD;Stella, Lorenzo&#xD;Kisin, Elena&#xD;Shvedova, Anna&#xD;Autio, Reija&#xD;Salminen-Mankonen, Heli&#xD;Lahesmaa, Riitta&#xD;Fadeel, Bengt&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;England&#xD;Sci Rep. 2018 Jan 18;8(1):1115. doi: 10.1038/s41598-018-19521-9.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.nature.com/articles/s41598-018-19521-9</style></url></related-urls></urls><custom2><style face="normal" font="default" size="100%">PMC5773626</style></custom2><electronic-resource-num><style face="normal" font="default" size="100%">10.1038/s41598-018-19521-9</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>628</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">628</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Bohr, Christoph</style></author><author><style face="normal" font="default" size="100%">Queraltó, Albert</style></author><author><style face="normal" font="default" size="100%">Frohnhoven, Robert</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mokkapati, Sudha</style></author><author><style face="normal" font="default" size="100%">Jagadish, Chennupati</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Chapter One - Inorganic Nanofibers by Electrospinning Techniques and Their Application in Energy Conversion and Storage Systems</style></title><secondary-title><style face="normal" font="default" size="100%">Semiconductors and Semimetals</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1-70</style></pages><volume><style face="normal" font="default" size="100%">98</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Electrospinning</style></keyword><keyword><style face="normal" font="default" size="100%">Nanofiber architectures</style></keyword><keyword><style face="normal" font="default" size="100%">Li-ion batteries</style></keyword><keyword><style face="normal" font="default" size="100%">Supercapacitors</style></keyword><keyword><style face="normal" font="default" size="100%">Solar fuel cells</style></keyword><keyword><style face="normal" font="default" size="100%">Energy conversion</style></keyword><keyword><style face="normal" font="default" size="100%">Energy storage</style></keyword><keyword><style face="normal" font="default" size="100%">Catalysis</style></keyword><keyword><style face="normal" font="default" size="100%">Transparent conductive electrodes</style></keyword><keyword><style face="normal" font="default" size="100%">Perovskites</style></keyword><keyword><style face="normal" font="default" size="100%">Core–shell</style></keyword><keyword><style face="normal" font="default" size="100%">Janus fibers</style></keyword><keyword><style face="normal" font="default" size="100%">Yarns</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">2018/01/01/</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">Elsevier</style></publisher><isbn><style face="normal" font="default" size="100%">0080-8784</style></isbn><abstract><style face="normal" font="default" size="100%">Electrospinning is a promising technique for producing ultrafine fibers of a large variety of one-dimensional materials that can be assembled into nonwoven architectures useful for various smart technologies and lightweight applications such as wearable and flexible electronics, lightweight batteries, and high-surface area substrates for catalysis and sensing. Self-integration of electrospun fibers into webs and yarns not only enhances their functionality but also opens new innovative directions ranging from energy and environment applications to regenerative medicine. This chapter presents a comprehensive account on the processing of single-phase and composite nanofibers and their manifold applications in batteries, supercapacitors, transparent conducting materials, photovoltaics, as well as solar fuels. Using multinozzle approaches in electrospinning, heterojunctions and sophisticated 3D architectures at the nanoscale can be achieved in a single process step by engineering the spinnerets and fiber collectors. Given its modular nature and variability of precursor chemistry, electrospinning enables scaled-up production of micro- and nanofibers at reasonable cost and represents a promising fabrication method for integrating functional nanomaterials into devices. Nanofibrous meshes of carbon, metal, metal oxide, and their mixtures have been obtained in different geometries such as core–shell, Janus-type fibers, and yarns to demonstrate the possibility of net shaping at the nanoscale and possible conversion of interconnected 1D networks into 3D structures. The insufficient strength of nanofiber meshes can be reinforced through infiltration of a secondary phase that also decreases the intrinsic porosity of electrospun mats thereby offering new experimental space to create multimaterial junctions and bulk heterostructures. The chapter also alludes to the future trends and existing challenges of shape control and retention of flexible and fibrous structure after heat treatment that is often mandatory to obtain crystalline materials.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0080878418300085</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/bs.semsem.2018.04.003</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>194</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">194</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ludwig, Tim</style></author><author><style face="normal" font="default" size="100%">Bohr, Christoph</style></author><author><style face="normal" font="default" size="100%">Queraltó, Albert</style></author><author><style face="normal" font="default" size="100%">Frohnhoven, Robert</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mokkapati, Sudha</style></author><author><style face="normal" font="default" size="100%">Jagadish, Chennupati</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Inorganic nanofibers by electrospinning techniques and their application in energy conversion and storage systems</style></title><secondary-title><style face="normal" font="default" size="100%">SEMI: Nanowires for Energy Applications</style></secondary-title></titles><edition><style face="normal" font="default" size="100%">1st</style></edition><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year></dates><publisher><style face="normal" font="default" size="100%">Elsevier Inc.</style></publisher><label><style face="normal" font="default" size="100%">Ludiwg2018</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>193</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">193</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Leduc, Jennifer</style></author><author><style face="normal" font="default" size="100%">Pacold, Joseph I.</style></author><author><style face="normal" font="default" size="100%">Shuh, David K.</style></author><author><style face="normal" font="default" size="100%">Dong, Chung-Li</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Lawrence Berkeley Natl Lab, Glenn T Seaborg Ctr, Chem Sci Div, Berkeley, CA 94720 USA&#xD;Tamkang Univ, Dept Phys, Tamsui, Taiwan</style></auth-address><titles><title><style face="normal" font="default" size="100%">Uranium Oxide Nanocrystals by Microwave-Assisted Thermal Decomposition: Electronic and Structural Properties</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für Anorganische und Allgemeine Chemie</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></full-title></periodical><pages><style face="normal" font="default" size="100%">12-18</style></pages><volume><style face="normal" font="default" size="100%">644</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2018, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">January</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">00442313</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000422797100004</style></accession-num><abstract><style face="normal" font="default" size="100%">Uranium oxides have attracted much attention not only in the context of nuclear energy generation but also for their application as pristine catalysts or as supports for other (transition metal) oxides and (precious) metals. Their propensity to adopt high coordination numbers and manifest multiple oxidation states (from +II to +VI) makes them attractive candidates for catalyzed transformation reactions. Herein, we report a new synthesis route to phase-pure, crystalline UO2 nanoparticles via microwave-assisted decomposition of a molecular uranium(IV) precursor. The electronic structure and optical absorption properties of these nanocrystals were investigated using spectroscopic methods to evaluate their suitability for photo(electro)catalytic applications.</style></abstract><label><style face="normal" font="default" size="100%">Leduc2018</style></label><notes><style face="normal" font="default" size="100%">Ft0fk&#xD;Times Cited:6&#xD;Cited References Count:41</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/zaac.201700294</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/zaac.201700294</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>192</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">192</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Konstantynovski, K.</style></author><author><style face="normal" font="default" size="100%">Njio, G.</style></author><author><style face="normal" font="default" size="100%">Börner, F.</style></author><author><style face="normal" font="default" size="100%">Lepcha, A.</style></author><author><style face="normal" font="default" size="100%">Fischer, T.</style></author><author><style face="normal" font="default" size="100%">Holl, G.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Appl Sci Bonn Rhein Sieg, Inst Detect Technol IDT, Von Liebig Str 20, D-53359 Rheinbach, Germany&#xD;Univ Cologne, Chair Inorgan &amp; Mat Chem, Greinstr 6, D-50937 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Bulk detection of explosives and development of customized metal oxide semiconductor gas sensors for the identification of energetic materials</style></title><secondary-title><style face="normal" font="default" size="100%">Sensors and Actuators B: Chemical</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Sensor Actuat B-Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1252--1266</style></pages><volume><style face="normal" font="default" size="100%">258</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2018, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">April</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09254005</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000424868700143</style></accession-num><abstract><style face="normal" font="default" size="100%">Based on previous work, a setup allowing discrimination between energetic and non-energetic materials was developed. In order to cover novel materials not yet included in databases, a library free approach was chosen. The evaluation of explosion hazards for solid and liquid samples in the lowest milligram range was carried out by relying on the response of the substances towards thermal activation rather than on their chemical nature. The reaction was monitored by a combination of metal oxide semiconductor (MOX) gas sensors, photodiodes and a pressure sensor. Utilization of ambient air as a carrier gas and indirect control over sample weight by the geometry of the heater allow uncomplicated handling under real working conditions. In the first phase readily available physical and chemical sensors were applied. The rate of correct assignments was 99.8% with no false negatives and only 1 false positive out of 475 experiments. The possibility of library free operation was also confirmed by an additional series of experiments on materials not used for training the system. In the second phase the readily available MOX gas sensors were replaced by custom designed ones, which allowed single substances and classes of energetic materials by means to be discriminated by means of principal component analysis (PCA). (C) 2017 Elsevier B.V. All rights reserved.</style></abstract><label><style face="normal" font="default" size="100%">Konstantynovski2018</style></label><notes><style face="normal" font="default" size="100%">Fv8wt&#xD;Times Cited:10&#xD;Cited References Count:29</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0925400517322475</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.snb.2017.11.116</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>629</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">629</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hoppius, Jan S.</style></author><author><style face="normal" font="default" size="100%">Bialuschewski, Danny</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ostendorf, Andreas</style></author><author><style face="normal" font="default" size="100%">Gurevich, Evgeny L.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Femtosecond laser crystallization of amorphous titanium oxide thin films</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Physics Letters</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">071904</style></pages><volume><style face="normal" font="default" size="100%">113</style></volume><number><style face="normal" font="default" size="100%">7</style></number><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">2018/08/13</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Institute of Physics</style></publisher><isbn><style face="normal" font="default" size="100%">0003-6951</style></isbn><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1063/1.5027899</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1063/1.5027899</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2021/02/03</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>190</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">190</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Heidemann, Tim</style></author><author><style face="normal" font="default" size="100%">Pantenburg, Ingo</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Influence of Metal Fragment Mobility and Solution Dynamics on Cationic Rearrangements in Multimetallic Alkoxide Frameworks</style></title><secondary-title><style face="normal" font="default" size="100%">ChemistrySelect</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chemistryselect</style></alt-title></titles><pages><style face="normal" font="default" size="100%">12064--12069</style></pages><volume><style face="normal" font="default" size="100%">3</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2018, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">January</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">23656549</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000419480300002</style></accession-num><abstract><style face="normal" font="default" size="100%">Multimetallic alkoxides show manifold dynamics in solution comprising ligand switching among different sites (terminal, doubly or triply bridging), coordination lability of alkoxometallate units ({M(OR)(x)(-)}) and rearrangement of metal centers. Solution behavior and structural investigations of heterobimetallic iodide isopropoxides [IM{Ce-2(OPri)(9)}](2) (M=Cd (1), Ba (2)) and corresponding potassium alkoxometallates of Sr and Al revealed equilibrium of several interconverting species that rearrange to form stable monomeric or dimeric trimetallic frameworks. Quantitative formation of dimeric heterotrimetallic alkoxides [{Cd(OPri)(3)}Sr{Ce-2(OPri)(9)}](2) (3), [{Cd(OPri)(3)}Ba{Ce-2(OPri)(9)}](2) (4) and monomeric [{Al(OPri)(4)}(HOPri)Ba{Ce-2(OPri)(9)}] (5) confirmed the tendency of metallo-fragments to rearrange themselves for achieving the maximum possible coordination number for constituent metals. Multinuclear NMR spectroscopy, elemental analysis, mass spectrometry and X-ray diffraction analyses verified the potential of electronically and sterically unsaturated alkoxometallate units in initiating the redistribution of metal centers.</style></abstract><label><style face="normal" font="default" size="100%">Hegemann2018</style></label><notes><style face="normal" font="default" size="100%">Fs0rb&#xD;Times Cited:1&#xD;Cited References Count:51</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/slct.201702252</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/slct.201702252</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>631</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">631</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Krakor, Eva</style></author><author><style face="normal" font="default" size="100%">Jurewicz, Anna</style></author><author><style face="normal" font="default" size="100%">Wulff, Veronika</style></author><author><style face="normal" font="default" size="100%">Kling, Lasse</style></author><author><style face="normal" font="default" size="100%">Christiansen, Silke</style></author><author><style face="normal" font="default" size="100%">Brodusch, Nicolas</style></author><author><style face="normal" font="default" size="100%">Gauvin, Raynald</style></author><author><style face="normal" font="default" size="100%">Wortmann, Laura</style></author><author><style face="normal" font="default" size="100%">Wolke, Martina</style></author><author><style face="normal" font="default" size="100%">Plum, Georg</style></author><author><style face="normal" font="default" size="100%">Schauss, Astrid</style></author><author><style face="normal" font="default" size="100%">Krautwurst, John</style></author><author><style face="normal" font="default" size="100%">Ruschewitz, Uwe</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hollow silica capsules for amphiphilic transport and sustained delivery of antibiotic and anticancer drugs</style></title><secondary-title><style face="normal" font="default" size="100%">RSC Advances</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">24883-24892</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">44</style></number><dates><year><style face="normal" font="default" size="100%">2018</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><abstract><style face="normal" font="default" size="100%">Hollow mesoporous silica capsules (HMSC) are potential drug transport vehicles due to their biocompatibility, high loading capacity and sufficient stability in biological milieu. Herein, we report the synthesis of ellipsoid-shaped HMSC (aspect ratio ∼2) performed using hematite particles as solid templates that were coated with a conformal silica shell through cross-condensation reactions. For obtaining hollow silica capsules, the iron oxide core was removed by acidic leaching. Gas sorption studies on HMSC revealed mesoscopic pores (main pore width ∼38 Å) and a high surface area of 308.8 m2 g−1. Cell uptake of dye-labeled HMSC was confirmed by incubating them with human cervical cancer (HeLa) cells and analyzing the internalization through confocal microscopy. The amphiphilic nature of HMSC for drug delivery applications was tested by loading antibiotic (ciprofloxacin) and anticancer (curcumin) compounds as model drugs for hydrophilic and hydrophobic therapeutics, respectively. The versatility of HMSC in transporting hydrophilic as well as hydrophobic drugs and a pH dependent drug release over several days under physiological conditions was demonstrated in both cases by UV-vis spectroscopy. Ciprofloxacin-loaded HMSC were additionally evaluated towards Gram negative (E. coli) bacteria and demonstrated their efficacy even at low concentrations (10 μg ml−1) in inhibiting complete bacterial growth over 18 hours.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/C8RA03716G</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C8RA03716G</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/C8RA03716G</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>630</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">630</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">M. Dolatyari</style></author><author><style face="normal" font="default" size="100%">A. Rostami</style></author><author><style face="normal" font="default" size="100%">S. Mathur</style></author><author><style face="normal" font="default" size="100%">A. Klein</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">UV/IR Dual-Wavelength Photodetector Design Based on ZnO/PMMA/PbSe Nanocomposites</style></title><secondary-title><style face="normal" font="default" size="100%">IEEE Transactions on Nanotechnology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">574-581</style></pages><volume><style face="normal" font="default" size="100%">17</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">boron</style></keyword><keyword><style face="normal" font="default" size="100%">discrete Fourier transforms</style></keyword><keyword><style face="normal" font="default" size="100%">filled polymers</style></keyword><keyword><style face="normal" font="default" size="100%">II-VI semiconductors</style></keyword><keyword><style face="normal" font="default" size="100%">infrared detectors</style></keyword><keyword><style face="normal" font="default" size="100%">infrared spectra</style></keyword><keyword><style face="normal" font="default" size="100%">IV-VI semiconductors</style></keyword><keyword><style face="normal" font="default" size="100%">lead compounds</style></keyword><keyword><style face="normal" font="default" size="100%">nanocomposites</style></keyword><keyword><style face="normal" font="default" size="100%">nanofabrication</style></keyword><keyword><style face="normal" font="default" size="100%">nanoparticles</style></keyword><keyword><style face="normal" font="default" size="100%">nanosensors</style></keyword><keyword><style face="normal" font="default" size="100%">photodetectors</style></keyword><keyword><style face="normal" font="default" size="100%">semiconductor doping</style></keyword><keyword><style face="normal" font="default" size="100%">semiconductor growth</style></keyword><keyword><style face="normal" font="default" size="100%">ultraviolet detectors</style></keyword><keyword><style face="normal" font="default" size="100%">ultraviolet spectra</style></keyword><keyword><style face="normal" font="default" size="100%">visible spectra</style></keyword><keyword><style face="normal" font="default" size="100%">wide band gap semiconductors</style></keyword><keyword><style face="normal" font="default" size="100%">zinc compounds</style></keyword><keyword><style face="normal" font="default" size="100%">poly(methyl methacrylate)</style></keyword><keyword><style face="normal" font="default" size="100%">simultaneous detection</style></keyword><keyword><style face="normal" font="default" size="100%">UV detection spherical nanoparticles</style></keyword><keyword><style face="normal" font="default" size="100%">boron-doped ZnO</style></keyword><keyword><style face="normal" font="default" size="100%">fabricated UV detector</style></keyword><keyword><style face="normal" font="default" size="100%">detector gain</style></keyword><keyword><style face="normal" font="default" size="100%">IR detector</style></keyword><keyword><style face="normal" font="default" size="100%">PbSe based detectors</style></keyword><keyword><style face="normal" font="default" size="100%">IR detection</style></keyword><keyword><style face="normal" font="default" size="100%">mid-IR range</style></keyword><keyword><style face="normal" font="default" size="100%">B-doping</style></keyword><keyword><style face="normal" font="default" size="100%">photodetector devices</style></keyword><keyword><style face="normal" font="default" size="100%">UV radiation</style></keyword><keyword><style face="normal" font="default" size="100%">IR radiation</style></keyword><keyword><style face="normal" font="default" size="100%">UV-visible range</style></keyword><keyword><style face="normal" font="default" size="100%">discrete Fourier transform calculations</style></keyword><keyword><style face="normal" font="default" size="100%">input wavelength</style></keyword><keyword><style face="normal" font="default" size="100%">incident wavelength</style></keyword><keyword><style face="normal" font="default" size="100%">UV-IR dual-wavelength photodetector design</style></keyword><keyword><style face="normal" font="default" size="100%">hexamethylenetetramine</style></keyword><keyword><style face="normal" font="default" size="100%">ZnO-PMMA-PbSe nanocomposites</style></keyword><keyword><style face="normal" font="default" size="100%">absorption intensity</style></keyword><keyword><style face="normal" font="default" size="100%">thioacetamide</style></keyword><keyword><style face="normal" font="default" size="100%">chemical factors</style></keyword><keyword><style face="normal" font="default" size="100%">surface modification</style></keyword><keyword><style face="normal" font="default" size="100%">optoelectronic performance</style></keyword><keyword><style face="normal" font="default" size="100%">wavelength 365.0 nm</style></keyword><keyword><style face="normal" font="default" size="100%">wavelength 4.0 mum</style></keyword><keyword><style face="normal" font="default" size="100%">ZnO:B-PbSe</style></keyword><keyword><style face="normal" font="default" size="100%">Zinc oxide</style></keyword><keyword><style face="normal" font="default" size="100%">II-VI semiconductor materials</style></keyword><keyword><style face="normal" font="default" size="100%">Detectors</style></keyword><keyword><style face="normal" font="default" size="100%">Absorption</style></keyword><keyword><style face="normal" font="default" size="100%">Orbits</style></keyword><keyword><style face="normal" font="default" size="100%">Photodetector</style></keyword><keyword><style face="normal" font="default" size="100%">nanomaterials</style></keyword><keyword><style face="normal" font="default" size="100%">UV detection</style></keyword><keyword><style face="normal" font="default" size="100%">PbSe</style></keyword><keyword><style face="normal" font="default" size="100%">mid-IR detection</style></keyword><keyword><style face="normal" font="default" size="100%">surface treatment</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year></dates><isbn><style face="normal" font="default" size="100%">1941-0085</style></isbn><abstract><style face="normal" font="default" size="100%">A UV/IR dual-wavelength photodetector based on a ZnO/PMMA/PbSe nanocomposite [PMMA = poly(methyl methacrylate)] for simultaneous detection of 365 nm UV and 4 μm IR radiation is presented. For UV detection spherical nanoparticles of boron-doped ZnO were synthesized and stabilized using hexamethylenetetramine. The absorption intensity in the UV-vis range is increased upon B doping and discrete Fourier transform calculations confirm the results. Responsivity of the fabricated UV detector is 7.8 AW-1 and the detector gain is 26.49 at a 365 nm input wavelength. For the synthesis of IR detecting PbSe a new method was worked out, including the stabilization of the particles with thioacetamide. The performance of the PbSe based IR detector turns out to be superior to previously reported PbSe based detectors synthesized by established methods. The responsivity and gain of the detector is 8 AW-1 and 3.31, respectively for 4 μm incident wavelength. The sensitivity is 30 for IR detection and overall this sensitivity is excellent for sensing in the mid-IR range. All three “chemical factors,” the B-doping, the synthesis conditions for nanoparticles, and the surface modification have contributed to the excellent optoelectronic performance of these new photodetector devices, while the polymethyl methacrylate layer turned out to be very effectively reducing the noise for IR detection.</style></abstract><urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1109/TNANO.2018.2827201</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>632</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">632</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Czympiel, Lisa</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Mettenbörger, Andreas</style></author><author><style face="normal" font="default" size="100%">Hühne, Sven-Martin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">High activity heterogeneous catalysts by plasma-enhanced chemical vapor deposition of volatile palladium complexes on biomorphic carbon</style></title><secondary-title><style face="normal" font="default" size="100%">Comptes Rendus Chimie</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">943-951</style></pages><volume><style face="normal" font="default" size="100%">21</style></volume><number><style face="normal" font="default" size="100%">10</style></number><keywords><keyword><style face="normal" font="default" size="100%">Pd precursor</style></keyword><keyword><style face="normal" font="default" size="100%">PECVD</style></keyword><keyword><style face="normal" font="default" size="100%">Solid-supported catalyst</style></keyword><keyword><style face="normal" font="default" size="100%">BioC</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">2018/10/01/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1631-0748</style></isbn><abstract><style face="normal" font="default" size="100%">Six new palladium complexes based on allyl and alkenolate ligands were synthesized and structurally characterized. Combination of delocalized allylic sp2-hybridized carbon centers and a strongly binding NˆO chelating unit (e.g., 3,3,3-trifluoro(pyridin-2-yl)propen-2-ol) offered a promising combination of high volatility and thermal lability not commonly observed in noble metal precursors. Application of the new Pd compounds in thermal metal–organic and plasma-enhanced chemical vapor deposition demonstrated their clean and efficient decomposition pathways, which in conjunction with their intriguing air stability made them efficient precursors for Pd films and clusters. Plasma-enhanced chemical vapor deposition of the palladium compounds on biomorphic carbon used as a porous substrate with high surface area and interconnected channels delivered recyclable carbon-supported Pd catalysts (Pd@BioC), which showed excellent selectivity, stability, and recyclability in CC coupling reactions.</style></abstract><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S1631074818301115</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.crci.2018.04.008</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>186</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">186</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bialuschewski, Danny</style></author><author><style face="normal" font="default" size="100%">Hoppius, Jan S.</style></author><author><style face="normal" font="default" size="100%">Frohnhoven, Robert</style></author><author><style face="normal" font="default" size="100%">Deo, Meenal</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Gurevich, Evgeny L.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;Ruhr Univ Bochum, Chair Appl Laser Technol, Univ Str 150, D-44801 Bochum, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Laser-Textured Metal Substrates as Photoanodes for Enhanced PEC Water Splitting Reactions</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Adv Eng Mater</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><volume><style face="normal" font="default" size="100%">1800167</style></volume><number><style face="normal" font="default" size="100%">9</style></number><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style face="normal" font="default" size="100%">Sep</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">14381656</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000445327200020</style></accession-num><abstract><style face="normal" font="default" size="100%">We demonstrate the effect of femtosecond laser structuring of titanium substrates to increase the absorption, photoconversion, and overall photoelectrochemical water splitting (PEC) performance compared to pristine metal substrates, independent of any additional top coat layers. The influence of ultra short laser pulse patterning on PEC efficiency is investigated toward spectroscopic (UV-Vis), microscopic (SEM), crystallographic (XRD), and compositional (XPS) properties. The beneficial effect of a periodically patterned substrate is attributed to enhanced specific surface area and improved in-plane light trapping when compared to flat surfaces. Photoanodes for water splitting experiments fabricated by titanium and iron oxide films on laser pre-patterned Ti substrates are also found to show enhanced PEC efficiency (0.057 mA cm(-2)) when compared to unpatterened substrates (0.028 mA cm(-2)). The lower absolute PEC efficiencies are due to extreme thin films.</style></abstract><label><style face="normal" font="default" size="100%">Bialuschewski2018</style></label><notes><style face="normal" font="default" size="100%">Gu5lo&#xD;Times Cited:4&#xD;Cited References Count:42</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/adem.201800167</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">ARTN 1800167&#xD;10.1002/adem.201800167</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>222</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">222</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zhao, Zhihan</style></author><author><style face="normal" font="default" size="100%">Chen, Shixing</style></author><author><style face="normal" font="default" size="100%">Wang, Jianbang</style></author><author><style face="normal" font="default" size="100%">Su, Jing</style></author><author><style face="normal" font="default" size="100%">Xu, Jiaqiang</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Fan, Chunhai</style></author><author><style face="normal" font="default" size="100%">Song, Shiping</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">NEST Lab, Department of Chemistry, Shanghai University, Shanghai 200444, China; Division of Physical Biology and Bioimaging Center, Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, 2019 Jialuo Road, Shanghai 201800, China.&#xD;Division of Physical Biology and Bioimaging Center, Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, 2019 Jialuo Road, Shanghai 201800, China.&#xD;NEST Lab, Department of Chemistry, Shanghai University, Shanghai 200444, China. Electronic address: xujiaqiang@shu.edu.cn.&#xD;Institute of Inorganic Chemistry, University of Cologne, D-50939 Cologne, Germany.&#xD;Division of Physical Biology and Bioimaging Center, Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, 2019 Jialuo Road, Shanghai 201800, China. Electronic address: spsong@sinap.ac.cn.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Nuclease-free target recycling signal amplification for ultrasensitive multiplexing DNA biosensing</style></title><secondary-title><style face="normal" font="default" size="100%">Biosensors and Bioelectronics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">605--608</style></pages><volume><style face="normal" font="default" size="100%">94</style></volume><edition><style face="normal" font="default" size="100%">2017/04/02</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2017, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">August</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09565663</style></isbn><accession-num><style face="normal" font="default" size="100%">28364707</style></accession-num><abstract><style face="normal" font="default" size="100%">Ultrasensitive biosensing technologies without gene amplification held great promise for direct detection of DNA. Herein we report a novel biosensing method, combining target recycling signal-amplification strategy and a homemade electrochemical device. Especially, the target recycling was achieved by a strand displacement process, no needing the help of any nucleases. In the presence of target DNA, the recycling system could be activated to generate a cascade of assembly steps with three hairpin DNA segments. Each recycling process were accompanied by a disassembly step that the last hairpin DNA segment displaces target DNA from the complex at the end of each circulation, freeing targets to activate the self-assembly of more trefoil DNA structures. This biosensing method could detect target DNA at aM level and can distinguish target DNA from interfering DNAs, demonstrating its high sensitivity and high selectivity. Importantly, the biosensing method could work well with serum samples.</style></abstract><label><style face="normal" font="default" size="100%">Zhao2017</style></label><notes><style face="normal" font="default" size="100%">Zhao, Zhihan&#xD;Chen, Shixing&#xD;Wang, Jianbang&#xD;Su, Jing&#xD;Xu, Jiaqiang&#xD;Mathur, Sanjay&#xD;Fan, Chunhai&#xD;Song, Shiping&#xD;eng&#xD;England&#xD;Biosens Bioelectron. 2017 Aug 15;94:605-608. doi: 10.1016/j.bios.2017.03.051. Epub 2017 Mar 25.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0956566317302178</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.bios.2017.03.051</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>221</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">221</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Su, Jing</style></author><author><style face="normal" font="default" size="100%">Wang, Dongfang</style></author><author><style face="normal" font="default" size="100%">Nörbel, Lena</style></author><author><style face="normal" font="default" size="100%">Shen, Jianlei</style></author><author><style face="normal" font="default" size="100%">Zhao, Zhihan</style></author><author><style face="normal" font="default" size="100%">Dou, Yanzhi</style></author><author><style face="normal" font="default" size="100%">Peng, Tianhuan</style></author><author><style face="normal" font="default" size="100%">Shi, Jiye</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Fan, Chunhai</style></author><author><style face="normal" font="default" size="100%">Song, Shiping</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Chinese Acad Sci, Div Phys Biol, Shanghai 201800, Peoples R China&#xD;Chinese Acad Sci, Bioimaging Ctr, Shanghai Synchrotron Radiat Facil, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Univ Oxford, Kellogg Coll, Oxford OX2 6PN, England</style></auth-address><titles><title><style face="normal" font="default" size="100%">Multicolor Gold–Silver Nano-Mushrooms as Ready-to-Use SERS Probes for Ultrasensitive and Multiplex DNA/miRNA Detection</style></title><secondary-title><style face="normal" font="default" size="100%">Analytical Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Anal Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2531--2538</style></pages><volume><style face="normal" font="default" size="100%">89</style></volume><number><style face="normal" font="default" size="100%">4</style></number><keywords><keyword><style face="normal" font="default" size="100%">2017, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">February</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0003-2700</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000394724700050</style></accession-num><abstract><style face="normal" font="default" size="100%">Uniform silver-containing metal nanostructures with strong and stable surface enhanced Raman scattering (SERS) signals hold great promise for developing ultrasensitive probes for biodetection. Nevertheless, the direct synthesis of such ready-to-use nanoprobes remains extremely challenging. Herein we report a DNA-mediated gold silver nanomushroom with interior nanogaps directly synthesized and used for multiplex and simultaneous SERS detection of various DNA and RNA targets. The DNA involved in the nanostructures can act as hot only gap DNA (mediated DNA) but also probe DNA (hybridized DNA), and DNA&apos;s involvement enables the nanostructures to have the inherent ability to recognize DNA and RNA targets. Importantly, we were the first to establish a new method for the generation of multicolor SERS probes using two different strategies. First Raman-labeled alkanethiol probe DNA was assembled on gold nanoparticles, and second, thiol-containing Raman reporters were coassembled with the probe DNA. The ready-to-use probes also give great potential to develop ultrasensitive detection methods for various biological molecules.</style></abstract><label><style face="normal" font="default" size="100%">Su2017</style></label><notes><style face="normal" font="default" size="100%">El6ig&#xD;Times Cited:116&#xD;Cited References Count:51</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/acs.analchem.6b04729</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.analchem.6b04729</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>220</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">220</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sivakov, G</style></author><author><style face="normal" font="default" size="100%">Mussabek, K</style></author><author><style face="normal" font="default" size="100%">Yermukhamed, D</style></author><author><style face="normal" font="default" size="100%">Dikhanbayev, K K</style></author><author><style face="normal" font="default" size="100%">Schleusener, A</style></author><author><style face="normal" font="default" size="100%">Mathur, S</style></author><author><style face="normal" font="default" size="100%">Sivakov, V</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Al Farabi Kazakh Natl Univ, Natl Nanotechnol Lab Open Type, 71 Al Farabi Av, Alma Ata 050040, Kazakhstan&#xD;Leibniz Inst Photon Technol, Albert Einstein Str 9, D-07745 Jena, Germany&#xD;Cologne Univ, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Self-organized growth of germanium nanocolumns</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Research Express</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Mater Res Express</style></alt-title></titles><pages><style face="normal" font="default" size="100%">35003</style></pages><volume><style face="normal" font="default" size="100%">4</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">2017, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">Mar</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2053-1591</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000415254800001</style></accession-num><abstract><style face="normal" font="default" size="100%">The crystalline germanium nanostructures were obtained on a silicon surface by the chemical vapor deposition technique using a germanium (IV) iso -propoxide ([Ge(O i Pr) 4 ]) metalorganic precursor as a germanium source. As was observed, the one-dimensional (1D) germanium nanostructures on the silicon surface form without using a metal catalyst, meaning that the formation of 1D nanostructures is based not on a vapor–liquid–solid (VLS) growth mechanism, but on self-organization processes which take place on the silicon surfaces during the CVD process of germanium iso -propoxide pyrolysis. Our observation suggests that the non-catalytic growth of germanium nanocolumns is strongly dependent on the CVD process temperature. The germanium phase composition and morphology have been investigated by x-ray diffraction (XRD) and x-ray photoelectron spectroscopy (XPS), and high resolution scanning electron microscopy (HRSEM), respectively. Our results provide a new way to grow 1D germanium nanostructures without contamination by a catalyst, which the vapor–liquid–solid growth mechanism is known to cause, allowing for the application of such materials in micro- and optoelectronics.</style></abstract><label><style face="normal" font="default" size="100%">Sivakov2017</style></label><notes><style face="normal" font="default" size="100%">Fm7ki&#xD;Times Cited:1&#xD;Cited References Count:36</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://stacks.iop.org/2053-1591/4/i=3/a=035003</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">ARTN 035003&#xD;10.1088/2053-1591/aa5ed6</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>219</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">219</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Schütz, Markus B.</style></author><author><style face="normal" font="default" size="100%">Xiao, Lisong</style></author><author><style face="normal" font="default" size="100%">Lehnen, Thomas</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Microwave-assisted synthesis of nanocrystalline binary and ternary metal oxides</style></title><secondary-title><style face="normal" font="default" size="100%">International Materials Reviews</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1--34</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2017, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">December</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0950-6608</style></isbn><label><style face="normal" font="default" size="100%">Schutz2017</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.tandfonline.com/doi/full/10.1080/09506608.2017.1402158</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>218</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">218</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sasinska, Alexander</style></author><author><style face="normal" font="default" size="100%">Ritschel, Daniel</style></author><author><style face="normal" font="default" size="100%">Czympiel, Lisa</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Metallic Copper Thin Films Grown by Plasma-Enhanced Atomic Layer Deposition of Air Stable Precursors</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Adv Eng Mater</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1600593</style></pages><volume><style face="normal" font="default" size="100%">19</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">February</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">14381656</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000394997400015</style></accession-num><abstract><style face="normal" font="default" size="100%">The authors, report here on the deposition of metallic copper thin films by plasma-assisted atomic layer deposition (ALD) with an air stable and volatile precursor-[Cu((Py)CHCOCF3)(2)](2) (Py=pyridine)-that stands out due to its facile synthesis and easy handling under ambient conditions. Copper thin films are obtained by decomposing [Cu((Py)CHCOCF3)(2)](2) in hydrogen plasma in a concomitant deposition and recrystallization process. The thermal stability of the precursor prevents thermally induced decomposition, which allows precise control over thickness and film homogeneity. Electrical measurements of the as-deposited samples show clear interdependence of sheet resistance on the substrates surface roughness, thereby, films with higher roughness show higher resistance. Combined X-Ray photoelectron spectroscopy of Cu 2p peak and Cu LMM peak, as well as resistivity values of 58(-1) confirm the high quality of copper films without the need of further annealing steps under reducing atmosphere.</style></abstract><label><style face="normal" font="default" size="100%">Sasinska2016</style></label><notes><style face="normal" font="default" size="100%">Em0gs&#xD;Times Cited:8&#xD;Cited References Count:43</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/adem.201600593</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">ARTN 1600593&#xD;10.1002/adem.201600593</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>217</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">217</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sasinska, Alexander</style></author><author><style face="normal" font="default" size="100%">Bialuschewski, Danny</style></author><author><style face="normal" font="default" size="100%">Islam, Mazharul M</style></author><author><style face="normal" font="default" size="100%">Singh, Trilok</style></author><author><style face="normal" font="default" size="100%">Deo, Meenal</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;Univ Bonn, Mulliken Ctr Theoret Chem, Beringstr 4-6, D-53115 Bonn, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Experimental and Theoretical Insights into Influence of Hydrogen and Nitrogen Plasma on the Water Splitting Performance of ALD Grown TiO2 Thin Films</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry C</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Phys Chem C</style></alt-title></titles><pages><style face="normal" font="default" size="100%">15538--15548</style></pages><volume><style face="normal" font="default" size="100%">121</style></volume><number><style face="normal" font="default" size="100%">29</style></number><keywords><keyword><style face="normal" font="default" size="100%">2017, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">July</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000406726200006</style></accession-num><abstract><style face="normal" font="default" size="100%">Specific effects of hydrogen and nitrogen plasma treatment on anatase TiO2 photoanodes, grown via atomic layer deposition (ALD), and their respective impact on water splitting properties are reported. ALD grown TiO2 samples were exposed to reactive hydrogen and nitrogen plasmas and the photoelectrochemical efficiency of the modified samples were comparatively analyzed. Both H-2 and N-2 plasma treatment enhanced the photocurrent values compared to pristine TiO2. Electron density at oxygen vacancy sites was decreased upon nitrogen incorporation, reflected in band gap modulation and decreased recombination probability as confirmed by spectral data. Surface modification via H-2 plasma induce more midgap states to augment the photoinduced charge carriers concentration that was supported by theoretical investigation performed on the electronic properties of both H-and N-doped TiO2 (anatase). First-principles calculations based on Hartree-Fock-Density-Functional Theory (HF-DFT) hybrid models showed good agreement with the experimental findings and confirmed electronic band gap reduction due to extra electron density introduced via H-2 and N incorporation in TiO2.</style></abstract><label><style face="normal" font="default" size="100%">Sasinska2017</style></label><notes><style face="normal" font="default" size="100%">Fc3gd&#xD;Times Cited:5&#xD;Cited References Count:67</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/acs.jpcc.7b03424</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.jpcc.7b03424</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>216</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">216</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Leduc, Jennifer</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Raauf, Aida</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Rare-Earth-Containing Materials for Photoelectrochemical Water Splitting Applications</style></title></titles><pages><style face="normal" font="default" size="100%">185--219</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2017, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year></dates><label><style face="normal" font="default" size="100%">Leduc2017</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0080878417300145</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>215</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">215</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kaur, Jasleen</style></author><author><style face="normal" font="default" size="100%">Tsvetkova, Yoanna</style></author><author><style face="normal" font="default" size="100%">Arroub, Karim</style></author><author><style face="normal" font="default" size="100%">Sahnoun, Sabri</style></author><author><style face="normal" font="default" size="100%">Kiessling, Fabian</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Cologne, Germany&#xD;RWTH Aachen Univ Hosp, Dept Expt Mol Imaging, Aachen, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Synthesis, characterization, and relaxation studies of Gd-DO3A conjugate of chlorambucil as a potential theranostic agent</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Biology &amp; Drug Design</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Biol Drug Des</style></alt-title></titles><pages><style face="normal" font="default" size="100%">269-276</style></pages><volume><style face="normal" font="default" size="100%">89</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2017, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">February</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">17470277</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000393958900008</style></accession-num><abstract><style face="normal" font="default" size="100%">DO3A-based macrocycles serve as attractive templates from which clinically useful theranostic agents can be obtained after coupling with molecular targeted therapeutic drugs. In this study, we describe the chemical synthesis, relaxation, and cytotoxicity studies of a new DO3A conjugate of chlorambucil (CHL) as a magnetic resonance imaging (MRI) theranostic agent. A convenient route of synthesis is reported, which allowed conjugation of the macrocyclic ligand (DO3A) to the chemotherapeutic drug (CHL) via tyrosine for the preparation of an attractive chelate-drug ensemble (DO3A-TR-CHL). The structures of all intermediates and final compound have been determined by H-1, C-13 NMR, and MS. The efficacy of DO3A-TR-CHL as a non-ionic magnetic contrast agent was tested by performing relaxometric studies on its gadolinium complex. The complex exhibited relaxivities (7.11 mm(-1)/s) higher than that of currently used MR contrast agents and showed enhanced contrast in T-1-weighted images. MTT assays revealed that both DO3A-TR-CHL and Gd(III)-DO3A-TR-CHL conjugates exhibited dose-dependent toxicity and an enhanced antiproliferative activity against tumor (A549 and HeLa) cell lines compared to that of parent drug (CHL), thereby demonstrating their potential to be used as a magnetic resonance imaging theranostic for improved molecular imaging and therapy of human cancers.</style></abstract><label><style face="normal" font="default" size="100%">Kaur2017</style></label><notes><style face="normal" font="default" size="100%">Ek5ia&#xD;Times Cited:4&#xD;Cited References Count:22</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1111/cbdd.12827</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1111/cbdd.12827</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>214</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">214</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jürgensen, Lasse</style></author><author><style face="normal" font="default" size="100%">Frank, Michael</style></author><author><style face="normal" font="default" size="100%">Pyeon, Myeongwhun</style></author><author><style face="normal" font="default" size="100%">Czympiel, Lisa</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Subvalent Iridium Precursors for Atom-Efficient Chemical Vapor Deposition of Ir and IrO2 Thin Films</style></title><secondary-title><style face="normal" font="default" size="100%">Organometallics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">2331--2337</style></pages><volume><style face="normal" font="default" size="100%">36</style></volume><number><style face="normal" font="default" size="100%">12</style></number><keywords><keyword><style face="normal" font="default" size="100%">2017, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">June</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0276-7333</style></isbn><label><style face="normal" font="default" size="100%">Jurgensen2017</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/acs.organomet.7b00275</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>213</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">213</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Heidemann, Tim</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Inst Inorgan Chem, Dept Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Three at a Time: Step by Step to Heterotermetallic Molecules</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Inorg Chem</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">234--240</style></pages><volume><style face="normal" font="default" size="100%">56</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2017, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">January</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000391248900027</style></accession-num><abstract><style face="normal" font="default" size="100%">New structural motifs in ternary metal alkoxides are demonstrated through synthetic strategies that enable overcoming statistical barriers and solution equilibrium. Tetradentate dimetalate unit, {M-2(OiP)(9)}(-) (M = Hf (1), Zr (2)), used to sequester the coordination sphere of the central metal atom (Ba), allowed step-by-step construction of termetallic molecules [{M&apos;(OiPr)(4)}(HOiPr)Ba{M-2(OiPr)(9)}] (M&apos; = Al (3), Ga (4), M = Hf; M&apos; = Al, M = Zr (5)). In contrast to a common coordinative-fit&quot; approach mainly used for bimetallic compounds, this stepwise rational construction using fast successive salt metathesis reactions circumvents general challenges in the syntheses of termetallic alkoxides by avoiding the thermodynamically preferred formation of bimetallic alkoxide molecules. The presented compounds exhibit for the first time gas phase stable termetallic alkoxide frameworks.</style></abstract><label><style face="normal" font="default" size="100%">Heidemann2017</style></label><notes><style face="normal" font="default" size="100%">Eg7sj&#xD;Times Cited:7&#xD;Cited References Count:59</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.6b02069</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.inorgchem.6b02069</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>212</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">212</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Graf, David</style></author><author><style face="normal" font="default" size="100%">Schläfer, Johannes</style></author><author><style face="normal" font="default" size="100%">Garbe, Simon</style></author><author><style face="normal" font="default" size="100%">Klein, Axel</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Interdependence of Structure, Morphology, and Phase Transitions in CVD Grown VO2 and V2O3 Nanostructures</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">5877--5885</style></pages><volume><style face="normal" font="default" size="100%">29</style></volume><number><style face="normal" font="default" size="100%">14</style></number><keywords><keyword><style face="normal" font="default" size="100%">2017, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">July</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000406573200018</style></accession-num><abstract><style face="normal" font="default" size="100%">Phase selective chemical vapor deposition of nanostructured vanadium dioxide (VO2) and sesquioxide (V2O3) was achieved by deploying [V(OR)(4)](n) (R = Bu-t, n = 1 (1), R = Et, n = 3 (2), R = Me, n = 4 (3)). Use of [V((OBu)-Bu-t)(4)] (1) produced thin films of monoclinic VO2 (Ml) at 700 and 800 degrees C consisting of anisotropic nanostructures with high crystallinity and small hysteresis in the metal-to-semiconductor transition (MST). Film morphologies manifested strong dependence on growth temperatures and exhibited pronounced texturing effects at high temperatures (&gt;700 degrees C). The microstructure of the films was found to significantly affect the MST behavior of VO2 films. DTA measurements of VO2 films showed MST at 63 degrees C (700 degrees C) and 65 degrees C (800 degrees C), much lower than the transition temperature observed in single crystal material (68 degrees C). Precursors were characterized in the solid state (XRD) and solution state (temperature dependent EPR, NMR) to reveal an association dissociation equilibrium in solution (complexes 2 and 3), involving monomeric, dimeric, and oligomeric species. Use of 2 and 3 as single precursors produced thin films of crystalline V2O3 consisting of nanosheets (5 nm) with a flower-like morphology.</style></abstract><label><style face="normal" font="default" size="100%">Graf2017</style></label><notes><style face="normal" font="default" size="100%">Fc1bu&#xD;Times Cited:17&#xD;Cited References Count:56</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/acs.chemmater.7b01018</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.chemmater.7b01018</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>211</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">211</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Garg, Rishabh</style></author><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Heterobimetallic Alkoxides (CdIIMV(OiPr)7)2 (M = Nb, Ta) as Potential Precursors to Pyrochlore Cd2M2O7</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">3383--3389</style></pages><volume><style face="normal" font="default" size="100%">2017</style></volume><number><style face="normal" font="default" size="100%">28</style></number><keywords><keyword><style face="normal" font="default" size="100%">2017, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">August</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">14341948</style></isbn><label><style face="normal" font="default" size="100%">Garg2017</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/ejic.201700331</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>210</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">210</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Czympiel, Lisa</style></author><author><style face="normal" font="default" size="100%">Lekeu, Jean-Marius</style></author><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Dept Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Oxidative halogenation of Sn(II)heteroaryl alkenolates: Formation of unusual trans-dihalo Sn(IV) complexes</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganica Chimica Acta</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Inorg Chim Acta</style></alt-title></titles><pages><style face="normal" font="default" size="100%">197--203</style></pages><volume><style face="normal" font="default" size="100%">455</style></volume><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">January</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">00201693</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000389167100024</style></accession-num><abstract><style face="normal" font="default" size="100%">A series of novel tin(IV)-heteroaryl alkenolates of the general formula [Sn(DMOTFP)(2)X-2] (3-6, X = F, Cl, Br, I) were prepared by direct oxidative halogenation of the corresponding tin(II) derivative [Sn-II(DMOTFP)(2)] (2) and by cleavage of the carbon-tin bonds in diphenyltin dichloride [Ph2SnCl2] by (4,5-dimethyloxazolyl)-1,1,1-trifluoropropen-2-ol, (H-DMOTFP, 1) with a subsequent halide exchange reaction. The molecular structures elucidated in solution (multi-nuclear NMR spectroscopy) and by single crystal X-ray diffraction confirmed the sixfold coordination of the tin(IV) center with a distorted octahedral arrangement of ligands. An unusual centrosymmetric octahedral trans-dihalo configuration was found for the compounds [Sn-IV(DMOTFP)(2)X-2] (X = Cl, Br, I), while the compound [Sn(DMOTFP)(2)F-2] adopted a cis-dihalide configuration. (C) 2016 Published by Elsevier B.V.</style></abstract><label><style face="normal" font="default" size="100%">Czympiel2017</style></label><notes><style face="normal" font="default" size="100%">1&#xD;Ed9cf&#xD;Times Cited:2&#xD;Cited References Count:62</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0020169316307265</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.ica.2016.10.023</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>209</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">209</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Büyükyazi, Mehtap</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Yu, Penmgei</style></author><author><style face="normal" font="default" size="100%">Coll, Mariona</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Institute of Inorganic Chemistry, University of Cologne, Greinstrasse 6, Cologne 50939, Germany. sanjay.mathur@uni-koeln.de.</style></auth-address><titles><title><style face="normal" font="default" size="100%">A cobalt(II)heteroarylalkenolate precursor for homogeneous Co3O4 coatings by atomic layer deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Dalton Trans.</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">12996--13001</style></pages><volume><style face="normal" font="default" size="100%">46</style></volume><number><style face="normal" font="default" size="100%">38</style></number><edition><style face="normal" font="default" size="100%">2017/09/22</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2017, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">Oct 14</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1477-9226</style></isbn><accession-num><style face="normal" font="default" size="100%">28933477</style></accession-num><abstract><style face="normal" font="default" size="100%">We present a robust approach to prepare conformal Co3O4 nanocoatings on high aspect ratio structures from a new cobalt metalorganic complex.</style></abstract><label><style face="normal" font="default" size="100%">Buyukyazi2017</style></label><notes><style face="normal" font="default" size="100%">Buyukyazi, Mehtap&#xD;Fischer, Thomas&#xD;Yu, Penmgei&#xD;Coll, Mariona&#xD;Mathur, Sanjay&#xD;eng&#xD;England&#xD;Dalton Trans. 2017 Oct 14;46(38):12996-13001. doi: 10.1039/c7dt02757e. Epub 2017 Sep 21.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.rsc.org/en/Content/ArticleLanding/2017/DT/C7DT02757E http://xlink.rsc.org/?DOI=C7DT02757E</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c7dt02757e</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>208</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">208</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Andón, Fernando T.</style></author><author><style face="normal" font="default" size="100%">Mukherjee, Sourav P.</style></author><author><style face="normal" font="default" size="100%">Gessner, Isabel</style></author><author><style face="normal" font="default" size="100%">Wortmann, Laura</style></author><author><style face="normal" font="default" size="100%">Xiao, Lisong</style></author><author><style face="normal" font="default" size="100%">Hultenby, Kjell</style></author><author><style face="normal" font="default" size="100%">Shvedova, Anna A.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Fadeel, Bengt</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hollow carbon spheres trigger inflammasome-dependent IL-beta secretion in macrophages</style></title><secondary-title><style face="normal" font="default" size="100%">Carbon</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">243--251</style></pages><volume><style face="normal" font="default" size="100%">113</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2017, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style face="normal" font="default" size="100%">March</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">00086223</style></isbn><label><style face="normal" font="default" size="100%">Andon2017</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0008622316310235</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>239</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">239</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Schläfer, J.</style></author><author><style face="normal" font="default" size="100%">Graf, D.</style></author><author><style face="normal" font="default" size="100%">Fornalczyk, G.</style></author><author><style face="normal" font="default" size="100%">Mettenbörger, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Institute of Inorganic Chemistry, University of Cologne Greinstrasse 6, D-50939 Cologne, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Fluorinated Cerium(IV) Enaminolates: Alternative Precursors for Chemical Vapor Deposition of CeO2 Thin Films</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">5422-5429</style></pages><volume><style face="normal" font="default" size="100%">55</style></volume><number><style face="normal" font="default" size="100%">11</style></number><edition><style face="normal" font="default" size="100%">2016/05/10</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2016, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun 6</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1520-510X (Electronic)&#xD;0020-1669 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">27159551</style></accession-num><abstract><style face="normal" font="default" size="100%">High-yield synthesis of four new fluorinated enaminones LH2 (RfC(O)C2H2NH)2C2H4 (Rf = CF3 (2a), C2F5 (2b), C3F7 (2c)) and (F3CC(O)C2H2NH)2C3H6 (2a&apos;) as dianionic ligands is described. The ligands were characterized in solution (via nuclear magnetic resoannce (NMR)) as well as in the solid state (via X-ray diffraction (XRD)). The ligating ability of the enaminones was verified by reacting them with [Ce2(O(i)Pr)8(HO(i)Pr)2], which resulted in monomeric cerium(IV) complexes [CeL2] (3a-c, 3a&apos;) based on tetradentate chelation of the ligands. Cerium enaminolates were comprehensively analyzed by NMR spectroscopy, mass spectrometry, and single-crystal XRD studies to verify their monomeric nature. High stability under ambient conditions and high volatility makes them a potential precursor for the gas-phase synthesis of CeO2. Complexes 3a and 3b were applied as precursors in thermal and plasma-enhanced chemical vapor deposition to obtain crystalline ceria films with different surface morphologies. The purity and surface states of the films were analyzed by X-ray photoelectron spectroscopy, which revealed a high amount of Ce(3+) on the subsurface of CeO2 films.</style></abstract><label><style face="normal" font="default" size="100%">Schlafer2016</style></label><notes><style face="normal" font="default" size="100%">Schlafer, J&#xD;Graf, D&#xD;Fornalczyk, G&#xD;Mettenborger, A&#xD;Mathur, S&#xD;eng&#xD;Inorg Chem. 2016 Jun 6;55(11):5422-9. doi: 10.1021/acs.inorgchem.6b00348. Epub 2016 May 9.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.6b00348</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.inorgchem.6b00348</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>238</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">238</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Saruhan, Bilge</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Metal Oxide (MO) and MO-integrated 1D Carbon Nano-Fibrils for increased Storage Capability</style></title><secondary-title><style face="normal" font="default" size="100%">5th International Workshop on Advanced Materials Challenges for Health and Alternative Energy Solutions -AMAES V</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2016, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year></dates><label><style face="normal" font="default" size="100%">Saruhan2016</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>237</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">237</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Saruhan, Bilge</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Capacitance Performance with Metal and Oxygen integrated 1D Carbon Nano-Fibrils</style></title><secondary-title><style face="normal" font="default" size="100%">NanoFIS 2016</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2016, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year></dates><label><style face="normal" font="default" size="100%">Saruhan2016a</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>236</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">236</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pyeon, Myeongwhun</style></author><author><style face="normal" font="default" size="100%">Wang, Meng</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Kaouk, Ali</style></author><author><style face="normal" font="default" size="100%">Jäckle, Sara</style></author><author><style face="normal" font="default" size="100%">Christiansen, Silke</style></author><author><style face="normal" font="default" size="100%">Hwang, Taejin</style></author><author><style face="normal" font="default" size="100%">Moon, KyoungIl</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Dept Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;Xi An Jiao Tong Univ, State Key Lab Multiphase Flow Power Engn, Int Res Ctr Renewable Energy, Xian 710049, Shaanxi, Peoples R China&#xD;Helmholtz Zentrum Berlin Mat &amp; Energie GmbH, Hahn Meitner Pl 1, D-14109 Berlin, Germany&#xD;Max Planck Inst Sci Light, Gunther Scharowsky Str 1, D-91058 Erlangen, Germany&#xD;Korea Inst Ind Technol KITECH, 320 Techno sunhwan Ro, Dalseong Gun 711880, Daegu, South Korea&#xD;Korea Inst Ind Technol KITECH, Siheung Ppuri Technol Supporting Ctr, Heat Treatment R&amp;D Grp, 113-5 Seohaean Ro, Siheung Si 429450, Gyeonggi Do, South Korea</style></auth-address><titles><title><style face="normal" font="default" size="100%">Design of multi-layered TiO2–Fe2O3 photoanodes for photoelectrochemical water splitting: patterning effects on photocurrent density</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Communications</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Mrs Commun</style></alt-title></titles><pages><style face="normal" font="default" size="100%">442--448</style></pages><volume><style face="normal" font="default" size="100%">6</style></volume><number><style face="normal" font="default" size="100%">04</style></number><keywords><keyword><style face="normal" font="default" size="100%">2016, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style face="normal" font="default" size="100%">December</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2159-6859</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000393127700016</style></accession-num><abstract><style face="normal" font="default" size="100%">We report the effect of patterning on photoelectrochemical (PEC) water-splitting performance. Oxide-oxide heterostructures based on horizontal and vertical heterojunctions were fabricated on transparent conductive oxide glass by sequential plasma enhanced chemical vapor deposition (PECVD) of individual metal oxide. Featured masks were employed to enable three-dimensional patternings of stripes and cross-bars structures formed by Fe2O3 and TiO2 layers. PEC measurement was carried out by a three-electrode cell. It was found that double layered TiO2//Fe2O3: FTO showed a decrease in PEC performance when compared with single Fe2O3: FTO layer, whereas triple-layered Fe2O3//TiO2//Fe2O3: FTO (both patterned and unpatterned samples) displayed enhanced photocurrent density. The results show that the existence of multiple phase boundaries does not always add up to PEC enhancement observed in single heterojunction.</style></abstract><label><style face="normal" font="default" size="100%">Pyeon2016</style></label><notes><style face="normal" font="default" size="100%">Ej3qw&#xD;Times Cited:7&#xD;Cited References Count:41</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.journals.cambridge.org/abstract{\_}S2159685916000549</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1557/mrc.2016.54</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>235</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">235</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Poirier, Stéphanie</style></author><author><style face="normal" font="default" size="100%">Czympiel, Lisa</style></author><author><style face="normal" font="default" size="100%">Bélanger-Desmarais, Nicolas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Reber, Christian</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Departement de chimie, Universite de Montreal, Montreal, Quebec H3C 3J7, Canada. christian.reber@umontreal.ca.&#xD;Institute of Inorganic Chemistry, University of Cologne, D-50939 Cologne, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Temperature and pressure variations of d–d luminescence band maxima of bis(pyridylalkenolato)palladium(II) complexes with different ligand substituents: opposite-signed trends</style></title><secondary-title><style face="normal" font="default" size="100%">Dalton Transactions</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Dalton Transactions</style></full-title></periodical><pages><style face="normal" font="default" size="100%">6574-6581</style></pages><volume><style face="normal" font="default" size="100%">45</style></volume><number><style face="normal" font="default" size="100%">15</style></number><edition><style face="normal" font="default" size="100%">2016/03/11</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2016, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style face="normal" font="default" size="100%">Apr 21</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1477-9234 (Electronic)&#xD;1477-9226 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">26961410</style></accession-num><abstract><style face="normal" font="default" size="100%">Luminescence spectra of two d8-configured bis(pyridylalkenolato)palladium(ii) complexes, Pd\PyCHC(C3F7)O\2 and Pd\PyCHC(CH3)O\2, are presented at variable temperature and pressure. Bands are assigned as d-d transitions. The heptafluoropropyl and methyl substituents on the ligands have different steric demands, influencing luminescence spectra. Broad bands with maxima at approximately 12 700 cm-1 (790 nm) for ligands with heptafluoropropyl substituents and 12 100 cm-1 (830 nm) for ligands with methyl substituents and widths of approximately 2100 cm-1 for both complexes are observed at 80 K. Quenching of the luminescence is observed as temperature increases. The maxima of Pd\PyCHC(C3F7)O\2 show a shift of -0.9 +/- 0.1 cm-1 K-1 due to broadening of the spectra to lower energy. The luminescence maxima of Pd\PyCHC(CH3)O\2 shift in the opposite direction by +7.2 +/- 0.7 cm-1 K-1. Shifts with different signs are also obtained from variable-pressure luminescence spectra, with values of +13 +/- 2 cm-1 kbar-1 and -15 +/- 7 cm-1 kbar-1 for Pd\PyCHC(C3F7)O\2 and Pd\PyCHC(CH3)O\2, respectively. The pressure-induced decrease is unusual and likely caused by intermolecular interactions involving the palladium(ii) center and a vinylic proton of a neighboring complex.</style></abstract><label><style face="normal" font="default" size="100%">poirier2016temperature</style></label><notes><style face="normal" font="default" size="100%">Poirier, Stephanie&#xD;Czympiel, Lisa&#xD;Belanger-Desmarais, Nicolas&#xD;Mathur, Sanjay&#xD;Reber, Christian&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;England&#xD;Dalton Trans. 2016 Apr 21;45(15):6574-81. doi: 10.1039/c5dt05068e.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.rsc.org/en/Content/ArticleLanding/2016/DT/C5DT05068E#!divAbstract</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c5dt05068e</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>233</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">233</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Miguel, F. L.</style></author><author><style face="normal" font="default" size="100%">Müller, R.</style></author><author><style face="normal" font="default" size="100%">Rosenkranz, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Mücklich, F.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Chair Funct Mat, D-66123 Saarbrucken, Germany&#xD;Univ Cologne, Chair Inorgan &amp; Mat Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Analysis and modelling of the dry-sliding friction and wear behaviour of electrodeposited Ni and Ni-matrix-nanocomposite films</style></title><secondary-title><style face="normal" font="default" size="100%">Wear</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Wear</style></alt-title></titles><pages><style face="normal" font="default" size="100%">87-98</style></pages><volume><style face="normal" font="default" size="100%">346-347</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2016, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan 15</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0043-1648</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000367235000010</style></accession-num><abstract><style face="normal" font="default" size="100%">The work here described aimed to assess the tribological behaviour of a Ni-matrix-nanocomposite film and to gain understanding of the role that the reinforcing phases play in it. The composite consisted of an array of Ag-coated SnO2 nanowires grown onto a substrate, around which the Ni matrix was galvanostatically deposited. Friction and wear were evaluated under dry sliding conditions using a linearly reciprocating ball-on-flat setup, with a diamond ball of 5.8µm radius as counterbody, subjected to loads ranging from 5 to 30mN. The surface and cross section of the wear tracks were characterised by scanning electron microscopy, energy-dispersive X-ray spectroscopy and white light interferometry. Ploughing-type abrasive wear was observed, with load-dependent dynamic friction coefficients, being this attributed to scale effect. Numerical models were developed for the analysis of wear volume and wear rate, as function of film hardness, applied load and wear track length. Due to their higher hardness, the composite films exhibited superior wear resistance with respect to Ni films produced using the exact same bath and deposition parameters as the composite׳s matrix. This was evidenced by reductions of up to 74 and 65\% in wear volume and rate, respectively.</style></abstract><label><style face="normal" font="default" size="100%">Miguel2016a</style></label><notes><style face="normal" font="default" size="100%">Cz6tx&#xD;Times Cited:6&#xD;Cited References Count:72</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0043164815004822</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.wear.2015.11.006</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>234</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">234</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Miguel, F. L.</style></author><author><style face="normal" font="default" size="100%">Müller, R.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Mücklich, F.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Chair Funct Mat, Campus D3-3, D-66123 Saarbrucken, Germany&#xD;Univ Cologne, Chair Inorgan &amp; Mat Chem, Greinstr 6, D-50937 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">On the thermal stability of electrodeposited Ni-matrix-nanocomposite films reinforced with Ag-coated SnO2 nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Surface and Coatings Technology</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Surf Coat Tech</style></alt-title></titles><pages><style face="normal" font="default" size="100%">93-102</style></pages><volume><style face="normal" font="default" size="100%">287</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2016, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style face="normal" font="default" size="100%">Feb 15</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0257-8972</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000370908600012</style></accession-num><abstract><style face="normal" font="default" size="100%">Ni-matrix-nanocomposite films were produced by constant-current electrodeposition from a sulphamate bath. The composite consisted of a disordered array of Ag-coated SnO2 nanowires grown onto a substrate by chemical vapour deposition, around which the Ni matrix was electrodeposited. The thermal stability of the films was analysed by non-isothermal annealing at up to 600°C and isothermally at 300 and 500°C for 10h, at high vacuum (10−7 to 10−6mbar). Pure Ni films were also analysed for comparison purposes. The microstructural evolution of the samples was characterised by means of X-ray diffraction and scanning electron microscopy assisted by electron backscatter diffraction. The composite showed higher thermal stability, evidenced by an increase of only 70\% in its average grain size after annealing at 500°C, against the 300\% observed for the pure Ni films, as a result of pinning of the matrix&apos;s grain boundaries by the Ag–SnO2 phase. Moreover, it retained its random crystallographic orientation, while Ni samples evolved from a &lt;100&gt; towards a &lt;111&gt; fibre texture due to surface energy minimisation.</style></abstract><label><style face="normal" font="default" size="100%">Miguel2016</style></label><notes><style face="normal" font="default" size="100%">De8tc&#xD;Times Cited:1&#xD;Cited References Count:58</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0257897215305156</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.surfcoat.2015.12.085</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>232</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">232</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mettenbörger, A.</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Y.</style></author><author><style face="normal" font="default" size="100%">Fischer, T.</style></author><author><style face="normal" font="default" size="100%">Heisig, T.</style></author><author><style face="normal" font="default" size="100%">Sasinska, A.</style></author><author><style face="normal" font="default" size="100%">Maccato, C.</style></author><author><style face="normal" font="default" size="100%">Carraro, G.</style></author><author><style face="normal" font="default" size="100%">Sada, C.</style></author><author><style face="normal" font="default" size="100%">Barreca, D.</style></author><author><style face="normal" font="default" size="100%">Mayrhofer, L.</style></author><author><style face="normal" font="default" size="100%">Moseler, M.</style></author><author><style face="normal" font="default" size="100%">Held, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Interfacial insight in multi-junction metal oxide photoanodes for water-splitting applications</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><pages><style face="normal" font="default" size="100%">415-427</style></pages><volume><style face="normal" font="default" size="100%">19</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2016, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year></dates><abstract><style face="normal" font="default" size="100%">Photoelectrochemical (PEC) properties of nanostructured hematite (Fe2O3) thin films prepared using plasma-enhanced chemical vapor deposition (PE-CVD) were investigated against the influence of processing parameters and post-synthesis heat-treatment procedures. Annealing at high temperatures (&gt;500°C) was found to substantially affect the micro-structure (grain growth and densification) and electronic (interdiffusion at the film/substrate interface) concomitantly manifested in an enhancement in the PEC behavior. The Sn impurity level in hematite films was found to increase with the annealing temperature with highest values achieved in samples heat-treated at 750°C, due to the interdiffusion and substitution of Sn(IV) species at Fe(III) sites. Sn:Fe2O3 films exhibited significantly high photocurrent density of 1.33mAcm−2 at the water oxidation level of 1.23V vs. RHE. The diffusion of Sn ions into iron oxide lattice altered the electronic properties of hematite films due to electron–donor behavior of the dopants that was verified by X-ray photoelectron spectroscopy and secondary ion mass spectroscopy (SIMS) analyses. Deposition of a thin overlayer of TiO2 (10nm) on hematite films by atomic layer deposition (ALD) was found to further improve the photocurrent density to 1.8mAcm−2 at 1.23V vs. RHE. Ab-initio calculations on the effect of substitutional Sn(IV) dopants in the Fe2O3 lattice on the electronic structure and the band alignment between hematite and the TiO2 over layer revealed that Sn-dopants led to the generation of localized Fe(II) centers augmenting the n-type behavior of hematite. No effect of the Sn-doping on the electrostatic potential was found on a macroscopic scale. However, the charge transfer from the Sn-doping to the Fe(II) centers would cause high electric fields on the nanometer scale and might hence play an important role in the efficient separation of electron and holes. The simulations showed that the hematite band edges are enclosed by the TiO2 band edges and therefore electron depletion at the surface–liquid interface is enhanced. This might lead to reduced recombination rates near the surface and consequently to increased photocurrents, since the Fe2O3/TiO2 interface constitutes a barrier for hole transport.</style></abstract><label><style face="normal" font="default" size="100%">Mettenborger2016</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S2211285515003791</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>231</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">231</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kaouk, Ali</style></author><author><style face="normal" font="default" size="100%">Ruoko, Tero-Petri</style></author><author><style face="normal" font="default" size="100%">Pyeon, Myeongwhun</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Kaunisto, Kimmo</style></author><author><style face="normal" font="default" size="100%">Lemmetyinen, Helge</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Tampere Univ Technol, Dept Chem &amp; Bioengn, Tampere 33710, Finland&#xD;German Aerosp Ctr DLR, Inst Mat Phys Space, D-51170 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">High Water-Splitting Efficiency through Intentional In and Sn Codoping in Hematite Photoanodes</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry C</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Phys Chem C</style></alt-title></titles><pages><style face="normal" font="default" size="100%">28345--28353</style></pages><volume><style face="normal" font="default" size="100%">120</style></volume><number><style face="normal" font="default" size="100%">49</style></number><keywords><keyword><style face="normal" font="default" size="100%">2016, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style face="normal" font="default" size="100%">December</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000390072100065</style></accession-num><abstract><style face="normal" font="default" size="100%">The effects of intermittent thin ITO layers on the water-splitting efficiency of alpha-Fe2O3 films grown by PECVD on FTO substrates are reported. The alpha-Fe2O3 was codoped with indium and tin by temperature-driven ionic transport and diffusion from the ultrathin ITO layer sputtered between the alpha-Fe2O3 layer and FTO substrate. The alpha-Fe2O3/ITO/FTO photoanodes showed a remarkable interdependence between the thickness of the ITO layer and PEC efficiency. Hematite photoanodes with a 32 nrn thick ITO underlayer showed the highest photocurrent density of 2.5 mA cm(-2), corresponding to an approximate 3-fold enhancement over pristine alpha-Fe2O3 at 1.23 V vs RHE, whereas the thinner (8 nm) ITO underlayer yielded the lowest onset potential at 0.6 V vs RHE. Although the electrode with a thicker 72 nm ITO underlayer showed a higher onset potential of 0.9 V vs RHE, it still showed an enhancement in the photocurrent density at higher bias voltages. alpha-Fe2O3 was also deposited on metallic titanium substrates with intermittent sputtered tin and ITO layers. The codoping with indium and tin from ITO was observed to yield greatly enhanced performance when compared with both alpha-Fe2O3 alone and tin-doped alpha-Fe2O3. Transient absorption decays in the sub-nanosecond time scale were not affected by the doping, indicating that the doping had little effect on the primary charge carrier generation and recombination. On the other hand, fewer trapped electrons on the microsecond to millisecond time scale and a greatly increased amount of long-lived surface photoholes were observed for the ITO-doped samples. The transient absorption results imply that the large increases in photoelectrochemical efficiency were obtained due to higher electron mobility, which reduces recombination and leads to more efficient electron extraction from the electrodes.</style></abstract><label><style face="normal" font="default" size="100%">Kaouk2016</style></label><notes><style face="normal" font="default" size="100%">Ef1ga&#xD;Times Cited:24&#xD;Cited References Count:50</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/10.1021/acs.jpcc.6b10432</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.jpcc.6b10432</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>230</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">230</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jamil, Aida</style></author><author><style face="normal" font="default" size="100%">Schläfer, Johannes</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Lepcha, Ashish</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Precursor-Derived Rare Earth Metal Pyrochlores: Nd2Sn2O7 Nanofibers and Thin Films As Efficient Photoabsorbers</style></title><secondary-title><style face="normal" font="default" size="100%">Cryst. Growth Des.</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Cryst Growth Des</style></alt-title></titles><pages><style face="normal" font="default" size="100%">5260–5267</style></pages><volume><style face="normal" font="default" size="100%">16</style></volume><number><style face="normal" font="default" size="100%">9</style></number><keywords><keyword><style face="normal" font="default" size="100%">2016, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style face="normal" font="default" size="100%">Sep</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1528-7483</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000382902400058</style></accession-num><abstract><style face="normal" font="default" size="100%">Single phase rare earth pyrochlores, Ln(2)M(2)O(7), were produced as nanofibers and thin films by electrospinning and spin-coating of chemical sols obtained from bimetallic metalorganic precursors, Ln(III)M(II)((OBu)-Bu-t)(5)Py (Ln(III) = La, Pr, Nd, Sm, Er, Yb; M-II = Ge, Sn, Pb; Py = pyridine). Compatibility of the metal ratio in the single-source compounds was confirmed by single crystal X-ray diffraction analyses and the ratio was preserved during the processing as the crystalline pyrochlore materials originated from an amorphous preceramic aggregate as confirmed by powder XRD and TEM studies. The photocatalytic activity of the Nd2Sn2O7 nanofibers was found to be significantly higher than that of TiO2. Nd2Sn2O7 thin films deposited on F:SnO2 as bilayered Nd2Sn2O7//Fe2O3 photoanodes showed superior photoelectrochemical (PEC) efficiency for water splitting reaction with an over 3-fold higher photocurrent density than bare Fe2O3 photoanodes.</style></abstract><label><style face="normal" font="default" size="100%">jamil2016ownprecursorderived</style></label><notes><style face="normal" font="default" size="100%">Dv4nn&#xD;Times Cited:17&#xD;Cited References Count:42</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/acs.cgd.6b00815</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.cgd.6b00815</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>229</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">229</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gonzalo-Juan, Isabel</style></author><author><style face="normal" font="default" size="100%">Detsch, Rainer</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ionescu, Emanuel</style></author><author><style face="normal" font="default" size="100%">Boccaccini, Aldo</style></author><author><style face="normal" font="default" size="100%">Riedel, Ralf</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">FB Material-und Geowissenschaften, Technische Universitat Darmstadt, Jovanka-Bontschits-Strasse 2, Darmstadt D-64287, Germany. gonzalo@materials.tu-darmstadt.de.&#xD;Department of Materials Science and Engineering, Institute of Biomaterials, University of Erlangen-Nuremberg, Cauerstrasse 6, Erlangen D-91058, Germany. rainer.detsch@fau.de.&#xD;Institute for Inorganic Chemistry, University of Cologne, Greinstrasse 6, Koln D-50939, Germany. sanjay.mathur@uni-koeln.de.&#xD;FB Material-und Geowissenschaften, Technische Universitat Darmstadt, Jovanka-Bontschits-Strasse 2, Darmstadt D-64287, Germany. ionescu@materials.tu-darmstadt.de.&#xD;Department of Materials Science and Engineering, Institute of Biomaterials, University of Erlangen-Nuremberg, Cauerstrasse 6, Erlangen D-91058, Germany. aldo.boccaccini@fau.de.&#xD;FB Material-und Geowissenschaften, Technische Universitat Darmstadt, Jovanka-Bontschits-Strasse 2, Darmstadt D-64287, Germany. riedel@materials.tu-darmstadt.de.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Synthesis and In Vitro Activity Assessment of Novel Silicon Oxycarbide-Based Bioactive Glasses</style></title><secondary-title><style face="normal" font="default" size="100%">Materials</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">959</style></pages><volume><style face="normal" font="default" size="100%">9</style></volume><number><style face="normal" font="default" size="100%">12</style></number><edition><style face="normal" font="default" size="100%">2017/08/05</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2016, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1996-1944</style></isbn><accession-num><style face="normal" font="default" size="100%">28774079</style></accession-num><abstract><style face="normal" font="default" size="100%">Novel bioactive glasses based on a Ca- and Mg-modified silicon oxycarbide (SiCaMgOC) were prepared from a polymeric single-source precursor, and their in vitro activity towards hydroxyapatite mineralization was investigated upon incubating the samples in simulated body fluid (SBF) at 37 degrees C. The as-prepared materials exhibit an outstanding resistance against devitrification processes and maintain their amorphous nature even after exposure to 1300 degrees C. The X-ray diffraction (XRD) analysis of the SiCaMgOC samples after the SBF test showed characteristic reflections of apatite after only three days, indicating a promising bioactivity. The release kinetics of the Ca(2+) and Mg(2+) and the adsorption of H(+) after immersion of SiCaMgOC in simulated body fluid for different soaking times were analyzed via optical emission spectroscopy. The results show that the mechanism of formation of apatite on the surface of the SiCaMgOC powders is similar to that observed for standard (silicate) bioactive glasses. A preliminary cytotoxicity investigation of the SiOC-based bioactive glasses was performed in the presence of mouse embryonic fibroblasts (MEF) as well as human embryonic kidney cells (HEK-293). Due to their excellent high-temperature crystallization resistance in addition to bioactivity, the Ca- and Mg-modified SiOC glasses presented here might have high potential in applications related to bone repair and regeneration.</style></abstract><label><style face="normal" font="default" size="100%">Gonzalo-Juan2016</style></label><notes><style face="normal" font="default" size="100%">Gonzalo-Juan, Isabel&#xD;Detsch, Rainer&#xD;Mathur, Sanjay&#xD;Ionescu, Emanuel&#xD;Boccaccini, Aldo R&#xD;Riedel, Ralf&#xD;eng&#xD;Switzerland&#xD;Materials (Basel). 2016 Nov 24;9(12). pii: ma9120959. doi: 10.3390/ma9120959.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.mdpi.com/1996-1944/9/12/959</style></url></related-urls></urls><custom2><style face="normal" font="default" size="100%">PMC5456995</style></custom2><electronic-resource-num><style face="normal" font="default" size="100%">10.3390/ma9120959</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>228</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">228</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fiz, Raquel</style></author><author><style face="normal" font="default" size="100%">Appel, Linus</style></author><author><style face="normal" font="default" size="100%">Gutiérrez-Pardo, Antonio</style></author><author><style face="normal" font="default" size="100%">Ramírez-Rico, Joaquín</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Institute of Inorganic Chemistry, University of Cologne , Greinstrasse 6, 50939, Cologne, Germany.&#xD;Departamento Fisica de la Materia Condensada-ICMS ( Universidad de Sevilla-CSIC ), Avda Reina Mercedes s/n, 41012 Seville, Spain.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Electrochemical Energy Storage Applications of CVD Grown Niobium Oxide Thin Films</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials \&amp; Interfaces</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">21423-21430</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">33</style></number><edition><style face="normal" font="default" size="100%">2016/07/16</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2016, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style face="normal" font="default" size="100%">Aug 24</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1944-8252 (Electronic)&#xD;1944-8244 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">27420568</style></accession-num><abstract><style face="normal" font="default" size="100%">We report here on the controlled synthesis, characterization, and electrochemical properties of different polymorphs of niobium pentoxide grown by CVD of new single-source precursors. Nb2O5 films deposited at different temperatures showed systematic phase evolution from low-temperature tetragonal (TT-Nb2O5, T-Nb2O5) to high temperature monoclinic modifications (H–Nb2O5). Optimization of the precursor flux and substrate temperature enabled phase-selective growth of Nb2O5 nanorods and films on conductive mesoporous biomorphic carbon matrices (BioC). Nb2O5 thin films deposited on monolithic BioC scaffolds produced composite materials integrating the high surface area and conductivity of the carbonaceous matrix with the intrinsically high capacitance of nanostructured niobium oxide. Heterojunctions in Nb2O5/BioC composites were found to be beneficial in electrochemical capacitance. Electrochemical characterization of Nb2O5/BioC composites showed that small amounts of Nb2O5 (as low as 5\%) in conjunction with BioCarbon resulted in a 7-fold increase in the electrode capacitance, from 15 to 104 F g–1, while imparting good cycling stability, making these materials ideally suited for electrochemical energy storage applications.</style></abstract><label><style face="normal" font="default" size="100%">doi:10.1021/acsami.6b03945</style></label><notes><style face="normal" font="default" size="100%">PMID: 27420568</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/acsami.6b03945</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acsami.6b03945</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>226</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">226</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Camurlu, H. Erdem</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Arslan, Osman</style></author><author><style face="normal" font="default" size="100%">Akarsu, Esin</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Akdeniz Univ, Dept Mech Engn, Dumlupinar Bulvari, TR-07058 Antalya, Turkey&#xD;Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany&#xD;Bilkent Univ UNAM, TR-06800 Ankara, Turkey&#xD;Akdeniz Univ, Fac Sci, Dept Chem, TR-07058 Antalya, Turkey</style></auth-address><titles><title><style face="normal" font="default" size="100%">Modification of hexagonal boron nitride nanoparticles with fluorosilane</style></title><secondary-title><style face="normal" font="default" size="100%">Ceramics International</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Ceram Int</style></alt-title></titles><pages><style face="normal" font="default" size="100%">6312-6318</style></pages><volume><style face="normal" font="default" size="100%">42</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">2016, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style face="normal" font="default" size="100%">Apr</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0272-8842</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000370884500085</style></accession-num><abstract><style face="normal" font="default" size="100%">Surfaces of hexagonal boron nitride (hBN) nanoparticles were modified with perfluorooctyl-triethoxysilane (FTS). Experiments were performed for 40–120min in 70–150°C range with FTS/hBN weight ratio in the range of 0.5–1.5. The products were analyzed by FT-IR, TGA, FESEM, HRTEM and EDX. Results of FT-IR analyses indicated that modification takes place in 80min at 150°C under reflux with a FTS/hBN ratio of 1.5. Presence of FTS on hBN nanoparticles was confirmed by the weight losses in TGA, and by TEM, TEM-EDX analyses.</style></abstract><label><style face="normal" font="default" size="100%">Camurlu2016a</style></label><notes><style face="normal" font="default" size="100%">De8ki&#xD;Times Cited:22&#xD;Cited References Count:23</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S027288421600047X</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.ceramint.2016.01.019</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>227</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">227</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Camurlu, H. Erdem</style></author><author><style face="normal" font="default" size="100%">Akarsu, Esin</style></author><author><style face="normal" font="default" size="100%">Arslan, Osman</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Akdeniz Univ, Dept Mech Engn, TR-07058 Antalya, Turkey&#xD;Akdeniz Univ, Dept Chem, Fac Sci, TR-07058 Antalya, Turkey&#xD;Bilkent Univ UNAM, TR-06800 Ankara, Turkey&#xD;Univ Cologne, Inst Inorgan Chem, Greinstr 6, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Nanocomposite glass coatings containing hexagonal boron nitride nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">Ceramics International</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Ceram Int</style></alt-title></titles><pages><style face="normal" font="default" size="100%">8856-8862</style></pages><volume><style face="normal" font="default" size="100%">42</style></volume><number><style face="normal" font="default" size="100%">7</style></number><keywords><keyword><style face="normal" font="default" size="100%">2016, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style face="normal" font="default" size="100%">May 15</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0272-8842</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000374075300131</style></accession-num><abstract><style face="normal" font="default" size="100%">Glass coatings composed of SiO2–K2O–Li2O, containing non-modified and fluorosilane modified hexagonal boron nitride (hBN) nanoparticles, were prepared on stainless steel plates through sol–gel spin-coating method. Coatings were examined by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, x-ray diffraction (XRD), atomic force microscopy (AFM) and thermo-gravimetric analysis (TGA). 1.3–2.5µm thick uniform coatings were obtained after curing at 500°C for 1h. The coatings adhered well to the steel substrates. It was determined by salt spray tests that the coatings enhance corrosion resistance. The aim of hydrophobic fluorosilane modification of hBN nanoparticles was to enrich hBN quantity on the top surface of the coatings. Coatings containing fluorosilane modified hBN nanoparticles presented slightly lower friction coefficient values than the other coatings.</style></abstract><label><style face="normal" font="default" size="100%">Camurlu2016</style></label><notes><style face="normal" font="default" size="100%">Dj2zx&#xD;Times Cited:7&#xD;Cited References Count:41</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0272884216300827</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.ceramint.2016.02.133</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>225</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">225</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Arslan, Osman</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Abalı, Yüksel</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanotechnology in Industry: ZnO Nanorods from Chemistry to Materialsitle</style></title><secondary-title><style face="normal" font="default" size="100%">INTERNATIONAL STRATEGIC RESEARCH CONGRESS</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2016, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year></dates><label><style face="normal" font="default" size="100%">Arslan2016a</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>224</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">224</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Arslan, Osman</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fabrication of the Ultrastable ZnO QD&apos;s for the Hybrid Nanomaterial Applications</style></title><secondary-title><style face="normal" font="default" size="100%">31.th Glass symposium</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2016, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year></dates><label><style face="normal" font="default" size="100%">Arslan2016</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>223</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">223</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Abbas, Yasmine</style></author><author><style face="normal" font="default" size="100%">Azzazy, Hassan M.E.</style></author><author><style face="normal" font="default" size="100%">Tammam, Salma</style></author><author><style face="normal" font="default" size="100%">Lamprecht, Alf</style></author><author><style face="normal" font="default" size="100%">Ali, Mohamed Ehab</style></author><author><style face="normal" font="default" size="100%">Schmidt, Annette</style></author><author><style face="normal" font="default" size="100%">Sollazzo, Silvio</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Department of Chemistry, School of Sciences &amp; Engineering, The American University in Cairo, Cairo, Egypt.&#xD;Department of Chemistry, School of Sciences &amp; Engineering, The American University in Cairo, Cairo, Egypt. Electronic address: hazzazy@aucegypt.edu.&#xD;Department of Chemistry, School of Sciences &amp; Engineering, The American University in Cairo, Cairo, Egypt; Laboratory of Pharmaceutical Technology and Biopharmaceutics, University of Bonn, Bonn, Germany.&#xD;Laboratory of Pharmaceutical Technology and Biopharmaceutics, University of Bonn, Bonn, Germany; Laboratory of Pharmaceutical Engineering, University of Franche-Comte, Besancon, France.&#xD;Laboratory of Pharmaceutical Technology and Biopharmaceutics, University of Bonn, Bonn, Germany; Department of Industrial Pharmacy, Faculty of Pharmacy, Assiut University, Assiut, Egypt.&#xD;Department of Chemistry, Institute of Physical Chemistry, University of Cologne, Cologne, Germany.&#xD;Department of Chemistry, Institute of Inorganic Chemistry, University of Cologne, Cologne, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Development of an Inhalable, Stimuli-Responsive Particulate System for Delivery to Deep Lung Tissue</style></title><secondary-title><style face="normal" font="default" size="100%">Colloids and Surfaces B: Biointerfaces</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">19-30</style></pages><volume><style face="normal" font="default" size="100%">146</style></volume><edition><style face="normal" font="default" size="100%">2016/06/01</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2016, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style face="normal" font="default" size="100%">Oct 1</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1873-4367 (Electronic)&#xD;0927-7765 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">27244047</style></accession-num><abstract><style face="normal" font="default" size="100%">Lung cancer, the deadliest solid tumor among all types of cancer, remains difficult to treat. This is a result of unavoidable exposure to carcinogens, poor diagnosis, the lack of targeted drug delivery platforms and limitations associated with delivery of drug to deep lung tissues. Development of a non-invasive, patient-convenient formula for the targeted delivery of chemotherapeutics to cancer in deep lung tissue is the aim of this study. The formulation consisted of inhalable polyvinylpyrrolidone (PVP)/maltodextrin (MD)-based microparticles (MPs) encapsulating chitosan (CS) nanoparticles (NPs) loaded with either drug only or drug and magnetic nanoparticles (MNPs). Drug release from CS NPs was enhanced with the aid of MNPs by a factor of 1.7 in response to external magnetic field. Preferential toxicity by CS NPs was shown towards tumor cells (A549) in comparison to cultured fibroblasts (L929). The prepared spray freeze dried (SFD) powders for CS NPs and CS MNPs were of the same size at ∼6$\mu$m. They had a fine particle fraction (FPF≤5.2$\mu$m) of 40–42\% w/w and mass median aerodynamic diameter (MMAD) of 5–6$\mu$m as determined by the Next Generation Impactor (NGI). SFD-MPs of CS MNPs possess higher MMAD due to the high density associated with encapsulated MNPs. The developed formulation demonstrates several capabilities including tissue targeting, controlled drug release, and the possible imaging and diagnostic values (due to its MNPs content) and therefore represents an improved therapeutic platform for drug delivery to cancer in deep lung tissue.</style></abstract><label><style face="normal" font="default" size="100%">Abbas2016</style></label><notes><style face="normal" font="default" size="100%">Abbas, Yasmine&#xD;Azzazy, Hassan M E&#xD;Tammam, Salma&#xD;Lamprecht, Alf&#xD;Ali, Mohamed Ehab&#xD;Schmidt, Annette&#xD;Sollazzo, Silvio&#xD;Mathur, Sanjay&#xD;eng&#xD;Netherlands&#xD;Colloids Surf B Biointerfaces. 2016 Oct 1;146:19-30. doi: 10.1016/j.colsurfb.2016.05.031. Epub 2016 May 12.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0927776516303563</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.colsurfb.2016.05.031</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>269</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">269</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zopes, David</style></author><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Schläfer, Johannes</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Institute of Inorganic Chemistry, University of Cologne, Greinstrasse 6, Cologne, 50939, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Single-Source Precursors for Alloyed Gold–Silver Nanocrystals - A Molecular Metallurgy Approach</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">3781-3787</style></pages><volume><style face="normal" font="default" size="100%">54</style></volume><number><style face="normal" font="default" size="100%">8</style></number><edition><style face="normal" font="default" size="100%">2015/04/10</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">April</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><accession-num><style face="normal" font="default" size="100%">25856772</style></accession-num><abstract><style face="normal" font="default" size="100%">Multiple silver(I)-aurates(I) have been prepared by salt metathesis reactions that act as efficient single-source precursors to colloidal gold silver alloys with the highest possible atom economy in the chemical synthesis of nanostructures. The CF3 group present on the Au cation acts as an in situ reducing agent and can be converted into CO ligands by simple hydrolysis. This ligand-mediated activation and subsequent decomposition of metal-organic precursors impose a molecular control over the nucleation process, producing homogeneously alloyed (Ag-Au) nanoparticles with an atomic Au:Ag ratio of 1:1. The concept also works for the Au-Cu system and acts as a pointer to replace Au (Ag) with less expensive (Cu) metals.</style></abstract><label><style face="normal" font="default" size="100%">zopes2015singlesource</style></label><notes><style face="normal" font="default" size="100%">Zopes, David&#xD;Hegemann, Corinna&#xD;Schlafer, Johannes&#xD;Tyrra, Wieland&#xD;Mathur, Sanjay&#xD;eng&#xD;Inorg Chem. 2015 Apr 20;54(8):3781-7. doi: 10.1021/ic502924s. Epub 2015 Apr 9.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/ic502924s</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/ic502924s</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>268</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">268</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Xiao, Lisong</style></author><author><style face="normal" font="default" size="100%">Mertens, Marianne</style></author><author><style face="normal" font="default" size="100%">Wortmann, Laura</style></author><author><style face="normal" font="default" size="100%">Kremer, Silke</style></author><author><style face="normal" font="default" size="100%">Valldor, Martin</style></author><author><style face="normal" font="default" size="100%">Lammers, Twan</style></author><author><style face="normal" font="default" size="100%">Kiessling, Fabian</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">daggerInstitute of Inorganic Chemistry, University of Cologne, D-50939 Cologne, Germany.&#xD;double daggerDepartment of Experimental Molecular Imaging, RWTH Aachen University Hospital, D-52074 Aachen, Germany.&#xD;section signMax-Planck-Institute for Chemical Physics and Solids, D-01187 Dresden, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Enhanced In Vitro and In Vivo Cellular Imaging with Green Tea Coated Water-Soluble Iron Oxide Nanocrystals</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></full-title></periodical><pages><style face="normal" font="default" size="100%">6530-6540</style></pages><volume><style face="normal" font="default" size="100%">7</style></volume><number><style face="normal" font="default" size="100%">12</style></number><edition><style face="normal" font="default" size="100%">2015/03/03</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">April</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><accession-num><style face="normal" font="default" size="100%">25729881</style></accession-num><abstract><style face="normal" font="default" size="100%">Fully green and facile redox chemistry involving reduction of colloidal iron hydroxide (Fe(OH)3) through green tea (GT) polyphenols produced water-soluble Fe3O4 nanocrystals coated with GT extracts namely epigallocatechin gallate (EGCG) and epicatechin (EC). Electron donating polyphenols stoichiometrically reduced Fe3+ ions into Fe2+ ions resulting in the formation of magnetite (Fe3O4) nanoparticles and corresponding oxidized products (semiquinones and quinones) that simultaneously served as efficient surface chelators for the Fe3O4 nanoparticles making them dispersible and stable in water, PBS and cell culture medium for extended time periods. As-formed iron oxide nanoparticles (2.5-6 nm) displayed high crystallinity and saturation magnetization as well as high relaxivity ratios manifested in strong contrast enhancement observed in T2-weighted images. Potential of green tea-coated super-paramagnetic iron oxide nanocrystals (SPIONs) as superior negative contrast agents was confirmed by in vitro and in vivo experiments. Primary human macrophages (J774A.1) and colon cancer cells (CT26) were chosen to assess cytotoxicity and cellular uptake of GT-, EGCGq- and ECq-coated Fe3O4 nanoparticles, which showed high uptake efficiencies by J774A.1 and CT26 cells without any additional transfection agent. Furthermore, the in vivo accumulation characteristics of GT-coated Fe3O4 nanoparticles were similar to those observed in clinical studies of SPIONs with comparable accumulation in epidermoid cancer-xenograft bearing mice. Given their promising transport and uptake characteristics and new surface chemistry, GT-SPIONs conjugates can be applied for multimodal imaging and therapeutic applications by anchoring further functionalities.</style></abstract><label><style face="normal" font="default" size="100%">xiao2015enhanced</style></label><notes><style face="normal" font="default" size="100%">Xiao, Lisong&#xD;Mertens, Marianne&#xD;Wortmann, Laura&#xD;Kremer, Silke&#xD;Valldor, Martin&#xD;Lammers, Twan&#xD;Kiessling, Fabian&#xD;Mathur, Sanjay&#xD;eng&#xD;Evaluation Study&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;ACS Appl Mater Interfaces. 2015 Apr 1;7(12):6530-40. doi: 10.1021/am508404t. Epub 2015 Mar 17.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/am508404t</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/am508404t</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>267</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">267</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Warwick, Michael E. A.</style></author><author><style face="normal" font="default" size="100%">Carraro, Giorgio</style></author><author><style face="normal" font="default" size="100%">Gasparotto, Alberto</style></author><author><style face="normal" font="default" size="100%">Maccato, Chiara</style></author><author><style face="normal" font="default" size="100%">Barreca, Davide</style></author><author><style face="normal" font="default" size="100%">Sada, Cinzia</style></author><author><style face="normal" font="default" size="100%">Bontempi, Elza</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Padua, Dept Chem, I-35131 Padua, Italy&#xD;INSTM, I-35131 Padua, Italy&#xD;Univ Padua, CNR, IENI, I-35131 Padua, Italy&#xD;Univ Padua, Dept Chem, INSTM, I-35131 Padua, Italy&#xD;Univ Padua, Dept Phys &amp; Astron, I-35131 Padua, Italy&#xD;Univ Brescia, Chem Technol Lab, I-25123 Brescia, Italy&#xD;INSTM, I-25123 Brescia, Italy&#xD;Univ Cologne, Dept Chem, Chair Inorgan &amp; Mat Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Interplay of thickness and photoelectrochemical properties in nanostructured alpha-Fe2O3 thin films</style></title><secondary-title><style face="normal" font="default" size="100%">physica status solidi (a)</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Phys Status Solidi A</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1501-1507</style></pages><volume><style face="normal" font="default" size="100%">212</style></volume><number><style face="normal" font="default" size="100%">7</style></number><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jul</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1862-6300</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000357679200015</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanostructured Fe2O3 thin films were grown by plasma enhanced-chemical vapor deposition (PE-CVD) from Ar/O-2 plasmas for photoelectrochemical (PEC) water splitting applications. Iron oxide coatings were deposited on fluorine-doped tin oxide (FTO) substrates at 300 degrees C under optimized conditions, and subsequently annealed ex situ in air at 650 degrees C. Structural and compositional analyses confirmed the formation of pure alpha-Fe2O3 (hematite), free from other crystalline iron oxide phases. Controlled variations of the deposition time enabled tuning of the thickness and nano-aggregate sizes in the resulting deposits and, correspondingly, their current-voltage characteristics. A maximum photocurrent density close to 1mAcm(-2) was achieved at 1.23V versus the reversible hydrogen electrode (RHE), without the need of any oxygen evolution catalyst or over/underlayer. The present findings revealed the key role played by the engineering of Fe2O3-based nanomaterials, resulting ultimately in a lowered carrier diffusion length, and in an optimal diffusion of tin from FTO into thinner layers. These features offer an amenable opportunity for harvesting radiant energy to trigger water photoelectrolysis and produce clean hydrogen in a carbonneutral fashion. (C) 2015 WILEY - VCH Verlag GmbH &amp; Co. KGaA, Weinheim</style></abstract><label><style face="normal" font="default" size="100%">Warwick2015a</style></label><notes><style face="normal" font="default" size="100%">Cm4ua&#xD;Times Cited:17&#xD;Cited References Count:42</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/pssa.201532366</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/pssa.201532366</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>266</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">266</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Warwick, M. E. A.</style></author><author><style face="normal" font="default" size="100%">Barreca, D.</style></author><author><style face="normal" font="default" size="100%">Bontempi, E.</style></author><author><style face="normal" font="default" size="100%">Carraro, G.</style></author><author><style face="normal" font="default" size="100%">Gasparotto, A.</style></author><author><style face="normal" font="default" size="100%">Maccato, C.</style></author><author><style face="normal" font="default" size="100%">Kaunisto, K.</style></author><author><style face="normal" font="default" size="100%">Ruoko, T.-P.</style></author><author><style face="normal" font="default" size="100%">Lemmetyinen, H.</style></author><author><style face="normal" font="default" size="100%">Sada, C.</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Y.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Department of Chemistry, Padova University and INSTM, 35131 Padova, Italy. alberto.gasparotto@unipd.it.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Pt-functionalized Fe2O3 photoanodes for solar water splitting: the role of hematite nano-organization and the platinum redox state</style></title><secondary-title><style face="normal" font="default" size="100%">Physical Chemistry Chemical Physics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">12899-12907</style></pages><volume><style face="normal" font="default" size="100%">17</style></volume><number><style face="normal" font="default" size="100%">19</style></number><edition><style face="normal" font="default" size="100%">2015/04/25</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">May 21</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1463-9076</style></isbn><accession-num><style face="normal" font="default" size="100%">25909639</style></accession-num><abstract><style face="normal" font="default" size="100%">Pt/[small alpha]-Fe2O3 nanocomposites were synthesized on fluorine-doped tin oxide (FTO) substrates by a sequential plasma enhanced-chemical vapor deposition (PE-CVD)/radio frequency (RF) sputtering approach, tailoring the overall Pt content as a function of sputtering time. The chemico-physical properties of the as-prepared systems were extensively investigated by means of complementary techniques, including X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field emission-scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDXS), secondary ion mass spectrometry (SIMS), and optical absorption spectroscopy, and compared to those of the homologous Pt/[small alpha]-Fe2O3 systems annealed in air prior and/or after sputtering. The obtained results evidenced that the material compositional, structural and morphological features, with particular regard to the Pt oxidation state and hematite nano-organization, could be finely tailored as a function of the adopted processing conditions. Pt/[small alpha]-Fe2O3 systems were finally tested as photoanodes in photoelectrochemical (PEC) water splitting experiments, evidencing a remarkable interplay between functional performances and the above-mentioned material properties, as also testified by transient absorption spectroscopy (TAS) results.</style></abstract><label><style face="normal" font="default" size="100%">Warwick2015</style></label><notes><style face="normal" font="default" size="100%">Warwick, M E A&#xD;Barreca, D&#xD;Bontempi, E&#xD;Carraro, G&#xD;Gasparotto, A&#xD;Maccato, C&#xD;Kaunisto, K&#xD;Ruoko, T-P&#xD;Lemmetyinen, H&#xD;Sada, C&#xD;Gonullu, Y&#xD;Mathur, S&#xD;eng&#xD;England&#xD;Phys Chem Chem Phys. 2015 May 21;17(19):12899-907. doi: 10.1039/c5cp01636c.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C5CP01636C</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c5cp01636c</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>265</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">265</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wang, Meng</style></author><author><style face="normal" font="default" size="100%">Pyeon, Myeongwhun</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Kaouk, Ali</style></author><author><style face="normal" font="default" size="100%">Shen, Shaohua</style></author><author><style face="normal" font="default" size="100%">Guo, Liejin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">International Research Center for Renewable Energy, State Key Laboratory of Multiphase Flow in Power Engineering, Xi&apos;an Jiaotong University, Shaanxi 710049, China. shshen_xjtu@mail.xjtu.edu.cn lj-guo@mail.xjtu.edu.cn.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Constructing Fe2O3/TiO2 core–shell photoelectrodes for efficient photoelectrochemical water splitting</style></title><secondary-title><style face="normal" font="default" size="100%">Nanoscale</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nanoscale</style></full-title></periodical><pages><style face="normal" font="default" size="100%">10094-10100</style></pages><volume><style face="normal" font="default" size="100%">7</style></volume><number><style face="normal" font="default" size="100%">22</style></number><edition><style face="normal" font="default" size="100%">2015/05/20</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun 14</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2040-3372 (Electronic)&#xD;2040-3364 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">25980730</style></accession-num><abstract><style face="normal" font="default" size="100%">In this study, plasma enhanced chemical vapor deposition (PECVD) was utilized to co-axially modify hydrothermally grown Fe2O3 nanorod arrays by depositing a TiO2 overlayer to create Fe2O3/TiO2 core-shell photoelectrodes. Comprehensive structural (XRD, SEM, TEM) and compositional (XPS) analyses were performed to understand the effects of the TiO2 shell on the PEC activities of the Fe2O3 core. It was revealed that the heterojunction structure formed between TiO2 and Fe2O3, significantly improved the separation efficiency of photo-induced charge carriers and the oxygen evolution kinetics. A maximum photocurrent density of ∼900 $\mu$A cm(-2) at 0.6 V vs. saturated calomel electrode (SCE) was obtained for the Fe2O3/TiO2 photoelectrodes, which was 5 and 18 times higher when compared to that of hydrothermally synthesized Fe2O3 and PECVD synthesized TiO2 electrodes, respectively. Moreover, the Fe2O3/TiO2 core-shell nanorod arrays displayed superior stability for PEC water splitting. During 5000 s PEC measurements, a steady decrease of the photocurrent was observed, mainly attributed to the evolution of oxygen bubbles adsorbed on the working electrodes. This observation was verified by the complete recovery of the PEC performance demonstrated for a second 5000 s PEC measurement carried out after a brief time interval (10 min) that allowed the electrode surface to regenerate.</style></abstract><label><style face="normal" font="default" size="100%">Wang2015</style></label><notes><style face="normal" font="default" size="100%">Wang, Meng&#xD;Pyeon, Myeongwhun&#xD;Gonullu, Yakup&#xD;Kaouk, Ali&#xD;Shen, Shaohua&#xD;Guo, Liejin&#xD;Mathur, Sanjay&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;England&#xD;Nanoscale. 2015 Jun 14;7(22):10094-100. doi: 10.1039/c5nr01493j. Epub 2015 May 18.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C5NR01493J</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c5nr01493j</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>264</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">264</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Stein, Benjamin</style></author><author><style face="normal" font="default" size="100%">Zopes, David</style></author><author><style face="normal" font="default" size="100%">Schmudde, Madlen</style></author><author><style face="normal" font="default" size="100%">Schneider, Ralf</style></author><author><style face="normal" font="default" size="100%">Mohsen, Ahmed</style></author><author><style face="normal" font="default" size="100%">Goroncy, Christian</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Graf, Christina</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Institut fur Chemie u. Biochemie, Freie Universitat Berlin, Takustrasse 3, 14195 Berlin, Germany. cmgraf@zedat.fu-berlin.de.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Kinetics of aggregation and growth processes of PEG-stabilised mono- and multivalent gold nanoparticles in highly concentrated halide solutions</style></title><secondary-title><style face="normal" font="default" size="100%">Faraday Discussions</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">85-102</style></pages><volume><style face="normal" font="default" size="100%">181</style></volume><edition><style face="normal" font="default" size="100%">2015/05/15</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year></dates><isbn><style face="normal" font="default" size="100%">1359-6640 (Print)&#xD;1359-6640 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">25972038</style></accession-num><abstract><style face="normal" font="default" size="100%">5-6 nm gold nanoparticles were prepared by hydrolytic decomposition of NMe4Au(CF3)2 and functionalized in situ with mono- and multivalent thiolated PEG ligands. Time-dependent changes of the nanoparticles were monitored in aqueous NaCl, NaBr, and NaI solutions by UV-Vis spectroscopy, TEM, and HRTEM. The purely sterically protected particles are stable in less-than-or-equal1 M NaCl and NaBr solutions, regardless of the valence of the ligands. At higher concentrations (greater-than-or-equal2 M), the monovalent stabilized particles show minor reaction limited colloidal aggregation. In NaBr but not in NaCl solutions a minor Ostwald ripening also occurs. The divalent stabilized particles remain colloidally stable in both halide solutions, even if the temperature is raised or the concentration is increased above 2 M. In less-than-or-equal1 M aqueous NaI solutions the particles remain stable. Above, the monovalent stabilized particles undergo an oxidative reaction, resulting in a time-dependent shift and broadening of the absorbance spectrum. Finally, this process slows down while the width of the spectra slightly narrows. The kinetics of this process can be described by a two-step sigmoidal process, comprising a slow induction period where active species are formed, followed by a fast growth and aggregation process. The increasing concentration of fused structures from the aggregates during this process results in a narrowing of the size distributions. The divalent stabilized particles show only some minor broadening and a slight shift of the absorbance spectra in less-than-or-equal3 M NaI solutions. These observations confirm the excellent stability of the multivalent stabilized particles from this chloride-free particle synthesis.</style></abstract><label><style face="normal" font="default" size="100%">stein2015kinetics</style></label><notes><style face="normal" font="default" size="100%">Stein, Benjamin&#xD;Zopes, David&#xD;Schmudde, Madlen&#xD;Schneider, Ralf&#xD;Mohsen, Ahmed&#xD;Goroncy, Christian&#xD;Mathur, Sanjay&#xD;Graf, Christina&#xD;eng&#xD;England&#xD;Faraday Discuss. 2015;181:85-102. doi: 10.1039/c5fd00024f. Epub 2015 May 14.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C5FD00024F</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c5fd00024f</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>262</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">262</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Singh, Trilok</style></author><author><style face="normal" font="default" size="100%">Müller, Ralf</style></author><author><style face="normal" font="default" size="100%">Singh, Jai</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Sejong Univ, Dept Nano Sci &amp; Technol, Inst Adv Mat Engn, Seoul 143747, South Korea</style></auth-address><titles><title><style face="normal" font="default" size="100%">Tailoring surface states in WO3 photoanodes for efficient photoelectrochemical water splitting</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Surface Science</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Appl Surf Sci</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Applied Surface Science</style></full-title></periodical><pages><style face="normal" font="default" size="100%">448-453</style></pages><volume><style face="normal" font="default" size="100%">347</style></volume><keywords><keyword><style face="normal" font="default" size="100%">Hydrogenation,Surface, modification,WO3,Water, splitting</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">August</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">01694332</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000356058500059</style></accession-num><abstract><style face="normal" font="default" size="100%">The dynamics of photo-induced charge carriers are significantly influenced by the surface states of WO3 thin films, which were synthesized by reactive sputtering of tungsten substrates in oxygen plasma. Tailoring the surface properties by (i) hydrogen plasma treatment and (ii) anchoring plasmonic nanoparticles (Au and Ag) altered the light harvesting and charge separation/transport processes of WO3 photoanodes. Upon hydrogen plasma-treatment and coating of noble metal clusters, WO3 films showed enhanced visible light absorption and consequently higher photocurrent density (1.4mAcm−2) compared to pristine WO3 (0.2mAcm−2). Enhancement in hydrogen treated WO3 sample was found to be due to the reduction of W(VI) into W(V) centers, which produced substoichiometric WO3−x phases, whereas noble metal particles contributed towards both resonant and non-resonant scattering of incident light thereby increasing photon-to-current conversion efficiency.</style></abstract><label><style face="normal" font="default" size="100%">Singh2015a</style></label><notes><style face="normal" font="default" size="100%">Ck2re&#xD;Times Cited:42&#xD;Cited References Count:45</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.apsusc.2015.04.126</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.apsusc.2015.04.126</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>261</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">261</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Singh, Trilok</style></author><author><style face="normal" font="default" size="100%">Lehnen, Thomas</style></author><author><style face="normal" font="default" size="100%">Leuning, Tessa</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Xi An Jiao Tong Univ, Sch Energy &amp; Power Engn, Int Res Ctr Renewable Energy, Xian 710049, Shaanxi, Peoples R China</style></auth-address><titles><title><style face="normal" font="default" size="100%">Atomic layer deposition grown MOx thin films for solar water splitting: Prospects and challenges</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Vacuum Science &amp; Technology A: Vacuum, Surfaces, and Films</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Vac Sci Technol A</style></alt-title></titles><pages><style face="normal" font="default" size="100%">10801</style></pages><volume><style face="normal" font="default" size="100%">33</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0734-2101</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000355735400056</style></accession-num><abstract><style face="normal" font="default" size="100%">The magnitude of energy challenge not only calls for efficient devices but also for abundant, inexpensive, and stable photoactive materials that can enable efficient light harvesting, charge sepn. and collection, as well as chem. transformations. Photoelectrochem. systems based on semiconductor materials have the possibility to transform solar energy directly into chem. energy the so-called &quot;solar hydrogen.&quot;. The current challenge lies in the harvesting of a larger fraction of electromagnetic spectrum by enhancing the absorbance of electrode materials. In this context, atomically precise thin films of metal oxide semiconductors and their multilayered junctions are promising candidates to integrate high surface areas with well-defined electrode-substrate interface. Given its self-limited growth mechanism, the at. layer deposition (ALD) technique offers a wide range of capabilities to deposit and modify materials at the nanoscale. In addn., it opens new frontiers for developing precursor chem. that is inevitable to design new processes. Herein, the authors review the properties and potential of metal oxide thin films deposited by ALD for their application in photoelectrochem. water splitting application. The first part of the review covers the basics of ALD processes followed by a brief discussion on the electrochem. of water splitting reaction. The second part focuses on different MOx films deposited by at. layer deposition for water splitting applications; in this section, The authors discuss the most explored MOx semiconductors, namely, Fe2O3, TiO2, WO3, and ZnO, as active materials and refer to their application as protective coatings, conductive scaffolds, or in heterojunctions. The third part deals with the current challenges and future prospects of ALD processed MOx thin films for water splitting reactions. (c) 2015 American Institute of Physics.</style></abstract><label><style face="normal" font="default" size="100%">singh2015atomic</style></label><notes><style face="normal" font="default" size="100%">Cj8fk&#xD;Times Cited:15&#xD;Cited References Count:56</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://scitation.aip.org/content/avs/journal/jvsta/33/1/10.1116/1.4904729</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Artn 010801&#xD;10.1116/1.4904729</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>260</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">260</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shen, Jianlei</style></author><author><style face="normal" font="default" size="100%">Su, Jing</style></author><author><style face="normal" font="default" size="100%">Yan, Juan</style></author><author><style face="normal" font="default" size="100%">Zhao, Bin</style></author><author><style face="normal" font="default" size="100%">Wang, Dongfang</style></author><author><style face="normal" font="default" size="100%">Wang, Siyi</style></author><author><style face="normal" font="default" size="100%">Li, Kun</style></author><author><style face="normal" font="default" size="100%">Liu, Mengmeng</style></author><author><style face="normal" font="default" size="100%">He, Yao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Fan, Chunhai</style></author><author><style face="normal" font="default" size="100%">Song, Shiping.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Div Phys Biol, Shanghai 201800, Peoples R China&#xD;Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Bioimaging Ctr, Shanghai 201800, Peoples R China&#xD;Soochow Univ, Inst Funct Nano &amp; Soft Mat FUNSOM, Suzhou 215123, Peoples R China&#xD;Soochow Univ, Jiangsu Key Lab Carbon Based Funct Mat &amp; Devices, Suzhou 215123, Peoples R China&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Bimetallic nano-mushrooms with DNA-mediated interior nanogaps for high-efficiency SERS signal amplification</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Research</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nano Res</style></alt-title></titles><pages><style face="normal" font="default" size="100%">731-742</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">Mar</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1998-0124</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000352448800003</style></accession-num><abstract><style face="normal" font="default" size="100%">Uniform silver-contg. metal nanostructures with well-defined nanogaps hold great promise for ultrasensitive surface-enhanced Raman scattering (SERS) analyses. Nevertheless, the direct synthesis of such nanostructures with strong and stable SERS signals remains extremely challenging. Here, we report a DNA-mediated approach for the direct synthesis of gold-silver nano-mushrooms with interior nanogaps. The SERS intensities of these nano-mushrooms were critically dependent on the area of the nanogap between the gold head and the silver cap. We found that the formation of nanogaps was finely tunable by controlling the surface d. of 6-carboxy-X-rhodamine (ROX) labeled single-stranded DNA (ssDNA) on the gold nanoparticles. We obtained nano-mushrooms in high yield with a high SERS signal enhancement factor of ∼1.0 × 109, much higher than that for Au-Ag nanostructures without nanogaps. Measurements for single nanomushrooms show that these structures have both sensitive and reproducible SERS signals. Figure not available: see fulltext.. on SciFinder(R)</style></abstract><label><style face="normal" font="default" size="100%">Shen2014</style></label><notes><style face="normal" font="default" size="100%">Cf3la&#xD;Times Cited:47&#xD;Cited References Count:50</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1007/s12274-014-0556-2</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1007/s12274-014-0556-2</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>259</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">259</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sasinska, Alexander</style></author><author><style face="normal" font="default" size="100%">Singh, Trilok</style></author><author><style face="normal" font="default" size="100%">Wang, Shuangzhou</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kraehnert, Ralph</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Tech Univ Berlin, Dept Chem, D-10623 Berlin, Germany&#xD;Xi An Jiao Tong Univ, Sch Energy &amp; Power Engn, Int Res Ctr Renewable Energy, Xian 710049, Shaanxi, Peoples R China</style></auth-address><titles><title><style face="normal" font="default" size="100%">Enhanced photocatalytic performance in atomic layer deposition grown TiO2 thin films via hydrogen plasma treatment</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Vacuum Science &amp; Technology A: Vacuum, Surfaces, and Films</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Vac Sci Technol A</style></alt-title></titles><pages><style face="normal" font="default" size="100%">01A152</style></pages><volume><style face="normal" font="default" size="100%">33</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0734-2101</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000355735400052</style></accession-num><abstract><style face="normal" font="default" size="100%">The authors report the effect of hydrogen plasma treatment on TiO2 thin films grown by at. layer deposition as an effective approach for modifying the photoanode materials in order to enhance their photoelectrochem. performance. Hydrogen plasma treated TiO2 thin films showed an improved absorption in the visible spectrum probably due to surface redn. XPS anal. confirmed the formation of Ti3+ states upon plasma treatment. Hydrogen plasma treatment of TiO2 films enhanced the measured photocurrent densities by a factor of 8 (1 mA/cm2 at 0.8 V vs. normal hydrogen electrode) when compared to untreated TiO2 (0.12 mA/cm2). The enhancement in photocurrent is attributed to the formation of localized electronic states in mid band-gap region, which facilitate efficient sepn. and transportation of photo excited charge carriers in the UV region of electromagnetic spectrum. (c) 2015 American Institute of Physics. [on SciFinder(R)]</style></abstract><label><style face="normal" font="default" size="100%">Sasinska2015</style></label><notes><style face="normal" font="default" size="100%">Cj8fk&#xD;Times Cited:18&#xD;Cited References Count:31</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://scitation.aip.org/content/avs/journal/jvsta/33/1/10.1116/1.4904503</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Artn 01a152&#xD;10.1116/1.4904503</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>258</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">258</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ohji, Tatsuki</style></author><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Gyekenyesi, Andrew L.</style></author><author><style face="normal" font="default" size="100%">Halbig, Michael</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Advanced Processing and Manufacturing Technologies for Nanostructured and Multifunctional Materials: Ceramic Engineering and Science Proceedings, Volume 35, Issue 6</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year></dates><publisher><style face="normal" font="default" size="100%">Wiley</style></publisher><isbn><style face="normal" font="default" size="100%">978-1-119-04026-2</style></isbn><label><style face="normal" font="default" size="100%">Ohji2015</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://eu.wiley.com/WileyCDA/WileyTitle/productCd-1119040264.html</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>257</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">257</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Miguel, F.L.</style></author><author><style face="normal" font="default" size="100%">Müller, R.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Mücklich, F.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Chair Funct Mat, D-66123 Saarbrucken, Germany&#xD;Univ Cologne, Chair Inorgan &amp; Mat Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Microstructure and mechanical properties of electrodeposited Ni and Ni–matrix-nanocomposite thin films</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Science and Engineering: A</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Mat Sci Eng a-Struct</style></alt-title></titles><pages><style face="normal" font="default" size="100%">254-262</style></pages><volume><style face="normal" font="default" size="100%">646</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">October</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09215093</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000362132000028</style></accession-num><abstract><style face="normal" font="default" size="100%">Ni and Ni-matrix-nanocomposite thin films were produced by constant-current electrodeposition from a sulphamate bath. The composite consisted of an array of Ag-coated SnO2 nanowires grown onto a substrate, around which the Ni matrix was deposited. The hardness and Young&apos;s modulus of the films were studied by microindentation, showing a strengthening of 66\% for the composite with respect to Ni films produced using the exact same bath and deposition parameters as the composite&apos;s matrix. A straightforward method for evaluating the stress–strain relationship from indentation data based on analytical and computational models available in the literature was proposed and evaluated. A thorough microstructure characterisation by scanning electron microscopy together with electron backscatter diffraction was conducted to assist in the interpretation of the mechanical response of the films. The Ag–SnO2 in the composite prevented the development of texture and was responsible for a grain size reduction of 85\%.</style></abstract><label><style face="normal" font="default" size="100%">miguel2015microstructure</style></label><notes><style face="normal" font="default" size="100%">Cs5qc&#xD;Times Cited:7&#xD;Cited References Count:59</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S092150931530321X</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.msea.2015.08.069</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>256</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">256</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Pyeon, Myeongwhun</style></author><author><style face="normal" font="default" size="100%">Wang, Meng</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Ohji, Tatsuki</style></author><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Perspectives of Nanostructured Metal Oxides and Their Heterostructures in Photoelectrochemical Water Splitting for Solar Hydrogen Production</style></title><secondary-title><style face="normal" font="default" size="100%">Engineered Ceramics: Current Status and Future Prospects</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">457-495</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year></dates><pub-location><style face="normal" font="default" size="100%">Hoboken, NJ, USA</style></pub-location><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Inc.</style></publisher><label><style face="normal" font="default" size="100%">Mathur2015</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/9781119100430.ch23</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>255</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">255</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mazharul, M. Islam</style></author><author><style face="normal" font="default" size="100%">Moazzem, Hossain</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Cultural and Materials Interfaces as Sustainable Solutions to Global Needs</style></title><secondary-title><style face="normal" font="default" size="100%">Sustainable Development: South Asian Conundrum</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">152</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year></dates><publisher><style face="normal" font="default" size="100%">IIDS Australia,IIMS Indiaand BEN Germany</style></publisher><isbn><style face="normal" font="default" size="100%">978 984 33 8819 3</style></isbn><label><style face="normal" font="default" size="100%">Mathur2015</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>254</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">254</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lepcha, A.</style></author><author><style face="normal" font="default" size="100%">Maccato, C.</style></author><author><style face="normal" font="default" size="100%">Mettenbörger, A.</style></author><author><style face="normal" font="default" size="100%">Andreu, T.</style></author><author><style face="normal" font="default" size="100%">Mayrhofer, L.</style></author><author><style face="normal" font="default" size="100%">Walter, M.</style></author><author><style face="normal" font="default" size="100%">Olthof, S.</style></author><author><style face="normal" font="default" size="100%">Ruoko, T.-P.</style></author><author><style face="normal" font="default" size="100%">Klein, A.</style></author><author><style face="normal" font="default" size="100%">Moseler, M.</style></author><author><style face="normal" font="default" size="100%">Meerholz, K.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author><author><style face="normal" font="default" size="100%">Barreca, D.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50859 Cologne, Germany&#xD;Univ Padua, Dept Chem, I-35131 Padua, Italy&#xD;INSTM, I-35131 Padua, Italy&#xD;Catalonia Inst Energy Res IREC, Barcelona, Spain&#xD;Fraunhofer IWM, Multiscale Mat Modelling &amp; Tribo Simulat, D-79108 Freiburg, Germany&#xD;Univ Cologne, Inst Phys Chem, D-50939 Cologne, Germany&#xD;Univ Padua, Dept Chem, CNR IENI, I-35151 Padua, Italy&#xD;Univ Padua, Dept Chem, INSTM, I-35151 Padua, Italy&#xD;Tampere Univ Technol, Dept Chem &amp; Bioengn, FI-33101 Tampere, Finland</style></auth-address><titles><title><style face="normal" font="default" size="100%">Electrospun Black Titania Nanofibers: Influence of Hydrogen Plasma-Induced Disorder on the Electronic Structure and Photoelectrochemical Performance</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry C</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Phys Chem C</style></alt-title></titles><pages><style face="normal" font="default" size="100%">18835-18842</style></pages><volume><style face="normal" font="default" size="100%">119</style></volume><number><style face="normal" font="default" size="100%">33</style></number><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">Aug 20</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000360026200002</style></accession-num><abstract><style face="normal" font="default" size="100%">This work encompasses a facile method for tailoring surface defects in electrospun TiO2 nanofibers by employing hydrogen plasma treatments. This amiable processing method was proven with SQUID, EPR, and XPS to be highly effective in generating oxygen vacancies, accompanied by the reduction of Ti4+ centers to Ti3+, resulting in the formation of black titania. The treatment temperature was found to affect the Ti3+/Ti4+ ratios and surface valence, while preserving the original 1D morphology of the titania fibers. Ab initio DFT calculations showed that a high concentration of oxygen vacancies is highly efficient in producing midgap states that enhance the system absorption over the whole visible range, as observed with UV/vis/NIR diffuse reflectance spectroscopy. Pristine TiO2 nanofibers produced a photocurrent density of ?0.02 mA/cm2 at 1.23 V vs RHE, whereas the hydrogen plasma treatment resulted in up to a 10-fold increase in the photoelectrochemical performance.</style></abstract><label><style face="normal" font="default" size="100%">lepcha2015electrospun</style></label><notes><style face="normal" font="default" size="100%">Cp6vl&#xD;Times Cited:44&#xD;Cited References Count:40</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/acs.jpcc.5b02767</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.jpcc.5b02767</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>253</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">253</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Leduc, Jennifer</style></author><author><style face="normal" font="default" size="100%">Ravithas, Rajitha</style></author><author><style face="normal" font="default" size="100%">Rathgeber, Lisa</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Chair Mat &amp; Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">New air-stable uranium(iv) complexes with enhanced volatility</style></title><secondary-title><style face="normal" font="default" size="100%">New Journal of Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">New J Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">7571-7574</style></pages><volume><style face="normal" font="default" size="100%">39</style></volume><number><style face="normal" font="default" size="100%">10</style></number><keywords><keyword><style face="normal" font="default" size="100%">2015, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year></dates><isbn><style face="normal" font="default" size="100%">1144-0546</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000362355200008</style></accession-num><abstract><style face="normal" font="default" size="100%">Herein we report the synthesis and characterization of new air-stable uranium(iv) complexes based on three different heteroarylalkenolate ligands namely DMOPFB (1) (1-(4,5-dimethyl-oxazol-2-yl)-3,3,4,4,4-pentafluoro-but-1-en-2-ol) with an elongated fluorinated alkyl chain compared to DMOTFP (2) (3,3,3-trifluoro-1-(4,5-dimethyloxazol-2-yl) propen-2-ol) and the tetradentate enaminone TFB-en (3) (N,N[prime or minute]-bis-(4,4,4-trifluorobut-1-en-3-on)-ethylenediamine). These new complexes exhibit sufficiently high volatilities, with respect to previously reported uranium compounds, and are thus promising precursors for chemical vapor deposition (CVD) of uranium oxide materials.</style></abstract><label><style face="normal" font="default" size="100%">Leduc2015</style></label><notes><style face="normal" font="default" size="100%">Cs8re&#xD;Times Cited:5&#xD;Cited References Count:29</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C5NJ00647C</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c5nj00647c</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>252</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">252</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kaouk, A.</style></author><author><style face="normal" font="default" size="100%">Ruoko, T.-P.</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Y.</style></author><author><style face="normal" font="default" size="100%">Kaunisto, K.</style></author><author><style face="normal" font="default" size="100%">Mettenbörger, A.</style></author><author><style face="normal" font="default" size="100%">Gurevich, E.</style></author><author><style face="normal" font="default" size="100%">Lemmetyinen, H.</style></author><author><style face="normal" font="default" size="100%">Ostendorf, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Tampere Univ Technol, Dept Chem &amp; Bioengn, Tampere 33710, Finland&#xD;Ruhr Univ Bochum, Lehrstuhl Laseranwendungstech, D-44801 Bochum, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Graphene-intercalated Fe2O3/TiO2 heterojunctions for efficient photoelectrolysis of water</style></title><secondary-title><style face="normal" font="default" size="100%">RSC Advances</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Rsc Adv</style></alt-title></titles><pages><style face="normal" font="default" size="100%">101401-101407</style></pages><volume><style face="normal" font="default" size="100%">5</style></volume><number><style face="normal" font="default" size="100%">123</style></number><keywords><keyword><style face="normal" font="default" size="100%">2015, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year></dates><accession-num><style face="normal" font="default" size="100%">WOS:000365952200020</style></accession-num><abstract><style face="normal" font="default" size="100%">Interfacial modification of small alpha-Fe2O3/TiO2 multilayer photoanodes by intercalating few-layer graphene (FLG) was found to improve water splitting efficiency due to superior transport properties, when compared to individual iron and titanium oxides and heterojunctions thereof. Both metal oxides and graphene sheets were grown by plasma-enhanced chemical vapor deposition. Compared to the onset potential achieved for small alpha-Fe2O3 films (1 V vs. RHE), the small alpha-Fe2O3/TiO2 bilayer structure yielded a better onset potential (0.3 V vs. RHE). Heterojunctioned bilayers exhibited a higher photocurrent density (0.32 mA cm-2 at 1.23 V vs. RHE) than the single small alpha-Fe2O3 layer (0.22 mA cm-2 at 1.23 V vs. RHE), indicating more efficient light harvesting and higher concentration of photogenerated charge carriers. For more efficient charge transport at the interface, a few layer graphene sheet was intercalated into the small alpha-Fe2O3/TiO2 interface, which substantially increased the photocurrent density to 0.85 mA cm-2 (1.23 V vs. RHE) and shifted the onset potential (0.25 V vs. RHE). Ultrafast transient absorption spectroscopy studies indicated that the incorporation of FLG between the small alpha-Fe2O3 and TiO2 layers resulted in reduced recombination in the small alpha-Fe2O3 layer. The results showed that graphene intercalation improved the charge separation and the photocurrent density of the FTO/small alpha-Fe2O3/FLG/TiO2 system.</style></abstract><label><style face="normal" font="default" size="100%">Kaouk2015</style></label><notes><style face="normal" font="default" size="100%">Cx8km&#xD;Times Cited:8&#xD;Cited References Count:34</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C5RA18330H</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c5ra18330h</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>251</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">251</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hemmer, Eva</style></author><author><style face="normal" font="default" size="100%">Cavelius, Christian</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">daggerInstitut National de la Recherche Scientifique-Energie Materiaux Telecommunications, Universite du Quebec, 1650 Boulevard Lionel-Boulet, Varennes, Quebec J3X 1S2, Canada.&#xD;double daggerLeibniz Institute of New Materials, Im Stadtwald, Building D2 2, 66123 Saarbruecken, Germany.&#xD;section signInstitute of Inorganic Chemistry, Saarland University, P.O. Box 151150, 66041 Saarbruecken, Germany.&#xD;parallelInstitute of Inorganic Chemistry, University of Cologne, Greinstrasse 6, 50939 Cologne, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Templating Influence of Molecular Precursors on Pr(OH)3 Nanostructures</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">6267-6280</style></pages><volume><style face="normal" font="default" size="100%">54</style></volume><number><style face="normal" font="default" size="100%">13</style></number><edition><style face="normal" font="default" size="100%">2015/06/13</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">July</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><accession-num><style face="normal" font="default" size="100%">26068779</style></accession-num><abstract><style face="normal" font="default" size="100%">Four new praseodymium alkoxo and amido compounds ([Pr3(mu3-OtBu)2(mu2-OtBu)3(OtBu)4(HOtBu)2] (1), [Pr{OC(tBu)3}3(THF)] (2), [PrCl{N(SiMe3)2}2(THF)]2 (3), and [PrCl{OC(tBu)3}2(THF)]2 (4)) were synthesized and structurally characterized by single-crystal X-ray diffraction analysis. Application of these compounds in solvothermal synthesis of praseodymium oxide/hydroxide nanostructures showed their templating influence on the morphology and phase composition of the resulting solid-state materials. Differential reactivity of the chosen alkoxide ligands toward water and the different arrangements of metal-oxygen units in the studied precursor compounds strongly influenced the kinetics of hydrolysis and cross-condensation reactions as manifested in the morphological changes and phase composition of the final products. Thermal decomposition studies of 1-4 confirmed their conversion into the corresponding oxide phases. Activation of compounds 1, 2, and 4 by either a base or a stoichiometric amount of water showed the distinct influence of their chemical configuration on the obtained nanopowders: whereas 1 solely produced nanorods of Pr(OH)3, 2 predominantly formed a mixture of rod-shaped and spherical particles. The solvothermal decomposition of 4 resulted in Pr(OH)2Cl or PrOCl due to the presence of Cl ligands in the molecular precursor. The resultant materials were thoroughly characterized to demonstrate the relationship between precursor chemistry and the processing parameters that are clearly manifested in the morphology and phase of the final ceramics.</style></abstract><label><style face="normal" font="default" size="100%">hemmer2015templating</style></label><notes><style face="normal" font="default" size="100%">Hemmer, Eva&#xD;Cavelius, Christian&#xD;Huch, Volker&#xD;Mathur, Sanjay&#xD;eng&#xD;Inorg Chem. 2015 Jul 6;54(13):6267-80. doi: 10.1021/acs.inorgchem.5b00529. Epub 2015 Jun 12.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.5b00529</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/acs.inorgchem.5b00529</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>250</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">250</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Guilera, Jordi</style></author><author><style face="normal" font="default" size="100%">Fàbrega, Cristian</style></author><author><style face="normal" font="default" size="100%">Casals, Olga</style></author><author><style face="normal" font="default" size="100%">Hernández-Ramírez, Francisco</style></author><author><style face="normal" font="default" size="100%">Wang, Shuangzhou</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Udrea, Florian</style></author><author><style face="normal" font="default" size="100%">De Luca, Andrea</style></author><author><style face="normal" font="default" size="100%">Ali, S. Zeeshan</style></author><author><style face="normal" font="default" size="100%">Romano-Rodríguez, Albert</style></author><author><style face="normal" font="default" size="100%">Prades, J. Daniel</style></author><author><style face="normal" font="default" size="100%">Morante, Joan R.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Catalonia Inst Energy Res, San Adria De Besos, Spain&#xD;Univ Barcelona, Dept Elect, Barcelona, Spain&#xD;Univ Barcelona, Inst Nanosci &amp; Nanotechnol IN2UB, Barcelona, Spain&#xD;Univ Cologne, Inst Inorgan Chem, Cologne, Germany&#xD;Univ Cambridge, Dept Engn, Cambridge CB2 1PZ, England&#xD;Cambridge CMOS Sensors Ltd, Cambridge, England</style></auth-address><titles><title><style face="normal" font="default" size="100%">Facile integration of ordered nanowires in functional devices</style></title><secondary-title><style face="normal" font="default" size="100%">Sensors and Actuators B: Chemical</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Sensor Actuat B-Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">104-112</style></pages><volume><style face="normal" font="default" size="100%">221</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">December</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09254005</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000362918100014</style></accession-num><abstract><style face="normal" font="default" size="100%">The integration of one-dimensional (1D) nanostructures of non-industry-standard semiconductors in functional devices following bottom-up approaches is still an open challenge that hampers the exploitation of all their potential. Here, we present a simple approach to integrate metal oxide nanowires in electronic devices based on controlled dielectrophoretic positioning together with proof of concept devices that corroborate their functionality. The method is flexible enough to manipulate nanowires of different sizes and compositions exclusively using macroscopic solution-based techniques in conventional electrode designs. Our results show that fully functional devices, which display all the advantages of single-nanowire gas sensors, photodetectors, and even field-effect transistors, are thus obtained right after a direct assembly step without subsequent metallization processing. This paves the way to low cost, high throughput manufacturing of general-purpose electronic devices based on non-conventional and high quality 1D nanostructures driving up many options for high performance and new low energy consumption devices.</style></abstract><label><style face="normal" font="default" size="100%">guilera2015facile</style></label><notes><style face="normal" font="default" size="100%">Ct6ja&#xD;Times Cited:20&#xD;Cited References Count:48</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0925400515008448</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.snb.2015.06.069</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>249</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">249</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Czympiel, Lisa</style></author><author><style face="normal" font="default" size="100%">Pfrommer, Johannes</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Schäfer, Mathias</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Department of Chemistry, Institute of Inorganic Chemistry and double daggerDepartment of Chemistry, Institute of Organic Chemistry, University of Cologne , 50939 Cologne, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Ligand-Modulated Chemical and Structural Implications in Four-, Five-, and Six-fold Coordinated Aluminum Heteroaryl Alkenolates</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">25-37</style></pages><volume><style face="normal" font="default" size="100%">54</style></volume><number><style face="normal" font="default" size="100%">1</style></number><edition><style face="normal" font="default" size="100%">2014/12/20</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">January</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><accession-num><style face="normal" font="default" size="100%">25525667</style></accession-num><abstract><style face="normal" font="default" size="100%">Synthesis and characterization (gas phase, solution, and solid-state) of a series of four-, five- and six-fold coordinated heteroaryl-alkenolato aluminum complexes were performed to demonstrate the delicate interplay of structural and chemical influences of ligands in the design of new precursors for chemical vapor deposition. We are investigating the properties of heteroaryl alkenols as O^N chelating ligands [where O^N is 3,3,3-trifluoro(pyridin-2-yl)propen-2-ol (H-PyTFP), 3,3,3-trifluoro(1,3-benzimidazol-2-yl)propen-2-ol (H-BITFP), 3,3,3-trifluoro(dimethyl-1,3-oxazol-2-yl)propen-2-ol (H-DMOTFP), 3,3,3-trifluoro(1,3-benzoxazol-2-yl)propen-2-ol (H-BOTFP), 3,3,3-trifluoro(1,3-benzthiazol-2-yl)propen-2-ol (H-BTTFP), and 3,3,3-trifluoro(dimethyl-1,3-thiazol-2-yl)propen-2-ol (H-DMTTFP)] to prepare volatile and air-stable compounds. All three methyl groups in highly reactive AlMe3 could be replaced by H-PyTFP, H-BITFP, H-DMOTFP, and H-BOTFP yielding octahedral complexes of the type Al(O^N)3; under similar conditions H-BTTFP and H-DMTTFP produced heteroleptic MeAl(O^N)2 compounds with five-fold coordinated aluminum centers. Various attempts to obtain tris-alkenolato derivatives by choosing higher temperatures and prolonged reaction times were not successful. The reaction of H-PyTFP with [Al(O(t)Bu)3]2 produced the dimeric heteroleptic [Al(PyTFP)(O(t)Bu)2]2 complex with Al atoms present in both octahedral (Oh) and tetrahedral (Td) coordination in a single molecular unit. The introduction of the chelating ligand H-PyTFP in the dimeric framework of [Al(O(t)Bu)3]2 enhanced the stability against hydrolyses significantly. The tendency of Al(III) centers to preferably coordinate in Td or Oh environment was elucidated by hydrolysis studies of monomeric Al(PyTFP)3, Al(BOTFP)3, and MeAl(BTTFP)2 that produced hydroxo-bridged dimers to retain the octahedral environment for Al atoms. Surprisingly, hydrolysis of monomeric MeAl(DMTTFP)2 yielded an oxo-bridged dimer with two five-fold coordinated aluminum centers. The structural features of all new complexes were investigated in solution, vapor, and solid state by multinuclear NMR spectroscopy, EI-MS spectrometry, and single-crystal X-ray diffraction analyses, respectively.</style></abstract><label><style face="normal" font="default" size="100%">czympiel2015ligandmodulated</style></label><notes><style face="normal" font="default" size="100%">Czympiel, Lisa&#xD;Pfrommer, Johannes&#xD;Tyrra, Wieland&#xD;Schafer, Mathias&#xD;Mathur, Sanjay&#xD;eng&#xD;Inorg Chem. 2015 Jan 5;54(1):25-37. doi: 10.1021/ic502549m. Epub 2014 Dec 19.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/ic502549m</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/ic502549m</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>248</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">248</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Büyükyazi, Mehtap</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">3D nanoarchitectures of alpha-LiFeO2 and alpha-LiFeO2/C nanofibers for high power lithium-ion batteries</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><pages><style face="normal" font="default" size="100%">28-35</style></pages><volume><style face="normal" font="default" size="100%">13</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year></dates><abstract><style face="normal" font="default" size="100%">Hydrodynamic structuring of alkoxide-based sols in an elec. field is a promising technique to fabricate one-dimensional materials as free-standing fiber mats with high surface area and precisely controlled microstructure. Hollow $\alpha$-LiFeO2 and composite $\alpha$-LiFeO2/C nanofibers were prepd. as self-supported 3D architectures of ceramic fibers by single-step electrospinning of metal alkoxide sols. The spinel fibers exhibited a cryst. spinel phase with uniform fiber diam. and morphol. that was modified by a thin sheath of amorphous carbon in the composite fibers that enhances the elec. cond. and also has a structure-holding influence. The at. scale mixing and pre-existing -Li-O-Fe- units in the spinning soln. were the delivers of obsd. phase purity and control over the surface properties verified by high resoln. TEM data. Galvanostatic and potentiostatic studies confirmed the superior electrochem. behaviors of $\alpha$-LiFeO2 and $\alpha$-LiFeO2/C nanofibers as high-energy d. anode materials in half-cell configuration. $\alpha$-LiFeO2/C composite nanofibers showed after 50 cycles a discharge capacity of 821 mAh/g at 0.1 C with a capacity retention of 75\% from the 2nd to 50th cycle, whereas the discharge capacity of $\alpha$-LiFeO2-hollow nanofibers was found to be 756 mAh/g with a capacity retention of 68\%. Flexible composite nanofiber networks are promising soln. enabling improved electronic and ionic cond. and mech. stability for the development of lithium-ion batteries with high power and energy densities. Investigations on the stability and rate capability of $\alpha$-LiFeO2/C-composite electrode studied at different rates of 0.1 C, 0.25 C and 0.5 C for 75 cycles also showed high capacity values that indicated their potential as anode materials. on SciFinder(R)</style></abstract><label><style face="normal" font="default" size="100%">Buyukyazi2015</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.nanoen.2015.02.005</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>636</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">636</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Barreca, Davide</style></author><author><style face="normal" font="default" size="100%">Carraro, Giorgio</style></author><author><style face="normal" font="default" size="100%">Gasparotto, Alberto</style></author><author><style face="normal" font="default" size="100%">Maccato, Chiara</style></author><author><style face="normal" font="default" size="100%">Warwick, Michael E. A.</style></author><author><style face="normal" font="default" size="100%">Kaunisto, Kimmo</style></author><author><style face="normal" font="default" size="100%">Sada, Cinzia</style></author><author><style face="normal" font="default" size="100%">Turner, Stuart</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Ruoko, Tero-Petri</style></author><author><style face="normal" font="default" size="100%">Borgese, Laura</style></author><author><style face="normal" font="default" size="100%">Bontempi, Elza</style></author><author><style face="normal" font="default" size="100%">Van Tendeloo, Gustaaf</style></author><author><style face="normal" font="default" size="100%">Lemmetyinen, Helge</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fe2O3–TiO2 Nano-heterostructure Photoanodes for Highly Efficient Solar Water Oxidation</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Materials Interfaces</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1500313</style></pages><volume><style face="normal" font="default" size="100%">2</style></volume><number><style face="normal" font="default" size="100%">17</style></number><keywords><keyword><style face="normal" font="default" size="100%">Fe2O3</style></keyword><keyword><style face="normal" font="default" size="100%">nano-heterostructures</style></keyword><keyword><style face="normal" font="default" size="100%">photoelectrochemistry</style></keyword><keyword><style face="normal" font="default" size="100%">TiO2</style></keyword><keyword><style face="normal" font="default" size="100%">water splitting</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">2015/11/01</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Ltd</style></publisher><isbn><style face="normal" font="default" size="100%">2196-7350</style></isbn><abstract><style face="normal" font="default" size="100%">Harnessing solar energy for the production of clean hydrogen by photo?electrochemical water splitting represents a very attractive, but challenging approach for sustainable energy generation. In this regard, the fabrication of Fe2O3?TiO2 photoanodes is reported, showing attractive performances [≈2.0 mA cm?2 at 1.23 V vs. the reversible hydrogen electrode in 1 M NaOH] under simulated one-sun illumination. This goal, corresponding to a tenfold photoactivity enhancement with respect to bare Fe2O3, is achieved by atomic layer deposition of TiO2 over hematite (α-Fe2O3) nanostructures fabricated by plasma enhanced-chemical vapor deposition and final annealing at 650 °C. The adopted approach enables an intimate Fe2O3?TiO2 coupling, resulting in an electronic interplay at the Fe2O3/TiO2 interface. The reasons for the photocurrent enhancement determined by TiO2 overlayers with increasing thickness are unraveled by a detailed chemico-physical investigation, as well as by the study of photo?generated charge carrier dynamics. Transient absorption spectroscopy shows that the increased photoelectrochemical response of heterostructured photoanodes compared to bare hematite is due to an enhanced separation of photogenerated charge carriers and more favorable hole dynamics for water oxidation. The stable responses obtained even in simulated seawater provides a feasible route in view of the eventual large-scale generation of renewable energy.</style></abstract><notes><style face="normal" font="default" size="100%">https://doi.org/10.1002/admi.201500313</style></notes><work-type><style face="normal" font="default" size="100%">https://doi.org/10.1002/admi.201500313</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1002/admi.201500313</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1002/admi.201500313</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2021/02/05</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>246</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">246</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Arslan, Osman</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Abalı, Yüksel</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Morfological Evolution of the 1D ZnO Nanostructures : Anionic Effects</style></title><secondary-title><style face="normal" font="default" size="100%">11th Nanoscience and Nanotechnology Conference</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2015, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year></dates><label><style face="normal" font="default" size="100%">Arslan2015</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.researchgate.net/publication/312372539_Morfological_Evolution_of_the_1D_ZnO_Nanostructures_Anionic_Effects</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>245</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">245</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Arslan, Osman</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Abalı, Yüksel</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fabrication of Nanorods by Nanoparticle Building Blocks</style></title><secondary-title><style face="normal" font="default" size="100%">1st International Conference on Green Chemistry and Sustainable Technologies</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2015, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year></dates><label><style face="normal" font="default" size="100%">Arslan2015a</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>244</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">244</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Arslan, O.</style></author><author><style face="normal" font="default" size="100%">Belkoura, L.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Univ Cologne, Inst Phys Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Swift synthesis, functionalization and phase-transfer studies of ultrastable, visible light emitting oleate@ZnO quantum dots</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry C</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Mater Chem C</style></alt-title></titles><pages><style face="normal" font="default" size="100%">11965-11973</style></pages><volume><style face="normal" font="default" size="100%">3</style></volume><number><style face="normal" font="default" size="100%">45</style></number><keywords><keyword><style face="normal" font="default" size="100%">2015, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year></dates><isbn><style face="normal" font="default" size="100%">2050-7526</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000364908600023</style></accession-num><abstract><style face="normal" font="default" size="100%">Stable oleate capped, visible light emitting ZnO quantum dots (QDs) have been synthesized by a modified sol-gel method and examined for large-scale synthesis. Surface chelation with oleate ligands and their implications on particle growth were investigated by comprehensive NMR experiments and photoluminescence measurements. High-resolution electron microscopy and X-ray diffraction confirmed the high crystallinity and well-dispersed character of the ZnO QDs. The here investigated ZnO nanocrystals were found to be suitable for phase transfer synthesis (non-polar to polar dispersion medium) even after prolonged storage time that was verified by unchanged visible light emission. The absorption wavelength could be tuned by adjusting the nucleation kinetics and upon anchoring bulky ligands that provide control over the surface defects responsible for the optical (visible) properties. The demonstrated phase transfer studies make visible light emitting ZnO QDs accessible for a wide range of applications like ink-jet printing for nano-electronics, cell labelling or theranostic studies.</style></abstract><label><style face="normal" font="default" size="100%">Arslan2015</style></label><notes><style face="normal" font="default" size="100%">Cw3re&#xD;Times Cited:15&#xD;Cited References Count:69</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C5TC03377B</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c5tc03377b</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>243</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">243</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Appel, Linus</style></author><author><style face="normal" font="default" size="100%">Leduc, Jennifer</style></author><author><style face="normal" font="default" size="100%">Webster, Christopher L.</style></author><author><style face="normal" font="default" size="100%">Ziller, Joseph W.</style></author><author><style face="normal" font="default" size="100%">Evans, William J.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Dept Mat &amp; Inorgan Chem, D-50939 Cologne, Germany&#xD;Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA</style></auth-address><titles><title><style face="normal" font="default" size="100%">Synthesis of Air-Stable, Volatile Uranium(IV) and (VI) Compounds and Their Gas-Phase Conversion To Uranium Oxide Films</style></title><secondary-title><style face="normal" font="default" size="100%">Angewandte Chemie International Edition</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Angew Chem Int Edit</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2209-2213</style></pages><volume><style face="normal" font="default" size="100%">54</style></volume><number><style face="normal" font="default" size="100%">7</style></number><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">Feb 9</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">14337851</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000349391000035</style></accession-num><abstract><style face="normal" font="default" size="100%">Four air-stable, volatile uranium heteroarylalkenolates have been synthesized and characterized by three synthetic approaches and their gas phase deposition to uranium oxide films has been examined.</style></abstract><label><style face="normal" font="default" size="100%">appel2015synthesis</style></label><notes><style face="normal" font="default" size="100%">Cb1me&#xD;Times Cited:18&#xD;Cited References Count:83</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/anie.201409606</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/anie.201409606</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>242</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">242</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Appel, Linus</style></author><author><style face="normal" font="default" size="100%">Fiz, Raquel</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Pantenburg, Ingo</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Chair Inorgan &amp; Mat Chem, D-50939 Cologne, Germany&#xD;Xi An Jiao Tong Univ, Sch Energy &amp; Power Engn, Int Res Ctr Renewable Energy, Xian 710049, Shaanxi, Peoples R China</style></auth-address><titles><title><style face="normal" font="default" size="100%">Design of Volatile Mixed-Ligand Tantalum(V) Compounds as Precursors to Ta2O5 Films</style></title><secondary-title><style face="normal" font="default" size="100%">Crystal Growth &amp; Design</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Cryst Growth Des</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1141-1149</style></pages><volume><style face="normal" font="default" size="100%">15</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">Mar</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1528-7483</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000350614400018</style></accession-num><abstract><style face="normal" font="default" size="100%">Synthesis and structural characterization of six monomeric, heteroleptic tantalum(V) complexes of the general formula Ta(OiPr)4(ArTFP), where Ar = pyridine (1), 4,5- dimethyloxazole (2), 4,5-dimethylthiazole (3), benzimidazole (4), benzoxazole (5), benzthiazole (6), and TFP = trifluoropropenol, are described. Introduction of a donor-functionalized \^{I}²-heteroarylalkenolate in the coordination sphere of Ta in the dimeric Ta2(OiPr)10 increases significantly the stability and volatility of these precursors, simplifying the depositions of Ta2O5. The molecular structures of 1\^{a} 6 exhibited a distorted octahedral coordination around the tantalum center by four isopropoxide groups and one \^{I}²-heteroarylalkenolate. Thermal decomposition studies (TG/DTA) and analysis of byproducts by NMR spectroscopy confirmed the decomposition mechanism and gas-phase stability of the heteroleptic compounds necessary for Ta2O5 depositions. Chemical vapor deposition studies with 1 and 2 demonstrated their suitability as efficient precursors for the growth of Ta2O5 thin films, whose properties were compared with Ta2O5 thin films obtained from homoleptic alkoxides.</style></abstract><label><style face="normal" font="default" size="100%">Appel2015</style></label><notes><style face="normal" font="default" size="100%">Cc8jl&#xD;Times Cited:6&#xD;Cited References Count:53</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/cg501438k</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/cg501438k</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>241</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">241</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Amini, Pegah</style></author><author><style face="normal" font="default" size="100%">Dolatyari, Mahboubeh</style></author><author><style face="normal" font="default" size="100%">Rostami, Ali</style></author><author><style face="normal" font="default" size="100%">Rostami, Ghasem</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Torabi, Pouneh</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Tabriz, OIC Res Grp, Tabriz 5166614761, Iran&#xD;ASEPE Co, SP EPT Labs, Tabriz 5364196795, Iran&#xD;Univ Cologne, Inst Anorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">High-Performance Solution Processed Inorganic Quantum-Dot LEDs</style></title><secondary-title><style face="normal" font="default" size="100%">IEEE Transactions on Nanotechnology</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Ieee T Nanotechnol</style></alt-title></titles><pages><style face="normal" font="default" size="100%">911-917</style></pages><volume><style face="normal" font="default" size="100%">14</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style face="normal" font="default" size="100%">September</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1536-125X</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000364504200019</style></accession-num><abstract><style face="normal" font="default" size="100%">In this research paper, fabrication of novel CdSe\ZnS QD-LEDs with solution processing method is presented, and the impact of trap energy levels in the electron and hole transport levels on these QD-LEDs brightness is investigated. Two types of QD-LEDs are fabricated with ITO as the transparent anode electrode, NiO nanoparticles as the hole transport layer (HTL), CdSe\ZnS QDs as the luminescent layer, ZnO:Ga as the electron transport layer (ETL), and Al as the cathode electrode. The NiO nanoparticles are synthesized by the sol-gel or alternatively the electrochemical method. Formation of different trap levels is observed in the crystal structures of the NiO nanoparticles synthesized by each of these methods. Considering the electrochemically prepared NiO nanoparticles, it is found that the density of trap levels is higher in the crystal structure of the NiO nanoparticles synthesized by sol-gel method, and the device fabricated by the latter material shows higher performance. Calculation of the electronic structure of ZnO:Ga by DFT methods (GGA-PBE) indicates that doping of Ga in the structure of crystalline ZnO creates new energy levels in conduction band and intermediate bands at the bandgap of ZnO host. It facilitates electron injection from Al cathode to the ZnO:Ga ETL layer and from this layer to the QD-luminescent layer. The fabricated devices show turn-on lower voltages than 5 V in which a peak brightness of 500 and 340 cd.m(-2) is measured for the LEDs fabricated with sol-gel and electrochemically synthesized NiO nanoparticles, respectively.</style></abstract><label><style face="normal" font="default" size="100%">Amini2015</style></label><notes><style face="normal" font="default" size="100%">Cv8cn&#xD;Times Cited:4&#xD;Cited References Count:27</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://ieeexplore.ieee.org/lpdocs/epic03/wrapper.htm?arnumber=7172534</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1109/Tnano.2015.2461025</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>240</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">240</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Abbas, Y. H.</style></author><author><style face="normal" font="default" size="100%">Azzazy, H. M. E.</style></author><author><style face="normal" font="default" size="100%">Tammam, S.</style></author><author><style face="normal" font="default" size="100%">Lamprecht, A.</style></author><author><style face="normal" font="default" size="100%">Ali, M. E.</style></author><author><style face="normal" font="default" size="100%">Schmidt, A. M.</style></author><author><style face="normal" font="default" size="100%">Sollazzo, S.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Inhalable Stimuli-Responsive Theranostic Nanoparticles for Targeting Cancer in Deep Lung Tissue</style></title><secondary-title><style face="normal" font="default" size="100%">TechConnect World Innovation</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2015, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2015</style></year></dates><abstract><style face="normal" font="default" size="100%">Lung cancer is the deadliest solid tumour, leading to the deaths of more individuals than the combination of the three next most lethal cancers which are colon, prostate and breast cancer. According to the IARC, in 2012 lung cancer accounted for 13\% (1.83 million) of cancer cases and caused 19\% (1.56 million) of cancer deaths worldwide. Despite advances in surgery and drug discovery lung cancer remains difficult to treat. This is a result of unavoidable exposure to carcinogens, poor diagnosis and the lack of targeted drug delivery platforms. Moreover, delivery of drug to deep lung tissue is limited by several factors including; transporters, defense mechanisms (beating cilia, local enzymes and macrophages) and mucus covering. The aim of this study was to develop a non-invasive, patient convenient platform for the targeted delivery of chemotherapeutics to cancer in deeper lung tissue. The formulation consisted of inhalable maltodextrin (MD)-based microparticles (MPs) encapsulating chitosan (CS) nanoparticles (NPs) loaded with ultra-small superparamagnetic iron oxide nanoparticles (USPIONs) and a chemotherapeutic drug. CS NPs were prepared using ionotropic gelation method. USPIONs of size 5 nm were synthesized via hydrothermal method using L-ascorbic acid as reducing agent and were characterized by scanning transmission electron microscopy (STEM) and dynamic light scattering (DLS). Synthesized USPIONs possessed hysteresis loop with magnetic saturation (Ms), coercivity (Hci) and retentivity (Mr) of 48.4 emu/g, 9.9 G and 0.5 emu/g; respectively. Fluorescein-loaded CS NPs provided a sustained release of drug, whereas USPIONs encapsulated in CS NPs were able to increase the NP drug release in response to an external magnetic field by 1.7 fold. Cell uptake studies conducted using lung cancer cells (A549) indicated that the CS NPs are rapidly uptaken, and show preferential toxicity to tumour cells in comparison to cultured fibroblasts. NPs were modified with anti-epidermal growth factor receptor antibodies and this modification showed to hinder cellular uptake of NPs. Afterwards, the prepared CS NPs and CS-USPIONs were co-spray freeze dried (SFD) with MD resulting in a dry powder with adequate aerodynamic properties suitable for deep pulmonary deposition. The prepared SFD powders had fine particle fraction (FPF≤5 µm) of 40-42 \% w/w and mass median aerodynamic diameter (MMAD) of 5-6 µm as determined by the next generation impactor (NGI). A mixture of CS NPs and CS-USPIONs could be able to provide a continuous sustained release of drug, with intermittent blouses of drug in response to external stimuli; a drug profile desirable in cancer therapy. In conclusion, the developed formulation may represent improved therapy for cancer in deep lung tissue due to the combined effect of tissue targeting, controlled drug release, and the possible imaging and prognostic values as a result of the USPIONs content.</style></abstract><label><style face="normal" font="default" size="100%">Y.H.AbbasH.ME.AzzazyS.TammamA.LamprechtM.E.AliA.M.SchmidtS.Sollazzo2015</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.researchgate.net/publication/278666910_Inhalable_Stimuli-Responsive_Theranostic_Nanoparticles_for_Targeting_Cancer_in_Deep_Lung_Tissue</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>300</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">300</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zhao, Bin</style></author><author><style face="normal" font="default" size="100%">Shen, Jianlei</style></author><author><style face="normal" font="default" size="100%">Chen, Shixing</style></author><author><style face="normal" font="default" size="100%">Wang, Dongfang</style></author><author><style face="normal" font="default" size="100%">Li, Fan</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Song, Shiping</style></author><author><style face="normal" font="default" size="100%">Fan, Chunhai</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Chinese Acad Sci, Div Phys Biol, Shanghai 201800, Peoples R China&#xD;Chinese Acad Sci, Shanghai Synchrotron Radiat Facil, Shanghai Inst Appl Phys, Bioimaging Ctr, Shanghai 201800, Peoples R China&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Gold nanostructures encoded by non-fluorescent small molecules in polyA-mediated nanogaps as universal SERS nanotags for recognizing various bioactive molecules</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Science</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Sci</style></alt-title></titles><pages><style face="normal" font="default" size="100%">4460-4466</style></pages><volume><style face="normal" font="default" size="100%">5</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><isbn><style face="normal" font="default" size="100%">2041-6520</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000343004300043</style></accession-num><abstract><style face="normal" font="default" size="100%">Surface-enhanced Raman scattering (SERS) has recently been used to design novel nanoprobes called &quot;SERS tags&quot; which hold great promise for the fields of biosensing and nanomedicine. More recent advances have shed new light on the synthesis of uniform nanostructures with interior nanogaps for stable SERS enhancement. However, producing interior nanogap-based SERS nanotags directly and controllably with strong and stable multiplex SERS signals as well as developing a multiplex anal. platform to recognize different types of bioactive mols. still remain highly challenging. To address this challenge, we herein develop a novel approach for the direct synthesis of nanogap-based universal SERS nanotags by mediating poly-adenine (polyA) and encoding non-fluorescent small mols. The universal nanotags were then functionalized by different types of biol. probes and used as SERS nanoprobes to recognize various bioactive mols. To the best of our knowledge, this is the first example of using SERS nanotags to develop a simultaneous multianal. platform for all of the major types of bioactive analytes, including nucleic acids, proteins and small mols. Furthermore, the nanotags show great promise for fluorescence-SERS bimodal bioanal. and bioimaging.</style></abstract><label><style face="normal" font="default" size="100%">zhao2014nanostructures</style></label><notes><style face="normal" font="default" size="100%">Aq7nk&#xD;Times Cited:92&#xD;Cited References Count:39</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://xlink.rsc.org/?DOI=C4SC01792G</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c4sc01792g</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>299</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">299</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wortmann, Laura</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Niznansky, Daniel</style></author><author><style face="normal" font="default" size="100%">Valldor, Martin</style></author><author><style face="normal" font="default" size="100%">Arroub, Karim</style></author><author><style face="normal" font="default" size="100%">Berger, Nadja</style></author><author><style face="normal" font="default" size="100%">Rahme, Kamil</style></author><author><style face="normal" font="default" size="100%">Holmes, Justin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Institute of Inorganic Chemistry, University of Cologne , Greinstrasse 6, Cologne 50939, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Bioconjugated Iron Oxide Nanocubes: Synthesis, Functionalization, and Vectorization</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">ACS Applied Materials &amp; Interfaces</style></full-title></periodical><pages><style face="normal" font="default" size="100%">16631-16642</style></pages><volume><style face="normal" font="default" size="100%">6</style></volume><number><style face="normal" font="default" size="100%">19</style></number><edition><style face="normal" font="default" size="100%">2014/09/04</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">October</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1944-8244</style></isbn><accession-num><style face="normal" font="default" size="100%">25184762</style></accession-num><abstract><style face="normal" font="default" size="100%">A facile bottom-up approach for the synthesis of inorganic/organic bioconjugated nanoprobes based on iron oxide nanocubes as the core with a nanometric silica shell is demonstrated. Surface coating and functionalization protocols developed in this work offered good control over the shell thickness (8-40 nm) and enabled biovectorization of SiO2@Fe3O4 core-shell structures by covalent attachment of folic acid (FA) as a targeting unit for cellular uptake. The successful immobilization of folic acid was investigated both quantitatively (TGA, EA, XPS) and qualitatively (AT-IR, UV-vis, $\zeta$-potential). Additionally, the magnetic behavior of the nanocomposites was monitored after each functionalization step. Cell viability studies confirmed low cytotoxicity of FA@SiO2@Fe3O4 conjugates, which makes them promising nanoprobes for targeted internalization by cells and their imaging.</style></abstract><label><style face="normal" font="default" size="100%">wortmann2014bioconjugated</style></label><notes><style face="normal" font="default" size="100%">Wortmann, Laura&#xD;Ilyas, Shaista&#xD;Niznansky, Daniel&#xD;Valldor, Martin&#xD;Arroub, Karim&#xD;Berger, Nadja&#xD;Rahme, Kamil&#xD;Holmes, Justin&#xD;Mathur, Sanjay&#xD;eng&#xD;ACS Appl Mater Interfaces. 2014 Oct 8;6(19):16631-42. doi: 10.1021/am503068r. Epub 2014 Sep 22.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/am503068r</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/am503068r</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>298</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">298</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Von Hagen, Robin</style></author><author><style face="normal" font="default" size="100%">Sneha, Mahima</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ink-jet Printing of Hollow SnO2 Nanospheres for Gas Sensing Applications</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the American Ceramic Society</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1035-1040</style></pages><volume><style face="normal" font="default" size="100%">97</style></volume><number><style face="normal" font="default" size="100%">4</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">April</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">00027820</style></isbn><abstract><style face="normal" font="default" size="100%">Hollow Sn-oxide (SnO2) nanospheres were synthesized by coating, C nanospheres (CNs) as hard templates, with a Sn(IV) sol obtained by partial hydrolysis of Sn(OBut)4 under ambient conditions. Formation of cryst. SnO2 spheres upon calcination was confirmed by powder x-ray diffraction data, whereas the hollow interiors of SnO2 particles were verified by scanning and TEM of both intact and broken spheres. The shell of SnO2 nanospheres sintered at 700° consisted of a single layer of nanocrystallites (∼6 nm) self-assembled in a ball-like superlattice. Sn-oxide hollow spheres showed an av. diam. of 150 nm and could be homogeneously dispersed in H2O/ethylene glycol (50:50 vol. mixt. to form stable inorg. inks viable for their use in com. ink-jet printers demonstrated by printing porous ceramic structures on an interdigitated sensor chip. The integration of large surface and nanoscopic voids in the final structures imparted higher sensitivity to the as-printed sensors toward both oxidizing (N dioxide) and reducing gases (methane and EtOH), which validates the enormous potential of printable inorgs. in functional applications.</style></abstract><label><style face="normal" font="default" size="100%">hagen2014inkjet</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1111/jace.12832</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>297</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">297</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Vomiero, Alberto</style></author><author><style face="normal" font="default" size="100%">Ferroni, Matteo</style></author><author><style face="normal" font="default" size="100%">Natile, Marta Maria</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Fiz, Raquel</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Sberveglieri, Giorgio.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">CNR INO, SENSOR Lab, I-25123 Brescia, Italy&#xD;Univ Brescia, Dept Informat Engn &amp; Mat, SENSOR Lab, I-25133 Brescia, Italy&#xD;CNR IENI, I-35131 Padua, Italy&#xD;Univ Padua, Dept Chem Sci, I-35131 Padua, Italy&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Sequential physical vapor deposition and chemical vapor deposition for the growth of In2O3–SnO2 radial and longitudinal heterojunctions</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Surface Science</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Appl Surf Sci</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Applied Surface Science</style></full-title></periodical><pages><style face="normal" font="default" size="100%">59-64</style></pages><volume><style face="normal" font="default" size="100%">323</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">Dec 30</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">01694332</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000345511600011</style></accession-num><abstract><style face="normal" font="default" size="100%">Heterostructures of In2O3 and SnO2 were produced by sequential application of the phys.- and CVD techniques usually adopted for nanowire fabrication. In2O3 nanowires exhibit a single crystal bcc. structure oriented along the 1 0 0 direction and grow epitaxially on $\alpha$-sapphire substrate by a transport and condensation method assisted by Au nanoparticles. Nucleation and growth occurred via direct vapor solid (VS) mechanism competing with catalyst-mediated vapor-liq.-solid (VLS). SnO2 nanowires were obtained in a single crystal tetragonal (cassiterite) structure and oriented along the 1 0 1 direction, the growth being promoted by the gold particle at the apex of the In2O3 nanowires. The size of the catalyst thereby dets. the main morphol. features of SnO2 wires. CVD deposition allows precise control of the geometrical features of the heterojunction, also limiting detrimental nucleation of SnO2 on the lateral sides of In2O3 nanowires due to lower longitudinal growth rate. These results can help in improving the ability of finely tuning the morphol. and structural properties of heterostructured oxide nanocrystals.</style></abstract><label><style face="normal" font="default" size="100%">vomiero2014sequential</style></label><notes><style face="normal" font="default" size="100%">Au3kj&#xD;Times Cited:6&#xD;Cited References Count:40</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S016943321401705X</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.apsusc.2014.07.177</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>295</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">295</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Singh, Trilok</style></author><author><style face="normal" font="default" size="100%">Wang, Shuangzhou</style></author><author><style face="normal" font="default" size="100%">Aslam, Nabeel</style></author><author><style face="normal" font="default" size="100%">Zhang, Hehe</style></author><author><style face="normal" font="default" size="100%">Hoffmann-Eifert, Susanne</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Xi An Jiao Tong Univ, Sch Energy &amp; Power Engn, Int Res Ctr Renewable Energy, Xian 710049, Shaanxi, Peoples R China&#xD;Forschungszentrum Julich, Peter Gruenberg Inst PGI 7, D-52425 Julich, Germany&#xD;JARA FIT, D-52425 Julich, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Atomic Layer Deposition of Transparent VOx Thin Films for Resistive Switching Applications</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Vapor Deposition</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Vapor Depos</style></alt-title></titles><pages><style face="normal" font="default" size="100%">291-297</style></pages><volume><style face="normal" font="default" size="100%">20</style></volume><number><style face="normal" font="default" size="100%">7-8-9</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">Sep</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09481907</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000342069800013</style></accession-num><abstract><style face="normal" font="default" size="100%">Atomic layer deposition (ALD) offers nearly pinhole-free, conformal, and with good thickness control, metal oxide nanometric thin films required for next-generation memory devices. Here we report on the ALD of VOx thin films grown at about 100°C from a vanadium tri-isopropoxide (VTIP) precursor, with water as the co-reactant, followed by their post-growth treatments, for potential applications in resistive switching (RS) devices. As-grown VOx films are amorphous, and transform into polycryst. layers upon annealing. Capacitor structures fabricated from amorphous VOx films show current-voltage (I-V) characteristics, interesting for RS applications. Depending on the electroforming conditions, bipolar-type memory switching with a resistance ratio ROFF/RON &gt; 103 is obtained, as well as a combination of memory and threshold switching. The latter is attractive for its highly non-linear I-V characteristics, which is attributed to the temp.-induced insulator-to-metal transition (IMT) in vanadium dioxide.</style></abstract><label><style face="normal" font="default" size="100%">singh2014atomic</style></label><notes><style face="normal" font="default" size="100%">Sp. Iss. SI&#xD;Ap4su&#xD;Times Cited:22&#xD;Cited References Count:42</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/cvde.201407122</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/cvde.201407122</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>296</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">296</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Singh, Trilok</style></author><author><style face="normal" font="default" size="100%">Lehnen, Thomas</style></author><author><style face="normal" font="default" size="100%">Leuning, Tessa</style></author><author><style face="normal" font="default" size="100%">Sahu, Diptiranjan</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan &amp; Mat Chem, D-50939 Cologne, Germany&#xD;Univ Witwatersrand, Sch Phys, ZA-2050 Johannesburg, South Africa&#xD;Univ Witwatersrand, DST NRF Ctr Excellence Strong Mat, ZA-2050 Johannesburg, South Africa</style></auth-address><titles><title><style face="normal" font="default" size="100%">Thickness dependence of optoelectronic properties in ALD grown ZnO thin films</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Surface Science</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Appl Surf Sci</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Applied Surface Science</style></full-title></periodical><pages><style face="normal" font="default" size="100%">27-32</style></pages><volume><style face="normal" font="default" size="100%">289</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan 15</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">01694332</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000328635700005</style></accession-num><abstract><style face="normal" font="default" size="100%">ZnO thin films with high cond. and high transparency were grown on Si(100) substrates by at. layer deposition. Thickness dependent (43-225 nm) changes in crystallog., optical, and elec. properties are reported and discussed. Increase in film thickness caused a decrease in the bandgap by relaxation of stress in the plane of the film and led to an improvement in crystallinity and cond. The optical studies showed a noticeable change towards the contribution of excitonic and phonon replica to the UV-emission band.</style></abstract><label><style face="normal" font="default" size="100%">singh2014thickness</style></label><notes><style face="normal" font="default" size="100%">274wa&#xD;Times Cited:50&#xD;Cited References Count:45</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0169433213019302</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.apsusc.2013.10.071</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>293</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">293</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Singh, Dileep</style></author><author><style face="normal" font="default" size="100%">Zhu, Dongming</style></author><author><style face="normal" font="default" size="100%">Kriven, Waltraud M.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Lin, Hua-Tay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Design, Development, and Applications of Structural Ceramics, Composites, and Nanomaterials: Ceramic Transactions, Volume 244</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><publisher><style face="normal" font="default" size="100%">Wiley</style></publisher><isbn><style face="normal" font="default" size="100%">978-1-118-77094-8</style></isbn><label><style face="normal" font="default" size="100%">singh2014design</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://eu.wiley.com/WileyCDA/WileyTitle/productCd-1118770943.html</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>294</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">294</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Singh, Dileep</style></author><author><style face="normal" font="default" size="100%">Timofeeva, Elena V.</style></author><author><style face="normal" font="default" size="100%">Moravek, Michael R.</style></author><author><style face="normal" font="default" size="100%">Cingarapu, Sreeram</style></author><author><style face="normal" font="default" size="100%">Yu, Wenhua</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Argonne Natl Lab, Nucl Engn Div, Argonne, IL 60439 USA&#xD;Argonne Natl Lab, Div Energy Syst, Argonne, IL 60439 USA&#xD;Univ Cologne, Inst Inorgan Chem, D-50923 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Use of metallic nanoparticles to improve the thermophysical properties of organic heat transfer fluids used in concentrated solar power</style></title><secondary-title><style face="normal" font="default" size="100%">Solar Energy</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Sol Energy</style></alt-title></titles><pages><style face="normal" font="default" size="100%">468-478</style></pages><volume><style face="normal" font="default" size="100%">105</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jul</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0038092X</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000337985700045</style></accession-num><abstract><style face="normal" font="default" size="100%">One of the approaches to enhance the efficiency, and consequently, reduce costs to produce electricity from concd. solar power (CSP) is by the development of advanced high temp. heat transfer fluids (HTFs). Incorporation of metallic nanoparticles into conventional heat transfer fluids could significantly improve the thermal transport properties of the HTFs. This study reports on the synthesis and investigation of copper nanoparticles synthesized inhouse and dispersed in two synthetic HTFs Therminol 59 (TH59) and Therminol 66 (TH66). Liq. phase redn. of a copper salt was used to produce copper nanoparticles. Suspensions with various copper nanoparticle loadings (0.5-2 vol.\%) were prepd. Characterizations such as the thermal cond., dynamic viscosity, mass sp. heat capacity, and fluid stability were performed on the suspensions. Thermal cond. enhancements over the base fluids were as high as approx. 20\% at a 2 vol.\% particle loading. These enhancements in the thermal cond. are higher than the predictions based on the Effective Medium Theory (EMT). Dynamic viscosity measurements showed that if good dispersion of nanoparticles is achieved, the composite fluids behave in a Newtonian manner and the dynamic viscosity increases over the base fluid are minor at temps. 125 °C and above. Stability of the suspensions with time was also investigated. Based on the measured properties of the suspensions, a figure of merit for heat transfer was calcd. to evaluate the viability of the suspensions.</style></abstract><label><style face="normal" font="default" size="100%">singh2014metallic</style></label><notes><style face="normal" font="default" size="100%">Aj8vj&#xD;Times Cited:38&#xD;Cited References Count:32</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0038092X14001248</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.solener.2014.02.036</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>292</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">292</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Schläfer, Johannes</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Octakis(tert-butoxo)dicerium(IV) [Ce2(OtBu)8]: Synthesis, Characterization, Decomposition, and Reactivity</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2751-2753</style></pages><volume><style face="normal" font="default" size="100%">53</style></volume><number><style face="normal" font="default" size="100%">6</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><abstract><style face="normal" font="default" size="100%">An advanced synthesis for the homometallic derivative [Ce2(OtBu)8] (1) starting from [Ce(OtBu)2(N(SiMe3)2)2] was developed. Structural characterization of a cerium(IV) complex and its decomposition products confirmed the coexistence of both ether elimination and Ce–O bond cleavage processes, which lead to the formation of [Ce3O(OtBu)10] and [Ce3(OtBu)11] (2) derivatives, respectively. Variable-temperature NMR spectroscopy under strict exclusion of moisture enabled insight into the decomposition processes in noncoordinating solvents and at elevated temperature. In addition, structural analysis of the heterovalent &quot;(2)&quot; and of two new complexes of the general formula [Ce2(OtBu)8(L)] [L = HOtBu (3), OCPh2 (4)] is described.</style></abstract><label><style face="normal" font="default" size="100%">schlafer2014octakis</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/ic4025876</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>291</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">291</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Schläfer, Johannes</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Correction to Octakis(tert-butoxo)dicerium(IV) [Ce2(OtBu)8]: Synthesis, Characterization, Decomposition, and Reactivity</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">8838-8838</style></pages><volume><style face="normal" font="default" size="100%">53</style></volume><number><style face="normal" font="default" size="100%">16</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">August</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><abstract><style face="normal" font="default" size="100%">On page 2752, the calcd. hydrodynamic radius contained an error; the correction is given.</style></abstract><label><style face="normal" font="default" size="100%">schlafer2014correction</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/ic501773f</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>290</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">290</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Raccis, Riccardo</style></author><author><style face="normal" font="default" size="100%">Wortmann, Laura</style></author><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Schläfer, Johannes</style></author><author><style face="normal" font="default" size="100%">Mettenbörger, Andreas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Geometry-based, n-type-enhanced p-type polymer/metal oxide nanocomposites for high-efficiency, high-specificity conductive systems</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Proceedings</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">mrsf13--1630--o3--37</style></pages><volume><style face="normal" font="default" size="100%">1630</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><isbn><style face="normal" font="default" size="100%">1946-4274</style></isbn><abstract><style face="normal" font="default" size="100%">Hematite ($\alpha$-Fe2O3) nanoparticles were diffused of two different shapes (spherical and cubical) in PEDOT:PSS matrices below the percolation threshold. Increases in conductivity within a distinct range in concentration were observed in the dark and under simulated solar illumination. The effect was ascribed to a generalized Poole-Frenkel effect in conjunction with basic properties of heterojunctions and electrostatic dipoles, and verified through data fitting. A difference in behaviour between sphere- and cube-based nanocomposites was also observed.</style></abstract><label><style face="normal" font="default" size="100%">raccis2014geometrybased</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1557/opl.2014.56</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>289</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">289</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Raccis, R.</style></author><author><style face="normal" font="default" size="100%">Wortmann, L.</style></author><author><style face="normal" font="default" size="100%">Ilyas, S.</style></author><author><style face="normal" font="default" size="100%">Schläfer, J.</style></author><author><style face="normal" font="default" size="100%">Mettenbörger, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Dipole-induced conductivity enhancement by n-type inclusion in a p-type system: alpha-Fe2O3-PEDOT:PSS nanocomposites</style></title><secondary-title><style face="normal" font="default" size="100%">Physical Chemistry Chemical Physics</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Phys Chem Chem Phys</style></alt-title></titles><pages><style face="normal" font="default" size="100%">15597-15607</style></pages><volume><style face="normal" font="default" size="100%">16</style></volume><number><style face="normal" font="default" size="100%">29</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><isbn><style face="normal" font="default" size="100%">1463-9076</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000339173700063</style></accession-num><abstract><style face="normal" font="default" size="100%">Hematite (alpha-Fe2O3) nanoparticles of two different shapes but of same size (ca. 40 nm) were dispersed in PEDOT:PSS matrices in various concentration ranges (0-7 wt to study the consequent changes in conductivity in the dark and under solar illumination conditions. Within a distinct range of concentration, a distinct increase in the conductivity was observed for both spherical and cubical particle population. We ascribed this effect to the generalized Poole-Frenkel theory of conduction in conjunction with the basic depletion width properties of heterojunctions and electrostatic dipole moments, and verified our assumptions through data fitting. A difference in conductivity between sphere-and cube-based alpha-Fe2O3-PEDOT: PSS nanocomposites was also observed and ascribed to the electrostatic edge effect on the nanoparticles. The dispersion of alpha-Fe2O3 nanocrystals was confirmed by high-resolution electron microscopy, whereas the electrical properties and modulations thereof were followed by recording current-voltage characteristics.</style></abstract><label><style face="normal" font="default" size="100%">raccis2014dipoleinduced</style></label><notes><style face="normal" font="default" size="100%">Al5ky&#xD;Times Cited:2&#xD;Cited References Count:35</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C4CP01093K</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c4cp01093k</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>288</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">288</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Miguel, F. L.</style></author><author><style face="normal" font="default" size="100%">Müller, R.</style></author><author><style face="normal" font="default" size="100%">Weinmann, M.</style></author><author><style face="normal" font="default" size="100%">Hempelmann, R.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Mücklich, F.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, D-66123 Saarbrucken, Germany&#xD;Univ Cologne, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Production and characterization of nanocomposite thin films based on Ni matrix reinforced with SnO2 single-crystalline nanowires for electrical contact applications</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Alloys and Compounds</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Alloy Compd</style></alt-title></titles><pages><style face="normal" font="default" size="100%">14-18</style></pages><volume><style face="normal" font="default" size="100%">603</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">Aug 5</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0925-8388</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000335505100003</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanocomposite thin films based on electrodeposited Ni matrix reinforced with SnO2 single-crystalline nanowires grown onto Si substrates by chemical vapor deposition were produced. The composites were characterized by means of scanning and transmission electron microscopy (for imaging, selected area diffraction and transmission Kikuchi diffraction), atomic force microscopy (for 3D surface profiling and roughness evaluation) and 4-point probe electrical resistivity measurements. The Ni matrices obtained were nanocrystalline in nature (41 nm crystallite mean size) even though low direct current electrode-position was used. The topography and roughness of the samples were strongly affected by the presence of the nanowires as so was the electrical resistivity, which could be improved by Ag-coating the nanowires. A comparison with pure Ni produced in the same way is presented for determining the effects of the SnO2 nanowires.</style></abstract><label><style face="normal" font="default" size="100%">miguel2014production</style></label><notes><style face="normal" font="default" size="100%">Ag6cc&#xD;Times Cited:3&#xD;Cited References Count:35</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.jallcom.2014.03.066</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.jallcom.2014.03.066</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>287</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">287</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mettenbörger, Andreas</style></author><author><style face="normal" font="default" size="100%">Singh, Trilok</style></author><author><style face="normal" font="default" size="100%">Singh, Aadesh P.</style></author><author><style face="normal" font="default" size="100%">Järvi, Tommi T.</style></author><author><style face="normal" font="default" size="100%">Moseler, Michael</style></author><author><style face="normal" font="default" size="100%">Valldor, Martin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Plasma-chemical reduction of iron oxide photoanodes for efficient solar hydrogen production</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Hydrogen Energy</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">4828-4835</style></pages><volume><style face="normal" font="default" size="100%">39</style></volume><number><style face="normal" font="default" size="100%">10</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><isbn><style face="normal" font="default" size="100%">03603199</style></isbn><abstract><style face="normal" font="default" size="100%">The authors demonstrate the effect of hydrogen plasma treatment on hematite films as a simple and effective strategy for modifying the existing substrate to improve significantly the band edge positions and photoelectrochem. (PEC) performance. Plasma treated hematite films were consist of mixed phases (Fe3O4:$\alpha$-Fe2O3) which was confirmed by XPS and Raman anal., treated films also showed higher absorption cross-section and are a promising photoelectrode material. The treated samples showed enhance photocurrent densities with max. of 3.5 mA/cm2 at 1.8 V/RHE and the photocurrent onset potentials were shifted from 1.68 VRHE (untreated) to 1.28 VRHE (treated). Hydrogen plasma treatment under nonequil. conditions induced a valence dynamics among Fe centers in the sub-surface region that was sustained by the incorporation of hydrogen in the hematite lattice as supported by the d. functional theory calcns.</style></abstract><label><style face="normal" font="default" size="100%">mettenborger2014plasmachemical</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S036031991400130X</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>285</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">285</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Hemmer, E.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Altmayer, J.</style></author><author><style face="normal" font="default" size="100%">Donia, N.</style></author><author><style face="normal" font="default" size="100%">Kumakiri, I.</style></author><author><style face="normal" font="default" size="100%">Lecerf, N.</style></author><author><style face="normal" font="default" size="100%">Bredesen, R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Microporous ZrO2 Membrane Preparation by Liquid-Injection MOCVD</style></title><secondary-title><style face="normal" font="default" size="100%">Progress in Nanotechnology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">157-167</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><pub-location><style face="normal" font="default" size="100%">Hoboken, NJ, USA</style></pub-location><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Inc.</style></publisher><isbn><style face="normal" font="default" size="100%">9780470588246</style></isbn><abstract><style face="normal" font="default" size="100%">Inorganic microporous membranes, presenting pores smaller than 2 nm, have an important potential for large-scale application in gas purification and separation. This chapter presents a membrane system based on the chemical vapor deposition of microporous zirconia on a-alumina / y-alumina supports prepared by slip casting and sol-gel. For this purpose, Zr(OBut)4\% was chosen as precursor for the deposition of nanocrystalline Z1O2 films. The as-deposited and post-annealed zirconia layers were investigated by EDX, XRD, SEM and AFM. First permporometry tests showed that the additional zirconia layer influenced the gas flux through the membrane in dependence of the CVD process parameters and resulted in a reduction of the total pore volume. The chapter presents a membrane of microporous zirconia on a-alumina / y-alumina supports was prepared by liquid-injection metal-organic chemical vapor deposition (LI-MOCVD).</style></abstract><label><style face="normal" font="default" size="100%">mathur2014microporous</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/9780470588246.ch25</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>286</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">286</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Solar Hydrogen and Nanotechnology IX</style></title></titles><volume><style face="normal" font="default" size="100%">9176</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><isbn><style face="normal" font="default" size="100%">9781628412031</style></isbn><label><style face="normal" font="default" size="100%">mathur2014solar</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://spie.org/Publications/Proceedings/Volume/9176</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>284</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">284</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Maleki, Mahboubeh</style></author><author><style face="normal" font="default" size="100%">Amani-Tehran, Mohammad</style></author><author><style face="normal" font="default" size="100%">Latifi, Masoud</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Department of Textile Engineering, Textile Excellence &amp; Research Centers, Amirkabir University of Technology (Tehran Polytechnic), Hafez Avenue, 1591634311, Tehran, Iran; Institute of Inorganic Chemistry, Inorganic and Materials Chemistry, University of Cologne, Greinstrasse 6, D-50939 Cologne, Germany. Electronic address: maleki.m83@gmail.com.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Drug release profile in core-shell nanofibrous structures: A study on Peppas equation and artificial neural network modeling</style></title><secondary-title><style face="normal" font="default" size="100%">Computer Methods and Programs in Biomedicine</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">92-100</style></pages><volume><style face="normal" font="default" size="100%">113</style></volume><number><style face="normal" font="default" size="100%">1</style></number><edition><style face="normal" font="default" size="100%">2013/11/21</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><isbn><style face="normal" font="default" size="100%">1872-7565</style></isbn><accession-num><style face="normal" font="default" size="100%">24252468</style></accession-num><abstract><style face="normal" font="default" size="100%">Release profile of drug constituent encapsulated in electrospun core-shell nanofibrous mats was modeled by Peppas equation and artificial neural network. Core-shell fibers were fabricated by co-axial electrospinning process using tetracycline hydrochloride (TCH) as the core and poly(l-lactide-co-glycolide) (PLGA) or polycaprolactone (PCL) as the shell materials. The density and hydrophilicity of the shell polymers, feed rates and concentrations of core and shell phases, the contribution of TCH in core material and electrical field were the parameters fed to the perceptron network to predict Peppas constants in order to derive release pattern. This study demonstrated the viability of the prediction tool in determining drug release profile of electrospun core-shell nanofibrous scaffolds.</style></abstract><label><style face="normal" font="default" size="100%">maleki2014release</style></label><notes><style face="normal" font="default" size="100%">Maleki, Mahboubeh&#xD;Amani-Tehran, Mohammad&#xD;Latifi, Masoud&#xD;Mathur, Sanjay&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;Ireland&#xD;Comput Methods Programs Biomed. 2014;113(1):92-100. doi: 10.1016/j.cmpb.2013.09.003. Epub 2013 Sep 14.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.cmpb.2013.09.003</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.cmpb.2013.09.003</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>282</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">282</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lehnen, Thomas</style></author><author><style face="normal" font="default" size="100%">Valldor, Martin</style></author><author><style face="normal" font="default" size="100%">Nižňanský, Daniel</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50931 Cologne, Germany&#xD;Univ Cologne, Phys Inst 2, D-50931 Cologne, Germany&#xD;Charles Univ Prague, Fac Sci, Dept Inorgan Chem, Prague, Czech Republic</style></auth-address><titles><title><style face="normal" font="default" size="100%">Hydrothermally grown porous FeVO4 nanorods and their integration as active material in gas-sensing devices</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Mater Chem A</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1862-1868</style></pages><volume><style face="normal" font="default" size="100%">2</style></volume><number><style face="normal" font="default" size="100%">6</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000329935700035</style></accession-num><abstract><style face="normal" font="default" size="100%">Controllable fabrication of highly porous iron vanadate (FeVO4) thick film consisting of disordered nanorods suitable for gas penetration and permeation was achieved by hydrothermal synthesis of fervanite-like FeVO4·1.1H2O. The subsequent dehydration to FeVO4 was studied by 57Fe Moessbauer spectroscopy ($\Delta$qS), DTA, magnetic susceptibility ($\chi$) and electron microscopy (REM/TEM). Their integration in gas sensing devices as porous layer via polymer-blended (PVDF) doctor-blading approach was successfully demonstrated followed by studies of their elec. properties and oxygen sensing capability. The probed I-U behavior and UV-visible measurements confirmed the semiconducting nature of triclinic FeVO4 (Eg = 2.72 eV) and exhibited an activation energy for elec. conduction of 0.46 eV. The best sensitivity of 0.29 ± 0.01 (m = -3.4 ± 0.1) could be obtained at an optimal working temp. of 250°.</style></abstract><label><style face="normal" font="default" size="100%">lehnen2014hydrothermally</style></label><notes><style face="normal" font="default" size="100%">292xj&#xD;Times Cited:33&#xD;Cited References Count:50</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://xlink.rsc.org/?DOI=C3TA12821K</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c3ta12821k</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>283</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">283</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lehnen, Thomas</style></author><author><style face="normal" font="default" size="100%">Schläfer, Johannes</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50931 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Rapid Microwave Synthesis of CeO2 Quantum Dots</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für Anorganische und Allgemeine Chemie</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Z Anorg Allg Chem</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></full-title></periodical><pages><style face="normal" font="default" size="100%">819-825</style></pages><volume><style face="normal" font="default" size="100%">640</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">April</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">00442313</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000333697200019</style></accession-num><abstract><style face="normal" font="default" size="100%">The synthesis and structural characterization of two new homo- and heteroleptic tetravalent Ce complexes with tert-butoxo and heteroarylalkenolate ligands Ce(OtBu)2-xLx+2 x = 2 (1), x = 0 (2) L = Dmox-CHC(CF3)O is described. Their thermal decompn. behavior as well as their potential as single-source precursor for the fabrication of nanostructured ceria was evaluated. By using the heteroleptic alkoxide complex 2 as metal org. precursor, an efficient synthesis of highly cryst. CeO2 QDs with a narrow size distribution was achieved by microwave assisted solvothermal synthesis in NMP. An expedient choice of precursor enabled the replacement of additives like bases or other mineralizer and opens an efficient pathway for controlled nucleation of metal oxide nanoparticles.</style></abstract><label><style face="normal" font="default" size="100%">lehnen2014rapid</style></label><notes><style face="normal" font="default" size="100%">Sp. Iss. SI&#xD;Ae1ai&#xD;Times Cited:12&#xD;Cited References Count:64</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/zaac.201300625</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/zaac.201300625</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>281</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">281</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Krais, Annette</style></author><author><style face="normal" font="default" size="100%">Wortmann, Laura</style></author><author><style face="normal" font="default" size="100%">Hermanns, Laura</style></author><author><style face="normal" font="default" size="100%">Feliu, Neus</style></author><author><style face="normal" font="default" size="100%">Vahter, Marie</style></author><author><style face="normal" font="default" size="100%">Stucky, Stefan</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Fadeel, Bengt</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Targeted uptake of folic acid-functionalized iron oxide nanoparticles by ovarian cancer cells in the presence but not in the absence of serum</style></title><secondary-title><style face="normal" font="default" size="100%">Nanomedicine: Nanotechnology, Biology, and Medicine</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1421-1431</style></pages><volume><style face="normal" font="default" size="100%">10</style></volume><number><style face="normal" font="default" size="100%">7</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><isbn><style face="normal" font="default" size="100%">1549-9642</style></isbn><abstract><style face="normal" font="default" size="100%">Targeted delivery of nanoparticles to cells or tissues of interest is arguably the &quot;holy grail&quot; of nanomedicine. Using primary human macrophages and ovarian cancer cells, we evaluated the biocompatibility and specific targeting of folic acid (FA)-conjugated iron oxide nanoparticles with organic poly(ethylene glycol), PEG or inorganic (SiO2) intermediate surface coatings. Reduction of folate receptor-$\alpha$ expression using specific siRNA resulted in a significant decrease in cellular uptake of the SiO2-coated nanoparticles, but did not affect uptake of PEG-coated nanoparticles. Notably, specific (i.e. FA-dependent) uptake was observed only in the presence of serum proteins. The strategy presented here for receptor-mediated uptake of nanoparticles with pre-defined surface chemistry may enable targeting of nanoparticles for therapeutic and imaging applications. From the clinical editor: In this study the receptor specific uptake of folic acid-functionalized iron oxide nanoparticles was determined in ovarian cancer cells. It was found that the presence of serum proteins is an absolute requirement for the uptake of these nanoparticles. The described strategy for receptor-mediated uptake of nanoparticles with pre-defined surface chemistry may enable a better targeting of nanoparticles for additional therapeutic and imaging applications.</style></abstract><label><style face="normal" font="default" size="100%">krais2014targeted</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.nano.2014.01.006</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>280</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">280</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jurewicz, Anna</style></author><author><style face="normal" font="default" size="100%">Arslan, Osman</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Evaluation Of Antibacterial Activity Of Metal Oxide Nanoparticles For Water Disinfection Applications</style></title><secondary-title><style face="normal" font="default" size="100%">38th International Conference and Expo on Advanced Ceramics and Composites</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2014, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><label><style face="normal" font="default" size="100%">Jurewicz2014</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>279</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">279</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Heidemann, Tim</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, Chair Inorgan &amp; Mat Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Air-Stable and Volatile Bis(pyridylalkenolato)germanium(II), -tin(II), and -lead(II) Complexes</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Eur J Inorg Chem</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">506-510</style></pages><volume><style face="normal" font="default" size="100%">2014</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1434-1948</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000329999400012</style></accession-num><abstract><style face="normal" font="default" size="100%">Homoleptic germanium(II), tin(II), and lead(II) complexes of the general formula M(2-PyCHCOCF3)(2) (M = Ge, Sn, Pb; Py = pyridine) were synthesized by treating the corresponding silyl amides [M{N(SiMe3)(2)}(2)] with two equivalents of a 3,3,3-trifluoro-1-(2-pyridyl)prop-1-en-2-ol (2-PyCHCOHCF3) ligand. Single-crystal X-ray diffraction revealed the bidentate chelation of 2-PyCHCOHCF3, which imposes a distorted trigonal bipyramidal geometry for all three molecular structures; this distortion is highest for the lead compound, probably as a result of the high s character of the lone pair of electrons present on the metal centers. The monomeric nature of the compounds in solution was confirmed by multinuclear NMR spectroscopy, whereas a polymeric structure is observed for the lead complex in the solid state.</style></abstract><label><style face="normal" font="default" size="100%">Heidemann2014</style></label><notes><style face="normal" font="default" size="100%">293uo&#xD;Times Cited:10&#xD;Cited References Count:30</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/ejic.201301054</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/ejic.201301054</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>277</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">277</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Govender, M.</style></author><author><style face="normal" font="default" size="100%">Mwakikunga, B. W.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Singh, T.</style></author><author><style face="normal" font="default" size="100%">Kaouk, A.</style></author><author><style face="normal" font="default" size="100%">Gönüllü, Y.</style></author><author><style face="normal" font="default" size="100%">Machatine, A. G. J.</style></author><author><style face="normal" font="default" size="100%">Kunert, H. W.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Selective room-temperature sensing of NO2 by WO3 film/graphene layers</style></title><secondary-title><style face="normal" font="default" size="100%">IEEE SENSORS 2014 Proceedings</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">301-304</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><abstract><style face="normal" font="default" size="100%">This is one of the first attempts of making WO3 thick film selective at low operating temperature by placing graphene sheets directly on the film surface. The WO3 film was prepared by DC magnetron reactive sputtering of a pure tungsten target and annealing in air. The thickness of the film averaged 507 nm from FIB cross-sectioning and STEM measurement. The film was characterized with XRD, XPS and Raman spectroscopy. Graphene was synthesized on copper foil using plasma enhanced chemical vapor deposition of methane gas, which was found to produce three monolayers of graphene sheets according to Raman spectroscopic analysis. The graphene was transferred onto the WO3 film and annealed. It was found that the pure WO3 sensed low concentrations of nitrogen dioxide at 30&amp;\#x00B0;C and 100&amp;\#x00B0;C operating temperature. The selectivity towards nitrogen dioxide over ammonia and carbon monoxide was achieved with graphene on the tungsten trioxide film at the compromise of sensitivity at both operating temperatures. The analysis of the graphene/WO3 composite orientation may lead to improved sensor capabilities as well as better understanding of the sensing mechanism.</style></abstract><label><style face="normal" font="default" size="100%">govender2014selective</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://ieeexplore.ieee.org/xpl/articleDetails.jsp?arnumber=6984993</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>278</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">278</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gönüllü, Yakup</style></author><author><style face="normal" font="default" size="100%">Kelm, Klemens</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Saruhan, Bilge</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Equivalent Circuit Models for Determination of the Relation between the Sensing Behavior and Properties of Undoped/Cr Doped TiO2 NTs</style></title><secondary-title><style face="normal" font="default" size="100%">Chemosensors</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">69-84</style></pages><volume><style face="normal" font="default" size="100%">2</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><isbn><style face="normal" font="default" size="100%">2227-9040</style></isbn><label><style face="normal" font="default" size="100%">Gonullu2014</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.mdpi.com/2227-9040/2/1/69/</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>276</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">276</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ghibelli, Lina</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Roma Tor Vergata, Dipartimento Biol, I-00173 Rome, Italy&#xD;Univ Cologne, Inst Inorgan Chem, Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Biological interactions of oxide nanoparticles: The good and the evil</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Bulletin</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Mrs Bull</style></alt-title></titles><pages><style face="normal" font="default" size="100%">949-954</style></pages><volume><style face="normal" font="default" size="100%">39</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0883-7694</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000345121300013</style></accession-num><abstract><style face="normal" font="default" size="100%">The biol. effects of engineered nanoparticles are presently a focus of interest in chem., biol., pharmacol., clin. medicine, and toxicol. due to the enormous therapeutic and diagnostic potential that the particulate nature of nanoparticles offers for selective drug delivery and controlled release. This raises unprecedented safety issues, calling for novel paradigms to face the biocompatibility anal. of particulate (as opposed to mol.) bioactive agents that vary in shape, surface, and charge, in addn. to chem. structure. This issue of MRS Bulletin focuses on the bioeffects of metal oxide nanostructures, whose high bioactivity can be exploited to design novel multifunctional devices for nanomedical applications, some of which are already undergoing testing in anticancer and antioxidant clin. trials. The ubiquitous application in research and technol. of these non-biodegradable structures has evoked concerns regarding their potential hazards, due to the same chem. activities that promise nanomedical developments. A Janus-type scenario is emerging, pointing to intricate networks of beneficial and detrimental effects following the biol. interactions of metal oxide nanoparticles.</style></abstract><label><style face="normal" font="default" size="100%">ghibelli2014biological</style></label><notes><style face="normal" font="default" size="100%">At7ml&#xD;Times Cited:0&#xD;Cited References Count:20</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1557/mrs.2014.250</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1557/mrs.2014.250</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>275</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">275</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gad, A.E.</style></author><author><style face="normal" font="default" size="100%">Hoffmann, M.W.G.</style></author><author><style face="normal" font="default" size="100%">Prades, J.D.</style></author><author><style face="normal" font="default" size="100%">Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Fiz, R.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Waag, A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Self-Powered Solar Diode Gas Sensors</style></title><secondary-title><style face="normal" font="default" size="100%">Extended Abstracts of the 2014 International Conference on Solid State Devices and Materials</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2014, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">September</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">The Japan Society of Applied Physics</style></publisher><label><style face="normal" font="default" size="100%">Gad2014</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://confit.atlas.jp/guide/organizer/ssdm/ssdm2014/subject/D-1-4/detail</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>274</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">274</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fornalczyk, Gregor</style></author><author><style face="normal" font="default" size="100%">Valldor, Martin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Max Planck Inst Chem Phys Fester Stoffe, D-01187 Dresden, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Monomeric Iron Heteroarylalkenolates: Structural Design Concepts and Investigations on Their Application in Chemical Vapor Deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Crystal Growth &amp; Design</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Cryst Growth Des</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1811-1818</style></pages><volume><style face="normal" font="default" size="100%">14</style></volume><number><style face="normal" font="default" size="100%">4</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">April</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1528-7483</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000333948000037</style></accession-num><abstract><style face="normal" font="default" size="100%">Aryl substituted beta-alkenol 1-(dimethyl-1,3-thiazol-2-yl)-3,3,3-trifluoropropenol (DMTTFP) was employed as an efficient metal chelator to obtain volatile monomeric precursors containing Fe-II and Fe-III centers. Fe(DMTTFP)(2) (1) and Fe(DMTTFP)(2)(OBut) (2) were synthesized by reacting suitable starting materials with DMTTFP. The molecular structures were elucidated by single-crystal X-ray diffraction analyses, which revealed a distorted tetrahedral and a trigonal-bipyramidal arrangement of ligands around iron atoms in 1 and 2, respectively. Magnetic investigations confirmed Fe(DMTTFP)(2) to exhibit a thermally populated spin-state transition that becomes apparent below 10 K. The high-spin state was gradually transferred to a low-spin state on cooling, suggesting a nonmagnetic ground state. Fe(DMTTFP)(2)(OBut) exhibited enhanced stability, sufficient volatility, and decomposition behavior serving as an efficient Fe-III precursor for the growth of iron oxide layers on an Al2O3 substrate via chemical vapor deposition.</style></abstract><label><style face="normal" font="default" size="100%">fornalczyk2014monomeric</style></label><notes><style face="normal" font="default" size="100%">Ae4jf&#xD;Times Cited:11&#xD;Cited References Count:38</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/cg401930n</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/cg401930n</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>273</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">273</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chyba, Jan</style></author><author><style face="normal" font="default" size="100%">Moravec, Zdenek</style></author><author><style face="normal" font="default" size="100%">Necas, Marek</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Pinkas, Jiri</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Masaryk Univ, Dept Chem, CZ-61137 Brno, Czech Republic&#xD;Masaryk Univ, CEITEC MU, CZ-61137 Brno, Czech Republic&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Nonaqueous synthesis of molecular zinc amide phosphate</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Organometallic Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Organomet Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">197-203</style></pages><volume><style face="normal" font="default" size="100%">749</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan 1</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0022328X</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000327939000030</style></accession-num><abstract><style face="normal" font="default" size="100%">Three new mol. zinc compds. were prepd. by nonaq. reactions of ZnN(SiMe3)22 and ZnEt2 with trimethylsilylesters of phosphoric acid, OP(OSiMe3)3 and OP(OSiMe3)2(OH). Single-crystal x-ray diffraction analyses of cryst. products revealed mol. structures of two mononuclear complexes ZnX2OP(OSiMe3)3 (X = N(SiMe3)2 (1), hexafluoroacetylacetonate (2)) and one dinuclear zinc phosphate (Zn\(py)N(SiMe3)2\\$\mu$2-O2P(OSiMe3)2\)2 (3). Compd. 1 is only the second structurally characterized adduct of zinc bisamide with an oxygen donor and a three-coordinate Zn atom. The cyclic inorg. core \Zn($\mu$2-O2PO2)\2 in 3 is a model for the most common single four-ring (S4R) building unit of open-framework zinc phosphates. The mol. of 3 possesses reactive amide and trimethylsiloxy groups that can be employed in further studies on the formation of extended structures by condensation reactions. Spectroscopic properties and thermal behavior of the mol. products were examd. Compds. 1 and 3 were converted to $\alpha$-Zn2P2O7 by calcination.</style></abstract><label><style face="normal" font="default" size="100%">chyba2014nonaqueous</style></label><notes><style face="normal" font="default" size="100%">265gu&#xD;Times Cited:3&#xD;Cited References Count:69</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.jorganchem.2013.09.040</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.jorganchem.2013.09.040</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>272</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">272</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chyba, Jan</style></author><author><style face="normal" font="default" size="100%">Moravec, Zdenek</style></author><author><style face="normal" font="default" size="100%">Necas, Marek</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Pinkas, Jiri</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Department of Chemistry, Faculty of Science, Masaryk University , Kotlarska 2, CZ-61137 Brno, Czech Republic.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Construction of Larger Molecular Aluminophosphate Cages from the Cyclic Four-Ring Building Unit</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">3753-3762</style></pages><volume><style face="normal" font="default" size="100%">53</style></volume><number><style face="normal" font="default" size="100%">7</style></number><edition><style face="normal" font="default" size="100%">2014/03/13</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style face="normal" font="default" size="100%">April</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1520-510X</style></isbn><accession-num><style face="normal" font="default" size="100%">24617956</style></accession-num><abstract><style face="normal" font="default" size="100%">New molecular aluminophosphates of different nuclearity are synthesized by a stepwise process and structurally characterized. The alkane elimination reaction of bis(trimethylsiloxy)phosphoric acid, OP(OH)(OSiMe3)2, with trialkylalanes, AlR3 (R = Me, Et, (i)Bu), provides the cyclic dimeric aluminophosphates, (AlR2\$\mu$2-O2P(OSiMe3)2\)2 (R = Me (1), Et (2), (i)Bu (3)). Unsymmetrically substituted cyclic aluminophosphonate (AlMe2\$\mu$2-O2P(OSiMe3)((c)Hex)\)2 (cis/trans-4) is prepared by dealkylsilylation reaction of (c)HexP(O)(OSiMe3)2 with AlMe3. Molecules 1-4 containing the Al2($\mu$2-O2P)2 inorganic core are structural and spectroscopic models for the single four-ring (S4R) secondary building units (SBU) of zeolite frameworks. Compound 1 serves as a starting point in construction of larger molecular units by reactions with OP(OH)(OSiMe3)2 as a cage-extending reagent and with diketones, such as Hhfacac (1,1,1,5,5,5-hexafluoropentan-2,4-dione) and Hacac (pentan-2,4-dione), as capping reagents. Reaction of 1 with 4 equiv of Hhfacac leads to new cyclic aluminophosphate (Al(hfacac)2\$\mu$2-O2P(OSiMe3)2\)2 (5), existing in two isomeric (D2 and C2h) forms. Reaction of 1 with 2 equiv of OP(OH)(OSiMe3)2 and 1 equiv of Hhfacac provides a molecular aluminophosphate AlMe\Al(hfacac)\2\$\mu$3-O3P(OSiMe3)\2\$\mu$2-O2P(OSiMe3)2\2ØP(OSiMe3)3\ (6), while by adding first the Hhfacac and using 3 equiv of OP(OH)(OSiMe3)2 we isolate Al\Al(hfacac)\2\$\mu$3-O3P(OSiMe3)\2\$\mu$2-O2P(OSiMe3)2\2HØP(O)(OSiMe3)2\2 (7). These molecules contain units in their cores that imitate 4=1 SBU of zeolite frameworks. Reaction with the order of component mixing 1, Hhfacac, OP(OH)(OSiMe3)2 at a 1:2:2 molar ratio lead to formation of a larger cluster (Al(AlMe)\Al(hfacac)\\$\mu$3-O3P(OSiMe3)\2\$\mu$2-O2P(OSiMe3)2\3)2 (8) containing both S4R and 4=1 structural units. Similarly, Hacac (pentan-2,4-dione) provides an isostructural (Al(AlMe)\Al(acac)\\$\mu$3-O3P(OSiMe3)\2\$\mu$2-O2P(OSiMe3)2\3)2 (9). Both molecules display Al centers in three different coordination environments.</style></abstract><label><style face="normal" font="default" size="100%">chyba2014construction</style></label><notes><style face="normal" font="default" size="100%">Chyba, Jan&#xD;Moravec, Zdenek&#xD;Necas, Marek&#xD;Mathur, Sanjay&#xD;Pinkas, Jiri&#xD;eng&#xD;Inorg Chem. 2014 Apr 7;53(7):3753-62. doi: 10.1021/ic500083a. Epub 2014 Mar 11.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/ic500083a</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/ic500083a</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>271</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">271</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Büyükyazi, Mehtap</style></author><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Lehnen, Thomas</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular Co(II) and Co(III) Heteroarylalkenolates as Efficient Precursors for Chemical Vapor Deposition of Co3O4 Nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">10928-10936</style></pages><volume><style face="normal" font="default" size="100%">53</style></volume><number><style face="normal" font="default" size="100%">20</style></number><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><isbn><style face="normal" font="default" size="100%">1520-510X</style></isbn><abstract><style face="normal" font="default" size="100%">Two new cobalt precursors, Co(II)(PyCHCOCF3)2(DMAP)2 (1) and Co(III)(PyCHCOCF3)3 (2), based on Co(II) and Co(III) centers were synthesized using a redox active ligand system. The different chemical configurations of 1 and 2 and differential valence states of cobalt were confirmed by crystal structure determination and comprehensive analytical studies. Whereas 1 could not be studied by NMR due to the paramagnetic nature of the central atom, 2 was unambiguously characterized by multinuclear 1D and 2D NMR experiments in solution. Both compounds are efficient precursors for catalyst-free growth of Co3O4 nanowires on Si and Al2O3 substrates by a chemical vapor deposition process. The different valence states of cobalt species influenced their chemical decomposition pathways in the gas phase; for instance, 1 was partially oxidized (Co(2+) → Co(3+)), and 2 underwent reduction (Co(3+) → Co(2+)) to form pure cobaltite in both cases that verified the metal-ligand redox interplay. Co3O4 nanowires with nanometric diameters (50-100 nm) were obtained irrespective of the chosen cobalt precursor. Investigations on the humidity sensing behavior of CVD deposits demonstrated their potential as promising sensor materials.</style></abstract><label><style face="normal" font="default" size="100%">buyukyazi2014molecular</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/ic501157e</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>270</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">270</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Aravindan, Vanchiappan</style></author><author><style face="normal" font="default" size="100%">Sundaramurthy, Jayaraman</style></author><author><style face="normal" font="default" size="100%">Kumar, Elumalai Naveen</style></author><author><style face="normal" font="default" size="100%">Kumar, Palaniswamy Suresh</style></author><author><style face="normal" font="default" size="100%">Ling, Wong Chui</style></author><author><style face="normal" font="default" size="100%">von Hagen, Robin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ramakrishna, Seeram</style></author><author><style face="normal" font="default" size="100%">Madhavi, Srinivasan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Does carbon coating really improves the electrochemical performance of electrospun SnO2 anodes?</style></title><secondary-title><style face="normal" font="default" size="100%">Electrochimica Acta</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">109-115</style></pages><volume><style face="normal" font="default" size="100%">121</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2014, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2014</style></year></dates><isbn><style face="normal" font="default" size="100%">0013-4686</style></isbn><abstract><style face="normal" font="default" size="100%">Abstract In this paper, we report the influence of carbon coating on the electrochemical performance of hollow structured SnO2 electrospun nanofibers. The electrospun nanofibers are subjected to plasma enhanced chemical vapour deposition for a conformal carbon coating of ∼6 nm thickness without destroying the one dimensional morphological features of the fiber mats. Li-storage properties are evaluated in half-cell configuration between two different potential windows i.e. 0.005-0.8 V and 0.005-2.5 V vs. Li. The potential regions tested corresponds to the alloying/de-alloying and alloying/de-alloying &amp; conversion reactions for former and latter cases, respectively. Very high reversibility over 3.6 moles of Li is feasible for both bare and carbon coated SnO2, without an obvious difference between the electrochemical profiles noted during cycling. In contrary, huge differences in the electrochemical performances are observed for bare and carbon coated SnO2 when the test cell is cycled for conversion reaction. This result clearly shows the importance of carbon coating for conversion reaction compared to alloying/de-alloying reaction.</style></abstract><label><style face="normal" font="default" size="100%">Aravindan2014109</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0013468613025942</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>338</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">338</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zopes, David</style></author><author><style face="normal" font="default" size="100%">Stein, Benjamin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Graf, Christina</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Department fur Chemie, Lehrstuhl fur Anorganische und Materialchemie, Universitat zu Koln , Greinstrasse 6, D-50939 Koln, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Improved Stability of &quot;Naked&quot; Gold Nanoparticles Enabled by in Situ Coating with Mono and Multivalent Thiol PEG Ligands</style></title><secondary-title><style face="normal" font="default" size="100%">Langmuir</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">11217-11226</style></pages><volume><style face="normal" font="default" size="100%">29</style></volume><number><style face="normal" font="default" size="100%">36</style></number><edition><style face="normal" font="default" size="100%">2013/08/03</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">September</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1520-5827</style></isbn><accession-num><style face="normal" font="default" size="100%">23906521</style></accession-num><abstract><style face="normal" font="default" size="100%">Unprotected (&quot;naked&quot;) gold nanoparticles with high monodispersity (d, 5.5± 0.5 nm) were obtained in a facile and single-step microwave-assisted hydrolytic decomposition of the molecular precursor NMe4Au(CF3)2. Given their chloride-free surface chemistry, the as-obtained gold nanoparticles were in situ functionalized with mono-, di-, and trivalent thiolated PEG ligands in order to study the influence of multivalent character of the ligands on the stability of the colloidal solutions. For this purpose, a novel tridentate ligand was synthesized and the previously reported syntheses of mono- and divalent thiol ligands were improved. Owing to the pristine character of the Au nanoparticles no ligand exchange was required, and the colloidal and chemical stability of the mono- and multivalent functionalized particles purely depended on the ligating ability of the thiolated groups. In situ-functionalized Au nanoparticles showed a strikingly (2 orders of magnitude higher) improved stability against small nucleophiles such as sodium cyanide compared to gold nanoparticles coated with citrate ligands and functionalized via a ligand-exchange reaction. The monovalent thiol PEG ligand produced most stable colloids against cyanide, which is explained by a strongly increased numerical ligand-density on the surface. Gold colloids stabilized by di- and trivalent ligands exhibited high stability in aqueous solutions with high NaCl concentrations (2 M) in contrast to those functionalized with the monovalent PEG ligand, which were only temporally stable in dilute NaCl solutions. The beneficial effect of the multivalence of the ligands was further demonstrated by the incorporation of an additional chelating ligand (dithiothreitol) to the colloidal dispersions.</style></abstract><label><style face="normal" font="default" size="100%">zopes2013improved</style></label><notes><style face="normal" font="default" size="100%">Zopes, David&#xD;Stein, Benjamin&#xD;Mathur, Sanjay&#xD;Graf, Christina&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;Langmuir. 2013 Sep 10;29(36):11217-26. doi: 10.1021/la4012058. Epub 2013 Aug 27.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/la4012058</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/la4012058</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>337</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">337</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zamani, Reza</style></author><author><style face="normal" font="default" size="100%">Fiz, Raquel</style></author><author><style face="normal" font="default" size="100%">Pan, Jun</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Morante, Joan Ramon</style></author><author><style face="normal" font="default" size="100%">Arbiol, Jordi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Oxide–oxide nanojunctions in coaxial SnO2/TiO2, SnO2/V2O3 and SnO2/(Ti0.5V0.5)2O3 nanowire heterostructures</style></title><secondary-title><style face="normal" font="default" size="100%">CrystEngComm</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">4532-4539</style></pages><volume><style face="normal" font="default" size="100%">15</style></volume><number><style face="normal" font="default" size="100%">22</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><isbn><style face="normal" font="default" size="100%">1466-8033</style></isbn><abstract><style face="normal" font="default" size="100%">A single-cryst. shell based on titanium and vanadium binary oxides with karelianite structure (Ti1-xVx)2O3 was successfully deposited onto SnO2 nanowires by sequential chem. vapor deposition (CVD). In comparison to single titanium or vanadium oxide shells, the binary Ti-V metal oxide overlayer overcomes the problems related to lattice mismatch and thermochem. stability, which usually take place in coaxial oxide-oxide heterostructures due to the at. diffusion between core and shell. The modulation of the titanium content in the binary (Ti1-xVx)2O3 karelianite shell results in a lower mismatch (∼1.5\%) and improves the epitaxial relationship with the rutile lattice of SnO2 core nanowires. Therefore, the presence of defects such as dislocations and strain fields, which in principle limit the carrier transport properties affecting the elec., optical and photocatalytic performance, is strongly reduced. Atomic model simulations confirm that structural characteristics related to lattice mismatch and strain accommodation at the heterojunction influence the thermochem. stability and were corroborated by detailed high resoln. transmission electron microscopy analyses of the different core-shell systems.</style></abstract><label><style face="normal" font="default" size="100%">zamani2013oxideoxide</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://xlink.rsc.org/?DOI=c3ce26672a</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>336</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">336</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">von Hagen, Robin</style></author><author><style face="normal" font="default" size="100%">Lepcha, Ashish</style></author><author><style face="normal" font="default" size="100%">Song, Xuefeng</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of electrode design on the electrochemical performance of Li3V2(PO4)3/C nanocomposite cathode in lithium ion batteries</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><pages><style face="normal" font="default" size="100%">304-313</style></pages><volume><style face="normal" font="default" size="100%">2</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><isbn><style face="normal" font="default" size="100%">22112855</style></isbn><abstract><style face="normal" font="default" size="100%">A new alkoxide-based sol contg. lithium isopropoxide, vanadyl isopropoxide, di-n-butyl-phosphate, acetic-acid and polyvinylpyrrolidone, was used for the synthesis of monoclinic $\alpha$-Li3V2(PO4)3/C composites by sol-gel and electrospinning techniques. The precursor mixt. was highly sol. in org. solvents and thereby suitable for different synthesis techniques like sol-gel electrospinning or conventional sol-gel synthesis, to generate $\alpha$-Li3V2(PO4)3/C nanocomposites with zero- and one-dimensionality. Electrospinning resulted in well-defined nanofibers and conventional sol-gel synthesis in polydisperse, isotropic nanoparticles. Phase compn. and morphol. in the composite nanostructures was examd. by XRD, TGA, FT-IR, Raman, SEM and HR-TEM anal. Comparative const.-current and cyclovoltammetric measurements of $\alpha$-Li3V2(PO4)3/C composite applied as conventional film electrodes (nanoparticles and nanofibers) and self-supporting nanofiber electrodes revealed the influence of electrode texturing on the electrochem. performances. The nanofibrous self-supported electrodes showed superior cycling stability giving an initial discharge capacity of 124 mA h g-1 at 0.2 °C with retention of 95\% after 50 cycles with rate variation in a voltage range of 3-4.3 V.</style></abstract><label><style face="normal" font="default" size="100%">vonhagen2013influence</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S2211285512002042</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>335</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">335</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tuomela, Soile</style></author><author><style face="normal" font="default" size="100%">Autio, Reija</style></author><author><style face="normal" font="default" size="100%">Buerki-Thurnherr, Tina</style></author><author><style face="normal" font="default" size="100%">Arslan, Osman</style></author><author><style face="normal" font="default" size="100%">Kunzmann, Andrea</style></author><author><style face="normal" font="default" size="100%">Andersson-Willman, Britta</style></author><author><style face="normal" font="default" size="100%">Wick, Peter</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Scheynius, Annika</style></author><author><style face="normal" font="default" size="100%">Krug, Harald F.</style></author><author><style face="normal" font="default" size="100%">Fadeel, Bengt</style></author><author><style face="normal" font="default" size="100%">Lahesmaa, Riitta</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Turku Centre for Biotechnology, University of Turku and Abo Akademi University, Turku, Finland.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Gene Expression Profiling of Immune-Competent Human Cells Exposed to Engineered Zinc Oxide or Titanium Dioxide Nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">PloS One</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">e68415</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">7</style></number><edition><style face="normal" font="default" size="100%">2013/07/31</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><isbn><style face="normal" font="default" size="100%">1932-6203</style></isbn><accession-num><style face="normal" font="default" size="100%">23894303</style></accession-num><abstract><style face="normal" font="default" size="100%">A comprehensive in vitro assessment of two commercial metal oxide nanoparticles, TiO2 and ZnO, was performed using human monocyte-derived macrophages (HMDM), monocyte-derived dendritic cells (MDDC), and Jurkat T cell leukemia-derived cell line. TiO2 nanoparticles were found to be non-toxic whereas ZnO nanoparticles caused dose-dependent cell death. Subsequently, global gene expression profiling was performed to identify transcriptional response underlying the cytotoxicity caused by ZnO nanoparticles. Analysis was done with doses 1 µg/ml and 10 µg/ml after 6 and 24 h of exposure. Interestingly, 2703 genes were significantly differentially expressed in HMDM upon exposure to 10 µg/ml ZnO nanoparticles, while in MDDCs only 12 genes were affected. In Jurkat cells, 980 genes were differentially expressed. It is noteworthy that only the gene expression of metallothioneins was upregulated in all the three cell types and a notable proportion of the genes were regulated in a cell type-specific manner. Gene ontology analysis revealed that the top biological processes disturbed in HMDM and Jurkat cells were regulating cell death and growth. In addition, genes controlling immune system development were affected. Using a panel of modified ZnO nanoparticles, we obtained an additional support that the cellular response to ZnO nanoparticles is largely dependent on particle dissolution and show that the ligand used to modify ZnO nanoparticles modulates Zn(2+) leaching. Overall, the study provides an extensive resource of transcriptional markers for mediating ZnO nanoparticle-induced toxicity for further mechanistic studies, and demonstrates the value of assessing nanoparticle responses through a combined transcriptomics and bioinformatics approach.</style></abstract><label><style face="normal" font="default" size="100%">tuomela2013expression</style></label><notes><style face="normal" font="default" size="100%">Tuomela, Soile&#xD;Autio, Reija&#xD;Buerki-Thurnherr, Tina&#xD;Arslan, Osman&#xD;Kunzmann, Andrea&#xD;Andersson-Willman, Britta&#xD;Wick, Peter&#xD;Mathur, Sanjay&#xD;Scheynius, Annika&#xD;Krug, Harald F&#xD;Fadeel, Bengt&#xD;Lahesmaa, Riitta&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;PLoS One. 2013 Jul 22;8(7):e68415. doi: 10.1371/journal.pone.0068415. Print 2013.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1371/journal.pone.0068415</style></url></related-urls></urls><custom2><style face="normal" font="default" size="100%">PMC3718780</style></custom2><electronic-resource-num><style face="normal" font="default" size="100%">10.1371/journal.pone.0068415</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>334</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">334</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tkach, Alexey V.</style></author><author><style face="normal" font="default" size="100%">Yanamala, Naveena</style></author><author><style face="normal" font="default" size="100%">Stanley, Shyla</style></author><author><style face="normal" font="default" size="100%">Shurin, Michael R.</style></author><author><style face="normal" font="default" size="100%">Shurin, Galina V.</style></author><author><style face="normal" font="default" size="100%">Kisin, Elena R.</style></author><author><style face="normal" font="default" size="100%">Murray, Ashley R.</style></author><author><style face="normal" font="default" size="100%">Pareso, Samantha</style></author><author><style face="normal" font="default" size="100%">Khaliullin, Timur</style></author><author><style face="normal" font="default" size="100%">Kotchey, Gregg P.</style></author><author><style face="normal" font="default" size="100%">Castranova, Vincent</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Fadeel, Bengt</style></author><author><style face="normal" font="default" size="100%">Star, Alexander</style></author><author><style face="normal" font="default" size="100%">Kagan, Valerian E.</style></author><author><style face="normal" font="default" size="100%">Shvedova, Anna A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Graphene Oxide, But Not Fullerenes, Targets Immunoproteasomes and Suppresses Antigen Presentation by Dendritic Cells</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Small</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1686-1690</style></pages><volume><style face="normal" font="default" size="100%">9</style></volume><number><style face="normal" font="default" size="100%">9-10</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><isbn><style face="normal" font="default" size="100%">1613-6829</style></isbn><abstract><style face="normal" font="default" size="100%">Graphene oxide (GO) and C60 - or C60 -TRIS fullerenes, internalized by murine dendritic cells (DCs), differently affect their abilities to present antigens to T-cells. While C60 -fullerenes stimulate the ovalbumin-specific MHC class I-restricted T-cell response, GO impairs the stimulatory potential of DCs. In contrast to C60 -fullerenes, GO decreases the intracellular levels of LMP7 immunoproteasome subunits required for processing of protein antigens. This is important for the development of DC-based vaccines.</style></abstract><label><style face="normal" font="default" size="100%">tkach2013graphene</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/smll.201201546</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>333</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">333</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Song, Xuefeng</style></author><author><style face="normal" font="default" size="100%">Pan, Jun</style></author><author><style face="normal" font="default" size="100%">Xiao, Lisong</style></author><author><style face="normal" font="default" size="100%">Gao, Lian</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">School of Materials Science and Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, People&apos;s Republic of China. songxfeng@sjtu.edu.cn</style></auth-address><titles><title><style face="normal" font="default" size="100%">A hierarchical hybrid design for high performance tin based Li-ion battery anodes</style></title><secondary-title><style face="normal" font="default" size="100%">Nanotechnology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">205401</style></pages><volume><style face="normal" font="default" size="100%">24</style></volume><number><style face="normal" font="default" size="100%">20</style></number><edition><style face="normal" font="default" size="100%">2013/04/20</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0957-4484</style></isbn><accession-num><style face="normal" font="default" size="100%">23598519</style></accession-num><abstract><style face="normal" font="default" size="100%">Novel hierarchical hybrids, tin dioxide@carbon hollow spheres with encapsulated tin nanoparticles (SnO2@HCS@Sn), were fabricated by combining solution and vapor phase techniques. The phase composition, morphological evolution and porosity of the hierarchical hybrids were characterized by x-ray diffraction, energy dispersive x-ray spectroscopy, scanning and transmission electron microscopy, and N2 adsorption–desorption analysis. The significantly improved electrochemical performance of this functional material is attributed to its heterogeneous architecture which unifies hollow carbon spheres with tin nanoparticles with a diameter of less than 20 nm, which are further conformally covered by ultra-small tin dioxide nanoplates. The ultrathin SnO2 nanoplates grown on the carbon spheres effectively increase the charge-transfer properties and shorten the transport lengths for both electrons and lithium ions. The mesoporous carbon spheres offer excellent conductivity and abundant void space to buffer the large volume change during cycling. High initial capacity (\~1766 mAh g−1 at 0.1 Ag−1), high initial Coulombic efficiency (56.4\%), and long cycle life (100 cycles with \~710 mAh g−1) have been realized in the hierarchical hybrid tin-based anodes.</style></abstract><label><style face="normal" font="default" size="100%">song2013hierarchical</style></label><notes><style face="normal" font="default" size="100%">Song, Xuefeng&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;England&#xD;Nanotechnology. 2013 May 24;24(20):205401. doi: 10.1088/0957-4484/24/20/205401. Epub 2013 Apr 19.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://stacks.iop.org/0957-4484/24/i=20/a=205401?key=crossref.159ca93dca003d8f48756dbe09b5839e</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1088/0957-4484/24/20/205401</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>332</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">332</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Singh, Trilok</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Singh, Jai</style></author><author><style face="normal" font="default" size="100%">Gurram, Sanjeev Kumar</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Kirihara, Soshu</style></author><author><style face="normal" font="default" size="100%">Widjaja, Sujanto</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Plasma Enhanced CVD of Transparent and Conductive Tin Oxide Thin Films</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology VII</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">99-105</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><label><style face="normal" font="default" size="100%">Singh2013</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/9781118807828.ch9</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>331</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">331</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Singh, Dileep</style></author><author><style face="normal" font="default" size="100%">Salem, Jonathan</style></author><author><style face="normal" font="default" size="100%">Halbig, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Mechanical Properties and Performance of Engineering Ceramics and Composites VII: Ceramic Engineering and Science Proceedings, Volume 33, Issue 2, 2012</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><publisher><style face="normal" font="default" size="100%">Wiley</style></publisher><isbn><style face="normal" font="default" size="100%">978-1-118-20588-4</style></isbn><abstract><style face="normal" font="default" size="100%">This collection of 33 papers deals with mechanical behaviors associated with systems ranging from diamond reinforced silicon carbide to rare earth pyrosilicates. Presented at The Mechanical Behavior and Performance of Ceramics &amp; Composites Symposium in January 2012 during the 36th International Conference on Advanced Ceramics and Composites (ICACC), it offers researchers from around the world the opportunity to explore new and emerging issues in all aspects of the field.</style></abstract><label><style face="normal" font="default" size="100%">singh2013mechanical</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://eu.wiley.com/WileyCDA/WileyTitle/productCd-111820588X.html</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>330</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">330</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hoffmann, Martin Wolfgang Georg</style></author><author><style face="normal" font="default" size="100%">Gad, Alaa Eldin Abd Eltawab Mohamed</style></author><author><style face="normal" font="default" size="100%">Prades Garcia,, Juan Daniel</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fluid detector and method for detecting fluids</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><abstract><style face="normal" font="default" size="100%">The present invention relates to a fluid detector comprising at least one semiconductor detector cell, the semiconductor detector cell including: - a photovoltaic semiconductor device with at least one portion made of a 1st semiconducting type material and at least one other portion made of a 2nd semiconducting type material, wherein the 1st and 2nd semiconducting type materials differ in their charge carrier types and/or the d. of their charge carriers and wherein the different portions adjoin each other with the formation of a junction between said different charge carrier types and/or charge carrier densities; and - a system for photo-induced electron transfer, the system comprising a plurality of semiconducting nanoparticles on at least one surface area of the portion made of the 2nd semiconducting type material, wherein said surface area is accessible for the fluid. The invention further relates to a corresponding detecting method.</style></abstract><label><style face="normal" font="default" size="100%">shen2013fluid</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://patents.google.com/patent/EP2565645A1/en</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">misc</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>329</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">329</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shao, F.</style></author><author><style face="normal" font="default" size="100%">Hoffmann, M. W. G.</style></author><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Zamani, R.</style></author><author><style face="normal" font="default" size="100%">Arbiol, J.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author><author><style face="normal" font="default" size="100%">Varechkina, E.</style></author><author><style face="normal" font="default" size="100%">Rumyantseva, M.</style></author><author><style face="normal" font="default" size="100%">Gaskov, A.</style></author><author><style face="normal" font="default" size="100%">Giebelhaus, I.</style></author><author><style face="normal" font="default" size="100%">Fischer, T.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Hernández-Ramírez, F.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Catalonia Inst Energy Res IREC, E-08930 St Adria Del Besos, Spain&#xD;Univ Barcelona, Dept Elect, E-08028 Barcelona, Spain&#xD;ICMAB CSIC, Inst Ciencia Mat Barcelona, E-08193 Bellaterra, Spain&#xD;ICREA, E-08010 Barcelona, Spain&#xD;Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119991, Russia&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Heterostructured p-CuO (nanoparticle)/n-SnO2 (nanowire) devices for selective H2S detection</style></title><secondary-title><style face="normal" font="default" size="100%">Sensors and Actuators B: Chemical</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Sensor Actuat B-Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">130-135</style></pages><volume><style face="normal" font="default" size="100%">181</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09254005</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000317941100019</style></accession-num><abstract><style face="normal" font="default" size="100%">Dihydrogen sulphide (H2S) is a dangerous pollutant released in fossil combustion processes. Here, p-CuO (particle)/n-SnO2 (nanowire) heterostructures were evaluated as selective H2S sensors, and the working principle behind their good performance was qualitatively modelled. It was concluded that the main sensing mechanism was dissimilar to standard redox reactions typical of simple metal oxide devices, but ascribable to the sulphurization of CuO and the consequent variation of the pn-junction band structure at the CuO-SnO2 interfaces. Experimental data showed that these H2S sensors suit well for alarm applications with extremely high selectivity and sensitivity to this gas for concentrations between 1 ppm and 10 ppm. (C) 2013 Elsevier B.V. All rights reserved.</style></abstract><label><style face="normal" font="default" size="100%">shao2013heterostructured</style></label><notes><style face="normal" font="default" size="100%">130st&#xD;Times Cited:98&#xD;Cited References Count:25</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.snb.2013.01.067</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.snb.2013.01.067</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>328</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">328</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Schläfer, Johannes</style></author><author><style face="normal" font="default" size="100%">Stucky, Stefan</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Institute of Inorganic Chemistry, University of Cologne, Greinstrasse 6, D-50939 Cologne, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Heterobi- and Trimetallic Cerium(IV) tert -Butoxides with Mono-, Di-, and Trivalent Metals (M = K(I), Ge(II), Sn(II), Pb(II), Al(III), Fe(III))</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">4002-4010</style></pages><volume><style face="normal" font="default" size="100%">52</style></volume><number><style face="normal" font="default" size="100%">7</style></number><edition><style face="normal" font="default" size="100%">2013/03/14</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">April</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1520-510X (Electronic)&#xD;0020-1669 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">23480730</style></accession-num><abstract><style face="normal" font="default" size="100%">The reaction of Cerium Ammonium Nitrate (CAN) with varying amounts of KO(t)Bu produced homometallic Ce(O(t)Bu)4(NC5H5)2 (1) and the heterometallic derivative KCe2(O(t)Bu)10 (3) characterized by X-ray diffraction and NMR spectroscopy. The oxo-alkoxide cluster Ce3O(O(t)Bu)9 (2) was obtained from a solution of cerium(IV) tetrakis(tert-butoxide) in n-heptane under stringent precautions to avoid any adventitious hydrolysis. Lewis acid-base reactions of in situ generated Ce(O(t)Bu)4(THF)2 (THF = tetrahydrofuran) with bi- and trivalent metal alkoxides M(O(t)Bu)xn (M = Ge, Sn; x = 2; n = 2; M = Pb, x = 2; n = 3; M = Al, Fe; x = 3; n = 2) resulted in volatile products of the general formula MCe(O(t)Bu)(4+x) (M = Al (4), Fe (5); x = 3; M = Ge (8), Sn (9), Pb (10); x = 2) in high yields. By dissolving 4 and 5 in pyridine the solvent adducts MCe(O(t)Bu)7(NC5H5) (M = Al (6), Fe (7)) were formed, whereas 8 and 9 reacted with Mo(CO)6 in boiling toluene to yield the termetallic complexes (CO)5MoM($\mu$2-O(t)Bu)3Ce(O(t)Bu)3 (M = Ge (11), Sn (12)). The new compounds were characterized by comprehensive spectral studies, mass spectroscopy, and single crystal X-ray diffraction analysis.</style></abstract><label><style face="normal" font="default" size="100%">schlafer2013heterobi</style></label><notes><style face="normal" font="default" size="100%">Schlafer, Johannes&#xD;Stucky, Stefan&#xD;Tyrra, Wieland&#xD;Mathur, Sanjay&#xD;eng&#xD;Inorg Chem. 2013 Apr 1;52(7):4002-10. doi: 10.1021/ic400030j. Epub 2013 Mar 12.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/ic400030j</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/ic400030j</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>326</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">326</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mwakikunga, Bonex Wakufwa</style></author><author><style face="normal" font="default" size="100%">Ray, Suprakas Sihna</style></author><author><style face="normal" font="default" size="100%">Mokwena, Malose</style></author><author><style face="normal" font="default" size="100%">Dewar, John</style></author><author><style face="normal" font="default" size="100%">Geibelhaus, Irina</style></author><author><style face="normal" font="default" size="100%">Singh, Trilok</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Tin dioxide nano-wire device for sensing kinetics of acetone and ethanol towards diabetes monitoring</style></title><secondary-title><style face="normal" font="default" size="100%">SENSORS, 2013 IEEE</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1-4</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><label><style face="normal" font="default" size="100%">mwakikunga2013dioxide</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://ieeexplore.ieee.org/lpdocs/epic03/wrapper.htm?arnumber=6688338</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>327</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">327</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Müller, R.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Graphene-SnO2 Nanocomposites for Lithium-Ion Battery Anodes</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology VII</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">67-73</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><label><style face="normal" font="default" size="100%">muller2013graphenesno2</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/9781118807828.ch6</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>325</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">325</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Miguel, F. L.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Soldera, F.</style></author><author><style face="normal" font="default" size="100%">Fischer, T.</style></author><author><style face="normal" font="default" size="100%">Müller, R.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Mücklich, F.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Chair Funct Mat, D-66123 Saarbrucken, Germany&#xD;Univ Cologne, Chair Inorgan &amp; Mat Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Electroless deposition of a Ag matrix on semiconducting one-dimensional nanostructures</style></title><secondary-title><style face="normal" font="default" size="100%">Thin Solid Films</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Thin Solid Films</style></alt-title></titles><pages><style face="normal" font="default" size="100%">54-56</style></pages><volume><style face="normal" font="default" size="100%">536</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun 1</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0040-6090</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000318974800006</style></accession-num><abstract><style face="normal" font="default" size="100%">Composite materials consisting of one-dimensional semiconducting nanostructures embedded in a Ag matrix were produced. The regarded nanostructures are hydrothermally grown TiO2 nanorods and SnO2 nanowires obtained by chemical vapor deposition with a vapor-liquid-solid growth process. The Ag was deposited by means of electroless plating, for which AgNO3 was employed as the Ag+ source and a glucose-based aqueous solution as the reducing agent. Cross-section micrographs obtained through scanning electron microscopy show homogeneous and compact Ag coatings, which penetrated down to the substrate level filling the space between the oxide structures. Additionally, the SnO2 composite was analyzed by focused ion beam nanotomography with a measured porosity of 0.1 The obtained materials are potential candidates for electrical contacts applications.</style></abstract><label><style face="normal" font="default" size="100%">miguel2013electroless</style></label><notes><style face="normal" font="default" size="100%">144xi&#xD;Times Cited:5&#xD;Cited References Count:7</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.tsf.2013.03.054</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.tsf.2013.03.054</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>320</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">320</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">von Hagen, Robin</style></author><author><style face="normal" font="default" size="100%">Müller, Ralf</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Reedijk, Jan</style></author><author><style face="normal" font="default" size="100%">Poeppelmeier, Ken</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">1D Inorganic Nanomaterials for Energy Applications</style></title><secondary-title><style face="normal" font="default" size="100%">Comprehensive Inorganic Chemistry II</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><publisher><style face="normal" font="default" size="100%">Elsevier</style></publisher><abstract><style face="normal" font="default" size="100%">Comprehensive Inorganic Chemistry II reviews and examines topics of relevance to today’s inorganic chemists. Covering more interdisciplinary and high impact areas, Comprehensive Inorganic Chemistry II includes biological inorganic chemistry, solid state chemistry, materials chemistry, and nanoscience. The work is designed to follow on, with a different viewpoint and format, from our 1973 work, Comprehensive Inorganic Chemistry, edited by Bailar, Emeléus, Nyholm, and Trotman-Dickenson, which has received over 2,000 citations. The new work will also complement other recent Elsevier works in this area, Comprehensive Coordination Chemistry and Comprehensive Organometallic Chemistry, to form a trio of works covering the whole of modern inorganic chemistry. Chapters are designed to provide a valuable, long-standing scientific resource for both advanced students new to an area and researchers who need further background or answers to a particular problem on the elements, their compounds, or applications. Chapters are written by teams of leading experts, under the guidance of the Volume Editors and the Editors-in-Chief. The articles are written at a level that allows undergraduate students to understand the material, while providing active researchers with a ready reference resource for information in the field. The chapters will not provide basic data on the elements, which is available from many sources (and the original work), but instead concentrate on applications of the elements and their compounds.</style></abstract><label><style face="normal" font="default" size="100%">mathur2013inorganic</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.researchgate.net/publication/256456373_1D_Inorganic_Nanomaterials_for_Energy_Applications</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>324</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">324</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Singh, Trilok</style></author><author><style face="normal" font="default" size="100%">Maleki, Mahboubeh</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Taubert, Andreas</style></author><author><style face="normal" font="default" size="100%">Mano, Joäo F.</style></author><author><style face="normal" font="default" size="100%">Rodríguez-Cabello, J. Carlos</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Plasma-Assisted Surface Treatments and Modifications for Biomedical Applications</style></title><secondary-title><style face="normal" font="default" size="100%">Biomaterials Surface Science</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">375-408</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><publisher><style face="normal" font="default" size="100%">Wiley-VCH Verlag GmbH &amp; Co. KGaA</style></publisher><isbn><style face="normal" font="default" size="100%">9783527649600</style></isbn><label><style face="normal" font="default" size="100%">mathur2013plasmaassisted</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/9783527649600.ch13</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>321</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">321</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ray, Suprakas Sinha</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology VI: Ceramic Engineering and Science Proceedings, Volume 33, Issue 7</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><isbn><style face="normal" font="default" size="100%">978-1-118-20597-6</style></isbn><label><style face="normal" font="default" size="100%">noauthororeditor2013nanostructured</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://eu.wiley.com/WileyCDA/WileyTitle/productCd-1118205979,subjectCd-CE80.html</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>322</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">322</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Kirihara, Soshu</style></author><author><style face="normal" font="default" size="100%">Widjaja, Sujanto</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology VII: Ceramic Engineering and Science Proceedings, Volume 34, Issue 7</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><publisher><style face="normal" font="default" size="100%">Wiley</style></publisher><isbn><style face="normal" font="default" size="100%">1118807626</style></isbn><label><style face="normal" font="default" size="100%">mathur2013nanostructured</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/9781118807828</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>323</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">323</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">One Dimensional Inorganic Nanomaterials for Energy Storage and Production</style></title><secondary-title><style face="normal" font="default" size="100%">International Photonics and Optoelectronics Meetings (POEM)</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">NSa2A.2</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2013, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><pub-location><style face="normal" font="default" size="100%">Washington, D.C.</style></pub-location><publisher><style face="normal" font="default" size="100%">OSA</style></publisher><isbn><style face="normal" font="default" size="100%">978-1-55752-976-3</style></isbn><label><style face="normal" font="default" size="100%">Mathur2013</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.osapublishing.org/abstract.cfm?uri=N3-2013-NSa2A.2</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>318</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">318</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Maleki, Mahboubeh</style></author><author><style face="normal" font="default" size="100%">Latifi, Masoud</style></author><author><style face="normal" font="default" size="100%">Amani-Tehran, Mohammad</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Amirkabir Univ Technol, Dept Text Engn, Tehran 1591634311, Iran&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Electrospun core-shell nanofibers for drug encapsulation and sustained release</style></title><secondary-title><style face="normal" font="default" size="100%">Polymer Engineering &amp; Science</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Polym Eng Sci</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1770-1779</style></pages><volume><style face="normal" font="default" size="100%">53</style></volume><number><style face="normal" font="default" size="100%">8</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">August</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">00323888</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000321821700023</style></accession-num><abstract><style face="normal" font="default" size="100%">Fabrication of core-shell nanofibers by coaxial electrospinning system suited for drug delivery applications was investigated based on tetracycline hydrochloride (TCH) as the core and poly(lactide-co-glycolide) as the shell materials. Comparison of drug release from monolithic fibers (blend electrospinning) and core-shell structures was performed to evaluate the efficacy of the core-shell morphol. The nanofibrous webs are potentially interesting for wound healing purposes since they can be maintained for an adequate length of time to gradually disinfect a local area without the need of bandage renewal. Further, our studies showed the potential of core-shell nanostructures for sustained drug release, which also suppressed the burst release effect from 62 to 44\% in the first 3 h by adding only 1 wt\% TCH to the polymeric shell. POLYM. ENG. SCI., 2013. © 2013 Society of Plastics Engineers.</style></abstract><label><style face="normal" font="default" size="100%">maleki2013electrospun</style></label><notes><style face="normal" font="default" size="100%">183nb&#xD;Times Cited:43&#xD;Cited References Count:58</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/pen.23426</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/pen.23426</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>317</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">317</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Maleki, Mahboubeh</style></author><author><style face="normal" font="default" size="100%">Amani-Tehran, Mohammad</style></author><author><style face="normal" font="default" size="100%">Latifi, Masoud</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Study on Electrospun Nanofibrous Mats for Local Antibiotic Delivery</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Materials Research</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">510-514</style></pages><volume><style face="normal" font="default" size="100%">829</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1662-8985</style></isbn><abstract><style face="normal" font="default" size="100%">The demand for novel antibiotic-loaded electrospun nanofibrous structures has increased extremely in the recent years and has engaged the interests of scientists and engineers into a blend configuration of antibiotic drug and biocompatible polymers due to their unique applications in future of better therapeutic effect, reduced toxicity and sustained local antibiotic release over a period of time. One method to produce these antibiotic-loaded networks is by electrospinning process. However, it is very important to know structural characteristics and morphol. of nanofibers for controlling the performance of the yields. In this paper, fabrication of electrospun nanofibers suited for antibiotic delivery system is investigated based on tetracycline hydrochloride as the antibiotic drug and poly (lactic-co-glycolic acid) as the biodegradable polymeric matrix. Furthermore, the effect of material and process parameters on morphol. and release behavior of produced nonwovens is investigated. The efficacy of the medicated scaffolds using a static system for bacterial growth on agar plates was also proved.</style></abstract><label><style face="normal" font="default" size="100%">maleki2013study</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.scientific.net/AMR.829.510</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>316</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">316</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Khan, Tamanna K.</style></author><author><style face="normal" font="default" size="100%">Bröring, Martin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ravikanth, Mangalampalli</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Tech Univ Carolo Wilhelmina Braunschweig, Inst Inorgan &amp; Analyt Chem, D-3810 Braunschweig, Germany&#xD;Indian Inst Technol, Dept Chem, Bombay 400076, Maharashtra, India</style></auth-address><titles><title><style face="normal" font="default" size="100%">Boron dipyrrin-porphyrin conjugates</style></title><secondary-title><style face="normal" font="default" size="100%">Coordination Chemistry Reviews</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Coordin Chem Rev</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Coordination Chemistry Reviews</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2348-2387</style></pages><volume><style face="normal" font="default" size="100%">257</style></volume><number><style face="normal" font="default" size="100%">15-16</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">August</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">00108545</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000321539200010</style></accession-num><abstract><style face="normal" font="default" size="100%">A review. Porphyrin/metalloporphyrin derivs. are a class of chromophores possessing favorable optical and redox properties for variety of applications ranging from materials to medicine. One drawback of porphyrin derivs. is their relatively poor absorption in the blue-green region of the spectrum (450-550 nm). One of the approaches for improving the absorption properties of porphyrin derivs. in blue-green region is their linking with chromophores that are capable of strongly absorbing in that region. B-dipyrrins (BODIPYs) are highly fluorescent dyes which absorb strongly in blue-green region and possess complementary properties with porphyrins. In recent times, covalently and noncovalently linked BODIPY-porphyrin conjugates on their own and in assocn. with other moieties such as fullerenes received lot of attention because of their use for various applications. Several synthetic strategies were developed to synthesize simple BODIPY-porphyrin conjugates to complex photonic wires and gates. Synthesis, properties, and potential applications of covalently and noncovalently linked conjugates contg. only BODIPY and porphyrin units as well as conjugates contg. BODIPY, porphyrin and other groups such as fullerenes are described.</style></abstract><label><style face="normal" font="default" size="100%">khan2013boron</style></label><notes><style face="normal" font="default" size="100%">179ro&#xD;Times Cited:76&#xD;Cited References Count:107</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0010854513000921</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.ccr.2013.04.007</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>315</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">315</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ilyas, Shaista</style></author><author><style face="normal" font="default" size="100%">Ilyas, Muhammad</style></author><author><style face="normal" font="default" size="100%">van der Hoorn, Renier A. L.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Max Planck Inst Plant Breeding Res, Plant Chemet Lab, D-50829 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Selective Conjugation of Proteins by Mining Active Proteomes through Click-Functionalized Magnetic Nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Nano</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Acs Nano</style></alt-title></titles><pages><style face="normal" font="default" size="100%">9655-9663</style></pages><volume><style face="normal" font="default" size="100%">7</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1936-0851</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000327752200014</style></accession-num><abstract><style face="normal" font="default" size="100%">Superparamagnetic iron oxide nanoparticles (SPIONs) coated with azide groups were functionalized at the surface with biotin (biotin@SPIONs) and cysteine protease inhibitor E-64 (E-64@SPIONs) with the purpose of developing nanoparticle-based assays for identifying cysteine proteases in proteomes. Magnetite particles (ca. 6 nm) were synthesized by microwave-assisted thermal decomposition of iron acetylacetonate and subsequently functionalized following a click chemistry protocol to obtain biotin and E-64 labeled particulate systems. Successful surface modification and covalent attachment of functional groups and molecules were confirmed by FT-IR spectroscopy and thermal gravimetric analysis. The ability of the surface-grafted biotin terminal groups to specifically interact with streptavidin (either horseradish peroxidase (HRP)-luminol-H2O2 or rhodamine) was confirmed by chemiluminescent assay. A quantitative assessment showed a capture limit of 0.55-1.65 $\mu$g protein/100 $\mu$g particles. Furthermore, E-64@SPIONs were successfully used to specifically label papain-like cysteine proteases from crude plant extracts. Owing to the simplicity and versatility of the technique, together with the superparamagnetic behavior of FeOx-nanoparticles, the results demonstrate that click chemistry on surface anchored azide group is a viable approach toward bioconjugations that can be extended to other nanoparticles surfaces with different functional groups to target specific therapeutic and diagnostic applications.</style></abstract><label><style face="normal" font="default" size="100%">ilyas2013selective</style></label><notes><style face="normal" font="default" size="100%">262qh&#xD;Times Cited:32&#xD;Cited References Count:37</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/nn402382g</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/nn402382g</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>314</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">314</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hoffmann, Martin W. G.</style></author><author><style face="normal" font="default" size="100%">Gad, Alaa Eldin</style></author><author><style face="normal" font="default" size="100%">Prades, J. Daniel</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Fiz, Raquel</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Barcelona, Dept Elect, E-08028 Barcelona, Spain&#xD;Catalonia Inst Energy Res IREC, Dept Adv Mat Energy Applicat, E-08930 Barcelona, Spain&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Tech Univ Carolo Wilhelmina Braunschweig, Inst Semicond Technol, D-38105 Braunschweig, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Solar diode sensor: Sensing mechanism and applications</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nano Energy</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><alt-periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></alt-periodical><pages><style face="normal" font="default" size="100%">514-522</style></pages><volume><style face="normal" font="default" size="100%">2</style></volume><number><style face="normal" font="default" size="100%">4</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jul</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">22112855</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000322937000012</style></accession-num><abstract><style face="normal" font="default" size="100%">Herein we report a solar diode sensor (SDS) based on new designed CdS@n-ZnO/p-Si nanoelements which unify gas sensing (CdS@n-ZnO) and solar energy harvesting (n-ZnO/p-Si diode) functionalities in a singular material unit and device. A novel The SDS sensing mechanism (change of open circuit voltage, $\Delta$Voc), in comparison to the well-known conductometric sensors (change of resistance, $\Delta$R), is systematically studied and explained in terms of gas-material surface interactions and the subsequent changes in the doping level (ND) of n-ZnO, which is manifested in the variation of Voc in CdS@n-ZnO/p-Si. The fabricated SDS was capable of quant. detecting oxidizing and reducing gases with reproducible response at room temp. and without the need of any other energy sources except solar illumination to deliver a self-sustained gas sensor.</style></abstract><label><style face="normal" font="default" size="100%">hoffmann2013solar</style></label><notes><style face="normal" font="default" size="100%">198qi&#xD;Times Cited:29&#xD;Cited References Count:38</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S2211285512002571</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.nanoen.2012.12.003</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>313</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">313</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Neudoerfl, Joerg-Martin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthetic and Structural Investigations on the Reactivity of the Cd-I Bond in ICdZr2(OPri)(9) to Construct New Mixed-Metal Alkoxides</style></title><secondary-title><style face="normal" font="default" size="100%">Organometallics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1654-1664</style></pages><volume><style face="normal" font="default" size="100%">32</style></volume><number><style face="normal" font="default" size="100%">6</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><abstract><style face="normal" font="default" size="100%">New mixed-metal alkoxides of general formula XCdZr-2(OPri)(9) (X = -C2F5, -C6F5, -C6F4-4-H, -NO3, -NCO, -SO3CF3, -O2CCF3, -O2CC2F5, -O2CCH3, -ClO4, -CN, -SO4; n = 1, 2) were obtained by the scission of the Cd-I bond in the iodo heterobimetallic isopropoxide ICdZr-2(OPri)(9) (1), whereby the underlying synthetic strategies involve metathesis reactions with silver salts or Lewis acid-base interactions between the Bronsted acid Zr-(OPri)(4)(HOPri)(2) and bis(fluoroorgano)cadmium (Cd(R-f)(2)) compounds. The new compounds were characterized by multinuclear NMR spectroscopy, elemental analysis, and mass spectrometry.</style></abstract><label><style face="normal" font="default" size="100%">hegemann2013synthetic</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/om301053b</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>312</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">312</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Giebelhaus, Irina</style></author><author><style face="normal" font="default" size="100%">Varechkina, Elena</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Rumyantseva, Marina</style></author><author><style face="normal" font="default" size="100%">Ivanov, Vladimir</style></author><author><style face="normal" font="default" size="100%">Gaskov, Alexander</style></author><author><style face="normal" font="default" size="100%">Morante, Joan Ramon</style></author><author><style face="normal" font="default" size="100%">Arbiol, Jordi</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Dept Chem, D-50939 Cologne, Germany&#xD;Moscow MV Lomonosov State Univ, Lab Chem &amp; Phys Semicond &amp; Sensor Mat, Dept Chem, Moscow 119991, Russia&#xD;Kurnakov Inst Gen &amp; Inorgan Chem RAS, Moscow 119991, Russia&#xD;Catalonia Inst Energy Res IREC, Dept Adv Mat Energy Applicat, E-08930 Barcelona, Spain&#xD;ICMAB CSIC, ICREA, E-08193 Bellaterra, Cat, Spain&#xD;ICMAB CSIC, Inst Ciencia Mat Barcelona, E-08193 Bellaterra, Cat, Spain</style></auth-address><titles><title><style face="normal" font="default" size="100%">One-dimensional CuO–SnO2 p–n heterojunctions for enhanced detection of H2S</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Mater Chem A</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></full-title></periodical><pages><style face="normal" font="default" size="100%">11261-11268</style></pages><volume><style face="normal" font="default" size="100%">1</style></volume><number><style face="normal" font="default" size="100%">37</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><isbn><style face="normal" font="default" size="100%">2050-7488</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000323765100023</style></accession-num><abstract><style face="normal" font="default" size="100%">Highly crystalline SnO2 nanowires were synthesized and functionalized with copper particles in a CVD using Sn(OBut)(4) and [Cu-II((C5H4N)(CHCOCF3))(2)](2) (1) as precursors respectively. Controlled oxidation of Cu to CuO led to the formation of CuO@SnO2 p-n heterojunctions, which were found to be highly sensitive and selective towards the detection of H2S gas. The change in the conductance upon exposure to H2S gas was attributed to the formation of CuS resulting in the shrinkage of the space charge region along the SnO2 nanowire and a concomitant increase of the conductivity channel in an individual nanowire.</style></abstract><label><style face="normal" font="default" size="100%">giebelhaus2013onedimensional</style></label><notes><style face="normal" font="default" size="100%">209nm&#xD;Times Cited:49&#xD;Cited References Count:48</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://xlink.rsc.org/?DOI=c3ta11867c</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c3ta11867c</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>311</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">311</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gad, Alaa Eldin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Self-Sustained NO2 Gas Sensor Operating at Room Temperatures Based on Solar Light activated p-NiO/n-Si Diode</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology VII</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">131-137</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Inc.</style></publisher><isbn><style face="normal" font="default" size="100%">9781118807828</style></isbn><abstract><style face="normal" font="default" size="100%">This chapter contains sections titled: * Introduction * Experimental * Results and Discussion * Conclusion * Acknowledgements</style></abstract><label><style face="normal" font="default" size="100%">gad2013selfsustained</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/9781118807828.ch12</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>310</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">310</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fiz, Raquel</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Lopez-Conesa, Lluis</style></author><author><style face="normal" font="default" size="100%">Estrade, Sonia</style></author><author><style face="normal" font="default" size="100%">Peiro, Francesca</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Dept Inorgan Chem, D-50939 Cologne, Germany&#xD;Univ Barcelona, Dept Elect, E-08028 Barcelona, Spain&#xD;IREC, Catalonia Inst Energy Res, Barcelona 08930, Spain&#xD;Univ Barcelona, CCiT, TEM MAT, Ctr Sci, E-08028 Barcelona, Spain&#xD;Univ Barcelona, CCiT, TEM MAT, Ctr Technol, E-08028 Barcelona, Spain</style></auth-address><titles><title><style face="normal" font="default" size="100%">Synthesis, Characterization, and Humidity Detection Properties of Nb2O5 Nanorods and SnO2/Nb2O5 Heterostructures</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry C</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Phys Chem C</style></alt-title></titles><pages><style face="normal" font="default" size="100%">10086-10094</style></pages><volume><style face="normal" font="default" size="100%">117</style></volume><number><style face="normal" font="default" size="100%">19</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">May 16</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000319649100063</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanostructured metal oxide semiconductors are ideally suited for their integration in different devices due to their high thermal and mech. stability, unique electronic characteristics, and low-cost fabrication. The modification of their surface allows the design of heterostructures with novel properties. The authors synthesized single-cryst. niobium pentoxide (Nb2O5) nanorods and niobium-pentoxide-coated tin oxide (Nb2O5/SnO2) heterostructures by CVD. HR-TEM anal. and computer simulation studies showed the low d. of defects and high crystallinity of the Nb2O5 nanorods, which exhibited high sensitivity toward humidity at low temps. (60°). The fabrication of SnO2/Nb2O5 core-shell heterostructures combines the high sensitivity of Nb2O5 shell toward moisture with the good elec. cond. of SnO2. The growth of the nanoscopic Nb2O5 overlayer on SnO2 nanowires introduces defects in the structure, which influence the electronic properties of the material and enable the design of more efficient humidity sensors.</style></abstract><label><style face="normal" font="default" size="100%">fiz2013synthesis</style></label><notes><style face="normal" font="default" size="100%">154cm&#xD;Times Cited:33&#xD;Cited References Count:42</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/jp3121066</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/jp3121066</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>309</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">309</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fiz, Raquel</style></author><author><style face="normal" font="default" size="100%">Appel, Linus</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Lin, Hua-Tay</style></author><author><style face="normal" font="default" size="100%">Hwang, Taejin</style></author><author><style face="normal" font="default" size="100%">Kirihara, Soshu</style></author><author><style face="normal" font="default" size="100%">Widjaja, Sujanto</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Photoinduced Hydrophilicity and Photocatalytic Properties of Nb2O5 Thin Films</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Ceramic Coatings and Materials for Extreme Environments III</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">47-53</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><label><style face="normal" font="default" size="100%">Fiz2013</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/9781118807651.ch5</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>308</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">308</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Singh, Aadesh P.</style></author><author><style face="normal" font="default" size="100%">Singh, Trilok</style></author><author><style face="normal" font="default" size="100%">Hernández-Ramírez, Francisco</style></author><author><style face="normal" font="default" size="100%">Prades, Daniel</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Carpenter, Michael A.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kolmakov, Andrei</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Metal Oxide Nano-architectures and Heterostructures for Chemical Sensors</style></title><secondary-title><style face="normal" font="default" size="100%">Metal Oxide Nanomaterials for Chemical Sensors</style></secondary-title><tertiary-title><style face="normal" font="default" size="100%">Integrated Analytical Systems</style></tertiary-title></titles><pages><style face="normal" font="default" size="100%">397-438</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><publisher><style face="normal" font="default" size="100%">Springer New York</style></publisher><isbn><style face="normal" font="default" size="100%">978-1-4614-5394-9</style></isbn><label><style face="normal" font="default" size="100%">fischer2013metal</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1007/978-1-4614-5395-6_13</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>307</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">307</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Czympiel, L.</style></author><author><style face="normal" font="default" size="100%">Gutiérrez-Pardo, A.</style></author><author><style face="normal" font="default" size="100%">Frank, M.</style></author><author><style face="normal" font="default" size="100%">Ramírez-Rico, J.</style></author><author><style face="normal" font="default" size="100%">Fernández, J. M.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Singh, J. P.</style></author><author><style face="normal" font="default" size="100%">Bansal, Narottam P.</style></author><author><style face="normal" font="default" size="100%">Bhalla, Amar S.</style></author><author><style face="normal" font="default" size="100%">Mahmoud, Morsi M.</style></author><author><style face="normal" font="default" size="100%">Manjooran, Navin Jose</style></author><author><style face="normal" font="default" size="100%">Singh, Gurpreet</style></author><author><style face="normal" font="default" size="100%">Lamon, Jacques</style></author><author><style face="normal" font="default" size="100%">Choi, Sung R.</style></author><author><style face="normal" font="default" size="100%">Pickrell, Gary</style></author><author><style face="normal" font="default" size="100%">Lu, Kathy</style></author><author><style face="normal" font="default" size="100%">Brennecka, Geoff</style></author><author><style face="normal" font="default" size="100%">Goto, Takashi</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Plasma Enhanced Chemical Vapor Deposition of Noble Metal Catalysts on Mesoporous Biomorphic Carbon</style></title><secondary-title><style face="normal" font="default" size="100%">Processing and Properties of Advanced Ceramics and Composites VI: Ceramic Transactions</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">115-122</style></pages><volume><style face="normal" font="default" size="100%">249</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><pub-location><style face="normal" font="default" size="100%">Hoboken, NJ, USA</style></pub-location><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Inc.</style></publisher><isbn><style face="normal" font="default" size="100%">111874411X</style></isbn><abstract><style face="normal" font="default" size="100%">Ceramic Transactions Volume 240, Processing and Properties of Advanced Ceramics and Composites VContains contributed 38 papers from the following seven symposia held during the 2012 Materials Science and Technology (MS&amp;T’12) meeting:Innovative Processing and Synthesis of Ceramics, Glasses and CompositesAdvances in Ceramic Matrix CompositesSolution Based Processing for Ceramic MaterialsNovel Sintering Processes and News in the Conventional Sintering and Grain GrowthNanotechnology for Energy, Healthcare and IndustryDielectric Ceramic Materials and Electronic DevicesControlled Synthesis, Processing, and Applications of Structure and Functional Nanomaterials</style></abstract><label><style face="normal" font="default" size="100%">czympiel2013plasma</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/9781118995433.ch12</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>306</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">306</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Cheah, Yan L.</style></author><author><style face="normal" font="default" size="100%">von Hagen, Robin</style></author><author><style face="normal" font="default" size="100%">Aravindan, Vanchiappan</style></author><author><style face="normal" font="default" size="100%">Fiz, Raquel</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Madhavi, Srinivasan</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Nanyang Technol Univ, Sch Mat Sci &amp; Engn, Singapore 639798, Singapore&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Nanyang Technol Univ, Energy Res Inst NTU ERI N, Singapore 637553, Singapore&#xD;Nanyang Technol Univ, TUM CREATE Ctr Electromobil, Singapore 637553, Singapore</style></auth-address><titles><title><style face="normal" font="default" size="100%">High-rate and elevated temperature performance of electrospun V2O5 nanofibers carbon-coated by plasma enhanced chemical vapour deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Nano Energy</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nano Energy</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></periodical><alt-periodical><full-title><style face="normal" font="default" size="100%">Nano Energy</style></full-title></alt-periodical><pages><style face="normal" font="default" size="100%">57-64</style></pages><volume><style face="normal" font="default" size="100%">2</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">22112855</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000318050500010</style></accession-num><abstract><style face="normal" font="default" size="100%">Vanadium pentoxide (V2O5) nanofibers (VNF) are synthesized by electrospinning technique and homogeneously coated with carbon by plasma enhanced chem. vapor deposition. The morphol. features of the VNF are analyzed by field emission scanning and transmission electron microscopy showed the presence of carbon layer over the VNF crystallites. Powder X-ray diffraction (XRD) patterns of the calcined nanofibers reveal the formation of V2O5 phase. Electrochem. Li-insertion behaviors of VNFs are explored as cathode in half-cell configuration by means of both potentiostatic and galvanostatic measurements. Carbon-coated VNF (C-VNF) showed the slightly less initial discharge capacity of ∼300 mA h g-1 with improved capacity retention of &gt;65\% after 50 cycles at 0.1 C rate, whereas native VNF showed only ∼40\% capacity retention under the same testing conditions. Enhanced high rate and elevated temp. performance of C-VNF is noted with overall capacity and capacity retention (&gt;60\%) characteristics than native fibers. Carbon-coating enables improved electronic cond. profiles and prevents undesired side reactions with electrolyte counterpart without hindering the Li-ion mobility reflected in the superior battery performance of C-VNF.</style></abstract><label><style face="normal" font="default" size="100%">cheah2013highrate</style></label><notes><style face="normal" font="default" size="100%">132ek&#xD;Times Cited:40&#xD;Cited References Count:48</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S2211285512001528</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.nanoen.2012.07.012</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>304</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">304</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Buerki-Thurnherr, Tina</style></author><author><style face="normal" font="default" size="100%">Xiao, Lisong</style></author><author><style face="normal" font="default" size="100%">Diener, Liliane</style></author><author><style face="normal" font="default" size="100%">Arslan, Osman</style></author><author><style face="normal" font="default" size="100%">Hirsch, Cordula</style></author><author><style face="normal" font="default" size="100%">Maeder-Althaus, Xenia</style></author><author><style face="normal" font="default" size="100%">Grieder, Kathrin</style></author><author><style face="normal" font="default" size="100%">Wampfler, Bruno</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Wick, Peter</style></author><author><style face="normal" font="default" size="100%">Krug, Harald F.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Empa, Swiss Federal Laboratories for Materials Testing and Technology, Laboratory for Materials-Biology Interactions, Lerchenfeldstrasse, St. Gallen, Switzerland. tina.buerki@empa.ch</style></auth-address><titles><title><style face="normal" font="default" size="100%">In vitro mechanistic study towards a better understanding of ZnO nanoparticle toxicity</style></title><secondary-title><style face="normal" font="default" size="100%">Nanotoxicology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">402-416</style></pages><volume><style face="normal" font="default" size="100%">7</style></volume><number><style face="normal" font="default" size="100%">4</style></number><edition><style face="normal" font="default" size="100%">2012/03/08</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1743-5404</style></isbn><accession-num><style face="normal" font="default" size="100%">22394310</style></accession-num><abstract><style face="normal" font="default" size="100%">ZnO nanoparticles (NPs) elicit significant adverse effects in various cell types, organisms and in the environment. The toxicity of nanoscale ZnO has often been ascribed to the release of zinc ions from the NPs but it is not yet understood to which extent these ions contribute to ZnO NP toxicity and what are the underlying mechanisms. Here, we take one step forward by demonstrating that ZnO-induced Jurkat cell death is largely an ionic effect involving the extracellular release of high amounts of Zn(II), their rapid uptake by the cells and the induction of a caspase-independent alternative apoptosis pathway that is independent of the formation of ROS. In addition, we identified novel coating strategies to reduce ZnO NP dissolution and subsequent adverse effects.</style></abstract><label><style face="normal" font="default" size="100%">buerkithurnherr2013vitro</style></label><notes><style face="normal" font="default" size="100%">Buerki-Thurnherr, Tina&#xD;Xiao, Lisong&#xD;Diener, Liliane&#xD;Arslan, Osman&#xD;Hirsch, Cordula&#xD;Maeder-Althaus, Xenia&#xD;Grieder, Kathrin&#xD;Wampfler, Bruno&#xD;Mathur, Sanjay&#xD;Wick, Peter&#xD;Krug, Harald F&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;England&#xD;Nanotoxicology. 2013 Jun;7(4):402-16. doi: 10.3109/17435390.2012.666575. Epub 2012 Mar 20.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.3109/17435390.2012.666575</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.3109/17435390.2012.666575</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>303</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">303</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Barreca, Davide</style></author><author><style face="normal" font="default" size="100%">Carraro, Giorgio</style></author><author><style face="normal" font="default" size="100%">Gasparotto, Alberto</style></author><author><style face="normal" font="default" size="100%">Maccato, Chiara</style></author><author><style face="normal" font="default" size="100%">Sada, Cinzia</style></author><author><style face="normal" font="default" size="100%">Singh, Aadesh P.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Mettenbörger, Andreas</style></author><author><style face="normal" font="default" size="100%">Bontempi, Elza</style></author><author><style face="normal" font="default" size="100%">Depero, Laura E.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Padua, IENI CNR, I-35131 Padua, Italy&#xD;Univ Padua, Dept Chem, INSTM, I-35131 Padua, Italy&#xD;Univ Padua, Dept Chem, I-35131 Padua, Italy&#xD;INSTM, I-35131 Padua, Italy&#xD;Univ Padua, Dept Phys &amp; Astron, I-35131 Padua, Italy&#xD;Univ Cologne, Dept Chem, Chair Inorgan &amp; Mat Chem, D-50939 Cologne, Germany&#xD;Univ Brescia, Chem Technol Lab, I-25123 Brescia, Italy&#xD;INSTM, I-25123 Brescia, Italy</style></auth-address><titles><title><style face="normal" font="default" size="100%">Columnar Fe2O3 arrays via plasma-enhanced growth: Interplay of fluorine substitution and photoelectrochemical properties</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Hydrogen Energy</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Int J Hydrogen Energ</style></alt-title></titles><pages><style face="normal" font="default" size="100%">14189-14199</style></pages><volume><style face="normal" font="default" size="100%">38</style></volume><number><style face="normal" font="default" size="100%">33</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">Nov 4</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">03603199</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000327578300006</style></accession-num><abstract><style face="normal" font="default" size="100%">A single-step plasma enhanced-chemical vapor deposition (PE-CVD) route for the synthesis of F-doped iron(III) oxide nanomaterials is presented. Growth experiments, performed from a fluorinated Fe(II) beta-diketonate precursor on Indium Tin Oxide (ITO) between 200 and 400 degrees C, yielded columnar beta-Fe2O3 arrays with a preferential (100) growth direction. The fluorine content in the deposits could be adjusted by the sole variation of the deposition temperature controlling, in turn, the optical absorption and energy bandgap. Photocurrent measurements and Mott-Schottky analyses, carried out in Na2SO4 solution under one sun illumination, evidenced a conductivity switch from n- to p-type upon increasing fluorine amount in the obtained nanomaterials. The sample photocurrent density, donor content and flatband potential support the hypothesis that a progressive substitution of oxygen by fluorine in the iron(III) oxide lattice can alter electronic structure and extend charge carrier lifetimes, making anion-doped beta-Fe2O3 an efficient water oxidation catalyst. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.</style></abstract><label><style face="normal" font="default" size="100%">barreca2013columnar</style></label><notes><style face="normal" font="default" size="100%">260er&#xD;Times Cited:53&#xD;Cited References Count:43</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0360319913021290</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.ijhydene.2013.08.119</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>302</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">302</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Arslan, Osman</style></author><author><style face="normal" font="default" size="100%">Singh, Aadesh P.</style></author><author><style face="normal" font="default" size="100%">Belkoura, Lhoussaine</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Univ Cologne, Inst Phys Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Cysteine-functionalized zwitterionic ZnO quantum dots</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Research</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Mater Res</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1947-1954</style></pages><volume><style face="normal" font="default" size="100%">28</style></volume><number><style face="normal" font="default" size="100%">14</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jul</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0884-2914</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000322021100009</style></accession-num><abstract><style face="normal" font="default" size="100%">Visible light emitting ZnO quantum dots (QDs) were synthesized by a modified sol-gel method and in situ coated with the amino acid cysteine to modify their surface chemistry and govern the crystal growth process. Surface chelation by a hydrophilic thiol such as cysteine offered a fine control over the particle size and modulated the optical emission and its stability by reducing the density of surfacial oxygen deficiencies and also induced the formation of hierarchical nanostructures in the solution. TEM and XRD results confirmed the formation of mono-dispersed and spherical ZnO QDs in the size range 2.5-3.8 nm. The modulation of band gap energies was manifested in the visible emission of cysteine modified QDs, which was found to be remarkably stable for cell labeling applications, when compared to the photoluminescence of conventional ZnO QDs.</style></abstract><label><style face="normal" font="default" size="100%">arslan2013cysteinefunctionalized</style></label><notes><style face="normal" font="default" size="100%">186db&#xD;Times Cited:12&#xD;Cited References Count:43</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1557/jmr.2013.161</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1557/jmr.2013.161</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>301</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">301</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Altmayer, Jessica</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Inst New Mat INM, D-66123 Saarbrucken, Germany&#xD;Vienna Univ Technol, Inst Mat Chem, A-1060 Vienna, Austria&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Influence of precursor chemistry on CVD grown TiO2 coatings: differential cell growth and biocompatibility</style></title><secondary-title><style face="normal" font="default" size="100%">RSC Advances</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Rsc Adv</style></alt-title></titles><pages><style face="normal" font="default" size="100%">11234-11239</style></pages><volume><style face="normal" font="default" size="100%">3</style></volume><number><style face="normal" font="default" size="100%">28</style></number><keywords><keyword><style face="normal" font="default" size="100%">2013, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2013</style></year></dates><isbn><style face="normal" font="default" size="100%">2046-2069</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000320782500018</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanocrystalline titanium oxide (TiO2) coatings with different phases and surface topographies were deposited using chemical vapor deposition (CVD) of different homo- and heteroleptic titanium precursors of general formula XTi((OPr)-Pr-i)(3) (X = Cl (1), -NEt2 (2), -N(SiMe3)(2) (3), -C5H5 (4), -(OPr)-Pr-i (5) and -(OBu)-Bu-t (6)) to elucidate the influence of molecular configuration on resulting material properties. The interdependence of precursor chemistry and materials features of the CVD deposits was verified by performing film growth under similar conditions using different precursor molecules (1-6). Studies on composition (XPS), structure (SEM, XRD) and bio-functional properties (cell tests) revealed that the decomposition process is markedly influenced by the auxiliary ligands, which led to incorporation of heteroelements (Si, Cl, N) in the films. Cell tests performed to evaluate the biocompatibility of the coatings towards the growth of bone cells showed a pronounced correlation between cell adhesion and surface morphology as well as the chemical composition. Growth of osteoblast cells was strongly enhanced on films obtained using Ti((OPr)-Pr-i)(4) and CpTi((OPr)-Pr-i)(3), whereas TiO2 coatings produced by ClTi((OPr)-Pr-i)(3) significantly inhibited the cell growth and their proliferation due to Cl contamination. Also, the nanomorphological features of the films were found to stimulate the cell adhesion and growth.</style></abstract><label><style face="normal" font="default" size="100%">altmayer2013influence</style></label><notes><style face="normal" font="default" size="100%">169lu&#xD;Times Cited:6&#xD;Cited References Count:32</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C3RA00050H</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c3ra00050h</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>368</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">368</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zopes, David</style></author><author><style face="normal" font="default" size="100%">Hegemann, Corinna</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">(CF3)4Au2(C5H5N)2 - a new alkyl gold(II) derivative with a very short Au-Au bond</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Communications</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">8805-8807</style></pages><volume><style face="normal" font="default" size="100%">48</style></volume><number><style face="normal" font="default" size="100%">70</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year></dates><isbn><style face="normal" font="default" size="100%">1364-548X</style></isbn><abstract><style face="normal" font="default" size="100%">A new gold(II) species (CF(3))(4)Au(2)(C(5)H(5)N)(2) with a very short unsupported Au-Au bond (250.62(9) pm) was generated by photo irradiation of a silver aurate, Ag(Py)(2)Au(CF(3))(2), unambiguously characterized by (19)F and (109)Ag NMR studies.</style></abstract><label><style face="normal" font="default" size="100%">zopes2012cf34au2c5h5n2</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C2CC33735E</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>367</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">367</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Wilfert, Jakob</style></author><author><style face="normal" font="default" size="100%">von Hagen, Robin</style></author><author><style face="normal" font="default" size="100%">Fiz, Raquel</style></author><author><style face="normal" font="default" size="100%">Jansen, Martin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany&#xD;Univ Cologne, Dept Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Electrospinning of preceramic polymers for the preparation of SiBNC felts and their modification with semiconductor nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Mater Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2099-2104</style></pages><volume><style face="normal" font="default" size="100%">22</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year></dates><isbn><style face="normal" font="default" size="100%">0959-9428</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000298970700053</style></accession-num><abstract><style face="normal" font="default" size="100%">Preceramic polymers obtained from the aminolysis of dichloroboryl-methyl-trichlorosilyl-amine (DMTA) were processed to ceramic felts of SiBNC by electrospinning, followed by curing in ammonia and subsequent pyrolysis. An amorphous ceramic with the compn. SiBN2.4C1.4 was obtained in 60\% yield, which was stable against crystn. and mass loss above 1565 °C. The pyrolyzed felts showed a fiber thickness ranging between 2 and 3 $\mu$m and revealed seamless connectivity among the fibers. The rheol. properties of the precursor could be tuned by adjusting the polymer/solvent ratio. Solns. with 40 wt\% polymer were reproducibly spun into preceramic felts, whereas lower concns. (10 wt\%) mainly led to agglomerated powders contg. few fibers. Given their intertwined morphol. and high-temp. stability, the SiBNC felts were used as substrates to grow tin oxide nanowires by chem. vapor deposition for potential application as electrode materials in gas sensing, demonstrated by preliminary expts.</style></abstract><label><style face="normal" font="default" size="100%">wilfert2012electrospinning</style></label><notes><style face="normal" font="default" size="100%">874pn&#xD;Times Cited:17&#xD;Cited References Count:33</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://xlink.rsc.org/?DOI=C1JM14497A</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c1jm14497a</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>366</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">366</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">von Hagen, Robin</style></author><author><style face="normal" font="default" size="100%">Lorrmann, Henning</style></author><author><style face="normal" font="default" size="100%">Möller, Kai-Christian</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electrospun LiFe1−yMnyPO4/C Nanofiber Composites as Self-Supporting Cathodes in Li-Ion Batteries</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Energy Materials</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Energy Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">553-559</style></pages><volume><style face="normal" font="default" size="100%">2</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">16146832</style></isbn><abstract><style face="normal" font="default" size="100%">LiFe1-yMnyPO4/C nanofiber composites are applied as cathode materials in Li-ion batteries and their electrochem. properties are explored. Nanofiber meshes are synthesized via electrospinning of com. available precursors (LiOH·H2O, FeSO4·7H2O, MnSO4·H2O, H3PO4, and polyvinylpyrrolidone). Nanofibers calcined at 850 °C under Ar/H2 (95/5 vol\%) atm. are directly used as self-supporting electrodes in Swagelok half cells without the need for any conductive additive or polymer binder. The morphol., phase, and chem. compn. of as-prepd. and heat-treated samples are analyzed by means of X-ray powder diffraction, thermogravimetric anal., and electron and scanning microscopy techniques. Brunauer-Emmett-Teller gas adsorption-desorption measurements show a high sp. surface area (111m2 g-1) for LiFe0.5Mn0.5PO4. The influence of different Fe/Mn ratios on the morphol., elec., and electrochem. performances are analyzed. on</style></abstract><label><style face="normal" font="default" size="100%">vonhagen2012electrospun</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/aenm.201100534</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>365</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">365</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Vomiero, Alberto</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Wang, Zhong Lin</style></author><author><style face="normal" font="default" size="100%">Diau, Eric Wei-Guang</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Functional Metal-Oxide Nanostructures: Volume 1406 (MRS Proceedings)</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2012, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year></dates><isbn><style face="normal" font="default" size="100%">978-1605113838</style></isbn><label><style face="normal" font="default" size="100%">vomiero2012functional</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>364</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">364</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tammam, Salma</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Afifi, Nagia</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Department of Pharmaceutical Technology, Faculty of Pharmacy and Biotechnology, German University in Cairo, Egypt.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Preparation and Biopharmaceutical Evaluation of Tacrolimus Loaded Biodegradable Nanoparticles for Liver Targeting</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Biomedical Nanotechnology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">439-449</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">3</style></number><edition><style face="normal" font="default" size="100%">2012/07/07</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">15507033</style></isbn><accession-num><style face="normal" font="default" size="100%">22764413</style></accession-num><abstract><style face="normal" font="default" size="100%">Tacrolimus (TAC) is a potent immunosuppressant used in liver transplantation. Its use is however hindered by its systemic side effects, mainly nephrotoxcity. Since antigen presentation occurs in the graft and lymphatics, then by targeting TAC to the liver and spleen graft survival and decreased side effects could both be achieved. Simultaneous targeting to liver and spleen could be obtained via the reticuloendothelial system (RES). The objective of this study was to formulate RES attractive TAC-loaded nanoparticles that could ultimately increase TAC concn. in the liver and spleen and decrease it in the kidneys. Tacrolimus was incorporated into Poly(lactic acid) nanoparticles via the emulsion-solvent evapn. method. Poly lactide tacrolimus nanoparticles (PLA-TAC-NP) were extensively characterized by dynamic light scattering (DLS), transmission, scanning and at. force microscopy (TEM, SEM and AFM) ensuring that they possessed the required characteristics rendering them RES attractive. Targeting efficiency of the formulated particles was assessed in-vitro by the evaluating their uptake by cultured human monocytes both qual. by TEM and quant. by HPLC-UV. DLS showed that particles had a mean diam. of 255 ± 4.58 nm with unimodal distribution. Results were confirmed by SEM, AFM and TEM. Zeta Potential was -60.08 ± 5.83 mV, whereas entrapment efficiency was 64.71 ± 4.27\%. TAC release pattern from PLA-NP was detd. by the dialysis bag method showing 77 ± 5.72\% drug release within 4 days. PLA-TAC-NP phagocytosis was confirmed by TEM. The extent of phagocytosis was detd. by HPLC anal. to be 80.48 ± 11.61\%. In conclusion, PLA-TAC-NP are promising carriers for TAC targeting to the liver and spleen via the reticuloendothelial system (RES).</style></abstract><label><style face="normal" font="default" size="100%">tammam2012preparation</style></label><notes><style face="normal" font="default" size="100%">Tammam, Salma&#xD;Mathur, Sanjay&#xD;Afifi, Nagia&#xD;eng&#xD;J Biomed Nanotechnol. 2012 Jun;8(3):439-49. doi: 10.1166/jbn.2012.1403.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1166/jbn.2012.1403</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1166/jbn.2012.1403</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>363</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">363</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Styskalik, Ales</style></author><author><style face="normal" font="default" size="100%">Skoda, David</style></author><author><style face="normal" font="default" size="100%">Pinkas, Jiri</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Masaryk Univ, Dept Chem, Brno, Czech Republic&#xD;Masaryk Univ, CEITEC MU, Brno, Czech Republic&#xD;Univ Cologne, Dept Chem, Fac Math &amp; Nat Sci, D-50931 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Non-hydrolytic synthesis of titanosilicate xerogels by acetamide elimination and their use as epoxidation catalysts</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Sol-Gel Science and Technology</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Sol-Gel Sci Techn</style></alt-title></titles><pages><style face="normal" font="default" size="100%">463-472</style></pages><volume><style face="normal" font="default" size="100%">63</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">Sep</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0928-0707</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000310162700020</style></accession-num><abstract><style face="normal" font="default" size="100%">Novel non-hydrolytic syntheses of titanosilicate xerogels by polycondensation of silicon acetate, Si(OAc)4, with titanium (IV) dimethylamide or diethylamide, Ti(NR2)4 (R = Me, Et), are presented. The reactions are based on acetamide elimination and yield gels with a high content of Si-O-Ti bonds in comparison with the ester elimination route. Although a ligand exchange was obsd., it was interestingly not followed by homo-condensation and during the synthesis the phase sepn. to SiO2 and TiO2 was avoided. The degree of condensation reached up to 68 \%. The xerogels prepd. for a comparison by ester elimination from Si(OAc)4 and titanium (IV) isopropoxide featured a significantly lower content of the Si-O-Ti bonds. The initial tests in the epoxidn. of cyclohexene by cumyl hydroperoxide (CHP) indicated a high selectivity and moderate activity of the xerogels. The catalytic properties were significantly improved by combining non-hydrolytic and hydrolytic methods yielding mesoporous and homogeneous Si/Ti mixed oxides. The catalysts prepd. by these methods provided a complete epoxidn. of cyclohexene in 2 h at 65 °C.</style></abstract><label><style face="normal" font="default" size="100%">styskalik2012nonhydrolytic</style></label><notes><style face="normal" font="default" size="100%">025cr&#xD;Times Cited:14&#xD;Cited References Count:40</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://link.springer.com/10.1007/s10971-012-2808-5</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1007/s10971-012-2808-5</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>362</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">362</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Singh, Aadesh P.</style></author><author><style face="normal" font="default" size="100%">Mettenbörger, Andreas</style></author><author><style face="normal" font="default" size="100%">Golus, Peter</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Dept Chem, D-50859 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Photoelectrochemical properties of hematite films grown by plasma enhanced chemical vapor deposition</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Hydrogen Energy</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Int J Hydrogen Energ</style></alt-title></titles><pages><style face="normal" font="default" size="100%">13983-13988</style></pages><volume><style face="normal" font="default" size="100%">37</style></volume><number><style face="normal" font="default" size="100%">19</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">Oct</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">03603199</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000309493600008</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanostructured $\alpha$-Fe2O3 thin films were grown by plasma-enhanced chem. vapor deposition (PE-CVD) using iron pentacarbonyl (Fe(CO)5) as precursor. Influence of the plasma parameters on photoelectrochem. (PEC) properties of the resulting hematite thin films toward solar oxidn. of water was investigated under one sun illumination in a basic (1 M NaOH) electrolyte. PEC data analyzed in conjunction with the data obtained by SEM, X-ray diffraction and Mott-Schottky anal. showed 100 W plasma power to be an optimal RF-power value for achieving a high photocurrent d. of ∼1098 $\mu$A/cm2 at 0.9 V/SCE external applied potential. The donor d., flat band potential, grain size and porosity of the films were obsd. to be highly affected by RF-power, which in turn resulted in enhanced photoresponse.</style></abstract><label><style face="normal" font="default" size="100%">singh2012photoelectrochemical</style></label><notes><style face="normal" font="default" size="100%">016bz&#xD;Times Cited:37&#xD;Cited References Count:31</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0360319912015157</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.ijhydene.2012.06.097</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>361</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">361</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shi, Jingwen</style></author><author><style face="normal" font="default" size="100%">Karlsson, Hanna L.</style></author><author><style face="normal" font="default" size="100%">Johansson, Katarina</style></author><author><style face="normal" font="default" size="100%">Gogvadze, Vladimir</style></author><author><style face="normal" font="default" size="100%">Xiao, Lisong</style></author><author><style face="normal" font="default" size="100%">Li, Jiangtian</style></author><author><style face="normal" font="default" size="100%">Burks, Terrance</style></author><author><style face="normal" font="default" size="100%">Garcia-Bennett, Alfonso</style></author><author><style face="normal" font="default" size="100%">Uheida, Abdusalam</style></author><author><style face="normal" font="default" size="100%">Muhammed, Mamoun</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Morgenstern, Ralf</style></author><author><style face="normal" font="default" size="100%">Kagan, Valerian E.</style></author><author><style face="normal" font="default" size="100%">Fadeel, Bengt</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Microsomal Glutathione Transferase 1 Protects Against Toxicity Induced by Silica Nanoparticles but Not by Zinc Oxide Nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Nano</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1925-1938</style></pages><volume><style face="normal" font="default" size="100%">6</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">March</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1936-0851</style></isbn><abstract><style face="normal" font="default" size="100%">Microsomal glutathione transferase 1 (MGST1) is an antioxidant enzyme located predominantly in the mitochondrial outer membrane and endoplasmic reticulum and has been shown to protect cells from lipid peroxidation induced by a variety of cytostatic drugs and pro-oxidant stimuli. We hypothesized that MGST1 may also protect against nanomaterial-induced cytotoxicity through a specific effect on lipid peroxidation. We evaluated the induction of cytotoxicity and oxidative stress by TiO(2), CeO(2), SiO(2), and ZnO in the human MCF-7 cell line with or without overexpression of MGST1. SiO(2) and ZnO nanoparticles caused dose- and time-dependent toxicity, whereas no obvious cytotoxic effects were induced by nanoparticles of TiO(2) and CeO(2). We also noted pronounced cytotoxicity for three out of four additional SiO(2) nanoparticles tested. Overexpression of MGST1 reversed the cytotoxicity of the main SiO(2) nanoparticles tested and for one of the supplementary SiO(2) nanoparticles but did not protect cells against ZnO-induced cytotoxic effects. The data point toward a role of lipid peroxidation in SiO(2) nanoparticle-induced cell death. For ZnO nanoparticles, rapid dissolution was observed, and the subsequent interaction of Zn(2+) with cellular targets is likely to contribute to the cytotoxic effects. A direct inhibition of MGST1 by Zn(2+) could provide a possible explanation for the lack of protection against ZnO nanoparticles in this model. Our data also showed that SiO(2) nanoparticle-induced cytotoxicity is mitigated in the presence of serum, potentially through masking of reactive surface groups by serum proteins, whereas ZnO nanoparticles were cytotoxic both in the presence and in the absence of serum.</style></abstract><label><style face="normal" font="default" size="100%">shi2012microsomal</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/nn2021056</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>359</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">359</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pan, Jun</style></author><author><style face="normal" font="default" size="100%">Zhang, Jun</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Xiong, Qihua</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Correction to “Switchable Wettability in SnO2 Nanowires and SnO2@SnO2 Heterostructures”</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry C</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">13835-13836</style></pages><volume><style face="normal" font="default" size="100%">116</style></volume><number><style face="normal" font="default" size="100%">25</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year></dates><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><label><style face="normal" font="default" size="100%">pan2012correction</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/jp305167t</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>360</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">360</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pan, Jun</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">One-Dimensional SnO2 Nanostructures: Synthesis and Applications</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Nanotechnology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1-12</style></pages><volume><style face="normal" font="default" size="100%">2012</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year></dates><isbn><style face="normal" font="default" size="100%">1687-9503</style></isbn><abstract><style face="normal" font="default" size="100%">A review. Nanoscale semiconducting materials such as quantum dots (0-dimensional) and one-dimensional (1D) structures, like nanowires, nanobelts, and nanotubes, have gained tremendous attention within the past decade. Among the variety of 1D nanostructures, tin oxide (SnO2) semiconducting nanostructures are particularly interesting because of their promising applications in optoelectronic and electronic devices due to both good cond. and transparence in the visible region. This article provides a comprehensive review of the recent research activities that focus on the rational synthesis and unique applications of 1D SnO2 nanostructures and their optical and elec. properties. We begin with the rational design and synthesis of 1D SnO2 nanostructures, such as nanotubes, nanowires, nanobelts, and some heterogeneous nanostructures, and then highlight a range of applications (e.g., gas sensor, lithium-ion batteries, and nanophotonics) assocd. with them. Finally, the review is concluded with some perspectives with respect to future research on 1D SnO2 nanostructures.</style></abstract><label><style face="normal" font="default" size="100%">pan2012onedimensional</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1155/2012/917320</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>358</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">358</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Müller, Ralf</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Du, Hongchu</style></author><author><style face="normal" font="default" size="100%">Mader, Werner</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of Precursor Chemistry on Morphology and Composition of CVD-Grown SnO2 Nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of Materials</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">4028-4035</style></pages><volume><style face="normal" font="default" size="100%">24</style></volume><number><style face="normal" font="default" size="100%">21</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><abstract><style face="normal" font="default" size="100%">Tin oxide (SnO2) nanowires (NWs) were synthesized via the gold-catalyzed CVD of tin(IV) and tin(II) precursors, namely, Sn(OtBu)4 (1) and Sn(OtBu)22 (2). Nanowires were deposited on gold-coated Si(001) substrates, following the vapor-liq.-solid mechanism. Energy-dispersive x-ray (EDX) anal. and high-resoln. TEM (HR-TEM) measurements on individual nanostructures showed that the change in tin valence from +IV to +II has significant influence on the morphol. and compn. of the resulting NWs. Whereas 1 led directly to the growth of SnO2 nanowires, 2 underwent a disproportionation reaction whereby the elemental phase (Sn0) reacted with Au nanoparticles to form a Au-Sn intermetallic catalyst. Comparative anal. of gas-sensing behaviors of nanowires grown from 1 and 2 illustrated that crystallog. imperfections, such as oxygen deficiency and a change in the oxidn. states of the cations, are subject to the precursor configurations (Sn:O ratio in 1 and 2) and can significantly alter the surface properties, such as transduction behavior and electronic transport, that are responsible for their sensitivity toward analyte gases.</style></abstract><label><style face="normal" font="default" size="100%">muller2012influence</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/cm300913h</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>357</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">357</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Monteiro-Riviere, N. A.</style></author><author><style face="normal" font="default" size="100%">Inman, A. O.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Muhammed, M.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">N Carolina State Univ, Ctr Chem Toxicol Res &amp; Pharmacokinet, Raleigh, NC 27695 USA&#xD;Univ Cologne, Inst Inorgan Chem, D-50931 Cologne, Germany&#xD;Royal Inst Technol, Dept Mat Sci &amp; Engn, Stockholm, Sweden&#xD;Karolinska Inst, Inst Environm Med, S-10401 Stockholm, Sweden</style></auth-address><titles><title><style face="normal" font="default" size="100%">Effects of eight nanoparticles of different sizes and shapes on human epidermal keratinocytes</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Investigative Dermatology</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Invest Dermatol</style></alt-title></titles><pages><style face="normal" font="default" size="100%">S52</style></pages><volume><style face="normal" font="default" size="100%">132</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, imported, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0022-202x</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000302866900308</style></accession-num><label><style face="normal" font="default" size="100%">monteiroriviere2012effects</style></label><notes><style face="normal" font="default" size="100%">Suppl. 1&#xD;926xv&#xD;306&#xD;Times Cited:0&#xD;Cited References Count:0</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.diva-portal.org/smash/record.jsf?pid=diva2%3A525162&amp;dswid=508</style></url></related-urls></urls><custom2><style face="normal" font="default" size="100%">&lt;Link&gt; urn:nbn:se:kth:diva-93907</style></custom2><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>356</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">356</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mettenbörger, Andreas</style></author><author><style face="normal" font="default" size="100%">Merod, Vanessa</style></author><author><style face="normal" font="default" size="100%">Singh, Aadesh P.</style></author><author><style face="normal" font="default" size="100%">Lemmetyinen, Helge</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ray, Suprakas Sinha</style></author><author><style face="normal" font="default" size="100%">Halbig, Michael</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Plasma-Assisted Chemical Vapor Deposition of Fe: TiO2 Films for Photoelectrochemical Hydrogen Production</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology VI</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">81-88</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year></dates><label><style face="normal" font="default" size="100%">Mettenborger2012</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/9781118217511.ch8</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>355</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">355</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Singh, Aadesh Pratap</style></author><author><style face="normal" font="default" size="100%">Müller, Ralf</style></author><author><style face="normal" font="default" size="100%">Leuning, Tessa</style></author><author><style face="normal" font="default" size="100%">Lehnen, Thomas</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Riedel, Ralf</style></author><author><style face="normal" font="default" size="100%">Chen, I. Wei</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Metal-Organic Chemical Vapor Deposition of Metal Oxide Films and Nanostructures</style></title><secondary-title><style face="normal" font="default" size="100%">Ceramics Science and Technology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">291-336</style></pages><volume><style face="normal" font="default" size="100%">3</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year></dates><pub-location><style face="normal" font="default" size="100%">Weinheim, Germany</style></pub-location><publisher><style face="normal" font="default" size="100%">Wiley-VCH Verlag GmbH &amp; Co. KGaA</style></publisher><isbn><style face="normal" font="default" size="100%">9783527311576</style></isbn><abstract><style face="normal" font="default" size="100%">A review on the development of chem. vapor deposition (CVD) processing and general CVD methods applicable to the formation of metal oxide thin films, with special ref. to the precursor-based techniques.</style></abstract><label><style face="normal" font="default" size="100%">mathur2012metalorganic</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/9783527631957.ch12</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>354</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">354</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lima, Enio</style></author><author><style face="normal" font="default" size="100%">Brito, Giancarlo E. S.</style></author><author><style face="normal" font="default" size="100%">Cavelius, Christian</style></author><author><style face="normal" font="default" size="100%">Sivakov, Vladimir</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Goya, Gerardo F.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Consejo Nacl Invest Cient &amp; Tecn, Ctr Atom Bariloche, RA-8400 San Carlos De Bariloche, RN, Argentina&#xD;Univ Sao Paulo, Inst Fis, BR-05315970 Sao Paulo, Brazil&#xD;Leibniz Inst New Mat, CVD Div, D-66123 Saarbrucken, Germany&#xD;Univ Zaragoza, INA, E-50009 Zaragoza, Spain</style></auth-address><titles><title><style face="normal" font="default" size="100%">Influence of the Substrate and Precursor on the Magnetic and Magneto-transport Properties in Magnetite Films</style></title><secondary-title><style face="normal" font="default" size="100%">Current Nanoscience</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Curr Nanosci</style></alt-title></titles><pages><style face="normal" font="default" size="100%">659-668</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">Oct</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">15734137</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000310390700002</style></accession-num><abstract><style face="normal" font="default" size="100%">We have investigated the magnetic and transport properties of nanoscaled Fe3O4 films obtained from Chem. Vapor Deposition (CVD) technique using [FeIIFeIII(OBut)8] and [Fe2III(OBut)6] precursors. Samples were deposited on different substrates (i.e., MgO (001), MgAl2O4 (001) and Al2O3 (0001)) with thicknesses varying from 50 to 350 nm. Atomic Force Microscopy anal. indicated a granular nature of the samples, irresp. of the synthesis conditions (precursor and deposition temp., Tpre) and substrate. Despite the similar morphol. of the films, magnetic and transport properties were found to depend on the precursor used for deposition. Using [FeIIFe2III(OBut)8] as precursor resulted in lower resistivity, higher MS and a sharper magnetization decrease at the Verwey transition (TV). The temp. dependence of resistivity was found to depend on the precursor and Tpre. We found that the transport is dominated by the d. of antiferromagnetic antiphase boundaries (AF-APB&apos;s) when [FeIIFe2III(OBut)8] precursor and Tpre = 363 K are used. On the other hand, grain boundary-scattering seems to be the main mechanism when [Fe2III(OBut)6] is used. The Magnetoresistance (MR(H)) displayed an approx. linear behavior in the high field regime (H &gt; 796 kA/m), with a max. value at room-temp. of ∼ 2-3 \% for H = 1592 kA/m, irresp. from the transport mechanism.</style></abstract><label><style face="normal" font="default" size="100%">lima2012influence</style></label><notes><style face="normal" font="default" size="100%">027yt&#xD;Times Cited:2&#xD;Cited References Count:30</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.2174/157341312802884544</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Doi 10.2174/157341312802884544</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>353</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">353</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Li, Jiangtian</style></author><author><style face="normal" font="default" size="100%">Hoffmann, Martin W. G.</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Fabrega, Cristian</style></author><author><style face="normal" font="default" size="100%">Prades, Joan Daniel</style></author><author><style face="normal" font="default" size="100%">Andreu, Teresa</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Univ Barcelona, Dept Elect, E-08028 Barcelona, Spain&#xD;Catalonia Inst Energy Res IREC, Dept Adv Mat Energy, E-08930 Barcelona, Spain</style></auth-address><titles><title><style face="normal" font="default" size="100%">Enhanced photoelectrochemical activity of an excitonic staircase in CdS@TiO2 and CdS@anatase@rutile TiO2 heterostructures</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Mater Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">20472-20476</style></pages><volume><style face="normal" font="default" size="100%">22</style></volume><number><style face="normal" font="default" size="100%">38</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year></dates><isbn><style face="normal" font="default" size="100%">0959-9428</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000308658600053</style></accession-num><abstract><style face="normal" font="default" size="100%">TiO2 nanorod arrays grown on conductive substrates were converted using chem. strategies into CdS@TiO2 and CdS@anatase@rutile TiO2 heterostructures to fabricate visible-light harvesting assemblies. Compared to pure TiO2 nanorods, CdS@TiO2 heterostructures evidently extended the absorption edge and exhibited enhanced photoelectrochem. (PEC) response in the visible region. Further enhancement of PEC performance was achieved by introducing an intermediate anatase TiO2 layer in the CdS@rutile TiO2 heterostructures. An excitonic cascade of band alignment (CdS, anatase-TiO2 and rutile-TiO2) was constituted by arranging different semiconductors to align the edges of their conducting band, which improved charge sepn. and suppressed the recombination processes by facilitating the transfer of forward electrons and limiting the reverse processes due to spatial sepn. of the electron and hole in different material regions.</style></abstract><label><style face="normal" font="default" size="100%">li2012enhanced</style></label><notes><style face="normal" font="default" size="100%">004cv&#xD;Times Cited:73&#xD;Cited References Count:24</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://xlink.rsc.org/?DOI=c2jm33404f</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c2jm33404f</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>352</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">352</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lehnen, Thomas</style></author><author><style face="normal" font="default" size="100%">Zopes, David</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Phase-selective microwave synthesis and inkjet printing applications of Zn2SnO4 (ZTO) quantum dots</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Mater Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">17732-17736</style></pages><volume><style face="normal" font="default" size="100%">22</style></volume><number><style face="normal" font="default" size="100%">34</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year></dates><isbn><style face="normal" font="default" size="100%">0959-9428</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000307305700049</style></accession-num><abstract><style face="normal" font="default" size="100%">An efficient synthesis of highly cryst. and single phase Zn2SnO4 quantum dots (ZTO QDs) with a narrow size distribution was achieved by microwave-assisted hydrothermal synthesis. Printed structures fabricated from aq. suspensions of ZTO QDs showed typical semiconducting I-V behaviors and were used for reproducible detection of humidity.</style></abstract><label><style face="normal" font="default" size="100%">lehnen2012phaseselective</style></label><notes><style face="normal" font="default" size="100%">985yf&#xD;Times Cited:27&#xD;Cited References Count:34</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://xlink.rsc.org/?DOI=c2jm32924g</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c2jm32924g</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>351</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">351</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hirsch, Cordula</style></author><author><style face="normal" font="default" size="100%">Buerki-Thurnherr, Tina</style></author><author><style face="normal" font="default" size="100%">Xiao, Lisong</style></author><author><style face="normal" font="default" size="100%">Arslan, Osman</style></author><author><style face="normal" font="default" size="100%">Wampfler, Bruno</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Roesslein, Matthias</style></author><author><style face="normal" font="default" size="100%">Wick, Peter</style></author><author><style face="normal" font="default" size="100%">Krug, Harald F.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">A comprehensive evaluation platform to assess nanoparticle toxicity in vitro</style></title><secondary-title><style face="normal" font="default" size="100%">Toxycology Letters</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Toxicol Lett</style></alt-title></titles><pages><style face="normal" font="default" size="100%">S41</style></pages><volume><style face="normal" font="default" size="100%">211</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun 17</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0378-4274</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000305173900133</style></accession-num><label><style face="normal" font="default" size="100%">hirsch2012comprehensive</style></label><notes><style face="normal" font="default" size="100%">Suppl. S&#xD;957pb&#xD;Times Cited:1&#xD;Cited References Count:0</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.toxlet.2012.03.172</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.toxlet.2012.03.172</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>350</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">350</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Prades, J.D.</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, R.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Morante, J.R.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Helwig, A.</style></author><author><style face="normal" font="default" size="100%">Spannhake, J.</style></author><author><style face="normal" font="default" size="100%">Mueller, G</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">MEMS hotplates sensors based on single metal oxide nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">The 14th International Meeting on Chemical Sensors</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year></dates><label><style face="normal" font="default" size="100%">hernandezramirez2012hotplates</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>349</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">349</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hemmer, Eva</style></author><author><style face="normal" font="default" size="100%">Kumakiri, Izumi</style></author><author><style face="normal" font="default" size="100%">Lecerf, Nicolas</style></author><author><style face="normal" font="default" size="100%">Bredesen, Rune</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Altmayer, Jessica</style></author><author><style face="normal" font="default" size="100%">Donia, Nicole</style></author><author><style face="normal" font="default" size="100%">Cavelius, Christian</style></author><author><style face="normal" font="default" size="100%">Soga, Kohei</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Leibniz Inst New Mat, CVD Technol, D-66123 Saarbrucken, Germany&#xD;SINTEF, N-0314 Oslo, Norway&#xD;Tokyo Univ Sci, Dept Mat Sci &amp; Technol, Chiba 2788510, Japan</style></auth-address><titles><title><style face="normal" font="default" size="100%">Nanostructured ZrO2 membranes prepared by liquid-injection chemical vapor deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Microporous and Mesoporous Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Micropor Mesopor Mat</style></alt-title></titles><pages><style face="normal" font="default" size="100%">229-236</style></pages><volume><style face="normal" font="default" size="100%">163</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">13871811</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000309625800029</style></accession-num><abstract><style face="normal" font="default" size="100%">Using the mol. compd. Zr(OBut)4 in a liq.-injection chem. vapor deposition process, microporous zirconia membranes were deposited on porous multi-layered alumina substrates consisting of a macroporous $\alpha$-alumina base covered with a mesoporous $\gamma$-alumina layer. The structure of nanocryst. zirconia (ZrO2), membranes formed by the thermal decompn. of the precursor varied depending on the decompn. temp. and the injection frequency. The deposited zirconia membranes were characterized by SEM, energy dispersive X-ray anal. (EDX), X-ray diffraction (XRD) and at. force microscopy (AFM). X-ray diffraction anal. patterns of the deposits obtained at 500 and 600°C indicated a mixt. of tetragonal and monoclinic ZrO2 phases, whereas the fraction of the monoclinic phase increased at higher substrate temp. and injection frequency. Morphol. and surface roughness are strongly dependent on the process parameters. ZrO2 membranes prepd. by the liq.-injection chem. vapor deposition had a microporous structure with less than 1 nm Kelvin diam. The liq.-injection chem. vapor deposition is a unique method to prep. microporous membranes in one step without any post-treatment.</style></abstract><label><style face="normal" font="default" size="100%">hemmer2012nanostructured</style></label><notes><style face="normal" font="default" size="100%">017xz&#xD;Times Cited:6&#xD;Cited References Count:61</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S1387181112004386</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.micromeso.2012.06.057</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>348</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">348</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Heinrich, Frank</style></author><author><style face="normal" font="default" size="100%">Keßler, Michael T.</style></author><author><style face="normal" font="default" size="100%">Dohmen, Stephan</style></author><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author><author><style face="normal" font="default" size="100%">Prechtl, Martin H. G.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Dept Chem, Chair Inorgan &amp; Mat Chem, D-50939 Cologne, Germany&#xD;NASA, Glenn Res Ctr, Ohio Aerosp Inst, Cleveland, OH 44135 USA</style></auth-address><titles><title><style face="normal" font="default" size="100%">Molecular Palladium Precursors for Pd0 Nanoparticle Preparation by Microwave Irradiation: Synthesis, Structural Characterization and Catalytic Activity</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Eur J Inorg Chem</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">6027-6033</style></pages><volume><style face="normal" font="default" size="100%">2012</style></volume><number><style face="normal" font="default" size="100%">36</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">Dec</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1099-0682</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000312291000013</style></accession-num><abstract><style face="normal" font="default" size="100%">Two new palladium complexes Pd(MEA)2Cl2 (1) and Pd(MEA)2Br2 (2) MEA = (2-methoxyethyl)amine were synthesized by the reaction of 2 equiv. of MEA with PdCl2 or (cod)PdBr2 (cod = cycloocta-1,5-diene), respectively. Single-crystal X-ray diffraction analysis of 1 and 2 revealed the formation of square-planar trans complexes with palladium coordinated by chloride/bromide ions and N-atoms of MEA bonded in a monodentate fashion. Given their molecular form and solubility, 1 and 2 act as intractable precursors to Pd nanoparticles by microwave-assisted synthesis. The influence of the reaction temperature, irradiation time and surfactant (PVP) concentration on the size (5–40 nm) of the resulting particles was studied by DLS (hydrodynamic diameter) and TEM analyses (particle size). The growth mechanism of the nanoparticles depended on the type of halide ligand. Powder X-ray diffractometry confirmed the formation of elemental Pd particles that were embedded in carbonized wood to examine their potential as a catalyst. The catalytic activity of these nanoscale particles was evaluated in carbon–carbon cross-coupling reactions by using Heck, Suzuki and Sonogashira reactions as benchmark models. The investigations included recycling experiments that resulted in total turnover numbers of 4321 (Heck), 6173 (Sonogashira) and 8223 (Suzuki).</style></abstract><label><style face="normal" font="default" size="100%">heinrich2012molecular</style></label><notes><style face="normal" font="default" size="100%">053ro&#xD;Times Cited:12&#xD;Cited References Count:48</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/ejic.201200380</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/ejic.201200380</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>347</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">347</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hackner, Angelika</style></author><author><style face="normal" font="default" size="100%">Beer, Sebastian</style></author><author><style face="normal" font="default" size="100%">Müller, Gerhard</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">EADS Innovat Works, D-81663 Munich, Germany&#xD;Univ Cologne, Inst Inorgan Chem, D-50923 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Surface ionization detection of amphetamine-type illicit drugs</style></title><secondary-title><style face="normal" font="default" size="100%">Sensors and Actuators B: Chemical</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Sensor Actuat B-Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">209-215</style></pages><volume><style face="normal" font="default" size="100%">162</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">Feb 20</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09254005</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000301214700031</style></accession-num><abstract><style face="normal" font="default" size="100%">We report on developments towards a novel miniaturized gas sensor system for the detection of amphetamine-type illicit drugs, operating on the principle of surface ionization. The detector is shown to feature good sensitivity to the target compds. as well as high selectivity against potential interfering species. The latter include in particular a set of possible solvent liqs. for the salt forms of the target substances. In a set of expts. using flash desorption on both solid and liq.-dissolved analytes, with subsequent gas phase detection, the potential of the detection method for field applications is demonstrated.</style></abstract><label><style face="normal" font="default" size="100%">hackner2012surface</style></label><notes><style face="normal" font="default" size="100%">904rd&#xD;Times Cited:15&#xD;Cited References Count:17</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0925400511011580</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.snb.2011.12.068</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>345</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">345</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gad, A. E.</style></author><author><style face="normal" font="default" size="100%">Hoffmann, M. W. G.</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Coaxial p-Si/n-ZnO nanowire heterostructures for energy and sensing applications</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Chemistry and Physics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">618-622</style></pages><volume><style face="normal" font="default" size="100%">135</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year></dates><publisher><style face="normal" font="default" size="100%">Elsevier BV</style></publisher><abstract><style face="normal" font="default" size="100%">Radial p-n nanowire heterojunction devices represent a favorable geometry to maximize the interfacial area and carrier separation due to the built-in field established across the junction. This report presents the functional characterization of a heterojunction device based on a single coaxial n-ZnO/p-Si nanowire that was integrated in a circuit by FIB nanolithography to study the electrical properties. The photovoltaic and gas sensing performances of these single p-n heterojunctions were preliminary assessed, showing for the first time that the sensing response could be modulated by changing the bias current through the device, showing a complementary functionality of these nanoarchitectured devices; with the maximum gas sensing response obtained at low reverse values. This working principle could be applied to many other one-dimensional p-n junction metal oxide nanostructures and used to tailor their gas sensor responses.</style></abstract><label><style face="normal" font="default" size="100%">gad2012coaxial</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.matchemphys.2012.05.034</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>346</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">346</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gad, Alaaeldin</style></author><author><style face="normal" font="default" size="100%">Hoffmann, Martin W. G.</style></author><author><style face="normal" font="default" size="100%">Leuning, Tessa</style></author><author><style face="normal" font="default" size="100%">Prades, J. Daniel</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Solar Driven Zinc Oxide Based Heterojunctions for Gas Sensing Applications</style></title><secondary-title><style face="normal" font="default" size="100%">14th International Meeting on Chemical Sensors - IMCS 2012</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1312-1315</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year></dates><abstract><style face="normal" font="default" size="100%">Zinc oxide-based heterojunctions are promising material systems for optoelectronic devices to overcome the challenges of growing stable p-type ZnO. In this work, CdS@n-ZnO/ p-Si nanowires heterojunctions were fabricated through a combination of wet-chemical etching (Si NWs) and atomic layer deposition (ZnO) techniques followed by chemical bath deposition (CdS). The electrical properties of the obtained heterojunctions were evaluated by analysing current-voltage (I–V) and capacitance-voltage (C–V) characteristics. The (I-V) characteristics in dark conditions at room temperature exhibited diode characteristics, while solar light illumination shifts the I-V characteristics to a photovoltaic effect. The sensing properties, tested under solar simulated light, toward oxidizing gases, showed a good and reproducible sensing response toward oxygen gas at room temperature. These heterojunction-based devices are potential candidates for the development of a new generation of solar driven gas sensors.</style></abstract><label><style face="normal" font="default" size="100%">gad2012solar</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.ama-science.org/proceedings/details/1213</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>344</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">344</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Cavelius, Christian</style></author><author><style face="normal" font="default" size="100%">Moh, Karsten</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;INM Leibniz Inst New Mat, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Chemically Designed Growth of Monodisperse Iron Oxide Nanocrystals</style></title><secondary-title><style face="normal" font="default" size="100%">Crystal Growth &amp; Design</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Cryst Growth Des</style></alt-title></titles><pages><style face="normal" font="default" size="100%">5948-5955</style></pages><volume><style face="normal" font="default" size="100%">12</style></volume><number><style face="normal" font="default" size="100%">12</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">Dec</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1528-7483</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000311858600017</style></accession-num><abstract><style face="normal" font="default" size="100%">The authors describe here a chem. controlled pathway for the designed synthesis of Fe oxide nanoparticles by thermal decompn. of Fe(II) and Fe(III) oxalates in high-boiling solvents in the presence of oleylamine and oleic acid acting as capping ligands. The phase compn. of the nanocrystals (Fe, FeO, Fe3O4, or $\alpha$-Fe2O3) could be precisely controlled by adjusting the synthesis conditions or by addn. of appropriate oxidants, such as trimethylamine-N-oxide (TMAO), which produced highly monodisperse Fe(III) oxide particles at 6-25 nm in good yields. The decompn. behavior of different precursor/TMAO mixts. was elucidated by DSC and TG, and resulting particles were characterized by comprehensive HR-TEM and XRD analyses.</style></abstract><label><style face="normal" font="default" size="100%">cavelius2012chemically</style></label><notes><style face="normal" font="default" size="100%">047rn&#xD;Times Cited:20&#xD;Cited References Count:32</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/cg300936t</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/cg300936t</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>342</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">342</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Brückmann, Lisa</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Stucky, Stefan</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Inorganic and Materials Chemistry, Institute of Inorganic Chemistry, University of Cologne, Greinstrasse 6, 50939 Cologne, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Novel Air-Stable and Volatile Bis(pyridylalkenolato)palladium(II) and -platinum(II) Derivatives</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">536-542</style></pages><volume><style face="normal" font="default" size="100%">51</style></volume><number><style face="normal" font="default" size="100%">1</style></number><edition><style face="normal" font="default" size="100%">2011/12/17</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">January</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><accession-num><style face="normal" font="default" size="100%">22171636</style></accession-num><abstract><style face="normal" font="default" size="100%">Six novel homoleptic palladium(II) and platinum(II) complexes of donor-substituted alkenol ligands PyCHC(R)OH; Py = pyridine, R = CH(3), CF(3), C(2)F(5), C(3)F(7) of the general formula MPyCHC(R)O(2) (M = Pd, Pt) were synthesized by reacting the deprotonated ligands with PdCl(2) and K(2)PtCl(4), respectively. Molecular structures, revealed by single-crystal X-ray diffraction analyses, showed a square-planar arrangement of ligands around palladium and platinum centers, with the pyridine-ring nitrogen atoms situated in a mutually trans position. The monomeric nature of the compounds in the solution state was confirmed by multinuclear ((1)H, (13)C, and (19)F) NMR spectroscopy. Thermal decomposition profiles recorded under a nitrogen atmosphere suggested their potential as volatile precursors to palladium and platinum materials. The volatility was increased upon elongation of the perfluoroalkyl chain, which suppressed the intermolecular interactions, as is evident in crystal packings. The volatility of these compounds was attributed to bidentate chelation of the alkenol units and cooperativity among the electron-back-donating nitrogen atom and interplay of electron-withdrawing C(x)F(y) groups, resulting in an effective steric shielding of the metal atoms.</style></abstract><label><style face="normal" font="default" size="100%">bruckmann2012novel</style></label><notes><style face="normal" font="default" size="100%">Bruckmann, Lisa&#xD;Tyrra, Wieland&#xD;Stucky, Stefan&#xD;Mathur, Sanjay&#xD;eng&#xD;Inorg Chem. 2012 Jan 2;51(1):536-42. doi: 10.1021/ic201996r. Epub 2011 Dec 15.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/ic201996r</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/ic201996r</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>341</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">341</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Brückmann, Lisa</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Berden, Giel</style></author><author><style face="normal" font="default" size="100%">Oomens, Jos</style></author><author><style face="normal" font="default" size="100%">Meijer, Anthony J. H. M.</style></author><author><style face="normal" font="default" size="100%">Schäfer, Mathias</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Examination of the Coordination Sphere of AlIII in Trifluoromethyl-Heteroarylalkenolato Complex Ions by Gas-Phase IRMPD Spectroscopy and Computational Modelling</style></title><secondary-title><style face="normal" font="default" size="100%">ChemPhysChem</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">2037-2045</style></pages><volume><style face="normal" font="default" size="100%">13</style></volume><number><style face="normal" font="default" size="100%">8</style></number><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">June</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">14394235</style></isbn><label><style face="normal" font="default" size="100%">bruckmann2012examination</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/cphc.201200132</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>340</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">340</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Appel, Linus</style></author><author><style face="normal" font="default" size="100%">Fiz, Raquel</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">University of Cologne, Institute of Inorganic and Materials Chemistry, Greinstrasse 6, 50939, Cologne, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">New iso-propoxides, tert-butoxides and neo-pentoxides of niobium(v): Synthesis, structure, characterization and stabilization by trifluoroheteroarylalkenolates and pyridine ligands</style></title><secondary-title><style face="normal" font="default" size="100%">Dalton Transactions</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Dalton Transactions</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1981-1990</style></pages><volume><style face="normal" font="default" size="100%">41</style></volume><number><style face="normal" font="default" size="100%">7</style></number><edition><style face="normal" font="default" size="100%">2011/12/20</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2012, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">Feb 21</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1477-9234</style></isbn><accession-num><style face="normal" font="default" size="100%">22180863</style></accession-num><abstract><style face="normal" font="default" size="100%">The synthesis and characterization of nine new heteroleptic alkoxides of niobium is described. Metathesis reactions of Nb(2)Cl(10) with (t)BuCH(2)OH and pyridine (py) or 4-dimethylaminopyridine (DMAP) affords monomeric octahedral complexes Nb(OCH(2)(t)Bu)(5)py (1) and Nb(OCH(2)(t)Bu)(5)DMAP (2), respectively, in high yields (&gt;60\%). The same reaction with (t)BuOH resulted in a chloro functionalized alkoxide Nb(O(t)Bu)(4)pyCl (3) and could not be pushed to complete removal of remaining Cl(-) ligand. The introduction of a chelating bidental ligand 3,3,3-trifluoro-1-(pyridine-2-yl)propen-2-ol (2-PyCHCOHCF(3)) (4&apos;&apos;) in the dimeric framework of Nb(2)(O(i)Pr)(10) (4&apos;) produced a heteroleptic, monomeric niobium complex Nb(O(i)Pr)(4)(2-PyCHCOCF(3)) (4) with significantly enhanced stability and volatility. As a comparison to (4), five different heteroaryl systems (5-9) with the same side chain have been synthesized and examined in order to understand the influence upon physio-chemical properties. All the new compounds (1-9) have been characterized by microanalysis, variable temperature multinuclear NMR spectroscopy, mass spectrometry, thermal analysis and single crystal X-ray diffraction studies ((3), (4) and (9)). The molecular structure of (3) revealed mononuclear species with Nb atoms present in the distorted octahedral environment of four (t)BuO, one chloride and one pyridine ligand. Compounds (4) and (9) consisting of four (i)PrO and a trifluoroheteroarylenolate exhibited a stronger distortion in the molecular geometry due to the rigidity of chelating $\beta$-alkenolate moiety.</style></abstract><label><style face="normal" font="default" size="100%">appel2012isopropoxides</style></label><notes><style face="normal" font="default" size="100%">Appel, Linus&#xD;Fiz, Raquel&#xD;Tyrra, Wieland&#xD;Mathur, Sanjay&#xD;eng&#xD;England&#xD;Dalton Trans. 2012 Feb 21;41(7):1981-90. doi: 10.1039/c1dt11668a. Epub 2011 Dec 16.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/c1dt11668a</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c1dt11668a</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>633</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">633</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Andon, Fernando Torres</style></author><author><style face="normal" font="default" size="100%">Xiao, Lisong</style></author><author><style face="normal" font="default" size="100%">Song, Xuefeng</style></author><author><style face="normal" font="default" size="100%">Kisin, Elena R.</style></author><author><style face="normal" font="default" size="100%">Murray, Ashley R.</style></author><author><style face="normal" font="default" size="100%">Shvedova, Anna A.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Fadeel, Bengt</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Carbon-based nanomaterials trigger interleukin-1β secretion in human macrophages</style></title><secondary-title><style face="normal" font="default" size="100%">Toxicology Letters</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">S203</style></pages><volume><style face="normal" font="default" size="100%">211</style></volume><dates><year><style face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style face="normal" font="default" size="100%">2012/06/17/</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0378-4274</style></isbn><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/pii/S0378427412008314</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">https://doi.org/10.1016/j.toxlet.2012.03.729</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>390</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">390</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zopes, David</style></author><author><style face="normal" font="default" size="100%">Kremer, Silke</style></author><author><style face="normal" font="default" size="100%">Scherer, Harald</style></author><author><style face="normal" font="default" size="100%">Belkoura, Lhoussaine</style></author><author><style face="normal" font="default" size="100%">Pantenburg, Ingo</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hydrolytic Decomposition of Tetramethylammonium Bis(trifluoromethyl)aurate(I), NMe4Au(CF3)2: A Route for the Synthesis of Gold Nanoparticles in Aqueous Medium</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">273-280</style></pages><volume><style face="normal" font="default" size="100%">2011</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year></dates><isbn><style face="normal" font="default" size="100%">14341948</style></isbn><abstract><style face="normal" font="default" size="100%">Monodisperse Au nanoparticles (AuNPs) were obtained by hydrolytic decompn. of a new mol. precursor, tetramethylammonium bis(trifluoromethyl)aurate(I), NMe4Au(CF3)2, which was characterized by spectroscopic and single-crystal x-ray diffraction analyses. On account of the simple and high-yield synthesis, the title compd. represents a versatile synthon and an alternative to the commonly used chloroauric acid (HAuCl4).</style></abstract><label><style face="normal" font="default" size="100%">zopes2011hydrolytic</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/ejic.201000863</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>389</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">389</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Xiao, Lisong</style></author><author><style face="normal" font="default" size="100%">Li, Jiangtian</style></author><author><style face="normal" font="default" size="100%">Brougham, Dermot F.</style></author><author><style face="normal" font="default" size="100%">Fox, Eoin K.</style></author><author><style face="normal" font="default" size="100%">Feliu, Neus</style></author><author><style face="normal" font="default" size="100%">Bushmelev, Alexey</style></author><author><style face="normal" font="default" size="100%">Schmidt, Annette</style></author><author><style face="normal" font="default" size="100%">Mertens, Natascha</style></author><author><style face="normal" font="default" size="100%">Kiessling, Fabian</style></author><author><style face="normal" font="default" size="100%">Valldor, Martin</style></author><author><style face="normal" font="default" size="100%">Fadeel, Bengt</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Chair Institute of Inorganic and Materials Chemistry, University of Cologne, D-50939 Cologne, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Water-Soluble Superparamagnetic Magnetite Nanoparticles with Biocompatible Coating for Enhanced Magnetic Resonance Imaging</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Nano</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">6315-6324</style></pages><volume><style face="normal" font="default" size="100%">5</style></volume><number><style face="normal" font="default" size="100%">8</style></number><edition><style face="normal" font="default" size="100%">2011/07/28</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style face="normal" font="default" size="100%">August</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1936-0851</style></isbn><accession-num><style face="normal" font="default" size="100%">21790153</style></accession-num><abstract><style face="normal" font="default" size="100%">Ultrasmall superparamagnetic Fe(3)O(4) nanoparticles (USIRONs) were synthesized by a novel, easily scalable chemical reduction of colloidal iron hydroxide under hydrothermal conditions. The average crystallite size (5.1 ± 0.5 nm) and good crystallinity of the samples were supported by HR-TEM analysis and the saturation magnetization value (47 emu g(-1)). Vitamin C, used as a chemical reducing agent, also served as a capping agent in the oxidized form (dehydroascorbic acid, DHAA) to impart nanoparticles with exceptional solubility and stability in water, PBS buffer, and cell culture medium. Detailed physicochemical analysis of the USIRON suspensions provided insight into the magnetic ordering phenomena within the colloid, arising from the formation of uniform clusters displaying a hydrodynamic size of 41 nm. Phantom experiments on the contrast agent (clinical 3 T MRI scanner) revealed an enhanced r(2)/r(1) ratio of 36.4 (r(1)= 5 s(-1) mM(-1) and r(2)= 182 s(-1) mM(-1)) when compared to the clinically approved agents. The potential of the DHAA-Fe(3)O(4) nanoparticles as negative contrast agents for MRI with optimal hydrodynamic size for extended blood circulation times was confirmed by strong contrast observed in T(2)- and T(2)*-weighted images. The cell tests performed with primary human immune-competent cells confirmed the excellent biocompatibility of USIRONs.</style></abstract><label><style face="normal" font="default" size="100%">xiao2011watersoluble</style></label><notes><style face="normal" font="default" size="100%">Xiao, Lisong&#xD;Li, Jiangtian&#xD;Brougham, Dermot F&#xD;Fox, Eoin K&#xD;Feliu, Neus&#xD;Bushmelev, Alexey&#xD;Schmidt, Annette&#xD;Mertens, Natascha&#xD;Kiessling, Fabian&#xD;Valldor, Martin&#xD;Fadeel, Bengt&#xD;Mathur, Sanjay&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;ACS Nano. 2011 Aug 23;5(8):6315-24. doi: 10.1021/nn201348s. Epub 2011 Aug 2.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/nn201348s</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/nn201348s</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>388</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">388</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Xia, Xin R.</style></author><author><style face="normal" font="default" size="100%">Monteiro-Riviere, Nancy A.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Song, Xuefeng</style></author><author><style face="normal" font="default" size="100%">Xiao, Lisong</style></author><author><style face="normal" font="default" size="100%">Oldenberg, Steven J.</style></author><author><style face="normal" font="default" size="100%">Fadeel, Bengt</style></author><author><style face="normal" font="default" size="100%">Riviere, Jim E.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Center for Chemical Toxicology Research and Pharmacokinetics, North Carolina State University, Raleigh, North Carolina 27607, USA.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Mapping the Surface Adsorption Forces of Nanomaterials in Biological Systems</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Nano</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">9074-9081</style></pages><volume><style face="normal" font="default" size="100%">5</style></volume><number><style face="normal" font="default" size="100%">11</style></number><edition><style face="normal" font="default" size="100%">2011/10/18</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1936-0851</style></isbn><accession-num><style face="normal" font="default" size="100%">21999618</style></accession-num><abstract><style face="normal" font="default" size="100%">The biological surface adsorption index (BSAI) is a novel approach to characterize surface adsorption energy of nanomaterials that is the primary force behind nanoparticle aggregation, protein corona formation, and other complex interactions of nanomaterials within biological systems. Five quantitative nanodescriptors were obtained to represent the surface adsorption forces (hydrophobicity, hydrogen bond, polarity/polarizability, and lone-pair electrons) of the nanomaterial interaction with biological components. We have mapped the surface adsorption forces over 16 different nanomaterials. When the five-dimensional information of the nanodescriptors was reduced to two dimensions, the 16 nanomaterials were classified into distinct clusters according their surface adsorption properties. BSAI nanodescriptors are intrinsic properties of nanomaterials useful for quantitative structure-activity relationship (QSAR) model development. This is the first success in quantitative characterization of the surface adsorption forces of nanomaterials in biological conditions, which could open a quantitative avenue in predictive nanomedicine development, risk assessment, and safety evaluation of nanomaterials.</style></abstract><label><style face="normal" font="default" size="100%">xia2011mapping</style></label><notes><style face="normal" font="default" size="100%">Xia, Xin R&#xD;Monteiro-Riviere, Nancy A&#xD;Mathur, Sanjay&#xD;Song, Xuefeng&#xD;Xiao, Lisong&#xD;Oldenberg, Steven J&#xD;Fadeel, Bengt&#xD;Riviere, Jim E&#xD;eng&#xD;R01 ES016138/ES/NIEHS NIH HHS/&#xD;R01 ES016138-01/ES/NIEHS NIH HHS/&#xD;Research Support, N.I.H., Extramural&#xD;Research Support, U.S. Gov&apos;t, Non-P.H.S.&#xD;ACS Nano. 2011 Nov 22;5(11):9074-81. doi: 10.1021/nn203303c. Epub 2011 Oct 27.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/nn203303c</style></url></related-urls></urls><custom2><style face="normal" font="default" size="100%">PMC3222732</style></custom2><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/nn203303c</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>387</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">387</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">von Hagen, R.</style></author><author><style face="normal" font="default" size="100%">Lepcha, A.</style></author><author><style face="normal" font="default" size="100%">Hoffmann, M.</style></author><author><style face="normal" font="default" size="100%">Di Biase, M.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ray, Suprakas Sinha</style></author><author><style face="normal" font="default" size="100%">Widjaja, Sujanto</style></author><author><style face="normal" font="default" size="100%">Singh, Dileep</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Morphology Controlled Electrospinning of V2O5 Nanofibres and their Gas Sensing Behavior</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured materials and nanotechnology V: Ceramic Engineering and Proceedings</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1-9</style></pages><volume><style face="normal" font="default" size="100%">32</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year></dates><pub-location><style face="normal" font="default" size="100%">Hoboken, N.J.</style></pub-location><publisher><style face="normal" font="default" size="100%">John Wiley &amp;amp; Sons</style></publisher><abstract><style face="normal" font="default" size="100%">Electrospinning of vanadyl acetylacetonate/polyvinylpyrrolidone hybrid nanofibers and calcination procedures design led to V2O5 nanofibers with control over their morphology. The fibers either consisted of densely joint nanorods or anisotropic nanocrystals forming porous nanofibers. They have been analyzed by thermogravimetric analysis, Fourier transform infrared spectroscopy, X-ray diffraction and scanning electron microscopy. Their dispersions in water/ethylene glycol could be used for inkjet printing of V2O5 gas sensors and the particle and film morphology influence on gas sensitivity was investigated.</style></abstract><label><style face="normal" font="default" size="100%">vonhagen2011morphology</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/9781118095362</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>386</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">386</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Song, Xuefeng</style></author><author><style face="normal" font="default" size="100%">Gao, Lian</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Chinese Acad Sci, State Key Lab High Performance Ceram &amp; Superfine, Shanghai Inst Ceram, Shanghai 200050, Peoples R China</style></auth-address><titles><title><style face="normal" font="default" size="100%">Synthesis, Characterization, and Gas Sensing Properties of Porous Nickel Oxide Nanotubes</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry C</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Phys Chem C</style></alt-title></titles><pages><style face="normal" font="default" size="100%">21730-21735</style></pages><volume><style face="normal" font="default" size="100%">115</style></volume><number><style face="normal" font="default" size="100%">44</style></number><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000296394300026</style></accession-num><abstract><style face="normal" font="default" size="100%">A novel approach was employed to synthesize porous NiO nanotubes with controllable interior voids based on an effective interplay of Kirkendall effect and vol. change upon phase transformation. For this purpose, nickel nanowires were chem. converted into Ni3S2/Ni core-shell structures, followed by a controlled oxidn., whereby the assocd. vol. change (Ni → NiO conversion) resulted in 1-dimensional porous structure with voids. The voids between the Ni core and Ni3S2 shell could be controlled by adjusting the oxidn. conditions that enabled fabrication of hollow and double-walled morphologies. Phase compn., morphol. evolution, and porosity of double-walled NiO nanotubes were analyzed by x-ray diffraction, scanning and TEM, and N2 adsorption-desorption studies. Gaseous sulfur oxides formed during the oxidn. of Ni3S2/Ni structures resulted in a perforated structure with multiple voids with pores ranging between 1 and 14 nm. The unique complex structure with the interpenetrating voids and the surface porosity resulted in a high sp. surface area of 161.6 m2 g-1. The gas sensing property of such double-walled structure was found to vary as a function of the concentric void between the core and the shell. Gas-sensing measurements in hollow porous core-shell NiO nanotubes exhibited excellent sensitivity toward ethanol, originating from efficient adsorption of target mols. in the interior voids and their rapid diffusion and transport through the porous structures.</style></abstract><label><style face="normal" font="default" size="100%">song2011synthesis</style></label><notes><style face="normal" font="default" size="100%">839ug&#xD;Times Cited:83&#xD;Cited References Count:45</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/jp208093s</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/jp208093s</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>385</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">385</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author><author><style face="normal" font="default" size="100%">Ohji, Tatsuki</style></author><author><style face="normal" font="default" size="100%">Asthana, Rajiv</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ceramic Integration and Joining Technologies: From Macro to Nanoscale</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style face="normal" font="default" size="100%">September</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Inc.</style></publisher><isbn><style face="normal" font="default" size="100%">9780470391228</style></isbn><abstract><style face="normal" font="default" size="100%">The article reviews the book &quot;Ceramic Integration and Joining Technologies: From Macro to Nanoscale&quot; edited by Mrityunjay Singh.</style></abstract><label><style face="normal" font="default" size="100%">singh2011ceramic</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">10.1002/9781118056776</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>384</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">384</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ramirez-Hernandez, Francisco</style></author><author><style face="normal" font="default" size="100%">Prades, J. Daniel</style></author><author><style face="normal" font="default" size="100%">Morante, Joan R.</style></author><author><style face="normal" font="default" size="100%">Hackner, Angelika</style></author><author><style face="normal" font="default" size="100%">Beer, Sebastian</style></author><author><style face="normal" font="default" size="100%">Müller, Gerhard</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Simultaneous Resistive and Ionization Readout of Single Metal Oxide Nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Procedia Engineering</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1489-1492</style></pages><volume><style face="normal" font="default" size="100%">25</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year></dates><isbn><style face="normal" font="default" size="100%">18777058</style></isbn><abstract><style face="normal" font="default" size="100%">Gas detection expts. were performed with individual tin dioxide (SnO2) nanowires specifically configured to observe surface ion (SI) emission response towards representative analyte species. These devices were found to work at much lower temps. (T ≈ 280°C) and bias voltages (V ≈ 2 V) than their micro-counterparts, thereby demonstrating the inherent potential of individual nanostructures in building functional nanodevices. The high selectivity of our miniaturized sensors emerges from the dissimilar sensing mechanisms of SI as compared to std. resistive (RES) type gas sensors. By employing this innovative detection principle (SI) together with conventional RES measurements, significantly improved selectivity can be attained with a single gas sensor device. Self-heating of the SnO2 nanowires moreover opens up a road towards ultra-low power consumption gas sensors.</style></abstract><label><style face="normal" font="default" size="100%">ramirezhernandez2011simultaneous</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S1877705811060371</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>383</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">383</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prades, J.D.</style></author><author><style face="normal" font="default" size="100%">Hernández-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Fischer, T.</style></author><author><style face="normal" font="default" size="100%">Hoffmann, M.</style></author><author><style face="normal" font="default" size="100%">Müller, R.</style></author><author><style face="normal" font="default" size="100%">López, N.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Simultaneous CO and Humidity Quantification with Self-Heated Nanowires in Pulsed Mode</style></title><secondary-title><style face="normal" font="default" size="100%">Procedia Engineering</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1485-1488</style></pages><volume><style face="normal" font="default" size="100%">25</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year></dates><isbn><style face="normal" font="default" size="100%">18777058</style></isbn><label><style face="normal" font="default" size="100%">prades2011simultaneous</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S187770581106036X</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>382</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">382</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pan, Jun</style></author><author><style face="normal" font="default" size="100%">Song, Xuefeng</style></author><author><style face="normal" font="default" size="100%">Zhang, Jun</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Xiong, Qihua</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Nanyang Technol Univ, Sch Phys &amp; Math Sci, Div Phys &amp; Appl Phys, Singapore 637371, Singapore&#xD;Nanyang Technol Univ, Sch Elect &amp; Elect Engn, Div Microelect, Singapore 639798, Singapore</style></auth-address><titles><title><style face="normal" font="default" size="100%">Switchable Wettability in SnO2 Nanowires and SnO2@SnO2 Heterostructures</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry C</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Phys Chem C</style></alt-title></titles><pages><style face="normal" font="default" size="100%">22225-22231</style></pages><volume><style face="normal" font="default" size="100%">115</style></volume><number><style face="normal" font="default" size="100%">45</style></number><keywords><keyword><style face="normal" font="default" size="100%">2011</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000296685800016</style></accession-num><abstract><style face="normal" font="default" size="100%">Tin oxide nanowires and heterostructures thereof were synthesized by sequential application of thermal and plasma-assisted chem. vapor deposition (CVD) methods. The wetting properties of surfaces based on individual nanowires, hyperbranched SnO2@SnO2 structures, and SnO2@SnO2@SiOx core-shell heterostructures could be modulated from superhydrophilic to superhydrophobic by changing both chem. compn. and the geometrical architecture of nanoheterostructures Whereas the randomly grown SnO2 nanowires with a contact angle of 3° exhibited superhydrophilicity, the contact angle of SnO2@SnO2 heterostructures synthesized by a two-step CVD process increased to 133°. The corresponding contact angle of SnO2@SnO2@SiOx heterostructures was enhance to 155.8° by a hydrophobic SiOx coating. Switchable surface wettability in SnO2@SnO2@SiOx heterostructures was obsd. by alteration of UV irradn., storage in dark, and O2 annealing, indicating that geometric microstructure was the major determinant in the switchable wettability. .The significant change in the surface wettability upon changing the geometrical features is of potential interest in functional coating such as antifinger print and self-cleaning surfaces.</style></abstract><label><style face="normal" font="default" size="100%">pan2011switchable</style></label><notes><style face="normal" font="default" size="100%">843pz&#xD;Times Cited:47&#xD;Cited References Count:36</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/jp207376t</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/jp207376t</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>380</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">380</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pan, Jun</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Werner, Ulf</style></author><author><style face="normal" font="default" size="100%">Prades, Joan Daniel</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Soldera, Flavio</style></author><author><style face="normal" font="default" size="100%">Mücklich, Frank</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Chair Inorgan &amp; Mat Chem, D-50939 Cologne, Germany&#xD;Leibniz Inst New Mat, D-66123 Saarbrucken, Germany&#xD;Univ Barcelona, Dept Elect, E-08028 Barcelona, Spain&#xD;Catalonia Inst Energy Res, Dept Adv Mat Energy Applicat, E-08930 Barcelona, Spain&#xD;Univ Saarland, Dept Mat Sci, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Heteroepitaxy of SnO2 Nanowire Arrays on TiO2 Single Crystals: Growth Patterns and Tomographic Studies</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry C</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Phys Chem C</style></alt-title></titles><pages><style face="normal" font="default" size="100%">15191-15197</style></pages><volume><style face="normal" font="default" size="100%">115</style></volume><number><style face="normal" font="default" size="100%">31</style></number><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style face="normal" font="default" size="100%">August</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000293419700010</style></accession-num><abstract><style face="normal" font="default" size="100%">Oriented SnO2 nanowire (NW) arrays were grown on TiO2(001) substrates by mol.-based CVD of Sn(OtBu)4. Preferred growth directions ([101], [-101], [011], and [0-11]) of SnO2 NWs were correlated to surface energy consideration and crystallog. relation between the substrate and NW material by comprehensive electron microscopy and bulk tomog. studies. The proposed growth incubation model (tilting of catalyst/NW interface due to driving force of surface energy) explains the formation mechanism of oriented SnO2 NWs on TiO2 substrates. These results allowed the authors to also study the I-V characteristics and gas-sensing properties of individual SnO2 NWs grown with a perfectly defined crystal orientation ([101]).</style></abstract><label><style face="normal" font="default" size="100%">pan2011heteroepitaxy</style></label><notes><style face="normal" font="default" size="100%">801em&#xD;Times Cited:24&#xD;Cited References Count:37</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/jp202685a</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/jp202685a</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>381</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">381</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pan, Jun</style></author><author><style face="normal" font="default" size="100%">Hühne, Sven-Martin</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Xiao, Lisong</style></author><author><style face="normal" font="default" size="100%">Born, Philip</style></author><author><style face="normal" font="default" size="100%">Mader, Werner</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Univ Bonn, Inst Inorgan Chem, D-53117 Bonn, Germany&#xD;Leibniz Inst New Mat, CVD Div, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">SnO2–TiO2 Core–Shell Nanowire Structures: Investigations on Solid State Reactivity and Photocatalytic Behavior</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry C</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Phys Chem C</style></alt-title></titles><pages><style face="normal" font="default" size="100%">17265-17269</style></pages><volume><style face="normal" font="default" size="100%">115</style></volume><number><style face="normal" font="default" size="100%">35</style></number><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style face="normal" font="default" size="100%">September</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000294386000005</style></accession-num><abstract><style face="normal" font="default" size="100%">Two-step chem. vapor deposition (CVD) in combination with metal-catalyzed vapor-liq.-solid (VLS) growth mechanism was used as a new approach to synthesize and modify the morphol. of SnO2-TiO2 core-shell nanowires. SnO2 nanowires were grown by decompn. of Sn(OtBu)4 precursor on Au-coated Al2O3 substrates followed by the growth of a TiO2 overlayer by the CVD of Ti(OiPr)4. Structural characterization of SnO2-TiO2 heterostructures by x-ray diffraction and high-resoln. TEM revealed the formation of mixed SnxTi1-xO2 compns. (x = 0.857-1.0) at the SnO2-TiO2 phase boundaries, where x depended on the annealing temps. The obsd. oriented attachment of TiO2 nanoclusters on single crystal SnO2 core was possibly due to low lattice mismatch. The photocatalytic studies suggested an enhanced activity in SnO2-TiO2 heterostructures due to higher surface area and change in the electronic structures caused by Sn4+ doping in TiO2.</style></abstract><label><style face="normal" font="default" size="100%">pan2011sno2tio2</style></label><notes><style face="normal" font="default" size="100%">813rq&#xD;Times Cited:72&#xD;Cited References Count:38</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/jp201901b</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/jp201901b</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>377</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">377</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Singh, Anirudh</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Investigations on homo- and heteroleptic isopropoxometallates of lead(II)</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the Indian Chemical Society</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1673-1678</style></pages><volume><style face="normal" font="default" size="100%">88</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year></dates><isbn><style face="normal" font="default" size="100%">0019-4522</style></isbn><abstract><style face="normal" font="default" size="100%">Novel homo- and hetero-leptic isopropoxometallates of lead(II) of the types \\Zr2(OPri)9\Pb($\mu$-F)\2 (1a), \\Nb(OPri)6\Pb($\mu$-F)\2 (1b), \\Al(OPri)4\Pb($\mu$-F)\2 (1c), \\Sn2(OPri)9\Pb($\mu$-F)\2 (1d), Pb\Zr2(OPri)9\2 (1e), Pb\Nb(OPri)6\2 (1f), Pb\Al(OPri)4\2 (1g) and Pb\Sn2(OPri)9\2 (1h) were prepd. for the first time by interactions of PbF2 and the appropriate potassium isopropoxometalate in 1 : 1 and 1 : 2 molar ratio. Fluoro-derivs. 1a, 1b and 1c undergo fluoride-alkoxide or isopropoxometalate exchange reactions to yield derivs. of the types \\Zr2(OPri)9\Pb($\mu$-OR)\2 (R = Pri (2a), But (2b)), \\Nb(OPri)6\Pb($\mu$-OPri)\2 (2c), \\Al(OPri)4\Pb($\mu$-OPri)\2 (2d), \Zr2(OPri)9\Pb\Al(OPri)4\ (2e), \Sn2(OPri)9\Pb\Zn2(OPri)9\ (2f), \Nb(OPri)6\Pb\Ta(OPri)6\ (2g), \Al(OPri)4\Pb\Nb(OPri)6\ (2h) and \Al(OPri)4\Pb\Sn2(OPri)9\ (2i). Characterization of new complexes is mainly based on elemental/isopropoxo group analyses, mol. wt. measurements, IR and multinuclear (1H, 13C, 19F, 27Al and 207Pb) NMR spectral studies.</style></abstract><label><style face="normal" font="default" size="100%">mathur2011investigations</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.researchgate.net/publication/287427002_Investigations_on_homo-_and_hetero-leptic_isopropoxometallates_of_leadII</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>379</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">379</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ruegamer, Thomas</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Dept Chem, D-50939 Cologne, Germany&#xD;Leibniz Inst New Mat INM, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Transparent and Scratch-Resistant C:ZrOx Coatings on Polymer and Glass by Plasma-Enhanced Chemical Vapor Deposition</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Applied Ceramic Technology</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Int J Appl Ceram Tec</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">International Journal of Applied Ceramic Technology</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1050-1058</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style face="normal" font="default" size="100%">Sep-Oct</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1546542X</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000297249200009</style></accession-num><abstract><style face="normal" font="default" size="100%">Transparent and scratch-resistant zirconium oxide thin films were deposited in radio-frequency plasma-enhanced chem. vapor deposition process on glass and polycarbonate substrates using zirconium-tetra-tert-butoxide, Zr(OtBu)4, as the precursor. Investigations on film morphol. (AFM), thickness (cross-sectional SEM), phase structure (x-ray diffraction), chem. compn. (XPS), and optical properties (UV/Vis, ellipsometry) revealed the interplay of process parameters (plasma power, gas compn., deposition time, and precursor flux) on the compn. and properties of the coatings. High-quality transparent coatings (&gt;90\%) with a tunable refractive index (n = 1.7-2.1) and abrasion-resistant properties were deposited on both polymer and glass substrates. Despite low deposition temps. (&lt;100°C), the coatings showed good adherence to the substrate and extraordinary barrier properties that were further improved by depositing intermediary SiOx-layers. Phase anal. of the predominantly amorphous films showed the incipient crystn. of ZrO2.</style></abstract><label><style face="normal" font="default" size="100%">mathur2011transparent</style></label><notes><style face="normal" font="default" size="100%">851ds&#xD;Times Cited:3&#xD;Cited References Count:27</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1111/j.1744-7402.2010.02537.x</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1111/j.1744-7402.2010.02537.x</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>378</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">378</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ray, Suprakas Sinha</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology V: Ceramic Engineering and Science Proceedings, Volume 32, Issue 7</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year></dates><isbn><style face="normal" font="default" size="100%">978-1-118-05992-0</style></isbn><abstract><style face="normal" font="default" size="100%">A collection of papers from The American Ceramic Society&apos;s 35th International Conference on Advanced Ceramics and Composites, held in Daytona Beach, Florida, January 23-28, 2011. This issue includes papers presented in the 5th International Symposium on Nanostructured Materials and Nanotechnology on topics such as Nanotubes, Nanorods, Nanowires and other One-dimensional Structures; Nanostructured Membranes, Thin Films, and Functional Coatings; Synthesis, Functionalization and Processing of Nanostructured Materials; and Advanced Applications</style></abstract><label><style face="normal" font="default" size="100%">mathur2011nanostructured</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://eu.wiley.com/WileyCDA/WileyTitle/productCd-1118059921.html</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>376</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">376</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Llosa, J.</style></author><author><style face="normal" font="default" size="100%">de Marigorta, M. Martínez</style></author><author><style face="normal" font="default" size="100%">Bécares, J.</style></author><author><style face="normal" font="default" size="100%">Monereo, O.</style></author><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Vilajosana, I.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Cirera, A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanomaterials make possible integrating gas sensors in wireless and ultralow power consumption motes</style></title><secondary-title><style face="normal" font="default" size="100%">Procedia Engineering</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1053-1056</style></pages><volume><style face="normal" font="default" size="100%">25</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year></dates><isbn><style face="normal" font="default" size="100%">18777058</style></isbn><abstract><style face="normal" font="default" size="100%">Power consumption is one of the most challenging issues that hamper the development of autonomous chemical and gas sensors. Here, we present the first prototypes of a new generation of fully autonomous gas sensor systems that combine self-heated nanosensors with wireless communications and energy harvesting systems for extended battery lifetime.</style></abstract><label><style face="normal" font="default" size="100%">llosa2011nanomaterials</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S1877705811059285</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>375</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">375</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Liu, Gang</style></author><author><style face="normal" font="default" size="100%">Lao, Ruojun</style></author><author><style face="normal" font="default" size="100%">Xu, Li</style></author><author><style face="normal" font="default" size="100%">Xu, Qin</style></author><author><style face="normal" font="default" size="100%">Li, Lanying</style></author><author><style face="normal" font="default" size="100%">Zhang, Min</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Fan, Chunhai</style></author><author><style face="normal" font="default" size="100%">Song, Shiping</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Shanghai Institute of Measurement and Testing Technology, Shanghai 201203, China. liug@simt.com.cn</style></auth-address><titles><title><style face="normal" font="default" size="100%">Detection of Single-Nucleotide Polymorphism on uidA Gene of Escherichia coli by a Multiplexed Electrochemical DNA Biosensor with Oligonucleotide-Incorporated Nonfouling Surface</style></title><secondary-title><style face="normal" font="default" size="100%">Sensors</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">8018-8027</style></pages><volume><style face="normal" font="default" size="100%">11</style></volume><number><style face="normal" font="default" size="100%">8</style></number><edition><style face="normal" font="default" size="100%">2011/12/14</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style face="normal" font="default" size="100%">August</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1424-8220</style></isbn><accession-num><style face="normal" font="default" size="100%">22164059</style></accession-num><abstract><style face="normal" font="default" size="100%">We report here a practical application of a multiplexed electrochemical DNA sensor for highly specific single-nucleotide polymorphism (SNP) detection. In this work, a 16-electrode array was applied with an oligonucleotide-incorporated nonfouling surfaces (ONS) on each electrode for the resistance of unspecific absorption. The fully matched target DNA templated the ligation between the capture probe assembled on gold electrodes and the tandem signal probe with a biotin moiety, which could be transduced to peroxidase-based catalyzed amperometric signals. A mutant site (T93G) in uidA gene of E. coli was analyzed in PCR amplicons. 10\% percentage of single mismatched mutant gene was detected, which clearly proved the selectivity of the multiplexed electrochemical DNA biosensor when practically applied.</style></abstract><label><style face="normal" font="default" size="100%">liu2011detection</style></label><notes><style face="normal" font="default" size="100%">Liu, Gang&#xD;Lao, Ruojun&#xD;Xu, Li&#xD;Xu, Qin&#xD;Li, Lanying&#xD;Zhang, Min&#xD;Shen, Hao&#xD;Mathur, Sanjay&#xD;Fan, Chunhai&#xD;Song, Shiping&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;Switzerland&#xD;Sensors (Basel). 2011;11(8):8018-27. doi: 10.3390/s110808018. Epub 2011 Aug 15.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.3390/s110808018</style></url></related-urls></urls><custom2><style face="normal" font="default" size="100%">PMC3231733</style></custom2><electronic-resource-num><style face="normal" font="default" size="100%">10.3390/s110808018</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>374</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">374</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernández-Ramírez, F.</style></author><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author><author><style face="normal" font="default" size="100%">Ohji, Tatsuki</style></author><author><style face="normal" font="default" size="100%">Asthana, Rajiv</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Integration of Nanowires in New Devices and Circuit Architectures: Recent Developments and Challenges</style></title><secondary-title><style face="normal" font="default" size="100%">Ceramic Integration and Joining Technologies</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">575-639</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Inc.</style></publisher><isbn><style face="normal" font="default" size="100%">9781118056776</style></isbn><abstract><style face="normal" font="default" size="100%">This chapter contains sections titled: * Introduction * 1-D Nanoscale Building Blocks: Synthesis and Growth Mechanism * Structure-Property Characterization and Relationship * Development of Nanodevice Architectures * Summary * Acknowledgments * References</style></abstract><label><style face="normal" font="default" size="100%">hernandezramirez2011integration</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/9781118056776.ch18</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>637</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">637</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Prades, Juan Daniel</style></author><author><style face="normal" font="default" size="100%">Hackner, Angelika</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mueller, Gerhard</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Morante, Joan Ramon</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Miniaturized ionization gas sensors from single metal oxide nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Nanoscale</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nanoscale</style></full-title></periodical><pages><style face="normal" font="default" size="100%">630-634</style></pages><volume><style face="normal" font="default" size="100%">3</style></volume><number><style face="normal" font="default" size="100%">2</style></number><dates><year><style face="normal" font="default" size="100%">2011</style></year></dates><publisher><style face="normal" font="default" size="100%">The Royal Society of Chemistry</style></publisher><isbn><style face="normal" font="default" size="100%">2040-3364</style></isbn><abstract><style face="normal" font="default" size="100%">Gas detection experiments were performed with individual tin dioxide (SnO2) nanowires specifically configured to observe surface ion (SI) emission response towards representative analyte species. These devices were found to work at much lower temperatures (T ≈ 280 °C) and bias voltages (V ≈ 2 V) than their micro-counterparts, thereby demonstrating the inherent potential of individual nanostructures in building functional nanodevices. High selectivity of our miniaturized sensors emerges from the dissimilar sensing mechanisms of those typical of standard resistive-type sensors (RES). Therefore, by employing this detection principle (SI) together with RES measurements, better selectivity than that observed in standard metal oxide sensors could be demonstrated. Simplicity and specificity of the gas detection as well as low-power consumption make these single nanowire devices promising technological alternatives to overcome the major drawbacks of solid-state sensor technologies.</style></abstract><work-type><style face="normal" font="default" size="100%">10.1039/C0NR00528B</style></work-type><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C0NR00528B</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/C0NR00528B</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>372</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">372</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hemmer, Eva</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author><author><style face="normal" font="default" size="100%">Adlung, Matthias</style></author><author><style face="normal" font="default" size="100%">Wickleder, Claudia</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Tokyo Univ Sci, Dept Mat Sci &amp; Technol, Chiba 2788510, Japan&#xD;Univ Saarland, Inst Inorgan Chem, D-66123 Saarbrucken, Germany&#xD;Univ Siegen, Inst Inorgan Chem, D-57068 Siegen, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Homo- and Heterometallic Terbium Alkoxides - Synthesis, Characterization and Conversion to Luminescent Oxide Nanostructures</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Eur J Inorg Chem</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2148-2157</style></pages><volume><style face="normal" font="default" size="100%">2011</style></volume><number><style face="normal" font="default" size="100%">13</style></number><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">14341948</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000290232700016</style></accession-num><abstract><style face="normal" font="default" size="100%">Terbium alkoxides in homometallic - [Tb-3(mu(3)-OtBu)(2)(mu(2)-OtBu)(3)(OtBu)(4) (HOtBu)(2)] (1), [Tb{OC(tBu)(3)}(3)(THF)] (2) - and heterometallic configurations - [TbAl(mu(2)-OiPr)(3)(OiPr)(3)(iP-rOH)](2) (3), [TbAl3(mu(2)-OiPr)(6)(OiPr)(6)] (4) - were synthesized and characterized by single- crystal X-ray diffraction. Decomposition of 1 and 2 under solvothermal conditions produced Tb(OH) 3 nanorods, whereby the material formation and crystallization were influenced by the steric profile of the organic ligand, which controlled the hydrolysis and condensation reactions of the precursor molecules. Monophasic terbium aluminate in the perovskite phase (TbAlO3) was obtained by the sol-gel processing of 3. Heterometallic frame-works present in 3 and 4 were, however, unstable under solvothermal conditions and resulted in hydroxide-oxide composites [Tb(OH)(3)/Al2O3/Al(OH)(3)]. Compound 4 exhibited sufficient vapour pressure to be used in the chemical vapour deposition (CVD) process to grow Tb-O-Al thin films. Crystalline compositions obtained on MgAl2O4 and SiO2 (quartz) substrates were garnet and perovskite phases, and were ascribed to the crystallographic relationship between the substrate and CVD deposits. The optical properties of the powders obtained were studied by photoluminescence spectroscopy.</style></abstract><label><style face="normal" font="default" size="100%">hemmer2011heterometallic</style></label><notes><style face="normal" font="default" size="100%">759ia&#xD;Times Cited:11&#xD;Cited References Count:71</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/ejic.201000963</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/ejic.201000963</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>371</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">371</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hackner, Angelika</style></author><author><style face="normal" font="default" size="100%">Beer, Sebastian</style></author><author><style face="normal" font="default" size="100%">Müller, Gerhard</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fast responding ephedrine detection with miniaturized surface ionization gas sensors</style></title><secondary-title><style face="normal" font="default" size="100%">Procedia Engineering</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1325--1328</style></pages><volume><style face="normal" font="default" size="100%">25</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year></dates><isbn><style face="normal" font="default" size="100%">18777058</style></isbn><abstract><style face="normal" font="default" size="100%">We report on novel kinds of miniaturized gas sensors whose operation is based on the principle of surface ionization (SI). In SI gas sensing adsorbed analyte species are ionized at a heated solid surface and the formed ions are extd. towards an oppositely charged collector electrode positioned a short distance from the emitting surface. Here, we show that SI sensors allow for a fast, sensitive and selective detection of illicit drugs in the presence of large concns. of solvent water.</style></abstract><label><style face="normal" font="default" size="100%">hackner2011responding</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S1877705811059960</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>370</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">370</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Giebelhaus, Irina</style></author><author><style face="normal" font="default" size="100%">Müller, Ralf</style></author><author><style face="normal" font="default" size="100%">Tyrra, Wieland</style></author><author><style face="normal" font="default" size="100%">Pantenburg, Ingo</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Chair Inorgan &amp; Mat Chem, Dept Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">First air stable tin(II) beta-heteroarylalkenolate: Synthesis, characterization and application in chemical vapor deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganica Chimica Acta</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Inorg Chim Acta</style></alt-title></titles><pages><style face="normal" font="default" size="100%">340-346</style></pages><volume><style face="normal" font="default" size="100%">372</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun 15</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">00201693</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000290943100047</style></accession-num><abstract><style face="normal" font="default" size="100%">Prepn. and crystal structure of bis(\$2-N,O-2-4,5-dimethyloxazolyl-1,1,1-trifluoro-propen-2-olato)tin SnII(Me2C3NO)(CHCOCF3)2 (1) that was obtained by reacting SnN(SiMe3)22 with 2 M equiv. of the \$-heteroarylalkenol (Me2C3NO)(CHCOHCF3) (2) are reported. The mol. structures of the ligand and the tin deriv. were elucidated by single crystal X-ray diffraction and multi-nuclear NMR spectroscopy that confirmed the monomeric nature and fourfold coordination of the tin(II) center with a pseudo-pyramidal geometry. The bidentate chelating mode of 2 imparted high air stability to 1, which together with its high volatility made it a suitable precursor for chem. vapor deposition. CVD of 1 on gold-coated Al2O3 substrates produced single cryst. SnO2 nanowires by vapor-liq.-solid growth mechanism. Transmission electron microscopy studies and X-ray diffraction data confirmed the high crystallinity of SnO2 nanowires possessing an av. diam. of 90 nm.</style></abstract><label><style face="normal" font="default" size="100%">giebelhaus2011first</style></label><notes><style face="normal" font="default" size="100%">Sp. Iss. SI&#xD;768nz&#xD;Times Cited:23&#xD;Cited References Count:29</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0020169311002131</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.ica.2011.02.052</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>369</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">369</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">El-Gamel, Nadia E. A.</style></author><author><style face="normal" font="default" size="100%">Wortmann, Laura</style></author><author><style face="normal" font="default" size="100%">Arroub, Karim</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Chemistry Department, Faculty of Science, Cairo University, 12613 Giza, Egypt. nadinealy@hotmail.com</style></auth-address><titles><title><style face="normal" font="default" size="100%">SiO2@Fe2O3 core-shell nanoparticles for covalent immobilization and release of sparfloxacin drug</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Communications</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">10076-10078</style></pages><volume><style face="normal" font="default" size="100%">47</style></volume><number><style face="normal" font="default" size="100%">36</style></number><edition><style face="normal" font="default" size="100%">2011/08/11</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2011, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style face="normal" font="default" size="100%">September</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1364-548X</style></isbn><accession-num><style face="normal" font="default" size="100%">21829847</style></accession-num><abstract><style face="normal" font="default" size="100%">Silica-coated Fe(2)O(3) nanoparticles were synthesized as carriers for the covalent immobilization and release of antimicrobial drug sparfloxacin (SPFX). SPFX-loaded nanoparticles exhibited time-dependent drug release, with no measurable in vitro cytotoxicity, making the drug@nanoparticle conjugates potentially relevant for nanomedicine applications.</style></abstract><label><style face="normal" font="default" size="100%">elgamel2011sio2fe2o3</style></label><notes><style face="normal" font="default" size="100%">El-Gamel, Nadia E A&#xD;Wortmann, Laura&#xD;Arroub, Karim&#xD;Mathur, Sanjay&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;England&#xD;Chem Commun (Camb). 2011 Sep 28;47(36):10076-8. doi: 10.1039/c1cc13708e. Epub 2011 Aug 10.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C1CC13708E</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c1cc13708e</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>415</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">415</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Zopes, David</style></author><author><style face="normal" font="default" size="100%">von Hagen, Robin</style></author><author><style face="normal" font="default" size="100%">Müller, Ralf</style></author><author><style face="normal" font="default" size="100%">Fiz, Raquel</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Division of Inorganic and Materials Chemistry, University of Cologne, Greinstrasse 6, D-50939 Koln, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Ink-jetable patterning of metal-catalysts for regioselective growth of nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Nanoscale</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Nanoscale</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2091-2095</style></pages><volume><style face="normal" font="default" size="100%">2</style></volume><number><style face="normal" font="default" size="100%">10</style></number><edition><style face="normal" font="default" size="100%">2010/08/05</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style face="normal" font="default" size="100%">Oct</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">2040-3372</style></isbn><accession-num><style face="normal" font="default" size="100%">20683541</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanosized (20-30 nm) colloidal gold, silver and their alloys were obtained by reductive transformation of corresponding metal salts. Dispersions of metal nanoparticles ($\sigma$ &lt; 4\%) in aqueous solutions were obtained by appropriate surface functionalization which led to inorganic inks with solid fraction ranging from 0.01-4\%. Judicious choice of a polymer additive (polyethylene glycol or carboxymethyl cellulose) was found to be crucial to avoid the agglomeration of nanocrystals in the ink-jetted structures upon solvent evaporation. The versatility of the nanoparticle-based printing technology was demonstrated by fabrication of dot-matrices and circuitry patterns on different substrates. Characterization of printed structures showed a homogeneous topography (AFM) and uniform distribution of metallic nanoparticles (SEM/TEM) within the ink-jetted microdrops. The site-specific patterning on silicon (001) substrates with nanoparticle (mono)layers could also be achieved by printing the linker molecule, aminopropyltriethoxysilane, followed by selective attachment of gold nanoparticles. Positionally ordered and chemically bonded gold catalyst patterns were used for the chemical vapour deposition (CVD) of nanowires, which led to site-specific growth of nanowires via the vapour-liquid-solid (VLS) mechanism and unlike in the case of spin-coated metal colloids no significant lateral diffusion of metal nanoparticles was observed, in chemically anchored Au nanoparticles. Nanoparticle containing inks allow a user-defined dilution to vary the density of CVD grown nanowires, which was utilized to show the differences in catalytic activities of silver and gold catalysts in the VLS growth.</style></abstract><label><style face="normal" font="default" size="100%">zopes2010inkjetable</style></label><notes><style face="normal" font="default" size="100%">Zopes, David&#xD;von Hagen, Robin&#xD;Muller, Ralf&#xD;Fiz, Raquel&#xD;Mathur, Sanjay&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;England&#xD;Nanoscale. 2010 Oct;2(10):2091-5. doi: 10.1039/c0nr00131g. Epub 2010 Aug 4.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/c0nr00131g</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/c0nr00131g</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>414</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">414</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Xiao, Lisong</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">von Hagen, Robin</style></author><author><style face="normal" font="default" size="100%">Pan, Jun</style></author><author><style face="normal" font="default" size="100%">Belkoura, Lhoussaine</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Microwave assisted fast and facile synthesis of SnO(2) quantum dots and their printing applications</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Communications</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">6509-6511</style></pages><volume><style face="normal" font="default" size="100%">46</style></volume><number><style face="normal" font="default" size="100%">35</style></number><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style face="normal" font="default" size="100%">September</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1364-548X</style></isbn><abstract><style face="normal" font="default" size="100%">An efficient synthesis of highly crystalline SnO(2) QDs with a narrow size distribution (4.27 +/- 0.67 nm) was achieved by microwave-assisted decomposition of Sn(OtBu)(4) in ionic liquid. Printed structures fabricated from SnO(2) QDs showed typical semiconducting I-V behaviors, and gas sensing properties.</style></abstract><label><style face="normal" font="default" size="100%">xiao2010microwave</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/C0CC01156H</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>412</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">412</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">von Hagen, R.</style></author><author><style face="normal" font="default" size="100%">Hoffmann, M.</style></author><author><style face="normal" font="default" size="100%">Lehnen, T.</style></author><author><style face="normal" font="default" size="100%">Xiao, L.</style></author><author><style face="normal" font="default" size="100%">Zopes, D.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Printable Silver Nanostructures: Fabrication and Plasma-Chemical Modification</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology IV: Ceramic Engineering and Science Proceedings</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">29-36</style></pages><volume><style face="normal" font="default" size="100%">31</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><label><style face="normal" font="default" size="100%">VonHagen2010</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/9780470944042.ch4</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>413</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">413</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">von Hagen, Robin</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ein Zwerg wird erwachsen</style></title><secondary-title><style face="normal" font="default" size="100%">Nachrichten aus der Chemie</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1115-1120</style></pages><volume><style face="normal" font="default" size="100%">58</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><isbn><style face="normal" font="default" size="100%">1439-9598</style></isbn><abstract><style face="normal" font="default" size="100%">A review. The concept of nanochem. is discussed, based on the perception, that the particle size influences the properties of a material. The nanochem. deals with the synthesis, characterization, and modification of nanoparticles and nanostructures. Different chem. methods for the development and functionalization of nanoparticles and nanostructures are described. Application examples are nanowires or nanotubes used in nanoelectronic or photovoltaic devices, nanocoatings, bio-functional surfaces for an increased cell adhesion, CVD, and nanocomposites.</style></abstract><label><style face="normal" font="default" size="100%">vonhagen2010nanochemistry</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/nadc.201075708</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>411</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">411</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Lecerf, Nicolas</style></author><author><style face="normal" font="default" size="100%">Huefner, Stefan</style></author><author><style face="normal" font="default" size="100%">Jilavi, Mohammad H.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">ChemInform Abstract: Single-Step Preparation of Oxide-Oxide Nanocomposites: Chemical Vapor Synthesis of LnAlO3/Al2O3 (Ln: Pr, Nd) Thin Films</style></title><secondary-title><style face="normal" font="default" size="100%">ChemInform</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">n/a</style></pages><volume><style face="normal" font="default" size="100%">33</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09317597</style></isbn><abstract><style face="normal" font="default" size="100%">ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</style></abstract><label><style face="normal" font="default" size="100%">veith2010cheminform</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/chin.200205233</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>410</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">410</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, M.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Mathur, C.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">ChemInform Abstract: New Perspectives in the Tailoring of Hetero (Bi- and Tri-) Metallic Alkoxide Derivatives</style></title><secondary-title><style face="normal" font="default" size="100%">ChemInform</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">n/a</style></pages><volume><style face="normal" font="default" size="100%">29</style></volume><number><style face="normal" font="default" size="100%">38</style></number><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><isbn><style face="normal" font="default" size="100%">09317597</style></isbn><label><style face="normal" font="default" size="100%">VEITH2010</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/chin.199838302</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>408</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">408</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, R.</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Cirera, A.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Individual Metal Oxide Nanowires in Chemical Sensing: Breakthroughs, Challenges and Prospects</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style face="normal" font="default" size="100%">September</style></date></pub-dates></dates><pub-location><style face="normal" font="default" size="100%">Hoboken, NJ, USA</style></pub-location><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Inc.</style></publisher><label><style face="normal" font="default" size="100%">prades2010individual</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/9780470909812.ch11</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>638</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">638</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Hernández-Ramírez, F.</style></author><author><style face="normal" font="default" size="100%">Fischer, T.</style></author><author><style face="normal" font="default" size="100%">Hoffmann, M.</style></author><author><style face="normal" font="default" size="100%">Müller, R.</style></author><author><style face="normal" font="default" size="100%">López, N.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Quantitative analysis of CO-humidity gas mixtures with self-heated nanowires operated in pulsed mode</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Physics Letters</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">243105</style></pages><volume><style face="normal" font="default" size="100%">97</style></volume><number><style face="normal" font="default" size="100%">24</style></number><dates><year><style face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style face="normal" font="default" size="100%">2010/12/13</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Institute of Physics</style></publisher><isbn><style face="normal" font="default" size="100%">0003-6951</style></isbn><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1063/1.3515918</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1063/1.3515918</style></electronic-resource-num><access-date><style face="normal" font="default" size="100%">2021/02/05</style></access-date></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>406</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">406</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pan, Jun</style></author><author><style face="normal" font="default" size="100%">Xiao, Lisong</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author><author><style face="normal" font="default" size="100%">Singh, Dileep</style></author><author><style face="normal" font="default" size="100%">Salem, Jonathan</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Mechanistic Studies on Chemical Vapor Deposition Grown Tin Oxide Nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology III: Ceramic Engineering and Science Proceedings</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">9-15</style></pages><volume><style face="normal" font="default" size="100%">30</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons</style></publisher><label><style face="normal" font="default" size="100%">Pan2010</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/9780470584378.ch2</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>405</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">405</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pan, J.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">CVD Grown Semiconductor Nanowires: Synthesis, Properties and Challenges</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured Materials and Systems</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">39-48</style></pages><volume><style face="normal" font="default" size="100%">214</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons</style></publisher><isbn><style face="normal" font="default" size="100%">9780470909812</style></isbn><abstract><style face="normal" font="default" size="100%">The Symposium on Nanostructured Materials and Systems was held during the 8th Pacific Rim Conference on Ceramic and Glass Technology (PACRIM 8) from May 31-June 5, 2009 in Vancouver, Canada. This symposium aimed to review the progress in the state-of-the-art of nanoscience and nanotechnology including synthesis, processing, modeling, applications and assessment of toxicological potential of nanomatter. More than 55 contributions (invited talks, oral presentations, and posters), were presented by participants, from all over the world, representing universities, research institutions, and indust.</style></abstract><label><style face="normal" font="default" size="100%">pan2010grown</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/9780470909812.ch4</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>407</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">407</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Pan, Jun</style></author><author><style face="normal" font="default" size="100%">Ganesan, Rajesh</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan &amp; Mat Chem, D-50939 Cologne, Germany&#xD;Leibniz Inst New Mat, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Plasma-Modified SnO2 Nanowires for Enhanced Gas Sensing</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry C</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Phys Chem C</style></alt-title></titles><pages><style face="normal" font="default" size="100%">8245-8250</style></pages><volume><style face="normal" font="default" size="100%">114</style></volume><number><style face="normal" font="default" size="100%">18</style></number><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style face="normal" font="default" size="100%">May 13</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000277280800019</style></accession-num><abstract><style face="normal" font="default" size="100%">Tin oxide (SnO2) nanowires grown by CVD were modified by Ar/O2 plasma treatment through preferential etching of the lattice oxygen atoms, which produced nonstoichiometric surface compns. that imparted a manyfold higher sensitivity toward gas absorption on such surfaces. Microstructures of as-grown and plasma-treated SnO2 nanowires confirmed the gradual change in the chem. compn. and morphologies. Surficial disorder caused by the bombardment of argon and oxygen ions present in the plasma was visible as a disordered overlayer in high-resoln. TEM micrographs, when compared to single cryst. as-grown SnO2 nanowires. Gas-sensing expts. on modified SnO2 nanostructures showed higher sensitivity for ethanol gas at lower operating temps. and exhibited an improved transduction response toward changing gas atms., attributed to the increased concn. of oxygen vacancies on the surface of SnO2 nanowires. Modulation of surface chem. was also supported by photoluminescence and x-ray photoemission spectroscopy studies.</style></abstract><label><style face="normal" font="default" size="100%">pan2010plasmamodified</style></label><notes><style face="normal" font="default" size="100%">591eb&#xD;Times Cited:98&#xD;Cited References Count:38</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/jp101072f</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/jp101072f</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>402</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">402</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Huefner, Stefan</style></author><author><style face="normal" font="default" size="100%">Jilavi, Mohammad H.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">ChemInform Abstract: Structural and Optical Properties of NdAlO3 Nanocrystals Embedded in an Al2O3 Matrix</style></title><secondary-title><style face="normal" font="default" size="100%">ChemInform</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">n/a</style></pages><volume><style face="normal" font="default" size="100%">33</style></volume><number><style face="normal" font="default" size="100%">20</style></number><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><isbn><style face="normal" font="default" size="100%">09317597</style></isbn><label><style face="normal" font="default" size="100%">Mathur2010</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/chin.200220004</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>401</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">401</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Haas, Michel</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Lecerf, Nicolas</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author><author><style face="normal" font="default" size="100%">Huefner, Stefan</style></author><author><style face="normal" font="default" size="100%">Haberkorn, Robert</style></author><author><style face="normal" font="default" size="100%">Beck, Horst P.</style></author><author><style face="normal" font="default" size="100%">Jilavi, Mohammad</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">ChemInform Abstract: Single-Source Sol-Gel Synthesis of Nanocrystalline ZnAl2O4: Structural and Optical Properties</style></title><secondary-title><style face="normal" font="default" size="100%">ChemInform</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">n/a</style></pages><volume><style face="normal" font="default" size="100%">32</style></volume><number><style face="normal" font="default" size="100%">50</style></number><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><isbn><style face="normal" font="default" size="100%">09317597</style></isbn><label><style face="normal" font="default" size="100%">Mathur2010</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/chin.200150017</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>403</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">403</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author><author><style face="normal" font="default" size="100%">Singh, Dileep</style></author><author><style face="normal" font="default" size="100%">Salem, Jonathan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology III: Ceramic Engineering and Science Proceedings, Volume 30, Issue 7</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><publisher><style face="normal" font="default" size="100%">Wiley</style></publisher><isbn><style face="normal" font="default" size="100%">978-0-470-45757-3</style></isbn><abstract><style face="normal" font="default" size="100%">This useful resource will help you understand the most valuable aspects of nanostructured materials and nanotechnology. Containing 16 peer-reviewed papers, this issue covers various aspects and the latest developments related to processing, modeling and manufacturing technologies of nanoscaled materials including CNT and clay-based composites, nanowire-based sensors, new generation photovoltaic cells, plasma processing of functional thin films, ceramic membranes and self-assembled functional nanostructures.</style></abstract><label><style face="normal" font="default" size="100%">mathur2010nanostructured</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://eu.wiley.com/WileyCDA/WileyTitle/productCd-0470457570.html</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>404</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">404</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ray, Suprakas Sinha</style></author><author><style face="normal" font="default" size="100%">Ohji, Tatsuki</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology IV: Ceramic Engineering and Science Proceedings, Volume 31, Issue 7</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><isbn><style face="normal" font="default" size="100%">978-0-470-59472-8</style></isbn><label><style face="normal" font="default" size="100%">mathur2010nanostructured</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://eu.wiley.com/WileyCDA/WileyTitle/productCd-0470594721.html</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>400</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">400</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Cavelius, Christian</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">ChemInform Abstract: CoGa2O4 Nanoparticles and Films Using a Single Molecular Source</style></title><secondary-title><style face="normal" font="default" size="100%">ChemInform</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">n/a</style></pages><volume><style face="normal" font="default" size="100%">41</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><isbn><style face="normal" font="default" size="100%">09317597</style></isbn><label><style face="normal" font="default" size="100%">Mathur2010</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/chin.201003016</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>399</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">399</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">López, N.</style></author><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Hernández-Ramírez, F.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author><author><style face="normal" font="default" size="100%">Pan, J.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Bidimensional versus tridimensional oxygen vacancy diffusion in SnO2-x under different gas environments</style></title><secondary-title><style face="normal" font="default" size="100%">Physical Chemistry Chemical Physics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">2401-2406</style></pages><volume><style face="normal" font="default" size="100%">12</style></volume><number><style face="normal" font="default" size="100%">10</style></number><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><abstract><style face="normal" font="default" size="100%">Metal oxides present oxygen defects that induce different chemical and physical properties. Experiments performed in SnO2-x sensors show that the dynamics of these vacancies are strongly affected by the presence of different gases in the environment. Experimentally, the electrical resistance of individual metal oxide SnO2-x nanowires shows modulation: when the environment is oxygen rich long term drifts (hours) are observed indicating extended vacancy dynamics. Instead, if CO is present, drifts disappear in minutes. Density functional theory indicates that changes in resistance follow the extension of reoxidation. For oxygen-poor environments, oxygen vacancy excorporation and healing are confined to the near-surface layer of SnO2-x (bidimensional or near-surface diffusion), and completed in short times. Under oxygen-rich conditions, tridimensional diffusion of oxygen vacancies towards the surface takes place at room temperature. In this case, a push-pull mechanism allows bulk-to-surface diffusion and as a consequence resistance drifts are longer and the vacancy quenching is more extensive.</style></abstract><label><style face="normal" font="default" size="100%">lopez2010bidimensional</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/B921213B</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>398</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">398</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hoffmann, M.</style></author><author><style face="normal" font="default" size="100%">von Hagen, R.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ray, Suprakas Sinha</style></author><author><style face="normal" font="default" size="100%">Ohji, Tatsuki</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Single Step Synthesis and Self-Assembly of Magnetite Nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology IV: Ceramic Engineering and Science Proceedings</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">21-27</style></pages><volume><style face="normal" font="default" size="100%">31</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><label><style face="normal" font="default" size="100%">Hoffmann2010</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/9780470944042.ch3</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>395</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">395</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Rodriguez-Diaz, R.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author><author><style face="normal" font="default" size="100%">Singh, Dileep</style></author><author><style face="normal" font="default" size="100%">Salem, Jonathan</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanowires as Building Blocks of New Devices: Present State and Prospects</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><label><style face="normal" font="default" size="100%">hernandezramirez2010nanowires</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/9780470584378.ch1</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>396</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">396</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Prades, Juan Daniel</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, Roman</style></author><author><style face="normal" font="default" size="100%">Casals, Olga</style></author><author><style face="normal" font="default" size="100%">Cirera, Albert</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author><author><style face="normal" font="default" size="100%">Morante, Joan Ramon</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fabrication of electrical contacts on individual metal oxide nanowires and novel device architectures</style></title><secondary-title><style face="normal" font="default" size="100%">Nanotechnology: Nanofabrication, Patterning and Self Assembly</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">293-308</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><publisher><style face="normal" font="default" size="100%">Nova Science Publishers, Inc.</style></publisher><abstract><style face="normal" font="default" size="100%">A review. Metal oxide nanowires exhibit novel properties due to their high surface-to-vol. ratio and high surface stability. For this reason, they are considered excellent candidates to be incorporated into a new generation of devices with improved performance. Nevertheless, reaching complete control of their phys., chem. and elec. properties is needed before they can be widely used in our everyday life. This objective can be only fulfilled if reproducible elec. measurements on individual nanomaterials are performed. However, the fabrication of elec. nanocontacts in a fast and well-controlled process is still an unsolved issue. In this chapter, the main nanofabrication techniques that are commonly used to elec. access individual metal oxide nanowires, and to study their intrinsic properties are presented. Advantages and limitations of these methodologies are discussed in detail. By integrating bottom-up and top-down techniques, the first functional prototypes based on individual nanowires have already been implemented, paving the way to the future developments of nanoscale electronics, optoelectronics and chem. sensing devices.</style></abstract><label><style face="normal" font="default" size="100%">hernandezramirez2010fabrication</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.researchgate.net/publication/224339763_Fabrication_of_electrical_contacts_on_individual_metal_oxide_nanowires_and_novel_device_architectures</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>397</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">397</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Prades, Joan Daniel</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Tarancon, Albert</style></author><author><style face="normal" font="default" size="100%">Casais, Olga</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, Roman</style></author><author><style face="normal" font="default" size="100%">Rodriguez, Jordi</style></author><author><style face="normal" font="default" size="100%">Pellicer, Eva</style></author><author><style face="normal" font="default" size="100%">Juli, Miguel Angel</style></author><author><style face="normal" font="default" size="100%">Andreu, Teresa</style></author><author><style face="normal" font="default" size="100%">Estrade, Sonia</style></author><author><style face="normal" font="default" size="100%">Rossinyo, Emma</style></author><author><style face="normal" font="default" size="100%">Morante, Joan Ramon.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fabrication of nanodevices based on individual SnO2 nanowires and their electrical characterization</style></title><secondary-title><style face="normal" font="default" size="100%">Metal Oxide Nanostructures and Their Applications</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">3-30</style></pages><volume><style face="normal" font="default" size="100%">3</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><publisher><style face="normal" font="default" size="100%">American Scientific Publishers</style></publisher><abstract><style face="normal" font="default" size="100%">A review on the fabrication and elec. characterization of devices based on individual tin oxide (SnO2) nanowires. The first part deals with the problem of obtaining reliable and small elec. nanocontacts to individual SnO2 nanowires. In the second part, the elec. characterization and modeling of SnO2 nanowires is discussed in detail, since the estn. of their key elec. parameters is essential to deepen the present knowledge of their properties as well as to avoid any undesired damage or irreversible modification during the measurements. The third section is an overview of the most significant examples of the use of SnO2 nanowire-based systems as functional devices, such as gas sensors or UV photodetectors. Finally, some important conclusions are summed up, and the main work guidelines that can pave the way to obtaining new and better devices are identified.</style></abstract><label><style face="normal" font="default" size="100%">hernandezramirez2010fabrication</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>392</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">392</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hemmer, Eva</style></author><author><style face="normal" font="default" size="100%">Soga, Kohei</style></author><author><style face="normal" font="default" size="100%">Konishi, Tomoya</style></author><author><style face="normal" font="default" size="100%">Watanabe, Tomoaki</style></author><author><style face="normal" font="default" size="100%">Taniguchi, Takaaki</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Tokyo Univ Sci, Dept Mat Sci &amp; Technol, Chiba 2788510, Japan&#xD;Anan Natl Coll Technol, Ctr Collaborat Res, Tokushima 7740017, Japan&#xD;Meji Univ, Sch Sci &amp; Technol, Dept Appl Chem, Tama Ku, Kawasaki, Kanagawa 2148571, Japan&#xD;Tokyo Inst Technol, Mat &amp; Struct Lab, Yokohama, Kanagawa 2268503, Japan&#xD;Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Influence of the Host Phase on the Vibrational Spectra of Europium-Doped Zirconia Prepared by Hydrothermal Processing</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the American Ceramic Society</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Am Ceram Soc</style></alt-title></titles><pages><style face="normal" font="default" size="100%">3873-3879</style></pages><volume><style face="normal" font="default" size="100%">93</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style face="normal" font="default" size="100%">Nov</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">00027820</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000283987400066</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanocryst. zirconia (ZrO2) powders doped with 0.5-5 mol\% europium (Eu3+) were prepd. by hydrothermal process using ZrCl4 and EuCl3·6H2O as starting materials. Optical emission and vibrational properties of as-prepd. and calcined samples were investigated by phonon sideband (PSB), FTIR and photoluminescence spectroscopy as well as lifetime measurements. We found that the doping degree had a strong effect on the cryst. phase, m- and t-ZrO2 of the host material, which also influenced on its shape and intensity of the PSB spectra. Residual water in the as-prepd. samples indicated by FT-IR spectra induced water relating vibrations in the PSB spectra. The obtained PSB were compared with the peaks in the recorded FT-IR spectra and related to the vibrational modes of m- and t-ZrO2.</style></abstract><label><style face="normal" font="default" size="100%">hemmer2010influence</style></label><notes><style face="normal" font="default" size="100%">677jl&#xD;Times Cited:11&#xD;Cited References Count:45</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1111/j.1551-2916.2010.03981.x</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1111/j.1551-2916.2010.03981.x</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>394</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">394</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hemmer, Eva</style></author><author><style face="normal" font="default" size="100%">Kohl, Yvonne</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Thielecke, Hagen</style></author><author><style face="normal" font="default" size="100%">Soga, Kohei</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Solvothermal Synthesis of Gadolinium Hydroxide and Oxide Powders and Their Potential for Biomedical Applications</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured Materials and Systems</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">27-37</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year></dates><pub-location><style face="normal" font="default" size="100%">Hoboken, NJ, USA</style></pub-location><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Inc.</style></publisher><label><style face="normal" font="default" size="100%">Hemmer2010</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/9780470909812.ch3</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>393</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">393</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hemmer, Eva</style></author><author><style face="normal" font="default" size="100%">Kohl, Yvonne</style></author><author><style face="normal" font="default" size="100%">Colquhoun, Victoria</style></author><author><style face="normal" font="default" size="100%">Thielecke, Hagen</style></author><author><style face="normal" font="default" size="100%">Soga, Kohei</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Department of Materials Science and Technology, Tokyo University of Science, 2641 Yamazaki, 278-8510 Chiba, Japan.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Probing Cytotoxicity of Gadolinium Hydroxide Nanostructures</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry B</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">4358-4365</style></pages><volume><style face="normal" font="default" size="100%">114</style></volume><number><style face="normal" font="default" size="100%">12</style></number><edition><style face="normal" font="default" size="100%">2010/03/12</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style face="normal" font="default" size="100%">April</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1520-5207</style></isbn><accession-num><style face="normal" font="default" size="100%">20218658</style></accession-num><abstract><style face="normal" font="default" size="100%">Gadolinium hydroxide, Gd(OH)(3), nanostructures were examined for their possible use in imaging and tracking of cells and tissues by investigating their cellular interactions and cytotoxic behaviors. For this purpose, Gd(OH)(3) nanorods (length, several hundred nanometers; diameter, approximately 40 nm) and spherical nanoparticles (average diameter, &lt;10 nm) were synthesized by solvothermal decomposition of gadolinium containing molecular precursors. After comprehensive characterization of material properties, human colon adenocarcinoma (Caco2) and human lung epithelial (A549) cells were incubated with Gd(OH)(3) nanostructures in concentrations up to 900 microg/mL to perform cytotoxicity assays (BrdU (5-bromo-2&apos;-deoxyuridine), WST-1 (4-3-(4-iodophenyl)-2-(4-nitrophenyl)-2H-5-tetrazolio-1,3-benzol-disulfonate)) and living/dead staining. As observed in all in vitro assays, the investigated Gd(OH)(3) nanostructures do not induce any significant cytotoxic effect, making them promising candidates for a new class of contrast agents, which may overcome the limitations of organic stains such as photobleaching and single usage.</style></abstract><label><style face="normal" font="default" size="100%">hemmer2010probing</style></label><notes><style face="normal" font="default" size="100%">Hemmer, Eva&#xD;Kohl, Yvonne&#xD;Colquhoun, Victoria&#xD;Thielecke, Hagen&#xD;Soga, Kohei&#xD;Mathur, Sanjay&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;J Phys Chem B. 2010 Apr 1;114(12):4358-65. doi: 10.1021/jp911607h.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/20218658</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/jp911607h</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>391</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">391</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ganesan, R.</style></author><author><style face="normal" font="default" size="100%">Donia, N.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Johnson, I.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanocatalytic effects in Gold/Tin functionalized tin oxide nanowires for enhanced co sensing</style></title><secondary-title><style face="normal" font="default" size="100%">2010 International Conference on Nanoscience and Nanotechnology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">49-50</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2010, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style face="normal" font="default" size="100%">February</style></date></pub-dates></dates><abstract><style face="normal" font="default" size="100%">Tin oxide (SnO2) nanowires were synthesized by a molecule based chemical vapour deposition process and the metallic additives Sn and Au were incorporated by treating nanowires in the mixture of Argon and O2 plasma. Tin inclusion in the SnO2 nanowires were achieved by preferential etching of the lattice oxygen atoms from the surface of SnO2 nanowires through the plasma treatment, which lead to chemically directed synthesis of Sn 0 / SnO2 nanocomposites. However, Gold incorporated nanowires were obtained by treating the Au sputtered samples (5 - 13 nm) at low plasma energy to induce nucleation of Au nanocrystals on SnO2 backbone. Investigations on Carbon-monoxide (CO) sensing behaviour of SnO2 nanostructures as a function of surface structure, composition and electronic properties are reported. Metal-functionalized nanowires showed better sensitivity for CO at lower operating temperature and exhibited higher transduction towards altering gas atmospheres attributed to a spill-over effect in Au incorporated tin oxide nanowires (AuTO), whereas the surface valence dynamics (Sn 0 / Sn 2+ / Sn 4+ ) is responsible for higher sensitivity of Sn incorporated system (SnTO).</style></abstract><label><style face="normal" font="default" size="100%">ganesan2010nanocatalytic</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1109/ICONN.2010.6045172</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>430</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">430</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prades, Joan Daniel</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, Roman</style></author><author><style face="normal" font="default" size="100%">Manzanares, Marta</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Cirera, Albert</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Morante, Joan Ramon.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">EME/XaRMAE/IN2UB, Departament d&apos;Electronica, Universitat de Barcelona, C/ Marti i Franques 1, Planta 2, E-08028 Barcelona, Spain. dprades@el.ub.es</style></auth-address><titles><title><style face="normal" font="default" size="100%">A model for the response towards oxidizing gases of photoactivated sensors based on individual SnO2 nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Physical Chemistry Chemical Physics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">10881-10889</style></pages><volume><style face="normal" font="default" size="100%">11</style></volume><number><style face="normal" font="default" size="100%">46</style></number><edition><style face="normal" font="default" size="100%">2009/11/20</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style face="normal" font="default" size="100%">Dec 14</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1463-9084</style></isbn><accession-num><style face="normal" font="default" size="100%">19924322</style></accession-num><abstract><style face="normal" font="default" size="100%">The paper presents a quantitative model to elucidate the role of impinging photons on the final response towards oxidizing gases of light-activated metal oxide gas sensors. The model is based on the competition between oxygen molecules in air and oxidizing target gases (such as NO(2)) for the same adsorption sites: the surface oxygen vacancies (OV). The model fairly reproduces the experimental measurements of both the steady-state and the dynamic response of individual SnO(2) nanowires towards oxidizing gases. Quantitative results indicate that: (1) at room temperature NO(2) adsorbs onto OV more avidly than oxygen; (2) the flux of photons and the NO(2) concentration determine the partition of the two gas populations at the surface; and (3) the band-to-band generation of electron-hole pairs plays a significant role in the photodesorption process of gas molecules. The model also offers a methodology to estimate some fundamental parameters, such as the adsorption rates and the photodesorption cross sections of oxidizing molecules interacting with the nanowires&apos; surface. All these results, enabled by the use of individual nanowires, provide deep insight about how to control the response of metal oxide nanowires towards oxidizing gases, paving the way to the development and consolidation of this family of low consumption conductometric sensors operable at room temperature.</style></abstract><label><style face="normal" font="default" size="100%">prades2009model</style></label><notes><style face="normal" font="default" size="100%">Prades, Joan Daniel&#xD;Jimenez-Diaz, Roman&#xD;Manzanares, Marta&#xD;Hernandez-Ramirez, Francisco&#xD;Cirera, Albert&#xD;Romano-Rodriguez, Albert&#xD;Mathur, Sanjay&#xD;Morante, Joan Ramon&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;England&#xD;Phys Chem Chem Phys. 2009 Dec 14;11(46):10881-9. doi: 10.1039/b915646a. Epub 2009 Oct 14.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/19924322</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/b915646a</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>426</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">426</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, R.</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Pan, J.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Inst Recerca Energia Catalunya, IREC, E-08019 Barcelona, Spain&#xD;Univ Barcelona, Dept Elect, EME XaRMAE IN2UB, E-08028 Barcelona, Spain&#xD;Elect Nanosyst SL, E-08028 Barcelona, Spain&#xD;Univ Cologne, Dept Inorgan Chem, D-50939 Cologne, Germany&#xD;Leibniz Inst New Mat, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Direct observation of the gas-surface interaction kinetics in nanowires through pulsed self-heating assisted conductometric measurements</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Physics Letters</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Appl Phys Lett</style></alt-title></titles><pages><style face="normal" font="default" size="100%">53101</style></pages><volume><style face="normal" font="default" size="100%">95</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style face="normal" font="default" size="100%">Aug 3</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0003-6951</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000268809400065</style></accession-num><abstract><style face="normal" font="default" size="100%">Dynamics of gas-surface interactions determine the limits of the fastest response times of sensors based on metal oxides. Here, the kinetics of adsorption and desorption of gaseous molecules onto the surface of metal oxide nanowires was analyzed through pulsed self-heating assisted conductometric measurements. This approach overcomes gas diffusion, which is typical of conventional porous film based devices, and provides thermal response times fast enough to evaluate the fundamental gas-surface reactions kinetics. Experimental response and recovery times of individual SnO2 nanowires toward oxidizing and reducing gases obtained with the here-proposed methodology were related to the reaction barriers predicted by theoretical models and other experimental techniques.</style></abstract><label><style face="normal" font="default" size="100%">prades2009direct</style></label><notes><style face="normal" font="default" size="100%">481kq&#xD;Times Cited:24&#xD;Cited References Count:34</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1063/1.3192358</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Artn 053101&#xD;10.1063/1.3192358</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>428</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">428</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, R.</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Fischer, T.</style></author><author><style face="normal" font="default" size="100%">Cirera, A.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author><author><style face="normal" font="default" size="100%">Pardo, Matteo</style></author><author><style face="normal" font="default" size="100%">Sberveglieri, Giorgio</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Self-Heating in Individual Nanowires: a Major Breakthrough in Sensors Technology</style></title><secondary-title><style face="normal" font="default" size="100%">AIP Conference Proceedings</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">127-129</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year></dates><publisher><style face="normal" font="default" size="100%">AIP</style></publisher><label><style face="normal" font="default" size="100%">Prades2009</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://scitation.aip.org/content/aip/proceeding/aipcp/10.1063/1.3156488</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>425</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">425</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, R.</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Pan, J.</style></author><author><style face="normal" font="default" size="100%">Cirera, A.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Barcelona, Dept Elect, EME, XaRMAE,IN2UB, Barcelona, Spain&#xD;IREC, Barcelona, Spain&#xD;Elect Nanosyst SL, Barcelona, Spain&#xD;Leibniz Inst New Mat, Saarbrucken, Germany&#xD;Natl Univ Ireland Univ Coll Cork, Dept Chem, Cork, Ireland&#xD;Univ Cologne, Dept Inorgan Chem, Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">An Experimental Method to Estimate the Temperature of Individual Nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal of Nanotechnology</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Int J Nanotechnol</style></alt-title></titles><pages><style face="normal" font="default" size="100%">860-869</style></pages><volume><style face="normal" font="default" size="100%">6</style></volume><number><style face="normal" font="default" size="100%">9</style></number><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year></dates><isbn><style face="normal" font="default" size="100%">1475-7435</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000268869900008</style></accession-num><abstract><style face="normal" font="default" size="100%">In this paper, the authors present an effective experimental method to estimate the temperature of individual metal oxide nanowires that can be used to quantify the heating produced in conductometric or other operating conditions. The here-proposed method is based on the analysis of the recovery time of the nanowire&apos;s resistance after exposure to a gas pulse (0.5 ppm of NO(2) in dry air). It is reproducible with different devices always with uncertainties below +/- 20 degrees C in the temperature range (70-300 degrees C) studied herein. The exploration of alternative gases and nanolithography techniques may help to extend its operating range and its applicability to other materials. In any case, the opportunity to probe temperatures at the nanoscale opens the door to a number of fundamental and applied advancements in the field of nanotechnology.</style></abstract><label><style face="normal" font="default" size="100%">prades2009experimental</style></label><notes><style face="normal" font="default" size="100%">482fl&#xD;Times Cited:11&#xD;Cited References Count:21</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1504/IJNT.2009.026745</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Doi 10.1504/Ijnt.2009.026745</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>427</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">427</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, R.</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Cirera, A.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Barcelona, Dept Elect, EME XaRMAE IN2UB, Barcelona, Spain&#xD;Elect Nanosyst SL, Barcelona, Spain&#xD;Leibniz Inst New Mat, Saarbrucken, Germany&#xD;Univ Cologne, Dept Inorgan Chem, Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Equivalence between thermal and room temperature UV light-modulated responses of gas sensors based on individual SnO2 nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Sensors and Actuators B: Chemical</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Sensor Actuat B-Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">337-341</style></pages><volume><style face="normal" font="default" size="100%">140</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jul 16</style></date></pub-dates></dates><accession-num><style face="normal" font="default" size="100%">WOS:000268215200001</style></accession-num><abstract><style face="normal" font="default" size="100%">We demonstrate that illuminating metal oxide gas sensors with ultra-violet light is a viable alternative not only to activate but also to modulate their response towards oxidizing gases. Here, the performance of individual monocrystalline SnO2 nanowires to NO2 at room temperature as function of the flux and the energy of photons is studied. The results reveal that nearly identical responses, similar to thermally activated sensor surfaces, can be achieved by choosing the optimal illumination conditions. On the basis these results, a qualitative model to explain the response of these sensors towards oxidizing gases is proposed. This finding paves the way to the development of conductometric gas sensors operating at room temperature.</style></abstract><label><style face="normal" font="default" size="100%">prades2009equivalence</style></label><notes><style face="normal" font="default" size="100%">473nw&#xD;Times Cited:141&#xD;Cited References Count:35</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0925400509003670</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.snb.2009.04.070</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>429</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">429</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, R.</style></author><author><style face="normal" font="default" size="100%">Andreu, T.</style></author><author><style face="normal" font="default" size="100%">Cirera, A.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Cornet, A.</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">UV photosensors based on individual semiconductor nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">2009 Spanish Conference on Electron Devices</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">410-411</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style face="normal" font="default" size="100%">February</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">IEEE</style></publisher><isbn><style face="normal" font="default" size="100%">978-1-4244-2838-0</style></isbn><label><style face="normal" font="default" size="100%">prades2009photosensors</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://ieeexplore.ieee.org/lpdocs/epic03/wrapper.htm?arnumber=4800520</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>424</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">424</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author><author><style face="normal" font="default" size="100%">Ohji, Tatsuki</style></author><author><style face="normal" font="default" size="100%">Wereszczak, Andrew</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology II: Ceramic Engineering and Science Proceedings, Volume 29, Issue 8</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year></dates><publisher><style face="normal" font="default" size="100%">Wiley</style></publisher><isbn><style face="normal" font="default" size="100%">978-0-470-34498-9</style></isbn><label><style face="normal" font="default" size="100%">2009nanostructured</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://eu.wiley.com/WileyCDA/WileyTitle/productCd-0470344989.html</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>421</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">421</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Erdem, Arzum</style></author><author><style face="normal" font="default" size="100%">Cavelius, Christian</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Altmayer, Jessica</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan &amp; Mat Chem, D-50939 Cologne, Germany&#xD;Leibniz Inst New Mat, D-66123 Saarbrucken, Germany&#xD;Ege Univ, Dept Analyt Chem, Fac Pharm, TR-35100 Izmir, Turkey</style></auth-address><titles><title><style face="normal" font="default" size="100%">Amplified electrochemical DNA-sensing of nanostructured metal oxide films deposited on disposable graphite electrodes functionalized by chemical vapor deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Sensors and Actuators B: Chemical</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Sensor Actuat B-Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">432-437</style></pages><volume><style face="normal" font="default" size="100%">136</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style face="normal" font="default" size="100%">Mar 2</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09254005</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000264089600025</style></accession-num><abstract><style face="normal" font="default" size="100%">Metal oxide nanostructures offer interesting possibilities to design functional surfaces for bio-sensing applications, for instance, through higher surface area leading to enhanced immobilization of biomols., which increases the detection limit. Herein, an amplified electrochem. sensing method was presented for the detection of DNA based on the readout resulting from chem. oxidn. of guanine on nanoscaled metal oxides (TiO2, SnO2, and Fe3O4) obtained by chem. vapor deposition (CVD) onto pencil graphite electrode (PGE) as electrochem. transducer. The proposed strategy is suitable to produce cost-effective disposable sensor elements enabling quant. detection of nanomolar concns. of DNA. When prepg. these metal oxide surfaces by CVD onto PGEs, the various exptl. conditions; such as, the effect of different concns. of 20 mer-bases DNA oligonucleotide (ODN20), and the surface pretreatment steps were studied to obtain better surface properties for DNA immobilization. The detection limit estd. for signal-to-noise ratios &gt;3 corresponds to 21.3, 53.9 and 45.8 nmole/mL ODN20 concns. for PGEs modified with TiO2, SnO2 and Fe3O4 films, resp. The electrochem. detection of DNA onto metal oxide@GEs is discussed together with the application potential.</style></abstract><label><style face="normal" font="default" size="100%">mathur2009amplified</style></label><notes><style face="normal" font="default" size="100%">417pw&#xD;Times Cited:41&#xD;Cited References Count:53</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S092540050800765X</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.snb.2008.11.049</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>423</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">423</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Cavelius, Christian</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Inst Inorgan Chem, D-50939 Cologne, Germany&#xD;Leibniz Inst New Mat, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">CoGa2O4 Nanoparticles and Films Using a Single Molecular Source</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Z Anorg Allg Chem</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2106-2111</style></pages><volume><style face="normal" font="default" size="100%">635</style></volume><number><style face="normal" font="default" size="100%">13-14</style></number><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">00442313</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000272341200004</style></accession-num><abstract><style face="normal" font="default" size="100%">Mixed-metal tert-butoxide, CoGa2(OtBu)8, was employed in the chem. vapor deposition (CVD) and sol-gel processes to obtain thin films and nanoparticles of spinel CoGa2O4 phase, resp. The appropriate Co:Ga ratio and intact vaporization (115-120°/10-2 Torr) of the mol. source produced cryst. deposits of CoGa2O4 at relatively low temps. (≈500°). A clean transformation of the heterometal precursor in spinel oxide of definite compn. was supported by TG/DTA anal. that showed no wt. loss &gt;470°. The SEM images of CoGa2O4 films showed homogeneous morphol. and dense microstructure constituted by nanometric grains (&lt;d&gt;, ≈35 nm). Hydrolytic decompn. of the precursor produced gels that upon heat-treatment (400-1200°) formed nanoscaled spinel. For comparison, CoGa2O4 was also prepd. by complexing Co2+ and Ga3+ ions with glycolate ligands, significant agglomeration effect, broader size dispersion and amorphous domains were obsd. indicating that low-temp. prepn. of monophasic materials following conventional chem. approaches is hampered by thermodn. impediments. The UV/Vis spectra of CoGa2O4 particles exhibit characteristic peaks corresponding to 4A2(F) to 4T1(P) transition in the divalent cobalt cation. The magnetization data of the CoGa2O4 nanoparticles showed as expected an antiferromagnetic behavior.</style></abstract><label><style face="normal" font="default" size="100%">mathur2009coga2o4</style></label><notes><style face="normal" font="default" size="100%">527bn&#xD;Times Cited:4&#xD;Cited References Count:40</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/zaac.200900167</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/zaac.200900167</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>422</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">422</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Cavelius, Christian</style></author><author><style face="normal" font="default" size="100%">Moh, Karsten</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Bauer, Jürgen</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Cologne, Dept Inorgan &amp; Mat Chem, D-50939 Cologne, Germany&#xD;Leibniz Inst New Mat, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Cobalt Ferrite Nanoparticles from Single and Multi-Component Precursor Systems</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Z Anorg Allg Chem</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></full-title></periodical><pages><style face="normal" font="default" size="100%">898-902</style></pages><volume><style face="normal" font="default" size="100%">635</style></volume><number><style face="normal" font="default" size="100%">6-7</style></number><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year></dates><isbn><style face="normal" font="default" size="100%">00442313</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000266556900015</style></accession-num><abstract><style face="normal" font="default" size="100%">Highly cryst. CoFe2O4 nanoparticles (&lt;d&gt; ∼ 5.6 nm) were synthesized by thermal decompn. of (i) single mol. precursor CoFe2(OtBu)8 and (ii) stoichiometric mixt. of individual metal precursors. The precursors were thermolyzed in a high-boiling solvent (Docosane, bp. 369°C) to produce uniformly dispersed cobalt ferrite nanoparticles in the case of mol. precursor, whereas bimodal distribution of nanoparticles was obtained in the multi-source synthesis. TG/DSC and HR-TEM revealed single- and multi-step decompn. profiles and differential nucleation steps in the two cases, which influence size dispersion and phase purity. on SciFinder(R)</style></abstract><label><style face="normal" font="default" size="100%">mathur2009cobalt</style></label><notes><style face="normal" font="default" size="100%">452qs&#xD;Times Cited:6&#xD;Cited References Count:26</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/zaac.200900010</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/zaac.200900010</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>420</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">420</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kohl, Yvonne</style></author><author><style face="normal" font="default" size="100%">Hemmer, Eva</style></author><author><style face="normal" font="default" size="100%">Soga, Kohei</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Thielecke, Hagen</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Biocompatibility of Eu3+-doped gadolinium hydroxide and oxide nanorods</style></title><secondary-title><style face="normal" font="default" size="100%">7th International Conference on f Elements, ICfE-7, Terrae Rarae</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1-9</style></pages><volume><style face="normal" font="default" size="100%">14</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year></dates><label><style face="normal" font="default" size="100%">kohl2009biocompatibility</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.researchgate.net/publication/233814649_Biocompatibility_of_Eu3-doped_gadolinium_hydroxide_and_oxide_nanorods</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>419</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">419</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Prades, J. Daniel</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, Roman</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Morante, Joan R.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">EME/XaRMAE/IN2UB, Departament d&apos;Electronica, Universitat de Barcelona, C/ Marti i Franques 1, Barcelona, Spain.</style></auth-address><titles><title><style face="normal" font="default" size="100%">On the role of individual metal oxide nanowires in the scaling down of chemical sensors</style></title><secondary-title><style face="normal" font="default" size="100%">Physical Chemistry Chemical Physics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">7105-7110</style></pages><volume><style face="normal" font="default" size="100%">11</style></volume><number><style face="normal" font="default" size="100%">33</style></number><edition><style face="normal" font="default" size="100%">2009/08/13</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style face="normal" font="default" size="100%">September</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1463-9076</style></isbn><accession-num><style face="normal" font="default" size="100%">19672516</style></accession-num><abstract><style face="normal" font="default" size="100%">Single-crystalline semiconductor metal oxide nanowires exhibit novel structural and electrical properties attributed to their reduced dimensions, well-defined geometry and the negligible presence of grain boundaries and dislocations in their inside. This favours direct chemical transduction mechanisms at their surfaces upon exposure to gas molecules, making them promising active device elements for a new generation of chemical sensors. Furthermore, metal oxide nanowires can be heated up to the optimal operating temperature for gas sensing applications with extremely low power consumption due to their small mass, giving rise to devices more efficient than their nanoparticle-based counterparts. Here, the current status of development of sensors based on individual metal oxide nanowires is surveyed, and the main technological challenges which act as bottleneck to their potential use in real applications are presented.</style></abstract><label><style face="normal" font="default" size="100%">hernandezramirez2009individual</style></label><notes><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco&#xD;Prades, J Daniel&#xD;Jimenez-Diaz, Roman&#xD;Fischer, Thomas&#xD;Romano-Rodriguez, Albert&#xD;Mathur, Sanjay&#xD;Morante, Joan R&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;England&#xD;Phys Chem Chem Phys. 2009 Sep 7;11(33):7105-10. doi: 10.1039/b905234h. Epub 2009 Jun 24.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/19672516</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/b905234h</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>418</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">418</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Prades, J. Daniel</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, Roman</style></author><author><style face="normal" font="default" size="100%">Fischer, Thomas</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Morante, Joan R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">ChemInform Abstract: On the Role of Individual Metal Oxide Nanowires in the Scaling Down of Chemical Sensors</style></title><secondary-title><style face="normal" font="default" size="100%">ChemInform</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">n/a</style></pages><volume><style face="normal" font="default" size="100%">40</style></volume><number><style face="normal" font="default" size="100%">44</style></number><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year></dates><isbn><style face="normal" font="default" size="100%">09317597</style></isbn><label><style face="normal" font="default" size="100%">Hernandez-Ramirez2009</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/chin.200944210</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>417</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">417</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Harnagea, Catalin</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Rosei, Federico</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">INRS-Energie, Materiaux et Telecommunications, Universite du Quebec, Varennes, Canada. sbarth76@gmail.com</style></auth-address><titles><title><style face="normal" font="default" size="100%">The elastic moduli of oriented tin oxide nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Nanotechnology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">115705</style></pages><volume><style face="normal" font="default" size="100%">20</style></volume><number><style face="normal" font="default" size="100%">11</style></number><edition><style face="normal" font="default" size="100%">2009/05/08</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style face="normal" font="default" size="100%">Mar 18</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1361-6528</style></isbn><accession-num><style face="normal" font="default" size="100%">19420453</style></accession-num><abstract><style face="normal" font="default" size="100%">Tin oxide nanowires (NWs) exhibit interesting electronic properties, which can be harnessed for applications in nanoelectronic devices and sensors. Oriented single crystalline tin oxide NWs were grown at 45 degrees from a titanium dioxide substrate. Their elastic properties were investigated in a two-point geometry using an atomic force microscope (AFM) coupled with a scanning electron microscope under ultrahigh vacuum conditions. Young&apos;s modulus was calculated by bending individual NWs and measuring the force exerted on the AFM tip during force-displacement measurements. For the NWs investigated, having radial dimensions below 45 nm and length up to 1.2 microm, we found an average value of 100 +/- 20 GPa, which is below the theoretical predictions calculated for different SnO(2) single crystal orientations, yet consistent with the indentation moduli of nanobelts. Finally, we discuss the effects of the nanowire-cantilever configuration on the measured Young&apos;s modulus.</style></abstract><label><style face="normal" font="default" size="100%">barth2009elastic</style></label><notes><style face="normal" font="default" size="100%">Barth, Sven&#xD;Harnagea, Catalin&#xD;Mathur, Sanjay&#xD;Rosei, Federico&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;England&#xD;Nanotechnology. 2009 Mar 18;20(11):115705. doi: 10.1088/0957-4484/20/11/115705. Epub 2009 Feb 25.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/19420453</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1088/0957-4484/20/11/115705</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>416</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">416</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Estrade, Sonia</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Peiro, Francesca</style></author><author><style face="normal" font="default" size="100%">Arbiol, Jordi</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author><author><style face="normal" font="default" size="100%">Morante, Joan Ramon</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Quebec, INRS Energie Mat &amp; Telecommun, Varennes, PQ J3X 1S2, Canada&#xD;Leibniz Inst New Mat, Dept CVD Technol, D-66123 Saarbrucken, Germany&#xD;Univ Barcelona, Dept Elect, EME XaRMAE INUB2, Barcelona, Spain&#xD;Elect Nanosyst SL, Barcelona, Spain&#xD;Univ Cologne, Inst Inorgan Chem, Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Studies on Surface Facets and Chemical Composition of Vapor Grown One-Dimensional Magnetite Nanostructures</style></title><secondary-title><style face="normal" font="default" size="100%">Crystal Growth &amp; Design</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Cryst Growth Des</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1077-1081</style></pages><volume><style face="normal" font="default" size="100%">9</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2009, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2009</style></year><pub-dates><date><style face="normal" font="default" size="100%">Feb</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1528-7483</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000263048200065</style></accession-num><abstract><style face="normal" font="default" size="100%">Studies on shape and chem. compn. of 1-dimensional magnetite nanostructures grown by a catalyst-assisted vapor phase procedure are reported. Intrinsic crystal chem. (preferred growth of most stable surfaces) could be modulated by seeding the magnetite growth through Au nanoclusters, which led to elongated nanostructures (VLS mode); however, the structures have similar facets as obsd. in uncatalyzed growth. Geometric and energetic contributions to the evolution of the predominately obsd. \111\ surface facets are discussed from high-angle annular dark field (HAADF) images and EELS. The Fe:O stoichiometry in magnetite nanowire was detd. by EELS, which manifested the reproducibility of nanowire growth by mol.-based CVD and the slightly nonstoichiometric nature of magnetite (Fe3O4-0.15). In combination with HAADF-TEM techniques, Au nanoclusters were identified on the surface of single-cryst. nanowires, which ably result from the surface diffusion of the catalyst (Au) material. Core-shell SnO2/Fe3O4 1 D nanostructures were fabricated by sequential deposition of Sn and Fe precursors. Cross sections of the coaxial nanostructures revealed polycryst. magnetite shells on single-cryst. SnO2 wires constituted by well-defined single-cryst. facetted grains of slightly nonstoichiometric magnetite.</style></abstract><label><style face="normal" font="default" size="100%">barth2009studies</style></label><notes><style face="normal" font="default" size="100%">402ye&#xD;Times Cited:27&#xD;Cited References Count:68</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/cg8009095</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/cg8009095</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>454</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">454</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sharma, Namita</style></author><author><style face="normal" font="default" size="100%">Sharma, Vinita</style></author><author><style face="normal" font="default" size="100%">Nagar, Meena</style></author><author><style face="normal" font="default" size="100%">Bohra, Rakesh</style></author><author><style face="normal" font="default" size="100%">Kaushik, Ajay</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Rajasthan, Dept Chem, Jaipur 302004, Rajasthan, India&#xD;MLV Text &amp; Engn Coll, Dept Chem, Bhilwara, Rajasthan, India&#xD;Leibniz Inst Neue Mat gGmbH, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Glycol modified cis-diisopropoxy-bis(N-phenylsalicylideneiminato)zirconium(IV): syntheses, characterization and low temperature transformation to nanocrystalline zirconia</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Coordination Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Coord Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2234-2245</style></pages><volume><style face="normal" font="default" size="100%">61</style></volume><number><style face="normal" font="default" size="100%">14</style></number><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year></dates><isbn><style face="normal" font="default" size="100%">0095-8972</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000257266600007</style></accession-num><abstract><style face="normal" font="default" size="100%">Zr(OPr(i))(4)center dot Pr(i)OH reacts with N-phenylsalicylideneimine in anhydrous benzene in 1 : 2 molar ratio to afford [Zr{O(C(6)H(4))CH=NPh}(2){OPr(i)}(2)] (1). Further reactions of 1 with various glycols yield heteroleptic complexes of the type [Zr{O(C(6)H(4))CH=NPh}(2){O-G-O}] [where-G-= (CH(2))(2) (2), (CH(2)CHCH(3)) (3), (CH(3)CHCHCH(3)) (4), (CH(2)CHC(2)H(5)) (5), (CH(2))(3) (6), (CH(2)CH(2)CHCH(3)) (7), and (CH(2))(6) (8)]. All new derivatives have been characterized by elemental analyses, FTIR and NMR ((1)H and (13)C{(1)H}) studies. FAB mass spectra of 1 and 7 revealed the monomeric nature of these complexes. Complete hydrolyses and low temperature transformations of 1 and 7 using Sol-Gel technique formed tetragonal phase of ZrO(2) at 700 degrees C, whereas transformation of tetragonal to monoclinic phase occurred at 900 degrees C. SEM observations of these samples indicate formation of agglomerates of nanocrystalline zirconia (Scherer analysis).</style></abstract><label><style face="normal" font="default" size="100%">sharma2008glycol</style></label><notes><style face="normal" font="default" size="100%">320wt&#xD;Times Cited:12&#xD;Cited References Count:53</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.tandfonline.com/doi/abs/10.1080/00958970801902483</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1080/00958970801902483</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>450</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">450</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Prades, Joan Daniel</style></author><author><style face="normal" font="default" size="100%">Tarancon, Albert</style></author><author><style face="normal" font="default" size="100%">Casals, Olga</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, Roman</style></author><author><style face="normal" font="default" size="100%">Juli, Miguel Angel</style></author><author><style face="normal" font="default" size="100%">Morante, Juan Ramon</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Helwig, Andreas</style></author><author><style face="normal" font="default" size="100%">Spannhake, Jan</style></author><author><style face="normal" font="default" size="100%">Mueller, Gerhard</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Bottom-up Fabrication of Individual SnO2 Nanowires-based Gas Sensors on Suspended Micromembranes</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Proceedings 2007</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1052-DD08-02</style></pages><volume><style face="normal" font="default" size="100%">1052</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year></dates><isbn><style face="normal" font="default" size="100%">1946-4274</style></isbn><label><style face="normal" font="default" size="100%">Romano-Rodriguez2008</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1557/PROC-1052-DD08-02</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>451</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">451</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Prades, Joan Daniel</style></author><author><style face="normal" font="default" size="100%">Tarancon, Albert</style></author><author><style face="normal" font="default" size="100%">Casals, Olga</style></author><author><style face="normal" font="default" size="100%">Jimenaz-Diaz, Roman</style></author><author><style face="normal" font="default" size="100%">Juli, Miguel Angel</style></author><author><style face="normal" font="default" size="100%">Morante, Juan Ramon</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Helwig, Andreas</style></author><author><style face="normal" font="default" size="100%">Spannhake, Jan</style></author><author><style face="normal" font="default" size="100%">Mueller, Gerhard</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Bottom-Up Fabrication of Individual SnO2 Nanowires-Based Gas Sensors on Suspended Micromembranes</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Research Society Symposium Proceedings</style></secondary-title></titles><volume><style face="normal" font="default" size="100%">1052</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year></dates><publisher><style face="normal" font="default" size="100%">Materials Research Society</style></publisher><abstract><style face="normal" font="default" size="100%">Bottom-up techniques were used to obtain gas sensors based on individual SnO2 nanowires placed over microhotplates with integrated heaters. These nanowires were elec. contacted to pre-patterned microelectrodes by means of Focused Ion Beam (FIB) nanofabrication methodologies. The performance of these sensors, which exhibit reproducible and stable responses, was evaluated as function of different gas atmospheres and dissipated power by the heater, demonstrating that this technol. approach could be used to develop functional devices based on nanomaterials.</style></abstract><label><style face="normal" font="default" size="100%">romanorodriguez2008bottomup</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1557/PROC-1052-DD08-02</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>452</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">452</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, Roman</style></author><author><style face="normal" font="default" size="100%">Prades, Joan Daniel</style></author><author><style face="normal" font="default" size="100%">Casals, Olga</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Gas Sensing Devices Based on 1D Metal-Oxide Nanostructures: Fabrication, Testing and Device Integration</style></title><secondary-title><style face="normal" font="default" size="100%">ECS Transactions</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">57-64</style></pages><volume><style face="normal" font="default" size="100%">13</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year></dates><abstract><style face="normal" font="default" size="100%">Individual tin oxide (SnO2) nanowires were electrically contacted with Focused Ion Beam (FIB) nanolithography techniques, their properties were characterized and their behavior as gas and ultraviolet light sensing devices was evaluated. These nanowires exhibited outstanding and reproducible responses to carbon monoxide and ultraviolet light, demonstrating that gas sensors and photodetectors based on this technology can be obtained. The combination of these nanowires with suspended microhotplates with integrated heaters is presented as a good solution to develop new nanowire-based devices.</style></abstract><label><style face="normal" font="default" size="100%">romanorodriguez2008sensing</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://ecst.ecsdl.org/cgi/doi/10.1149/1.2908616</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>453</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">453</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, Roman</style></author><author><style face="normal" font="default" size="100%">Casals, Olga</style></author><author><style face="normal" font="default" size="100%">Tarancon, Alberto</style></author><author><style face="normal" font="default" size="100%">Prades, Joan-Daniel</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Juli, Miquel-Angel</style></author><author><style face="normal" font="default" size="100%">Helwig, Andreas</style></author><author><style face="normal" font="default" size="100%">Spannhake, Jan</style></author><author><style face="normal" font="default" size="100%">Müller, Gerhard</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Portable Bottom-up Gas Sensor Based on the Integration of Individual SnO2 Nanowires with Microhotplates</style></title><secondary-title><style face="normal" font="default" size="100%">Ceramic and Electrochemical Sensors</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year></dates><label><style face="normal" font="default" size="100%">romanorodriguez2008portable</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://ma.ecsdl.org/content/MA2008-01/38/1198.abstract</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>449</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">449</key></foreign-keys><ref-type name="Book Section">5</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ramachandran, Anup</style></author><author><style face="normal" font="default" size="100%">Poppendieck, Wigand</style></author><author><style face="normal" font="default" size="100%">Koch, Klaus Peter</style></author><author><style face="normal" font="default" size="100%">Donia, Nicole</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author><author><style face="normal" font="default" size="100%">Salem, Janathan</style></author><author><style face="normal" font="default" size="100%">Zhu, Dongming</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Investigations on the Stability of Platinum Nanostructures on Implantable Microelectrodes- A First Approach</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology: Ceramic and Engineering Science Proceedings</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">65-72</style></pages><volume><style face="normal" font="default" size="100%">28</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year></dates><pub-location><style face="normal" font="default" size="100%">Hoboken, NJ, USA</style></pub-location><publisher><style face="normal" font="default" size="100%">John Wiley &amp; Sons, Inc.</style></publisher><label><style face="normal" font="default" size="100%">Ramachandran2008</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/9780470339701.ch8</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">incollection</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>448</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">448</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Promnimit, S.</style></author><author><style face="normal" font="default" size="100%">Cavelius, C.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Dutta, J.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Asian Inst Technol, Sch Engn &amp; Technol, Ctr Excellence Nanotechnol, Klongluang 12120, Pathumthani, Thailand&#xD;Leibniz Inst New Mat, CVD Div, D-66121 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Growth of gold/zinc sulphide multilayer films using layer-by-layer assembly of colloidal nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">Physica E: Low-dimensional Systems and Nanostructures</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Physica E</style></alt-title></titles><pages><style face="normal" font="default" size="100%">285-291</style></pages><volume><style face="normal" font="default" size="100%">41</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style face="normal" font="default" size="100%">Dec</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1386-9477</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000261481800021</style></accession-num><abstract><style face="normal" font="default" size="100%">Fabrication of multilayer thin films through layer-by-layer (Ibl) deposition of charged nanoparticles on tin-doped indium oxide (ITO) coated and uncoated glass substrates are reported. The thin films were constructed by alternately dipping a substrate into a colloidal suspension of chitosan capped zinc sulphide (ZnS) nanoparticles (similar to 30 nm) and citrate stabilized colloidal gold (Au) nanoparticles (similar to 20 nm) leading to electrostatic interactions between the oppositely charged nanoparticle layers. Thin films consisting of up to 200 deposition cycles by multiple dipping have been studied and surface morphology, changes in the optical absorption characteristics, thickness, uniformity, toughness and electrical characteristics are reported. The niultilayered assemblies, attached to the surface by strong ionic bonds, were highly stable and could not be removed by moderate scratching. The current-voltage characteristics in the forward and reverse bias conditions demonstrated rectifying behaviors in the onset of conduction voltage which makes these films attractive for future electronic devices. (C) 2008 Elsevier B.V. All rights reserved.</style></abstract><label><style face="normal" font="default" size="100%">promnimit2008growth</style></label><notes><style face="normal" font="default" size="100%">380rb&#xD;Times Cited:8&#xD;Cited References Count:31</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S1386947708002555</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.physe.2008.07.013</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>447</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">447</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prades, Joan Daniel</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, Roman</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Fernandez-Romero, Luis</style></author><author><style face="normal" font="default" size="100%">Andreu, Teresa</style></author><author><style face="normal" font="default" size="100%">Cirera, Albert</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author><author><style face="normal" font="default" size="100%">Cornet, Albert</style></author><author><style face="normal" font="default" size="100%">Morante, Joan Ramon</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Barcelona, Dept Elect, EME XaRMAE UB IN2, E-08028 Barcelona, Spain&#xD;Leibniz Inst New Mat, D-66123 Saarbrucken, Germany&#xD;Univ Cologne, Dept Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Toward a Systematic Understanding of Photodetectors Based on Individual Metal Oxide Nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Physical Chemistry C</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Phys Chem C</style></alt-title></titles><pages><style face="normal" font="default" size="100%">14639-14644</style></pages><volume><style face="normal" font="default" size="100%">112</style></volume><number><style face="normal" font="default" size="100%">37</style></number><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style face="normal" font="default" size="100%">September</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1932-7447</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000259140700060</style></accession-num><abstract><style face="normal" font="default" size="100%">The authors present a set of criteria to optimize photodetectors based on n-type metal oxide nanowires and a comparison methodol. capable of overcoming the present lack of systematic studies dealing with such devices. The response of photoconductors is enhanced following different fabrication strategies, such as diminishing the distance between the elec. contacts, increasing the width of the photoactive area, or improving the elec. mobility of the nanomaterials. The validity of the theor. background is verified by exptl. results obtained with devices based on ZnO nanowires. The performances of the devices show that the normalized gain of single ZnO nanowire-based photodetectors exceeds those of thin films.</style></abstract><label><style face="normal" font="default" size="100%">prades2008toward</style></label><notes><style face="normal" font="default" size="100%">347kt&#xD;Times Cited:114&#xD;Cited References Count:43</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/jp804614q</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/jp804614q</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>446</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">446</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, R.</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Cirera, A.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Barcelona, EME XaRMAE IN2UB, Dept Elect, E-08028 Barcelona, Spain&#xD;Elect Nanosyst SL, E-08028 Barcelona, Spain&#xD;Leibniz Inst New Mat, D-66123 Saarbrucken, Germany&#xD;Univ Cologne, Dept Inorgan Chem, D-50939 Cologne, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Ultralow power consumption gas sensors based on self-heated individual nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Physics Letters</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Appl Phys Lett</style></alt-title></titles><pages><style face="normal" font="default" size="100%">123110</style></pages><volume><style face="normal" font="default" size="100%">93</style></volume><number><style face="normal" font="default" size="100%">12</style></number><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style face="normal" font="default" size="100%">Sep 22</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0003-6951</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000259799100071</style></accession-num><abstract><style face="normal" font="default" size="100%">Dissipated power in metal oxide nanowires (r(NW) &lt; 45 nm) often causes &lt;p&gt; important self-heating effects and as a result, undesired aging and &lt;p&gt; failure of the devices. Nevertheless, this effect can be used to &lt;p&gt; optimize the sensing conditions for the detection of various gaseous &lt;p&gt; species, avoiding the requirement of external heaters. In this letter, &lt;p&gt; the sensing capabilities of self-heated individual SnO(2) nanowires &lt;p&gt; toward NO(2) are presented. These proof-of-concept systems exhibited &lt;p&gt; responses nearly identical to those obtained with integrated &lt;p&gt; microheaters, demonstrating the feasibility of taking advantage of &lt;p&gt; self-heating in nanowires to develop ultralow power consumption &lt;p&gt; integrated devices.</style></abstract><label><style face="normal" font="default" size="100%">prades2008ultralow</style></label><notes><style face="normal" font="default" size="100%">356sy&#xD;Times Cited:145&#xD;Cited References Count:18</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://scitation.aip.org/content/aip/journal/apl/93/12/10.1063/1.2988265</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Artn 123110&#xD;10.1063/1.2988265</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>445</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">445</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Hüfner, Stefan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Single-Step Preparation of Nanosized Ceramics and Composites from Metal–Organic Precursors</style></title><secondary-title><style face="normal" font="default" size="100%">26th Annual Conference on Composites, Advanced Ceramics, Materials, and Structures: B: Ceramic Engineering and Science Proceedings</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">557-568</style></pages><volume><style face="normal" font="default" size="100%">23</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2002, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year></dates><label><style face="normal" font="default" size="100%">Mathur2002</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/9780470294758.ch61</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>440</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">440</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Ruegamer, T.</style></author><author><style face="normal" font="default" size="100%">Donia, N.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Department of Nanocrystalline Materials and Thin Film Systems, Leibniz-Institute of New Materials, 66041 Saarbruecken, Germany.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Functional Metal Oxide Coatings by Molecule-Based Thermal and Plasma Chemical Vapor Deposition Techniques</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Nanoscience and Nanotechnology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">2597-2603</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">5</style></number><edition><style face="normal" font="default" size="100%">2008/06/25</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1533-4880 (Print)&#xD;1533-4880 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">18572690</style></accession-num><abstract><style face="normal" font="default" size="100%">Deposition of thin films through vaccum processes plays an important role in industrial processing of decorative and functional coatings. Many metal oxides have been prepared as thin films using different techniques, however obtaining compositionally uniform phases with a control over grain size and distribution remains an enduring challenge. The difficulties are largely related to complex compositions of functional oxide materials, which makes a control over kinetics of nucleation and growth processes rather difficult to control thus resulting in non-uniform material and inhomogeneous grain size distribution. Application of tailor-made molecular precursors in low pressure or plasma-enhanced chemical vapor deposition (CVD) techniques offers a viable solution for overcoming thermodynamic impediments involved in thin film growth. In this paper molecule-based CVD of functional coatings is demonstrated for iron oxide (Fe2O3, Fe3O4), vanadium oxide (V2O5, VO2) and hafnium oxide (HfO2) phases followed by the characterization of their microstructural, compositional and functional properties which support the advantages of chemical design in simplifying deposition processes and optimizing functional behavior.</style></abstract><label><style face="normal" font="default" size="100%">mathur2008functional</style></label><notes><style face="normal" font="default" size="100%">Mathur, S&#xD;Ruegamer, T&#xD;Donia, N&#xD;Shen, H&#xD;eng&#xD;J Nanosci Nanotechnol. 2008 May;8(5):2597-603. doi: 10.1166/jnn.2008.633.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.ingentaconnect.com/content/asp/jnn/2008/00000008/00000005/art00061?token=0047123168275c277b42573a674c7d3f3462702a6e46592f653b672c57582a72752d701</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1166/jnn.2008.633</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>442</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">442</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Werner, Ulf</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Wurzburg, Dept Inorgan Chem, D-97074 Wurzburg, Germany&#xD;Leibniz Inst New Mat, Dept Nanocrystalline Mat &amp; Thin Film Syst, D-66123 Saarbrucken, Germany&#xD;Univ Barcelona, Dept Elect, IN2UB, E-08028 Barcelona, Spain&#xD;Univ Barcelona, Dept Elect, EME, CErMAE,CEMIC, E-08028 Barcelona, Spain&#xD;NTEC106 SL, Lhospitalet De Llobregat 08903, Spain</style></auth-address><titles><title><style face="normal" font="default" size="100%">Chemical Vapor Growth of One-dimensional Magnetite Nanostructures</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Adv Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1550-1554</style></pages><volume><style face="normal" font="default" size="100%">20</style></volume><number><style face="normal" font="default" size="100%">8</style></number><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style face="normal" font="default" size="100%">April</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09359648</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000255694200028</style></accession-num><abstract><style face="normal" font="default" size="100%">One-dimensional nanoscopic Fe3O4 architectures are grown by molecule-based chemical vapor deposition CVD using Fe(OBut)32 precursor and Au particles as growth templates. Growth of magnetite shell on tin oxide nanowires is also achieved, obtaining magnetic–semiconductor heterostructures. Structural characterization of the different nanostructures and the first electrical measurements on an individual magnetite nanowire are reported.</style></abstract><label><style face="normal" font="default" size="100%">mathur2008chemical</style></label><notes><style face="normal" font="default" size="100%">298nk&#xD;Times Cited:81&#xD;Cited References Count:43</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/adma.200701448</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/adma.200701448</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>443</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">443</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">INM Leibniz Inst Neue Mat gGmgH, D-66123 Saarbrucken, Germany&#xD;Univ Wurzburg, Dept Chem, D-97074 Wurzburg, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">One-Dimensional Semiconductor Nanostructures: Growth, Characterization and Device Applications</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für Physikalische Chemie</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Z Phys Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">307-317</style></pages><volume><style face="normal" font="default" size="100%">222</style></volume><number><style face="normal" font="default" size="100%">2-3</style></number><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style face="normal" font="default" size="100%">February</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0942-9352</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000253465200005</style></accession-num><abstract><style face="normal" font="default" size="100%">One dimensional (1D) inorg. materials are gaining increasing attention because of their unique structural features and interesting functional properties. Given the structural stability, they show promising application potential in vacuum as well as in oxidizing atmospheres, which provides them a competitive edge over their carbon-based counterparts. A no. of synthetic procedures have been developed and demonstrated for 1D nanostructures that have led to intriguing morphol. variations (wires, tubes, belts, rods, etc.), however the control over radial and axial dimensions remains a continuing challenge. In addn., the choice of material is rather limited. We have developed a generic approach for the size-selective and site-specific growth of nanowires by combining vapor-liq.-solid (VLS) approach with mol.-based chem. vapor deposition. The synthesis of nanowires (NWs) is based on the decompn. of discrete mol. species, which allows growing nanowires at low temps. with a precise control over their diam. and length. The precursor chem. can be tuned to facilitate the stripping of org. ligands and to achieve complete decompn. that is crit. for maintaining the gas phase super-satn. necessary for 1D growth. High-yield synthesis of elemental (Ge) and compd. semiconductors (SnO2, Fe3O4, V2O5, In2O3) was performed by the chem. vapor deposition of appropriate metal-org. precursors. Axial and radial dimensions of the NWs were varied by adjusting the precursor feedstock, deposition temp., and catalyst size. Finally, the device potential of these building blocks as photo- and gas sensors was investigated by integrating individual nanowires in elec. circuits using focussed ion beam (FIB) assisted nano-lithog.</style></abstract><label><style face="normal" font="default" size="100%">mathur2008onedimensional</style></label><notes><style face="normal" font="default" size="100%">266vl&#xD;Times Cited:10&#xD;Cited References Count:27</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.degruyter.com/doi/10.1524/zpch.2008.222.2-3.307</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1524/zpch.2008.222.2-3.307</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>439</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">439</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lima Jr., E.</style></author><author><style face="normal" font="default" size="100%">Martins, T. B.</style></author><author><style face="normal" font="default" size="100%">Rechenberg, H. R.</style></author><author><style face="normal" font="default" size="100%">Goya, G. F.</style></author><author><style face="normal" font="default" size="100%">Cavelius, C.</style></author><author><style face="normal" font="default" size="100%">Rapalaviciute, R.</style></author><author><style face="normal" font="default" size="100%">Hao, S.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Numerical simulation of magnetic interactions in polycrystalline YFeO3</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Magnetism and Magnetic Materials</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">622-629</style></pages><volume><style face="normal" font="default" size="100%">320</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year></dates><abstract><style face="normal" font="default" size="100%">The magnetic behavior of polycrystalline yttrium orthoferrite was studied from the experimental and theoretical points of view. Magnetization measurements up to 170 kOe were carried out on a single-phase YFeO3 sample synthesized from heterobimetallic alkoxides. The complex interplay between weak-ferromagnetic and antiferromagnetic interactions, observed in the experimental M(H) curves, was successfully simulated by locally minimizing the magnetic energy of two interacting Fe sublattices. The resulting values of exchange field (H-E = 5590 kOe), anisotropy field (H-A = 0.5 kOe) and Dzyaloshinsky-Moriya antisymmetric field (H-D = 149 kOe) are in good agreement with previous reports on this system.</style></abstract><label><style face="normal" font="default" size="100%">limajr2008numerical</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.jmmm.2007.07.024</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>438</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">438</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lima Jr., E.</style></author><author><style face="normal" font="default" size="100%">Arelaro, A. D.</style></author><author><style face="normal" font="default" size="100%">Rechenberg, H. R.</style></author><author><style face="normal" font="default" size="100%">Duarte, E. L.</style></author><author><style face="normal" font="default" size="100%">Itri, R.</style></author><author><style face="normal" font="default" size="100%">Cavelius, C.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Goya, G. F.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Magnetic characterization of ferrihydrite nanoparticles synthesized by hydrolysis of Fe metal-organic precursor</style></title><secondary-title><style face="normal" font="default" size="100%">Physica B: Condensed Matter</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">4156-4159</style></pages><volume><style face="normal" font="default" size="100%">403</style></volume><number><style face="normal" font="default" size="100%">23-24</style></number><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year></dates><abstract><style face="normal" font="default" size="100%">We investigate the formation of ferrihydrite nanoparticles (NPs) by hydrolysis of the Fe(III) alkoxide Fe(O(t)Bu)(3). Controlled amounts of water, up to 3.0 vol were added to the precursor solution yielding a series of hydrolyzed samples ranging from P0.0 (the unreacted precursor) to P3.0. X-ray diffraction (XRD) analysis evidenced the formation of high-crystalline ferrihydrite NP in sample P3.0, with grain size estimate of about 3.2 nm. The transition from the molecular precursor to the formation of crystalline magnetic NPs was followed through magnetization measurements M(T) and M(H), as well as Mossbauer spectroscopy (MS). M(T) measurements indicate a paramagnetic (PM) behavior for sample P0.0, characteristic of binuclear Fe-O-Fe units, which evolves to a superparamagnetic (SPM) behavior, with an energy barrier for the blocking process estimated for sample P3.0 as E(a) = 4.9 x 10(-21) J (E(a)/k(B) = 355 K), resulting in a high effective anisotropy constant K(eff) = 290 kJ/m(3). Magnetization loops at 5 K progressively change from PM-like to ferromagnetic-like shape upon increasing the hydrolysis process, although hysteresis (H(c) approximate to 500 Oe) only is apparent for P2.0 and higher. MS spectra at room temperature are PM/SPM doublets for all samples, while the MS spectra at T = 4.2 K reveal increasingly well-defined magnetic ordering as hydrolysis of the precursor stepwise progresses until well-crystallized ferrihydrite particles are formed.</style></abstract><label><style face="normal" font="default" size="100%">lima2008magnetic</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0921452608003876</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>435</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">435</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jimenez-Diaz, R.</style></author><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Casals, O.</style></author><author><style face="normal" font="default" size="100%">Tarancon, A.</style></author><author><style face="normal" font="default" size="100%">Pellicer, E.</style></author><author><style face="normal" font="default" size="100%">Rodriguez, J.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author><author><style face="normal" font="default" size="100%">Juli, M. A.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Helwig, A.</style></author><author><style face="normal" font="default" size="100%">Spannhake, J.</style></author><author><style face="normal" font="default" size="100%">Müller, G.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Single-nanowire based portable gas-sensors and photodetectors</style></title><secondary-title><style face="normal" font="default" size="100%">The 34th International Conference on Micro- and Nano-Engineering</style></secondary-title></titles><volume><style face="normal" font="default" size="100%">86</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year></dates><label><style face="normal" font="default" size="100%">jimenezdiaz2008singlenanowire</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.researchgate.net/publication/259361393_Single-nanowire_based_portable_gas-sensors_and_photodetectors</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>436</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">436</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jimenez-Diaz, Roman</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Juli, Miguel Angel</style></author><author><style face="normal" font="default" size="100%">Prades, Juan Daniel</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Casals, Olga</style></author><author><style face="normal" font="default" size="100%">Andreu, Teresa</style></author><author><style face="normal" font="default" size="100%">Tarancon, Alberto</style></author><author><style face="normal" font="default" size="100%">Morante, Juan Ramon</style></author><author><style face="normal" font="default" size="100%">Pellicer, Eva</style></author><author><style face="normal" font="default" size="100%">Helwig, Andreas</style></author><author><style face="normal" font="default" size="100%">Spannhake, Jan</style></author><author><style face="normal" font="default" size="100%">Mueller, Gerhard</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Design and Fabrication of a Portable Prototype of Gas Sensor and UV Photodetector based on Individual Semiconductor Nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Spring meeting 2008</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year></dates><label><style face="normal" font="default" size="100%">jimenezdiaz2008design</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://www.researchgate.net/publication/259361434_Design_and_Fabrication_of_a_Portable_Prototype_of_Gas_Sensor_and_UV_Photodetector_based_on_Individual_Semiconductor_Nanowires</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>434</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">434</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Huch, V.</style></author><author><style face="normal" font="default" size="100%">Kumar, R.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Ratnani, R.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">MDS Univ Ajmer, Dept Pure &amp; Appl Chem, Ajmer 305009, India&#xD;Leibniz Inst New Mat, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Trans-dichlorodioxobis(triphenylphosphate)molybdenum(VI), MoO2Cl2(OP(OPh)3)2</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Chemical Crystallography</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Chem Crystallogr</style></alt-title></titles><pages><style face="normal" font="default" size="100%">605-608</style></pages><volume><style face="normal" font="default" size="100%">38</style></volume><number><style face="normal" font="default" size="100%">8</style></number><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style face="normal" font="default" size="100%">Aug</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1074-1542</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000257456100008</style></accession-num><abstract><style face="normal" font="default" size="100%">The molecular structure of trans-dichlorodioxobis(triphenylphosphate) molybdenum(VI), MoO2Cl2(OP(OPh)3)2 has been determined. Crystal data: Monoclinic, Pn, a = 11.767(2), b = 10.341(2), c = 15.682(3) \AA, $\beta$ = 92.27(3)°, V = 1906.8(7) \AA−3, Z = 2. Trans-dichlorodioxobis(triphenylphosphate)molybdenum(VI) was obtained by the reaction of molybdenum oxide, HCl and triphenylphosphate and was characterized by elemental analysis, IR, and 1H-NMR spectroscopy.</style></abstract><label><style face="normal" font="default" size="100%">huch2008transdichlorodioxobistriphenylphosphatemolybdenumvi</style></label><notes><style face="normal" font="default" size="100%">323oo&#xD;Times Cited:0&#xD;Cited References Count:12</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1007/s10870-008-9354-6</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1007/s10870-008-9354-6</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>433</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">433</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Prades, Joan Daniel</style></author><author><style face="normal" font="default" size="100%">Tarancon, Albert</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Casals, Olga</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, Roman</style></author><author><style face="normal" font="default" size="100%">Pellicer, Eva</style></author><author><style face="normal" font="default" size="100%">Rodriguez, Jordi</style></author><author><style face="normal" font="default" size="100%">Morante, Joan Ramon</style></author><author><style face="normal" font="default" size="100%">Juli, Miguel Angel</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Barcelona, Dept Elect, EME Xa RMAE IN2UB, E-08028 Barcelona, Spain&#xD;NTEC106 SL, Lhospitalet De Llobregat 08903, Spain&#xD;Leibniz Inst New Mat, Dept Nanocrystalline Mat &amp; Thin Film Syst, D-66123 Saarbrucken, Germany&#xD;Univ Cologne, Inst Inorgan Chem, D-97074 Wurzburg, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Insight into the Role of Oxygen Diffusion in the Sensing Mechanisms of SnO2 Nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Functional Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Adv Funct Mater</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Functional Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2990-2994</style></pages><volume><style face="normal" font="default" size="100%">18</style></volume><number><style face="normal" font="default" size="100%">19</style></number><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style face="normal" font="default" size="100%">Oct 9</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1616301X</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000260398300017</style></accession-num><abstract><style face="normal" font="default" size="100%">The role of oxygen diffusion in the response of individual SnO2 nanowires to this gas was studied. Different oxygen partial pressures lead to strong changes of their elec. resistance, even at room temp. Since surface models fail to explain the exptl. obsd. long-term resistance transients, it is necessary to make a description of the interaction mechanisms between oxygen species and SnO2 nanowires by taking ion diffusion into account. The model correctly describes the exptl. measured dependence of the nanowire resistance with oxygen partial pressure, and it can be applied to the characterization of other metal oxide materials.</style></abstract><label><style face="normal" font="default" size="100%">hernandezramirez2008insight</style></label><notes><style face="normal" font="default" size="100%">365ie&#xD;Times Cited:85&#xD;Cited References Count:42</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/adfm.200701191</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/adfm.200701191</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>432</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">432</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Donia, Nicole</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Method for producing one-dimensional coaxial Ge/SiCxNy heterostructures, corresponding structure and use of said structure</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year></dates><abstract><style face="normal" font="default" size="100%">The invention relates to a method for producing 1-dimensional (1D) coaxial Ge/SiCxNy heterostructures, to a corresponding structure and to the use of the structure. The aim of the invention is to provide a method for producing 1-dimensional coaxial Ge/SiCxNy heterostructures. To achieve this aim, the precursor GeN(SiMe3)2 or homologs thereof are used in CVD. The invention allows for the 1st time monocryst. Ge nanowires having a chem. and mech. stable shell of SiCxNy to be produced. The 1-step process according to the invention is based on mol.-based CVD using GeN(SiMe3)2 as the precursor and allows the direct prodn. of coaxial Ge/SiCxNy heterostructures.</style></abstract><label><style face="normal" font="default" size="100%">donia2008method</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">https://patents.google.com/patent/WO2008077386A2/en</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">misc</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>431</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">431</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dhayal, Veena</style></author><author><style face="normal" font="default" size="100%">Bohra, Rakesh</style></author><author><style face="normal" font="default" size="100%">Nagar, Meena</style></author><author><style face="normal" font="default" size="100%">Kaushik, Ajay</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Leibniz Inst Neue Mat gGmbH, D-66123 Saarbrucken, Germany&#xD;Univ Rajasthan, Dept Chem, Jaipur 302004, Rajasthan, India&#xD;MLV Text &amp; Engn Coll, Dept Chem, Bhilwara, Rajasthan, India</style></auth-address><titles><title><style face="normal" font="default" size="100%">Low-temperature sol-gel transformation of methyl silicon precursors to silica-based hybrid materials</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Organometallic Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Appl Organomet Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">629-636</style></pages><volume><style face="normal" font="default" size="100%">22</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">2008, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2008</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">02682605</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000260336600004</style></accession-num><abstract><style face="normal" font="default" size="100%">Six new Me Si(IV) precursors MeSiØN:C(R)Ar\3 when R = Me, Ar = 2-C5H4N (1), 2-C4H3O (2) or 2-C4H3S (3); and when R = H, Ar = 2-C5H4N (4), 2-C4H3O (5) or 2-C4H3S (6) were prepd. and structurally characterized by various spectroscopic techniques. Mol. wt. measurements and FAB (Fast At. Bombardment) mass spectral studies indicated their monomeric nature. 1H and 13C\1H\ NMR spectral studies suggested the oximate ligands to be monodentate in soln., which was confirmed by 29Si\1H\ NMR signals in the region expected for tetracoordinated methylsilicon(IV) derivs. TGA of 1 revealed the complex to be thermally labile, decompg. to a hybrid material of definite compn. Two representative compds. (2 and 4) were studied as single source mol. precursor for low-temp. transformation to SiO2-based hybrid materials using sol-gel technique. Formation of homogeneous Me-bonded SiO2 materials (MeSiO3/2) at low sintering temp. was obsd. The TGA of the methylsilica material indicated that Si-Me bond is thermally stable up to a temp. of 400°. Reaction of 2 and Al(OPri)3 in equimolar ratio in anhyd. toluene yielded a brown-colored viscous liq. MeSiØN:CMeC4H3O\3,Al(OPri)3. Spectroscopic techniques 1H, 13C\1H\, 27Al\1H\ and 29Si\1H\ NMR spectra of the viscous product indicated the presence of tetracoordination around both Si and Al atoms. On hydrolysis it yielded methylated aluminosilicate material with high sp. surface area (464 m2/g). Scanning electron microg. confirmed a regular porous structure with porosity in the nanometric range.</style></abstract><label><style face="normal" font="default" size="100%">dhayal2008lowtemperature</style></label><notes><style face="normal" font="default" size="100%">364lg&#xD;Times Cited:3&#xD;Cited References Count:39</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/aoc.1448</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/aoc.1448</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>472</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">472</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Hernández-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Tarancón, A.</style></author><author><style face="normal" font="default" size="100%">Casals, O.</style></author><author><style face="normal" font="default" size="100%">Prades, D.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fabrication Strategies and Electrical Characterization of Nanodevices Contacted Using Focused Ion Beam Techniques</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Science &amp; Technology 2007 Conference and Exhibition</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">2883-2890</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year></dates><label><style face="normal" font="default" size="100%">romanorodriguez2007fabrication</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>471</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">471</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, R.</style></author><author><style face="normal" font="default" size="100%">Casals, O.</style></author><author><style face="normal" font="default" size="100%">Tarancon, A.</style></author><author><style face="normal" font="default" size="100%">Juli, M. A.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Helwig, A.</style></author><author><style face="normal" font="default" size="100%">Spannhake, J.</style></author><author><style face="normal" font="default" size="100%">Muller, G.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fabrication of bottom-up gas sensors based on individual SnO2 nanowires and suspended microhotplates</style></title><secondary-title><style face="normal" font="default" size="100%">Microprocesses and Nanotechnology, 2007 Digest of papers</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">490-491</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year></dates><publisher><style face="normal" font="default" size="100%">IEEE</style></publisher><isbn><style face="normal" font="default" size="100%">978-4-9902472-4-9</style></isbn><label><style face="normal" font="default" size="100%">Romano-Rodriguez2007</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://ieeexplore.ieee.org/lpdocs/epic03/wrapper.htm?arnumber=4456318</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>470</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">470</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nielsch, Kornelius</style></author><author><style face="normal" font="default" size="100%">Bachmann, Julien</style></author><author><style face="normal" font="default" size="100%">Daub, Mihaela</style></author><author><style face="normal" font="default" size="100%">Jing, Jing</style></author><author><style face="normal" font="default" size="100%">Knez, Mato</style></author><author><style face="normal" font="default" size="100%">Gösele, Ulrich</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Escrig, Juan</style></author><author><style face="normal" font="default" size="100%">Altbir, Dora</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ferromagnetic Nanostructures by Atomic Layer Deposition: From Thin Films Towards Core-Shell Nanotubes</style></title><secondary-title><style face="normal" font="default" size="100%">ECS Transactions</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">139-148</style></pages><volume><style face="normal" font="default" size="100%">11</style></volume><number><style face="normal" font="default" size="100%">7</style></number><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year></dates><abstract><style face="normal" font="default" size="100%">Nickel, cobalt and iron oxide nanotubes were obtained by atomic layer deposition (ALD) into the pores of alumina membranes. Initially, a metal oxide film was grown by the reaction of a precursor vapor of NiCp2 (nickelocene), CoCp2 (cobaltocene) or FeCp2 (ferrocene) with ozone, respectively. Subsequently, the metal oxide film was reduced in hydrogen atmosphere and converted to a metallic ferromagnetic phase with low-degree of surface roughness. In a similar manner, Fe3O4 films have also been obtained by the atomic layer deposition of Fe2O3 films based on the reaction of water and iron(III) tert-butoxide (Fe2(OtBu)6), followed by a hydrogen reduction to Fe3O4 after the ALD process. By conformal coating of self-ordered Al2O3 membranes, arrays of magnetic nanotubes with diameters down to 30 nm and wall thicknesses of less than 3 nm have been achieved. The magnetic properties of the nanotube arrays as a function of wall thickness and tube diameter have been studied by SQUID magnetometry. Atomic layer deposition (ALD) was proven to be a very suitable method for the conformal deposition of magnetic thin films in pore structures of high aspect ratio, while offering high uniformity and precise tuning of the layer thickness and the magnetic properties.</style></abstract><label><style face="normal" font="default" size="100%">nielsch2007ferromagnetic</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://ecst.ecsdl.org/cgi/doi/10.1149/1.2779078</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>466</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">466</key></foreign-keys><ref-type name="Book">6</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Singh, Mrityunjay</style></author><author><style face="normal" font="default" size="100%">Salem, Jonathan</style></author><author><style face="normal" font="default" size="100%">Zhu, Dongming</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanostructured Materials and Nanotechnology: Ceramic Engineering and Science Proceedings, Volume 28, Issue 6</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year></dates><publisher><style face="normal" font="default" size="100%">Wiley</style></publisher><isbn><style face="normal" font="default" size="100%">978-0-470-19637-3</style></isbn><label><style face="normal" font="default" size="100%">mathur2007nanostructured</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://eu.wiley.com/WileyCDA/WileyTitle/productCd-0470196378.html</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">book</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>467</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">467</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Donia, Nicole</style></author><author><style face="normal" font="default" size="100%">Rügamer, Thomas</style></author><author><style face="normal" font="default" size="100%">Sivakov, Vladimir</style></author><author><style face="normal" font="default" size="100%">Werner, Ulf</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Institute of New Materials, Saarbruecken, Germany. sanjay.mathur@inm-gmbh.de</style></auth-address><titles><title><style face="normal" font="default" size="100%">One-step Chemical Vapor Growth of Ge/SiC(x)N(y) Nanocables</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the American Chemical Society</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">9746-9752</style></pages><volume><style face="normal" font="default" size="100%">129</style></volume><number><style face="normal" font="default" size="100%">31</style></number><edition><style face="normal" font="default" size="100%">2007/07/17</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style face="normal" font="default" size="100%">August</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0002-7863</style></isbn><accession-num><style face="normal" font="default" size="100%">17629271</style></accession-num><abstract><style face="normal" font="default" size="100%">Single-step synthesis of one-dimensional Ge/SiCxNy core-shell nanocables was achieved by chemical vapor deposition of the molecular precursor Ge\N(SiMe3)2\2. Single crystalline Ge nanowires (diameter approximately 60 nm) embedded in uniform SiCxNy shells were obtained in high yields, whereby the growth process was not influenced by the nature of substrates. The shell material exhibited high oxidation and chemical resistance at elevated temperatures (up to 250 degrees C) resulting in the preservation of size-dependent semiconductor properties of germanium nanowires, such as intact transport of charge carriers and reduction of energy consumption, when compared to pure Ge nanowires.</style></abstract><label><style face="normal" font="default" size="100%">mathur2007onestep</style></label><notes><style face="normal" font="default" size="100%">Mathur, Sanjay&#xD;Shen, Hao&#xD;Donia, Nicole&#xD;Rugamer, Thomas&#xD;Sivakov, Vladimir&#xD;Werner, Ulf&#xD;eng&#xD;J Am Chem Soc. 2007 Aug 8;129(31):9746-52. doi: 10.1021/ja071931e. Epub 2007 Jul 13.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/ja071931e</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/ja071931e</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>464</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">464</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Altmayer, Jessica</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Inst New Mat, Saarbrucken, Germany&#xD;Wuerzburg Univ, Dept Chem, Wurzburg, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Nanostructured functional ceramic coatings by molecule-based chemical vapor deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Reviews on Advanced Materials Science</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Rev Adv Mater Sci</style></alt-title></titles><pages><style face="normal" font="default" size="100%">16-23</style></pages><volume><style face="normal" font="default" size="100%">15</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style face="normal" font="default" size="100%">Sep</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1606-5131</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000250547100004</style></accession-num><abstract><style face="normal" font="default" size="100%">Thin film deposition by chem. vapor deposition (CVD) techniques plays a dominant role in the development of both protective and functional coatings, important for their technol. implications. Commonly, multi-component materials are prepd. from a mixt. of precursors, however the efficiency of such processes is hampered by the mis-match of chem. reactivity such as differential thermal stability and vapor pressure of individual precursor species. Consequently, phase sepn. and elemental segregation are usually obsd. in coatings produced by CVD. De-mixing of elements in multi-component systems is thermodynamically driven and sensitive to the chem. behavior of the precursors. Transformation of precursor compds. possessing bonding features inherent to the solid-state lowers the need of diffusion and counterbalances the thermodn. impediments. We discuss here the role of pre-defined chem. precursors in reducing the constraints imposed on conventional CVD techniques, which require rather high deposition temps. and generally offer marginal control over microstructure and surface topog. Examples dealing with the decompn. of mol. sources in CVD process to deposit gas sensing, photocatalytic and bio-compatible coatings are also presented.</style></abstract><label><style face="normal" font="default" size="100%">mathur2007nanostructured</style></label><notes><style face="normal" font="default" size="100%">225vu&#xD;Times Cited:7&#xD;Cited References Count:28</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.ipme.ru/e-journals/RAMS/</style></url></related-urls></urls><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>462</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">462</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Rügamer, Thomas</style></author><author><style face="normal" font="default" size="100%">Braunschweig, Holger</style></author><author><style face="normal" font="default" size="100%">D&apos;Andola, Giovanni</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Wurzburg, Inst Anorgan Chem, D-97074 Wurzburg, Germany&#xD;Leibniz Inst New Mat, Dept Nanocrystalline Mat &amp; Thin Film Syst, Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Investigations on Chemical Vapour Deposition of Magnesium-Boron-Containing Metal-Organic Precursors</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Z Anorg Allg Chem</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2459-2462</style></pages><volume><style face="normal" font="default" size="100%">633</style></volume><number><style face="normal" font="default" size="100%">13-14</style></number><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year></dates><isbn><style face="normal" font="default" size="100%">00442313</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000250266900057</style></accession-num><abstract><style face="normal" font="default" size="100%">Single-mol. Mg-B precursors Mg(C3H6-BC8H14)2 and Mg\C3H6-B(C6H11)2\2 were applied in CVD processes and characterized using SEM, XRD, XPS, AFM and MS methods towards their fragmentation behavior, film morphol., phase formation and film compn. Deposition procedures at 500-1000° produced smooth and thin films with Mg and B in the ration 1:2. It could be shown that the contamination of the deposits by a considerably fraction of residual C could be reduced by post-deposition in-situ tempering or addnl. sputter processes which may lead to improved deposition of MgB2-films.</style></abstract><label><style face="normal" font="default" size="100%">mathur2007investigations</style></label><notes><style face="normal" font="default" size="100%">221zw&#xD;Times Cited:1&#xD;Cited References Count:18</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/zaac.200700368</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/zaac.200700368</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>468</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">468</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ruegamer, Thomas</style></author><author><style face="normal" font="default" size="100%">Grobelsek, Ingrid</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Inst New Mat, Dept Nanorystalline Mat &amp; Thin Film Syst, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Phase-Selective CVD of Vanadium Oxide Nanostructures</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Vapor Deposition</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Vapor Depos</style></alt-title></titles><pages><style face="normal" font="default" size="100%">42-47</style></pages><volume><style face="normal" font="default" size="100%">13</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09481907</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000244062200007</style></accession-num><abstract><style face="normal" font="default" size="100%">Phase-selective synthesis of cryst. V oxides is achieved by the CVD of V oxo-tri-isopropoxide VO(OiPr)3. Preformed V-O and V=O units and their differential thermal stability present in the precursor enabled precise modulation of the V/O stoichiometry in the products of the CVD. No addnl. O carrier is employed during the deposition processes. Subject to deposition temp. (400-700°), different phase compns. (V2O5, V7O13, and VO2) are directly obtained and are studied regarding structural and elec. properties. Hall measurements on VO2 films show a sharp metal-to-semiconductor transition at 78° (single crystal, 68°) depending on their microstructure formed by an oriented aggregation of individual crystallites.</style></abstract><label><style face="normal" font="default" size="100%">mathur2007phaseselective</style></label><notes><style face="normal" font="default" size="100%">134dg&#xD;Times Cited:35&#xD;Cited References Count:30</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/cvde.200606578</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/cvde.200606578</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>469</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">469</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Ganesan, Rajesh</style></author><author><style face="normal" font="default" size="100%">Grobelsek, Ingrid</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Ruegamer, Thomas</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Leibniz Inst New Mat, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Plasma-Assisted Modulation of Morphology and Composition in Tin Oxide Nanostructures for Sensing Applications</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Adv Eng Mater</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Advanced Engineering Materials</style></full-title></periodical><pages><style face="normal" font="default" size="100%">658-663</style></pages><volume><style face="normal" font="default" size="100%">9</style></volume><number><style face="normal" font="default" size="100%">8</style></number><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style face="normal" font="default" size="100%">Aug</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">14381656</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000249173500007</style></accession-num><abstract><style face="normal" font="default" size="100%">The controlled growth of single crystal tin oxide platelets followed by modulation of their morphol. and compn. induced by argon and oxygen plasma is described. Nanoscopic SnO2 platelets were grown by a CVD of a mol. source, Sn(OtBu)4, on polycryst. alumina substrates. Tin oxide deposits were treated in Ar/O2 plasma to modulate morphol. and chem. compn. in the samples and to investigate the changes in their chem. sensing ability. Plasma treatment of nanoplates changed the plate-like morphol. to globular particles and granular structures possibly due to a sputter-redeposition mechanism, which also altered the wetting behavior of the surfaces. Higher Sn:O ratio was obtained in the plasma treated samples, due to preferential sputtering of lattice oxygen, which led to the formation of metallic tin as a minor phase embedded in tin oxide matrix. This microstructure augmented the cond. of the samples at room temp. Consequently, the plasma treated samples showed higher sensitivity at lower operating temp. and improved transducing response towards changing gas atmospheres. Plasma treated SnO2 nanoplates yielded stable performance and enhanced gas sensing characteristics due to increased charge carrier concn. which effectively improved oxygen chemisorption. However, surface treatment with high energy plasma (&gt; 40 W) increased the formation of elemental tin which was found to be detrimental for the semiconductor properties of the samples and influenced their ethanol sensing properties.</style></abstract><label><style face="normal" font="default" size="100%">mathur2007plasmaassisted</style></label><notes><style face="normal" font="default" size="100%">206hc&#xD;Times Cited:28&#xD;Cited References Count:28</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/adem.200700086</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/adem.200700086</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>465</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">465</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Donia, Nicole</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanostructured materials and coatings through chemistry: from molecules to product applications</style></title><secondary-title><style face="normal" font="default" size="100%">Nanotechnology in industrial applications: Euro Nano Forum 2007</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">105-109</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year></dates><label><style face="normal" font="default" size="100%">mathur2007nanostructured</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://bookshop.europa.eu/de/euronanoforum-2007-pbKINA22833/;pgid=Iq1Ekni0.1lSR0OOK4MycO9B000010mELhMm;sid=yk5M0AwnnfFM0louxD3Sd24CzZ1KA0FE1Dw=?CatalogCategoryID=w2wKABst3XAAAAEjfJEY4e5L</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>463</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">463</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Institute of New Materials, Im Stadtwald, Building D2 2, 66123 Saarbruecken, Germany. s.mathur@uni-wuerzburg.de</style></auth-address><titles><title><style face="normal" font="default" size="100%">Molecule-based chemical vapor growth of aligned SnO2 nanowires and branched SnO2/V2O5 heterostructures</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Small</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2070-2075</style></pages><volume><style face="normal" font="default" size="100%">3</style></volume><number><style face="normal" font="default" size="100%">12</style></number><edition><style face="normal" font="default" size="100%">2007/11/23</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style face="normal" font="default" size="100%">Dec</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1613-6829</style></isbn><accession-num><style face="normal" font="default" size="100%">18033716</style></accession-num><abstract><style face="normal" font="default" size="100%">Aligned SnO2 nanowire arrays and individual 1D structures were grown by a combination of mol.-based CVD and catalyst-assisted growth techniques on TiO2 substrates. Hierarchical branched SnO2/V2O5 heterostructures (see image) were obtained by a two-step process without secondary catalyst deposition leading to a red shift in the photoconductance of the SnO2/V2O5 structures compared to the pure SnO2 NWs.</style></abstract><label><style face="normal" font="default" size="100%">mathur2007moleculebased</style></label><notes><style face="normal" font="default" size="100%">Mathur, Sanjay&#xD;Barth, Sven&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;Germany&#xD;Small. 2007 Dec;3(12):2070-5. doi: 10.1002/smll.200700213.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/18033716</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/smll.200700213</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>461</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">461</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Altmayer, J.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Mueller, M.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Campus, CVD Div, Leibniz Inst New Mat, Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Nanostructured metal oxide surfaces for bio-medical applications: Modulation of surface properties through chemical precursor design</style></title><secondary-title><style face="normal" font="default" size="100%">Tissue Engineering</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Tissue Eng</style></alt-title></titles><pages><style face="normal" font="default" size="100%">906</style></pages><volume><style face="normal" font="default" size="100%">13</style></volume><number><style face="normal" font="default" size="100%">4</style></number><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style face="normal" font="default" size="100%">April</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1076-3279</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000245680900129</style></accession-num><label><style face="normal" font="default" size="100%">mathur2007nanostructured</style></label><notes><style face="normal" font="default" size="100%">156wp&#xD;Times Cited:0&#xD;Cited References Count:4</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1089/ten.2006.9999</style></url></related-urls></urls><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>458</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">458</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Tarancon, A.</style></author><author><style face="normal" font="default" size="100%">Casals, Olga</style></author><author><style face="normal" font="default" size="100%">Pellicer, E.</style></author><author><style face="normal" font="default" size="100%">Rodriguez, J.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Barcelona, IN 2, E-08028 Barcelona, Spain&#xD;Univ Barcelona, Dept Elect, EME CErM CEMIC, E-08028 Barcelona, Spain&#xD;Wuerzburg Univ, Dept Inorgan Chem, D-97074 Wurzburg, Germany&#xD;Leibniz Inst Neue Materialien, Dept Nanocrystalline Mat &amp; Thin Film Syst, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Electrical properties of individual tin oxide nanowires contacted to platinum electrodes</style></title><secondary-title><style face="normal" font="default" size="100%">Physical Review B</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Phys Rev B</style></alt-title></titles><pages><style face="normal" font="default" size="100%">085429</style></pages><volume><style face="normal" font="default" size="100%">76</style></volume><number><style face="normal" font="default" size="100%">8</style></number><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style face="normal" font="default" size="100%">Aug</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1098-0121</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000249155400127</style></accession-num><abstract><style face="normal" font="default" size="100%">A simple and useful experimental alternative to field-effect transistors for measuring electrical properties (free electron concentration n(d), electrical mobility mu, and conductivity sigma) in individual nanowires has been developed. A combined model involving thermionic emission and tunneling through interface states is proposed to describe the electrical conduction through the platinum-nanowire contacts, fabricated by focused ion beam techniques. Current-voltage (I-V) plots of single nanowires measured in both two- and four-probe configurations revealed high contact resistances and rectifying characteristics. The observed electrical behavior was modeled using an equivalent circuit constituted by a resistance placed between two back-to-back Schottky barriers, arising from the metal-semiconductor-metal (M-S-M) junctions. Temperature-dependent I-V measurements revealed effective Schottky barrier heights up to Phi(BE)=0.4 eV.</style></abstract><label><style face="normal" font="default" size="100%">hernandezramirez2007electrical</style></label><notes><style face="normal" font="default" size="100%">206ad&#xD;Times Cited:93&#xD;Cited References Count:22</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://link.aps.org/doi/10.1103/PhysRevB.76.085429</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">ARTN 085429&#xD;10.1103/PhysRevB.76.085429</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>459</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">459</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Prades, J. D.</style></author><author><style face="normal" font="default" size="100%">Tarancon, A.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Casals, O.</style></author><author><style face="normal" font="default" size="100%">Jimenez-Diaz, R.</style></author><author><style face="normal" font="default" size="100%">Pellicer, E.</style></author><author><style face="normal" font="default" size="100%">Rodriguez, J.</style></author><author><style face="normal" font="default" size="100%">Juli, M. A.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Helwig, A.</style></author><author><style face="normal" font="default" size="100%">Spannhake, J.</style></author><author><style face="normal" font="default" size="100%">Mueller, G.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">EME/IN2UB Departament d&apos;Electronica, Universitat de Barcelona, C/Martii Franques 1, E-08028 Barcelona, Spain. fhernandezra@gmail.com</style></auth-address><titles><title><style face="normal" font="default" size="100%">Portable microsensors based on individual SnO2 nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Nanotechnology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">495501</style></pages><volume><style face="normal" font="default" size="100%">18</style></volume><number><style face="normal" font="default" size="100%">49</style></number><edition><style face="normal" font="default" size="100%">2007/12/12</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style face="normal" font="default" size="100%">Dec 12</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1361-6528 (Electronic)&#xD;0957-4484 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">20442472</style></accession-num><abstract><style face="normal" font="default" size="100%">Individual SnO2 nanowires were integrated in suspended micromembrane-based bottom-up devices. Electrical contacts between the nanowires and the electrodes were achieved with the help of electron- and ion-beam-assisted direct-write nanolithography processes. The stability of these nanomaterials was evaluated as function of time and applied current, showing that stable and reliable devices were obtained. Furthermore, the possibility of modulating their temperature using the integrated microheater placed in the membrane was also demonstrated, enabling these devices to be used in gas sensing procedures. We present a methodology and general strategy for the fabrication and characterization of portable and reliable nanowire-based devices.</style></abstract><label><style face="normal" font="default" size="100%">hernandezramirez2007portable</style></label><notes><style face="normal" font="default" size="100%">Hernandez-Ramirez, F&#xD;Prades, J D&#xD;Tarancon, A&#xD;Barth, S&#xD;Casals, O&#xD;Jimenez-Diaz, R&#xD;Pellicer, E&#xD;Rodriguez, J&#xD;Juli, M A&#xD;Romano-Rodriguez, A&#xD;Morante, J R&#xD;Mathur, S&#xD;Helwig, A&#xD;Spannhake, J&#xD;Mueller, G&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;England&#xD;Nanotechnology. 2007 Dec 12;18(49):495501. doi: 10.1088/0957-4484/18/49/495501. Epub 2007 Nov 2.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1088/0957-4484/18/49/495501</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1088/0957-4484/18/49/495501</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>460</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">460</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, F.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Tarancon, A.</style></author><author><style face="normal" font="default" size="100%">Casals, O.</style></author><author><style face="normal" font="default" size="100%">Pellicer, E.</style></author><author><style face="normal" font="default" size="100%">Rodriguez, J.</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, A.</style></author><author><style face="normal" font="default" size="100%">Morante, J. R.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">IN2UB and EME/CErMAE/CEMIC Departament d&apos;Electronica, Universitat de Barcelona UB, C/MartiI Franques 1, E-08028 Barcelona, Spain.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Water vapor detection with individual tin oxide nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Nanotechnology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">424016</style></pages><volume><style face="normal" font="default" size="100%">18</style></volume><number><style face="normal" font="default" size="100%">42</style></number><edition><style face="normal" font="default" size="100%">2007/10/24</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style face="normal" font="default" size="100%">Oct 24</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0957-4484 (Print)&#xD;0957-4484 (Linking)</style></isbn><accession-num><style face="normal" font="default" size="100%">21730449</style></accession-num><abstract><style face="normal" font="default" size="100%">Individual tin oxide nanowires (NWs), contacted to platinum electrodes using focused ion beam assisted nanolithography, were used for detecting water vapor (1500-32 000 ppm) in different gaseous environments. Responses obtained in synthetic air (SA) and nitrogen atmospheres suggested differences in the sensing mechanism, which were related to changes in surface density of the adsorbed oxygen species in the two cases. A model describing the different behaviors has been proposed together with comparative evaluation of NW responses against sensors based on bulk tin oxide. The results obtained on ten individual devices (tested &gt; 6 times) revealed the interfering effect of water in the detection of carbon monoxide and illustrated the intrinsic potential of nanowire-based devices as humidity sensors. Investigations were made on sensitivity, recovery time and device stability as well as surface-humidity interactions. This is the first step towards fundamental understanding of single-crystalline one-dimensional (1D) tin oxide nanostructures for sensor applications, which could lead to integration in real devices.</style></abstract><label><style face="normal" font="default" size="100%">hernandezramirez2007water</style></label><notes><style face="normal" font="default" size="100%">Hernandez-Ramirez, F&#xD;Barth, S&#xD;Tarancon, A&#xD;Casals, O&#xD;Pellicer, E&#xD;Rodriguez, J&#xD;Romano-Rodriguez, A&#xD;Morante, J R&#xD;Mathur, S&#xD;eng&#xD;England&#xD;Nanotechnology. 2007 Oct 24;18(42):424016. doi: 10.1088/0957-4484/18/42/424016. Epub 2007 Sep 19.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1088/0957-4484/18/42/424016</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1088/0957-4484/18/42/424016</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>457</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">457</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chauhan, H. P. S.</style></author><author><style face="normal" font="default" size="100%">Shaik, N. M.</style></author><author><style face="normal" font="default" size="100%">Singh, U. P.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Zimmer, M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and Spectroscopic [IR, Solid-State NMR (1-H, 13-C &amp; 31-P)] Studies of 1,3-Dithia-2-Stannacyclopentane Diorganodithiophosphates</style></title><secondary-title><style face="normal" font="default" size="100%">Main Group Metal Chemistry</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">269-278</style></pages><volume><style face="normal" font="default" size="100%">30</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year></dates><abstract><style face="normal" font="default" size="100%">1,3-dithia-2-stannacyclopentane derivatives of diorganodithiophosphates of the, types SCH2CH2SSnS2P(OR)(2)Cl (I) and SCH2CH2SSnS2P(OR)(2)(2) (II) where R = Et, n-Pr, i-Pr, n-Bu, i-Bu and Ph have been synthesized (in 78-95\% yields) by the reaction of 2,2-dichloro-1,3-dithia-2-stannacyclopentane and sodium/ammonium salts of diorganodithiophosphates in 1:1 and 1:2 molar ratios respectively, in anhydrous benzene. All these newly synthesized complexes are insoluble in common organic solvents and are difficult to be analysed by conventional techniques. We have applied elemental analyses, IR and solid-state NMR (H-1, C-13 and P-31) techniques to obtain structural information of these complexes.</style></abstract><label><style face="normal" font="default" size="100%">chauhan2007synthesis</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1515/MGMC.2007.30.5.269</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>455</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">455</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bachmann, J.</style></author><author><style face="normal" font="default" size="100%">Jing, J.</style></author><author><style face="normal" font="default" size="100%">Escrig, J.</style></author><author><style face="normal" font="default" size="100%">Knez, M.</style></author><author><style face="normal" font="default" size="100%">Nielsch, K.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ordered arrays of magnetic iron oxide nanotubes</style></title><secondary-title><style face="normal" font="default" size="100%">Max Planck Institute of Microstructure Physics - Annual Reports 2007</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">36-37</style></pages><keywords><keyword><style face="normal" font="default" size="100%">2007, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2007</style></year></dates><abstract><style face="normal" font="default" size="100%">Although atomic layer deposition (ALD) has been available for thirty years for the preparation of thin dielectric and semiconduc-tor films 1, more complex structures and more varied materials systems have remained marginal applications of the technique. Its self-limiting nature, however, enables one to coat substrates of complex geometry confor-mally. Consequently, templates of controlled structure may be utilized for creating well-defined nanoobjects. This capability is at-tractive in the field of magnetic data stor-age, where structures are sought in which shape anisotropy overcomes superparamag-netism while maintaining small lateral sizes. We have developed ALD reactions appli-cable to growing films and nanostructures of Fe 2 O 3 (Fig. 1). The hydrolysis of iron(III) tert-butoxide, Fe 2 (O t Bu) 6 , occurs in ALD mode at temperatures near 150 • C with a growth rate of 0.26(±0.04 A per cycle 2. The combus-tion of ferrocene, Cp 2 Fe, by ozone, O 3 , fur-nishes a practical alternative in cases where slightly more elevated temperatures (∼200 • C) are tolerable. When applied to a porous an-odic alumina (AA) template 3, both meth-ods yield composites consisting of Fe 2 O 3 nan-otubes embedded in an Al 2 O 3 matrix. As-pect ratios ≥100 are accessible. Subsequently, Fe 2 O 3 is reduced to Fe 3 O 4 by H 2 . The trans-formation can be followed visually by a color change from golden or coppery brown to grey or black, and analytically by X-ray photo-electron spectroscopy (XPS). The tubes ex-hibit smooth walls of well-defined thickness d w , which can be adjusted between 1 and 40 nm proportionally to the number of ALD cy-cles performed. Their other geometric param-eters, length and diameter, are also tunable and are determined by the preparation of the tem-plate. Fig. 1 displays structural aspects of vari-ous tubes and allows one to evaluate the homo-geneity of the geometric parameters through-out each sample as well as the parallel align-ment.</style></abstract><label><style face="normal" font="default" size="100%">bachmann2007ordered</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www-old.mpi-halle.mpg.de/mpi/mpi_f_pub.html</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>640</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">640</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bachmann, Julien</style></author><author><style face="normal" font="default" size="100%">Jing,</style></author><author><style face="normal" font="default" size="100%">Knez, Mato</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Gösele, Ulrich</style></author><author><style face="normal" font="default" size="100%">Nielsch, Kornelius</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Ordered Iron Oxide Nanotube Arrays of Controlled Geometry and Tunable Magnetism by Atomic Layer Deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the American Chemical Society</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">9554-9555</style></pages><volume><style face="normal" font="default" size="100%">129</style></volume><number><style face="normal" font="default" size="100%">31</style></number><dates><year><style face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style face="normal" font="default" size="100%">2007/08/01</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><isbn><style face="normal" font="default" size="100%">0002-7863</style></isbn><urls><related-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/ja072465w</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/ja072465w</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>476</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">476</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Sivakov, V.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Cavelius, C.</style></author><author><style face="normal" font="default" size="100%">Nilsson, A.</style></author><author><style face="normal" font="default" size="100%">Kuhn, P.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Inst Neue Mat, CVD Div, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Nanostructured films of iron, tin and titanium oxides by chemical vapor deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Thin Solid Films</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Thin Solid Films</style></alt-title></titles><pages><style face="normal" font="default" size="100%">88-93</style></pages><volume><style face="normal" font="default" size="100%">502</style></volume><number><style face="normal" font="default" size="100%">1-2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2006, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2006</style></year><pub-dates><date><style face="normal" font="default" size="100%">Apr 28</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0040-6090</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000236309200018</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanostructured films of iron, tin and titanium oxides were grown on glass and quartz by gas phase decomposition of Fe(O&apos;Bu)(3)(2), Sn(O&apos;Bu)(4) and Ti(O&apos;Pr)(4), respectively. Films obtained exhibit good adhesion and homogeneous morphology with structural features in the nanometer range. The influence of microstructure and phase on optical (alpha-Fe2O3 and Fe3O4), gas sensing (SnO2) and photocatalytic (TiO2) properties was systematically studied to explore the potential of these coatings for technological applications.</style></abstract><label><style face="normal" font="default" size="100%">mathur2006nanostructured</style></label><notes><style face="normal" font="default" size="100%">026an&#xD;Times Cited:76&#xD;Cited References Count:32</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:000236309200018</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.tsf.2005.07.249</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>484</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">484</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Rapalaviciute, Rasa</style></author><author><style face="normal" font="default" size="100%">Agne, Thomas</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Inst New Mat, CVD Div, D-66123 Saarbrucken, Germany&#xD;Univ Saarland, Inst Inorgan Chem, D-66123 Saarbrucken, Germany&#xD;Univ Saarland, Inst Tech Phys, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Structural and Optical Properties of Highly Nd-Doped Yttrium Aluminum Garnet Ceramics from Alkoxide and Glycolate Precursors</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the American Ceramic Society</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Am Ceram Soc</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2027-2033</style></pages><volume><style face="normal" font="default" size="100%">89</style></volume><number><style face="normal" font="default" size="100%">6</style></number><keywords><keyword><style face="normal" font="default" size="100%">2006, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2006</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0002-7820</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000237812100038</style></accession-num><abstract><style face="normal" font="default" size="100%">Yttrium aluminum garnet (YAG) nanopowders doped with high neodymium (Nd) content (3 at.\%) were synthesized by the sol-gel processing of (i) alkoxide precursors and (ii) metal chelates formed by complexing the cations with polyethylene glycol. A stoichiometric YAG compn. was obtained following both procedures; however, the agglomeration of particles was significantly higher in glycolate synthesis, which shielded residual orgs. from oxidn. (elemental analyses). Distribution of Nd3+ ions in the YAG matrix, as shown by the absorption of pump energy and photoluminescence spectra of Nd:YAG ceramics, was more homogeneous in alkoxide-derived powders. The segregation of Nd centers in the glycolate-derived sample was supported by the pptn. of a cryst. Nd2O3 phase (X-ray diffraction) during sintering. High-resoln. absorption spectra (4I9/2(1) → 4F9/2(1)) of the powders showed that a higher absorption cross-section of glycolate-derived powders is due to Nd3+-Nd3+ ion pairing, which leads to the quenching of photoluminescence. Owing to the better dispersion of optically active centers, the photoluminescence signal was substantially enhanced in alkoxide-derived Nd:YAG ceramics.</style></abstract><label><style face="normal" font="default" size="100%">mathur2006structural</style></label><notes><style face="normal" font="default" size="100%">046lc&#xD;Times Cited:25&#xD;Cited References Count:48</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1111/j.1551-2916.2006.01000.x</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1111/j.1551-2916.2006.01000.x</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>477</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">477</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Donia, Nicole</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chemical Nanotechnology: From Molecules to Applications</style></title><secondary-title><style face="normal" font="default" size="100%">ECS Transactions</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">3-13</style></pages><volume><style face="normal" font="default" size="100%">3</style></volume><number><style face="normal" font="default" size="100%">9</style></number><keywords><keyword><style face="normal" font="default" size="100%">2006, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2006</style></year></dates><abstract><style face="normal" font="default" size="100%">The article reviews the potential of bottom-up chemical methodologies in synthesizing nanoscopic materials, and evaluates the influence of chemistry involved in materials processing on functional and structural properties of ceramics. Application of molecular sources in preparation of nanomaterials allows an intrinsic chemical encodingl in the initial stages of molecule-to- material transformation which plays an important role in tuning the properties of nanomaterials. Salient examples describing the precursor-structure-property-application relationship have been discussed to support the above arguments.</style></abstract><label><style face="normal" font="default" size="100%">mathur2006chemical</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://ecst.ecsdl.org/cgi/doi/10.1149/1.2357091</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>481</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">481</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Donia, Nicole</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Vayssieres, Lionel</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">One-dimensional semiconductor nanostructures: growth, characterization, and device applications</style></title><secondary-title><style face="normal" font="default" size="100%">Proceedings of SPIE-The International Society for Optical Engineering</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">634008</style></pages><volume><style face="normal" font="default" size="100%">6340</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2006, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2006</style></year><pub-dates><date><style face="normal" font="default" size="100%">August</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">SPIE-The International Society for Optical Engineering</style></publisher><abstract><style face="normal" font="default" size="100%">Molecule-based CVD is applied for the development of 1D semiconducting nanowires. By virtue of the chemical design of the metal-organic precursors, it is possible to achieve the required supersaturation ratio of phase-constituting elements in the gas phase, which allows to grow anisotropic structures with precisely controlled dimension and composition. [Ge(C5H5)2] with labile Ge-C bonds was thermolysed at 300 °C to grow single crystalline Ge nanowires (NWs). For tin oxide nanostructures, [Sn(OBut)4] with relatively strong and preformed Sn-O bonds was employed to synthesize anisotropic rutile phase. Determination of I-V characteristics of Ge NWs in different environments indicate surface passivation, possibly through hydrogen. Radial dimension of SnO2 NWs was varied in the range 30-1000 nm by choosing appropriate size of catalyst particles. Photo-conductance studies on different NW samples revealed a significant &apos;blue shift&apos; with shrinking wire diameters. Tin oxide nanowires were coated with vanadium oxide by CVD of [VO(OPri)3] on as-grown tin oxide nanowires. Composite SnO2/VOx 1D nanostructures showed a shift to higher wavelength in photo-response peak, when compared to pure SnO2 NWs. We also demonstrate the integration of single NW on pre-patterned electrodes for evaluating sensing and electrical properties on individual nanoobjects.</style></abstract><label><style face="normal" font="default" size="100%">mathur2006onedimensional</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1117/12.678325</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>479</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">479</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Cavelius, Christian</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Inorganic nanomaterials through chemical design</style></title><secondary-title><style face="normal" font="default" size="100%">SPIE Newsroom</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2006, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2006</style></year></dates><isbn><style face="normal" font="default" size="100%">18182259</style></isbn><label><style face="normal" font="default" size="100%">Mathur2006</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.spie.org/x8864.xml</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>480</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">480</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular routes to one dimensional nanostructures</style></title><secondary-title><style face="normal" font="default" size="100%">Ceramic Transactions</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">139--148</style></pages><volume><style face="normal" font="default" size="100%">172</style></volume><number><style face="normal" font="default" size="100%">Ceramic Nanomaterials and Nanotechnologies IV</style></number><keywords><keyword><style face="normal" font="default" size="100%">2006, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2006</style></year></dates><isbn><style face="normal" font="default" size="100%">1042-1122</style></isbn><abstract><style face="normal" font="default" size="100%">We have developed a facile synthetic technique based on the gas phase decompn. of mol. clusters on metal or metal oxide nanoparticles in the chem. vapor deposition process to produce high quality 1D nanostructures. The chem. compn. and dimensions (radial and axial) of the nanowires can be easily controlled by regulating the supersatn. rate of catalyst/source materials. The synthetic approach has been applied to grow germanium and tin oxide nanowires. The results show the obtained nanowires to be single crystals with a narrow diam. size-distribution. Investigation on the growth mechanism and size-dependent phys. properties are also discussed. on</style></abstract><label><style face="normal" font="default" size="100%">mathur2006molecular</style></label><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>478</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">478</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kuhn, Patrick</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">CVD of titanium oxide coatings: Comparative evaluation of thermal and plasma assisted processes</style></title><secondary-title><style face="normal" font="default" size="100%">Surface and Coatings Technology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">807-814</style></pages><volume><style face="normal" font="default" size="100%">201</style></volume><number><style face="normal" font="default" size="100%">3-4</style></number><keywords><keyword><style face="normal" font="default" size="100%">2006, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2006</style></year></dates><isbn><style face="normal" font="default" size="100%">02578972</style></isbn><abstract><style face="normal" font="default" size="100%">Deposition of titanium oxide (TiO2) films has been investigated in a pulsed DC plasma assisted CVD process (PACVD) using titanium isopropoxide, Ti(OPri)4, as the metal-org. source. The coatings were compared with TiO2 films obtained by a thermally activated decompn. of Ti(OPri)4 in a LPCVD process and characterized with respect to their morphol., microstructure, chem. compn. and mech. properties by SEM, at. force microscopy (AFM), x-ray diffraction (XRD), photoelectron spectroscopy (XPS) and micro-indentation studies, resp. While nanostructured deposits of cryst. TiO2 could be obtained in the LPCVD process at temps. as low as 350°, the PACVD films were identified to be amorphous under different deposition conditions. On the other hand, the plasma assisted CVD produced dense and mech. stable TiO2 films at temps. below 200° showing less residual carbon contamination when compared to LPCVD coatings. Despite the similar chem. compn., the precursor fragmentation and surface reactions (diffusion, nucleation and grain growth) were different in the two cases and found to be sensitive to the energy mode. Whereas high substrate temps. forced nucleation and crystn. in thermally activated process, incomplete decompn. of org. ligands caused high carbon contamination in the films. The fragmentation of precursor was found to be more effective in PACVD process as indicated by low residual carbon contamination in the films. Nevertheless, the PACVD films possessed an amorphous character and a post-annealing step was necessary to obtain cryst. deposits, which showed hydrophilic behavior stimulated by UV irradn. While the deposition temp. was found to be a key parameter for the LPCVD process which affects morphol. and microstructure, the chem. and mech. properties in the PACVD process were strongly influenced by plasma power variations, e.g. discharge voltage and gas compn.</style></abstract><label><style face="normal" font="default" size="100%">mathur2006titanium</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0257897205014027</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>483</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">483</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Pyun, Jae-Chul</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Size- and Surface-dependent Photoresistance in SnO2 Nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Proceedings 2005</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">0901--Rb15--02</style></pages><volume><style face="normal" font="default" size="100%">901</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2006, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2006</style></year></dates><isbn><style face="normal" font="default" size="100%">1946-4274</style></isbn><abstract><style face="normal" font="default" size="100%">Nanostructured one-dimensional materials, such as nanowires, tubes and rods, are gaining increasing attention due to interesting properties and confinement effects, however controlled synthesis of these structures is still limited to a few methods. We present here the synthesis of SnO2 nanowires (Ø, 50 – 1000 nm) at moderate temperatures (550 – 900 °C) using a molecular source Sn(OBut)4 with pre-existent Sn-O bonds. The growth occurs via a catalyst driven vapor-solid-solid mechanism. Size-selective synthesis of NWs in high areal density was achieved by choosing Au particles of appropriate size. HR-TEM analysis reveals the single crystalline behaviour of wires with a preferred growth direction 100. Use of SnO2 nanowires as potential optical switches for UV applications was demonstrated by the photo-response measurements. Determination of band gap values confirmed the blue-shift of the main photo-response peak with shrinking radial dimensions of the wires. Furthermore, deposition of vanadium oxide onto SnO2 led to a red-shift of the main conduction value of the nanowires.</style></abstract><label><style face="normal" font="default" size="100%">mathur2006surfacedependent</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1557/PROC-0901-Rb15-02</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>482</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">482</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Altmayer, Jessica</style></author><author><style face="normal" font="default" size="100%">Hemmer, Eva</style></author><author><style face="normal" font="default" size="100%">Donia, Nicole</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Rügamer, Thomas</style></author><author><style face="normal" font="default" size="100%">Kuhn, Patrick</style></author><author><style face="normal" font="default" size="100%">Cavelius, Christian</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Protective and bio-compatible nanostructured surfaces by CVD techniques: controlled modulation of surface and phase structures</style></title><secondary-title><style face="normal" font="default" size="100%">6th International Conference on Coatings on Glass and Plastics: Advanced Coatings for Large-Area or High-Volume Products</style></secondary-title></titles><volume><style face="normal" font="default" size="100%">133-134</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2006, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2006</style></year></dates><label><style face="normal" font="default" size="100%">mathur2006protective</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>475</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">475</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernández-Ramírez, Francisco</style></author><author><style face="normal" font="default" size="100%">Tarancón, Albert</style></author><author><style face="normal" font="default" size="100%">Casals, Olga</style></author><author><style face="normal" font="default" size="100%">Rodríguez, Jordi</style></author><author><style face="normal" font="default" size="100%">Romano-Rodríguez, Albert</style></author><author><style face="normal" font="default" size="100%">Morante, Joan R.</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Choi, Tae Y.</style></author><author><style face="normal" font="default" size="100%">Poulikakos, Dimos</style></author><author><style face="normal" font="default" size="100%">Callegari, Victor</style></author><author><style face="normal" font="default" size="100%">Nellen, Philipp M.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">EME/CErMAE/CEMIC, Departament d&apos;Electronica, University of Barcelona, E-08028 Barcelona, Spain.</style></auth-address><titles><title><style face="normal" font="default" size="100%">Fabrication and electrical characterization of circuits based on individual tin oxide nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Nanotechnology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">5577-5583</style></pages><volume><style face="normal" font="default" size="100%">17</style></volume><number><style face="normal" font="default" size="100%">22</style></number><edition><style face="normal" font="default" size="100%">2006/11/28</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2006, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2006</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0957-4484</style></isbn><accession-num><style face="normal" font="default" size="100%">21727327</style></accession-num><abstract><style face="normal" font="default" size="100%">Two- and four-probe electrical measurements on individual tin oxide (SnO(2)) nanowires were performed to evaluate their conductivity and contact resistance. Electrical contacts between the nanowires and the microelectrodes were achieved with the help of an electron- and ion-beam-assisted direct-write nanolithography process. High contact resistance values and the nonlinear current-bias (I-V) characteristics of some of these devices observed in two-probe measurements can be explained by the existence of back-to-back Schottky barriers arising from the platinum-nanowire contacts. The nanoscale devices described herein were characterized using impedance spectroscopy, enabling the development of an equivalent circuit. The proposed methodology of nanocontacting and measurements can be easily applied to other nanowires and nanometre-sized materials.</style></abstract><label><style face="normal" font="default" size="100%">hernandezramirez2006fabrication</style></label><notes><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco&#xD;Tarancon, Albert&#xD;Casals, Olga&#xD;Rodriguez, Jordi&#xD;Romano-Rodriguez, Albert&#xD;Morante, Joan R&#xD;Barth, Sven&#xD;Mathur, Sanjay&#xD;Choi, Tae Y&#xD;Poulikakos, Dimos&#xD;Callegari, Victor&#xD;Nellen, Philipp M&#xD;eng&#xD;England&#xD;Nanotechnology. 2006 Nov 28;17(22):5577-83. doi: 10.1088/0957-4484/17/22/009. Epub 2006 Oct 26.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/21727327</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1088/0957-4484/17/22/009</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>474</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">474</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hernandez-Ramirez, Francisco</style></author><author><style face="normal" font="default" size="100%">Tarancon, Albert</style></author><author><style face="normal" font="default" size="100%">Casals, Olga</style></author><author><style face="normal" font="default" size="100%">Pellicer, Eva</style></author><author><style face="normal" font="default" size="100%">Romano-Rodriguez, Albert</style></author><author><style face="normal" font="default" size="100%">Morante, Joan R</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Electrical gas sensor characterization of individual tin oxide nanowires contacted by focused ion beam techniques</style></title><secondary-title><style face="normal" font="default" size="100%">Matererials Science and Technology 2006 Conference and Exhibition</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1013-1024</style></pages><volume><style face="normal" font="default" size="100%">2</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2006, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2006</style></year></dates><publisher><style face="normal" font="default" size="100%">Minerals, Metals &amp; Materials Society</style></publisher><abstract><style face="normal" font="default" size="100%">Elec. properties of individual tin-oxide nanowires contacted using Focused Ion Beam techniques have been evaluated, observing in most of these devices high contact resistances and nonlinear current-bias (I-V) responses. This behavior can be explained by the existence of back-to-back Schottky barriers in platinum-nanowire contacts, whose elec. responses can be modeled using thermoionic emission theory. Impedance spectroscopy measurements allowed the development of an equiv. circuit of our devices, composed by a const. capacitance parallel to a variable resistance. The elec. ac- response were obsd. under different gas atmospheres (synthetic air, nitrogen, carbon monoxide), demonstrating their potential as reliable gas sensors. According to the obtained results, the existence of oxygen vacancies at the tin-oxide nanowires surfaces is demonstrated.</style></abstract><label><style face="normal" font="default" size="100%">hernandezramirez2006electrical</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>473</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">473</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chauhan, H. P. S.</style></author><author><style face="normal" font="default" size="100%">Singh, U. P.</style></author><author><style face="normal" font="default" size="100%">Shaik, N. M.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Huch, V.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Devi Ahilya Univ, Sch Chem Sci, Indore 452017, India&#xD;Leibniz Inst New Mat, Nanocrystalline Mat &amp; Thin Film Syst Div, D-66123 Saarbrucken, Germany&#xD;Univ Saarland, Inst Inorgan Chem, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Synthetic, spectroscopic, X-ray structural and antimicrobial studies of 1,3-dithia-2-stibacyclopentane derivatives of phosphorus based dithiolato ligands</style></title><secondary-title><style face="normal" font="default" size="100%">Polyhedron</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Polyhedron</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2841-2847</style></pages><volume><style face="normal" font="default" size="100%">25</style></volume><number><style face="normal" font="default" size="100%">15</style></number><keywords><keyword><style face="normal" font="default" size="100%">2006, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2006</style></year><pub-dates><date><style face="normal" font="default" size="100%">Nov 3</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0277-5387</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000241475100005</style></accession-num><abstract><style face="normal" font="default" size="100%">Some mixed 1,3-dithia-2-stibacyclopentane derivatives with phosphorus based dithiolato ligands of the types (SCH2CH2SS) over bar bS (S) (POGO) over bar where G = -CH(Me)-CH(Me)- and -C(Me)(2)-C(Me)(2)- and (SCH2SS) over bar bS(S)P(OR)(2) where R = Pr `&apos;, Bu `&apos; and Ph have been synthesized by the reaction of 2-chloro-1,3-dithia-2-stibacyclopentane and the ammonium/sodium salt of the corresponding phosphorus based ligands in an equimolar ratio in anhydrous benzene solution. These yellow crystalline solid/semi-solid derivatives have been characterized by elemental analysis (C, H, S and Sb), molecular weights, melting point as well as spectral UV, IR and NMR (H-1, C-13 and P-31) studies. Single crystal X-ray diffraction analyses of 1,3-dithia-2-stibacyclopentane 2,3-butylenedithiophosphate revealed a monodentate mode of bonding of the dithiophosphate ligand in the complex. The free ligands and their antimony(111) complexes have also been screened for their antibacterial and antifungal activities. (C) 2006 Elsevier Ltd. All rights reserved.</style></abstract><label><style face="normal" font="default" size="100%">chauhan2006synthetic</style></label><notes><style face="normal" font="default" size="100%">097us&#xD;Times Cited:15&#xD;Cited References Count:34</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.poly.2006.04.027</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.poly.2006.04.027</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>495</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">495</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yu, Fayou</style></author><author><style face="normal" font="default" size="100%">Mücklich, Frank</style></author><author><style face="normal" font="default" size="100%">Li, Ping</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Lehr, Claus-Michael</style></author><author><style face="normal" font="default" size="100%">Bakowsky, Udo</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Department of Materials Science and Department of Biopharmaceutics and Pharmaceutical Technology, Saarland University, D-66123 Saarbrucken, Germany. fayou.yu@hella.de</style></auth-address><titles><title><style face="normal" font="default" size="100%">In vitro cell response to a polymer surface micropatterned by laser interference lithography</style></title><secondary-title><style face="normal" font="default" size="100%">Biomacromolecules</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1160-1167</style></pages><volume><style face="normal" font="default" size="100%">6</style></volume><number><style face="normal" font="default" size="100%">3</style></number><edition><style face="normal" font="default" size="100%">2005/05/10</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2005, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style face="normal" font="default" size="100%">May-Jun</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1525-7797</style></isbn><accession-num><style face="normal" font="default" size="100%">15877329</style></accession-num><abstract><style face="normal" font="default" size="100%">This presentation will introduce laser interference lithography to prepare a periodic line and point micropatterns for study of cell-surface interactions. This process provides a straightforward micropatterning technique based on selective laser ablation of polymers utilizing the periodic energy distribution of two or more beam interference patterns. The micropatterns were characterized by atomic force microscopy, while the surface chemical modification was analyzed using X-ray photoelectron spectroscopy. Human pulmonary fibroblasts cultured on the surface of polycarbonate bearing line micropatterns were elongated, spindlelike, and oriented themselves along the line patterns with all different groove widths. In contrast, cells cultured on point patterns were also bipolar but showed no orientation. Further investigations demonstrated that human pulmonary fibroblast cells cultured on line and point micropatterns showed inflammatory response.</style></abstract><label><style face="normal" font="default" size="100%">yu2005vitro</style></label><notes><style face="normal" font="default" size="100%">Yu, Fayou&#xD;Mucklich, Frank&#xD;Li, Ping&#xD;Shen, Hao&#xD;Mathur, Sanjay&#xD;Lehr, Claus-Michael&#xD;Bakowsky, Udo&#xD;eng&#xD;Comparative Study&#xD;Congress&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;Biomacromolecules. 2005 May-Jun;6(3):1160-7. doi: 10.1021/bm049324w.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/15877329</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/bm049324w</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>496</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">496</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yu, Fayou</style></author><author><style face="normal" font="default" size="100%">Li, Ping</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Lehr, Claus-Michael</style></author><author><style face="normal" font="default" size="100%">Bakowsky, Udo</style></author><author><style face="normal" font="default" size="100%">Mücklich, Frank</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Dept Mat Sci, D-66123 Saarbrucken, Germany&#xD;Univ Saarland, Dept Biopharmaceut &amp; Pharmaceut Technol, D-66123 Saarbrucken, Germany&#xD;Leibniz Inst New Mat, CVD Div, D-66041 Saarbrucken, Germany&#xD;Univ Marburg, Dept Pharmaceut, D-35032 Marburg, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Laser interference lithography as a new and efficient technique for micropatterning of biopolymer surface</style></title><secondary-title><style face="normal" font="default" size="100%">Biomaterials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Biomaterials</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2307-2312</style></pages><volume><style face="normal" font="default" size="100%">26</style></volume><number><style face="normal" font="default" size="100%">15</style></number><keywords><keyword><style face="normal" font="default" size="100%">2005, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0142-9612</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000226698400013</style></accession-num><abstract><style face="normal" font="default" size="100%">Laser interference lithography (LIL) is a straightforward technique to prepare linear micropatterns for regulating cellular adhesion behaviors on polymer substratum. This process is based on selective laser ablation directly duplicating the interference patterns of two or more coherent laser beams onto the polymer surface. Micropatterns prepared by LIL on poly(ethylene terephthalate) and Thermanox were characterized using atomic force microscopy (AFM) and white light interferometer while the chemical surface modification induced by laser was analyzed by X-ray photoelectron spectroscopy (XPS). The AFM photographs show that the micropatterns are well-defined and of great consistency. Polymer properties and laser parameters related to LIL as well as laser ablation mechanisms are discussed in this technical note.</style></abstract><label><style face="normal" font="default" size="100%">yu2005laser</style></label><notes><style face="normal" font="default" size="100%">893db&#xD;Times Cited:62&#xD;Cited References Count:26</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/15585233</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.biomaterials.2004.07.021</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>494</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">494</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sivakov, Vladimir</style></author><author><style face="normal" font="default" size="100%">Petersen, Christian</style></author><author><style face="normal" font="default" size="100%">Daniel, Claus</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Mücklich, Frank</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Inst New Mat, CVD Div, D-66123 Saarbrucken, Germany&#xD;Univ Saarland, Dept Mat Sci Funct Mat, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Laser induced local and periodic phase transformations in iron oxide thin films obtained by chemical vapour deposition</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Surface Science</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Appl Surf Sci</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Applied Surface Science</style></full-title></periodical><pages><style face="normal" font="default" size="100%">513-517</style></pages><volume><style face="normal" font="default" size="100%">247</style></volume><number><style face="normal" font="default" size="100%">1-4</style></number><keywords><keyword><style face="normal" font="default" size="100%">2005, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jul 15</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">01694332</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000230098300080</style></accession-num><abstract><style face="normal" font="default" size="100%">Iron oxide films have been deposited on Si(100) substrates by chem. vapor deposition (CVD) of iron(III) tert-butoxide (Fe(OtBu)32) in the temp. range 350-450°C. The precursor flux and substrate temp. were varied to control the phase compn., av. grain size and film thickness. The nature of substrate and deposition temp. markedly influence the morphol. and iron-oxygen stoichiometry in the CVD deposits. Phase transformations in iron oxide films were achieved through precise local and periodic heating of the films by interfering laser beams. The interaction of iron oxide films with short laser pulses (Nd:YAG, 355 nm) induced partial transformation of hematite ($\alpha$-Fe2O3) to magnetite (Fe3O4) or magnetite to wustite (Fe1-xO), resp. The phase characterization and morphol. of the hematite and magnetite films were investigated before and after laser irradn. by X-ray diffractometry, high resoln. SEM and white light interferometry.</style></abstract><label><style face="normal" font="default" size="100%">sivakov2005laser</style></label><notes><style face="normal" font="default" size="100%">939uq&#xD;Times Cited:30&#xD;Cited References Count:23</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0169433205001546</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.apsusc.2005.01.088</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>492</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">492</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Leleckaite, Asta</style></author><author><style face="normal" font="default" size="100%">Beganskiene, Aldona</style></author><author><style face="normal" font="default" size="100%">Kareiva, Aivaras</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Vilnius Univ, Dept Gen &amp; Inorgan Chem, LT-03011 Vilnius, Lithuania&#xD;Leibniz Inst New Mat, CVD Div, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Low-temperature synthesis and characterization of yttrium–gallium garnet Y3Ga5O12 (YGG)</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Research Bulletin</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Mater Res Bull</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Materials Research Bulletin</style></full-title></periodical><pages><style face="normal" font="default" size="100%">439-446</style></pages><volume><style face="normal" font="default" size="100%">40</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">2005, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style face="normal" font="default" size="100%">Mar 8</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">00255408</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000227582500004</style></accession-num><abstract><style face="normal" font="default" size="100%">To obtain yttrium-gallium garnet (Y3Ga5O12, YGG) a simple chimie douce method was developed. This sol-gel method yielded excellent starting gel precursor for the fabrication of YGG phase, which could be used as host material for optical applications. The pattern of x-ray diffraction anal. of the ceramic sample sintered for 10 h at 1000° showed the formation of monophasic Y3Ga5O12 phase. The phase transformations, compn., and microstructural features in the gels and polycryst. sample were studied by thermoanal. methods (TGA/DTA), powder x-ray diffraction anal. (XRD), IR spectroscopy, and SEM. The quality of the resulting products (homogeneity, crystn. temp., grain size, grain size distribution, etc.) is discussed.</style></abstract><label><style face="normal" font="default" size="100%">mathur2005lowtemperature</style></label><notes><style face="normal" font="default" size="100%">905pv&#xD;Times Cited:21&#xD;Cited References Count:17</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0025540804003630</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.materresbull.2004.12.002</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>490</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">490</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Hemmer, Eva</style></author><author><style face="normal" font="default" size="100%">Ruegamer, Thomas</style></author><author><style face="normal" font="default" size="100%">Holzapfel, Christian</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Influence of Precursor Design on the Growth of Nanomaterials</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Proceedings 2004</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">55-60</style></pages><volume><style face="normal" font="default" size="100%">848</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2005, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2005</style></year></dates><pub-location><style face="normal" font="default" size="100%">Pittsburgh, Pa.</style></pub-location><publisher><style face="normal" font="default" size="100%">Materials Research Society</style></publisher><abstract><style face="normal" font="default" size="100%">Chem. processing of inorg. materials demands an understanding of the precursor chem. at the mol. level. Although chem. compds. imitating at. compn. or bonding features of solid phases are efficient templates for a controlled evolution of nanomatter, the intrinsic advantages of this approach, such as at. level mixing of the constituents and phase-selective synthesis, rely on the chem. involved in the transformation of mols. to materials. Therefore, a better understanding of principles underlying chem. processing is necessary to enable a rational synthesis of materials. The authors have deposited MgAl2O4 thin films by the CVD of two Mg-Al alkoxide precursors, [MgAl2(OPri)8] and [MgAl2(OBut)8], which reveal that precursor attributes such as vapor pressure and ligand elimination mechanisms influence the microstructure and material properties of the spinel films. Under similar growth conditions, [MgAl2(OPri)8] produces rough and poorly cryst. spinel films, whereas cryst. deposits and dense microstructure were obtained in the case of [MgAl2(OBut)8]. The films were characterized by XRD, SEM, TEM, XPS and nano-indentation studies.</style></abstract><label><style face="normal" font="default" size="100%">mathur2005influence</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1557/PROC-848-FF1.10</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>491</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">491</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Inorganic Nanomaterials from Molecular Templates</style></title><secondary-title><style face="normal" font="default" size="100%">ChemInform</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">n/a</style></pages><volume><style face="normal" font="default" size="100%">36</style></volume><number><style face="normal" font="default" size="100%">12</style></number><keywords><keyword><style face="normal" font="default" size="100%">2005, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style face="normal" font="default" size="100%">March</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0931-7597</style></isbn><label><style face="normal" font="default" size="100%">Mathur2005</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/chin.200512255</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>493</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">493</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Pyun, Jae-Chul</style></author><author><style face="normal" font="default" size="100%">Werner, Ulf</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Institute of New Materials, Saarland University Campus, Im Stadtwald, 66123 Saarbruecken, Germany. smathur@inm-gmbh.de</style></auth-address><titles><title><style face="normal" font="default" size="100%">Size-dependent photoconductance in SnO2 nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Small</style></full-title></periodical><pages><style face="normal" font="default" size="100%">713-717</style></pages><volume><style face="normal" font="default" size="100%">1</style></volume><number><style face="normal" font="default" size="100%">7</style></number><edition><style face="normal" font="default" size="100%">2006/12/29</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2005, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jul</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1613-6829</style></isbn><accession-num><style face="normal" font="default" size="100%">17193512</style></accession-num><abstract><style face="normal" font="default" size="100%">Single-cryst. SnO2 nanowires were synthesized in high yields and with a control over diam. and morphol. by using a mol. precursor, Sn(OtBu)4, in a chem. vapor deposition process. The wires formed by a vapor-liq.-solid growth model, which is supported by the presence of an alloy droplet on the tip of the nanowires. A precise control over the wire diams. in the range 50-1000 nm was achieved by tuning the size of gold particles that act as growth templates for the obsd. one-dimensional morphol. Under const. precursor flux, chem. vapor growth of one-dimensional structures was achieved in the range 550-750°C, whereas deposition of granular films was obsd. at &lt;525°C. The catalyst particles were produced by annealing sputtered Au layers of specific thickness, which demands an acute control of the deposition parameters. The photoconductance of the SnO2 nanowires showed a strong modulation that is dependent on the av. radial dimensions. The photoresponse exhibited a blue-shift with decreasing nanowire diam.</style></abstract><label><style face="normal" font="default" size="100%">mathur2005sizedependent</style></label><notes><style face="normal" font="default" size="100%">Mathur, Sanjay&#xD;Barth, Sven&#xD;Shen, Hao&#xD;Pyun, Jae-Chul&#xD;Werner, Ulf&#xD;eng&#xD;Research Support, Non-U.S. Gov&apos;t&#xD;Germany&#xD;Small. 2005 Jul;1(7):713-7. doi: 10.1002/smll.200400168.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/17193512</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1002/smll.200400168</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>489</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">489</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Barth, Sven</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Inst Neue Mat, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Chemical Vapor Growth of NiGa2O4 Films: Advantages and Limitations of a Single Molecular Source</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Vapor Deposition</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Vapor Depos</style></alt-title></titles><pages><style face="normal" font="default" size="100%">11-16</style></pages><volume><style face="normal" font="default" size="100%">11</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2005, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0948-1907</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000226964600002</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanocryst. NiGa2O4 films were deposited on silicon substrates by the CVD of a new heterometal alkoxide, NiGa2(OtBu)8. Thermogravimetric anal. (TGA) and DTA showed a single-step decompn. behavior for the mol. precursor at low temp. (240°C), suitable for a CVD process. NiGa2(OtBu)8 is monomeric in solid state with a tetrahedral Ni2+ center coordinated by two monoanionic Ga(OtBu)4-moieties. Despite an adequate vapor pressure, the gas-phase transport of NiGa2(OtBu)8 is susceptible to the distance and geometry of the effective diffusion path. Investigations on CVD deposits obtained using different transport pathways (reservoir → substrate) show that gas-phase travel through a long (39 cm) and angular reactor tube induces fragmentation of the heterometal compd., which yields minor amts. of Ni, NiO, and Ga2O3 (amorphous), besides the target (NiGa2O4) compn. Shortened reservoir → substrate path length (13 cm) produced stoichiometric NiGa2O4 films, apparently due to reduced collision probabilities and a laminar flow. In both cases, the chem. compn. was detd. using energy-dispersive X-ray (EDX) and XPS, while the structure was evaluated using powder X-ray diffraction (XRD) and SEM. From these, the advantages and limitations of the single mol. source in the growth of NiGa2O4 films could be detd.</style></abstract><label><style face="normal" font="default" size="100%">mathur2005chemical</style></label><notes><style face="normal" font="default" size="100%">896wj&#xD;Times Cited:16&#xD;Cited References Count:39</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/cvde.200306314</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">DOI 10.1002/cvde.200306314</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>488</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">488</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gulbinski, W.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Suszko, T.</style></author><author><style face="normal" font="default" size="100%">Gilewicz, A.</style></author><author><style face="normal" font="default" size="100%">Warcholinski, B.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Inst New Mat, D-66041 Saarbrucken, Germany&#xD;Tech Univ Koszalin, PL-75620 Koszalin, Poland</style></auth-address><titles><title><style face="normal" font="default" size="100%">Evaluation of phase, composition, microstructure and properties in TiC/a-C : H thin films deposited by magnetron sputtering</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Surface Science</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Appl Surf Sci</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Applied Surface Science</style></full-title></periodical><pages><style face="normal" font="default" size="100%">302-310</style></pages><volume><style face="normal" font="default" size="100%">239</style></volume><number><style face="normal" font="default" size="100%">3-4</style></number><keywords><keyword><style face="normal" font="default" size="100%">2005, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan 31</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0169-4332</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000226219200009</style></accession-num><abstract><style face="normal" font="default" size="100%">Titanium carbide/amorphous-carbon (TiC/a-C:H) nanocomposite coatings deposited by pulsed unbalanced reactive magnetron sputtering have been investigated in terms of structure, chemical and phase composition by AFM, TEM, XPS and XRD analyses. Subject to total carbon content, metallic titanium, titanium carbide and amorphous-carbon phases were found in the deposited coatings, which contributed to the observed microstructures and morphologies. The specific resistivity of nanocomposite coatings scales up with increasing amount of matrix-forming carbon. Hardness profiles of the different compositions revealed that nearly stoichiometric TiC films with average crystallite size of 70 nm exhibit the maximum hardness, whereas the lowest friction coefficient (mu containing smaller TiC nanocrystallites ( similar to 10 nm).</style></abstract><label><style face="normal" font="default" size="100%">gulbinski2005evaluation</style></label><notes><style face="normal" font="default" size="100%">886ib&#xD;Times Cited:126&#xD;Cited References Count:22</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.apsusc.2004.05.278</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.apsusc.2004.05.278</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>487</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">487</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Goya, G. F.</style></author><author><style face="normal" font="default" size="100%">Veith, M.</style></author><author><style face="normal" font="default" size="100%">Rapalavicuite, R.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Sao Paulo, Inst Fis, BR-05315970 Sao Paulo, Brazil&#xD;Univ Saarland, Inst Neue Mat, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Thermal hysteresis of spin reorientation at Morin transition in alkoxide derived hematite nanoparticles</style></title><secondary-title><style face="normal" font="default" size="100%">Applied Physics A-Materials Science &amp; Processing</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Appl Phys a-Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1523-1526</style></pages><volume><style face="normal" font="default" size="100%">80</style></volume><number><style face="normal" font="default" size="100%">7</style></number><keywords><keyword><style face="normal" font="default" size="100%">2005, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style face="normal" font="default" size="100%">Apr</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0947-8396</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000227908400024</style></accession-num><abstract><style face="normal" font="default" size="100%">We present results on the structural and magnetic properties of highly crystalline alpha-Fe2O3 nanoparticles of average size similar to 200 nm, synthesized from a novel sol-gel method using metal alkoxide precursor. These particles are multi-domain, showing the weak ferromagnetic antiferromagnetic (WF-AF) transition (i.e., the Morin transition) at T-M = 256 ( 2) K. Mossbauer measurements revealed a jump in hyperfine parameters ( HP&apos;s) at T similar to T-M, which also displays thermal hysteresis upon cooling or heating the sample. The analysis of HP&apos;s as a function of temperature allowed us to discard temperature gradients as well as the coexistence of WF/AF phases as possible origins of this hysteretic behaviour. Instead, the hysteresis can be qualitatively explained by the small size and high-crystallinity of the particles, which hinder the nucleation of the WF or AF phases yielding metastable states beyond T-M.</style></abstract><label><style face="normal" font="default" size="100%">goya2005thermal</style></label><notes><style face="normal" font="default" size="100%">910cz&#xD;Times Cited:27&#xD;Cited References Count:20</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1007/s00339-003-2381-4</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1007/s00339-003-2381-4</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>486</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">486</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Garskaite, E.</style></author><author><style face="normal" font="default" size="100%">Moravec, Z.</style></author><author><style face="normal" font="default" size="100%">Pinkas, J.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Kazlauskas, R.</style></author><author><style face="normal" font="default" size="100%">Kareiva, A.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Vilnius State Univ, Dept Gen &amp; Inorgan Chem, LT-03225 Vilnius, Lithuania&#xD;Masaryk Univ Brno, Dept Inorgan Chem, CZ-61137 Brno, Czech Republic&#xD;Leibniz Inst New Mat, CVD Div, D-66123 Saarbrucken, Germany&#xD;Vilnius State Univ, Dept Analyt &amp; Environm Chem, LT-03225 Vilnius, Lithuania</style></auth-address><titles><title><style face="normal" font="default" size="100%">Synthesis and evolution of crystalline garnet phases in Y3Sc5-xGaxO12</style></title><secondary-title><style face="normal" font="default" size="100%">Philosophical Magazine Letters</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Phil Mag Lett</style></alt-title></titles><pages><style face="normal" font="default" size="100%">557-562</style></pages><volume><style face="normal" font="default" size="100%">85</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">2005, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0950-0839</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000234228300001</style></accession-num><abstract><style face="normal" font="default" size="100%">Mixed-metal oxides with the composition Y3ScxGa5-xO12 (x = 2.0, 2.1, 2.2, 2.25, 2.3, 2.4, 2.5, and 3.0) have been prepared by an aqueous sol - gel method. The effects of scandium substitution on the garnet phase formation were studied by IR spectroscopy and X-ray powder diffraction (XRD). The XRD data indicate that single-phase Y3ScxGa5-xO12 ceramic samples were obtained for x = 2.0, 2.1, 2.2, 2.25, 2.3, and 2.4. The results also show that the formation of Y3ScxGa5-xO12 garnets depends on the molar ratio of scandium and gallium in the investigated composition, and consequently on the mean cationic radius at the Al3+ sites. The variation of lattice parameters for the Y3ScxGa5-xO12 phases with different x is reported.</style></abstract><label><style face="normal" font="default" size="100%">garskaite2005synthesis</style></label><notes><style face="normal" font="default" size="100%">997er&#xD;Times Cited:12&#xD;Cited References Count:29</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.tandfonline.com/doi/abs/10.1080/09500830500398389</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1080/09500830500398389</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>485</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">485</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Chauhan, H. P. S.</style></author><author><style face="normal" font="default" size="100%">Kori, Kavita</style></author><author><style face="normal" font="default" size="100%">Shaik, Nagulu Meera</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Devi Ahilya Univ, Sch Chem Sci, Indore 452017, India&#xD;Univ Saarland, Inst Inorgan Chem, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Dialkyldithiocarbamate derivatives of toluene-3,4-dithiolato arsenic(III) and -bismuth(III): synthetic, spectral and single crystal X-ray structural studies</style></title><secondary-title><style face="normal" font="default" size="100%">Polyhedron</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Polyhedron</style></alt-title></titles><pages><style face="normal" font="default" size="100%">89-95</style></pages><volume><style face="normal" font="default" size="100%">24</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2005, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2005</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan 6</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0277-5387</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000226542200007</style></accession-num><abstract><style face="normal" font="default" size="100%">We report here on dialkyldithiocarbamates complexes of the type [C6H3(CH3)S2MS2CNR2] (M = As and Bi; R = CH3, C2H5 and CH2–CH2), prepared by the reaction of toluene-3,4-dithiolatoarsenic(III) and -bismuth(III) chlorides [C6H3(CH3)S2MCl] (M = As and Bi) with sodium/ammonium salts of dialkyldithiocarbamates [XS2CNR2] (X = Na and NH4; R = CH3, C2H5 and CH2–CH2). The new derivatives were characterized by melting point, elemental analysis (C, H, N, S and As/Bi) and spectroscopic studies (IR, 1H and 13C NMR). Single crystal X-ray diffraction analyses of toluene-3,4-dithiolatoarsenic(III) dimethyldithiocarbamate and toluene-3,4-dithiolatoarsenic(III) pyrrolidine-dithiocarbamate revealed a monodentate chelating mode of the dimethyl as well as the pyrrolidine-dithiocarbamate moieties in these complexes.</style></abstract><label><style face="normal" font="default" size="100%">Chauhan200589</style></label><notes><style face="normal" font="default" size="100%">890wq&#xD;Times Cited:24&#xD;Cited References Count:36</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/j.poly.2004.10.007</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/j.poly.2004.10.007</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>510</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">510</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">König, Peter</style></author><author><style face="normal" font="default" size="100%">Cavelius, Christian</style></author><author><style face="normal" font="default" size="100%">Biegler, Julia</style></author><author><style face="normal" font="default" size="100%">Rammo, Andreas</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Schmid, Günter</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Anorgan Chem, D-66041 Saarbrucken, Germany&#xD;Univ Duisburg Essen, Fachbereich Anorgan Chem 8, D-45117 Essen, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Template-assisted ordering of Pb nanoparticles prepared from molecular-level colloidal processing</style></title><secondary-title><style face="normal" font="default" size="100%">Comptes Rendus Chimie</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Cr Chim</style></alt-title></titles><pages><style face="normal" font="default" size="100%">509-519</style></pages><volume><style face="normal" font="default" size="100%">7</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">16310748</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000222224500008</style></accession-num><abstract><style face="normal" font="default" size="100%">Lead nanoparticles ranging from 10-200 nm were prepd. by reacting Pb\N(SiMe3)2\2 with the reducing agent tert-butoxy alane, H2Al(OCMe3)2, in nonaq. media. By this reaction, Pb nuclei on the mol. scale can be produced imparting a high regularity of shape and size to the resulting nanoparticles. The amino-alkoxo-alane $\backslash$$\backslash$\(Me3Si)2NMe3C-OAl-H\2 is formed as the main mol. byproduct. The mol. structure of this amino-alkoxo-alane was detd. by single crystal x-ray diffraction techniques revealing a centro-sym. mol. with a central Al2O2 ring (Al-O = 1.848(1) \AA) to which tert-Bu (on oxygen) and hexamethyldisilazyl and hydrogen atoms (on Al) are bonded. Colored sols of lead particles were obtained using donor solvents contg. N, S and O atoms. The optical absorption spectra of colloids obtained at different concns. of the starting materials indicate that the color change (yellow - orange - burgundy red) is related to the particle size and/or the aggregation of particles in more concd. solns. The particles are nanoscopic and can be redispersed after a short ultrasonic treatment. This phase-sepn. is related to the nature of Pb-ligand interactions and to the aggregation of particles in the colloidal soln. Particle growth and inter-particle aggregation were obsd. by electron microscopy studies and absorption spectra of lead particles present in different solns. A variation of concn. of lead clusters present in the colloids shows a shift in the absorption spectra related to plasmon-plasmon interaction typically obsd. in the aggregates of metal nanoparticles. Porous anodic alumina membranes were filled with lead nanoparticles either by vacuum-induced infiltration of lead particles or by redn. of the Pb(II) precursor within the pores. The latter approach proved to be more successful in obtaining Pb/Al2O3 composites. The chem. compn. and morphol. of Pb particles in colloidal solns. and those present in and on the porous alumina membrane were studied by XRD, FTIR, SEM and TEM anal. $\backslash$$\backslash$\(Me3Si)2NtBuOAl-H\2 crystallizes in the monoclinic space group P21/c with Z = 2, a = 11.264(2), b = 14.518(3), c = 10.337(2) \AA, $\beta$ = 99.86(3)°, V = 1665.4(6) \AA3.</style></abstract><label><style face="normal" font="default" size="100%">veith2004templateassisted</style></label><notes><style face="normal" font="default" size="100%">831vm&#xD;Times Cited:6&#xD;Cited References Count:40</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S1631074804000815</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">DOI 10.1016/j.crci.2004.03.002</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>502</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">502</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Ruegamer, Thomas</style></author><author><style face="normal" font="default" size="100%">Hemmer, Eva</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibnitz Inst New Mat, CVD Div, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Chemical Vapor Deposition of MgAl2O4 Thin Films Using Different Mg−Al Alkoxides: Role of Precursor Chemistry</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1304-1312</style></pages><volume><style face="normal" font="default" size="100%">16</style></volume><number><style face="normal" font="default" size="100%">7</style></number><keywords><keyword><style face="normal" font="default" size="100%">2004, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year><pub-dates><date><style face="normal" font="default" size="100%">Apr 6</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000220634400022</style></accession-num><abstract><style face="normal" font="default" size="100%">We have studied the chem. and material aspects of mol. precursor-derived materials taking the example of the spinel MgAl2O4. Three Mg-Al alkoxides, MgAl2(OPri)8, MgAl2(OBut)8 and MgAl2(OBut)4H4 were used as single mol. precursors in the gas-phase synthesis of the MgAl2O4 films. A comparative evaluation of the growth rates, morphol., microstructure, av. particle size, consistency of elemental ratio, and carbon contamination in the films shows that material properties of the CVD deposits are a function of the chem. design of the precursor mol. The intrinsic precursor properties (phys. state, vapor pressure, decompn. temp., etc.) can be tuned by a judicious choice of ligand(s) or their combination. For instance, MgAl2(OPri)8 based on isopropoxide ligands displays a potential to oligomerize upon aging due to the presence of an unsatd. metal center (Mg) in the precursor framework. Nevertheless, the liq. state of MgAl2(OPri)8 provides adequate vapor pressure for growing high-quality spinel films. In contrast, the bulkier tert-butoxide groups in MgAl2(OBut)8 make it thermally and structurally more stable, however causing a lower vapor pressure and higher decompn. temp. MgAl2(OBut)4H4 exhibits substantially high vapor pressure but the films obtained contain small amts. of residual orgs., although the combination of hydride and tert-butoxide ligands in MgAl2(OBut)4H4 induces a designed ligand elimination, based on the $\beta$-hydride elimination. Despite the fact that microstructured MgAl2O4 films with sufficient crystallinity and a columnar microstructure could be obtained by tuning the growth parameters of the three Mg-Al compds., this study underscores the importance of precursor chem. in designing an efficient CVD process.</style></abstract><label><style face="normal" font="default" size="100%">mathur2004chemical</style></label><notes><style face="normal" font="default" size="100%">809ka&#xD;Times Cited:52&#xD;Cited References Count:42</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/cm0311675</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/cm0311675</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>507</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">507</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Rapalaviciute, Rasa</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Goya, Gerardo F.</style></author><author><style face="normal" font="default" size="100%">Martins Filho, Waldir L.</style></author><author><style face="normal" font="default" size="100%">Berquo, Thelma S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Inst New Mat, CVD Div, D-66123 Saarbrucken, Germany&#xD;Univ Saarland, Inst Inorgan Chem, D-66123 Saarbrucken, Germany&#xD;Univ Sao Paulo, Inst Phys, BR-05389970 Sao Paulo, Brazil</style></auth-address><titles><title><style face="normal" font="default" size="100%">Molecule Derived Synthesis of Nanocrystalline YFeO3 and Investigations on Its Weak Ferromagnetic Behavior</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1906-1913</style></pages><volume><style face="normal" font="default" size="100%">16</style></volume><number><style face="normal" font="default" size="100%">10</style></number><keywords><keyword><style face="normal" font="default" size="100%">2004, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year><pub-dates><date><style face="normal" font="default" size="100%">May 18</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000221386500014</style></accession-num><abstract><style face="normal" font="default" size="100%">A new Y-Fe alkoxide, YFe(OPri)6(PriOH)2, was used in the sol-gel process to obtain the orthoferrite, YFeO3. The Y/Fe stoichiometry (1:1) and Y-O(R)-Fe chem. links in the single mol. precursor kinetically control the formation of metastable YFeO3 which is otherwise difficult to prep. due to the easy formation of the garnet compn., Y3Fe5O12. TG/DTA anal. showed the crystn. of YFeO3 at 680°, which was confirmed by XRD data. The powders obtained were nanocryst. (TEM) and the only cryst. compd. present between 600 and 1300° was monophasic YFeO3. The absence of garnet and other iron-contg. residual phases obsd. in previous studies was confirmed by temp.-dependent Moessbauer and magnetization measurements. The magnetization data support a weak ferromagnetic behavior and reveal low- and high-field regimes in M-T and M-H curves, corresponding to magnetocryst. and antisym.-exchange anisotropy, resp.</style></abstract><label><style face="normal" font="default" size="100%">mathur2004molecule</style></label><notes><style face="normal" font="default" size="100%">820kb&#xD;Times Cited:141&#xD;Cited References Count:52</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/cm0311729</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/cm0311729</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>506</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">506</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Werner, Ulf</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Low Temperature Gas Phase Synthesis of Germanium Nanowires</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Proceedings 2003</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">377-382</style></pages><volume><style face="normal" font="default" size="100%">789</style></volume><number><style face="normal" font="default" size="100%">Quantum Dots, Nanoparticles and Nanowires</style></number><keywords><keyword><style face="normal" font="default" size="100%">2004, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year></dates><isbn><style face="normal" font="default" size="100%">0272-9172</style></isbn><abstract><style face="normal" font="default" size="100%">Single crystal Ge nanowires were obtained in high yield by gas phase decompn. of germanium di-cyclopentadienylide at 325° on iron substrates. High-resoln. SEM/TEM showed the Ge nanowires to be uniform in terms of diam. 20 nm and length &gt;25 $\mu$m. The wire growth was selective and appeared to be governed by a Ge-Fe alloy epilayer formed by the reaction between Ge clusters and iron substrate during the initial stages of the CVD process. The supersatn. of Ge-Fe solid soln. with respect to Ge induces the spontaneous formation of single crystal germanium nuclei that act as templates for the nanowire growth. X-ray and electron diffraction revealed the nanowires to be single crystals of cubic germanium with a preferred growth direction 11̅2. The proposed base-growth model on Fe substrate is supported by TEM, EDX and XPS studies.</style></abstract><label><style face="normal" font="default" size="100%">mathur2004lowtemperature</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1557/PROC-789-N15.38</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>508</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">508</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanocrystalline Bimetallic Oxides from Molecular Precursors</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Metastable and Nanocrystalline Materials</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">118-126</style></pages><volume><style face="normal" font="default" size="100%">20-21</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2004, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year></dates><isbn><style face="normal" font="default" size="100%">1422-6375</style></isbn><abstract><style face="normal" font="default" size="100%">Synthesis of bimetallic oxides from individual components poses a challenge on the conventional material processing methods largely due to the differences in the intrinsic chem. behavior of the starting materials that leads to undesired stoichiometries and residual monometal phases in the final material. To a large extent, this limitation can be overcome by employing metalorg. precursors that contain all at. constituents, required to form the target solid-state phase, in a single mol. The fact that the extended solid-state structure is derived from mol. building blocks substantiates the inherent advantages of chem. methods due to controlled and defined reaction chem. The authors have examd. the single-step conversion of various heterometal alkoxides via sol-gel process to obtain nanocryst. bimetallic oxides with homogeneous particle sizes and narrow size-distributions.</style></abstract><label><style face="normal" font="default" size="100%">mathur2004nanocrystalline</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.scientific.net/JMNM.20-21.118</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>503</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">503</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Sivakov, Vladimir</style></author><author><style face="normal" font="default" size="100%">Werner, Ulf</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Inst Neue Mat, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Germanium Nanowires and Core−Shell Nanostructures by Chemical Vapor Deposition of Ge(C5H5)2</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2449-2456</style></pages><volume><style face="normal" font="default" size="100%">16</style></volume><number><style face="normal" font="default" size="100%">12</style></number><keywords><keyword><style face="normal" font="default" size="100%">2004, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year><pub-dates><date><style face="normal" font="default" size="100%">June</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000221976400017</style></accession-num><abstract><style face="normal" font="default" size="100%">High-yield synthesis of germanium nanowires (NWs) and core-shell structures is achieved by the chemical vapor deposition (CVD) of dicyclopentadienyl germanium (Ge(C5H5)2). The one-dimensional (1D) nanostructures are formed on an iron substrate following a base-growth model in which an Fe-Ge epilayer functions as a catalytic bed. The wire growth is selective and no catalyst particles are observed at the tip of the NWs, which is contrary to the characteristic feature of a 1D growth based on the vapor-liquid-solid (VLS) mechanism. The diameter and length of the NWs were in the ranges 15-20 nm and 25-40 µm, respectively, as found by high-resolution electron microscopy. Both axial and radial dimensions of the NWs can be controlled by adjusting the precursor feedstock, deposition temperature, and size of alloy nuclei in the Fe-Ge epilayer. High precursor flux produced coaxial heterostructures where single-crystalline Ge cores are covered with an overlayer of nanocrystalline Ge. Single-crystal Ge nanowires exhibit a preferred growth direction 112 h confirmed by X-ray and electron diffraction patterns. When compared to bulk Ge, the micro- Raman spectra of Ge NWs show a low field shift, probably due to the dimensional confinement. Patterned growth of Ge NWs was achieved by shadow-masking the Fe substrate with a carbon film, which prevents the formation of Fe-Ge nuclei, thereby inhibiting the nanowire growth.</style></abstract><label><style face="normal" font="default" size="100%">mathur2004germanium</style></label><notes><style face="normal" font="default" size="100%">828mc&#xD;Times Cited:100&#xD;Cited References Count:40</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/cm031175l</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/cm031175l</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>505</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">505</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Rapalaviciute, Rasa</style></author><author><style face="normal" font="default" size="100%">Kareiva, Aivaras</style></author><author><style face="normal" font="default" size="100%">Donia, Nicole</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Leibniz Inst New Mat, D-66123 Saarbrucken, Germany&#xD;Univ Saarland, Inst Inorgan Chem, D-66123 Saarbrucken, Germany&#xD;Vilnius State Univ, Dept Gen &amp; Inorgan Chem, LT-2006 Vilnius, Lithuania</style></auth-address><titles><title><style face="normal" font="default" size="100%">Kinetically controlled synthesis of metastable YAlO3 through molecular level design</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Mater Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">3259-3265</style></pages><volume><style face="normal" font="default" size="100%">14</style></volume><number><style face="normal" font="default" size="100%">21</style></number><keywords><keyword><style face="normal" font="default" size="100%">2004, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year></dates><isbn><style face="normal" font="default" size="100%">0959-9428</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000224735700025</style></accession-num><abstract><style face="normal" font="default" size="100%">Heterometal alkoxide YAl(OPri)6(PriOH)2 has been used as a mol. template for the controlled and selective synthesis of metastable yttrium aluminate (YAlO3, YAP) in nanocryst. form. The results indicate that the strict control over the Y:Al ratio (1:1) in the precursor suppresses the formation of other Y:Al compns. (Y3Al5O12, YAG and Y4Al2O9, YAM) that are thermodynamically favored over YAP in the conventional synthesis.</style></abstract><label><style face="normal" font="default" size="100%">mathur2004kinetically</style></label><notes><style face="normal" font="default" size="100%">865wu&#xD;Times Cited:39&#xD;Cited References Count:47</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://xlink.rsc.org/?DOI=b406760f</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1039/b406760f</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>504</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">504</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Nalwa, Hari Singh</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Inorganic nanomaterials from molecular templates</style></title><secondary-title><style face="normal" font="default" size="100%">Encyclopedia of Nanoscience and Nanotechnology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">131-191</style></pages><volume><style face="normal" font="default" size="100%">4</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2004, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year></dates><publisher><style face="normal" font="default" size="100%">American Scientific Publishers</style></publisher><abstract><style face="normal" font="default" size="100%">A review. Discussion focuses on the state of the art of mol. concepts developed to obtain inorg. nanoparticles or nanostructured films by chem. routes. The research reviewed here is focused on mol. routes to inorg. nanomaterials and will not refer to the progress of mol. nanotechnol.</style></abstract><label><style face="normal" font="default" size="100%">mathur2004inorganic</style></label><urls></urls><custom2><style face="normal" font="default" size="100%">ISBN: 1-58883-001-2</style></custom2><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>509</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">509</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Altmayer, Jessica</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Nanostructured ZrO2 and Zr-C-N Coatings from Chemical Vapor Deposition of Metal-Organic Precursors</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2042-2048</style></pages><volume><style face="normal" font="default" size="100%">630</style></volume><number><style face="normal" font="default" size="100%">12</style></number><keywords><keyword><style face="normal" font="default" size="100%">2004, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year></dates><isbn><style face="normal" font="default" size="100%">0044-2313</style></isbn><abstract><style face="normal" font="default" size="100%">Nanocryst. zirconium carbonitride (Zr-C-N) and zirconium oxide (ZrO2) films were deposited by chem. vapor deposition (CVD) of zirconium-tetrakis-diethylamide (Zr(NEt2)4) and -tert-butoxide (Zr(OBut)4), resp. The films were deposited on iron substrates and characterized by SEM, x-ray diffraction (XRD) and XPS. The Zr-C-N films show blue, golden brown or bronze colors, with color stability depending upon the precursor compn. (pure metal amide or mixed with Et2NH). The deposition temp. showed no pronounced effect on the granular morphol. of the Zr-C-N films. The XRD data of the films correspond to the formation of carbonitride phase whereas the XPS analyses revealed a strong surface oxidn. and incorporation of oxygen in the film. The films deposited using a mixt. of Zr(NEt2)4 and Et2NH showed higher N content, better adhesion and scratch resistance when compared to films obtained from the CVD of pure Zr(NEt2)4. Subject to the precursor compn. and deposition temp. (550-750 °C), the microhardness values of Zr-C-N films were found to be in the range 2.11-5.65 GPa. For ZrO2 films, morphol. and phase compn. strongly depend on the deposition temp. The CVD deposits obtained at 350 °C show tetragonal ZrO2 to be the only cryst. phase. Upon increasing the deposition temp. to 450 °C, a mixt. of tetragonal and monoclinic modifications was formed with morphol. made up of interwoven elongated grains. At higher temps. (550 and 650 °C), pure monoclinic phase was obtained with facetted grains and developed texture.</style></abstract><label><style face="normal" font="default" size="100%">mathur2004nanostructured</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/zaac.200400271</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>501</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">501</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Komarneni, S.</style></author><author><style face="normal" font="default" size="100%">Parker, J. C.</style></author><author><style face="normal" font="default" size="100%">Watkins, J. J.</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecule Derived Nanomaterials: Chemical Concepts for Composition, Morphology and Particle Size Control</style></title><secondary-title><style face="normal" font="default" size="100%">MRS Proceedings 2003</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">43-48</style></pages><volume><style face="normal" font="default" size="100%">788</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2004, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year></dates><abstract><style face="normal" font="default" size="100%">Conventional material synthesis procedures rely on the intrinsic chemical behaviours (e.g., different hydrolysis rates of the reactants in solution phase reactions or different vapour pressure or thermal stability in the gas phase reactions) of the different components, which make the material properties susceptible to inaccuracies due to an increased number of process variables. As a consequence, phase separation and element segregation are present at the nanometer scale, although the global stoichiometry of the product may correspond to the desired composition. In this context, the use of well-defined molecular precursors is a promising approach to grow extended solid-state structures from atomic constituents.</style></abstract><label><style face="normal" font="default" size="100%">mathur2004molecule</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1557/PROC-788-L1.6</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>500</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">500</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Guceri, Selcuk</style></author><author><style face="normal" font="default" size="100%">Gogotsi, Yuri G.</style></author><author><style face="normal" font="default" size="100%">Kuznetsov, Vladmir</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular chemical concepts for the synthesis of nanocrystalline ceramics</style></title><secondary-title><style face="normal" font="default" size="100%">Nanoengineered Nanofibrous Materials</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">425-442</style></pages><volume><style face="normal" font="default" size="100%">169</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2004, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year></dates><label><style face="normal" font="default" size="100%">mathur2004molecular</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>499</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">499</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Faber, Stefan</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Nonninger, Ralph</style></author><author><style face="normal" font="default" size="100%">Meyer, Frank</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Preparation of doped mixed metal oxides and their use in CO2 sensors</style></title></titles><keywords><keyword><style face="normal" font="default" size="100%">2004, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year></dates><abstract><style face="normal" font="default" size="100%">Mixed metal oxides having the general formula AXO3 with A being Ba, Li, La, or Y, and X being Ce, Ti, Zr, Mn, In, or Sn, are prepd. Preferably, the mixed metal oxide is BaCeO3 having a particle size of &lt; 100 nm, preferably &lt; 50 nm. The mixed metal oxide is doped, preferably with Cu. The mixed oxides are prepd. by the single-source-precursor technique. The doped mixed oxides can be used for the manuf. of gas sensors, esp. for the detn. of CO2, by applying them onto a substrate.</style></abstract><label><style face="normal" font="default" size="100%">faber2004preparation</style></label><urls></urls><custom3><style face="normal" font="default" size="100%">misc</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>498</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">498</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Barth, S.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthese, Charakterisierung und Gasphasenverhalten eines neuen Heterometallalkoxids NiGa2(OBut)8</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1709</style></pages><volume><style face="normal" font="default" size="100%">630</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">2004, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year></dates><label><style face="normal" font="default" size="100%">barth2004synthese</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/zaac.200470036</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>497</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">497</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Altmayer, J.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Heteroleptische Alkoxo-Amido-Verbindungen: Synthese, Charakterisierung und Einsatz in der Materialforschung</style></title><secondary-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Zeitschrift für anorganische und allgemeine Chemie</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1708</style></pages><volume><style face="normal" font="default" size="100%">630</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">2004, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2004</style></year><pub-dates><date><style face="normal" font="default" size="100%">September</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0044-2313</style></isbn><label><style face="normal" font="default" size="100%">altmayer2004heteroleptische</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/zaac.200470035</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>515</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">515</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Muliuoliene, I.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Jasaitis, D.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Sivakov, V.</style></author><author><style face="normal" font="default" size="100%">Rapalaviciute, R.</style></author><author><style face="normal" font="default" size="100%">Beganskiene, A.</style></author><author><style face="normal" font="default" size="100%">Kareiva, A.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany&#xD;Vilnius State Univ, Dept Gen &amp; Inorgan Chem, LT-2006 Vilnius, Lithuania</style></auth-address><titles><title><style face="normal" font="default" size="100%">Evidence of the formation of mixed-metal garnets via sol-gel synthesis</style></title><secondary-title><style face="normal" font="default" size="100%">Optical Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Opt Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">241-250</style></pages><volume><style face="normal" font="default" size="100%">22</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">2003, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2003</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0925-3467</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000182288400009</style></accession-num><abstract><style face="normal" font="default" size="100%">A sol-gel method based on in situ generation of mixed-metal chelates by complexing metal ions with 1,2-ethanediol in aqueous media has been developed to prepare pure and substituted yttrium aluminium garnets: Y3Al5O12 (YAG), Y3Sc2Al1Ga2O12 (YSAGG-3212), Y3Sc1Al3Ga1O12 (YSAGG-3131), Y3Sc2Al3O12 (YSAG), Y3Al3Ga2O12 (YAGG), Y3Sc2.5Ga2.5O12 (YSGG). The XRD patterns of the powders sintered at 1000 degreesC showed the formation of monophasic garnet material except in the case of YSGG sample. The thermal behaviour, phase transformations, composition and micro-structural features in the gels and polycrystalline samples were studied by TG/DTA, XRD, FT-IR, SEM and EDX analysis. These new materials doped with different active elements could be potential candidates as laser materials for solid-state lasers.</style></abstract><label><style face="normal" font="default" size="100%">muliuoliene2003evidence</style></label><notes><style face="normal" font="default" size="100%">668jy&#xD;Times Cited:47&#xD;Cited References Count:36</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/S0925-3467(02)00271-9</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1016/S0925-3467(02)00271-9</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>514</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">514</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Sivakov, Vladimir</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author><author><style face="normal" font="default" size="100%">Hartmann, Uwe</style></author><author><style face="normal" font="default" size="100%">Gao, Hai-Bin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Phase Selective Deposition and Microstructure Control in Iron Oxide Films Obtained by Single-Source CVD</style></title><secondary-title><style face="normal" font="default" size="100%">ChemInform</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">n/a</style></pages><volume><style face="normal" font="default" size="100%">34</style></volume><number><style face="normal" font="default" size="100%">9</style></number><keywords><keyword><style face="normal" font="default" size="100%">2003, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2003</style></year><pub-dates><date><style face="normal" font="default" size="100%">March</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0931-7597</style></isbn><label><style face="normal" font="default" size="100%">Mathur2003</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://doi.wiley.com/10.1002/chin.200309016</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>513</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">513</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kumara Swamy, K. C.</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">School of Chemistry, University of Hyderabad, Hyderabad-500046, India. kckssc@uohyd.ernet.in</style></auth-address><titles><title><style face="normal" font="default" size="100%">Structural Motifs in (t-butoxy)Zirconium Phosphinates, Arsinates, and Phosphates</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">5837-5843</style></pages><volume><style face="normal" font="default" size="100%">42</style></volume><number><style face="normal" font="default" size="100%">19</style></number><edition><style face="normal" font="default" size="100%">2003/09/16</style></edition><keywords><keyword><style face="normal" font="default" size="100%">2003, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2003</style></year><pub-dates><date><style face="normal" font="default" size="100%">Sep 22</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><accession-num><style face="normal" font="default" size="100%">12971751</style></accession-num><abstract><style face="normal" font="default" size="100%">Reaction of zirconium tetrakis(tert-butoxide) (1) with dicylohexylphosphinic acid in toluene leads to the dinuclear compound Zr(mu,mu&apos;-O(2)P(cycl-C(6)H(11))(2))(O-t-Bu)(3)(2) (2) in which the zirconium is pentacoordinated. An analogous reaction using diphenylphosphinic acid in tetrahydrofuran also leads to a dinuclear complex Zr(mu,mu&apos;-O(2)PPh(2))(THF)((O-t-Bu)(3)(2).C(6)H(5)CH(3) (3.C(6)H(5)CH(3)), in which zirconium is hexacoordinated. A novel exchange of tert-butoxy and phenoxy groups occurs when 1 is treated with diphenyl phosphate (PhO)(2)PO(2)H leading to the isolation of the exchange product Zr(mu,mu&apos;-O(2)P(O-t-Bu)(OPh))(mu-OPh)(O-t-Bu)(2)(2) (4). In contrast to the above, trinuclear zirconium compounds Zr(3(mu,mu&apos;-O(2)AsMe(2))(2)(mu2,mu&apos;-O(2)AsMe(2))(O-t-Bu)(7)(mu-O-t-Bu)(2) (5) and Zr(3(mu,mu&apos;-O(2)P(O-t-Bu)(2))(5)(O-t-Bu)(7).(1)/(2)C(6)H(5)CH(3) (6.(1)/(2)C(6)H(5)CH(3)) have been isolated from the reaction of 1 with cacodylic acid and di-tert-butyl phosphate, respectively. The X-ray structures of 2, 3, 5, and 6 have been determined; although the X-ray structural analysis of 4 could not be satisfactorily finished, it reveals the disposition of the substituents. The solution state NMR data suggest that these compounds undergo structural changes in solution. Possible relationships among the various structures are discussed.</style></abstract><label><style face="normal" font="default" size="100%">kumaraswamy2003structural</style></label><notes><style face="normal" font="default" size="100%">Kumara Swamy, K C&#xD;Veith, Michael&#xD;Huch, Volker&#xD;Mathur, Sanjay&#xD;eng&#xD;Inorg Chem. 2003 Sep 22;42(19):5837-43. doi: 10.1021/ic034458o.</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/ic034458o</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/ic034458o</style></electronic-resource-num></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>512</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">512</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kareiva, A.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Jørgensen, J.-E.</style></author><author><style face="normal" font="default" size="100%">Tautkus, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Vilnius State Univ, Dept Gen &amp; Inorgan Chem, LT-2006 Vilnius, Lithuania&#xD;Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany&#xD;Univ Aarhus, Dept Chem, DK-8000 Aarhus C, Denmark&#xD;Vilnius State Univ, Dept Analyt &amp; Environm Chem, LT-2006 Vilnius, Lithuania</style></auth-address><titles><title><style face="normal" font="default" size="100%">Effect of strontium substitution on superconductivity in YBa2Cu4O8</style></title><secondary-title><style face="normal" font="default" size="100%">Philosophical Magazine</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Philos Mag</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1917-1927</style></pages><volume><style face="normal" font="default" size="100%">83</style></volume><number><style face="normal" font="default" size="100%">16</style></number><keywords><keyword><style face="normal" font="default" size="100%">2003, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2003</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun 1</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1478-6435</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000183544900004</style></accession-num><abstract><style face="normal" font="default" size="100%">Superconducting powders with the composition Y(Ba1-xSrx)(2)Cu4O8 (x = 0.00-0.50) have been prepared by an aqueous sol-gel method. The effects of strontium substitution on the properties of compounds were studied by resistivity measurements, X-ray powder diffraction, thermogravimetric analysis, electron microscopy and elemental analysis. The data indicate that single-phase Y(Ba1-xSrx)(2)Cu4O8 superconducting samples were obtained. They also show that doping with strontium has a strong effect on the superconducting properties of the YBa2Cu4O8 phase. The critical temperature is enhanced from 78 K (for a non-substituted sample) to 88 K (for Y(Ba1-xSrx)(2)Cu4O8). Elemental analysis data clearly indicate that small amounts of strontium enter the copper sites in the Y(Ba1-xSrx)(2)Cu4O8 compounds. A point-defect chemistry approach, which explains the enhancement, of T-c by substituting strontium for barium, is presented.</style></abstract><label><style face="normal" font="default" size="100%">kareiva2003effect</style></label><notes><style face="normal" font="default" size="100%">690jl&#xD;Times Cited:7&#xD;Cited References Count:51</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1080/1478643031000105638</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1080/1478643031000105638</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>511</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">511</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Auvray, Nicolas</style></author><author><style face="normal" font="default" size="100%">Braunstein, Pierre</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Hüfner, Stefan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thin films by metal organic deposition of Fe–Mo–S molecular clusters: synthesis and crystal structure of Cp2MoFe2(µ3-S)2(CO)6</style></title><secondary-title><style face="normal" font="default" size="100%">New Journal of Chemistry</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">155-160</style></pages><volume><style face="normal" font="default" size="100%">27</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2003, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2003</style></year></dates><isbn><style face="normal" font="default" size="100%">11440546</style></isbn><abstract><style face="normal" font="default" size="100%">The new cluster Cp2MoFe2(mu(3)-S)(2)(CO)(6) (1) was obtained by the reaction of Fe-2(mu(2)-eta(2)-S-2)(CO)(6) with Cp2MoH2. Its ``double-star&apos;&apos; shape was established by single crystal X-ray diffraction analysis. It possesses a pseudo mirror plane passing through the Mo atom and the middle of the Fe Fe bond. This cluster and the known tetranuclear cluster Cp2Mo2Fe2(mu(3)-S)(2)(CO)8 ( 2) have been used as precursors for the formation of thin films, using the Metal Organic Deposition ( MOD) process on silicon or borosilicate glass substrates. After thermal treatment of the films, the mixed-metal oxide phase Fe2MoxOz (3 (XRD) in the deposit. The elemental composition and morphology of the film materials were obtained from X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM), respectively.</style></abstract><label><style face="normal" font="default" size="100%">auvray2003films</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://xlink.rsc.org/?DOI=b206923g</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>528</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">528</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Venkatesh, C.</style></author><author><style face="normal" font="default" size="100%">Ila, H.</style></author><author><style face="normal" font="default" size="100%">Junjappa, H.</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Domino Carbocationic Rearrangement of Aryl-2-(1- N-methyl/benzyl-3-indolyl)cyclopropyl Ketones: A Serendipitous Route to 1H -Cyclopentaccarbazole Framework</style></title><secondary-title><style face="normal" font="default" size="100%">The Journal of Organic Chemistry</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">9477-9480</style></pages><volume><style face="normal" font="default" size="100%">67</style></volume><number><style face="normal" font="default" size="100%">26</style></number><keywords><keyword><style face="normal" font="default" size="100%">2002, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2002</style></year></dates><isbn><style face="normal" font="default" size="100%">0022-3263</style></isbn><abstract><style face="normal" font="default" size="100%">Aryl-2-(N-methyl/benzyl-3-indolyl)cyclopropyl ketones, e.g., I, are shown to undergo a novel unexpected domino carbocationic rearrangement in the presence of SnCl4/CH3NO2 yielding 2-aroyl-3-aryl-1H-cyclopentaccarbazoles, e.g., II, in good yields. The possible mechanistic pathway for this interesting transformation involves a series of cascade events, (a) electrophilic ring opening of cyclopropyl ketone, (b) intermol. enol capture of the resulting zwitterionic intermediate, (c) electrophilic dimerization of indole moieties to give tetrahydrocarbazole intermediate and its subsequent aromatization by elimination of an indole moiety and dehydrogenation, and (d) intramol. aldol condensation of the side chain to give a cyclopentene ring. The overall transformation involves formation of three carbon-carbon bonds along with a fused benzene and a substituted cyclopentene ring in one-pot operation from simple indole precursors.</style></abstract><label><style face="normal" font="default" size="100%">venkatesh2002domino</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/jo025827l</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>527</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">527</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Molecular ways to nanoscale particles and films</style></title><secondary-title><style face="normal" font="default" size="100%">Journal de Physique IV</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Phys Iv</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1-8</style></pages><volume><style face="normal" font="default" size="100%">12</style></volume><number><style face="normal" font="default" size="100%">Pr4</style></number><keywords><keyword><style face="normal" font="default" size="100%">2002, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2002</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1155-4339</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000176979500002</style></accession-num><abstract><style face="normal" font="default" size="100%">Chemical routes for the synthesis of nanoparticles and films are proving to be highly efficient and versatile in tailoring the elemental combination and intrinsic properties of the target materials. The use of molecular compounds allows a controlled interaction of atoms or molecules, when compared to the solid-state methods, resulting in the formation of compositionally homogeneous deposits or uniform solid particles. Assembling all the elements forming the material in a single molecular compound, the so-called single-source approach augments the formation of nanocrystalline phases at low temperatures with atomically precise structures. To this end, we have shown that predefined reaction (decomposition) chemistry of precursors enforces a molecular level homogeneity in the obtained materials. Following the single-step conversions of appropriate molecular sources, we have obtained films and nanoparticles of oxides (Fe3O4, BaTiO3, ZnAl2O4, CoAl2O4), metal/oxide composites (Ge/GeO2) and ceramic-ceramic composites (LnAlO(3)/Al2O3; Ln = Pr, Nd). For a comparative evaluation, CoAl2O4 nanoparticles were prepared by both single- and multi-component routes; whereas the single-source approach yielded monophasic high purity spinels, phase contamination, due to monometal phases, was observed in the ceramic obtained from multicomponent mixture. An account of the size-controlled synthesis and characterisation of the new ceramics and composites is presented.</style></abstract><label><style face="normal" font="default" size="100%">shen2002molecular</style></label><notes><style face="normal" font="default" size="100%">575zz&#xD;Times Cited:2&#xD;Cited References Count:14</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1051/jp4:20020070</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1051/jp4:20020070</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>526</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">526</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Meng, X. K.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Vehoff, H.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Ngan, A. H. W.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Nanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Peoples R China&#xD;Univ Saarland, Inst Mat Sci &amp; Methods, D-66041 Saarbrucken, Germany&#xD;Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany&#xD;Univ Hong Kong, Dept Mech Engn, Hong Kong, Hong Kong, Peoples R China</style></auth-address><titles><title><style face="normal" font="default" size="100%">Fractography, elastic modulus, and oxidation resistance of Novel metal-intermetallic Ni/Ni3Al multilayer films</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Research</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Mater Res</style></alt-title></titles><pages><style face="normal" font="default" size="100%">790-796</style></pages><volume><style face="normal" font="default" size="100%">17</style></volume><number><style face="normal" font="default" size="100%">4</style></number><keywords><keyword><style face="normal" font="default" size="100%">2002, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2002</style></year><pub-dates><date><style face="normal" font="default" size="100%">April</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0884-2914</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000174805700014</style></accession-num><abstract><style face="normal" font="default" size="100%">Novel metal-intermetallic Ni/Ni3Al multilayer films are synthesized by a magnetron sputtering technique. The fractography, elastic modulus, and the oxidation resistance of the multilayer films are studied by a series of experimental tests. The scanning electron microscopy fractography of the films shows that both Ni and Ni3Al layers fracture with the appearance of ductile metal failure. No metal-intermetallic delamination appears in the multilayered films. Fluted dimpling in each Ni and Ni3Al layer is evident and continuous, layer through layer, illustrating very good adherence among the constituent layers. Such adherence makes the toughness of the Ni layers capable of transferring into the Ni3Al layers. Young&apos;s modulus of the Ni/Ni3Al film is found to be 226 and 253 +/- 10 GPa by nanoindentation and laser acoustic techniques, respectively. The continuity of elastic modulus between the two phases is revealed by nanoindentation test. The modulus continuity indicates an excellent integration of the constituent layers with similar crystal structure and close lattice constants. This integration makes the multilayers unsurpassed in comprehensive mechanical properties. Sheet resistance measurements show a good protective ability of the Ni/Ni3Al multilayers during high temperature oxidation. X-ray photoelectron spectroscopy spectra suggest that crystallized Al2O3/Ni scales formed during the deposition and subsequent annealing processes are apparently responsible for the stability of these films under oxidative conditions. The appearance of the crystallized Al2O3/Ni thin scales on the top of Ni3Al layers provides the Ni/Ni3Al multilayers good thermal oxidation resistance without lowering the fracture toughness.</style></abstract><label><style face="normal" font="default" size="100%">meng2002fractography</style></label><notes><style face="normal" font="default" size="100%">538fz&#xD;Times Cited:5&#xD;Cited References Count:35</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://hdl.handle.net/10722/42408</style></url></related-urls></urls><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>522</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">522</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Sivakov, Vladimir</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author><author><style face="normal" font="default" size="100%">Hartmann, Uwe</style></author><author><style face="normal" font="default" size="100%">Gao, H.-B.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany&#xD;Univ Saarland, Inst Expt Phys, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Phase-Selective Deposition and Microstructure Control in Iron Oxide Films Obtained by Single-Source CVD</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Vapor Deposition</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Vapor Depos</style></alt-title></titles><pages><style face="normal" font="default" size="100%">277-283</style></pages><volume><style face="normal" font="default" size="100%">8</style></volume><number><style face="normal" font="default" size="100%">6</style></number><keywords><keyword><style face="normal" font="default" size="100%">2002, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2002</style></year><pub-dates><date><style face="normal" font="default" size="100%">Dec</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09481907</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000180009600010</style></accession-num><abstract><style face="normal" font="default" size="100%">Iron(III) tert-butoxide was used as a single source for iron and oxygen to obtain nanocryst. Fe2O3 or Fe3O4 films by low-pressure CVD. The decompn. profile of the mol. precursor and crystn. temp. of iron oxide were derived from thermogravimetry/DTA. The substrate temp. markedly influenced the morphol. and Fe/O stoichiometry in the deposited films. The morphol. features and phase identification of the grown films were obtained by SEM and x-ray diffraction, resp. The compn. identity of the phases was detd. by the XPS of the CVD deposits. Annealing the films ex-situ under reducing or oxidizing conditions allows selective interconversion (Fe2O3 ↔ Fe3O4) among the deposited phases with no grain size variation. The interplay between the rate of precursor delivery and substrate temp. controlled the mean particle size in the films. Fe3O4 film with a mean grain size of 10 nm was obtained on silicon at 450°. Formation of larger grains and grain clusters was obsd. at higher temps. High coercivity (4000 Oe) and low satn. magnetization (0.3 emu/g) of the Fe3O4 film confirmed superparamagnetic behavior due to small grain size. Absorption spectra of the films deposited on glass show them to be transparent to visible light. The sheet resistance of nanocryst. Fe3O4 and Fe2O3 films was 2.4 k$Ømega$ and 2 M$Ømega$, resp.</style></abstract><label><style face="normal" font="default" size="100%">mathur2002phaseselective</style></label><notes><style face="normal" font="default" size="100%">628re&#xD;Times Cited:66&#xD;Cited References Count:58</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/1521-3862(20021203)8:6&lt;277::AID-CVDE277&gt;3.0.CO;2-8</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Doi 10.1002/1521-3862(20021203)8:6&lt;277::Aid-Cvde277&gt;3.0.Co;2-8</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>525</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">525</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Hüfner, Stefan</style></author><author><style face="normal" font="default" size="100%">Jilavi, Mohammad H.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany&#xD;Univ Saarland, Inst Expt Phys, D-66041 Saarbrucken, Germany&#xD;Univ Saarland, Inst New Mat, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Structural and Optical Properties of NdAlO3 Nanocrystals Embedded in an Al2O3 Matrix</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">568-582</style></pages><volume><style face="normal" font="default" size="100%">14</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2002, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2002</style></year><pub-dates><date><style face="normal" font="default" size="100%">Feb</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000173998500019</style></accession-num><abstract><style face="normal" font="default" size="100%">Fabrication of an oxide-oxide nanocomposite, contg. a homogeneous dispersion of NdAlO3 nanocrystals in an Al2O3 matrix, is achieved by employing a single mol. compd., NdAl3(OPri)12(PriOH), in the sol-gel process. x-ray diffraction patterns of the composite material show NdAlO3 to be the only cryst. phase, up to 1200°, with an equimolar part of amorphous Al2O3. The crystn. of alumina ($\delta$-, $\gamma$- and $\kappa$-phases) occurs at higher temps. (&gt;1300°). TEM investigations reveal a bimodal distribution of particles where NdAlO3 crystallites are uniformly dispersed in an amorphous Al2O3 matrix. HR-TEM anal. shows a composite structure formed by NdAlO3 nanocrystals (50-60 nm) homogeneously incorporated in a matrix of smaller alumina particles (10-12 nm). The existence of two chem. different Al(III) species (Al2O3 and NdAlO3), in the composite, is proven by 27Al solid-state NMR and XPS studies. The line deconvolution of the Al 2p XPS spectrum reveals two components in a 1:2 ratio with binding energies corresponding to pure NdAlO3 and Al2O3. The diphasic nature of the oxide composite is also established by oxygen content anal. The influence of the alumina matrix on the structural and optical properties of NdAlO3 dispersoids was evaluated by comparing the results of grain growth and photoluminescence of the NdAlO3/Al2O3 nanocomposite (NA3) with those for a nanocryst. sample of monophasic neodymium aluminate (NA), obtained by the hydrolytic decompn. of the mol. precursor NdAl(OPri)6(PriOH)2. The absorption and photoluminescence (PL) spectra of NA and NA3 systems exhibit an enhanced performance in the composite material due to the effect of the NdAlO3-Al2O3 interface and the fact that the Al2O3 matrix functions as a spacer among the NdAlO3 nanocrystals. The PL efficiency was nearly 35 times higher in NA3 than in NA, which is attributed to the control of the min. Nd-Nd sepn. within and on the surface of NdAlO3 nanocrystals coupled with the cooperative energy transfer of the absorbed pumping energy from Al3+ to Nd3+ ions via the F+ centers present in the alumina matrix. The results illustrate that the use of single-source precursors can impose a strict stoichiometry control at the nanometer scale in monophasic ceramics and a homogeneous dispersion of one phase into another in nanocomposites.</style></abstract><label><style face="normal" font="default" size="100%">mathur2002structural</style></label><notes><style face="normal" font="default" size="100%">524ec&#xD;Times Cited:66&#xD;Cited References Count:68</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/cm0111433</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">10.1021/cm0111433</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>524</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">524</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Hüfner, Stefan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Single-step preparation of nanosized ceramics and composites from metal-organic precursors</style></title><secondary-title><style face="normal" font="default" size="100%">Ceramic Engineering and Science Proceedings</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">557--568</style></pages><volume><style face="normal" font="default" size="100%">23</style></volume><number><style face="normal" font="default" size="100%">4</style></number><keywords><keyword><style face="normal" font="default" size="100%">ceramic, composite, metal, myown, nanosized, org, precur, prepn</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2002</style></year></dates><isbn><style face="normal" font="default" size="100%">0196-6219</style></isbn><abstract><style face="normal" font="default" size="100%">The synthesis of nanoparticles with a precise control over compn., size, size distribution and morphol. poses a fundamental scientific challenge. The chem. reactions based on a controlled interaction of atoms or mols. in vapor or liq. phase are currently the popular alternatives to obtain nanostructured films or particles. The success of soft chem. methods is attributed to defined and in some cases designed mol. compds. that transform into nanocryst. ceramics or composites via thermolysis (Chem. Vapor Deposition) and hydrolysis (Sol-Gel) reactions. The synthesis of solid materials from mols. requires much lower temps. than those required for conventional powder syntheses or mech. procedures. Further, the flexibility to combine different ligands or metal combinations allows the precursor designing - the so-called single-source approach - to meet the demands of the target material. To this end, we have examd. the single-step conversion of various mol. sources to obtain oxides, biphasic metal/oxide composites and oxide-oxide composites. The results illustrate that a predefined reaction (decompn.) chem. of the precursors enforces a remarkable control over morphol., compn. and particle size.</style></abstract><label><style face="normal" font="default" size="100%">mathur2002singlestep</style></label><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>523</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">523</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Hufner, Stefan</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Ma, E.</style></author><author><style face="normal" font="default" size="100%">Atzmon, M.</style></author><author><style face="normal" font="default" size="100%">Koch, C. C.</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Single-Step Preparation of Nanocomposites</style></title><secondary-title><style face="normal" font="default" size="100%">Metastable, Mechanically Alloyed and Nanocrystalline Materials</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">341-346</style></pages><volume><style face="normal" font="default" size="100%">386-388</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2002, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2002</style></year></dates><abstract><style face="normal" font="default" size="100%">Single-step fabrication of thin films of Ge/GeO2 and NdAlO3/Al2O3 nanocomposites is achieved by the chemical vapour deposition of single molecular compounds Ge(OBui)(2)(2) and NdAl3(OPri)(12)((PrOH)-O-i), respectively. The Ge/GeO2 film is constituted by the distribution of Ge crystals in a GeO2 matrix. Since the biphasic composite is formed by the disproportionation of a single metastable species, a self-organization of the two phases is observed. The structural elucidation by X-ray photoelectron spectroscopy and nanoindentation studies confirmed a core-shell type constitution of the composite particles. The oxide-oxide composite is formed by a homogeneous dispersion of NdAlO3 nanocrystals in an amorphous Al2O3 matrix. Al-27 solid-state NMR and XPS studies established the diphasicity of the system. HR-TEM analysis revealed a composite structure formed by NdAlO3 nanocrystals evenly distributed in a matrix of alumina particles. NdAlO3/Al2O3 composite exhibits a higher absorption and photo luminescence efficiency than monophasic NdAlO3, which is attributed to the isolation of NdAlO3 crystals by the alumina matrix, and a cooperative energy transfer of the absorbed pump energy from Al3+ to Nd3+ ions.</style></abstract><label><style face="normal" font="default" size="100%">mathur2002singlestep</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.ttp.net/978-0-87849-892-5.html</style></url></related-urls></urls><custom2><style face="normal" font="default" size="100%">ISBN-13: 978-0-87849-892-5</style></custom2><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>517</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">517</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Veith, M.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular level synthesis of binary oxides: nanocrystalline powders of BaTiO3, ZnAl2O4 and GdFeO3</style></title><secondary-title><style face="normal" font="default" size="100%">Semiconductor Conference, 2002. CAS 2002 Proceedings. International</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">147-150</style></pages><volume><style face="normal" font="default" size="100%">1</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2002, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2002</style></year></dates><publisher><style face="normal" font="default" size="100%">IEEE</style></publisher><isbn><style face="normal" font="default" size="100%">0-7803-7440-1</style></isbn><abstract><style face="normal" font="default" size="100%">Chemical routes are becoming increasingly popular for the synthesis of nanomaterials because they allow to initiate the growth of the tar, target nanomaterial at rather low temperatures when compared to the conventional material synthesis procedures that require extensive heat-treatments and repeated (grinding steps for the nucleus formation. The use of well-defined inorganic clusters, containing the phase-forming elements in a discrete molecular, assembly, as Single-Source precursors further substantiates the potential of soft chemistry routes by enabling the construction or molecular templating, of the required ceramic material at the atomic scale.</style></abstract><label><style face="normal" font="default" size="100%">mathur2002molecular</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://ieeexplore.ieee.org/lpdocs/epic03/wrapper.htm?arnumber=1105821</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>521</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">521</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Lecerf, Nicolas</style></author><author><style face="normal" font="default" size="100%">Kjekshus, Arne</style></author><author><style face="normal" font="default" size="100%">Fjellvåg, H.</style></author><author><style face="normal" font="default" size="100%">Goya, G. F.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66123 Saarbrucken, Germany&#xD;Univ Oslo, Dept Chem, N-0315 Oslo, Norway&#xD;Univ Sao Paulo, Inst Phys, BR-05389970 Sao Paulo, Brazil</style></auth-address><titles><title><style face="normal" font="default" size="100%">Nanocrystalline Orthoferrite GdFeO3 from a Novel Heterobimetallic Precursor</style></title><secondary-title><style face="normal" font="default" size="100%">Advanced Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Adv Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1405-1409</style></pages><volume><style face="normal" font="default" size="100%">14</style></volume><number><style face="normal" font="default" size="100%">19</style></number><keywords><keyword><style face="normal" font="default" size="100%">2002, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2002</style></year><pub-dates><date><style face="normal" font="default" size="100%">Oct 2</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09359648</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000178609300016</style></accession-num><abstract><style face="normal" font="default" size="100%">The single-step hydrolytic decompn. of mixed-metal gadolinium iron isopropoxide precursor GdFe(OPri)6(HOPri)2 resulted in a size-controlled synthesis of nanocryst. GdFeO3 particles with high compositional and morphol. homogeneity. The temp. required for the formation of cryst. orthoferrite phase was significantly lower than that for a solid-state synthesis. The expected superparamagnetic behavior was not obsd. in the nanocryst. GdFeO3 samples contg. grains with mean particle size of &gt;40 nm.</style></abstract><label><style face="normal" font="default" size="100%">mathur2002nanocrystalline</style></label><notes><style face="normal" font="default" size="100%">604gt&#xD;Times Cited:79&#xD;Cited References Count:51</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/1521-4095(20021002)14:19&lt;1405::AID-ADMA1405&gt;3.0.CO;2-B</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Doi 10.1002/1521-4095(20021002)14:19&lt;1405::Aid-Adma1405&gt;3.0.Co;2-B</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>518</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">518</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Lecerf, N.</style></author><author><style face="normal" font="default" size="100%">Jilavi, M. H.</style></author><author><style face="normal" font="default" size="100%">Cauniene, V.</style></author><author><style face="normal" font="default" size="100%">Jørgensen, J.-E.</style></author><author><style face="normal" font="default" size="100%">Kareiva, A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sol-Gel Synthesis Route for the Praparation of Y(Ba1-xSrx)2Cu4O8 Superconducting Oxides</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Sol-Gel Science and Technology</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">57-68</style></pages><volume><style face="normal" font="default" size="100%">24</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">2002, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2002</style></year></dates><isbn><style face="normal" font="default" size="100%">09280707</style></isbn><label><style face="normal" font="default" size="100%">mathur2002solgel</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://link.springer.com/10.1023/A:1015113616733</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>519</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">519</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Structural and Physical Properties of La2/3Ca1/3MnO3 Prepared via a Modified Sol-Gel Method</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Sol-Gel Science and Technology</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Sol-Gel Sci Techn</style></alt-title></titles><pages><style face="normal" font="default" size="100%">147-157</style></pages><volume><style face="normal" font="default" size="100%">25</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2002, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2002</style></year><pub-dates><date><style face="normal" font="default" size="100%">Sep</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0928-0707</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000177697600006</style></accession-num><abstract><style face="normal" font="default" size="100%">High purity powder of manganese perovskite, La2/3Ca1/3MnO3, is prepared using a modified sol-gel synthesis based on the dissolution and homogenisation of metal salts in ethanol-acetic acid mixture without using any complexing aid (e.g., polyol or polyhydroxy acid, etc.), which is essentially used in the polymeric precursor routes. This modification minimises the organic contamination in the resulting ceramic that is formed as single perovskite at 650degreesC, after short calcination time periods. The formation of a monophasic material and absence of second phases or phase segregation was confirmed by powder X-ray diffraction, energy dispersive X-ray and electron microscopy of the ceramic calcined at higher temperatures (800-1400degreesC). The calcined samples are nanocrystalline up to 1000degreesC (average particle size, similar to44 nm) however, significant particle growth is observed at higher temperatures with micron-sized grains present in the sample sintered at 1400degreesC. The sample exhibits the characteristic colossal magnetoresistance behaviour. Owing to the high chemical and structural purity of the obtained ceramic, the intrinsic bulk features like metal-insulator transition and ferromagnet-antiferromagnet behaviour of the polycrystalline sample are comparable to those observed in the single crystal La2/3Ca1/3MnO3 specimen, used as a reference. The single-crystal-like properties are also corroborated by the observation of a sharp metallic fermi edge in the UPS measurements. The variable temperature photoemission spectra reveal a temperature dependent redistribution of spectral weight close to the fermi level corroborating the temperature dependent resistance and magnetoresistance of the sample. The material shows a homogeneous grain size and a high sinterability as shown by TEM and SEM studies, respectively. XPS study indicates a charge carrier hopping between Mn3+(3d(4)) and Mn4+(3d(3)) sites.</style></abstract><label><style face="normal" font="default" size="100%">mathur2002structural</style></label><notes><style face="normal" font="default" size="100%">588jd&#xD;Times Cited:33&#xD;Cited References Count:42</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1023/A:1019916413562</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Doi 10.1023/A:1019916413562</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>520</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">520</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Pauleau, Yves</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Thin Film Deposition By Sol-Gel and CVD Processing of Metal-Organic Precursors</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Physics of Thin Film Deposition Processes for Micro- and Nanotechnologies</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">91-118</style></pages><volume><style face="normal" font="default" size="100%">55</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2002, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2002</style></year></dates><abstract><style face="normal" font="default" size="100%">The application of metal-organic chemistry has played a major role in the development of thin film deposition by Chemical Vapour Deposition (CVD) and Sol-Gel techniques [1–2]. The success of chemical synthesis routes is largely attributed to the availability of molecular compounds that can be transformed via solution (Sol-Gel) [3–6] or gas phase (CVD) [7,8] reactions into high-purity coatings of desired ceramics or composites. In contrast to the solid-state reactions, the reactions in vapor or liquid phase allow a controlled interaction of atoms or molecules to form uniform films or particles. Further, the flexibility to combine different ligand or metal combinations allows the precursor designing to meet the demands of the target material. Assembling all the phase-forming elements in a single molecular source augments the advantages of chemical processing and simultaneously reduces the process parameters. In addition, the molecule-to-material transformation requires much lower temperatures than those required for the conventional (mixing, grinding and calcining) methods [9]. The clear practical implications of nanostructured materials [10,11] with a precise control over composition, size, size distribution and morphology has led to an upsurge of research activity in the synthesis and chemical processing of molecular precursors [12–17]. Among the various inorganic compounds—halides, nitrates, acetates, carboxylates, ß-diketonates, alkyls, alkoxides—used in the synthesis of metal oxides, metal alkoxides (M(0R)n) are especially attractive as precursors [18–24]. Some of their salient features include high purity, easy transformation into oxides with formation of volatile byproducts, ability to form homogeneous solution in different solvents and conditions and more importantly the facile formation of heterometal species useful for the synthesis of multicomponent materials [25]. The present article is intended to provide a brief account of the recent developments in the field of heterometal alkoxide chemistry and their applications in obtaining nanocrystalline thin films.</style></abstract><label><style face="normal" font="default" size="100%">mathur2002deposition</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1007/978-94-010-0353-7_5</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>516</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">516</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Jasaitis, D.</style></author><author><style face="normal" font="default" size="100%">Muliuoliene, I.</style></author><author><style face="normal" font="default" size="100%">Sivakov, V.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Rapalaviciute, R.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Kareiva, A</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">From Precursors to Ceramic Materials: Sol-gel Chemistry Approach in the Preparation of Precursors for the Advanced Optical Materials</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Science</style></secondary-title></titles><keywords><keyword><style face="normal" font="default" size="100%">2002, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2002</style></year></dates><label><style face="normal" font="default" size="100%">jasaitis2002precursors</style></label><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>533</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">533</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Lecerf, Nicolas</style></author><author><style face="normal" font="default" size="100%">Hüfner, Stefan</style></author><author><style face="normal" font="default" size="100%">Jilavi, Mohammad H.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Single-Step Preparation of Oxide−Oxide Nanocomposites: Chemical Vapor Synthesis of LnAlO3/Al2O3 (Ln = Pr, Nd) Thin Films</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of Materials</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">4041-4052</style></pages><volume><style face="normal" font="default" size="100%">13</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">2001, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2001</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><abstract><style face="normal" font="default" size="100%">Thin films contg. nanometer-sized PrAlO3 or NdAlO3 crystals evenly dispersed in an amorphous Al2O3 matrix were grown by chem. vapor deposition (CVD) of heterometal alkoxides, Ln\Al(OPri)4\3(PriOH) (Ln = Pr (1), Nd (2)). The lanthanoid to aluminum ratio in the precursors, established by single-crystal X-ray diffraction and chem. analyses of the cryst. products, enables the formation of a stoichiometric 1:1 composite of the general formula LnAlO3/Al2O3 in a single-stage synthesis. The gas-phase thermolysis of 1 and 2 in a cold-wall reactor gave amorphous films of formal compn. LnAl3O6, suggesting intact vaporization and decompn. of the heterometal frameworks on the substrates. Online mass spectral anal. of the gaseous products formed during the CVD process revealed iso-Pr alc., acetone, propene, and dihydrogen as the main byproducts. The electron spectroscopy for chem. anal. and energy-dispersive X-ray anal. confirmed the film compns. to be LnAl3O6, which was shown to be homogeneous through the film bulk by glow discharge mass spectrometry. The surface imaging (SEM/at. force microscopy) exhibits films with a regular globulated morphol. The annealing of as-deposited films at 800 °C shows PrAlO3 and NdAlO3 to be the only cryst. phases (X-ray diffraction) with av. grain sizes of 14 and 12 nm, resp. The residual Al component (Al2O3) remains amorphous until 1200 °C; however, the evolution of transition aluminas (mixt. of $\kappa$-, $\delta$-, and $\gamma$-phases) was obsd. at higher temps. (&gt;1200 °C). The ceramic-glass (cryst.-amorphous) nature of the system was established by high-resoln. transmission electron microscopy studies, while the compns. of the phases were detd. by spatially resolved energy dispersive spectra. The IR and solid-state 27Al MAS NMR data of the film material showed spectral patterns formed by an overlapping of the signals corresponding to LnAlO3 and Al2O3 phases. The ellipsometric studies revealed the refractive indexes to be 1.76 and 1.67 for the Pr-O-Al and Nd-O-Al systems, resp. The film growth rates were found to be in the range 1.7-1.8 $\mu$m/h at 500 °C.</style></abstract><label><style face="normal" font="default" size="100%">veith2001singlestep</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/cm011092</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>530</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">530</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Veith, M.</style></author><author><style face="normal" font="default" size="100%">Sivakov, V.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Gao, H. B.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany&#xD;Univ Saarland, Inst Expt Phys, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Composition, morphology and particle size control in nanocrystalline iron oxide films grown by single-source CVD</style></title><secondary-title><style face="normal" font="default" size="100%">Journal de Physique IV</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Phys Iv</style></alt-title></titles><pages><style face="normal" font="default" size="100%">487-494</style></pages><volume><style face="normal" font="default" size="100%">11</style></volume><number><style face="normal" font="default" size="100%">Pr3</style></number><keywords><keyword><style face="normal" font="default" size="100%">2001, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2001</style></year><pub-dates><date><style face="normal" font="default" size="100%">August</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1155-4339</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000171140300063</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanocrystalline iron oxide films have been deposited onto various substrates in a cold-wall CVD reactor using iron (III) tert-butoxide as a single-source for iron and oxygen. Influence of the CVD parameters on the growth rate, chemical composition, morphology and crystalline phases has been investigated. The Fe:O stoichiometry in the films is sensitive to the deposition conditions, For instance, the interplay between precursor flux/deposition temperature allows a fine control over deposition of different iron oxide phases (hematite, maghemite and magnetite) and their interconversion. The different iron oxides could be detected by their typical morphological features and confirmed by XRD and XPS data of the deposits. At 350 degreesC and below, ultrafine amorphous iron oxide grains with size lower than 10 mn are produced which, can be transformed to crystalline hematite or magnetite phases by ex-situ annealing. Spinel-type Fe3O4 was formed as a singular phase on copper at 450 degreesC, which could be converted to Fe2O3 upon annealing. On silicon, a mixture of magnetite and hematite was formed at 450 degreesC while a solid solution of the two phases resulted at 500 degreesC. Transmission spectra of films deposited on glass show them to be transparent to visible light. The results are discussed in the light of XRD, SEM-EDX, XPS, AFM and elemental analysis.</style></abstract><label><style face="normal" font="default" size="100%">mathur2001composition</style></label><notes><style face="normal" font="default" size="100%">475aw&#xD;Times Cited:16&#xD;Cited References Count:21</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1051/jp4:2001362</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">DOI 10.1051/jp4:2001362</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>531</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">531</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Veith, M.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Lecerf, N.</style></author><author><style face="normal" font="default" size="100%">Hüfner, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany&#xD;Univ Saarland, Inst Expt Phys, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Effect of Al2O3 matrix on the optical properties of NdAlO3 in NdAlO3/Al2O3 ceramic-ceramic composite</style></title><secondary-title><style face="normal" font="default" size="100%">Scripta Materialia</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Scripta Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2105-2109</style></pages><volume><style face="normal" font="default" size="100%">44</style></volume><number><style face="normal" font="default" size="100%">8-9</style></number><keywords><keyword><style face="normal" font="default" size="100%">2001, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2001</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">13596462</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000169389400189</style></accession-num><label><style face="normal" font="default" size="100%">mathur2001effect</style></label><notes><style face="normal" font="default" size="100%">444fl&#xD;Times Cited:15&#xD;Cited References Count:11</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S1359646201008831</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Doi 10.1016/S1359-6462(01)00883-1</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>532</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">532</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Haas, Michel</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Lecerf, Nicolas</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author><author><style face="normal" font="default" size="100%">Hüfner, Stefan</style></author><author><style face="normal" font="default" size="100%">Haberkorn, Robert</style></author><author><style face="normal" font="default" size="100%">Beck, Horst P.</style></author><author><style face="normal" font="default" size="100%">Jilavi, Mohammad</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem Geb 23 1, D-66123 Saarbrucken, Germany&#xD;Univ Saarland, Inst Expt Phys, D-66123 Saarbrucken, Germany&#xD;Univ Saarland, Inst Inorgan &amp; Analyt Radiochem, D-66123 Saarbrucken, Germany&#xD;Univ Saarland, Inst New Mat, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Single-Source Sol-Gel Synthesis of Nanocrystalline ZnAl2O4: Structural and Optical Properties</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the American Ceramic Society</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Am Ceram Soc</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1921-1928</style></pages><volume><style face="normal" font="default" size="100%">84</style></volume><number><style face="normal" font="default" size="100%">9</style></number><keywords><keyword><style face="normal" font="default" size="100%">2001, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2001</style></year><pub-dates><date><style face="normal" font="default" size="100%">Sep</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1551-2916</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000170962600002</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanometer-sized zinc aluminate (ZnAl2O4) particles were synthesized from heterometal alkoxides, [ZnAl2(OR)8], possessing an ideal cation stoichiometry for the ZnAl2O4 spinel. ZnAl2O4 is formed at 400°C, which is the lowest temperature reported for the formation of monophasic ZnAl2O4. 27Al magic-angle spinning nuclear magnetic resonance spectroscopy revealed that ZnAl2O4 possesses an inverse structure at &lt;900°C, while the normal spinel phase is observed at higher temperatures. The homogeneity of the in-depth composition and Zn:Al stoichiometry (1:2) was confirmed by electron spectroscopy for chemical analysis. Evaluation of the valence-band spectra of ZnAl2O4 and ZnS suggested that the hybridization of O 2p and Zn 3d orbitals is responsible for lowering the bandgap in the latter. The average crystallite size showed an exponential relationship to the calcination temperature (X-ray diffractometry and transmission electron microscopy data). The optical spectra of different spinel powders (average particle sizes, 20–250 nm) showed that the absorption edge exhibits a blue shift as particle size decreases.</style></abstract><label><style face="normal" font="default" size="100%">JACE:JACE1921</style></label><notes><style face="normal" font="default" size="100%">472bf&#xD;Times Cited:176&#xD;Cited References Count:27</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1111/j.1151-2916.2001.tb00938.x</style></url></related-urls></urls><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>529</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">529</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lecerf, N.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Shen, H.</style></author><author><style face="normal" font="default" size="100%">Veith, M.</style></author><author><style face="normal" font="default" size="100%">Hüfner, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany&#xD;Univ Saarland, Inst Expt Phys, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Chemical vapour and sol-gel syntheses of nano-composites and -ceramics using metal-organic precursors</style></title><secondary-title><style face="normal" font="default" size="100%">Scripta Materialia</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Scripta Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2157-2160</style></pages><volume><style face="normal" font="default" size="100%">44</style></volume><number><style face="normal" font="default" size="100%">8-9</style></number><keywords><keyword><style face="normal" font="default" size="100%">2001, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2001</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">13596462</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000169389400200</style></accession-num><abstract><style face="normal" font="default" size="100%">Nano-sized alloy-metal oxide composite and ceramics were prepared using single source alkoxide precursors. The molecule, Ni2Sn2(OBut)(8). has been used in a low-pressure CVD process to grow composite thin films where the binary alloy Ni3Sn4 is dispersed in a SnO2 matrix. The characterization of the layers by several analytical methods confirmed the biphasic nature of the obtained material and a homogeneous interdispersion of Ni3Sn4 and SnO2 crystallites. The mixed-metal alkoxides BaZr(OH)(OPri)(5)((PrOH)-O-i)(3)(2). BaTi(OH)(OPri),((PrOH)-O-i)(3)(2) and Ba2TiZr(OPri)(12) were used as molecular precursors for a size-controlled synthesis (Sol-Gel) of the ceramics BaTiO3. BaZrO3 and BaZr0.5Ti0.5O3. respectively. The complete crystallization of the pervoskite structure is clearly observed at relatively lower temperature of 600 degreesC for the binary oxides and at 400 degreesC for the ternary oxide system. Analytical electron microscopy investigations on the samples revealed a homogeneous stoichiometry on the nanometer level and narrow crystallite size distributions.</style></abstract><label><style face="normal" font="default" size="100%">lecerf2001chemical</style></label><notes><style face="normal" font="default" size="100%">444fl&#xD;Times Cited:25&#xD;Cited References Count:14</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S1359646201009137</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Doi 10.1016/S1359-6462(01)00913-7</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>536</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">536</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Lecerf, Nicolas</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author><author><style face="normal" font="default" size="100%">Decker, Timo</style></author><author><style face="normal" font="default" size="100%">Beck, Horst P.</style></author><author><style face="normal" font="default" size="100%">Eiser, Wolfgang</style></author><author><style face="normal" font="default" size="100%">Haberkorn, Robert</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66123 Saarbrucken, Germany&#xD;Univ Saarland, Inst Analyt &amp; Radiochem, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Sol-Gel Synthesis of Nano-Scaled BaTiO3, BaZrO3 and BaTi0.5Zr0.5O3 Oxides via Single-Source Alkoxide Precursors and Semi-Alkoxide Routes</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Sol-Gel Science and Technology</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Sol-Gel Sci Techn</style></alt-title></titles><pages><style face="normal" font="default" size="100%">145-158</style></pages><volume><style face="normal" font="default" size="100%">17</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2000, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2000</style></year><pub-dates><date><style face="normal" font="default" size="100%">Feb</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0928-0707</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000085543400006</style></accession-num><abstract><style face="normal" font="default" size="100%">Sol-gel synthesis of nano-sized BaTiO3, BaZrO3 and BaTi0.5Zr0.5O3 ceramics using alkoxide and semi-alkoxide routes has been investigated and the perovskites obtained have been compared with respect to crystn. temp., crystallite size and compositional purity. Heterometal alkoxides contg. two (for BaTiO3 and BaZrO3) and three (for BaTi0.5Zr0.5O3) different metals were used as single-source precursors in the alkoxide route while semi-alkoxide synthesis was performed by reacting barium hydroxide or acetate with Ti and/or Zr alkoxides. Semi-alkoxide synthesis also produces stoichiometric and phase-pure oxides, however, at temps. higher than 1000°C. At temps. below 1000°C, BaCO3 and small amts. of other undesired phases (e.g., BaTi2O4) were present in the oxides derived from semi-alkoxide synthesis. Thermal behavior, studied by TGA/DTA measurements, shows that thermal decompn. occurs in three major steps and depends on the educt compn. and the synthesis route. Among alkoxide derived powders, cryst. BaTi0.5Zr0.5O3 phase is formed at 400°C while complete crystn. of BaMO3 ceramics occurs around 600°C. The cubic to tetragonal phase transition for BaTiO3 is clearly obsd. at relatively low-temp. of 800°C. The stoichiometry and phase homogeneity of the obtained powders were demonstrated by energy dispersive X-ray anal. and powder diffractometry. The averaged crystallite size of the obtained nano-ceramics was evaluated using the FormFit program. SEM and TEM observations revealed a high microstructural uniformity.</style></abstract><label><style face="normal" font="default" size="100%">veith2000solgel</style></label><notes><style face="normal" font="default" size="100%">288cc&#xD;Times Cited:171&#xD;Cited References Count:45</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1023/A:1008795419020</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Doi 10.1023/A:1008795419020</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>537</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">537</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Lecerf, Nicolas</style></author><author><style face="normal" font="default" size="100%">Bartz, Karsten</style></author><author><style face="normal" font="default" size="100%">Heintz, Manuela</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem Geb 231, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Synthesis of a NdAlO3/Al2O3 Ceramic−Ceramic Composite by Single-Source Precursor CVD</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">271-274</style></pages><volume><style face="normal" font="default" size="100%">12</style></volume><number><style face="normal" font="default" size="100%">2</style></number><keywords><keyword><style face="normal" font="default" size="100%">2000, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2000</style></year><pub-dates><date><style face="normal" font="default" size="100%">Feb</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000085502900005</style></accession-num><abstract><style face="normal" font="default" size="100%">The thin films of nanoscaled NdAlO3/Al2O3 composite were deposited by gas-phase pyrolysis of Nd\Al(OPri)4\3(PriOH) using low-pressure CVD. The growth rates were 5-7 $\mu$m/h at 500°, and films of thickness 500nm-10$\mu$m were deposited on different substrates at this temp. The films obtained at lower temps. showed a high org. contamination (up to 4 at.\%), whereas at higher deposition temps. (&gt;550°) the adhesion of the films on the target substrate was poor and a significant amt. of the product decompd. in the gas phase before reaching the target. The films obtained were purple colored with glassy appearance. The carbon content in heat treated (800°) films was &lt;0.3\%. The XRD, AFM, TEM, EDX, electron diffraction and mass-spectroscopy proved the formal compn. of the deposit being NdAl3O6 with NdAlO3 as the only cryst. phase and Al2O3 to be the second with a high amorphous content. The characteristic grain sizes are 20-40 (Al2O3) and 200-300 (NdAlO3) nm. The use of hetero-metal alkoxides, generally used for producing high-homogeneity in the single-phase ceramics, to obtain a ceramic-ceramic composite of two distinct nanocryst. phases was demonstrated.</style></abstract><label><style face="normal" font="default" size="100%">veith2000synthesis</style></label><notes><style face="normal" font="default" size="100%">287jn&#xD;Times Cited:39&#xD;Cited References Count:20</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/cm991149g</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">DOI 10.1021/cm991149g</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>535</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">535</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Lecerf, Nicolas</style></author><author><style face="normal" font="default" size="100%">Donia, Nicole</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Hüfner, Stefan</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular Routes to Advanced Materials: Synthesis of NdAlO3 Ceramic and NdAlO3/Al2O3 Composite From Single Source Precursors</style></title><secondary-title><style face="normal" font="default" size="100%">Ceramics - Processing, Reliability, Tribology and Wear</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">282-288</style></pages><volume><style face="normal" font="default" size="100%">12</style></volume><keywords><keyword><style face="normal" font="default" size="100%">2000, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2000</style></year></dates><publisher><style face="normal" font="default" size="100%">Wiley-VCH Verlag GmbH</style></publisher><abstract><style face="normal" font="default" size="100%">Heterometal Nd-Al alkoxides were used as single-source precursors for the sol-gel prepn. of nanoscale NdAlO3 and NdAlO3/Al2O3 ceramics. The principle conclusion to be drawn is that the well-defined heterometal alkoxides form gels by a controlled polymn. without breaking down into sep constituents. Apparently, the retention of Nd-(O)-Al bridges in the gels is responsible for the easy and low-temp. conversion of green precursors to cryst. ceramics.</style></abstract><label><style face="normal" font="default" size="100%">mathur2000molecular</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/3527607293.ch48</style></url></related-urls></urls><custom3><style face="normal" font="default" size="100%">inproceedings</style></custom3></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>534</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">534</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kareiva, A.</style></author><author><style face="normal" font="default" size="100%">Barkauskas, J.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Vilnius State Univ, Dept Gen &amp; Inorgan Chem, LT-2006 Vilnius, Lithuania&#xD;Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Oxygen content and superconducting properties of Hg-based superconductors synthesized by sol-gel method</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Physics and Chemistry of Solids</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Phys Chem Solids</style></alt-title></titles><pages><style face="normal" font="default" size="100%">789-797</style></pages><volume><style face="normal" font="default" size="100%">61</style></volume><number><style face="normal" font="default" size="100%">5</style></number><keywords><keyword><style face="normal" font="default" size="100%">2000, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">2000</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0022-3697</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000085859000019</style></accession-num><abstract><style face="normal" font="default" size="100%">The superconducting properties and structural changes of HgBa2CaCu2O6+delta and HgBa2Ca2Cu3O8+delta systems synthesized by the sol-gel method were studied as a function of post-annealing in oxygen flow using thermogravimetric, X-ray diffraction and magnetic susceptibility studies. The point defect chemistry approach which explains the results obtained is presented.</style></abstract><label><style face="normal" font="default" size="100%">kareiva2000oxygen</style></label><notes><style face="normal" font="default" size="100%">293nl&#xD;Times Cited:12&#xD;Cited References Count:66</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/S0022-3697(99)00305-4</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Doi 10.1016/S0022-3697(99)00305-4</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>543</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">543</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Kareiva, Aivaras</style></author><author><style face="normal" font="default" size="100%">Jilavi, Mohammad</style></author><author><style face="normal" font="default" size="100%">Zimmer, Michael</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany&#xD;Vilnius State Univ, Dept Gen &amp; Inorgan Chem, LT-2006 Vilnius, Lithuania&#xD;Inst New Mat Gmbh, D-66132 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Low temperature synthesis of nanocrystalline Y3Al5O12 (YAG) and Ce-doped Y3Al5O12 via different sol–gel methods</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Mater Chem</style></alt-title></titles><pages><style face="normal" font="default" size="100%">3069-3079</style></pages><volume><style face="normal" font="default" size="100%">9</style></volume><number><style face="normal" font="default" size="100%">12</style></number><keywords><keyword><style face="normal" font="default" size="100%">1999, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1999</style></year></dates><isbn><style face="normal" font="default" size="100%">09599428</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000083921700020</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanocrystalline yttrium aluminium garnet (YAG, Y3Al5O12) and Ce-doped YAG ceramics were synthesized by two &apos;soft chemistry&apos; sol-gel processes using (i) mixtures of inorganic salts or oxides and (ii) mixtures of alkoxides of the respective elements. In the first approach the metal ions, generated by dissolving metal oxides or nitrates in acetic acid and/or water, were complexed by ethylene glycol to obtain the precursors for pure and doped YAG samples. In the alkoxide route monolithic gels were obtained by hydrolysis and condensation of a compositional mixture of Al, Y and Ce alkoxides in a (PrOH)-O-i solution. The molecular level mixing and the tendency of partially hydrolysed alkoxide species to form extended networks of cross-linked metal centers facilitates the structure evolution thereby lowering the crystallization temperature, in the latter case. The X-ray diffraction (XRD) patterns of the ceramic sintered at 700 degrees C were identical with the stoichiometric YAG composition which is the lowest temperature reported for the synthesis of crystalline and single phase Y3Al5O12 while well developed YAG phases in the non-alkoxide synthesis were obtained only at 1000 degrees C. Cerium doped YAG powders (CeO2 + Y3Al5O12) were synthesized using [NH4](2)[Ce(NO3)(6)] (8 mol%) and [Ce-3(OBut)(9)((BuOH)-O-t)(2)] (5 mol%), as dopants. A homogeneous distribution of cerium in the YAG lattice was achieved in both cases. The thermal behaviour, phase transformations, composition and microstructural features in the gels and polycrystalline samples were studied by TG/DTA, XRD, FT-IR, solid-state Al-27 MAS NMR spectroscopy, SEM, TEM, energy dispersive X-ray analysis and high resolution electron microscopy studies. The quality of the resulting products (homogeneity, crystallization temperature, grain size, grain size distribution, etc.) and economical aspects (synthetic skill, cost of precursors, etc.) of the two approaches are discussed.</style></abstract><label><style face="normal" font="default" size="100%">veith1999temperature</style></label><notes><style face="normal" font="default" size="100%">259yn&#xD;Times Cited:266&#xD;Cited References Count:72</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/A903664D</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">DOI 10.1039/a903664d</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>544</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">544</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Charu</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Unusual Sandwiching of the Cyclopentadienyl Anion in [K4(C5H5)2M2(OBut)6(CH3OCH2CH2OCH3)2]n (M = Ge, Sn)</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">5461-5463</style></pages><volume><style face="normal" font="default" size="100%">38</style></volume><number><style face="normal" font="default" size="100%">23</style></number><keywords><keyword><style face="normal" font="default" size="100%">1999, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1999</style></year></dates><abstract><style face="normal" font="default" size="100%">[Sn(OBut)2]2 and [Ge(OBut)2]2 react with CpK to give heterometal coordination polymer contg. sandwiching of the cyclopentadienyl anion, e.g., [K4(C5H5)2M2(OBut)6(CH3OCH2CH2OCH3)2]n [M = Sn (I), Ge, resp.]. I was characterized by x-ray crystallog.</style></abstract><label><style face="normal" font="default" size="100%">doi:10.1021/ic9814120</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/ic9814120</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>542</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">542</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Lecerf, Nicolas</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Shen, Hao</style></author><author><style face="normal" font="default" size="100%">Hüfner, Stefan</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany&#xD;Univ Saarland, Inst Phys Expt, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Incorporation of a Binary Alloy in an Oxide Matrix via Single Source Precursor CVD Process</style></title><secondary-title><style face="normal" font="default" size="100%">Chemistry of Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">3103-3112</style></pages><volume><style face="normal" font="default" size="100%">11</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">1999, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1999</style></year><pub-dates><date><style face="normal" font="default" size="100%">November</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0897-4756</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000083776000018</style></accession-num><abstract><style face="normal" font="default" size="100%">Using a Ni-Sn heterometal alkoxide, Ni2Sn2(OtBu)8, in a chem. vapor deposition (CVD) process, thin films of biphasic composite, Ni3Sn4/SnO2, have been obtained. Due to the presence of two metal atoms in a single mol., the decompn. occurs at a mol. level resulting in homogeneous incorporation of intermetallic Ni3Sn4 in an SnO2 matrix. The CVD expts. performed at different temps. (450-550 °C) show that the obtained composite results from two chem. processes: (i) disproportionation of Sn(II) species and (ii) the redox reactions occurring between Sn(II) and Ni(II) species. Fragmentation of the precursor and disproportionation of the tin(II) component dominate up to 500 °C, resulting in the formation of NiO, Sn(0), and SnO2. Redox reactions are favored at higher temp. (550 °C) which lead to the formation of the Ni3Sn4 alloy. This alloy-metal oxide composite has been deposited on different substrates (steel, copper, silicon wafer), and no heterogeneity was obsd. on a micrometer level (energy-dispersive X-ray anal.). Powder X-ray diffraction patterns of the deposits obtained at 550 °C show Ni3Sn4 and SnO2 as the only cryst. phases. The scanning electron micrograph images reveal a microstructured surface with a fibrous morphol. High-resoln. transmission electron microscope investigations show a bimodal mixt. where the Ni3Sn4 crystallites (ca. 60-80 nm) are uniformly dispersed in a SnO2 matrix (30-45 nm). Well-developed lattice fringes, for both particle types, corroborate the cryst. nature of the two phases. The isomeric shift in the Mossbauer spectrum of the CVD deposit, when compared with the Ni3Sn4 and SnO2 stds., confirms the biphasic nature of the obtained material and shows the compn. to be Ni3Sn4/SnO2. Electron spectroscopy for chem. anal. (ESCA) studies performed on both (i) as obtained and (ii) argon sputtered samples established the elemental compn., the oxidn. states of the Ni and Sn atoms, and the effect of atm. oxidn. on the metal atoms located on the surface of the layers. Further characterization of the Ni-Sn intermetallic phase was achieved by detailed ESCA and high-resoln. transmission electron microscopy (HR-TEM) studies. on SciFinder(R)</style></abstract><label><style face="normal" font="default" size="100%">veith1999incorporation</style></label><notes><style face="normal" font="default" size="100%">257hg&#xD;Times Cited:33&#xD;Cited References Count:38</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/cm991034c</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">DOI 10.1021/cm991034c</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>540</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">540</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, M.</style></author><author><style face="normal" font="default" size="100%">Bartz, K.</style></author><author><style face="normal" font="default" size="100%">Heintz, M.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Pillong, F.</style></author><author><style face="normal" font="default" size="100%">Altherr, A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Glow Discharge Mass Spectrometry – A Powerful Tool in Solid Sample and Thin Layer Analysis</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured materials</style></secondary-title></titles><volume><style face="normal" font="default" size="100%">98</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">1999, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1999</style></year></dates><label><style face="normal" font="default" size="100%">veith1999discharge</style></label><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>541</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">541</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, M.</style></author><author><style face="normal" font="default" size="100%">Altherr, A.</style></author><author><style face="normal" font="default" size="100%">Lecerf, N.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Valtchev, K.</style></author><author><style face="normal" font="default" size="100%">Fritscher, E.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Molecular precursor approach to nano-scaled ceramics and metal/metal oxide composites</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nanostruct Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">191-194</style></pages><volume><style face="normal" font="default" size="100%">12</style></volume><number><style face="normal" font="default" size="100%">1-4</style></number><keywords><keyword><style face="normal" font="default" size="100%">1999, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1999</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jul</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0965-9773</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000081912100043</style></accession-num><abstract><style face="normal" font="default" size="100%">Heterometal alkoxides are used as single-source precursors to obtain nanoscaled thin layers and powders of a variety of oxide ceramics and composites. The hydride alkoxide [MgH2Al(OBu&apos;)22] has been used for low-temperature deposits of crystalline MgAl2O4 spinel. The mixed-metal alkoxide [BaZr(OPri)5(OH)(PriOH)3]2, based on 1:1 stoichiometry of the metals, has been used for clean and selective synthesis (sol-gel) of nanocrystalline BaZrO3 ceramic. Using heterometal alkoxide [Ni2Sn2(OBut)8] in a CVD process gave a binary intermetallic compound (Ni3Sn4) in an oxide matrix (SnO2). The composite system Ni/Al2O3 obtained on reducing NiO with [H2Al(OBut)]2 shows remarkably high catalytic activity in hydrogenation of C-C double bonds. Thin layers of a composite containing nano-sized Ni/Al2O3 have been deposited using [NiAl(OPri)42] in a CVD process.</style></abstract><label><style face="normal" font="default" size="100%">veith1999molecular</style></label><notes><style face="normal" font="default" size="100%">A Sp. Iss. SI&#xD;224rm&#xD;Times Cited:30&#xD;Cited References Count:9</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.sciencedirect.com/science/article/pii/S0965977399000963</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Doi 10.1016/S0965-9773(99)00096-3</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>539</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">539</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Meyer, Frank</style></author><author><style face="normal" font="default" size="100%">Hempelmann, Rolf</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Veith, Michael</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Microemulsion mediated sol-gel synthesis of nano-scaled MAl2O4 (M=Co, Ni, Cu) spinels from single-source heterobimetallic alkoxide precursors</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1755-1763</style></pages><volume><style face="normal" font="default" size="100%">9</style></volume><number><style face="normal" font="default" size="100%">8</style></number><keywords><keyword><style face="normal" font="default" size="100%">1999, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1999</style></year></dates><isbn><style face="normal" font="default" size="100%">09599428</style></isbn><abstract><style face="normal" font="default" size="100%">Nanocryst. aluminate spinels with cobalt, nickel or copper as bivalent cations have been prepd. in different particle sizes using single-source heterometal alkoxides of the type [M\{Al(OR)4\}2] (MII=Co, Ni, Cu; R=Pri, But) in a microemulsion assisted sol-gel process. The compatibility of the metal stoichiometry in the precursor mols. with respect to the spinel requirement was established by elemental, spectroscopic and single crystal X-ray diffraction analyses. Synthesis of CoAl2O4 using both single- and multi-component routes gave different results: whereas the single-source precursor approach yielded monophasic high purity spinels, phase contamination was evident in the diffractograms of ceramics obtained using a mixt. of individual components. The alkoxide precursors were hydrolyzed in a homogeneous dispersion of colloidal water droplets in a non-aq. phase. The diam. of water droplets in the microemulsion can be tuned, inter alia, by varying the hydrophilic chain length of the surfactant mols. which influences the size distribution of nanoparticles in the MAl2O4 ceramics. This parameter is used to obtain nano-spinels with particle sizes in the range 5-45 nm and reveals a qual. correlation between the initial droplet size and the crystallite size of the resulting spinels. TG-DTA measurements showed the thermal decompn. to be a 3 step process with crystn. of the spinel phase occurring around 900 °C. 27Al MAS NMR spectra reveal the inverse nature of the obtained spinels. XRD, TEM, SEM, EDX, FTIR and UV-VIS spectral studies were used for characterization of the powders.</style></abstract><label><style face="normal" font="default" size="100%">meyer1999microemulsion</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://xlink.rsc.org/?DOI=a900014c</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>538</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">538</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Meyer, F.</style></author><author><style face="normal" font="default" size="100%">Dierstein, A.</style></author><author><style face="normal" font="default" size="100%">Beck, Ch.</style></author><author><style face="normal" font="default" size="100%">Härtl, W.</style></author><author><style face="normal" font="default" size="100%">Hempelmann, R.</style></author><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Veith, M.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, D-66123 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Size-controlled synthesis of nanoscaled aluminium spinels using heterobimetallic alkoxide precursors via water/oil microemulsions</style></title><secondary-title><style face="normal" font="default" size="100%">Nanostructured Materials</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nanostruct Mater</style></alt-title></titles><pages><style face="normal" font="default" size="100%">71-74</style></pages><volume><style face="normal" font="default" size="100%">12</style></volume><number><style face="normal" font="default" size="100%">1-4</style></number><keywords><keyword><style face="normal" font="default" size="100%">1999, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1999</style></year><pub-dates><date><style face="normal" font="default" size="100%">January</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">09659773</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000081912100015</style></accession-num><abstract><style face="normal" font="default" size="100%">Nanosized spinels of type MAl2O4 (M = Mg, Co, Ni, Cu) were prepared by a sol-gel type hydrolysis of alkoxides in the inverse micelles of w/o microemulsions. Heterobimetallic alkoxides M[AI(OPri)(4)](2) containing both metallic elements in the desired stoichiometric ratio were employed as single-source precursors. The structure and thus metal stoichiometry in the molecules was established by single crystal X-ray diffraction analysis. By varying the hydrophilic chain length of the detergent, the diameter of the water droplets can be tuned in the nanometer range, as determined by dynamic light scattering. The size of the resulting spinel nano-particles as evaluated from XRD peak profile analysis, correlates to the droplet size. The results of the ceramic syntheses using the different types of alkoxide precursors were compared which reveal the advantage of a single source approach. (C) 1999 Acta Metallurgica Inc.</style></abstract><label><style face="normal" font="default" size="100%">meyer1999sizecontrolled</style></label><notes><style face="normal" font="default" size="100%">A Sp. Iss. SI&#xD;224rm&#xD;Times Cited:31&#xD;Cited References Count:12</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0965977399000689</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Doi 10.1016/S0965-9773(99)00068-9</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>546</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">546</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Mathur, Charu</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis, Structure, and Reactivity of Iodo-Functionalized Heterobimetallic Alkoxides of Tin(IV): X-ray Crystal Structures of [I2Sn(Al(OPri)4)2], [I2Sn(Ti(OPri)5)2], [I3Sn(Zr(OPri)5(PriOH))], and [I2Sn(Mo(C5H5)(CO)3)2]</style></title><secondary-title><style face="normal" font="default" size="100%">Organometallics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1044-1051</style></pages><volume><style face="normal" font="default" size="100%">17</style></volume><number><style face="normal" font="default" size="100%">6</style></number><keywords><keyword><style face="normal" font="default" size="100%">1998, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1998</style></year></dates><abstract><style face="normal" font="default" size="100%">New iodide heterobimetallic isopropoxides [I2Sn{Al(OPri)4}2] (1), [I2Sn{Ti(OPri)5}2] (2), [I2Sn{Nb(OPri)6}2] (3), and [I3Sn{Zr(OPri)5(PriOH)}] (4) obtained on reacting SnI4 with stoichiometric amts. of alkali-metal reagents [KAl(OPri)4]n, [KTi(OPri)5]n, [KZr(OPri)5]n, and [KNb(OPri)6]n, resp., is reported. The monomeric formulation and hexacoordination of Sn proposed for 1-4, from microanal., cryoscopic, and multinuclear (1H, 13C, 27Al, and 119Sn) NMR spectral data, was established for 1, 2, and 4 by single-crystal x-ray diffraction anal. The solid-state structures of 1 and 2 feature an approx. octahedral Sn(IV) center bearing two terminal iodide ligands and two bidentate {Al(OPri)4}- and {Ti(OPri)5}- moieties, contg. Al or Ti atoms in a distorted tetrahedral or trigonal-bipyramidal environment of OPri ligands, resp. The crystal structure of 4 represents a bioctahedron formed by the face-sharing interaction of two slightly distorted octahedra built around Sn(IV) and Zr(IV) centers. Compds. 1 and 2, when allowed to react (1:2) with the transition-metal deriv. Na[Mo(C5H5)(CO)3], afford the Sn-Mo-bonded cluster [I2Sn{Mo(C5H5)(CO)3}2] (5) as the only isolable product, in both the cases.</style></abstract><label><style face="normal" font="default" size="100%">doi:10.1021/om970948a</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/om970948a</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>545</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">545</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Mathur, Charu</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">New perspectives in the tailoring of hetero (bi- and tri-) metallic alkoxide derivatives</style></title><secondary-title><style face="normal" font="default" size="100%">Polyhedron</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Polyhedron</style></alt-title></titles><pages><style face="normal" font="default" size="100%">1005-1034</style></pages><volume><style face="normal" font="default" size="100%">17</style></volume><number><style face="normal" font="default" size="100%">5-6</style></number><keywords><keyword><style face="normal" font="default" size="100%">1998, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1998</style></year></dates><isbn><style face="normal" font="default" size="100%">02775387</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000073069500043</style></accession-num><abstract><style face="normal" font="default" size="100%">Metal alkoxides containing more than one sort of metallic element are predominantly known in the field of heterobimetallic derivatives. In order to pass to heterotrimetallic homoleptic alkoxides bimetallic alkoxides have to be prepared which are at the same time heterobimetallic and heteroleptic. They serve as starting materials in salt elimination reactions leading to heterotrimetallic homoleptic alkoxides. The structural entity serving as a building block in these reactions must be kinetically stable in order to survive in the synthetic procedures. Besides heterotermetallic alkoxides, heterobimetallic alkoxides with halides and cyclopentadienyl as ancillary ligands and transition metal complexes of new mixed-metal alkoxy derivatives are presented. Besides the syntheses and the structural characterization reactivity, spectral aspects in view of dynamic or static structures and applications of hetero(bi- and tri-)metallic alkoxides are discussed.</style></abstract><label><style face="normal" font="default" size="100%">veith1998perspectives</style></label><notes><style face="normal" font="default" size="100%">Zh074&#xD;Times Cited:125&#xD;Cited References Count:103</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1016/S0277-5387(97)00272-6</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Doi 10.1016/S0277-5387(97)00272-6</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>547</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">547</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author><author><style face="normal" font="default" size="100%">Decker, Timo</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Tuning Metal Stoichiometry in Heterometal Alkoxides: First Structurally Characterised Molecular Precursor to BaZrO3</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Eur J Inorg Chem</style></alt-title></titles><periodical><full-title><style face="normal" font="default" size="100%">European Journal of Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">1327-1332</style></pages><volume><style face="normal" font="default" size="100%">1998</style></volume><number><style face="normal" font="default" size="100%">9</style></number><keywords><keyword><style face="normal" font="default" size="100%">1998, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1998</style></year><pub-dates><date><style face="normal" font="default" size="100%">September</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1434-1948</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000075696900016</style></accession-num><abstract><style face="normal" font="default" size="100%">Manipulable metal ratios are accessible in a series of heterometal Ba-Zr alkoxides by changing the size and the charge of the ligands. The synthesis and characterization of 4 mixed-metal Ba-Zr species BaZr2(OtBu)10 (I), Ba2Zr(OtBu)8(tBuOH)(THF)2 (II), BaZr(OtBu)6(THF)2 (III), and BaZr(OH)(OiPr)5(iPrOH)32 (IV), based on different Ba/Zr stoichiometries, are reported. The crystal and mol. structures of I, II, and IV were detd. by single-crystal x-ray diffraction studies. I exhibits a bow-tie structural motif in which a trigonally distorted 6-coordinate Ba atom is chelated by 2 bipyramidal \Zr(OtBu)5\- units. II reveals a triangular Ba2Zr($\mu$3-OtBu)2($\mu$2-OtBu)3 core structure formed by the fusion of 3 octahedra built about 2 Ba atoms and a Zr atom. The structure is unique in terms of the distribution of terminal ligands at each of the metal centers. One of the Ba atoms possesses 1 -OtBu and 1 tBuOH as terminal ligands, while the terminal ligands on the 2nd Ba atom are 2 THF mols.; the Zr center bears -OtBu groups as the terminal ligands. Hydrolysis of compd. III with 1 equiv. of water, followed by alcoholysis (iPrOH) of the resulting product, gave IV. The structure of IV shows a planar tetrametallic Ba2Zr2 frame capped by 2 $\mu$3-hydroxo ligands. The coordination figure of the Zr atoms resembles a distorted octahedron, whereas the geometry of the Ba centers is best described as capped trigonal prisms. Both III and IV are excellent precursors to morphol. pure BaZrO3 ceramic by the sol-gel process.</style></abstract><label><style face="normal" font="default" size="100%">veith1998tuning</style></label><notes><style face="normal" font="default" size="100%">115zr&#xD;Times Cited:32&#xD;Cited References Count:42</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1002/(SICI)1099-0682(199809)1998:9&lt;1327::AID-EJIC1327&gt;3.0.CO;2-U</style></url></related-urls></urls><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>554</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">554</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Mathur, Charu</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis, reactivity and structures of hafnium-containing homo- and hetero- (bi- and tri-) metallic alkoxides based on edge- and face-sharing bioctahedral alkoxometalate ligands</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the Chemical Society, Dalton Transactions</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Chem Soc Dalton</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2101-2108</style></pages><number><style face="normal" font="default" size="100%">12</style></number><keywords><keyword><style face="normal" font="default" size="100%">1997, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1997</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jun 21</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0300-9246</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:A1997XH76600016</style></accession-num><abstract><style face="normal" font="default" size="100%">Using Hf(OPri)4(PriOH)2 as a building-block precursor, a series of homo- and hetero-metallic alkoxides of hafnium has been prepared and characterised using elemental analyses, infrared, multinuclear (1H, 7Li, 13C and 113Cd) NMR and single-crystal X-ray diffraction studies. The solid-state structure of Hf2(OPri)8(PriOH)2 1 reveals an edge-shared bioctahedral structure with the co-ordinated alcohol forming a hydrogen bridge across the dinuclear unit. The reactions of 1 with other nitrogen- or oxygen-containing donors gave monosubstituted products of the general formula Hf2(OPri)8(PriOH)L (L = C5H5N 2 or C4H8O2 3) which retain the dinuclear edge-sharing bioctahedral structure as determined for 2 by X-ray crystallography. Compound 1 reacted (1 : 2) with LiBun or LiOPri to afford dimeric LiHf(OPri)52 4. The molecular structure of 4 can be conceived as a dianionic Hf2(OPri)102- unit that binds two Li+ one on each side of the Hf-Hf vector which are additionally co-ordinated by the bridging OPri groups to display a trigonal-pyramidal geometry at the lithium atoms. The Hf2O6Li2 core in 4 comprises two analogous seconorcubane subunits sharing a common face defined by a Hf2O2 ring. Equimolar reaction of CuCl2 and KHf2(OPri)9 afforded the monomeric halide heterobimetallic derivative CuHf2Cl(OPri)9 5. Compound 5 is paramagnetic and follows Curie law behaviour as inferred by a variable-temperature 1H NMR study. In the solid state its molecular geometry could be formally seen as a tetradentate interaction of the distorted confacial bioctahedron Hf2(OPri)9- with a CuCl+ fragment. Each Hf is six-co-ordinated; Cu is five-co-ordinated and displays a distorted trigonal-bipyramidal geometry. The reaction (1 : 1) of CdHf2I(OPri)9 with KSr(OPri)3 produced a new heterotermetallic derivative Cd(OPri)3SrHf2(OPri )92 6. This involves the switching of central metal atoms between the two precursors and the Hf2(OPri)9 unit in 6 binds to Sr rather than Cd as anticipated. The centrosymmetric dimeric form of 6 is made up of a Sr(small micro-OPri)2Cd(small micro-OPri)2 Cd(small micro-OPri)2Sr2+ spirocyclic unit capped at both the ends by Hf2(OPri)9- moieties.</style></abstract><label><style face="normal" font="default" size="100%">A700833C</style></label><notes><style face="normal" font="default" size="100%">Xh766&#xD;Times Cited:41&#xD;Cited References Count:31</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1039/A700833C</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">DOI 10.1039/a700833c</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>548</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">548</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Hugh, Volker</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A Sr(II)-Zr(IV)-Cd(II) Alkoxide Cluster: Synthesis and X-Ray Structure of [(Cd(OPri)3)Sr(Zr2(OPri)9)]2</style></title><secondary-title><style face="normal" font="default" size="100%">Phosphorus, Sulfur, and Silicon and the Related Elements</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">493-496</style></pages><volume><style face="normal" font="default" size="100%">124</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">1997, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1997</style></year><pub-dates><date><style face="normal" font="default" size="100%">January</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">1042-6507</style></isbn><abstract><style face="normal" font="default" size="100%">New heterotrimetallic alkoxide \Cd(OPri)3\Sr\Zr2(OPri)9\2 (1) was obtained quant. in an anion-exchange reaction involving well-characterized iodide heterobimetallic alkoxide ICd\Zr2(OPri)9\ and the alkali metal reagent KSr(OPri)3. The formation of 1 is accompanied with an exchange of metals (Cd(II) and Sr(II)) between the constituting fragments (Cd\Zr2(OPri)9\+ and Sr(OPri)3-) and the chelating Zr2(OPri)9- anion, in 1, coordinates to Sr2+ in contrast to the precursor ICdZr2(OPri)9 where it is bound to Cd2+. The heterotrimetallic nature of 1 is unambiguously established by multinuclear (1H, 13C and 113Cd) NMR spectral data and a single crystal x-ray diffraction anal.</style></abstract><label><style face="normal" font="default" size="100%">veith1997sriizrivcdii</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.tandfonline.com/doi/abs/10.1080/10426509708545667</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>551</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">551</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and Characterization of New Alkoxotitanates of Yttrium, Barium, and Copper: Single Crystal X-ray Diffraction Structures of Cl2YTi2(OPri)9, Ti(OPri)5BaTi2(OPri)9, and ClCuTi2(OPri)9</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">2391-2399</style></pages><volume><style face="normal" font="default" size="100%">36</style></volume><number><style face="normal" font="default" size="100%">11</style></number><keywords><keyword><style face="normal" font="default" size="100%">1997, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1997</style></year></dates><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><abstract><style face="normal" font="default" size="100%">The synthesis and characterization of new mixed-metal alkoxides of Ti with Y, Ba, and Cu, achieved via salt elimination and acid-base reactions, is described. The metathesis reactions of KTi2(OPri)9 with anhyd. YCl3 (1:1 and 2:1) and CuCl2 (1:1) afford chloro-functionalized heterobimetallic alkoxides Cl2Y\Ti2(OPri)9\ (1), ClY\Ti2(OPri)9\2 (2), and ClCu\Ti2(OPri)9\ (3), resp., in high yields. The Ba-Ti derivs. Ba\Ti2(OPri)10\2 (4), \Ti2(OPri)9\Ba\Ti(OPri)5\ (5), and Ba\Ti2(OPri)9\2 (6) result from the reaction between Ba(OPri)2n and Ti(OPri)4 in 1:2, 1:3, and 1:4 molar ratios, resp. All the new derivs. (1-6) were characterized by elemental analyses, variable-temp. 1H and 13C NMR, IR spectroscopy, cryoscopy, and single crystal x-ray diffraction studies for 1, 3, and 5. The crystallog. study of 1 reveals a mononuclear species where the Y atom, coordinated by four alkoxide O atoms of the \Ti2(OPri)9\- unit and two chloride ligands, is in a pseudo-octahedral arrangement. The NMR (1H and 13C) and cryoscopic data for 1 indicate that the bioctahedral \Ti2(OPri)9\ framework, as obsd. in the solid state structure, is retained in soln. The x-ray structure of Cu deriv. 3 exhibits a triangular heterometallic core CuTi2($\mu$2-OPri)3($\mu$3-OPri)2 with chloride as a terminal ligand on Cu. Each Ti bears two terminal OPri groups and displays a distorted octahedral geometry, whereas Cu has a pseudotrigonal bipyramidal environment. The high-temp. NMR studies for the paramagnetic 3 are in agreement with Curie law behavior; the isotropic shifts indicate that the OPri groups bound directly to the CuII center experience a greater paramagnetic influence in comparison to OPri groups attached to Ti only. Ba titanates reveal an interesting observation of structural and stoichiometry (Ba/Ti) change. The dimeric compd. 4 (Ba/Ti, 1:2) reacts with 1 mol of Ti(OPri)4 to offer mononuclear 5 with a Ba/Ti stoichiometry of 1:3; on further addn. of 1 mol of Ti(OPri)4, 5 is converted to 6 (Ba/Ti, 1:4). X-ray crystallog. performed on 5 shows the mol. structure to be formed by the coordination of monoanionic \Ti(OPri)5\- and \Ti2(OPri)9\- units to Ba2+ in bi- and tetradentate fashion, resp. The coordination figure of the central atom, Ba, corresponds to a trigonal prism distorted toward an octahedron. Crystal data for 1: monoclinic space group Cc, a 21.618(14), b 9.878(5), c 19.949(13) \AA, $\beta$ 109.51(4)°, Z = 4. Crystal data for 3: triclinic space group P̅1, a 10.085(2), b 10.210(2), c 21.551(4) \AA, $\alpha$ 84.40(3), $\beta$ 84.03(3), $\gamma$ 60.86(3)°, Z = 2. Crystal data for 5: triclinic space group P̅1, a 11.850(2), b 13.888(3), c 18.716(4) \AA, $\alpha$ 86.08(3), $\beta$ 89.15(3), $\gamma$ 83.36(3)°, Z = 4.</style></abstract><label><style face="normal" font="default" size="100%">veith1997synthesis</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/ic9613218</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>549</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">549</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Novel ionogenic heterometal alkoxide derivatives</style></title><secondary-title><style face="normal" font="default" size="100%">Chemical Communications</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Chem Commun</style></alt-title></titles><pages><style face="normal" font="default" size="100%">2197-2198</style></pages><number><style face="normal" font="default" size="100%">22</style></number><keywords><keyword><style face="normal" font="default" size="100%">1997, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1997</style></year><pub-dates><date><style face="normal" font="default" size="100%">Nov 21</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">13597345</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:A1997YG75800033</style></accession-num><abstract><style face="normal" font="default" size="100%">The first examples of hydrocarbon sol. heterometal cation-anion systems contg. metal alkoxide clusters as isolated ions are reported. The reaction of SnI4 with KTi(OPri)5, or KTi2(OPri)9, or with KOPri and Ti(OPri)4 gave the ionic complex Ti3(OPri)11+Sn2I6(OPri)3- (1). Reactions of SnCl2 with ClSn(M2(OPri)9)2 gave ionic complexes SnM2(OPri)9+SnCl3- (M = Ti (2), Zr (3)). 1 And 2 were characterized by x-ray crystallog. (triclinic, space group P̅1, R = 0.081 (1·2PhMe); R = 0.0469 (2)).</style></abstract><label><style face="normal" font="default" size="100%">veith1997novel</style></label><notes><style face="normal" font="default" size="100%">Yg758&#xD;Times Cited:13&#xD;Cited References Count:16</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://xlink.rsc.org/?DOI=a705345b</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">DOI 10.1039/a705345b</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>552</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">552</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Charu</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis, Characterization, and Reactivity of New Heteroleptic Heterobimetallic Alkoxide Derivatives of Tin(II): X-ray Crystal Structures of [ClSn(M2(OPri)9)]2 (M = Zr, Hf), [(C5H5)Sn(Zr2(OPri)9)], and [(C5H5)Pb(μ2-OBut)2Sn(OBut)]</style></title><secondary-title><style face="normal" font="default" size="100%">Organometallics</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1292-1299</style></pages><volume><style face="normal" font="default" size="100%">16</style></volume><number><style face="normal" font="default" size="100%">6</style></number><keywords><keyword><style face="normal" font="default" size="100%">1997, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1997</style></year></dates><abstract><style face="normal" font="default" size="100%">The synthesis of new cyclopentadienyl-containing heterobimetallic alkoxides has been accomplished by employing the alkoxide precursors toward cyclopentadienyl reagents (NaCp and (C5H5)SnCl). The equimolar reactions of anhydrous SnX2 (X = Cl, I) and KM2(OPri)9 (M = Zr, Hf) offer halide heterobimetallic isopropoxides [XSn{M2(OPri)9}]2 (1, M = Hf, X = Cl; 2, M = Hf, X = I; 3, M = Zr, X = Cl) in quantitative yields. Both 1 and 3 react with NaCp in benzene/THF to give (C5H5)Sn{M2(OPri)9} (4, M = Hf; 5, M = Zr). Alternatively, 4 and 5 are conveniently obtained by the equimolar reaction of (C5H5)SnCl with KM2(OPri)9 (M = Zr, Hf). Although the reaction (1:1) of (C5H5)SnCl with [KGe(OBut)3]n affords the expected product (C5H5)Sn(μ2-OBut)2Ge(OBut) (6), the reaction with [KPb(OBut)3]n shows a transfer of cyclopentadienyl ring from tin to lead to provide (C5H5)Pb(μ2-OBut)2Sn(OBut) (7). The new derivatives have been readily characterized by elemental analysis, multinuclear (1H, 13C, 119Sn, and 207Pb) NMR studies, molecular weight measurements, and volatility. A single-crystal X-ray diffraction study is reported for the compounds 1, 3, and 5, 7. The solid state structures of 1, 3, and 5 exhibit varying coordination behavior of M2(OPri)9- units to SnX+ (X = C5H5, Cl) fragments. In the structural framework of the tert-butoxide derivatives, the four membered MM&apos;(μ2-OBut)2 (6, M = Ge, M&apos; = Sn; 7, M = Pb, M&apos; = Sn) ring is terminated at the metal ends by cyclopentadienyl and tert-butoxide ligands and each of the metals, bearing a stereochemically active lone pair, displays a pyramidal geometry.</style></abstract><label><style face="normal" font="default" size="100%">doi:10.1021/om9606193</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://dx.doi.org/10.1021/om9606193</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>550</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">550</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Charu</style></author><author><style face="normal" font="default" size="100%">Hugh, Volker</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Saarland, Inst Inorgan Chem, D-66041 Saarbrucken, Germany</style></auth-address><titles><title><style face="normal" font="default" size="100%">Reactivity of a Cyclopentadienyl Containing Heterobimetallic Alkoxide</style></title><secondary-title><style face="normal" font="default" size="100%">Phosphorus, Sulfur, and Silicon and the Related Elements</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Phosphorus Sulfur</style></alt-title></titles><pages><style face="normal" font="default" size="100%">489-492</style></pages><volume><style face="normal" font="default" size="100%">124</style></volume><number><style face="normal" font="default" size="100%">1</style></number><keywords><keyword><style face="normal" font="default" size="100%">1997</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1997</style></year></dates><isbn><style face="normal" font="default" size="100%">1042-6507</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:000074130100062</style></accession-num><abstract><style face="normal" font="default" size="100%">The synthesis of the new heteroleptic heterotrimetallic cluster, [(C5H5)Sn(mu-OBut)(2)Ge(OBut)Mo(CO)(5)] (1) has been achieved by a thermally induced CO substitution of the transition metal derivative, Mo(CO)(6), by the basic germanium atom of the cyclopentadienyl heterobimetallic alkoxide, [(C5H5)Sn(mu-OBut)(2)Ge(OBut)]. The microanalysis, molecular weight (monomer in benzene), IR and multinuclear NMR data and X-ray diffraction study is consistent with the formulation of 1. The Sn atom has a trigonal pyramidal coordination environment formed by a aysmmterically pi-bonded terminal C5H5 ring and two symmetrically bridged tert-butoxy groups. The four-coordinate Ge atom lies at the centre of a distorted tetrahedron and is terminally attached to a tert-butoxy group and a Mo(CO)(S)(-)fragment.</style></abstract><label><style face="normal" font="default" size="100%">veith1997reactivity</style></label><notes><style face="normal" font="default" size="100%">Zt812&#xD;Times Cited:5&#xD;Cited References Count:3</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://www.tandfonline.com/doi/abs/10.1080/10426509708545666</style></url></related-urls></urls><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>557</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">557</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and Spectroscopic Characterization of Novel Heterotermetallic Isopropoxides: X-ray Crystal Structures of ICd2(OPri)9 and (OPri)32(OPri)92 (M = Ti, Hf)</style></title><secondary-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></secondary-title></titles><periodical><full-title><style face="normal" font="default" size="100%">Inorganic Chemistry</style></full-title></periodical><pages><style face="normal" font="default" size="100%">7295-7303</style></pages><volume><style face="normal" font="default" size="100%">35</style></volume><number><style face="normal" font="default" size="100%">25</style></number><keywords><keyword><style face="normal" font="default" size="100%">1996, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1996</style></year></dates><isbn><style face="normal" font="default" size="100%">0020-1669</style></isbn><abstract><style face="normal" font="default" size="100%">Metathesis reactions between CdI2 and KM2(OPri)9 (M = Ti, Hf) in toluene produce monomeric iodo-heterobimetallic isopropoxides ICdM2(OPri)9 (1, M = Ti; 2, M = Hf) which were characterized by soln. (1H, 13C, and 113Cd) and solid state (13C and 113Cd) CP MAS NMR spectroscopy, microanal., cryoscopic mol. wt. detn., and single crystal x-ray diffraction study. Both 1 and 2 in the solid state represent the 1st structurally characterized examples of halide heterobimetallic alkoxides based on \{Ti2(OPri)9\}- and \{Hf2(OPri)9\}- bioctahedral subunits, resp. The overall mol. geometry of 1 and 2 can be viewed formally as an interaction of the CdI+ fragment with \{M2(OPri)9\}- substructures via two terminal and two bridging ($\mu$2-) isopropoxy groups. Reaction of 1 and 2 with equimolar KBa(OPri)3 in toluene afforded novel heterotermetallic isopropoxides [\{Cd(OPri)3\}Ba\{M2(OPri)9\}]2 (3, M = Ti; 4, M = Hf). Formation of heterotermetallic frameworks involves an interesting rearrangement of the central metal atoms between the two precursor mols., which is probably commanded by the tendency of barium to achieve higher coordination nos. The dimeric forms of 3 and 4 as shown by cryoscopy and 113Cd soln. and solid state CP MAS NMR studies are confirmed by crystallog. The x-ray crystal structures of 3 and 4 reveal, as a common feature, a central Ba($\mu$2-OPri)2Cd($\mu$2-OPri)2Cd($\mu$2-OPri)2Ba unit formed by a spirocyclic linking of two LBa(OPri)2 (3, L = Ti2(OPri)9; 4, L = Hf2(OPri)9) units to a four membered, Cd2(OPri)2, ring. Crystal data: for 1, monoclinic, space group P21/m, a 11.71(2), b 15.78(3), c 12.16(2) \AA, $\beta$ 116.69(14)°, Z = 2; for 2, triclinic, space group P̅1, a 9.825(2), b 11.428, c 20.619 \AA, $\alpha$ 95.619(12), $\beta$ 99.915(11), $\gamma$ 111.347(11)°, Z = 2; for 3, monoclinic, space group P21/c, a 22.68(2), b 12.603(11), c 19.00(2) \AA, $\beta$ 96.83(8)°, Z = 2; for 4, monoclinic, space group P21/c, a 23.197(5), b 12.886(3), c 19.378(4) \AA, $\beta$ 97.18(3)°, Z = 2.</style></abstract><label><style face="normal" font="default" size="100%">veith1996synthesis</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/ic960116p</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>556</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">556</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and characterisation of novel heterobimetallic halide isopropoxides based on M2(OPri)9- (M = Sn, Zr or Ti) anions: crystal and molecular structures of CdI2(OPri)9 and 2(OPri)92</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the Chemical Society, Dalton Transactions</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">2485-2490</style></pages><number><style face="normal" font="default" size="100%">12</style></number><keywords><keyword><style face="normal" font="default" size="100%">1996, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1996</style></year></dates><isbn><style face="normal" font="default" size="100%">0300-9246</style></isbn><abstract><style face="normal" font="default" size="100%">New heterobimetallic halide isopropoxides based on the interaction of M2(OPri)9- (M = SnIV, ZrIV or TiIV) units with CdII, SnII and PbII were prepd. These complexes were characterized by multinuclear soln. and solid-state cross polarization magic angle spinning (CP MAS) NMR spectroscopy, elemental analyses and cryoscopy. Single-crystal x-ray diffraction studies were performed for CdI\Sn2(OPri)9\ (1) and \SnIZr2(OPri)9\2 (2). 1 Consists of a face-sharing bioctahedral Sn2(OPri)9- unit which interacts with the central metal atom, cadmium, using two $\mu$- and two terminal OPri groups. The cadmium atom is within a distorted trigonal bipyramid of oxygen and iodine atoms. The 113Cd chem. shifts in the soln. and solid-state CP MAS NMR spectra of 1 are consistent with the retention of its heterometallic nature in soln. In contrast to the monomeric form of 1, compd. 2 exists as an iodo-bridged dimer in the solid state. Cryoscopic measurements for 2 indicate a monomer-dimer equil. ($\eta$ = 1.6) in soln. which was confirmed by variable-temp. 119Sn NMR studies. In the solid state the ligating mode of the Zr2(OPri)9- unit in 2 is different from isostructural Sn2(OPri)9- and it binds to tin via only three OPri groups, the 4th M-OPri interaction being hindered by the stereochem. active lone pair of electrons present at SnII. The central SnI2O6 core in 2 can be viewed as two SnI2O3 octahedra fused along a common axial-equatorial edge where one of the axial coordination sites in each is occupied by the nonbonding electron pair of SnII. on SciFinder(R)</style></abstract><label><style face="normal" font="default" size="100%">veith1996synthesis</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://xlink.rsc.org/?DOI=dt9960002485</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>555</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">555</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Veith, Michael</style></author><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Huch, Volker</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Designed Synthesis and Molecular Structure of the First Heterotermetallic Alkoxide</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the American Chemical Society</style></secondary-title><alt-title><style face="normal" font="default" size="100%">J Am Chem Soc</style></alt-title></titles><pages><style face="normal" font="default" size="100%">903-904</style></pages><volume><style face="normal" font="default" size="100%">118</style></volume><number><style face="normal" font="default" size="100%">4</style></number><keywords><keyword><style face="normal" font="default" size="100%">1996, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1996</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jan 31</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0002-7863</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:A1996TT38100027</style></accession-num><abstract><style face="normal" font="default" size="100%">KZr2(OPri)9, prepd. from Zr2(OPri)8(iPrOH)2 and KOPri, reacted with CdI2 gave ICdZr2(OPri)9 (I). I reacted with KBa(OPri)3 to give \Cd(OPri)3\Ba\Zr2(OPRi)9\2 (II). I is triclinic, space group P̅1, Z = 2, Rw = 0.0470. II is monoclinic, space group P21/c, Z = 2, Rw = 0.0772. I is a monomer in which Cd is the central atom with a terminal I and with a face-sharing bioctahedral Zr2(OPri)9- unit via 2 triply and 2 doubly bridging isopropoxy groups. In II 2 ($\mu$2-OPri)2CdBaZr2($\mu$3-OPri)2($\mu$2-OPri)3($\mu$-OPri)4 + fragments are linked together by 2 isopropoxy groups bridging the Cd centers.</style></abstract><label><style face="normal" font="default" size="100%">veith1996designed</style></label><notes><style face="normal" font="default" size="100%">Tt381&#xD;Times Cited:71&#xD;Cited References Count:25</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://pubs.acs.org/doi/abs/10.1021/ja953255z</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">DOI 10.1021/ja953255z</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>558</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">558</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Singh, A.</style></author><author><style face="normal" font="default" size="100%">Mehrotra, R. C.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and Characterization of Nonaisopropoxodiziconatotin(IV) Coplexes</style></title><secondary-title><style face="normal" font="default" size="100%">Indian Journal of Chemistry-Section A: Inorganic, physical, theoretical &amp; analytical</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">454-458</style></pages><volume><style face="normal" font="default" size="100%">34</style></volume><number><style face="normal" font="default" size="100%">6</style></number><keywords><keyword><style face="normal" font="default" size="100%">1995, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1995</style></year></dates><label><style face="normal" font="default" size="100%">Mathur1995</style></label><urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>560</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">560</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Singh, Anirudh</style></author><author><style face="normal" font="default" size="100%">Mehrotra, Ram C.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Synthesis and characterization of the first heteroleptic tin(II) isopropoxometallates</style></title><secondary-title><style face="normal" font="default" size="100%">Polyhedron</style></secondary-title></titles><pages><style face="normal" font="default" size="100%">1073-1077</style></pages><volume><style face="normal" font="default" size="100%">12</style></volume><number><style face="normal" font="default" size="100%">9</style></number><keywords><keyword><style face="normal" font="default" size="100%">1993, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1993</style></year><pub-dates><date><style face="normal" font="default" size="100%">May</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">02775387</style></isbn><label><style face="normal" font="default" size="100%">mathur1993synthesis</style></label><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0277538700871867</style></url></related-urls></urls></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>559</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">559</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, S.</style></author><author><style face="normal" font="default" size="100%">Singh, A</style></author><author><style face="normal" font="default" size="100%">Mehrotra, R C</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Rajasthan,Dept Chem,Jaipur 302004,Rajasthan,India</style></auth-address><titles><title><style face="normal" font="default" size="100%">Synthesis, Reactions and Spectroscopic Studies of Some Novel Hetero(bi- and tri) metal Alkoxides of Tin(IV) with Niobium and Tantalum</style></title><secondary-title><style face="normal" font="default" size="100%">Indian Journal of Chemistry Section</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Indian J Chem A</style></alt-title></titles><pages><style face="normal" font="default" size="100%">58</style></pages><volume><style face="normal" font="default" size="100%">32</style></volume><number><style face="normal" font="default" size="100%">A</style></number><keywords><keyword><style face="normal" font="default" size="100%">1993, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1993</style></year><pub-dates><date><style face="normal" font="default" size="100%">Jul</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">0376-4710</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:A1993LK93200008</style></accession-num><abstract><style face="normal" font="default" size="100%">Novel (chloro)isopropoxo niobates and -tantalates of tin(IV) with the formulae Cl4-nSn{M(OPri)6}n, (n = 1 - 3) have been synthesized by the reactions of SnCl4 with an appropriate potassium hexaisopropoxometallate, KM(OPri)6 (M = Nb/Ta) in the required molar ratios. These chloro precursors have been used to obtain derivatives of the types (RO)2Sn{M(OPri)6}2 (R = Me, Pr(i), Bu(t)), {Ta(OPri)6}2Sn{Nb(OPri)6}2 and {Al(OPri)4}ClSn{Nb(OPri)6}2 by the replacement reaction of the chloride with appropriate potassium alkoxide or isopropoxometallate. Characterization of these novel complexes has been carried out on the basis of elemental and alkoxo group analyses, IR and multinuclear (H-1, C-14, Al-27 and Sn-119) NMR data and molecular weight studies.</style></abstract><label><style face="normal" font="default" size="100%">mathur1993synthesis</style></label><notes><style face="normal" font="default" size="100%">Lk932&#xD;Times Cited:7&#xD;Cited References Count:27</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">&lt;Go to ISI&gt;://WOS:A1993LK93200008</style></url></related-urls></urls><language><style face="normal" font="default" size="100%">English</style></language></record><record><database name="Publications-Mathur_2024-07-02.enl" path="C:\Users\naina\OneDrive\Desktop\Website Literaturstellen\02.07.24\Publications-Mathur_2024-07-02.enl">Publications-Mathur_2024-07-02.enl</database><source-app name="EndNote" version="21.3">EndNote</source-app><rec-number>561</rec-number><foreign-keys><key app="EN" db-id="f9zxt2zdisrs5xe5p565e92vrt5rdsr9fzaz">561</key></foreign-keys><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mathur, Sanjay</style></author><author><style face="normal" font="default" size="100%">Singh, Anirudh</style></author><author><style face="normal" font="default" size="100%">Mehrotra, Ram C.</style></author></authors></contributors><auth-address><style face="normal" font="default" size="100%">Univ Rajasthan,Dept Chem,Jaipur 302004,Rajasthan,India</style></auth-address><titles><title><style face="normal" font="default" size="100%">Synthesis, characterization and reactions of some alkoxoaluminates of tin(IV)</style></title><secondary-title><style face="normal" font="default" size="100%">Polyhedron</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Polyhedron</style></alt-title></titles><pages><style face="normal" font="default" size="100%">341-345</style></pages><volume><style face="normal" font="default" size="100%">11</style></volume><number><style face="normal" font="default" size="100%">3</style></number><keywords><keyword><style face="normal" font="default" size="100%">1992, myown</style></keyword></keywords><dates><year><style face="normal" font="default" size="100%">1992</style></year><pub-dates><date><style face="normal" font="default" size="100%">January</style></date></pub-dates></dates><isbn><style face="normal" font="default" size="100%">02775387</style></isbn><accession-num><style face="normal" font="default" size="100%">WOS:A1992HE58200005</style></accession-num><abstract><style face="normal" font="default" size="100%">Novel heterometal alkoxides of tin(IV) with the compositions [Cl4-nSn{Al(OPri)4}n] (where n = 1-3) and [Cl2Sn{Al(OBut)4}2] have been synthesized by the reactions of SnCl4 with the appropriate potassium alkoxoaluminate in the requisite molar ratio.  Replacement of chloride in these derivatives has yielded heterometal (bi- or tri-) derivatives of the types [(OR)4-nSn{Al(OPri)4}n] (R = Pr(i), Bu(t); n = 2 or 3) and [{Zr2(OPri)9} Sn{Al(OPri)4}3].  The new heterometal alkoxides have been characterized by elemental analyses, molecular weight measurements, IR and multinuclear (H-1, C-13, Al-27 and Sn-119) NMR spectral studies.</style></abstract><label><style face="normal" font="default" size="100%">mathur1992synthesis</style></label><notes><style face="normal" font="default" size="100%">He582&#xD;Times Cited:16&#xD;Cited References Count:23</style></notes><urls><related-urls><url><style face="normal" font="default" size="100%">http://linkinghub.elsevier.com/retrieve/pii/S0277538700831794</style></url></related-urls></urls><electronic-resource-num><style face="normal" font="default" size="100%">Doi 10.1016/S0277-5387(00)83179-4</style></electronic-resource-num><language><style face="normal" font="default" size="100%">English</style></language></record></records></xml>