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  • 1
    Publication Date: 2019
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2016-05-14
    Description: Atomically dispersed noble metal catalysts often exhibit high catalytic performances, but the metal loading density must be kept low (usually below 0.5%) to avoid the formation of metal nanoparticles through sintering. We report a photochemical strategy to fabricate a stable atomically dispersed palladium-titanium oxide catalyst (Pd1/TiO2) on ethylene glycolate (EG)-stabilized ultrathin TiO2 nanosheets containing Pd up to 1.5%. The Pd1/TiO2 catalyst exhibited high catalytic activity in hydrogenation of C=C bonds, exceeding that of surface Pd atoms on commercial Pd catalysts by a factor of 9. No decay in the activity was observed for 20 cycles. More important, the Pd1/TiO2-EG system could activate H2 in a heterolytic pathway, leading to a catalytic enhancement in hydrogenation of aldehydes by a factor of more than 55.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Liu, Pengxin -- Zhao, Yun -- Qin, Ruixuan -- Mo, Shiguang -- Chen, Guangxu -- Gu, Lin -- Chevrier, Daniel M -- Zhang, Peng -- Guo, Qing -- Zang, Dandan -- Wu, Binghui -- Fu, Gang -- Zheng, Nanfeng -- New York, N.Y. -- Science. 2016 May 13;352(6287):797-801. doi: 10.1126/science.aaf5251.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, Engineering Research Center for Nano-Preparation Technology of Fujian Province, National Engineering Laboratory for Green Chemical Productions of Alcohols, Ethers, and Esters, and Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China. ; Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China. ; Department of Chemistry, Dalhousie University, Halifax, Nova Scotia B3H 4R2, Canada. ; State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, Engineering Research Center for Nano-Preparation Technology of Fujian Province, National Engineering Laboratory for Green Chemical Productions of Alcohols, Ethers, and Esters, and Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China. nfzheng@xmu.edu.cn gfu@xmu.edu.cn.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/27174982" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2017-09-07
    Description: The electrochemical conversion of CO 2 and H 2 O into syngas using renewably generated electricity is an attractive approach to simultaneously achieve chemical fixation of CO 2 and storage of renewable energy. Developing cost-effective catalysts for selective electroreduction of CO 2 into CO is essential to the practical applications of the approach. We report a simple synthetic strategy for the preparation of ultrathin Cu/Ni(OH) 2 nanosheets as an excellent cost-effective catalyst for the electrochemical conversion of CO 2 and H 2 O into tunable syngas under low overpotentials. These hybrid nanosheets with Cu(0)-enriched surface behave like noble metal nanocatalysts in both air stability and catalysis. Uniquely, Cu(0) within the nanosheets is stable against air oxidation for months because of the presence of formate on their surface. With the presence of atomically thick ultrastable Cu nanosheets, the hybrid Cu/Ni(OH) 2 nanosheets display both excellent activity and selectivity in the electroreduction of CO 2 to CO. At a low overpotential of 0.39 V, the nanosheets provide a current density of 4.3 mA/cm 2 with a CO faradaic efficiency of 92%. No decay in the current is observed for more than 22 hours. The catalysts developed in this work are promising for building low-cost CO 2 electrolyzers to produce CO.
    Electronic ISSN: 2375-2548
    Topics: Natural Sciences in General
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  • 4
    Publication Date: 2019
    Description: 〈p〉Weyl semimetals are crystalline solids that host emergent relativistic Weyl fermions and have characteristic surface Fermi-arcs in their electronic structure. Weyl semimetals with broken time reversal symmetry are difficult to identify unambiguously. In this work, using angle-resolved photoemission spectroscopy, we visualized the electronic structure of the ferromagnetic crystal Co〈sub〉3〈/sub〉Sn〈sub〉2〈/sub〉S〈sub〉2〈/sub〉 and discovered its characteristic surface Fermi-arcs and linear bulk band dispersions across the Weyl points. These results establish Co〈sub〉3〈/sub〉Sn〈sub〉2〈/sub〉S〈sub〉2〈/sub〉 as a magnetic Weyl semimetal that may serve as a platform for realizing phenomena such as chiral magnetic effects, unusually large anomalous Hall effect and quantum anomalous Hall effect.〈/p〉
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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