通过设计活性位点周围的分子环境来控制催化的机会:无定形和结晶沸石硅酸盐支撑的阳离子

Q1 Materials Science
Nicolás A. Grosso‐Giordano, S. Zones, Alexander Katz
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引用次数: 3

摘要

对非晶二氧化硅和沸石硅酸盐支撑的催化活性位点的分子结构进行综合控制的机会进行了严格的研究,并评估了支撑结晶度对催化性能的影响。我们首先总结了硅酸盐载体上活性位点的结构特征,并将非晶态二氧化硅表面固有的无序性与结晶型的有序性进行了对比。然后,我们在工业实践中所选用的催化系统的背景下,分析这些结构如何影响分离活性位点的内外球环境,以及这些环境如何影响催化活性和下一代催化剂的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Opportunities for controlling catalysis by designing molecular environments around active sites: cations supported on amorphous versus crystalline zeolitic silicate supports
Opportunities for synthetically controlling the molecular architecture of catalytic active sites supported on amorphous silica versus zeolitic silicates are critically examined, and the role that support crystallinity could play on catalytic properties is assessed. We first summarize structural features of active sites on silicate supports and contrast the inherent disorder of amorphous silica surfaces to the order of crystalline zeotypes. We then analyze, within the context of selected catalytic systems currently employed in industrial practice, how these structures affect inner- and outer-sphere environments of isolated active sites, and how these environments could impact catalytic activity and the development of next generation catalysts.
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来源期刊
Catalysis Structure & Reactivity
Catalysis Structure & Reactivity CHEMISTRY, PHYSICAL-
CiteScore
4.80
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