二硫化钼
催化作用
石油化工
钼
氢
分子
GSM演进的增强数据速率
吡啶
二硫键
化学
活动站点
海水
材料科学
结晶学
无机化学
计算机科学
有机化学
冶金
地质学
海洋学
电信
生物化学
作者
Hemamala I. Karunadasa,E. Montalvo,Yujie Sun,Marcin Majda,Jeffrey R. Long,Christopher J. Chang
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2012-02-09
卷期号:335 (6069): 698-702
被引量:1156
标识
DOI:10.1126/science.1215868
摘要
Inorganic solids are an important class of catalysts that often derive their activity from sparse active sites that are structurally distinct from the inactive bulk. Rationally optimizing activity is therefore beholden to the challenges in studying these active sites in molecular detail. Here, we report a molecule that mimics the structure of the proposed triangular active edge site fragments of molybdenum disulfide (MoS(2)), a widely used industrial catalyst that has shown promise as a low-cost alternative to platinum for electrocatalytic hydrogen production. By leveraging the robust coordination environment of a pentapyridyl ligand, we synthesized and structurally characterized a well-defined Mo(IV)-disulfide complex that, upon electrochemical reduction, can catalytically generate hydrogen from acidic organic media as well as from acidic water.
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