甲酸
催化作用
氢氧化物
化学
无机化学
吸附
钌
氢
氢气储存
金属
活动中心
物理化学
有机化学
作者
Kohsuke Mori,Tomohisa Taga,Hiromi Yamashita
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2017-03-24
卷期号:7 (5): 3147-3151
被引量:238
标识
DOI:10.1021/acscatal.7b00312
摘要
In order to achieve an economical CO2-mediated hydrogen energy cycle, the development of heterogeneous catalysts for CO2 hydrogenation to formic acid is an urgent and challenging task. In this study, a stable and well-defined single-site Ru catalyst on the surface of a layered double hydroxide (LDH) in a basic medium is proven to be efficient for selective hydrogenation of CO2 to formic acid under mild reaction conditions (2.0 MPa, 100 °C). The electron-donating ability of triads of basic hydroxyl ligands with a particular location is crucial for an active electron-rich Ru center. There is a strong correlation between catalytic activity and adjustable CO2 adsorption capacity in the vicinity of the Ru center. Such electronic metal–support interactions and a CO2 concentration effect result in a significant positive influence on the catalytic activity.
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