选择性
水煤气变换反应
催化作用
化学工程
烧结
甲醇
甲烷化
材料科学
可再生能源
粒径
钌
粒子(生态学)
化学
有机化学
冶金
地质学
工程类
电气工程
海洋学
作者
Rui Tang,Zhijie Zhu,Chaoran Li,Mengqi Xiao,Zhiyi Wu,Dake Zhang,Chengcheng Zhang,Yi Xiao,Mingyu Chu,Alexander Genest,Günther Rupprechter,Liang Zhang,Xiaohong Zhang,Le He
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2021-10-27
卷期号:3 (12): 1652-1659
被引量:38
标识
DOI:10.1021/acsmaterialslett.1c00523
摘要
Cascade catalysis of reverse water gas shift (RWGS) and well-established CO hydrogenation holds promise for the conversion of greenhouse gas CO2 and renewable H2 into liquid hydrocarbons and methanol under mild conditions. However, it remains a big challenge to develop low-temperature RWGS catalysts with high activity, selectivity, and stability. Here, we report the design of an efficient RWGS catalyst by encapsulating ruthenium clusters with the size of 1 nm inside hollow silica shells. The spatially confined structure prevents the sintering of Ru clusters while the permeable silica layer allows the diffusion of gaseous reactants and products. This catalyst with reduced particle sizes not only inherits the excellent activity of Ru in CO2 hydrogenation reactions but also exhibits nearly 100% CO selectivity and superior stability at 200-500 °C. The ability to selectively produce CO from CO2 at relatively low temperatures paves the way for the production of value-added fuels from CO2 and renewable H2.
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