催化作用
甲醇
二氧化碳
多相催化
化学
化学工程
材料科学
铜
无机化学
有机化学
工程类
作者
Feng Sha,Zhe Han,Shan Tang,Jijie Wang,Can Li
出处
期刊:Chemsuschem
[Wiley]
日期:2020-11-04
卷期号:13 (23): 6160-6181
被引量:154
标识
DOI:10.1002/cssc.202002054
摘要
The increasing atmospheric CO2 level makes CO2 reduction an urgent challenge facing the world. Catalytic transformation of CO2 into chemicals and fuels utilizing renewable energy is one of the promising approaches toward alleviating CO2 emissions. In particular, the selective hydrogenation of CO2 to methanol utilizing renewable hydrogen potentially enables large scale transformation of CO2 . The Cu-based catalysts have been extensively investigated in CO2 hydrogenation. However, it is not only limited by long-term instability but also displays unsatisfactory catalytic performance. The supported metal-based catalysts (Pd, Pt, Au, and Ag) can achieve high methanol selectivity at low temperatures. The mixed oxide catalysts represented by Ma ZrOx (Ma =Zn, Ga, and Cd) solid solution catalysts present high methanol selectivity and catalytic activity as well as excellent stability. This Review focuses on the recent advances in developing Non-Cu-based heterogeneous catalysts and current understandings of catalyst design and catalytic performance. First, the thermodynamics of CO2 hydrogenation to methanol is discussed. Then, the progress in supported metal-based catalysts, bimetallic alloys or intermetallic compounds catalysts, and mixed oxide catalysts is discussed. Finally, a summary and a perspective are presented.
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