Active copper structures in ZnO-Cu interfacial catalysis: CO2 hydrogenation to methanol and reverse water-gas shift reactions

被引:0
|
作者
Wei Xiong
Zongfang Wu
Xuanye Chen
Jieqiong Ding
Aiai Ye
Wenhua Zhang
Weixin Huang
机构
[1] University of Science and Technology of China,Key Laboratory of Precision and Intelligent Chemistry, iChEM, Key Laboratory of Surface and Interface Chemistry and Energy Catalysis of Anhui Higher Education Institutes and School of Chemistry and Materials Sc
[2] University of Science and Technology of China,Hefei National Research Center for Physical Sciences at the Microscale
[3] Jiangxi Academy of Sciences,Research Institute of Applied Chemistry
来源
Science China Chemistry | 2024年 / 67卷
关键词
CO; hydrogenation; copper; zinc; reaction mechanisms; nanocrystals;
D O I
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中图分类号
学科分类号
摘要
Cu-ZnO-based catalysts are widely used to catalyze the CO2 hydrogenation to methanol and reverse water-gas shift (RWGS) reactions. Herein, via a combined experimental and theoretical calculation study of various Cu nanocrystals (NCs) with well-defined Cu facets and corresponding ZnO/Cu NC inverse catalysts, we demonstrate the Cu{110} facets as the most active facet for ZnO-Cu interfacial catalysis in the CO2 hydrogenation to methanol with an apparent activation energy as low as 25.3±3 kJ mol−1 and the Cu{100} facets as the most active facet for both ZnO-Cu interfacial catalysis and Cu catalysis in the RWGS reaction. Although the ZnO-Cu interface is more active in catalyzing the RWGS reaction than the Cu surface, the RWGS reaction occurs mainly on the bare Cu surface of ZnO/Cu inverse catalysts under the CO2 hydrogenation to methanol instead of that at the ZnO-Cu interface. This fundamental understanding will greatly help to fabricate efficient Cu-ZnO-based catalysts for the CO2 hydrogenation to methanol.
引用
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页码:715 / 723
页数:8
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