Electronic Metal-Support Interactions Between CuxO and ZnO for CuxO/ZnO Catalysts With Enhanced CO Oxidation Activity

被引:9
作者
Lyu, Shuai [1 ,2 ]
Zhang, Yuhua [1 ,2 ]
Li, Zhe [1 ,2 ]
Liu, Xinyue [1 ,2 ]
Tian, Zhenfang [3 ]
Liu, Chengchao [1 ,2 ]
Li, Jinlin [1 ,2 ]
Wang, Li [1 ,2 ]
机构
[1] South Cent Minzu Univ, Key Lab Catalysis, Energy Mat Chem, Minist Educ, Wuhan, Peoples R China
[2] South Cent Minzu Univ, Hubei Key Lab Catalysis & Mat Sci, Wuhan, Peoples R China
[3] Huanggang Normal Univ, Hubei Key Lab Proc & Applicat Catalyt Mat, Huanggang, Peoples R China
基金
中国国家自然科学基金;
关键词
metal-support interactions; Cu species; CO oxidation; ZnO; supported catalysts; CARBON-MONOXIDE OXIDATION; FISCHER-TROPSCH SYNTHESIS; ZINC OXIDE CATALYSTS; METHANOL SYNTHESIS; CU/ZNO CATALYSTS; HYDROGENATION; COPPER; NANOPARTICLES; PERFORMANCE; BEHAVIOR;
D O I
10.3389/fchem.2022.912550
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal-support interaction has been one of the main topics of research on supported catalysts all the time. However, many other factors including the particle size, shape and chemical composition can have significant influences on the catalytic performance when considering the role of metal-support interaction. Herein, we have designed a series of CuxO/ZnO catalysts as examples to quantitatively investigate how the metal-support interaction influences the catalytic performance. The electronic metal-support interactions between CuxO and ZnO were regulated successfully without altering the structure of CuxO/ZnO catalyst. Due to the lower work function of ZnO, electrons would transfer from ZnO to CuO, which is favorable for the formation of higher active Cu species. Combined experimental and theoretical calculations revealed that electron-rich interface result from interaction was favorable for the adsorption of oxygen and CO oxidation reaction. Such strategy represents a new direction to boost the catalytic activity of supported catalysts in various applications.
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页数:12
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