Optimizing C―C Coupling on Cu0/Cu+/Ga Interfaces by Enhancing Active Hydrogen Absorption for Excellent CO2-to-C2+ Electrosynthesis

被引:0
|
作者
Qi, Xiaoshuang [1 ,2 ]
Yang, Yikai [2 ]
Lan, Yupeng [3 ]
Bu, Xiuming [2 ]
Yang, Siwei [3 ]
Yin, Di [4 ]
Huang, Hongwen [1 ]
Ho, Johnny C. [4 ]
Wang, Xianying [2 ]
机构
[1] Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Ceram, CAS Key Lab Mat Energy Convers, Shanghai 200050, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Microsyst & Informat Technol, State Key Lab Mat Integrated Circuits, Shanghai 200050, Peoples R China
[4] City Univ Hong Kong, Dept Mat Sci & Engn, Hong Kong 999077, Peoples R China
关键词
asymmetric coupling; Cu+/Cu-0; electrocatalytic CO2 reduction; ethylene; SELECTIVE PRODUCTION; CO2; ETHYLENE;
D O I
10.1002/smll.202500538
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electrocatalytic reduction of CO2 (CO2RR) to high-value chemicals and fuels offers a promising route for a clean carbon cycle. However, it often suffers from low catalytic activity and poor selectivity. Heterostructure construction has been shown to be an effective strategy for producing multi-carbon products, but the synergistic mechanisms between multiple active sites resulting from the reconstruction process remain unclear. In this study, a Ga2O3/CuO heterostructure is established via a simple sol-gel method to produce C2+ products. Experimental results demonstrate that Ga2O3 stabilizes Cu+ to form Cu-0/Cu+/Ga active centers and enhances water-splitting ability during the reaction. The improved hydrogen absorption on the Ga site shifts the C & horbar;C coupling reaction pathway from *OCCO to the asymmetric *OCCHO coupling path with a lower energy barrier. As a result, the catalysts exhibit superior CO2RR performance, achieving a 70.1% C2+ Faradaic efficiency at -1.2 V-RHE in a flow cell, with ethylene Faradaic efficiency reaching 58.3% and remaining stable for 10 h.
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页数:8
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