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 Cu0/Cu+/Ga active centers and enhances water-splitting ability during the reaction. The improved hydrogen absorption on the Ga site shifts the C─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 VRHE in a flow cell, with ethylene Faradaic efficiency reaching 58.3% and remaining stable for 10 h.
| 源语言 | 英语 |
|---|---|
| 文章编号 | 2500538 |
| 期刊 | Small |
| 卷 | 21 |
| 期 | 15 |
| DOI | |
| 出版状态 | 已出版 - 16 4月 2025 |
| 已对外发布 | 是 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
-
可持续发展目标 7 经济适用的清洁能源
指纹
探究 'Optimizing C─C Coupling on Cu0/Cu+/Ga Interfaces by Enhancing Active Hydrogen Absorption for Excellent CO2-to-C2+ Electrosynthesis' 的科研主题。它们共同构成独一无二的指纹。引用此
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver