光催化
铜
电化学
材料科学
氧化还原
选择性
吸收(声学)
化学工程
价(化学)
光化学
可见光谱
氧化物
氧化铜
密度泛函理论
催化作用
电极
光电子学
化学
复合材料
物理化学
有机化学
冶金
计算化学
工程类
作者
Yuting Yin,Wenhao Jing,Feng Wang,Ya Liu,Liejin Guo
出处
期刊:Carbon
[Elsevier BV]
日期:2023-07-25
卷期号:214: 118317-118317
被引量:16
标识
DOI:10.1016/j.carbon.2023.118317
摘要
Coupling light absorber with an efficient cocatalyst is the most common way to fabricate composite photocatalyst. The light absorber supplies electrons and holes, while the cocatalyst domains chemical reactions. Inspired by the results from electrochemical CO2 reduction, Cu-based materials are the most promising cocatalysts for photocatalytic CO2 reduction. However, oxide-derived copper (OD-Cu) hasn't been introduced into photocatalytic systems yet, due to easily undergoing valence changes once exposed to air. Herein, we find that OD-Cu could be decorated on photocatalyst, polymeric C3N4 (PCN), by a self-designed in-situ electroreduction method. The as-prepared OD-Cu/PCN presents better visible light absorption than the one without in-situ electroreduction and prefers multi-carbon products. According to CO2RR measurements, the highest selectivity to C2H5OH is 58%. Density functional theory calculation further indicates that the unique structure between OD-Cu and PCN leads to a low energy barrier of C–C coupling due to the enhanced *CO dimerization and thus promotes the production of C2H5OH. Moreover, this optimized sample achieves a solar-to-fuel efficiency, of up to 0.94%, which is 1.69 times the pristine PCN.
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