催化作用
化学
电化学
原位
铜
还原(数学)
金属
傅里叶变换红外光谱
残余物
化学工程
碳纤维
过渡金属
曲面重建
选择性
无机化学
反应机理
电化学能量转换
电极
反应中间体
红外线的
红外光谱学
傅里叶变换
双金属片
循环伏安法
化石燃料
盐(化学)
作者
Qunmei Zhang,Haiyan Zhu,Tingjie Mao,Mengxiao Yan,Shun Wang,Xiaofang Song,Juan Wang,Huile Jin
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2026-02-19
卷期号:65 (8): 4650-4657
被引量:3
标识
DOI:10.1021/acs.inorgchem.5c05879
摘要
Electrochemical CO 2 reduction reaction (CO 2 RR), which enables the directional conversion of CO 2 into high-value-added fuels and chemicals, has emerged as a highly promising cutting-edge approach to mitigating fossil fuel consumption and curbing carbon emissions. Copper (Cu)-based catalysts have been extensively studied in the CO 2 RR, yet the in situ reconstruction mechanism of the catalysts remains an overlooked critical aspect. In this study, we employed diverse metal salt precursors to synthesize CuO catalysts, aiming to investigate the influence of residual elements on the surface reconstruction of catalysts during the CO 2 RR. Furthermore, with the aid of in situ Fourier transform infrared (FTIR) spectroscopy, the key intermediates in the CH 4 formation pathway (*CH 2 O) and the characteristic intermediate in the C 2 H 4 generation pathway (*OCCHO) were successfully captured, thereby elucidating the impact of residual elements on the CO 2 RR pathways. This study provides in-depth insights into catalyst surface reconstruction and offers effective strategies for the design of CO 2 RR catalysts.
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