铜
材料科学
乙醇
钴
无机化学
核化学
化学工程
化学
有机化学
工程类
冶金
作者
Zi Yang,Deguang Ji,Zhi Li,Zidong He,Yang Hu,Jie Yin,Yichao Hou,Pinxian Xi,Chun‐Hua Yan
出处
期刊:Small
[Wiley]
日期:2023-06-03
卷期号:19 (40): e2303099-e2303099
被引量:67
标识
DOI:10.1002/smll.202303099
摘要
Abstract Copper‐based electrocatalysts effectively produce multicarbon (C 2+ ) compounds during the electrochemical CO 2 reduction (CO 2 RR). However, big challenges still remain because of the chemically unstable active sites. Here, cerium is used as a self‐sacrificing agent to stabilize the Cu + of CuS, due to the facile Ce 3+ /Ce 4+ redox. CeO 2 ‐modified CuS nanoplates achieve high ethanol selectivity, with FE up to 54% and FE C2+ ≈ 75% in a flow cell. Moreover, in situ Raman spectroscopy and in situ Fourier‐transform infrared spectroscopy indicate that the stable Cu + species promote CC coupling step under CO 2 RR. Density functional theory calculations further reveal that the stronger * CO adsorption and lower CC coupling energy, which is conducive to the selective generation of ethanol products. This work provides a facile strategy to convert CO 2 into ethanol by retaining Cu + species.
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