Design strategy of a Cu-based catalyst for optimizing the performance in the electrochemical CO2 reduction reaction to multicarbon alcohols

被引:12
作者
Ni, Zhiyuan [1 ]
Wang, Peng [1 ,2 ]
Quan, Fan [1 ,2 ]
Guo, Rui [1 ,2 ]
Liu, Chunming [1 ]
Liu, Xuanwen [1 ]
Mu, Wenning [1 ,2 ]
Lei, Xuefei [1 ,2 ]
Li, Qingjun [3 ]
机构
[1] Northeastern Univ, Sch Mat Sci & Engn, Shenyang 110819, Peoples R China
[2] Northeastern Univ Qinhuangdao, Sch Resources & Mat, Key Lab Dielect & Electrolyte Funct Mat Hebei Pro, Qinhuangdao 066004, Hebei, Peoples R China
[3] Xusai Environm Technol Hebei Co Ltd, Qinhuangdao 066000, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
BOUNDARY-RICH COPPER; CARBON-DIOXIDE; ELECTROCATALYSTS; ELECTROREDUCTION; SELECTIVITY; CHALLENGES; CONVERSION; PATHWAYS; ETHYLENE;
D O I
10.1039/d2nr04826d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electrochemical CO2 reduction reaction (ECRR) is a promising method to reduce excessive CO2 emissions and achieve a sustainable carbon cycle. Due to the high reaction kinetics and efficiency, copper-based catalysts have shown great application potential for preparing multicarbon (C2+) products. C2+ alcohols have high economic value and use-value, playing an essential role in modern industry. Therefore, we summarize the latest research progress of the ECRR to synthesize C2+ alcohols on Cu-based catalysts and discuss the state-of-the-art catalyst design strategies to improve CO2 reduction performance. Moreover, we analyzed in detail the specific reaction pathways for the conversion of CO2 to C2+ alcohols based on DFT calculations. Finally, we propose the problems and possible solutions for synthesizing C2+ alcohols with copper-based catalysts. We hope that this review can provide ideas for devising ECRR catalysts for C2+ alcohols.
引用
收藏
页码:16376 / 16393
页数:18
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