Electrochemical interfaces during CO2 reduction on copper electrodes

被引:5
|
作者
Ligt, Bianca [1 ]
Hensen, Emiel J. M. [1 ]
Figueiredo, Marta Costa [1 ,2 ]
机构
[1] Eindhoven Univ Technol, Dept Chem Engn & Chem, Lab Inorgan Mat & Catalysis, Eindhoven, Netherlands
[2] Eindhoven Univ Technol, Eindhoven Inst Renewable Energy Syst EIRES, Eindhoven, Netherlands
基金
荷兰研究理事会;
关键词
CO2; electroreduction; Copper; Electrocatalysis; CARBON-DIOXIDE; ETHYLENE; CONVERSION; INSIGHTS; ELECTROREDUCTION; SELECTIVITY; PRESSURE; CATALYST; ALCOHOLS; ETHANOL;
D O I
10.1016/j.coelec.2023.101351
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Copper has received significant attention for decades as electrode material for the electrochemical reduction of carbon dioxide (CO2RR) because of its capability to form multi-carbon products (C2+). However, despite substantial research, CO2RR with Cu-based electrocatalysts has yet to be commercialized. Understanding the physical and chemical changes of the catalyst surface and the dynamics of the electrochemical interface during CO2RR is key to improve the activity and selectivity. This review article focuses on recent studies that provide important insights of the surfaces and interfaces during reduction using ex-situ, in-situ and operando characterization techniques.
引用
收藏
页数:8
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