Review-Non-Noble Metal-Based Single-Atom Catalysts for Efficient Electrochemical CO2 Reduction Reaction

被引:26
|
作者
Choi, Hyeonuk [1 ,2 ,3 ]
Lee, Dong-Kyu [1 ,2 ,3 ]
Han, Mi-Kyung [1 ,2 ,3 ]
Janani, Gnanaprakasam [1 ,2 ,3 ]
Surendran, Subramani [1 ,2 ,3 ]
Kim, Jin Hyeok [1 ,2 ]
Kim, Jung Kyu [4 ]
Cho, Hoonsung [1 ]
Sim, Uk [1 ,2 ,3 ]
机构
[1] Chonnam Natl Univ, Engn Res Ctr, Dept Mat Sci & Engn, Gwangju 61186, South Korea
[2] Chonnam Natl Univ, Optoelect Convergence Res Ctr, Gwangju 61186, South Korea
[3] Chonnam Natl Univ, Coll AI Convergence, Future Energy Engn Convergence, Gwangju 61186, South Korea
[4] Sungkyunkwan Univ SKKU, Sch Chem Engn, Suwon 16419, South Korea
基金
新加坡国家研究基金会;
关键词
ELECTROCATALYTIC REDUCTION; ACTIVE-CENTERS; CARBON-DIOXIDE; ELECTROREDUCTION; SITES; IRON; SELECTIVITY; AMMONIA; LAYER; SHELL;
D O I
10.1149/1945-7111/abc593
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Single-atom catalysts (SACs), as the name suggests, indicate that only one element participates in the catalytic reaction. The characteristic feature of SACs is that it has immobilized active sites with specific properties, such as unexpected catalytic activity, high product selectivity, and reduced energy barrier. SACs for electrochemical CO2 reduction reactions (CO2RR) should have isolated metal atoms acting as active sites to maximize the efficiency of metal use. Conventional metal catalysts with nano-sized metal particles, however, contain a variety of inactive sites showing inferior efficiency of metal use. Therefore, systematic synthesis and analysis of high-efficiency SACs have been an interesting challenge in the CO2RR. To address these issues, many researchers have attempted to synthesize SACs through various methods and employed numerous characterization techniques to identify single atoms and their electrochemical properties. In this review, we discuss recent trends in the synthesis strategies and analyzing techniques of SACs and explain the influence of SACs on electrochemical CO2RR mechanisms of various C1 and C2 products.
引用
收藏
页数:21
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