Dual-atom catalysts for oxygen electrocatalysis

被引:122
|
作者
Wang, Juan [1 ,2 ]
Zhao, Chang-Xin [3 ]
Liu, Jia-Ning [3 ]
Song, Yun-Wei [3 ]
Huang, Jia-Qi [1 ,2 ]
Li, Bo-Quan [1 ,2 ]
机构
[1] Beijing Inst Technol, Sch Mat Sci & Engn, Beijing 100081, Peoples R China
[2] Beijing Inst Technol, Adv Res Inst Multidisciplinary Sci, Beijing 100081, Peoples R China
[3] Tsinghua Univ, Dept Chem Engn, Beijing Key Lab Green Chem React Engn & Technol, Beijing 100084, Peoples R China
关键词
Dual -atom catalysts; Electrocatalysis; Oxygen reduction reaction; Oxygen evolution reaction; BIFUNCTIONAL AIR ELECTRODE; DENSITY-FUNCTIONAL THEORY; ATOMICALLY DISPERSED FE; METAL-SITE CATALYSTS; REDUCTION REACTION; DOPED CARBON; EVOLUTION REACTION; HYDROGEN-EVOLUTION; ACTIVE-SITES; EFFICIENT ELECTROCATALYST;
D O I
10.1016/j.nanoen.2022.107927
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
Oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) are involved in various electrochemical devices but are severely sluggish in kinetics. Dual-atom catalysts demonstrate unique advantages in terms of high intrinsic electrocatalytic activity, maximum atomic efficiency, high chemical diversity, and positive synergy between the dual atoms. As a result, dual-atom catalysts have attracted wide-spread attention as advanced ORR and OER electrocatalysts. This review systematically summarizes the current advances of dual-atom catalysts for ORR and OER electrocatalysis. The intrinsic advantages of dual-atom catalysts are first discussed following three proposed mechanisms focusing on the electronic structure of active sites. The structure-activity relationship is comprehensively discussed based on theoretical simulations and experimental results to afford a methodology for rational structural design. Following that, the current synthesis methods and a transverse performance com-parison are presented. Finally, several perspectives are highlighted for propelling the development of advanced dual-atom catalysts for ORR and OER electrocatalysis.
引用
收藏
页数:14
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