Epoxidized Single-Atom Co-N-C Catalysts Promote the Oxygen Reduction Reaction via a Two-Electron Pathway

被引:2
|
作者
Wang, Qian [1 ,2 ,3 ]
Feng, Jingyu [1 ,2 ,3 ]
Yang, Tao [1 ,2 ,3 ]
Qin, Yao [1 ,2 ,3 ]
Xie, Jiacheng [1 ,2 ,3 ]
Wei, Zengxi [1 ,2 ,3 ]
Zhao, Shuangliang [1 ,2 ,3 ]
机构
[1] Guangxi Univ, State Key Lab Featured Met Mat & Lifecycle Safety, Nanning 530004, Peoples R China
[2] Guangxi Univ, Guangxi Key Lab Petrochem Resource Proc & Proc Int, Nanning 530004, Peoples R China
[3] Guangxi Univ, Sch Chem & Chem Engn, Nanning 530004, Peoples R China
基金
中国国家自然科学基金;
关键词
Co-N-C configuration; epoxy group; two-electron pathway; hydrogen peroxide; densityfunctional theory; HYDROGEN-PEROXIDE; ENERGY CALCULATIONS; H2O2; ELECTROCATALYSTS; WATER;
D O I
10.1021/acsami.4c17354
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Coordination structure and group modifications of single-atom catalysts are essential for regulating superficial electronic structures and reaction activities. Epoxy group-modified single-atom Co-N-C configuration demonstrates exceptional catalytic performance for hydrogen peroxide production. Through the manipulation of the coordination structure of Co-N-C and the doped epoxy groups, we elucidate the origin of catalytic activity in epoxygroup-modified Co-N-C configurations. Theoretical results indicate that the second coordination sphere of the Co-N-C structure is essential for the regulation of the two-electron pathway by the epoxy groups acting as cocatalysts. This cocatalytic mechanism originates from hydrogen bonding interactions between the epoxy groups and the OOH intermediates. Three epoxy groups within the second coordination sphere of Co-N-C configuration lead to the achievement of the optimal G *OOH (similar to 4.22 eV) for hydrogen peroxide production. This study offers novel insights into the design of catalytic materials for the electrosynthesis of hydrogen peroxide as well as the engineering of their surface structures.
引用
收藏
页码:68221 / 68228
页数:8
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