Sulfur-bridge ligands altering the microenvironment of single-atom CoN3S sites to boost the oxygen reduction reaction

被引:8
|
作者
Liu, Feng [1 ]
Guo, Yingchun [2 ]
Zhong, Yan [1 ]
Li, Jingsha [1 ]
Zhang, Heng [1 ]
Shi, Lei [3 ]
Lin, Xuanni [4 ]
Ye, Fenghui [4 ]
Ge, Kai [5 ]
Yuan, Shuai [6 ]
Hu, Chuangang [4 ]
Guo, Chunxian [1 ]
机构
[1] Suzhou Univ Sci & Technol, Inst Mat Sci & Devices, Sch Mat Sci & Engn, Suzhou 215009, Peoples R China
[2] Huzhou Univ, Dept Mat Engn, Huzhou 313000, Peoples R China
[3] CAS Ctr Excellence Nanosci, Natl Ctr Nanosci & Technol, CAS Key Lab Nanosyst & Hierarch Fabricat, Beijing 100190, Peoples R China
[4] Beijing Univ Chem Technol, Coll Chem Engn, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[5] Hebei Univ Technol, Inst Polymer Sci & Engn, Hebei Key Lab Funct Polymers, Tianjin 300130, Peoples R China
[6] Peking Univ, Sch Software & Microelect, Beijing 102600, Peoples R China
基金
中国国家自然科学基金;
关键词
IRON;
D O I
10.1039/d4cc00854e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report here an asymmetric N,S-coordinated cobalt-based single-atom catalyst with sulfur (S)-bridge ligands (Co-N/S-C) for the oxygen reduction reaction (ORR). The Co-N/S-C exhibits a half-wave potential (E-1/2) of 0.908 V versus RHE, outperforming most state-of-the-art ORR catalysts. Theoretical calculations indicate that the CoN3SC10-S moiety facilitates the ORR kinetics by optimizing the adsorption of intermediates. This work provides new insights into the design of single-atom catalysts for electrocatalysis through heteroatom-bridge ligand engineering.
引用
收藏
页码:4064 / 4067
页数:4
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