Charge-asymmetry Fe1Cu single-atom alloy catalyst for efficient oxygen reduction reaction

被引:23
作者
Niu, Xudong [1 ]
Wei, Jian [2 ]
Xu, Dongyao [1 ]
Pei, Jiajing [3 ]
Sui, Rui [4 ]
机构
[1] China Univ Min & Technol, Sch Chem & Environm Engn, Beijing 100083, Peoples R China
[2] Chinese Res Inst Environm Sci, Inst Water Ecol & Environm, Beijing 100083, Peoples R China
[3] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
[4] Tsinghua Univ, Dept Chem, Engn Res Ctr Adv Rare Earth Mat, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Fe1Cu single-atom alloy (SAA); electrocatalysis; oxygen reduction reaction; charge-asymmetry; CU NANOPARTICLES; CARBON; COPPER; SITES; PERFORMANCE;
D O I
10.1007/s12274-023-6317-3
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
The development of high-efficient and low-cost oxygen reduction reaction (ORR) electrocatalysts is crucial for the practical applications of metal-air batteries. One promising way is to develop Fe single-atom catalysts. However, the single active center and inherent electronic structure of Fe single-atom catalysts lead to the undesirable adsorption of multiple ORR intermediates. Herein, a charge-asymmetry single-atom alloy (SAA) catalyst with Fe-Cu dual sites supported on nitrogen-doped carbon nanosheet (Fe1Cu SAA/NC) was constructed. Various characterizations manifest the existence of electron interaction between Fe and Cu in Fe1Cu SAA/NC, which facilitates the adsorption of ORR intermediate for fast kinetics. Consequently, the charge-asymmetry Fe1Cu SAA/NC exhibits much faster ORR kinetics with a half-wave potential of 0.917 V vs. reversible hydrogen electrode (RHE), outperforming its counterparts in the references. Furthermore, Fe1Cu SAA/NC still maintains a high half-wave potential with only a drop of 5 mV after 5000 cycles, indicating excellent stability. This work provides a new strategy to design highly active and non-noble metal ORR electrocatalysts, which hold great potential for various catalytic applications.
引用
收藏
页码:4702 / 4710
页数:9
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