不对称
催化作用
氧还原反应
合金
电荷(物理)
Atom(片上系统)
氧气
材料科学
氧原子
还原(数学)
化学
光化学
冶金
物理化学
物理
电化学
电极
分子
有机化学
计算机科学
几何学
数学
量子力学
嵌入式系统
作者
Xudong Niu,Jian Wei,Dongyao Xu,Jiajing Pei,Rui Sui
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2024-02-23
卷期号:17 (6): 4702-4710
被引量:39
标识
DOI:10.1007/s12274-023-6317-3
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.
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