反键分子轨道
拉伤
催化作用
原子轨道
氧气
Atom(片上系统)
材料科学
部分
氧还原反应
化学
纳米技术
电子
结晶学
物理化学
物理
立体化学
有机化学
医学
生物化学
电极
量子力学
计算机科学
内科学
电化学
嵌入式系统
作者
Lingfeng Li,Jiaming Zhu,Fanpeng Kong,Li Wang,Cong Kang,Ming Xu,Chunyu Du,Geping Yin
出处
期刊:Matter
[Elsevier]
日期:2024-02-08
卷期号:7 (4): 1517-1532
被引量:12
标识
DOI:10.1016/j.matt.2024.01.019
摘要
Summary
Elucidating how the local strain environment of single atoms affects their impact on a sluggish acidic oxygen reduction reaction (ORR) is important for the design and construction of highly active electrocatalysts. Here, we report that the atomic strain geometry of Fe single sites is exclusively regulated by the communicative effects of dual atoms. Theoretical analysis reveals that Fe-Ru dual atoms in a moderate strain environment achieve the lowest Gibbs free energy barrier during an ORR. Impressively, FeRu-N-C with an FeRuN8 moiety exhibits the highest acidic ORR performance, with a half-wave potential (E1/2) of 0.860 V and only a 17-mV loss in E1/2 after 50,000 potential cycles. Operando characterization and electronic configuration analysis demonstrate that moderately strained Fe sites promote hydrogenation desorption of (oxy-)hydroxyl by enabling more electrons to occupy antibonding orbitals. This study describes a promising way of investigating high-performance single-atom-based catalysts by tailoring the atomic strain environment.
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