催化作用
电解质
吸附
介孔材料
氧还原反应
活动站点
化学
化学工程
材料科学
曲率
Atom(片上系统)
无机化学
氧气
组合化学
物理化学
电极
电化学
有机化学
几何学
数学
计算机科学
工程类
嵌入式系统
作者
Jingjing Li,Wei Xia,Yanna Guo,Ruijuan Qi,Xingtao Xu,Dong Jiang,Tao Wang,Yoshiyuki Sugahara,Jianping He,Yusuke Yamauchi
标识
DOI:10.1016/j.cej.2023.146841
摘要
Iron-based single-atom catalysts (Fe-SACs) containing Fe–N4 active sites have shown immense potential in the oxygen reduction reaction (ORR). However, the limited ability to adsorb O2 and catalyze subsequent O–O bond breaking on Fe–N4 sites has hindered their full potential, especially in acidic electrolytes. Here, we present an approach by utilizing a tunable curved surface to enhance the activity of Fe–N4 active sites, with theoretical calculations, demonstrating that Fe–N4 sites anchored on low–curvature surfaces (lc-Fe-N4) is favirable for ORR. Experimental results show that the catalyst exhibits excellent catalytic activity and stability for ORR in acidic electrolytes, with a half-wave potential of 0.82 V vs. RHE, approaching that of commercial Pt/C. This work develops an approach for promoting the catalytic activity by anchoring atomically dispersed Fe–N4 sites, unlocking their potential for extended use in electrocatalytic and energy storage applications.
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