Proximity defect inductive effect of atomic Ni-N3 sites by Te atoms doping for efficient oxygen reduction and hydrogen evolution

被引:0
|
作者
Li, Min [1 ]
Zheng, Xiuhui [1 ]
Guo, Han [1 ]
Feng, Xiang [1 ]
Liu, Yunqi [1 ]
Pan, Yuan [1 ]
机构
[1] China Univ Petr East China, State Key Lab Heavy Oil Proc, Qingdao 266580, Shandong, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Proximity defect engineering; Single atom catalyst; Heteroatom doping; Oxygen reduction reaction; Hydrogen evolution reaction; TRANSITION;
D O I
10.1016/j.jechem.2025.03.003
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The development of single atom catalysts (SACs) with asymmetric active sites by defect regulation provides an encourage potential for oxygen reduction reaction (ORR) and hydrogen evolution reaction (HER), but highly challenging. Herein, N-doped carbon (N-C) anchored atomically dispersed Ni-N3 site with proximity defects (Ni-N3D) induced by Te atoms doping is reported. Benefitting from the inductive effect of proximity defect, the Ni-N3D/Te-N-C catalyst performs excellent ORR and HER performance in alkaline and acid condition. Both in situ characterization and theoretical calculation reveal that the existence of proximity defect effect is conducive to lower rate-determining-step energy barrier of ORR and HER, thus accelerating the multielectron reaction kinetics. This work paves a novel strategy for constructing highactivity bifunctional SACs by defect engineering for development of sustainable energy. (c) 2025 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
引用
收藏
页码:446 / 454
页数:9
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