In situ growth of iron-nickel nitrides on carbon nanotubes with enhanced stability and activity for oxygen evolution reaction

被引:42
作者
Chen, Xu [1 ]
Gao, Pengfei [2 ]
Liu, Huan [1 ]
Xu, Jingjing [1 ]
Zhang, Bo [1 ]
Zhang, Yang [2 ]
Tang, Yuhai [1 ]
Xiao, Chunhui [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Sci, Dept Appl Chem, Xian 710049, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Sci, Dept Appl Phys, Xian 710049, Shaanxi, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Oxygen evolution reaction; Powdery catalyst; Iron-nickel nitride; CNTs; Galvanic replacement; ELECTRONIC-STRUCTURE; EFFICIENT CATALYST; ELECTROCATALYSTS; NANOSHEETS; OXIDATION; ARRAY; FOAM; XPS; IRIDIUM; OER;
D O I
10.1016/j.electacta.2018.01.192
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The efficiency of energy storage technologies such as water splitting and metal-air batteries is limited by the sluggish dynamics of the oxygen evolution reaction (OER). Herein, we report a galvanic replacement-mediated method for in-situ growth of iron-nickel nitride on carbon nanotubes (CNTs) as a powdery catalyst for OER. This in-situ grown structure creates intimate interaction between the active substance of Fe2Ni2N and CNTs so as to accelerate charge transfer in the catalytical interface. First-principles calculations reveal that the Fe2Ni2N is intrinsically metallic, and the contribution mainly derives from the Fe atoms at corner sites of crystal structures. A good synergistic effect between metallic Fe2Ni2N with excellent intrinsic activity and conductive CNTs lead to outstanding electrochemical performance with a low overpotential (eta(10) (mAcm-2) = 282 mV) and Tafel slope (38 mV dec(-1)), as well as good long-term stability. (c) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:8 / 14
页数:7
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