NiFe-LDH@Ni3S2 supported on nickel foam as highly active electrocatalysts for oxygen evolution reaction

被引:18
作者
Fauzi, Akhmat [1 ,2 ]
Geng, Shuo [2 ]
Tian, Fenyang [2 ]
Liu, Yequn [3 ]
Li, Haibo [1 ]
Yu, Yongsheng [1 ]
Li, Jiaming [1 ]
Yang, Weiwei [2 ]
机构
[1] Jilin Normal Univ, Key Lab Funct Mat Phys & Chem, Minist Educ, Changchun 130103, Jilin, Peoples R China
[2] Harbin Inst Technol, Sch Chem & Chem Engn, MIIT Key Lab Crit Mat Technol New Energy Convers &, Harbin 150001, Heilongjiang, Peoples R China
[3] Chinese Acad Sci, Inst Coal Chem, Analyt Instrumentat Ctr, State Key Lab Coal Convers, Taiyuan 030001, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrocatalyst; Oxygen evolution reaction; Water splitting; SURFACE-AREA; EFFICIENT ELECTROCATALYST; HYDROGEN; NI3S2; ELECTROLYSIS; CATALYST; FILMS;
D O I
10.1016/j.ijhydene.2022.09.305
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Interface engineering is an efficient strategy for synthesis of high efficiency catalysts which can combine the advantages of each part for improving the catalytic activity. Herein, we fabricate the heterostructure NiFe-LDH@Ni3S2 by interface engineering through a simple hydrothermal combined with electrodeposition method. Combining the high conductivity of Ni3S2 and high intrinsic OER activity of NiFe-LDH at the interface, the NiFe-LDH@Ni3S2 electrode exhibits a relatively low overpotential of 240 mV for OER at a current density of 200 mA cm-2 which is lower than NiFe-LDH and Ni3S2. In addition, the overall water splitting unit provides a potential of 1.47 V at 10 mA cm-2. Furthermore, after 24 h of electrolysis in 1.0 M KOH, the current density remains 98% of the original value. This work paves a new way for synthesis of more heterostructure catalysts.(c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1370 / 1379
页数:10
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