Cu2S/Ni3S2 ultrathin nanosheets on Ni foam as a highly efficient electrocatalyst for oxygen evolution reaction

被引:17
|
作者
Tang, Mengyi [1 ]
Liu, Yu [1 ]
Cao, Heng [1 ]
Zheng, Qiaoji [1 ]
Wei, Xijun [2 ]
Lam, Kwok Ho [3 ]
Lin, Dunmin [1 ]
机构
[1] Sichuan Normal Univ, Coll Chem & Mat Sci, Chengdu 610066, Peoples R China
[2] Southwest Univ Sci & Technol, Sch Mat Sci & Engn, State Key Lab Environm Friendly Energy Mat, Mianyang 621010, Sichuan, Peoples R China
[3] Hong Kong Polytech Univ, Dept Elect Engn, Hung Hom, Kowloon, Hong Kong 999077, Peoples R China
关键词
Cu2S/Ni3S2; Nano sheets; Non-noble metal catalysts; Oxygen evolution reaction; FACILE SYNTHESIS; BIFUNCTIONAL ELECTROCATALYST; HIGH-PERFORMANCE; WATER; ELECTRODES; NANOTUBES; ARRAYS; CONSTRUCTION; HYDROXIDE; CARBON;
D O I
10.1016/j.ijhydene.2021.10.244
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
It is an inevitable choice to find efficient and economically-friendly electrocatalysts to reduce the high overpotential of oxygen evolution reaction (OER), which is the key to improve the energy conversion efficiency of water splitting. Herein, we synthesized Cu2S/Ni3S2 catalysts on nickel foam (NF) with different molar ratios of Ni/Cu by a simple two-step hydrothermal method. Cu2S/Ni3S2-0.5@NF (CS/NS-0.5@NF) effectively reduces the overpotential of OER, displaying small overpotentials (237 mV@100 mA cm(-2) and 280 mV@500 mA cm(-2)) in an alkaline solution, along with a low Tafel slope of 44 mV dec CS/NS-0.5@NF also presents an excellent durability at a relatively high current density of 100 mA cm(-2) for 100 h. The excellent performance is benefited by the prominent structural advantages and desirable compositions. The nanosheet has a high electrochemical active surface area and the porous structure is conducive to electrolyte penetration and product release. This work provides an economically-friendly Cu-based sulfide catalyst for effective electrosynthesis of OER. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3013 / 3021
页数:9
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