NiCoP coated on NiCo2S4 nanoarrays as electrode materials for hydrogen evolution reaction

被引:17
|
作者
Su, Hui [1 ]
Du, Xiaoqiang [2 ]
Zhang, Xiaoshuang [3 ]
机构
[1] North Univ China, Sch Environm & Safety, Taiyuan 030051, Shanxi, Peoples R China
[2] North Univ China, Sch Chem Engn & Technol, Taiyuan 030051, Shanxi, Peoples R China
[3] North Univ China, Sch Sci, Taiyuan 030051, Shanxi, Peoples R China
基金
美国国家科学基金会;
关键词
NiCo2S4@NiCoP; Electrocatalytic; Urea splitting; Nickel foam; Stability; EFFICIENT BIFUNCTIONAL ELECTROCATALYST; NICKEL FOAM; CONTROLLABLE SYNTHESIS; WATER OXIDATION; CONSTRUCTION; PERFORMANCE; ARRAYS; NANOSTRUCTURES; CONVERSION; NANOSHEETS;
D O I
10.1016/j.ijhydene.2019.10.046
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 very important to exploit robust electrocatalysts for the urea splitting in an alkaline medium. Hence, the NiCo2S4@NiCoP nanoarrays on Ni foam (NiCo2S4@NiCoP/NF) was successfully synthesized for the first time and used as an efficient and stable difunctional electrocatalyst for the overall urea splitting. As one of the most promising bifunctional electrocatalysts reported, NiCo2S4@NiCoP only needs 108 mV to reach current density of 10 mA cm(-2) for hydrogen evolution reaction. Moreover, such NiCo2S4@NiCoP//NiCo2S4@NiCoP electrodes couple display superior urea splitting performance with the requirement of a cell voltage of 1.53 V to drive a catalytic current density of 10 mA cm(-2). In addition, the NiCo2S4@NiCoP material presents high long-term electrocatalytic stability keeping its performance at 11 mA cm(-2) for 12 h. The experimental results demonstrate that the sluggish Volmer step has been improved by incorporating the NiCoP to the NiCo2S4. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:30910 / 30916
页数:7
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