Oxygen vacancies engineered CoMoO4 nanosheet arrays as efficient bifunctional electrocatalysts for overall water splitting

被引:89
|
作者
Chi, Kai [1 ]
Tian, Xin [1 ]
Wang, Qijun [1 ]
Zhang, Zheye [1 ]
Zhang, Xiangyu [1 ]
Zhang, Yan [1 ]
Jing, Feng [1 ]
Lv, Qiying [1 ]
Yao, Wei [2 ]
Xia, Fei [1 ,2 ]
Wang, Shua [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Key Lab Mat Chem Energy Convers & Storage, State Key Lab Digital Mfg Equipment & Technol, Sch Chem & Chem Engn,Minist Educ,FERC,Sch Mech Sc, Wuhan 430074, Peoples R China
[2] Shenzhen Huazhong Univ Sci & Technol, Res Inst, Shenzhen 518000, Peoples R China
关键词
Oxygen vacancy; Cobalt molybdate; Nanosheet arrays; Bifunctional electrocatalysts; Water electrolysis; LAYERED DOUBLE HYDROXIDE; HYDROGEN-EVOLUTION; NICKEL FOAM; NANOWIRE ARRAYS; ELECTRODE; CATALYSTS; GRAPHENE; CARBON; CO; NANOPARTICLES;
D O I
10.1016/j.jcat.2019.10.025
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
The development of highly efficient, stable and earth-abundant bifunctional electrocatalysts for water splitting is of great significance for confronting the environmental and energy crisis. In this work, we reported the design and synthesis of oxygen vacancies engineered CoMoO4 nanosheet arrays grown on three-dimension (3D) porous Ni foam (NF) support by hydrothermal synthesis followed by reducing gas heat treatment used H-2 or NH3, and explored their practical application as bifunctional electrocatalysts for water splitting. The unique 3D nanosheet array can facilitate the interfacial electron transfer and ion transport, as well as promote hydrogen and oxygen gas diffusion, and the formation of oxygen vacancies in CoMoO4 nanosheets can significantly improve efficiency of both hydrogen evolution reaction and oxygen evolution reaction. When using as self-supported bifunctional electrocatalyst to make an electrolyzer, NF/H-CoMoO4 approached 10 mA cm(-2) under the cell voltages of 1.56 V, along with excellent durability in an alkaline water electrolyzer, which hold great promise in energy conversion application. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:44 / 52
页数:9
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