Electrodeposition synthesis of cobalt-molybdenum bimetallic phosphide on nickel foam for efficient water splitting

被引:23
作者
Guo, Desheng [1 ]
Wen, Lingling [1 ]
Wang, Tiantian [1 ]
Li, Xin [1 ]
机构
[1] Harbin Inst Technol, Sch Chem & Chem Engn, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
关键词
Transition metal phosphides; Electrodeposition; Heterogeneous interface; Synergistic effect; Water splitting; OXYGEN EVOLUTION; HYDROGEN EVOLUTION; ELECTROCATALYST; CATALYST; DESIGN; ARRAYS; PERFORMANCE; FABRICATION; LAYER;
D O I
10.1016/j.jcis.2023.09.173
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
A reasonable design of excellent bifunctional catalyst is an effective strategy for large-scale hydrogen production. In this study, a two-stage electrodeposition method was used to prepare a crystalline-amorphous structure cobalt molybdenum phosphide layered particles with different sizes on a nickel foam (NF) substrate. Electron rearrangement at the Co/CoMoP2@CoMoO4 heterogeneous interface can reduce the reaction energy barrier for HER and OER, and accelerate the catalytic reaction kinetics. The doping of Mo can promote the synergistic effect between Co and Mo, thereby optimizing the Gibbs free energy of hydrogen adsorption/desorption. This layered arrangement of different size particles greatly improves the active area of the catalyst. In alkaline solution, achieving a current density of 10 mA cm-2 only required overpotentials of 40 mV for HER and 278 mV for OER, respectively. The cell voltage required for the CoMo-P/NF||CoMo-P/NF electrolytic cell is only 1.53 V at 10 mA cm-2. This study provides a reference for the rapid, efficient, and environmentally friendly preparation of highactivity water splitting catalysts with large surface areas.
引用
收藏
页码:707 / 717
页数:11
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