Nickel-manganese bimetallic phosphides porous nanosheet arrays as highly active bifunctional hydrogen and oxygen evolution electrocatalysts for overall water splitting

被引:47
|
作者
Jiang, Deli [1 ]
Ma, Wanxia [1 ]
Yang, Rong [1 ]
Quan, Biao [1 ]
Li, Di [2 ]
Meng, Suci [1 ]
Chen, Min [1 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Xuefu Rd 301, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Jiangsu Univ, Inst Energy Res, Xuefu Rd 301, Zhenjiang 212013, Jiangsu, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Bimetal phosphides; Porous nanosheet arrays; Electronic interaction; Water splitting; NANOWIRE ARRAYS; GENERATING HYDROGEN; LDH NANOSHEET; EFFICIENT; CATALYST; NANOPARTICLES; ALKALINE; ELECTROLYSIS; CATHODE;
D O I
10.1016/j.electacta.2019.135121
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The development of active, stable, and cost-effective overall water splitting catalysts consisting of earth-abundant materials is of paramount importance for renewable energy production. Herein, we demonstrate the synthesis of bimetallic nickel manganese phosphide porous nanosheet arrays (PNAs) grown on 3D Ni foam (Ni-Mn-P PNAs). Benefiting from the typical 3D PNAs structure and electronic interaction between Ni and Mn, the optimal Ni2Mn1P PNAs shows small overpotentials of 80 and 120 mV to reach 10 mA cm(-2) for hydrogen evolution reaction in acidic and alkaline media, respectively. The Ni-Mn-P PNAs also shows a high activity toward oxygen evolution reaction in the alkaline media with a low overpotential of 250 mV to drive 20 mA cm(-2). The Ni-Mn-P PNAs-based overall water splitting can achieve a current density of 10 mA cm(-2) at a low cell voltage of 1.6 V and excellent durability in alkaline solution, outperforming the benchmark Ir/C||Pt/C electrolyzer. This work highlights the formation of Mn-containing ternary metal phosphides PNAs structure as highly active and stable bifunctional electrocatalysts for overall water splitting. (C) 2019 Elsevier Ltd. All rights reserved.
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页数:8
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