MOF-derived V-CoxP@NC nanoarchitectures for highly enhanced electrocatalytic water splitting through electronical tuning

被引:32
作者
Guo, Wan Hui [1 ]
Zhang, Qing [1 ]
Wang, Xiao Hu [1 ]
Yang, Yu Xian [1 ]
Li, Xiao Lin [1 ]
Li, Ling Jie [2 ]
Luo, Hong Qun [1 ]
Li, Nian Bing [1 ]
机构
[1] Southwest Univ, Sch Chem & Chem Engn, Chongqing 400715, Peoples R China
[2] Chongqing Univ, Sch Chem & Chem Engn, Chongqing 400044, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal phosphides; Electrocatalysts; Vanadium doping; Water splitting; HYDROGEN EVOLUTION REACTION; BIFUNCTIONAL ELECTROCATALYSTS; ROBUST ELECTROCATALYST; DOPED COP; ONE-STEP; EFFICIENT; PHOSPHIDE; CARBON; NANOSHEETS; CO2P;
D O I
10.1016/j.electacta.2020.136850
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Achieving overall water splitting in the same electrolyte remains a challenge for a cost-effective and durable bifunctional catalyst. Doping foreign element into intrinsic materials is an effective way to enhance the electrocatalytic activity, thus we design a facile method to synthesize a novel vanadium doped mixture of CoP and Co2P nanoparticles encapsulated in zeolitic imidazolate framework-67 (ZIF-67) derived nitrogen doped carbon (V-CoxP@NC NPs) in this work for the first time. Benefiting from the protection of carbon shell and regulation of electronic structure through doping vanadium and phase-mixing CoP and Co2P, the V-CoxP@NC NPs show excellent electrocatalytic performance in both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in 1.0 M KOH. Using V-CoxP@NC NPs to construct overall water splitting (OWS) device, the electrolyzer achieves the current density of 10 mA cm(-2) with a small cell voltage of 1.54 V, exhibiting remarkable activity and continuous work for 20 h without obvious fluctuation. (C) 2020 Elsevier Ltd. All rights reserved.
引用
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页数:9
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