Interface and composition engineering of vanadium doped cobalt nickel sulfide/phosphide heterostructure for efficient water splitting

被引:22
|
作者
Suo, Na [1 ]
Dou, Zhiyu [1 ]
Cui, Lili [1 ]
机构
[1] Changchun Univ Sci & Technol, Sch Chem & Environm Engn, Key Lab Appl Chem & Nanotechnol Univ Jilin Prov, Changchun 130022, Peoples R China
基金
中国博士后科学基金;
关键词
Heterostructure; Transition metal dichalcogenides; Transition metal phosphides; Overall water splitting; HIGHLY EFFICIENT; NANOSHEET ARRAY; ELECTROCATALYST; HYDROGEN; CARBON; OXIDATION; CONSTRUCTION; CATALYST;
D O I
10.1016/j.electacta.2020.137602
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Developing efficient and robust non-noble electrocatalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is desirable for future green energy systems of electrochemical water splitting technology. Thus, the vanadium doped cobalt nickel sulfide/phosphide heterostructure catalyst supported on nickel foam (V-CNS/P/NF) is fabricated by sulfidation reaction, followed by phosphorization from the layer double hydroxide (LDH) precursor. After V doping, the peak position of Ni and Co shifts negatively. Simultaneously, it is noted that the introduction of V into CNS/P can result in the enhanced electrochemical surface area and improved conductivity of CNS/P. Importantly, the optimal electrocatalyst of V-CNS/P/N exhibits excellent performance in alkaline condition with small overpotentials of 38 mV and 210 mV to achieve 10 mA cm(-2) for HER and OER, respectively. Remarkably, V-CNS/P/NF needs lower overpotential than that of Pt/C to reach higher current density of 500 mA cm(-2). A two-electrode system both assembled by as-prepared V-CNS/P/NF for electrochemical water splitting requires a cell voltage of 1.56 V to reach 10 mA cm(-2) . (C) 2020 Elsevier Ltd. All rights reserved.
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页数:10
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