Mo-decorated cobalt phosphide nanoarrays as bifunctional electrocatalysts for efficient overall water/seawater splitting

被引:68
|
作者
Yu, Y. [1 ]
Li, J. [1 ]
Luo, J. [1 ]
Kang, Z. [1 ]
Jia, C. [1 ]
Liu, Z. [1 ]
Huang, W. [1 ]
Chen, Q. [1 ]
Deng, P. [1 ]
Shen, Y. [1 ]
Tian, X. [1 ]
机构
[1] Hainan Univ, State Key Lab Marine Resource Utilizat South Chin, Hainan Prov Key Lab Fine Chem, Sch Chem Engn & Technol, Haikou 570228, Hainan, Peoples R China
基金
中国国家自然科学基金; 海南省自然科学基金;
关键词
Transition metal phosphides; Bifunctional electrocatalysts; Overall seawater splitting; Synergistic effect; Corrosion resistance; HYDROGEN EVOLUTION; SURFACE;
D O I
10.1016/j.mtnano.2022.100216
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Transition metal phosphides (TMPs) are emerging as the indispensable electrocatalysts for overall water/seawater splitting, while there are ongoing challenges resulting from the poor catalytic activity and low stability, especially the electrode corrosion caused by the side reactions of chloride evolution reaction (ClER). Herein, Mo-decorated CoPX nanoarrays on nickel foam (Mo-CoPX/NF) is prepared by an in situ hydrothermal-phosphorylation method. Profiting from the unique self-supported nanoarrays, plenty of bimetallic active sites, and high conductivity, Mo-CoPX/NF nanosheet arrays show low overpotential as bifunctional electrocatalyst in water/seawater electrolytes. The Mo-CoPX/NF parallel to Mo-CoPX/NF pair only needs 1.49 and 2.01 V to drive an overall water splitting of 10 and 100 mA cm(-2), respectively, which is much better than the commercial catalysts. Moreover, with the strong inhibiting effect of CIER and corrosion resistance benefited from the synergistic effect of bimetallic atoms in phosphide, Mo-CoPX/NF parallel to Mo-CoPX/NF pair has superb catalytic durability for seawater electrolysis. (C) 2022 Elsevier Ltd. All rights reserved.
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页数:8
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