Iron-substituted Co-Ni phosphides immobilized on Ni foam as efficient self-supported 3D hierarchical electrocatalysts for oxygen evolution reaction

被引:55
|
作者
Zhou, Chenmin [1 ]
Mu, Jianshuai [1 ]
Qi, Yu-Feng [1 ]
Wang, Qian [1 ]
Zhao, Xiao-Jun [1 ,2 ]
Yang, En-Cui [1 ]
机构
[1] Tianjin Normal Univ, Coll Chem, Key Lab Inorgan Organ Hybrid Funct Mat Chem, Minist Educ,Tianjin Key Lab Struct & Performance, Tianjin 300387, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300071, Peoples R China
关键词
Trimetallic phosphide; Fe-substitution; Hierarchical nanomaterials; Oxygen evolution reaction; BIFUNCTIONAL ELECTROCATALYST; HIGHLY EFFICIENT; NANOSHEET ARRAYS; NICKEL PHOSPHIDE; HIGH-PERFORMANCE; NANOWIRE ARRAYS; P ALLOY; WATER; HYDROGEN; ENERGY;
D O I
10.1016/j.ijhydene.2019.02.053
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
Electrocatalytic water splitting for hydrogen evolution is significantly impeded by the kinetically sluggish oxygen evolution reaction (OER). Thus, the development of highly efficient and durably stable non-noble-metal OER electrocatalyst is necessary and challenging for the large-scale electrocatalytic water splitting. Herein, a series of iron-substituted cobalt-nickel phosphides grown on Ni foam (FeCoNi-P/NFs) were easily prepared though successive hydrothermal and phosphorization treatments. The chemical compositions, crystalline and electronic structures as well as surface morphologies of these resulting electrocatalysts are strongly related with the iron substitution ratio. More interestingly, the FeCoNi-P/NF-2 nanosheet arrays prepared from equivalent molar ratio of iron and cobalt precursors exhibit the best OER performance with a low overpotential of 266 mV to produce a current density of 50 mA cm(-2) and a low Tafel slope of 61.2 mV dec(-1) in 1.0 M KOH condition, which is comparable to the reported state-of-the-art OER electrocatalysts. Additionally, the FeCoNi-P/NF-2 nanosheet arrays also show satisfactory long-term durability over 60 h. The superior OER activity of the electrocatalyst is essentially attributed to the heteroatomic substitution and the unique three-dimensional hierarchical morphology, which greatly increase the electrical conductivity, afford more active sites and facilitate the efficient charge transfer ability. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:8156 / 8165
页数:10
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