Self-supported Ni2P nanosheets on low-cost three-dimensional Fe foam as a novel electrocatalyst for efficient water oxidation

被引:57
作者
Zhang, Mengrong [1 ]
Wang, Taotao [1 ]
Cao, Hongyun [1 ]
Cui, Shengsheng [1 ]
Du, Pingwu [1 ,2 ]
机构
[1] Univ Sci & Technol China, iChEM Collaborat Innovat Ctr Chem Energy Mat, Dept Mat Sci & Engn, Hefei Natl Lab Phys Sci Microscale,CAS Key Lab Ma, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Anhui, Peoples R China
来源
JOURNAL OF ENERGY CHEMISTRY | 2020年 / 42卷
基金
中国国家自然科学基金;
关键词
Low-cost electrocatalyst; Metal phosphide; Fe foam; Water oxidation; OXYGEN EVOLUTION; PHOSPHIDE; HYDROGEN; CATALYST; NANOPARTICLES; REDUCTION; HYDROXIDE; IRIDIUM; ARRAYS; IRON;
D O I
10.1016/j.jechem.2019.06.010
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Electrochemical water splitting into hydrogen and oxygen is a promising strategy for future renewable energy conversion devices. The oxygen evolution reaction (OER) is considered as the bottleneck reaction in an overall water splitting system because it involves 4e(-) and 4H(+) transfer processes. Currently, it is highly desirable to explore low-cost alternative catalysts for OER at ambient conditions. Herein, we report for the first time that nickel phosphide (Ni2P) nanosheets can be facilely grown on Fe foam (FF) as an efficient electrocatalyst for OER with excellent durability and catalytic activity under alkaline conditions. To reach a current density of 10 mA/cm(2), the Ni2P-FF catalyst required a low overpotential of only 198 mV for OER. The catalyst's high OER activity and durability were well maintained at a high current density. The required overpotentials were only 267 and 313 mV to achieve the current densities of 100 and 300 mA/cm(2), respectively. The combination of low-cost Fe foam with Ni(2)xP provides a promising low-cost catalyst for large-scale application of electrocatalytic water splitting. (C) 2019 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.
引用
收藏
页码:71 / 76
页数:6
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