Development of Ni-Fe based ternary metal hydroxides as highly efficient oxygen evolution catalysts in AEM water electrolysis for hydrogen production

被引:55
|
作者
Loh, Adeline [1 ]
Li, Xiaohong [1 ]
Taiwo, Oluwadamilola O. [2 ]
Tariq, Farid [2 ]
Brandon, Nigel P. [2 ]
Wang, Peican [3 ]
Xu, Ke [3 ]
Wang, Baoguo [3 ]
机构
[1] Univ Exeter, Coll Engn Math & Phys Sci, Renewable Energy Grp, Penryn Campus, Penryn TR10 9FE, Cornwall, England
[2] Imperial Coll London, Earth Sci & Engn, London SW11 2AZ, England
[3] Tsinghua Univ, Dept Chem Engn, Beijing 100084, Peoples R China
基金
英国工程与自然科学研究理事会;
关键词
Oxygen evolution reaction; NiFeCo ternary metal hydroxide; Cathodic electrodeposition; Anion exchange membrane (AEM); Water electrolyser; Hydrogen production; X-RAY PHOTOELECTRON; XPS SPECTRA; NICKEL METAL; ELECTROCATALYTIC PROPERTIES; ANODIC EVOLUTION; COBALT HYDROXIDE; ACTIVITY TRENDS; CURRENT-DENSITY; O-2; EVOLUTION; OXIDE;
D O I
10.1016/j.ijhydene.2020.06.253
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
A number of mixed metal hydroxide oxygen evolution reaction (OER) catalysts i.e. Ni-Fe, Ni-Co, Ni-Cr, Ni-Mo, Ni-Fe-Co, Ni-Fe-Mo and Ni-Fe-Cr were prepared by cathodic electrodeposition and characterised by SEM, TEM, EDS, XPS and micro X-CT. The compositions of selected catalysts were optimised to give lower OER overpotentials in alkaline media. Further optimisation of Ni-Fe based ternary metal hydroxide catalysts such as Ni-Fe-Co and Ni-Fe-Mo was carried out, showing improved performance at high current densities up to 1 A cm(-2) in 1 M NaOH, 333 K. The influence of electrodeposition parameters such as current density, pH, electrodeposition time and temperature on the electrocatalytic performance of ternary Ni-Fe-Co metal hydroxide was further investigated and optimised. The durability of the optimised catalyst was tested at a current density of 0.5 A cm(-2) in an anion exchange membrane (AEM) water electrolyser cell at 4 M NaOH, 333 K, demonstrating stable performance over 3.5 h. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:24232 / 24247
页数:16
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