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Hierarchically Structured FeNiO x H y Electrocatalyst Formed by In Situ Transformation of Metal Phosphate for Efficient Oxygen Evolution Reaction

A simple and low-cost fabrication method is needed to obtain effective and robust heterogeneous catalysts for the oxygen evolution reaction (OER). In this study, an electrocatalyst FeNiO H with a hierarchical structure is synthesized on nickel foam by a simple fabrication method through anion exchan...

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Bibliographic Details
Published in:ChemSusChem 2018-06, Vol.11 (11), p.1761-1767
Main Authors: Wu, Xiujuan, Zhao, Yimeng, Xing, Tongyu, Zhang, Peili, Li, Fusheng, Lee, Husileng, Li, Fei, Sun, Licheng
Format: Article
Language:English
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Summary:A simple and low-cost fabrication method is needed to obtain effective and robust heterogeneous catalysts for the oxygen evolution reaction (OER). In this study, an electrocatalyst FeNiO H with a hierarchical structure is synthesized on nickel foam by a simple fabrication method through anion exchange from a metal phosphate to a metal hydroxide. The as-fabricated FeNiO H electrode requires overpotentials of 206 and 234 mV to deliver current densities of 10 and 50 mA cm , respectively. The catalytic performance of FeNiO H is superior to that of most previously reported FeNi-based catalysts, including NiFe layered double hydroxide. The catalyst also shows good long-term durability at a current density of 50 mA cm over 50 h with no activity decay under 1 m KOH. By comparison to the directly electrodeposited FeNi hydroxide in morphology and electrochemical properties, the improved activity of the catalyst could be mainly attributed to an enhancement of its intrinsic activity, which was caused by the anion exchange of phosphate to (oxy)hydroxide. Further studies by cyclic voltammetry indicated a stronger interaction between Ni and Fe from the negative shift of the oxidation peak of Ni /Ni in comparison with reported FeNiO H , which promoted the generation of active Ni species more easily. This work may provide a new approach to the simple preparation of effective and robust OER catalysts by anion exchange.
ISSN:1864-5631
1864-564X
DOI:10.1002/cssc.201800407