Synthesis and Characterization of Fe3+ and CeO2 Co-decorated NiOOH Electrocatalysts Supported by Nickel Foam for the Oxygen Evolution Reaction

被引:15
作者
Zhang, Haoyu [1 ]
Du, Jingguang [1 ]
Niu, Dongfang [1 ]
Hu, Shuozhen [1 ]
Zhang, Xinsheng [1 ]
机构
[1] East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
来源
INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE | 2019年 / 14卷 / 07期
关键词
Oxygen Vacancy; Cerium Oxide; Fe3+ Dopant; NiOOH; Oxygen Evolution Reaction; WATER OXIDATION CATALYSIS; IN-SITU FORMATION; OXIDE CATALYSTS; OXYHYDROXIDE; HYDROXIDE; COBALT; FILMS; REDUCTION; DESIGN; TRENDS;
D O I
10.20964/2019.07.52
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Inexpensive and non-noble metal catalysts for the oxygen evolution reaction (OER) with high activity and stability must be developed to enhance water electrolysis for hydrogen production. Herein, Fe3+ dopants and flower-shaped CeO2-decorated NiOOH catalysts are synthesized, and the synergetic effect of Fe3+ dopants and CeO2 are investigated. The presence of both Fe3+ dopants and CeO2 produces more NiOOH species and more oxygen vacancies in the NiOOH structure as measured by X-ray photoelectron spectroscopy. Electrochemical measurements illustrate that the increase in oxygen vacancies in NiOOH significantly increases the conductivity and activity of the catalyst and reduces the OER overpotential. Among the catalysts studied in this research, CeO2-NiFeOH/NF, which is modified by both Fe3+ dopants and CeO2, hosts the highest number of oxygen vacancies. It also has the lowest overpotential (280 mV), the highest current density, and excellent stability with high performance for the OER.
引用
收藏
页码:6532 / 6545
页数:14
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