Nanocomposites Based on CoSe2-Decorated FeSe2 Nanoparticles Supported on Reduced Graphene Oxide as High-Performance Electrocatalysts toward Oxygen Evolution Reaction

被引:159
作者
Zhu, Guoxing [1 ]
Xie, Xulan [1 ]
Li, Xiaoyun [1 ]
Liu, Yuanjun [2 ]
Shen, Xiaoping [1 ]
Xu, Keqiang [1 ]
Chen, Shaowei [3 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[2] Jiangsu Univ Sci & Technol, Sch Environm & Chem Engn, Zhenjiang 202018, Peoples R China
[3] Univ Calif Santa Cruz, Dept Chem & Biochem, 1156 High St, Santa Cruz, CA 95064 USA
基金
中国国家自然科学基金;
关键词
catalysis; composite materials; electrode; oxygen evolution reaction; heterointerfaces; LAYERED DOUBLE HYDROXIDE; WATER OXIDATION; BIFUNCTIONAL ELECTROCATALYSTS; EFFICIENT ELECTROCATALYST; HYDROGEN EVOLUTION; DOPED NISE2; IRON; COBALT; CATALYST; NANOSHEETS;
D O I
10.1021/acsami.8b04024
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
FeCo-based materials are promising candidates as efficient, affordable, and sustainable electrocatalysts for oxygen evolution reaction (OER). Herein, a composite based on FeSe2@CoSe2 particles supported on reduced graphene oxide (rGO) was successfully prepared as an OER catalyst. In the catalyst, the CoSe2 phase was located on the FeSe2 surface, forming a large number of exposed heterointerfaces with acidic iron sites because of strong charge interaction between CoSe2 and FeSe2. It is believed that the exposed heterointerfaces act as catalytic active sites for OER via a two-site mechanism, manifesting an overpotential as low as 260 mV to reach the current density of 10 inA cm(-2) in 1 M KOH and excellent stability for at least 6 h, which is superior to those of CoSe2/rGO, FeSe2/rGO, as well as most of the FeNi- and FeCo-based electrocatalysts reported in recent literatures. It was demonstrated that the most optimal composite electrocatalysts release more Fe species into the electrolyte during the OER process, whereas the releasing of Co species is negligible. When the FeSe2@CoSe2/rGO catalysts were loaded on a alpha-Fe2O3 photoanode, the photocurrent density was increased by three times. These results may open up a promising avenue into the design and engineering of highly active and durable catalysts for water oxidation.
引用
收藏
页码:19258 / 19270
页数:13
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