Core-Shell NiO/C@NiFe-LDH Nanocomposite as an Efficient Electrocatalyst for Oxygen Evolution Reaction

被引:24
作者
Li, Xue [1 ]
Fan, Mingli [1 ]
Wei, Danan [1 ]
Wang, Xiaolong [1 ]
Wang, Yinling [1 ]
机构
[1] Anhui Normal Univ, Coll Chem & Mat Sci, Anhui Key Lab Chemobiosensing, Wuhu 241000, Peoples R China
关键词
LAYERED DOUBLE-HYDROXIDE; HIGH-SURFACE-AREA; N-DOPED CARBON; HIGHLY-EFFICIENT; ENERGY-STORAGE; NANOSHEETS; NICKEL; ARRAYS; HETEROSTRUCTURE; FRAMEWORKS;
D O I
10.1149/1945-7111/ab61eb
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Highly efficient and low-cost oxygen evolution reaction (OER) electrocatalysts have been urgently needed for the development of renewable hydrogen energy via water electrolysis. Herein, a core-shell NiO nanoparticles decorated carbon sphere (NiO/C) and NiFe-layered double hydroxide (NiFe-LDH) nanocomposite (NiO/C@NiFe-LDH) was prepared by a calcination-hydrothermal synthesis approach. In this nanocomposite, NiO/C as the core were derived from Ni based metal organic frameworks (Ni-MOFs), which not only provide a porous and conductive carbon support for NiFe-LDH nanosheets to expose active sites, but also offer a synergistic active site for NiFe-LDH nanosheets. The structure and morphology of NiO/C@NiFe-LDH were mainly characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and nitrogen adsorption-desorption test. The OER catalytic activity of NiO/C@NiFe-LDH was optimized by adjusting the ratio between NiO/C and NiFe-LDH and adding bridging agents. Under the optimum conditions, the overpotential at 10 mA cm(-2) for NiO/C@NiFe-LDHs is only 299 mV(vs RHE), lower than that of commercial RuO2 (330 mV). Besides, the NiO/C@NiFe-LDH exhibits a good stability in 10-hour testing. These results show that the ingenious combination of different OER catalysts may be an effective strategy to prepare low-cost OER catalysts with good performance. (C) 2020 The Electrochemical Society ("ECS"). Published on behalf of ECS by IOP Publishing Limited.
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页数:8
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