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Research Article

Mesoporous nickel–iron binary oxide nanorods for efficient electrocatalytic water oxidation

Guang LiuXusheng GaoKaifang WangDongying HeJinping Li( )
Research Institute of Special ChemicalsTaiyuan University of TechnologyTaiyuan030024China
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Abstract

The design and fabrication of low-cost, high-efficiency, and stable oxygen-evolving catalysts are essential for promoting the overall efficiency of water electrolysis. In this study, mesoporous Ni1–x Fe x O y (0 ≤ x ≤ 1, 1 ≤ y ≤ 1.5) nanorods were synthesized by the facile thermal decomposition of Ni–Fe-based coordination polymers. These polymers passed their nanorod-like morphology to oxides, which served as active catalysts for oxygen evolution reaction (OER). Increasing the Fe-doping amount to 33 at.% decreased the particle size and charge-transfer resistance and increased the surface area, resulting in a reduced overpotential (~302 mV) at 10 mA/cm2 and a reduced Tafel slope (~42 mV/dec), which were accompanied by a far improved OER activity compared with those of commercial RuO2 and IrO2 electrocatalysts. At Fe-doping concentrations higher than 33 at.%, the trend of the electrocatalytic parameters started to reverse. The shift in the dopant concentration of Fe was further reflected in the structural transformation from a NiO (< 33 at.% Fe) rock-salt structure to a biphasic NiO/NiFe2O4 (33 at.% Fe) heterostructure, a NiFe2O4 (66 at.% Fe) spinel structure, and eventually to α-Fe2O3 (100 at.% Fe). The efficient water-oxidation activity is ascribed to the highly mesoporous one-dimensional nanostructure, large surface area, and optimal amounts of the dopant Fe. The merits of abundance in the Earth, scalable synthesis, and highly efficient electrocatalytic activity make mesoporous Ni–Fe binary oxides promising oxygen-evolving catalysts for water splitting.

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Nano Research
Pages 2096-2105
Cite this article:
Liu G, Gao X, Wang K, et al. Mesoporous nickel–iron binary oxide nanorods for efficient electrocatalytic water oxidation. Nano Research, 2017, 10(6): 2096-2105. https://doi.org/10.1007/s22274-016-1398-x

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Received: 23 August 2016
Revised: 08 November 2016
Accepted: 28 November 2016
Published: 01 March 2017
© Tsinghua University Press and Springer-Verlag Berlin Heidelberg 2016
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