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Research Article

Acid-stable antimonate based catalysts for the electrocatalytic oxygen evolution reaction

Xiaoping Gao1,2Huang Zhou2Zhe Wang3( )Gang Zhou4 ( )Jin Wang1( )Yuen Wu2 ( )
College of Materials Science and Engineering, Shenzhen University, Shenzhen 518071, China
School of Chemistry and Materials Science, University of Science and Technology of China, Hefei 230026, China
Preservation Technology, Advanced Research Center, Hefei Hualing Co., Ltd, Hefei 230000, China
School of Science, Hubei University of Technology, Wuhan 430068, China
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Abstract

Acid-stable and highly active catalysts for the electrocatalytic oxygen evolution reaction (OER) are paramount to the advancement of electrochemical technologies for clean energy conversion and utilization. In this work, based on the density functional theory (DFT) calculations, we systematically investigated the MSb2O6 (M = Fe, Co, and Ni) and transition metal (TM) doped MSb2O6 (TM-MSb2O6, TM = Mn, Fe, Co, Ni, Cu, Zn, Ru, Rh, Pd, Ir, and Pt) as potential antimonate-based electrocatalysts for the OER. The stability and OER activity of these considered electrocatalysts were systematically studied under acidic conditions. It was found that Rh-NiSb2O6, Pt-CoSb2O6, Rh-FeSbO4, and Co-NiSb2O6 can serve as efficient and stable OER electrocatalysts, and their OER catalytic activities are better than that of the current state-of-the-art OER catalyst (IrO2). Our findings highlight a family of promising antimonate-based OER electrocatalysts for future experimental verification.

Graphical Abstract

The Rh-NiSb2O6, Pt-CoSb2O6, Rh-FeSbO4, and Co-NiSb2O6 are screened out as promising oxygen evolution reaction electrocatalysts with good stability and high activity under acidic condition.

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Nano Research
Pages 4691-4697

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Cite this article:
Gao X, Zhou H, Wang Z, et al. Acid-stable antimonate based catalysts for the electrocatalytic oxygen evolution reaction. Nano Research, 2023, 16(4): 4691-4697. https://doi.org/10.1007/s12274-022-5132-6
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Received: 12 September 2022
Revised: 30 September 2022
Accepted: 01 October 2022
Published: 29 November 2022
© Tsinghua University Press 2022