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Review | Open Access

Recent progress of manganese dioxide based electrocatalysts for the oxygen evolution reaction

Yunlong HeaZhenye Kanga ( )Jing LiaYawei Lib ( )Xinlong Tiana ( )
State Key Laboratory of Marine Resource Utilization in South China Sea, Hainan Provincial Key Lab of Fine Chemistry, School of Chemical Engineering and Technology, Hainan University, Haikou 570228, China
School of Chemistry and Chemical Engineering, Shanxi University, Taiyuan 030006, China
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Abstract

The oxygen evolution reaction (OER) represents an anodic reaction for a variety of sustainable energy conversion and storage technologies, such as hydrogen production, CO2 reduction, etc. To realize the large-scale implementation of these technologies, the sluggish kinetics of the OER resulting from multi-step proton/electron transfer and occurring at the gas–liquid–solid triple-phase boundary needs to be accelerated. Manganese oxide-based (MnOx) materials, especially MnO2, have become promising non-precious metal electrocatalysts for the OER under acidic conditions due to the good trade-off between catalytic activity and stability. This paper reviews the recent progress of MnO2-based materials to catalyze the OER through either the traditional adsorbent formation mechanism (AEM) or the emerging lattice-oxygen-mediated mechanism (LOM). Pure manganese dioxide OER catalysts with different crystalline structures and morphologies are summarized, while MnO2-based composite structures are also discussed, and the application of MnO2-based catalysts in PEMWEs is summarized. Critical challenges and future research directions are presented to hopefully help future research.

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Industrial Chemistry & Materials
Pages 312-331

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Cite this article:
He Y, Kang Z, Li J, et al. Recent progress of manganese dioxide based electrocatalysts for the oxygen evolution reaction. Industrial Chemistry & Materials, 2023, 1(3): 312-331. https://doi.org/10.1039/d3im00034f

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Received: 19 March 2023
Accepted: 11 May 2023
Published: 11 May 2023
© 2023 The Author(s). Co‐published by the Institute of Process Engineering, Chinese Academy of Sciences and the Royal Society of Chemistry

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.