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Mini Review | Open Access

Cutting-edge methods for amplifying the oxygen evolution reaction during seawater electrolysis: a brief synopsis

Xiang Lyu ( ), Alexey Serov
Electrification and Energy Infrastructures Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA
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Abstract

Electrochemical water splitting has been considered a clean and continual way for hydrogen (H2) production. Direct seawater electrolysis is a potentially attractive technology due to the ample access to seawater and scarce freshwater resources in some regions. However, the presence of impurities (e.g., Cl−, Mg2+) and the resulting corrosion and side reactions, such as the chloride oxidation reaction (ClOR), makes seawater electrocatalysis more challenging than that of fresh or alkaline water due to competition with the oxygen evolution reaction (OER) at the anode. Consequently, much effort has been devoted to developing approaches to enhance OER performance and suppress the ClOR. In this minireview, we summarize three general strategies for enhancing OER activity and selectivity in seawater electrolysis based on three different concepts: (1) the sole development of robust and high-performance OER catalysts in pure seawater electrolytes, (2) the introduction of additives to seawater electrolytes (e.g., alkalis and/or salts without chloride) to enhance the potential equilibrium gap between the ClOR and OER in combination with regular highly active OER catalysts, and (3) a combination of approaches (1) and (2). Finally, the current challenges and potential opportunities for green H2 production from seawater electrolysis are briefly presented.

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Industrial Chemistry & Materials
Pages 475-485

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Cite this article:
Lyu X, Serov A. Cutting-edge methods for amplifying the oxygen evolution reaction during seawater electrolysis: a brief synopsis. Industrial Chemistry & Materials, 2023, 1(4): 475-485. https://doi.org/10.1039/d3im00071k

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Received: 29 June 2023
Accepted: 10 August 2023
Published: 17 August 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 3.0 Unported Licence.