Rotating Ring-Disk Electrode Voltammetry for Determining the COR-OER Selectivity in Seawater Electrolysis under Neutral to Alkaline Conditions

被引:2
|
作者
Fujita, Wataru [1 ]
Yamaguchi, Maho [1 ]
Tanaka, Saki [1 ]
Nakayama, Masaharu [1 ,2 ]
机构
[1] Yamaguchi Univ, Grad Sch Sci & Technol Innovat, Dept Appl Chem, 2-16-1 Tokiwadai, Ube 7558611, Japan
[2] Blue Energy Ctr SGE Technol BEST, Ube 7558611, Japan
基金
日本学术振兴会;
关键词
OXYGEN EVOLUTION REACTION; OXIDE;
D O I
10.1149/1945-7111/acc13c
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Hydrogen production through the direct electrolysis of seawater is gaining attention as a method for achieving carbon neutrality. The Cl- anion oxidation reaction (COR) in seawater, which occurs at the counter electrode (anode) of hydrogen production and generates active chlorine species with a corrosive nature, should be suppressed as much as possible for hydrogen production and replaced with the oxidation of water, i.e., oxygen evolution reaction (OER). The COR and OER proceed competitively at the anode; however, no studies have separately investigated their behavior in a pH region close to that of seawater. This study uses a simple electrochemical method with a rotating ring-disk electrode (RRDE) to determine the independent behavior of COR and OER with respect to potential and pH in an aqueous NaCl solution, where IrO2 (COR dominant) and MnO2 (OER dominant) are used as catalysts. The results obtained based on the RRDE voltammetry in aqueous NaCl solutions at various pH values were consistent with the COR selectivity determined from product analysis. Thus, the described method will be a valid electrochemical protocol. (c) 2023 The Electrochemical Society ("ECS"). Published on behalf of ECS by IOP Publishing Limited.
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页数:7
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