Impact of applied potential range on corrosion behavior of stainless steel oxygen evolution electrode under potential cycle loading

被引:0
|
作者
Todoroki, Naoto [1 ]
Wadayama, Toshimasa [1 ]
机构
[1] Tohoku Univ, Grad Sch Environm Studies, Sendai 9808579, Japan
关键词
Alkaline water electrolysis; Anode; Oxygen evolution reaction; Stainless steel; Corrosion; Potential fluctuation; Potential cycle loading; LAYERED DOUBLE HYDROXIDE; OXIDE; CATALYST; ELECTROCATALYSTS; MEMBRANE; ENERGY;
D O I
10.1016/j.jpowsour.2024.234854
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We investigated the corrosion behavior of 310S stainless steel anode for alkaline water electrolyzer under various triangle-wave potential cycle loadings by changing the lower (x) and higher (y) vertex potentials to simulate the power fluctuation characteristics of renewable energy sources. The anode was subjected to the loadings of x = 0.5-1.5 and y = 1.8-2.5 V in 7 M KOH solution. The dissolution of Fe and Cr into the electrolyte depended significantly on x. Notably, under conditions of x >= 1.35 V, the total dissolution amounts of Fe and Cr after the 20,000 potential cycles decreased to approximately 7 % of the condition where x = 0.5 V. Conversely, y had less influence on the total dissolution amounts. Interestingly, the molar ratios of the eluted Fe and Cr into the electrolyte depended on both x and y, suggesting distinct corrosion behaviors of the stainless steel induced by the potential cycles of x <= 1.35 and y = 1.8 V, compared to those at x >= 1.35 and y = 2.5 V. These findings suggest the importance of precise potential control of the stainless steel anode in alkaline water electrolysis for preventing potential fluctuation-induced corrosion.
引用
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页数:7
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