Hydrogen Crossover in PEM and Alkaline Water Electrolysis: Mechanisms, Direct Comparison and Mitigation Strategies

渗透 渡线 过饱和度 电解水 聚合物电解质膜电解 电解 电解法 溶解度 扩散 化学 电解质 化学工程 无机化学 分析化学(期刊) 色谱法 计算机科学 热力学 电极 工程类 物理化学 人工智能 有机化学 物理 生物化学
作者
Patrick Trinke,Philipp Haug,Jörn Brauns,Boris Bensmann,Richard Hanke‐Rauschenbach,Thomas Turek
出处
期刊:Journal of The Electrochemical Society [Institute of Physics]
卷期号:165 (7): F502-F513 被引量:301
标识
DOI:10.1149/2.0541807jes
摘要

This study provides a direct comparison of hydrogen crossover in PEM (Nafion 117) and alkaline water electrolysis (Zirfon) at a temperature of applying state-of-the-art separating unit materials. To this end, occurring crossover mechanisms are described first, before experimental data of the anodic hydrogen content are shown in dependence of current density, system pressure and process management strategy. The results suggest that permeation in PEM electrolyzers is mainly governed by diffusion due to a supersaturated concentration of dissolved hydrogen within the catalyst layer, showing a share of 98} of the total permeation flux at and atmospheric pressure. Permeation in alkaline electrolyzers also exhibits a significant influence of supersaturation, but the overall crossover is mainly influenced by mixing the electrolyte cycles, which makes up a share of 90} at and . Generally it becomes evident that hydrogen permeation across the separating unit is more than one order of magnitude smaller in alkaline electrolysis, which is mainly a consequence of the significantly lower hydrogen solubility in concentrated KOH electrolyte. Finally, this study concludes with an assessment of the impact of separating unit thickness and provides mitigation strategies to reduce hydrogen crossover.
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