Current density effect on hydrogen permeation in PEM water electrolyzers

被引:130
作者
Trinke, P. [1 ]
Bensmann, B. [1 ]
Hanke-Rauschenbach, R. [1 ]
机构
[1] Leibniz Univ Hannover, Elect Energy Storage Syst, Welfengarten 1, D-30167 Hannover, Germany
关键词
PEM electrolyzer; Water electrolysis; Hydrogen permeation; Crossover; Supersaturation; Current density; SOLID-POLYMER-ELECTROLYTE; MEMBRANE FUEL-CELLS; IN-SITU MEASUREMENT; GAS-DIFFUSION; PRESSURE; SUPERSATURATION; TEMPERATURE; OXYGEN; PERMEABILITY; TRANSPORT;
D O I
10.1016/j.ijhydene.2017.03.231
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
Hydrogen permeation is an important phenomena for PEM water electrolyzers, due to several reasons as safety issues and efficiency loss. The present contribution deals with the measurement of hydrogen volume fraction within the anode product gas during PEM water electrolysis for different temperatures and cathode pressures. High cathode pressures lead to high anode hydrogen volume fractions close to the lower explosion limit of hydrogen in oxygen, which are caused by increased hydrogen permeation. It is shown that the results of the hydrogen volume fraction measurements can be easily converted into hydrogen permeation rates. Additionally, the experimental obtained permeation data indicate that hydrogen permeation increases linear with increasing current density. The impact of current density on the hydrogen permeation is very strong in comparison to the effects of temperature and pressure e.g. a current density increase of 1 A/cm(2) can causes a permeation increase comparable to a cathode pressure increase of 20 bar. In the second part of this contribution different theories to explain this strong dependence on current density are discussed. The most probable explanation is that due to mass transfer limitations a supersaturation of dissolved gas within the catalyst ionomer film arises that causes the investigated increase in permeation. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:14355 / 14366
页数:12
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