聚合物电解质膜电解
电解质
电解
降级(电信)
阳极
功率密度
电流密度
电解水
材料科学
化学工程
化学
氢
聚合物
复合材料
电极
功率(物理)
电气工程
热力学
有机化学
物理化学
工程类
物理
量子力学
作者
Christoph Rakousky,Uwe Reimer,Klaus Wippermann,Susanne Kuhri,Marcelo Carmo,Wiebke Lueke,Detlef Stolten
标识
DOI:10.1016/j.jpowsour.2016.11.118
摘要
Polymer electrolyte membrane (PEM) water electrolysis generates ‘green’ hydrogen when conducted with electricity from renewable - but fluctuating - sources like wind or solar photovoltaic. Unfortunately, the long-term stability of the electrolyzer performance is still not fully understood under these input power profiles. In this study, we contrast the degradation behavior of our PEM water electrolysis single cells that occurs under operation with constant and intermittent power and derive preferable operating states. For this purpose, five different current density profiles are used, of which two were constant and three dynamic. Cells operated at 1 A cm−2 show no degradation. However, degradation was observed for the remaining four profiles, all of which underwent periods of high current density (2 A cm−2). Hereby, constant operation at 2 A cm−2 led to the highest degradation rate (194 μV h−1). Degradation can be greatly reduced when the cells are operated with an intermittent profile. Current density switching has a positive effect on durability, as it causes reversible parts of degradation to recover and results in a substantially reduced degradation per mole of hydrogen produced. Two general degradation phenomena were identified, a decreased anode exchange current density and an increased contact resistance at the titanium porous transport layer (Ti-PTL).
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