膜
电解质
燃料电池
聚合物
材料科学
高分子化学
化学工程
化学
复合材料
电极
物理化学
生物化学
工程类
作者
N. Nambi Krishnan,Anastasiia Konovalova,David Aili,Qingfeng Li,Hyun S. Park,Jong Hyun Jang,Hyoung‐Juhn Kim,Dirk Henkensmeier
标识
DOI:10.1016/j.memsci.2019.117218
摘要
The degradation pathway of phosphoric acid doped polybenzimidazole membranes in high temperature polymer electrolyte membrane fuel cells depends on the acid contents. If it is high, creep is discussed as the main reason. If it is low (membranes prepared by solvent evaporation and post-doping), the main cause may be loss of acid due to evaporation. The net transport of acid to the anode side at high current densities should also lead to local softening of the membrane, which could be mitigated by crosslinking the membrane. Here we show that sulfonated para-polybenzimidazole membranes can be stabilized by curing at 350 °C. In contrast to meta-polybenzimidazole and sulfonated para-polybenzimidazole, crosslinked sulfonated para-polybenzimidazole is insoluble in dimethylacetamide at room temperature and phosphoric acid at 160 °C. At 160 °C and 5% relative humidity the conductivity of crosslinked sulfonated para-polybenzimidazole and meta-polybenzimidazole is 214 mS cm−1 and 147 mS cm−1, respectively. At 600 mA cm−2, the voltage decay rate is 16 μV h−1, much lower than published for commercial meta-polybenzimidazole (308 μV h−1). Furthermore, the average voltage at 600 mA cm−2 is 523 mV, while a previously published cured meta-polybenzimidazole membrane only reaches 475 mV.
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