膜
乙醚
化学
芳基
高分子化学
质子
酮
质子交换膜燃料电池
激进的
位阻效应
化学稳定性
有机化学
烷基
生物化学
量子力学
物理
作者
Qian Liu,Shouhai Zhang,Lin Zhuo,Zhaoqi Wang,Chenghao Wang,Fenchen Sun,Kang Niu,Peiqi Xu,Xuefu Che,Jie Zhang,Xigao Jian
标识
DOI:10.1016/j.memsci.2023.121767
摘要
The application of sulfonated poly(aryl ether)s proton exchange membranes in fuel cells is hampered by the inadequate oxidation stability and the trade-off effect between proton-conducting performance and physicochemical stability. So the sulfonated N-heterocyclic poly(aryl ether ketone)s (SPBPEK-Ps) membranes possessing fine proton-conducting behavior and radical tolerance are manufactured by the elaborate design of molecular backbones. The hydrophilic units containing proton-conducting groups in pendant moieties in SPBPEK-Ps contribute to constructing developed proton-conducting channels, in which the multiple interactions between sulfonic groups and N-heterocycles further promote proton conduction with the conductivity of up to 125 mS cm−1. The fuel cells loading SPBPEK-Ps membranes perform a power density of up to 1210 mW cm−2 with hypo-sensitivity to temperature and oxidized gas. A couple of steric hindrances from pendant proton-conducting groups and the diminished affinity of radicals for molecular chains resulting from the introduction of N-heterocyclic structure enhance the oxidation stability of SPBPEK-Ps membranes, and the break time of the membranes at 80 °C ranges in 2.5–7.8 h. The combination of the pendant proton-conducting groups and N-heterocycles with the electron-withdrawing effect would contribute to improving proton-conducting performance and oxidation stability and attenuating the trade-off effect between them.
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