膜
电导率
烷基
联苯
侧链
离子交换
极限抗拉强度
透射电子显微镜
高分子化学
阳离子聚合
化学工程
化学
材料科学
电化学
离子
纳米技术
有机化学
复合材料
聚合物
电极
生物化学
物理化学
工程类
作者
Qiao Liu,Wenli Ma,Lin Tian,Junmin Li,Lincan Yang,Fanghui Wang,Zhiqian Wang,Jing Li,Zhongming Wang,Hong Zhu
标识
DOI:10.1016/j.jpowsour.2022.232105
摘要
To achieve high-performance anion exchange membranes (AEMs) with superior conductivity and stability, a series of novel poly(biphenyl piperidinium) (PBP-n-Pip) membranes are synthesized by tethering cationic groups to the backbone utilizing flexible hydrophobic alkyl spacers with various lengths. All of the membranes exhibit excellent film-forming ability and tensile strength (42.34–53.49 MPa). Well-defined microphase separation is confirmed by transmission electron microscopy (TEM) and atomic force microscopy (AFM). The PBP-6-Pip membrane exhibits the conductivity of 117.1 mS cm−1 at 80 °C due to the most excellent microphase-separated morphology and highest water uptake. The long-term alkali resistance of AEMs can be improved by extending the length of the flexible alkyl chains appropriately. After immersion in 2 M NaOH at 80 °C for 1500 h, the initial conductivity of PBP-6-Pip with intermediate spacer chains and PBP-8-Pip with longer spacer chains both remains above 84%. Furthermore, the PBP-6-Pip membrane with the highest conductivity achieves a peak power density of 307 mW cm−2 at 80 °C in the H2/O2 single fuel cell. A long-term life test of this MEA shows a voltage decay rate of 2.87 mV/h over 40 h of operation under 0.2 A cm−2 at 60 °C.
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