哌啶
膜
化学
芳基
高分子化学
离子
离子交换
生物物理学
有机化学
生物化学
烷基
生物
作者
Xiaoqin Ma,Aidi Liu,Jingtao Si,Qiong Xiang,Wei Yuan,Xiaoli Lu,Caili Yuan,Baoshu Chen,Wei Luo,Jianchuan Wang,Zidong Wei
出处
期刊:Macromolecules
[American Chemical Society]
日期:2024-09-19
卷期号:57 (19): 9346-9354
被引量:16
标识
DOI:10.1021/acs.macromol.4c01260
摘要
As a key component of anion exchange membrane fuel cells, anion exchange membranes (AEMs) must exhibit outstanding comprehensive performance. Hyperbranched AEMs have garnered increasing attention due to their superior hydroxide conductivity compared to linear AEMs. However, while the loose chain entanglement of hyperbranched AEMs effectively reduces the mass transfer resistance, it also leads to excessive water uptake and high membrane swelling. Herein, a series of alkyl chains with different lengths are introduced into the hyperbranched AEMs to regulate their hydrophobicity, further affecting the membrane performance. Enhancing hydrophobicity effectively controls water absorption (52.8–15%@80 °C) and achieves extremely low membrane swelling (4.6%@80 °C). Although hydroxide conductivity is impacted by the enhanced hydrophobicity, hbQPTP-Cn AEMs still maintain high ion conductivity (>200 mS/cm@80 °C) due to the construction of ionic clusters induced by the hydrophobic phase. Regulating the hydrophobicity of AEMs also benefits the enhancement of alkaline resistance and water management during fuel cell operation.
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