膜
电解
离子交换
碱性水电解
离子电导率
化学工程
碱性燃料电池
离子键合
材料科学
互穿聚合物网络
化学
电导率
聚合物
无机化学
离子
电解质
电极
复合材料
有机化学
物理化学
工程类
生物化学
作者
Sarthak Mishra,Shubham Mishra,Riddhi Sainda,Prafulla K. Jha,Vaibhav Kulshrestha
出处
期刊:Small
[Wiley]
日期:2025-10-08
卷期号:: e04320-e04320
标识
DOI:10.1002/smll.202504320
摘要
Abstract Degradation of anion exchange membranes (AEMs) in alkaline medium is an issue to be resolved for the durability and performance of anion exchange membrane water electrolyzers (AEMWEs). This study presents the development of interpenetrating polymer network type anion exchange membranes (IPN‐AEMs) with improved alkaline stability, contrived with varying thicknesses (110, 80, and 40 µm) for alkaline and seawater electrolysis. Among the fabricated membranes, IPN‐AEM‐40 demonstrated superior physicochemical properties, including water uptake (33%), ion exchange capacity (1.3 meq g −1 ), and ionic conductivity (5.5 × 10 −2 S cm −1 ). The alkaline stability tests of IPN‐AEM‐40 in 5 m KOH at 80 °C indicated 75% retention of ionic conductivity over 90 days, with nucleophilic substitution identified as the predominant degradation pathway, corroborated by FT‐IR spectroscopy and computational analysis. Electrolysis performance evaluation revealed a current density of 850 mA cm −2 at 2 V in 1 m KOH at 80 °C, along with optimal seawater electrolysis with a current density achieving 600 mA cm −2 at 80 °C. These findings underscore the potential of IPN‐AEM‐40 for high‐performance and durable hydrogen generation with anion exchange membrane water electrolyzers (AEMWEs).
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