阳离子聚合
氢氧化物
限制
膜
离子键合
离子交换
耐久性
化学
离子电导率
材料科学
化学工程
纳米技术
组合化学
离子
计算机科学
无机化学
高分子化学
工程类
有机化学
机械工程
复合材料
物理化学
生物化学
电极
电解质
作者
Qihang Zhang,Rong Ren,Liqiang Yin,Licheng Sun
标识
DOI:10.1002/chem.202404264
摘要
Anion exchange membranes (AEMs) based energy conversion and storage devices have attracted attention as an innovative technology due to their advantageous alkaline catalytic kinetics and cost‐effectiveness. AEMs play a crucial role in these devices and have shown significant progress in terms of ionic conductivity, mechanical properties, alkaline stability, and other essential characteristics. Nevertheless, their durability remains a limiting factor preventing the large‐scale deployment of AEMs based devices. The attack of hydroxide ions on the cations is an inherent issue that needs to be addressed to enhance the lifetime of the AEMs. Therefore, the design of more stable cationic groups is essential to maintain the initial properties of AEMs and extend the device lifetime. This concept systematically summarizes the development and stability enhancement strategies of the cationic groups for AEMs in recent years, with particular emphasis on the emerging cyclic cationic groups. Furthermore, the stability differences of cations in small molecules versus AEMs are systematically discussed, as well as prospective research toward stable AEMs.
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