氢氧化物
膜
离子交换
化学工程
离子液体
共价键
热稳定性
混合材料
材料科学
离子键合
离子
化学
共价有机骨架
氧化物
离子电导率
无机化学
高分子化学
纳米技术
有机化学
电极
电解质
物理化学
催化作用
工程类
生物化学
作者
Jia Chen,Ping Li,Ningxin Zhang,Shaokun Tang
标识
DOI:10.1016/j.electacta.2021.138962
摘要
Anion exchange membranes with potentially high conductivity and stability are urgently demanded in alkaline anion exchange membrane fuel cells (AEMFCs). However, the design and preparation of novel hydroxide-conducting material remain grand challenges. Herein, we demonstrate a significantly enhanced hydroxide conduction hybrid membrane with multi-ion nanochannels assembled by embedding two-dimensional covalent organic framework (COF) sheets into one-dimensional comb-shaped poly (2,6-dimethyl-1,4-phenylene oxide) (PPO) chains. Hydrophilic imidazole-based ionic liquids (im-IL) in-situ polymerize within the ordered pores of COF PI-2, forming long-range continuous ion channels. Then the poly ionic liquid-loaded covalent organic frameworks ([email protected]) as a novel filler is embedded into imPPO to construct hybrid membranes with multi-ion nanochannels. A remarkable hydroxide conductivity of 147 mS/cm (80 °C and 100% RH) and a maximum power density of 140 mW/cm2 are readily achieved for the hybrid membrane with 5 wt% [email protected] content. Particularly, the chemical stability, thermal stability, mechanical properties, and swelling resistance of the hybrid membrane are dramatically promoted by the introduction of [email protected] Meanwhile, the transfer of hydroxide in hybrid AEM is investigated by molecular dynamics simulations, which clarify the significant role of PI-2 one-dimensional channels in elevating hydroxide transport.
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