膜
氢氧化物
结晶度
铵
材料科学
化学工程
氢氧化铵
肿胀 的
共价键
离子键合
离子交换
单体
高分子化学
无机化学
化学
聚合物
离子
有机化学
复合材料
生物化学
工程类
作者
Wanting Chen,Qiang Liu,Bo Pang,Fujun Cui,Leilei Wang,Fang-Jie Zhou,Gaohong He,Xuemei Wu
出处
期刊:Small
[Wiley]
日期:2024-11-28
标识
DOI:10.1002/smll.202407260
摘要
Abstract Quaternary ammonium functionalized covalent organic frameworks (COFs) have great potential to enhance hydroxide transport owing to crystalline ordered 1D nanochannels, however, suffer from limited quaternary ammonium functional monomers and poor membrane‐forming ability. In this work, a novel aminopropyl quaternary ammonium‐functionalized COF (DCOF) is designed and synthesized via a bottom‐up strategy. The self‐supporting DCOF membrane exhibits high crystallinity with a dense and orderly arrangement of quaternary ammonium groups (IEC, 2.07 mmol g −1 ), achieving a high hydroxide conductivity of 172.5 mS cm −1 and an extremely low water swelling of 5.3% at 80 °C. The exfoliated DCOF colloidal suspension is further incorporated into quaternary ammonium di‐cation grafted polybenzimidazoles (DPBI) matrix. Molecular simulations reveal strong electrostatic and van der Waals interfacial interactions between DCOF and DPBI, which enable a high doping content of 20 wt.% and interconnected ionic channels through the surface and nanochannels of the DCOF. The DCOF/DPBI‐20% membrane exhibits a tensile strength of 29.7 MPa, a hydroxide conductivity of 135.3 mS cm −1 , and a low swelling ratio of 37.2% at 80 °C. A H 2 /O 2 single cell assembled with the membrane reaches a peak power density of 323 mW cm − 2 , surpassing most recently reported COF‐based membranes.
科研通智能强力驱动
Strongly Powered by AbleSci AI