无水的
磷酸
质子
质子输运
膜
质子交换膜燃料电池
电导率
氢键
共价键
氢
化学
化学工程
材料科学
无机化学
分子
有机化学
物理化学
生物化学
物理
量子力学
工程类
作者
Xiao Pang,Benbing Shi,Yawei Liu,Hong Wu,Jianliang Shen,Jingyuan Guan,Xiaoyao Wang,Chunyang Fan,Zhen Li,Tianhao Zhu,Yan Kong,Zhongyi Jiang
标识
DOI:10.1002/anie.202423458
摘要
Phosphoric acid (H3PO4) doping is a widely employed strategy to facilitate anhydrous proton transport in high‐temperature proton exchange membrane fuel cells (HT‐PEMFCs). However, significant H3PO4 leaching during long‐term operation poses critical challenges to maintaining membrane stability and proton conductivity. Herein, H3PO4 is incorporated into positively charged nanochannels of quaternized covalent organic framework membranes (QACOFMs), leveraging strong electrostatic interactions and confinement effects to achieve exceptional H3PO4 retention under hydration conditions. Moreover, the shortened hydrogen bond length between H3PO4 (O‐H…O <2.7 Å) and the highly interconnected hydrogen bond network in the H3PO4@QACOFMs facilitate ultra‐fast anhydrous proton transport. As a result, the H3PO4@QACOFMs exhibit superior anhydrous proton transport in a broader temperature range (60‐200 oC) and the highest proton conductivity reaches about 379.7 mS cm‐1 at 200 oC.
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