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研究论文

物理限域与化学锚定协同的POSS交联膦酸化聚苯并咪唑高温质子交换膜

靳蔚宜, 唐逸, 杨天奇, 黄子恒, 宫琛亮*   

  1. 兰州大学化学化工学院 天然产物化学全国重点实验室 兰州 730000
  • 投稿日期:2026-06-10
  • 作者简介:纪念兰州大学化学学科创建80周年”专辑
  • 基金资助:
    甘肃省自然科学基金重点项目(24JRRA391)专项资助.

POSS-crosslinked Phosphonated Polybenzimidazole High-temperature Proton Exchange Membrane with Synergistic Physical Confinement and Chemical Anchoring

Jin Weiyi, Tang Yi, Yang Tianqi, Huang Ziheng, Gong Chenliang*   

  1. State Key Laboratory of Natural Product Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, 730000
  • Received:2026-06-10
  • Contact: * E-mail: gongchl@lzu.edu.cn
  • Supported by:
    Key Project of the Natural Science Foundation of Gansu Province (24JRRA391).

磷酸掺杂聚苯并咪唑(PA/PBI)是高温质子交换膜燃料电池(HT-PEMFCs)中最具应用潜力的电解质材料,但其在高磷酸掺杂量下存在磷酸易流失与膜过度溶胀的问题,严重影响电池的长期稳定性。针对上述问题,本研究设计了一种结合物理空间限制与化学固定作用的协同改性方案,以环氧多面体低聚倍半硅氧烷(epoxy-POSS)为刚性交联节点,与含羟基聚苯并咪唑(OHPBI)构筑三维交联网络,同时引入含膦酸基团的小分子二乙基(4-羟基苯基)磷酸酯(HDP),实现磷酸的稳定锚定与质子传输通道的构建。系统研究了交联网络与膦酸基团对膜结构与性能的影响。结果表明,EP10膜在磷酸吸收率达261%的条件下,溶胀率仅为112%,相较于纯OHPBI实现了高负载与低溶胀的协同优化。在180 ℃无水条件下,EP10膜的质子传导率达101.9 mS cm-1,活化能低至13.3 kJ mol-1,单电池峰值功率密度为1.013 W cm-2,约为纯OHPBI的两倍。冷启动热循环与加速应力测试进一步证实该膜在动态工况下具有优异的运行稳定性。上述结果表明,基于环氧POSS与膦酸小分子的双效协同策略,为构建高性能、高稳定性高温质子交换膜提供了可行路径。

关键词: 高温质子交换膜, 聚苯并咪唑, 多面体低聚倍半硅氧烷(POSS), 膦酸固定化, 交联

Phosphoric acid-doped polybenzimidazole (PA/PBI) is one of the most promising electrolyte materials for high-temperature proton exchange membrane fuel cells (HT-PEMFCs). However, it suffers from severe phosphoric acid leakage and excessive membrane swelling under high doping levels, which critically impair long-term stability. To address this challenge, this work proposes a synergistic strategy combining “physical confinement” and “chemical anchoring”. An epoxy-functionalized polyhedral oligomeric silsesquioxane (epoxy-POSS) was employed as a rigid crosslinking node to construct a three-dimensional crosslinked network with hydroxyl-containing polybenzimidazole (OHPBI). Meanwhile, a phosphonic acid-containing small molecule, 4-hydroxyphenyl dihydrogen phosphate (HDP), was introduced to achieve stable phosphoric acid anchoring and to build efficient proton transport pathways. The effects of the crosslinked network and phosphonic acid groups on membrane structure and performance were systematically investigated. The results show that the EP10 membrane achieves a phosphoric acid uptake of 261% while exhibiting a swelling ratio as low as 112%, demonstrating an excellent balance between high acid loading and dimensional stability compared to pristine OHPBI. Under anhydrous conditions at 180 °C, the EP10 membrane exhibits a proton conductivity of 101.9 mS cm-1 with an activation energy as low as 13.3 kJ mol-1. The single-cell peak power density reaches 1.013 W cm-2, approximately twice that of pristine OHPBI. Cold-start thermal cycling and accelerated stress tests further confirm the excellent operational stability of the membrane under dynamic conditions. These results demonstrate that the dual synergistic strategy based on epoxy-POSS crosslinking and phosphonic acid immobilization provides a viable route toward high-performance and durable high-temperature proton exchange membranes.

Key words: High-temperature proton exchange membrane, Polybenzimidazole, Polyhedral oligomeric silsesquioxane (POSS), Phosphonic acid immobilization, Crosslinking