共聚物
第四纪
铵
质子交换膜燃料电池
膜
质子
化学工程
高分子化学
化学
材料科学
聚合物
有机化学
地质学
古生物学
生物化学
物理
量子力学
工程类
作者
Binghui Liu,Qian Liu,Yang Pang,Tong Mu,Chengji Zhao
出处
期刊:Macromolecules
[American Chemical Society]
日期:2024-10-23
卷期号:57 (21): 10338-10348
被引量:1
标识
DOI:10.1021/acs.macromol.4c02047
摘要
Polybenzimidazole (PBI) exhibits considerable advantages as a leading membrane material for high-temperature proton exchange membrane fuel cells (HT-PEMFCs). However, their harsh synthesis conditions and high processing costs have greatly restricted the large-scale commercialization of HT-PEMFCs. Therefore, developing high-performance and durable membrane materials as alternatives to PBI has been recognized as the key technical challenge for the advancement of HT-PEMFC technology. In this study, a series of novel multiblock copolymers QPSBI-b-xTMA, consisting of acidophobic pentafluorophenyl, acidophilic quaternary ammonium groups, and high free-volume spirobisindane, were synthesized by a straightforward polymerization process involving two kinds of low-molecular-weight oligomers with different structures. The resulting multiblock membranes QPSBI-b-xTMA demonstrate well-defined microporous properties, and the PA-doped membranes exhibit a microphase separation structure, which effectively facilitates proton conduction (75.45 mS cm–1@200 °C). The HT-PEMFCs based on the QPSBI-b-xTMA/PA membrane can operate efficiently within the temperature range of 160–220 °C, achieving a high peak power density of 0.84 W cm–2 without external pressure and humidity. Notably, owing to the siphoning effect of the micropores and the strong quaternary ammonium-biphosphate ion pairs, the fuel cell exhibits a stable performance at a high current density of 0.5 A cm–2 at 160 °C, with a minimal voltage degradation rate of merely 4.7 μV h–1. Thus, the newly developed QPSBI-b-xTMA/PA materials present a promising avenue for HT-PEMFC applications.
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