材料科学
电解质
共价有机骨架
热重分析
化学工程
傅里叶变换红外光谱
电导率
介电谱
质子输运
共价键
聚合物
质子
膜
电化学
复合材料
物理化学
电极
有机化学
多孔性
化学
物理
工程类
生物化学
量子力学
作者
Yuki Okamura,Y. Tanada,M. Sasano,Keita Akagi,M. Isobe,Satoshi Tsuchiya,Naohiko Takimoto,Fumiya Kobayashi,Makoto Tadokoro,Kaname Kanai
标识
DOI:10.1002/admi.202400928
摘要
Abstract Recently, hexaazatriphenylene (HA)‐based covalent organic frameworks have garnered attention as polymer electrolyte membranes (PEMs) in polymer electrolyte fuel cells due to their robust framework and strong ion‐trapping capabilities. In this study, quinone‐functionalized HA‐based covalent organic frameworks (HAQ‐COFs) are synthesized by hydrothermal synthesis. This method is much simpler than the synthesis methods previously reported, and is also suitable for mass production. X‐ray diffraction (XRD) and Fourier‐transform infrared measurements reveal that HAQ‐COF exhibits a crystal structure where 2D molecular layers, formed by HA units and bridging paraquinone units, are stacked, creating pores that align to form channels for ion transport. Thermogravimetry and XRD measurements, as a function of temperature, demonstrate that HAQ‐COF exhibits high water retention capacity at room temperature and atmospheric pressure and has greater thermal stability than other PEMs. Electrochemical impedance spectroscopy measurements indicate that the proton conductivity of HAQ‐COF remains nearly unaffected by changes in external humidity, allowing it to sustain high proton conductivity even under sudden humidity drops. Moreover, the activation energy for proton hopping conduction in HAQ‐COF is significantly lower compared to that of similar proton conductors.
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