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通过表面引发聚合制备连续超薄两性离子共价有机框架膜以实现优异的保水性能

Continuous Ultrathin Zwitterionic Covalent Organic Framework Membrane Via Surface-Initiated Polymerization Toward Superior Water Retention.

作者信息

Liu Lin, Ma Yu, Li Bo, Yin Liying, Zang Hong-Ying, Zhang Ning, Bi Hai, Wang Shaolei, Zhu Guangshan

机构信息

Faculty of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China.

Ji Hua Laboratory, Foshan, 528200, P. R. China.

出版信息

Small. 2024 Apr;20(16):e2308499. doi: 10.1002/smll.202308499. Epub 2023 Nov 27.

DOI:10.1002/smll.202308499
PMID:38009797
Abstract

Efficient construction of proton transport channels in proton exchange membranes maintaining conductivity under varied humidity is critical for the development of fuel cells. Covalent organic frameworks (COFs) hold great potential in providing precise and fast ion transport channels. However, the preparation of continuous free-standing COF membranes retaining their inherent structural advantages to realize excellent proton conduction performance is a major challenge. Herein, a zwitterionic COF material bearing positive ammonium ions and negative sulphonic acid ions is developed. Free-standing COF membrane with adjustable thickness is constructed via surface-initiated polymerization of COF monomers. The porosity, continuity, and stability of the membranes are demonstrated via the transmission electron microscopy (TEM), atomic force microscopy (AFM), and scanning electron microscopy (SEM) characterization. The rigidity of the COF structure avoids swelling in aqueous solution, which improves the chemical stability of the proton exchange membranes and improves the performance stability. In the higher humidity range (50-90%), the prepared zwitterionic COF membrane exhibits superior capability in retaining the conductivity compared to COF membrane merely bearing sulphonic acid group. The established strategy shows the potential for the application of zwitterionic COF in the proton exchange membrane fuel cells.

摘要

在质子交换膜中高效构建质子传输通道,使其在不同湿度下保持导电性,这对燃料电池的发展至关重要。共价有机框架(COF)在提供精确且快速的离子传输通道方面具有巨大潜力。然而,制备能够保留其固有结构优势以实现优异质子传导性能的连续自支撑COF膜是一项重大挑战。在此,开发了一种带有正铵离子和负磺酸离子的两性离子COF材料。通过COF单体的表面引发聚合构建了厚度可调的自支撑COF膜。通过透射电子显微镜(TEM)、原子力显微镜(AFM)和扫描电子显微镜(SEM)表征证明了膜的孔隙率、连续性和稳定性。COF结构的刚性避免了在水溶液中的溶胀,这提高了质子交换膜的化学稳定性并改善了性能稳定性。在较高湿度范围(50 - 90%)内,与仅带有磺酸基团的COF膜相比,所制备的两性离子COF膜在保持导电性方面表现出卓越的能力。所建立的策略显示了两性离子COF在质子交换膜燃料电池中的应用潜力。

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