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Novel anion exchange membranes exhibit enhanced performance in electrochemical devices, indicating significant improvements in efficiency.
Anion exchange membranes (AEMs) with high ionic conductivity, good mechanical properties, and dimensional stability are crucial for preparing the corresponding high-performance electrochemical devices, such as anion exchange membrane water electrolyzers (AEMWEs) and anion exchange membrane fuel cells (AEMFCs). In this study, we have developed a series of novel cross-linking AEMs based on two commercial engineering plastics, polybenzimidazole (PBI) and polysulfone (PSF), in which the functionalized PBI (PBI-Pip) was employed as a highly hydrophilic basic polymer and the chloromethylated PSF was employed as a macromolecular cross-linker. The membranes displayed distinct hydrophilic/hydrophobic micro-phase separation given the effective aggregation of the hydrophilic domains, which was driven by the hydrophilic PBI-Pip. In comparison to the reported PBI-based AEMs, the (PBI-Pip)-PSF-3 membrane exhibited higher hydroxide conductivity of 136.1 mS/cm with a much lower swelling ratio of 28% at 80 °C. Furthermore, this membrane demonstrated excellent mechanical properties with the tensile strength at break of 34.56 MPa and elongation at break of 19.2% under wet state. The cross-linking structure and the highly hydrophilic basic polymer were important for the performance of the membranes. After being assembled with (PBI-Pip)-PSF-3, the AEMWE achieved a maximum current density of 3.0 A/cm 2 at 2.0 V at 80 °C and the corresponding AEMFC exhibited a peak power density of nearly 500 mW/cm 2 at 80 °C.
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Gao et al. (2026) studied this question.
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