Abstract
Issues of unsatisfactory ionic conductivity and chemical stability should be solved for anion exchange membranes (AEMs) in practical fuel cell applications. A series of flexible spacers, homologous multi-cationic cross-linkers with different lengths, were designed and synthesized from 1,4-diazabicyclo(2.2.2)octane (DABCO) and 1,6-dibromohexane, and subsequently used to fabricate a series of flexible multi-cationic cross-linked poly(aryl ether sulfone) (CQPAES) AEMs. The CQPAES membranes fabricated by simultaneous cross-linking and membrane formation are tough and pliable. The length and number of cations of the cross-linkers show noticeable effects on the comprehensive membrane performance. The CQPAES membranes display more distinct nano-phase separation morphology and well-developed ion transfer channels due to the higher mobility and hydrophilicity of the flexible long-chain multi-cationic segments. As a result, the CQPAES membranes exhibit gradually increased water uptake and ionic conductivity with the increase of cross-linker length. Furthermore, DABCO and hexyl segments in the cross-linker greatly enhance the steric hindrance and electron cloud density of the quaternary ammonium groups, which inhibit the Hoffmann elimination reaction. Consequently, the CQPAES membranes display a significant improvement in alkali stability than conventional benzyl-substituted quaternary ammonium group type AEMs.
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