摘要
Anion exchange membranes (AEMs), which serve as critical components in hydrogen conversion devices, have attracted considerable attention as next-generation energy materials. In this work, flexible alkyl chains were incorporated into rigid polybiphenyl backbones to synthesize a series of block poly(aryl-co-alkyl imidazolium)-based AEMs (denoted as b-PPxPEy-Im) with a well-balanced rigidity–flexibility combination. Owing to their ether-free backbones and stable imidazolium groups, these block AEMs exhibited excellent alkaline stability. The introduction of a block copolymer architecture enabled clear hydrophilic/hydrophobic microphase separation. As a result, b-PP1PE1-Im showed higher conductivity, improved flexibility, increased water uptake, superior device performance, and lower dimensional swelling than its random copolymer counterpart (r-PP1PE1-Im) at a similar ion exchange capacity. The single H 2 /O 2 fuel cell with b-PP1PE3-Im membrane achieved a peak power density of 1.08 W cm −2 at 80 °C. Moreover, an AEM water electrolyzer (AEMWE) system assembled with b-PP1PE3-Im demonstrated promising performance, reaching 2 A cm −2 at 2.24 V and 60 °C. This study offers an effective strategy for designing durable AEMs with well-rounded properties, underscoring their significant potential for application in fuel cells and water electrolyzers.
危险品化学品经营许可证(带存储)