Cui Yang
(, ), Yu Huang
(, ), Wanjie Song
(, ), Mingyue Wu
(, ), Jinyu Nie
(, ), Yaoming Wang
(, ), Liang Wu
(, ), Xiaolin Ge
(, ), Tongwen Xu
(, )
{"title":"Enhanced OH− conductivity and alkaline stability of AEM by pyrene stacking backbone for water electrolysis","authors":"Cui Yang \n (, ), Yu Huang \n (, ), Wanjie Song \n (, ), Mingyue Wu \n (, ), Jinyu Nie \n (, ), Yaoming Wang \n (, ), Liang Wu \n (, ), Xiaolin Ge \n (, ), Tongwen Xu \n (, )","doi":"10.1007/s40843-025-3504-1","DOIUrl":null,"url":null,"abstract":"<div><p>A burgeoning hydrogen technology utilizing anion exchange membranes (AEMs) has attracted increasing interest owing to its potential for cost-effective commercial values. Nonetheless, there are still challenges pertaining to conductivity and persistent stability. Herein, an innovative approach has been introduced to enhance the alkaline resistance and conductivity of AEMs via π-π interactions. The synergistic π-stacking networks in the polymer backbone induce long-range cation aggregation through directed self-assembly, generating ionic cluster microdomains. These nanoconfined environments elevate local hydroxide concentration, leading to the increased density of accessible ion hopping sites within the localized regions. Furthermore, the electron-donating effects of pyrene effectively reduce the electrostatic potential of the β-H adjacent to quaternary ammonium cations, thus increasing the energy barrier for OH<sup>−</sup> nucleophilic attack. The obtained AEMs demonstrate exceptional performance, exhibiting both high conductivity (160 mS/cm) and excellent alkaline stability (merely 0.35% conductivity degradation after 1950 h in 2 M KOH at 80 °C). These good properties enable the membrane electrode assembly (MEA) to achieve the current density of 2.58 A/cm<sup>2</sup> at 1.8 V, while maintaining stable operation for over 700 h in durability testing.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":773,"journal":{"name":"Science China Materials","volume":"68 10","pages":"3657 - 3666"},"PeriodicalIF":7.4000,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science China Materials","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s40843-025-3504-1","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
A burgeoning hydrogen technology utilizing anion exchange membranes (AEMs) has attracted increasing interest owing to its potential for cost-effective commercial values. Nonetheless, there are still challenges pertaining to conductivity and persistent stability. Herein, an innovative approach has been introduced to enhance the alkaline resistance and conductivity of AEMs via π-π interactions. The synergistic π-stacking networks in the polymer backbone induce long-range cation aggregation through directed self-assembly, generating ionic cluster microdomains. These nanoconfined environments elevate local hydroxide concentration, leading to the increased density of accessible ion hopping sites within the localized regions. Furthermore, the electron-donating effects of pyrene effectively reduce the electrostatic potential of the β-H adjacent to quaternary ammonium cations, thus increasing the energy barrier for OH− nucleophilic attack. The obtained AEMs demonstrate exceptional performance, exhibiting both high conductivity (160 mS/cm) and excellent alkaline stability (merely 0.35% conductivity degradation after 1950 h in 2 M KOH at 80 °C). These good properties enable the membrane electrode assembly (MEA) to achieve the current density of 2.58 A/cm2 at 1.8 V, while maintaining stable operation for over 700 h in durability testing.
期刊介绍:
Science China Materials (SCM) is a globally peer-reviewed journal that covers all facets of materials science. It is supervised by the Chinese Academy of Sciences and co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China. The journal is jointly published monthly in both printed and electronic forms by Science China Press and Springer. The aim of SCM is to encourage communication of high-quality, innovative research results at the cutting-edge interface of materials science with chemistry, physics, biology, and engineering. It focuses on breakthroughs from around the world and aims to become a world-leading academic journal for materials science.