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dc.contributor.authorMara , Muhammad Ikhsan-
dc.contributor.authorYang, Chaeyeon-
dc.contributor.authorGhotia, Kamal-
dc.contributor.authorEgert, Franz-
dc.contributor.authorAnsar, Syed-Asif-
dc.contributor.author?urowska, Olga-
dc.contributor.authorR?zga, Maria-
dc.contributor.authorMichalak, Artur-
dc.contributor.authorKraglund, Mikkel Rykær-
dc.contributor.authorAili, David-
dc.contributor.authorPark, Hyun S.-
dc.contributor.authorRazmjooei, Fatemeh-
dc.contributor.authorHenkensmeier, Dirk-
dc.date.accessioned2025-10-16T11:00:19Z-
dc.date.available2025-10-16T11:00:19Z-
dc.date.created2025-10-13-
dc.date.issued2025-10-
dc.identifier.issn2058-7546-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/153338-
dc.description.abstractIon solvating membranes based on polybenzimidazole (PBI) are alternatives to diaphragms in alkaline water electrolysers but can typically only operate with electrolyte concentrations of 15-30 wt% KOH. Sulfonation of the membrane broadens the operational range to 0.1 wt%-30 wt%; however, the swelling of sulfonated para-PBI means that crosslinkers are needed, complicating membrane fabrication and decreasing alkaline stability. Here we report a non-crosslinked PBI membrane with a 50% degree of sulfonation that shows a high room temperature conductivity in 1 M KOH of 135 mS cm-1. We did not observe degradation in a 6-month alkaline stability test at 80 °C. Using this membrane in an anion-exchange membrane water electrolyser, we report a current density of 4.8 A cm-2 at 2 V (3 M KOH at 80 °C; Pt and NiFe electrode catalysts); the H2 crossover to the O2 side remained <2%. Using non-platinum group metal electrodes and a polyphenylene sulfide-reinforced membrane, a cell operated for >1,000 h without failure. 1Center for-
dc.languageEnglish-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleSulfonated polybenzimidazole for low-alkalinity ion solvating membrane water electrolysis-
dc.typeArticle-
dc.identifier.doi10.1038/s41560-025-01876-9-
dc.description.journalClass1-
dc.identifier.bibliographicCitationNature Energy-
dc.citation.titleNature Energy-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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