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Base tolerant polybenzimidazolium hydroxide membranes for solid alkaline-exchange membrane fuel cells

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dc.contributor.authorLee, Ju Yeon-
dc.contributor.authorLim, Dong-Hee-
dc.contributor.authorChae, Ji Eon-
dc.contributor.authorChoi, Jieun-
dc.contributor.authorKim, Bo Hyun-
dc.contributor.authorLee, So Young-
dc.contributor.authorYoon, Chang Won-
dc.contributor.authorNam, Sang Yong-
dc.contributor.authorJang, Jong Hyun-
dc.contributor.authorHenkensmeier, Dirk-
dc.contributor.authorYoo, Sung Jong-
dc.contributor.authorKim, Jin-Young-
dc.contributor.authorKim, Hyoung-Juhn-
dc.contributor.authorHam, Hyung Chul-
dc.date.accessioned2022-12-26T20:03:04Z-
dc.date.available2022-12-26T20:03:04Z-
dc.date.issued2016-09-
dc.identifier.issn0376-7388-
dc.identifier.issn1873-3123-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/15263-
dc.description.abstractPoly(dibenzylated benzimidazolium) bromides (Bz-PBI-Br) were converted successfully to OH- ion conducting poly(dibenzylated benzimidazolium) hydroxides (Bz-PBI-hydroxides) by the treatment of KOH. The Bz-PBI-hydroxides obtained in this study showed an excellent alkali tolerance compared to previously synthesized poly(dimethylated benzimidazolium) hydroxides (Me-PBI-hydroxides). According to H-1-NMR analysis, Me-PBI-hydroxides were decomposed during KOH treatment. In order to find out the reason, density functional theory (DFT) calculations of two benzimidazolium structures, e.g., di-methylated benzimidazolium (Me-BI+) and dibenzylated benzimidazolium (Bz-BI+), were performed. Bz-BI+ showed lower electron affinity and OH--binding energies at the C2 position of the benzimidazolium ring than Me-BI+ These DFT results strongly confirm that Bz-BI+ is less vulnerable to an OH attack than Me-BI+; this contributes to the enhanced stability and OH- ion conductivity of the Bz-PBI-hydroxides. (C) 2016 Elsevier B.V. All rights reserved.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleBase tolerant polybenzimidazolium hydroxide membranes for solid alkaline-exchange membrane fuel cells-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.memsci.2016.05.012-
dc.identifier.scopusid2-s2.0-84968725200-
dc.identifier.wosid000378060100040-
dc.identifier.bibliographicCitationJournal of Membrane Science, v.514, pp 398 - 406-
dc.citation.titleJournal of Membrane Science-
dc.citation.volume514-
dc.citation.startPage398-
dc.citation.endPage406-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusINITIO MOLECULAR-DYNAMICS-
dc.subject.keywordPlusTOTAL-ENERGY CALCULATIONS-
dc.subject.keywordPlusAUGMENTED-WAVE METHOD-
dc.subject.keywordPlusIMIDAZOLIUM CATIONS-
dc.subject.keywordPlusBASIS-SET-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordPlusPOLYMER-
dc.subject.keywordPlusMETALS-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordAuthorPoly(dibenzylated benzimidazolium) hydroxide-
dc.subject.keywordAuthorSolid alkaline membrane fuel cell-
dc.subject.keywordAuthorOH- ion conductivity-
dc.subject.keywordAuthorDensity functional theory-
dc.subject.keywordAuthorElectron affinity-
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