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dc.contributor.authorChoe, Seunghoe-
dc.contributor.authorLee, Byung-Seok-
dc.contributor.authorCho, Min Kyung-
dc.contributor.authorKim, Hyoung-Juhn-
dc.contributor.authorHenkensmeier, Dirk-
dc.contributor.authorYoo, Sung Jong-
dc.contributor.authorKim, Jin Young-
dc.contributor.authorLee, So Young-
dc.contributor.authorPark, Hyun S.-
dc.contributor.authorJang, Jong Hyun-
dc.date.accessioned2024-01-19T22:33:16Z-
dc.date.available2024-01-19T22:33:16Z-
dc.date.created2021-09-03-
dc.date.issued2018-06-
dc.identifier.issn0926-3373-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/121312-
dc.description.abstractIn this study, IrO2-coated Ti mesh (e-IrO2/Ti) is proposed to be an efficient and durable oxygen electrode for high-temperature polymer-membrane-electrolyte water electrolyzers (HT-PEMWEs). A thin IrO2 film of submicron thickness was uniformly coated onto a porous Ti mesh substrate by anodic electrodeposition. The electrodeposited IrO2 film plays the dual role of a catalyst layer for the oxygen evolution reaction (OER), and a corrosion-protection layer that prevents oxidation of the inner Ti. The e-IrO2/Ti exhibited high performance (0.97 A cm(-2) at 1.6 V) despite a low IrO2 loading (0.4 mg cm(-2)) in single-cell tests conducted at 120 degrees C, which is comparable to that of conventional electrodes with greater catalyst loadings (0.8-5 mg cm(-2)). Furthermore, corrosion polarization tests reveal that the IrO2 coating physically blocks exposure of the Ti diffusion layer, thereby reducing Ti corrosion by 82% in 0.5 M H2SO4 at 25 degrees C. The low degradation rate (1.5 mA cm(-2) h(-1) (0.11% h(-1))) obtained in aging experiments at 120 degrees C and 1.72 V (voltage efficiency of 85%) confirms the excellent stability of this electrode.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.titleElectrodeposited IrO2/Ti electrodes as durable and cost-effective anodes in high-temperature polymer-membrane-electrolyte water electrolyzers-
dc.typeArticle-
dc.identifier.doi10.1016/j.apcatb.2017.12.037-
dc.description.journalClass1-
dc.identifier.bibliographicCitationAPPLIED CATALYSIS B-ENVIRONMENTAL, v.226, pp.289 - 294-
dc.citation.titleAPPLIED CATALYSIS B-ENVIRONMENTAL-
dc.citation.volume226-
dc.citation.startPage289-
dc.citation.endPage294-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000425476800031-
dc.identifier.scopusid2-s2.0-85039706617-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEngineering, Environmental-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.type.docTypeArticle-
dc.subject.keywordPlusOXYGEN EVOLUTION REACTION-
dc.subject.keywordPlusIRIDIUM OXIDE LOADINGS-
dc.subject.keywordPlusCOMPOSITE MEMBRANE-
dc.subject.keywordPlusSTEAM ELECTROLYSIS-
dc.subject.keywordPlusCATALYST-SUPPORT-
dc.subject.keywordPlusBIPOLAR PLATES-
dc.subject.keywordPlusNANOSIZED IROX-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusELECTROCATALYSTS-
dc.subject.keywordPlusOPERATION-
dc.subject.keywordAuthorPolymer-electrolyte-membrane water electrolysis-
dc.subject.keywordAuthorHigh temperature-
dc.subject.keywordAuthorMembrane electrode assembly-
dc.subject.keywordAuthorIrO2 catalyst-
dc.subject.keywordAuthorElectrodeposition-
dc.subject.keywordAuthorTitanium-
dc.subject.keywordAuthorCorrosion-
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KIST Article > 2018
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