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Crack-Engineered Microporous Layer for Mitigating Cathode Flooding in Polymer Electrolyte Fuel Cells

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dc.contributor.authorPark, Young Je-
dc.contributor.authorChoi, Won Young-
dc.contributor.authorPark, Seong Hyun-
dc.contributor.authorChoi, Hyunguk-
dc.contributor.authorChoi, Seo Won-
dc.contributor.authorJyoung, Jy-Young-
dc.contributor.authorLee, Eunsook-
dc.contributor.authorPark, Jae-ll-
dc.contributor.authorKo, Min Jae-
dc.contributor.authorLee, Kang Taek-
dc.contributor.authorJung, Chi-Young-
dc.date.accessioned2026-01-02T02:30:15Z-
dc.date.available2026-01-02T02:30:15Z-
dc.date.issued2025-06-
dc.identifier.issn2380-8195-
dc.identifier.issn2380-8195-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/210204-
dc.description.abstractCrack engineering within the microporous layer (MPL) of the gas diffusion layer (GDL) has emerged as a promising strategy to alleviate severe cathode flooding in polymer electrolyte fuel cells (PEFCs), especially under high current operation. Here, we report a connected-crack MPL architecture that forms continuous liquid water highways, extending from the catalyst layer (CL) to the GDL backing layer, effectively separating the liquid/gas transport. Three-dimensional reconstruction using X-ray computed tomography reveals that the microengineered cracks significantly reduce flooding at the CL-MPL interface by providing efficient drainage. Compared to the noncrack GDL, the connected-crack GDL (C-GDL) exhibits 20% higher peak power density of 1.23 W cm-2. Pore-scale simulations further validate the antiflooding capabilities of C-GDL, showing a 25-fold enhancement in water removal. This crack-engineered GDL thus offers an efficient and scalable route to water management challenges, enabling robust and high-performance PEFCs suitable for heavy-duty vehicle electrification.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleCrack-Engineered Microporous Layer for Mitigating Cathode Flooding in Polymer Electrolyte Fuel Cells-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acsenergylett.5c01202-
dc.identifier.scopusid2-s2.0-105008374275-
dc.identifier.wosid001508709500001-
dc.identifier.bibliographicCitationACS Energy Letters, v.10, no.7, pp 3241 - 3248-
dc.citation.titleACS Energy Letters-
dc.citation.volume10-
dc.citation.number7-
dc.citation.startPage3241-
dc.citation.endPage3248-
dc.type.docTypeArticle; Early Access-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaElectrochemistry-
dc.relation.journalResearchAreaEnergy & Fuels-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryElectrochemistry-
dc.relation.journalWebOfScienceCategoryEnergy & Fuels-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusGAS-DIFFUSION-LAYER-
dc.subject.keywordPlusOXYGEN REDUCTION REACTION-
dc.subject.keywordPlusTRANSPORT-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acsenergylett.5c01202-
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