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Modulating Lithium Metal Interphase Structures via Functional Design of Polymeric Ionic Liquids for Quasi-Solid-State Batteries

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dc.contributor.authorJeong, Wooyoung-
dc.contributor.authorKim, Young-Jun-
dc.contributor.authorLee, Jong-Won-
dc.date.accessioned2025-03-05T06:00:15Z-
dc.date.available2025-03-05T06:00:15Z-
dc.date.issued2025-02-
dc.identifier.issn2574-0962-
dc.identifier.issn2574-0962-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/206679-
dc.description.abstractDespite the great potential of Li-metal anodes, the high reactivity of Li metal and dendritic Li growth hinder the stable operation of Li-metal batteries. Artificial Li protective layers have been introduced as a solution to stabilize the interface between the electrolyte and the Li-metal anode. In this study, we propose a functionally designed polymeric ionic liquid (PIL) for the interfacial stabilization of Li-metal anodes in quasi-solid-state batteries. Polycationic PILs are designed to form conductive and robust interphases at the PIL/Li while serving as an effective electrostatic shield to suppress dendrite growth. In addition to the optimized composition for facile Li+ transport kinetics in the PIL, the anion configurations in the PIL are engineered to produce highly ionic-conductive Li3N and to increase the concentration of LiF in the solid-electrolyte interphase. A PIL-coated Li-metal electrode (PIL thickness similar to 5 mu m) exhibits reduced interfacial resistance and enhanced cycling performances for the Li symmetric cell and full cell with a quasi-solid-state electrolyte and a high-loading LiNi0.8Co0.1Mn0.1O2 cathode (4 mAh cm-2). These findings provide insights into the design of protective PIL layers for constructing a stable interface between the electrolyte and the Li-metal anode.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherAMER CHEMICAL SOC-
dc.titleModulating Lithium Metal Interphase Structures via Functional Design of Polymeric Ionic Liquids for Quasi-Solid-State Batteries-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acsaem.4c03341-
dc.identifier.scopusid2-s2.0-85217580473-
dc.identifier.wosid001417474300001-
dc.identifier.bibliographicCitationACS Applied Energy Materials, v.8, no.4, pp 2638 - 2646-
dc.citation.titleACS Applied Energy Materials-
dc.citation.volume8-
dc.citation.number4-
dc.citation.startPage2638-
dc.citation.endPage2646-
dc.type.docTypeArticle; Early Access-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEnergy & Fuels-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEnergy & Fuels-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusELECTROLYTES-
dc.subject.keywordAuthorLi-metal anode-
dc.subject.keywordAuthorprotective layer-
dc.subject.keywordAuthorpolymericionic liquid-
dc.subject.keywordAuthorsolid-electrolyte interphase-
dc.subject.keywordAuthorinterfacial stabilization-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acsaem.4c03341-
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