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High-Energy Quasi-Solid-State Lithium-Sulfur Batteries Based on Electrostatic-Nucleophilic Synergy

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dc.contributor.authorZhang, Yi-
dc.contributor.authorSong, Xiaosheng-
dc.contributor.authorZhao, Yong-
dc.contributor.authorPark, Geon-Tae-
dc.contributor.authorSun, Yang-Kook-
dc.date.accessioned2026-06-23T00:30:28Z-
dc.date.available2026-06-23T00:30:28Z-
dc.date.issued2026-03-
dc.identifier.issn2380-8195-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/214321-
dc.description.abstractQuasi-solid-state-polymer-electrolyte-based (QSSE-based) quasi-solid-state lithium-sulfur batteries (QSSLSBs) are an emerging research focus because they are safe and deliver high energy density. However, sluggish interfacial reaction kinetics involving the sulfur cathode and QSSE remains a core developmental bottleneck. Herein, we reveal that the cations and anions of tetrabutylammonium iodide (TBAI) promote S3 center dot- generation via a synergistic electrostatic-nucleophilic catalysis mechanism that accelerates lithium polysulfide conversion. Accordingly, we innovatively introduced TBAI into the cathode-QSSE interface to construct an QSSE with a catalytically active interfacial layer that realized enhanced interface reaction kinetics. The cycling performance of the assembled QSSLSBs: an average decay rate of only 0.038% per cycle over 1600 stable long cycles at 0.2 C; a capacity retention of 70.5% after 100 cycles at 0.1 C under a high sulfur loading of 6.5 mg<middle dot>cm-2. The synergistic electrostatic-nucleophilic catalysis strategy developed herein provides innovative insight that addresses the sluggish interfacial kinetics of the QSSLSB cathode.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherAMER CHEMICAL SOC-
dc.titleHigh-Energy Quasi-Solid-State Lithium-Sulfur Batteries Based on Electrostatic-Nucleophilic Synergy-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acsenergylett.5c04332-
dc.identifier.scopusid2-s2.0-105032741670-
dc.identifier.wosid001686297400001-
dc.identifier.bibliographicCitationACS ENERGY LETTERS, v.11, no.3, pp 2924 - 2934-
dc.citation.titleACS ENERGY LETTERS-
dc.citation.volume11-
dc.citation.number3-
dc.citation.startPage2924-
dc.citation.endPage2934-
dc.type.docTypeArticle-
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.keywordPlusELECTROLYTE-
dc.subject.keywordPlusCONDUCTIVITY-
dc.subject.keywordPlusSOLVATION-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acsenergylett.5c04332-
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