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High-Energy Quasi-Solid-State Lithium-Sulfur Batteries Based on Electrostatic-Nucleophilic Synergy
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Zhang, Yi | - |
| dc.contributor.author | Song, Xiaosheng | - |
| dc.contributor.author | Zhao, Yong | - |
| dc.contributor.author | Park, Geon-Tae | - |
| dc.contributor.author | Sun, Yang-Kook | - |
| dc.date.accessioned | 2026-06-23T00:30:28Z | - |
| dc.date.available | 2026-06-23T00:30:28Z | - |
| dc.date.issued | 2026-03 | - |
| dc.identifier.issn | 2380-8195 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/214321 | - |
| dc.description.abstract | Quasi-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.extent | 11 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | AMER CHEMICAL SOC | - |
| dc.title | High-Energy Quasi-Solid-State Lithium-Sulfur Batteries Based on Electrostatic-Nucleophilic Synergy | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1021/acsenergylett.5c04332 | - |
| dc.identifier.scopusid | 2-s2.0-105032741670 | - |
| dc.identifier.wosid | 001686297400001 | - |
| dc.identifier.bibliographicCitation | ACS ENERGY LETTERS, v.11, no.3, pp 2924 - 2934 | - |
| dc.citation.title | ACS ENERGY LETTERS | - |
| dc.citation.volume | 11 | - |
| dc.citation.number | 3 | - |
| dc.citation.startPage | 2924 | - |
| dc.citation.endPage | 2934 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalResearchArea | Electrochemistry | - |
| dc.relation.journalResearchArea | Energy & Fuels | - |
| dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
| dc.relation.journalResearchArea | Materials Science | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
| dc.relation.journalWebOfScienceCategory | Electrochemistry | - |
| dc.relation.journalWebOfScienceCategory | Energy & Fuels | - |
| dc.relation.journalWebOfScienceCategory | Nanoscience & Nanotechnology | - |
| dc.relation.journalWebOfScienceCategory | Materials Science, Multidisciplinary | - |
| dc.subject.keywordPlus | ELECTROLYTE | - |
| dc.subject.keywordPlus | CONDUCTIVITY | - |
| dc.subject.keywordPlus | SOLVATION | - |
| dc.identifier.url | https://pubs.acs.org/doi/10.1021/acsenergylett.5c04332 | - |
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