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Article: In situ formation of polymer-inorganic solid-electrolyte interphase for stable polymeric solid-state lithium-metal batteries

TitleIn situ formation of polymer-inorganic solid-electrolyte interphase for stable polymeric solid-state lithium-metal batteries
Authors
Keywordscomposite polymer electrolyte
interfacial chemistry
lithium batteries
lithium dendrite
SDG11: Sustainable cities and communities
SDG7: Affordable and clean energy
SDG9: Industry innovation and infrastructure
solid-electrolyte interphase
Issue Date2021
Citation
Chem, 2021, v. 7, n. 11, p. 3052-3068 How to Cite?
AbstractComposite polymer electrolytes (CPEs) for solid-state Li-metal batteries (SSLBs) still suffer from gradually increased interface resistance and unconstrained Li-dendrite growth. Herein, we addressed the challenges by designing a LiF-rich inorganic solid-electrolyte interphase (SEI) through introducing a fluoride-salt-concentrated interlayer on CPE film. The rigid but flexible CPE helps accommodate the volume change of electrodes, while the polymeric highly concentrated electrolyte (PHCE) surface-layer regulates Li-ion flux due to the formation of a stable LiF-rich SEI via anion reduction. The designed CPE-PHCE presents enhanced ionic conductivity and high oxidation stability of >5.0 V (versus Li/Li+). Furthermore, it dramatically reduces the interfacial resistance and achieves a high critical current density of 4.5 mA cm−2. The SSLBs, fabricated with thin CPE-PHCE membranes (<100 μm) and Co-free LiNiO2 cathodes, exhibit exceptional electrochemical performance and long cycling stability. This approach of SEI design can also be applied to other types of batteries.
Persistent Identifierhttp://hdl.handle.net/10722/355430
ISSN
2023 SCImago Journal Rankings: 6.556

 

DC FieldValueLanguage
dc.contributor.authorDeng, Tao-
dc.contributor.authorCao, Longsheng-
dc.contributor.authorHe, Xinzi-
dc.contributor.authorLi, Ai Min-
dc.contributor.authorLi, Dan-
dc.contributor.authorXu, Jijian-
dc.contributor.authorLiu, Sufu-
dc.contributor.authorBai, Panxing-
dc.contributor.authorJin, Ting-
dc.contributor.authorMa, Lin-
dc.contributor.authorSchroeder, Marshall A.-
dc.contributor.authorFan, Xiulin-
dc.contributor.authorWang, Chunsheng-
dc.date.accessioned2025-04-08T03:40:40Z-
dc.date.available2025-04-08T03:40:40Z-
dc.date.issued2021-
dc.identifier.citationChem, 2021, v. 7, n. 11, p. 3052-3068-
dc.identifier.issn2451-9308-
dc.identifier.urihttp://hdl.handle.net/10722/355430-
dc.description.abstractComposite polymer electrolytes (CPEs) for solid-state Li-metal batteries (SSLBs) still suffer from gradually increased interface resistance and unconstrained Li-dendrite growth. Herein, we addressed the challenges by designing a LiF-rich inorganic solid-electrolyte interphase (SEI) through introducing a fluoride-salt-concentrated interlayer on CPE film. The rigid but flexible CPE helps accommodate the volume change of electrodes, while the polymeric highly concentrated electrolyte (PHCE) surface-layer regulates Li-ion flux due to the formation of a stable LiF-rich SEI via anion reduction. The designed CPE-PHCE presents enhanced ionic conductivity and high oxidation stability of >5.0 V (versus Li/Li+). Furthermore, it dramatically reduces the interfacial resistance and achieves a high critical current density of 4.5 mA cm−2. The SSLBs, fabricated with thin CPE-PHCE membranes (<100 μm) and Co-free LiNiO2 cathodes, exhibit exceptional electrochemical performance and long cycling stability. This approach of SEI design can also be applied to other types of batteries.-
dc.languageeng-
dc.relation.ispartofChem-
dc.subjectcomposite polymer electrolyte-
dc.subjectinterfacial chemistry-
dc.subjectlithium batteries-
dc.subjectlithium dendrite-
dc.subjectSDG11: Sustainable cities and communities-
dc.subjectSDG7: Affordable and clean energy-
dc.subjectSDG9: Industry innovation and infrastructure-
dc.subjectsolid-electrolyte interphase-
dc.titleIn situ formation of polymer-inorganic solid-electrolyte interphase for stable polymeric solid-state lithium-metal batteries-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.chempr.2021.06.019-
dc.identifier.scopuseid_2-s2.0-85118863312-
dc.identifier.volume7-
dc.identifier.issue11-
dc.identifier.spage3052-
dc.identifier.epage3068-
dc.identifier.eissn2451-9294-

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