Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/98938
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dc.contributorDepartment of Applied Physicsen_US
dc.contributorResearch Institute for Smart Energyen_US
dc.creatorHou, Zen_US
dc.creatorZhou, Ren_US
dc.creatorYao, Yen_US
dc.creatorMin, Zen_US
dc.creatorLu, Zen_US
dc.creatorZhu, Yen_US
dc.creatorTarascon, JMen_US
dc.creatorZhang, Ben_US
dc.date.accessioned2023-06-06T00:54:35Z-
dc.date.available2023-06-06T00:54:35Z-
dc.identifier.issn1433-7851en_US
dc.identifier.urihttp://hdl.handle.net/10397/98938-
dc.language.isoenen_US
dc.publisherWiley-VCHen_US
dc.rights© 2022 Wiley-VCH GmbHen_US
dc.rightsThis is the peer reviewed version of the following article: Hou, Z., Zhou, R., Yao, Y., Min, Z., Lu, Z., Zhu, Y., Tarascon, J.-M., & Zhang, B. (2022). Correlation between Electrolyte Chemistry and Solid Electrolyte Interphase for Reversible Ca Metal Anodes. Angewandte Chemie International Edition, 61(50), e202214796, which has been published in final form at https://doi.org/10.1002/anie.202214796. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.en_US
dc.subjectCa deposition/strippingen_US
dc.subjectElectrolyte formulationen_US
dc.subjectSolid electrolyte interphaseen_US
dc.subjectSolvation structureen_US
dc.titleCorrelation between electrolyte chemistry and solid electrolyte interphase for reversible Ca metal anodesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume61en_US
dc.identifier.issue50en_US
dc.identifier.doi10.1002/anie.202214796en_US
dcterms.abstractThe development of rechargeable Ca metal batteries (RCMBs) is hindered by the Ca2+ passivating solid electrolyte interphases (SEIs). The cation solvation structure dictated by electrolyte chemistry plays a critical role in the SEIs properties. While a relatively weak cation-solvent binding is preferred in Li metal anodes to promote anion-derived SEIs, we demonstrate an enhanced Ca deposition/stripping reversibility under a strong cation-solvent interaction, which is materialized in strongly-solvating solvent and highly-dissociated salt combinations. Such electrolyte formulations benefit the formation of solvent-occupied solvation structure and minimize the anion reduction, resulting in organic-rich/CaF2-poor SEIs for reversible Ca metal anodes. Furthermore, RCMBs paired with an organic cathode using the optimized electrolytes are demonstrated as a proof-of-concept. Our work reveals the paradigm shift in SEIs design for Ca metal anodes, opening up new opportunities for emerging RCMBs.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAngewandte chemie international edition, 12 Dec. 2022, v. 61, no. 50, e202214796en_US
dcterms.isPartOfAngewandte chemie international editionen_US
dcterms.issued2022-12-12-
dc.identifier.scopus2-s2.0-85143217094-
dc.identifier.pmid36259391-
dc.identifier.eissn1521-3773en_US
dc.identifier.artne202214796en_US
dc.description.validate202306 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumbera2080-
dc.identifier.SubFormID46489-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryGreen (AAM)en_US
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