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Article: Salt-in-presalt electrolyte solutions for high-potential non-aqueous sodium metal batteries

TitleSalt-in-presalt electrolyte solutions for high-potential non-aqueous sodium metal batteries
Authors
Issue Date2025
Citation
Nature Nanotechnology, 2025, v. 20, n. 3, p. 388-396 How to Cite?
AbstractRoom-temperature non-aqueous sodium metal batteries are viable candidates for cost-effective and safe electrochemical energy storage. However, they show low specific energy and poor cycle life as the use of conventional organic-based non-aqueous electrolyte solutions enables the formation of interphases that cannot prevent degradations at the positive and negative electrodes. Here, to promote the formation of inorganic NaF-rich interphases on both negative and positive electrodes, we propose the salt-in-presalt (SIPS) electrolyte formulation strategy. In SIPS, sodium bis(fluorosulfonyl)imide (NaFSI) salt is dissolved in the liquid precursor of the sodium bis(trifluoromethylsulfonyl)imide (NaTFSI) salt, that is, N,N-dimethyltrifluoromethane-sulfonamide, called PreTFSI. The prepared 0.5 M NaFSI in PreTFSI (SIPS5) electrolyte solution shows an electrochemical stability up to 6.7 V versus Na|Na+ and enables a Na stripping/plating average Coulombic efficiency of 99.7% at 2.0 mA cm−2 and 4.0 mAh cm−2 in Na||Al cell configuration. By testing SIPS5 in Na metal and ‘anode-less’ coin and pouch cell configurations using NaNi0.6Mn0.2Co0.2O2 or sulfurized polyacrylonitrile as positive electrode active materials, we demonstrate the ability of the SIPS strategy to deliver improved specific discharge capacity and capacity retentions at high cell potentials and moderate applied specific currents for cell cycle life up to 1,000 cycles.
Persistent Identifierhttp://hdl.handle.net/10722/355452
ISSN
2023 Impact Factor: 38.1
2023 SCImago Journal Rankings: 14.577

 

DC FieldValueLanguage
dc.contributor.authorLi, Ai Min-
dc.contributor.authorZavalij, Peter Y.-
dc.contributor.authorOmenya, Fred-
dc.contributor.authorLi, Xiaolin-
dc.contributor.authorWang, Chunsheng-
dc.date.accessioned2025-04-08T03:40:48Z-
dc.date.available2025-04-08T03:40:48Z-
dc.date.issued2025-
dc.identifier.citationNature Nanotechnology, 2025, v. 20, n. 3, p. 388-396-
dc.identifier.issn1748-3387-
dc.identifier.urihttp://hdl.handle.net/10722/355452-
dc.description.abstractRoom-temperature non-aqueous sodium metal batteries are viable candidates for cost-effective and safe electrochemical energy storage. However, they show low specific energy and poor cycle life as the use of conventional organic-based non-aqueous electrolyte solutions enables the formation of interphases that cannot prevent degradations at the positive and negative electrodes. Here, to promote the formation of inorganic NaF-rich interphases on both negative and positive electrodes, we propose the salt-in-presalt (SIPS) electrolyte formulation strategy. In SIPS, sodium bis(fluorosulfonyl)imide (NaFSI) salt is dissolved in the liquid precursor of the sodium bis(trifluoromethylsulfonyl)imide (NaTFSI) salt, that is, N,N-dimethyltrifluoromethane-sulfonamide, called PreTFSI. The prepared 0.5 M NaFSI in PreTFSI (SIPS5) electrolyte solution shows an electrochemical stability up to 6.7 V versus Na|Na+ and enables a Na stripping/plating average Coulombic efficiency of 99.7% at 2.0 mA cm−2 and 4.0 mAh cm−2 in Na||Al cell configuration. By testing SIPS5 in Na metal and ‘anode-less’ coin and pouch cell configurations using NaNi0.6Mn0.2Co0.2O2 or sulfurized polyacrylonitrile as positive electrode active materials, we demonstrate the ability of the SIPS strategy to deliver improved specific discharge capacity and capacity retentions at high cell potentials and moderate applied specific currents for cell cycle life up to 1,000 cycles.-
dc.languageeng-
dc.relation.ispartofNature Nanotechnology-
dc.titleSalt-in-presalt electrolyte solutions for high-potential non-aqueous sodium metal batteries-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1038/s41565-024-01848-2-
dc.identifier.pmid39849064-
dc.identifier.scopuseid_2-s2.0-85217167045-
dc.identifier.volume20-
dc.identifier.issue3-
dc.identifier.spage388-
dc.identifier.epage396-
dc.identifier.eissn1748-3395-

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