Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/110332
PIRA download icon_1.1View/Download Full Text
DC FieldValueLanguage
dc.contributorDepartment of Applied Physics-
dc.creatorChe, L-
dc.creatorHu, ZW-
dc.creatorZhang, T-
dc.creatorDai, PM-
dc.creatorChen, CY-
dc.creatorShen, C-
dc.creatorHuang, HT-
dc.creatorJiao, LF-
dc.creatorJin, T-
dc.creatorXie, KY-
dc.date.accessioned2024-12-03T03:34:01Z-
dc.date.available2024-12-03T03:34:01Z-
dc.identifier.issn2768-1688-
dc.identifier.urihttp://hdl.handle.net/10397/110332-
dc.language.isoenen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_US
dc.rights© 2024 The Authors. Battery Energy published by Xijing University and John Wiley & Sons Australia, Ltd.en_US
dc.rightsThe following publication Che L, Hu Z, Zhang T, et al. Regulating the interfacial chemistry of graphite in ethyl acetate-based electrolyte for low-temperature Li-ion batteries. Battery Energy. 2024; 3:20230064 is available at https://dx.doi.org/10.1002/bte2.20230064.en_US
dc.subjectEthyl acetate (EA)en_US
dc.subjectGraphiteen_US
dc.subjectInorganic-Rich SEIen_US
dc.subjectLithium-Ion batteriesen_US
dc.subjectLow-temperature electrolyteen_US
dc.titleRegulating the interfacial chemistry of graphite in ethyl acetate-based electrolyte for low-temperature Li-ion batteriesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume3-
dc.identifier.issue3-
dc.identifier.doi10.1002/bte2.20230064-
dcterms.abstractLithium-ion batteries suffer from severe capacity loss and even fail to work under subzero temperatures, which is mainly due to the sluggish Li+ transportation in the solid electrolyte interphase (SEI) and desolvation process. Ethyl acetate (EA) is a highly promising solvent for low-temperature electrolytes, yet it has poor compatibility with graphite (Gr) anode. Here, we tuned the interfacial chemistry of EA-based electrolytes via synergies of anions. ODFB- with low solvation numbers, participates in the solvation sheath, significantly reducing the desolvation energy. Meanwhile, combined with the high dissociation of FSI-, the reduction of both anions constructs an inorganic-rich SEI to improve interfacial stability. The electrolyte enables Gr anode to deliver a capacity of 293 mA h g(-1) and 2.5 Ah LiFePO4-
dcterms.abstractGr pouch cell to exhibit 96.85% capacity retention at -20 degrees C. Remarkably, LiFePO4-
dcterms.abstractGr pouch cell with the designed electrolyte can still retain 66.28% of its room-temperature capacity even at -40 degrees C.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBattery energy, May 2024, v. 3, no. 3, 20230064-
dcterms.isPartOfBattery energy-
dcterms.issued2024-05-
dc.identifier.isiWOS:001155056500001-
dc.identifier.eissn2768-1696-
dc.identifier.artn20230064-
dc.description.validate202412 bcrc-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextFundamental Research Funds for the Central Universities; National Key Research and Development Program of China; Hong Kong Polytechnic University; Natural Science Foundation of Chongqing; Natural Science Basic Research Plan in Shaanxi Province of China; Hong Kong Scholars Programen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
Appears in Collections:Journal/Magazine Article
Files in This Item:
File Description SizeFormat 
Che_Regulating_Interfacial_Chemistry.pdf2.68 MBAdobe PDFView/Open
Open Access Information
Status open access
File Version Version of Record
Access
View full-text via PolyU eLinks SFX Query
Show simple item record

Page views

84
Citations as of Feb 9, 2026

Downloads

122
Citations as of Feb 9, 2026

WEB OF SCIENCETM
Citations

12
Citations as of Apr 23, 2026

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.