Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/110332
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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
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