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Facile Modification of LiAlCl4 Electrolytes for Mg-Li Hybrid Batteries by the Conditioning-Free Method

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dc.contributor.authorCho, Jae-Hyun-
dc.contributor.authorHa, Jung Hoon-
dc.contributor.authorOh, Jinwoo-
dc.contributor.authorLee, Sue Bin-
dc.contributor.authorKim, Kwang-Bum-
dc.contributor.authorLee, Kwan-Young-
dc.contributor.authorLee, Jae Kyun-
dc.date.accessioned2021-08-30T07:54:26Z-
dc.date.available2021-08-30T07:54:26Z-
dc.date.created2021-06-18-
dc.date.issued2020-11-25-
dc.identifier.issn1932-7447-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/51450-
dc.description.abstractLithium aluminum chloride complexes (LACCs) are excellent electrolyte candidates for Mg-Li hybrid batteries (MgHBs) because they can simultaneously conduct electrochemical reactions both at Mg anodes and Li+- insertion cathodes. However, to ensure compatibility with Mg anodes, LACCs must first undergo a cumbersome conditioning process; this severely lowers their productivity and limits any improvement in the electrolyte performance. To resolve this issue, we employed a conditioning-free process for the facile modification of LACCs. The conditioning-free process was conducted by reacting LACCs and metallic Mg powder with a small amount of CrCl3 that promotes the rapid and high-degree substitution of oxidation states between anionic Al3+ complexes and Mg. The newly generated Mg2+ ions in the conditioning-free LACC (cf-LACC) reached a high concentration of up to 1.2 M and formed anionic complexes that function as charge carriers for Mg anodes. Moreover, the cf-LACC electrolyte successfully demonstrated its applicability to the MgHB system, which used a high voltage cathode material LiFePO4, by exhibiting excellent rate capability and cyclability.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.titleFacile Modification of LiAlCl4 Electrolytes for Mg-Li Hybrid Batteries by the Conditioning-Free Method-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Kwan-Young-
dc.identifier.doi10.1021/acs.jpcc.0c07914-
dc.identifier.scopusid2-s2.0-85096566785-
dc.identifier.wosid000595545800009-
dc.identifier.bibliographicCitationJOURNAL OF PHYSICAL CHEMISTRY C, v.124, no.47, pp.25738 - 25747-
dc.relation.isPartOfJOURNAL OF PHYSICAL CHEMISTRY C-
dc.citation.titleJOURNAL OF PHYSICAL CHEMISTRY C-
dc.citation.volume124-
dc.citation.number47-
dc.citation.startPage25738-
dc.citation.endPage25747-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
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