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Germanium and Tin Selenide Nanocrystals for High-Capacity Lithium Ion Batteries: Comparative Phase Conversion of Germanium and Tin

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dc.contributor.authorIm, Hyung Soon-
dc.contributor.authorLim, Young Rok-
dc.contributor.authorCho, Yong Jae-
dc.contributor.authorPark, Jeunghee-
dc.contributor.authorCha, Eun Hee-
dc.contributor.authorKang, Hong Seok-
dc.date.accessioned2021-09-05T05:01:10Z-
dc.date.available2021-09-05T05:01:10Z-
dc.date.created2021-06-15-
dc.date.issued2014-09-25-
dc.identifier.issn1932-7447-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/97371-
dc.description.abstractGermanium and tin sulfide nanostructures are considered the most promising candidates for useful alternative materials in commercial Li-graphite anodes of lithium ion batteries. Selenides have received less attention, but the electrochemical reaction mechanism is still being debated. We report the novel synthesis of GeSex and SnSex (x = 1 and 2) nanocrystals by a gas-phase laser photolysis reaction and their 0.8 excellent reversible capacity for lithium ion batteries. The capacity was 400-800 (mA h)/g after 70 cycles, which is close to the theoretical capacity (Li4.4Ge or Li4.4Sn). Remarkably, SnSex exhibited higher rate capabilities than GeSex. Ex situ X-ray diffraction and Raman spectroscopy revealed the cubic-tetragonal phase conversion of Ge and Sn upon lithiation/delithiation to support their distinctive lithium ion battery capacities. First-principles calculations of the Li intercalation volume change indicate that the smallest volume expansion in the cubic Sn phase can guarantee the enhanced cycling capability of the Sn compounds.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.subjectLI-
dc.subjectELECTRODES-
dc.subjectSTORAGE-
dc.subjectOXIDE-
dc.subjectGE-
dc.subjectPERFORMANCE-
dc.subjectANODE-
dc.subjectCOMPOSITE-
dc.subjectPOWDERS-
dc.titleGermanium and Tin Selenide Nanocrystals for High-Capacity Lithium Ion Batteries: Comparative Phase Conversion of Germanium and Tin-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Jeunghee-
dc.identifier.doi10.1021/jp507337c-
dc.identifier.scopusid2-s2.0-84949117250-
dc.identifier.wosid000342396300017-
dc.identifier.bibliographicCitationJOURNAL OF PHYSICAL CHEMISTRY C, v.118, no.38, pp.21884 - 21888-
dc.relation.isPartOfJOURNAL OF PHYSICAL CHEMISTRY C-
dc.citation.titleJOURNAL OF PHYSICAL CHEMISTRY C-
dc.citation.volume118-
dc.citation.number38-
dc.citation.startPage21884-
dc.citation.endPage21888-
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-
dc.subject.keywordPlusLI-
dc.subject.keywordPlusELECTRODES-
dc.subject.keywordPlusSTORAGE-
dc.subject.keywordPlusOXIDE-
dc.subject.keywordPlusGE-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusANODE-
dc.subject.keywordPlusCOMPOSITE-
dc.subject.keywordPlusPOWDERS-
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