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dc.contributor.authorChang, SG-
dc.contributor.authorLee, HJ-
dc.contributor.authorKang, H-
dc.contributor.authorPark, SM-
dc.date.accessioned2016-03-31T13:18:18Z-
dc.date.available2016-03-31T13:18:18Z-
dc.date.created2009-03-13-
dc.date.issued2001-05-20-
dc.identifier.issn0253-2964-
dc.identifier.other2001-OAK-0000002017-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/19527-
dc.description.abstractSurface films formed prior to bulk reduction of lithium have been studied at gold, platinum, and copper electrodes in rigorously dried propylene carbonate solutions using electrochemical quartz crystal microbalance (EQCM) and secondary ion mass spectrometry experiments. The results indicate that the passive film formation takes place at a potential as positive as about 2.0 V vs. Li/Li+, and the passive film thus formed in this potential region is thicker than a monolayer. Quantitative analysis of the EQCM results indicates that electrogenerated lithium reacts with solvent molecules to produce a passive film consisting of lithium carbonate and other compounds of larger molecular weights. The presence of lithium carbonate is verified by SIMS, whereas the lithium compounds of low molecular weights, including lithium hydroxide and oxide, are not detected. Further lithium reduction takes place underneath the passive film at potentials lower than 1.2 V with a voltammetric current peak at about 0.6 V.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherKOREAN CHEMICAL SOC-
dc.relation.isPartOfBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.subjectsurface films-
dc.subjectpassivation-
dc.subjectlithium reduction-
dc.subjectpropylene carbonate-
dc.subjectelectrochemical quartz crystal microbalance-
dc.subjectsecondary ion mass spectrometry-
dc.subjectGRAPHITE INTERCALATION COMPOUNDS-
dc.subjectELECTROCHEMICAL-BEHAVIOR-
dc.subjectUNDERPOTENTIAL DEPOSITION-
dc.subjectCATHODIC DECOMPOSITION-
dc.subjectACETONITRILE SOLUTIONS-
dc.subjectORGANIC ELECTROLYTES-
dc.subjectNEGATIVE ELECTRODE-
dc.subjectHYPERTHERMAL CS+-
dc.subjectBATTERIES-
dc.subjectLI-
dc.titleCharacterization of surface films formed prior to bulk reduction of lithium in rigorously dried propylene carbonate solutions-
dc.typeArticle-
dc.contributor.college화학과-
dc.author.googleChang, SG-
dc.author.googleLee, HJ-
dc.author.googleKang, H-
dc.author.googlePark, SM-
dc.relation.volume22-
dc.relation.issue5-
dc.relation.startpage481-
dc.relation.lastpage487-
dc.contributor.id10200281-
dc.relation.journalBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.22, no.5, pp.481 - 487-
dc.identifier.wosid000169010900013-
dc.date.tcdate2019-01-01-
dc.citation.endPage487-
dc.citation.number5-
dc.citation.startPage481-
dc.citation.titleBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.citation.volume22-
dc.contributor.affiliatedAuthorPark, SM-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc4-
dc.type.docTypeArticle-
dc.subject.keywordPlusGRAPHITE INTERCALATION COMPOUNDS-
dc.subject.keywordPlusELECTROCHEMICAL-BEHAVIOR-
dc.subject.keywordPlusUNDERPOTENTIAL DEPOSITION-
dc.subject.keywordPlusCATHODIC DECOMPOSITION-
dc.subject.keywordPlusACETONITRILE SOLUTIONS-
dc.subject.keywordPlusORGANIC ELECTROLYTES-
dc.subject.keywordPlusNEGATIVE ELECTRODE-
dc.subject.keywordPlusHYPERTHERMAL CS+-
dc.subject.keywordPlusBATTERIES-
dc.subject.keywordPlusLI-
dc.subject.keywordAuthorsurface films-
dc.subject.keywordAuthorpassivation-
dc.subject.keywordAuthorlithium reduction-
dc.subject.keywordAuthorpropylene carbonate-
dc.subject.keywordAuthorelectrochemical quartz crystal microbalance-
dc.subject.keywordAuthorsecondary ion mass spectrometry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.description.journalRegisteredClassother-
dc.relation.journalResearchAreaChemistry-

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