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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/1103
DC FieldValueLanguage
dc.contributor.authorBlizanac, B.en
dc.contributor.authorMentus, Slavkoen
dc.contributor.authorCvijetićanin, N.en
dc.contributor.authorPavlović, N.en
dc.date.accessioned2022-12-16T17:30:07Z-
dc.date.available2022-12-16T17:30:07Z-
dc.date.issued2003-01-01en
dc.identifier.issn0352-5139en
dc.identifier.urihttps://dspace.ffh.bg.ac.rs/handle/123456789/1103-
dc.description.abstractGraphite Lonza KS44 in a solution 1 M LiC1O4 in a propoylene carbonate - ethylene carbonate (1 M:1 M) mixture was lithiated and delithiated galvanostatically at room temperature and at the elevated temperature of 55°C. Voltage-time profiles and complex impedance diagrams were recorded and are discussed for this particular system. It was confirmed that this type of graphite shows a relatively small current loss consumed by exfoliation, if lithiated at room temperature. However, the voltage-time curve of the first charging at 55°C shows a long voltage plateau at 0.7 V vs. Li/Li-, which corresponds to 540 mAh g-1 of irreversible capacity attributed to exfoliation. The solid electrolyte layer formed at elevated temperature, although less protecting in the sense of electrolyte reduction, shows a remarkably higher electrical resistance than that formed at room temperature. A comparison of the impedance diagrams of lithiated and delithiated samples allows the conclusion that mass transfer through the graphite, not that through the solid electrolyte layer, plays a dominant role in the mass transfer limitations.en
dc.relation.ispartofJournal of the Serbian Chemical Societyen
dc.subjectGalvanostatic chargingen
dc.subjectGraphiteen
dc.subjectLithiationen
dc.subjectReversible capacityen
dc.subjectSolid electrolyte layeren
dc.titleTemperature effect on graphite KS44 lithiation in ethylene carbonate + propylene carbonate solution: Galvanostatic and impedance studyen
dc.typeArticleen
dc.identifier.doi10.2298/JSC0302119Ben
dc.identifier.scopus2-s2.0-0037251384en
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/0037251384en
dc.relation.firstpage119en
dc.relation.lastpage130en
dc.relation.issue2en
dc.relation.volume68en
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeArticle-
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University of Belgrade
Faculty of Physical Chemistry
Studentski trg 12-16
11158 Belgrade 118
PAC 105305
SERBIA
University of Belgrade Faculty of Physical Chemistry