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dc.contributor.author선양국-
dc.date.accessioned2018-03-10T16:04:22Z-
dc.date.available2018-03-10T16:04:22Z-
dc.date.issued2013-02-
dc.identifier.citationJournal of power sources, Feb 2013, 223, P.1-8en_US
dc.identifier.issn0378-7753-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0378775312014383?via%3Dihub-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/44807-
dc.description.abstractFacile synthesis of rhombohedral type FeF3 introduced via two consecutive steps is introduced: i) acidic treatment of Fe2O3 followed by thermal evaporation at 80 degrees C resulting in hydrated beta-FeF3 center dot 3H(2)O and ii) a simple thermal decomposition of the as-received beta-FeF3 center dot 3H(2)O at 400 degrees C under an Ar atmosphere. A Rietveld refinement of x-ray diffraction data for the as-synthesized FeF3 indicates the formation of a highly crystalline FeF3 structure with a R (3) over barc space group. To overcome the high ionicity and improve the diffusivity, FeF3 is ball-milled with the aid of carbon (acetylene black). The electrochemical performance of nanosized FeF3 is not favored in voltage range of 1.5-4.5 V been_US
dc.description.sponsorshipcause the repetitive intercalation-conversion reaction accelerates the structural disruption within a few cycles, although a high capacity (518 mAh (g-fluoride)(-1) at 20 mA g(-1)) is observed, assisted by the three-electron redox of Fe3+/0. Raising the lower cut-off voltage to 2 V. which allows only intercalation reaction, the FeF3 delivers a high capacity of 224 mAh g(-1) with significantly improved capacity retention (71% at 100th cycle). (C) 2012 Elsevier B.V. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherElsevier Science B.V., Amsterdam.en_US
dc.subjectEvaporation synthesisen_US
dc.subjectIron trifluorideen_US
dc.subjectIntercalationen_US
dc.subjectConversionen_US
dc.subjectLithiumen_US
dc.subjectBatteryen_US
dc.titleIron trifluoride synthesized via evaporation method and its application to rechargeable lithium batteriesen_US
dc.typeArticleen_US
dc.relation.volume223-
dc.identifier.doi10.1016/j.jpowsour.2012.09.027-
dc.relation.page1-8-
dc.relation.journalJOURNAL OF POWER SOURCES-
dc.contributor.googleauthorMyung, S. T.-
dc.contributor.googleauthorSakurada, S.-
dc.contributor.googleauthorYashiro, H.-
dc.contributor.googleauthorSun, Y. K.-
dc.relation.code2013010943-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF ENGINEERING[S]-
dc.sector.departmentDEPARTMENT OF ENERGY ENGINEERING-
dc.identifier.pidyksun-
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COLLEGE OF ENGINEERING[S](공과대학) > ENERGY ENGINEERING(에너지공학과) > Articles
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