Formation of core-shell structure in the BaTiO3-SrTiO3 system

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dc.contributor.authorKim, JSko
dc.contributor.authorKang, Suk-Joong Lko
dc.date.accessioned2013-03-03T00:40:09Z-
dc.date.available2013-03-03T00:40:09Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1999-04-
dc.identifier.citationJOURNAL OF THE AMERICAN CERAMIC SOCIETY, v.82, no.4, pp.1085 - 1088-
dc.identifier.issn0002-7820-
dc.identifier.urihttp://hdl.handle.net/10203/76291-
dc.description.abstractWhen a 1-mol%-Fe2O3-added 0.67BaTiO(3)-0.33SrTiO(3) (mole ratio) powder compact was sintered at 1380 degrees C, a core-shell structure was developed. The core phase formed via solid-state interdiffusion of barium and strontium ions between BaTiO3 and SrTiO3 particles. In contrast, the shell phase formed via a solution-precipitation process in the presence of an Fe2O3-containing liquid phase. Energy-dispersive X-ray analysis showed that the core was a strontium-rich paraelectric phase and the shell was a barium-rich ferroelectric phase at room temperature. The core-shell structure developed in the BaTiO3-SrTiO3 system suggests the possibility of obtaining a variety of phase distributions with different Curie temperatures.-
dc.languageEnglish-
dc.publisherAMER CERAMIC SOC-
dc.subjectBARIUM-TITANATE CERAMICS-
dc.subjectDIELECTRIC-PROPERTIES-
dc.subjectZIRCONIA-
dc.subjectBATIO3-
dc.titleFormation of core-shell structure in the BaTiO3-SrTiO3 system-
dc.typeArticle-
dc.identifier.wosid000079929000043-
dc.identifier.scopusid2-s2.0-0032668110-
dc.type.rimsART-
dc.citation.volume82-
dc.citation.issue4-
dc.citation.beginningpage1085-
dc.citation.endingpage1088-
dc.citation.publicationnameJOURNAL OF THE AMERICAN CERAMIC SOCIETY-
dc.contributor.localauthorKang, Suk-Joong L-
dc.contributor.nonIdAuthorKim, JS-
dc.type.journalArticleArticle-
dc.subject.keywordPlusBARIUM-TITANATE CERAMICS-
dc.subject.keywordPlusDIELECTRIC-PROPERTIES-
dc.subject.keywordPlusZIRCONIA-
dc.subject.keywordPlusBATIO3-
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