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dc.contributor.authorHwang, Seong-Mee-
dc.contributor.authorLim, Jong-Chan-
dc.contributor.authorKim, Sang-il-
dc.contributor.authorKim, Jeong-Yeon-
dc.contributor.authorHwang, Jihyun-
dc.contributor.authorLee, Chung-hyun-
dc.contributor.authorKwon, Namhee-
dc.contributor.authorKim, Inseo-
dc.contributor.authorLee, Kimoon-
dc.contributor.authorPark, Soohyung-
dc.contributor.authorBae, Seung-Muk-
dc.contributor.authorHwang, Jin-Ha-
dc.contributor.authorLee, Kiyoung-
dc.contributor.authorKim, Hyun-Sik-
dc.date.accessioned2024-05-30T08:00:06Z-
dc.date.available2024-05-30T08:00:06Z-
dc.date.created2024-05-30-
dc.date.issued2024-08-
dc.identifier.issn0955-2219-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/149943-
dc.description.abstractLa-doped BaTiO3 ceramics are essential materials in electronic devices, finding applications in multilayer ceramic capacitors and positive temperature coefficient thermistors. While the electrical properties of La-doped BaTiO3 have been investigated, the impact of its room-temperature resistivity anomaly on dielectric properties remains unclear. We synthesized pristine and La-doped BaTiO3 (0.1 - 0.5 mol%) powders via hydrothermal methods, and then sintered bulk samples. Their resistivities (DC and AC), Curie temperature, room-temperature dielectric constant, and lattice volume with varying La doping concentrations were characterized. Beyond 0.3 mol%, the shift from electronic to ionic charge compensation mechanisms resulted in abrupt changes in resistivities, Curie temperature, and dielectric constant near 0.3 mol%. Given minimal changes in average grain size and relative density near 0.3 mol% La, the dominant factor influencing the dielectric constant peaking near this concentration was the shift in charge compensation mechanism.-
dc.languageEnglish-
dc.publisherElsevier BV-
dc.titleImpact of the change in charge compensation mechanism on the electrical, dielectric, and structural properties of La-doped BaTiO3 ceramics-
dc.typeArticle-
dc.identifier.doi10.1016/j.jeurceramsoc.2023.12.029-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJournal of the European Ceramic Society, v.44, no.9, pp.5471 - 5479-
dc.citation.titleJournal of the European Ceramic Society-
dc.citation.volume44-
dc.citation.number9-
dc.citation.startPage5471-
dc.citation.endPage5479-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid001226378500001-
dc.identifier.scopusid2-s2.0-85179820427-
dc.relation.journalWebOfScienceCategoryMaterials Science, Ceramics-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusBARIUM-TITANATE-
dc.subject.keywordPlusHYDROTHERMAL SYNTHESIS-
dc.subject.keywordPlusCRYSTAL-STRUCTURE-
dc.subject.keywordPlusPOWDERS-
dc.subject.keywordPlusSIZE-
dc.subject.keywordPlusTEMPERATURE-
dc.subject.keywordPlusBEHAVIOR-
dc.subject.keywordPlusPARTICLE-
dc.subject.keywordPlusDY-
dc.subject.keywordAuthorLa -doped BaTiO 3-
dc.subject.keywordAuthorMultilayer ceramic capacitor-
dc.subject.keywordAuthorResistivity-
dc.subject.keywordAuthorDielectric constant-
dc.subject.keywordAuthorCharge compensation-
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