Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/29470
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dc.contributor.authorSinkruason T.
dc.contributor.authorLuangpangai A.
dc.contributor.authorCharoenthai N.
dc.contributor.authorRittidech A.
dc.contributor.authorPulphol P.
dc.contributor.authorVittayakorn N.
dc.contributor.authorBongkarn T.
dc.contributor.otherSrinakharinwirot University
dc.date.accessioned2023-11-15T02:08:42Z-
dc.date.available2023-11-15T02:08:42Z-
dc.date.issued2023
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85165616625&doi=10.1080%2f02670836.2023.2238415&partnerID=40&md5=2177bea8e03a9197a39fc4138176c477
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/29470-
dc.description.abstractThis report investigates the effect of firing temperatures on the phase formation, microstructure, electrical, and energy storage properties of lead-free Sr0.3(Bi0.7Na0.67Li0.03)0.5TiO3 (SBNLT) ceramics, synthesised by combustion technique. The samples were calcined between 700°C and 900°C for 2 h and sintered between 1100°C and 1200°C for 2 h. The ceramics exhibited coexisting rhombohedral and tetragonal phases, which were confirmed by the Rietveld refinement technique. A morphotropic phase boundary (MPB) of the rhombohedral and tetragonal phases, with a ratio of 49:51, was obtained at the sintering temperature of 1175°C. The highest maximum dielectric constant (ε max= 4667), polarisation (P max= 28.80 µC/cm2) and energy density (W = 0.95 J/cm3), with a breakdown strength of 70 kV/cm, were achieved from the sample sintered at 1175°C. © 2023 Institute of Materials, Minerals and Mining.
dc.publisherTaylor and Francis Ltd.
dc.subjectdielectric
dc.subjectferroelectric
dc.subjectSBNLT
dc.subjectsolid-state combustion
dc.titlePhase formation and electrical properties of SBNLT ceramics prepared via combustion technique
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationMaterials Science and Technology (United Kingdom). Vol 39, No.18 (2023), p.3065-3075
dc.identifier.doi10.1080/02670836.2023.2238415
Appears in Collections:Scopus 2023

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