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Phase formation and electrical properties of SBNLT ceramics prepared via combustion technique

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dc.contributor.author Sinkruason T.
dc.contributor.author Luangpangai A.
dc.contributor.author Charoenthai N.
dc.contributor.author Rittidech A.
dc.contributor.author Pulphol P.
dc.contributor.author Vittayakorn N.
dc.contributor.author Bongkarn T.
dc.contributor.other Srinakharinwirot University
dc.date.accessioned 2023-11-15T02:08:42Z
dc.date.available 2023-11-15T02:08:42Z
dc.date.issued 2023
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-85165616625&doi=10.1080%2f02670836.2023.2238415&partnerID=40&md5=2177bea8e03a9197a39fc4138176c477
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/29470
dc.description.abstract This 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.publisher Taylor and Francis Ltd.
dc.subject dielectric
dc.subject ferroelectric
dc.subject SBNLT
dc.subject solid-state combustion
dc.title Phase formation and electrical properties of SBNLT ceramics prepared via combustion technique
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Materials Science and Technology (United Kingdom). Vol 39, No.18 (2023), p.3065-3075
dc.identifier.doi 10.1080/02670836.2023.2238415


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