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dc.contributor.authorKachaporn Sanjoomen_US
dc.contributor.authorGobwute Rujijanagulen_US
dc.date.accessioned2018-09-04T09:30:47Z-
dc.date.available2018-09-04T09:30:47Z-
dc.date.issued2013-01-01en_US
dc.identifier.issn15635112en_US
dc.identifier.issn00150193en_US
dc.identifier.other2-s2.0-84891750584en_US
dc.identifier.other10.1080/00150193.2013.842778en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84891750584&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/52704-
dc.description.abstractThe BiFeO3was prepared by a mixed oxide, solid-state reaction method. Excess Bi2O3(1-7wt%) was introduced prior to powder calcination to compensate for any Bi2O3that may have been lost from the samples due to volatilization during heat treatments. Various heating rates (1-10°C/min) were performed at the calcination state. X-ray diffraction analysis revealed that pure phase BFO was observed for the samples calcined at a low heating rate (1°C/min) and contained lower amount of Bi2O3.The higher levels of excess Bi2O3produced an increased in dielectric constant and dielectric loss. Further, ferroelectric behavior was improved for higher amount Bi2O3contented samples. © 2013 Copyright Taylor and Francis Group, LLC.en_US
dc.subjectMaterials Scienceen_US
dc.subjectPhysics and Astronomyen_US
dc.titleEffects of process parameter and excess Bi<inf>2</inf>O<inf>3</inf>on phase formation and electrical properties of BiFeO<inf>3</inf>ceramicsen_US
dc.typeJournalen_US
article.title.sourcetitleFerroelectricsen_US
article.volume454en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsCommission on Higher Educationen_US
Appears in Collections:CMUL: Journal Articles

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