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dc.contributor.authorT. Bongkarnen_US
dc.contributor.authorG. Rujijanagulen_US
dc.contributor.authorS. J. Milneen_US
dc.date.accessioned2018-09-10T03:48:41Z-
dc.date.available2018-09-10T03:48:41Z-
dc.date.issued2008-03-14en_US
dc.identifier.issn00036951en_US
dc.identifier.other2-s2.0-40549110595en_US
dc.identifier.other10.1063/1.2890060en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=40549110595&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/60740-
dc.description.abstractThe irreversibility of the antiferroelectric (AFE) to FE phase transition in Pb1-x Bax Zr O3, x=0.75-0.1, compositions is shown to be a consequence of lattice vacancies arising from PbO evaporation during ceramic processing. Previously, the absence of a FE→AFE cooling transition was thought to be due to the transformational strain and the fragmentation of ferroelectric domains. Appropriate compensating levels of excess PbO added to starting powders generate the FE→AFE transition. For lower levels of Ba2+ substitution, x=0.05, the transition is reversible in noncompensated samples, but PbO compensation raises the FE→AFE transition temperature by ∼25 °C. © 2008 American Institute of Physics.en_US
dc.subjectPhysics and Astronomyen_US
dc.titleAntiferroelectric-ferroelectric phase transitions in Pb1-x Bax Zr O3 ceramics: Effect of PbO contenten_US
dc.typeJournalen_US
article.title.sourcetitleApplied Physics Lettersen_US
article.volume92en_US
article.stream.affiliationsNaresuan Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversity of Leedsen_US
Appears in Collections:CMUL: Journal Articles

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