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dc.contributor.authorSong, Dongshengen_US
dc.contributor.authorLiu, Heng-Juien_US
dc.contributor.authorKovacs, Andrasen_US
dc.contributor.authorDunin-Borkowski, Rafal E.en_US
dc.contributor.authorChu, Ying-Haoen_US
dc.contributor.authorZhu, Jingen_US
dc.date.accessioned2020-01-02T00:04:19Z-
dc.date.available2020-01-02T00:04:19Z-
dc.date.issued1970-01-01en_US
dc.identifier.issn0002-7820en_US
dc.identifier.urihttp://dx.doi.org/10.1111/jace.16937en_US
dc.identifier.urihttp://hdl.handle.net/11536/153376-
dc.description.abstractOxygen octahedral tilting has been recognized to strongly interact with spin, charge, orbital, and lattice degrees of freedom in perovskite oxides. Here, we observe a strain-driven stripe-like morphology of two supertetragonal (monoclinic Cc and Cm) phases in the strained BiFeO3/LaAlO3 thin films. The two supertetragonal phases have a similar giant axial ratio but differences in oxygen pyramid tilting mode. Especially, the competition between polar instability and oxygen pyramid tilting is identified using atomically resolved scanning transmission electron microscopy, leading to the polarization rotation across the phase boundary. In addition, microtwins are observed in the Cc phase. Our findings provide new insights of the coupling between ferroelectric polarization and oxygen pyramid tilting in oxide thin films and will help to design novel phase morphology with desirable ferroelectric polarization and properties for new applications in perovskite oxides.en_US
dc.language.isoen_USen_US
dc.subjectferroelectricityen_US
dc.subjectferroelectric materialsen_US
dc.subjectmultiferroicsen_US
dc.subjectperovskitesen_US
dc.subjectpolarizationen_US
dc.subjectthin filmsen_US
dc.titleObservation of oxygen pyramid tilting induced polarization rotation in strained BiFeO3 thin filmen_US
dc.typeArticleen_US
dc.identifier.doi10.1111/jace.16937en_US
dc.identifier.journalJOURNAL OF THE AMERICAN CERAMIC SOCIETYen_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000502396000001en_US
dc.citation.woscount0en_US
Appears in Collections:Articles