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dc.contributor.authorLi, Mingqiangen_US
dc.contributor.authorCheng, Xiaoxingen_US
dc.contributor.authorLi, Ningen_US
dc.contributor.authorLiu, Heng-Juien_US
dc.contributor.authorHuang, Yen-Linen_US
dc.contributor.authorLiu, Kaihuien_US
dc.contributor.authorChu, Ying-Haoen_US
dc.contributor.authorYu, Dapengen_US
dc.contributor.authorChen, Long-Qingen_US
dc.contributor.authorIkuhara, Yuichien_US
dc.contributor.authorGao, Pengen_US
dc.date.accessioned2018-08-21T05:53:41Z-
dc.date.available2018-08-21T05:53:41Z-
dc.date.issued2018-05-25en_US
dc.identifier.issn2469-9950en_US
dc.identifier.urihttp://dx.doi.org/10.1103/PhysRevB.97.180103en_US
dc.identifier.urihttp://hdl.handle.net/11536/145029-
dc.description.abstractThe effective screening of the polarization bound charge is a prerequisite to stabilize the ferroelectricity in ferroelectric thin films. Here, by combining annular bright field imaging and electron energy-loss spectroscopy (EELS) in an aberration-corrected scanning transmission electron microscope with phase-field simulations, we investigate the screening mechanism by quantitatively measuring the structural relaxation at Pb(Zr0.2Ti0.8)O-3/SrTiO3 interfaces. We find that the thickness of the interfacial layer is similar to 3.5 unit cells (similar to 1.4 nm) in a domain with upward polarization and similar to 5.5 unit cells (similar to 2.2 nm) in a domain with downward polarization. Phase-field simulations, an EELS analysis, and a lattice parameter analysis verify the existence of interfacial oxygen vacancies accounting for the narrower interfacial layer in the domain with upward polarization. Our study indicates the internal structural relaxation at the interface is the dominant mechanism for the polarization charge screening for ferroelectric films grown on insulating substrates and has implications for our understanding of domain switching in ferroelectric devices.en_US
dc.language.isoen_USen_US
dc.titleAtomic-scale mechanism of internal structural relaxation screening at polar interfacesen_US
dc.typeArticleen_US
dc.identifier.doi10.1103/PhysRevB.97.180103en_US
dc.identifier.journalPHYSICAL REVIEW Ben_US
dc.citation.volume97en_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:000433061700002en_US
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