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dc.contributor.authorZhu, Y. M.en_US
dc.contributor.authorKe, D.en_US
dc.contributor.authorYu, R.en_US
dc.contributor.authorHsieh, Y. H.en_US
dc.contributor.authorLiu, H. J.en_US
dc.contributor.authorLiu, P. P.en_US
dc.contributor.authorChu, Y. H.en_US
dc.contributor.authorZhan, Q.en_US
dc.date.accessioned2014-12-08T15:29:45Z-
dc.date.available2014-12-08T15:29:45Z-
dc.date.issued2013-03-18en_US
dc.identifier.issn0003-6951en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.4796037en_US
dc.identifier.urihttp://hdl.handle.net/11536/21377-
dc.description.abstractThe pattern configuration and interface structure in epitaxial BiFeO3-CoFe2O4 heterostructures grown on (010) pc NdGaO3 substrates have been investigated systematically by transmission electron microscopy and chemical analysis. The crystal orientation of CoFe2O4 variants was tuned to [111](CFO), while BiFeO3 kept [010](pc) matching the substrate. Triangular prism-shaped CoFe2O4 embedded in the BiFeO3 matrix grew as an equilibrium island mode with {111}(CFO) as its surfaces and interfaces. Two types of BiFeO3-CoFe2O4 orientation relationships were determined as (001)[010](BFO)//(0-22)[111](CFO) and (101)[010](BFO)//(similar to 220)[111](CFO). The results reveal that the dominant factors controlling the growth orientation of the present vertical heterostructures are surface energy anisotropy and atomic structure continuity. (C) 2013 American Institute of Physics. [http://dx.doi.org/10.1063/1.4796037]en_US
dc.language.isoen_USen_US
dc.titleSelf-assembled perovskite-spinel heterostructure on a highly distorted substrateen_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.4796037en_US
dc.identifier.journalAPPLIED PHYSICS LETTERSen_US
dc.citation.volume102en_US
dc.citation.issue11en_US
dc.citation.epageen_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:000316544900028-
dc.citation.woscount3-
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