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Structural and electrical properties of c-axis epitaxial and polycrystalline Sr3Bi4Ti6O21 thin films

dc.contributor.authorZhang, S. T.en_US
dc.contributor.authorChen, Y. F.en_US
dc.contributor.authorSun, H. P.en_US
dc.contributor.authorPan, Xiaoqingen_US
dc.contributor.authorTan, W. S.en_US
dc.contributor.authorLiu, Zhi-Guoen_US
dc.contributor.authorMing, N. B.en_US
dc.date.accessioned2006-12-19T18:57:05Z
dc.date.available2006-12-19T18:57:05Z
dc.date.issued2003-03-05en_US
dc.identifier.citationZhang, S T; Chen, Y F; Sun, H P; Pan, X Q; Tan, W S; Liu, Z G; Ming, N B (2003). "Structural and electrical properties of c-axis epitaxial and polycrystalline Sr3Bi4Ti6O21 thin films." Journal of Physics: Condensed Matter. 15(8): 1223-1233. <http://hdl.handle.net/2027.42/48891>en_US
dc.identifier.issn0953-8984en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/48891
dc.description.abstractc-axis epitaxial and polycrystalline Sr3Bi4Ti6O21 (SBTi) thin films were fabricated on (001)SrTiO3 (STO) single-crystal substrates and Pt/Ti2/SiO2/Si substrates respectively, by pulsed laser deposition (PLD). Structures of the films were systematically characterized by x-ray diffraction (XRD), including θ– 2θ-scans, rocking curve scans and φ-scans, atomic force microscopy and transmission electron microscopy (TEM). The epitaxial orientation relation of the SBTi films on STO is established by selected-area electron diffraction and XRD φ-scans to be (001)SBTi ∥ (001)STO, [1 _1 0]SBTi ∥ [010]STO. Cross-sectional high-resolution TEM studies on the epitaxial SBTi film revealed that SBTi is a single-phase material. A special kind of irrational atomic shift along the [001] direction was observed and is discussed in detail. By using an evanescent microwave probe (EMP), the room-temperature dielectric constant of the epitaxial SBTi film was measured to be 211 ± 20. Excellent electrical properties of the polycrystalline SBTi films with Pt bottom and top electrodes were exhibited: the Pr and Ec values were 4.1 μC cm−2 and 75 kV cm−1 respectively, the nonvolatile polarizations decreased by less than 5% after 2.22 × 109 switching cycles and the dielectric constant and loss tangent were 363 and 0.04 at 100 kHz.en_US
dc.format.extent3118 bytes
dc.format.extent296531 bytes
dc.format.mimetypetext/plain
dc.format.mimetypeapplication/pdf
dc.language.isoen_US
dc.publisherIOP Publishing Ltden_US
dc.titleStructural and electrical properties of c-axis epitaxial and polycrystalline Sr3Bi4Ti6O21 thin filmsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Materials Science and Engineering, The University of Michigan, Ann Arbor, MI 48109-2136, USAen_US
dc.contributor.affiliationumDepartment of Materials Science and Engineering, The University of Michigan, Ann Arbor, MI 48109-2136, USAen_US
dc.contributor.affiliationotherNational Laboratory of Solid State Microstructures and Department of Materials Science and Engineering, Nanjing University, Nanjing 210093, Chinaen_US
dc.contributor.affiliationotherNational Laboratory of Solid State Microstructures and Department of Materials Science and Engineering, Nanjing University, Nanjing 210093, Chinaen_US
dc.contributor.affiliationotherNational Laboratory of Solid State Microstructures and Department of Physics, Nanjing University, Nanjing 210093, Chinaen_US
dc.contributor.affiliationotherNational Laboratory of Solid State Microstructures and Department of Materials Science and Engineering, Nanjing University, Nanjing 210093, Chinaen_US
dc.contributor.affiliationotherNational Laboratory of Solid State Microstructures and Department of Materials Science and Engineering, Nanjing University, Nanjing 210093, Chinaen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/48891/2/c30807.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1088/0953-8984/15/8/307en_US
dc.identifier.sourceJournal of Physics: Condensed Matter.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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