3
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

      Ferromagnetic and multiferroic interfaces in granular perovskite composite xLa0.5Sr0.5CoO3-(1−x)BiFeO3

      1 , 2 , 1 , 1
      Journal of Applied Physics
      AIP Publishing

      Read this article at

      ScienceOpenPublisher
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Related collections

          Most cited references42

          • Record: found
          • Abstract: found
          • Article: not found

          Epitaxial BiFeO3 multiferroic thin film heterostructures.

          Enhancement of polarization and related properties in heteroepitaxially constrained thin films of the ferroelectromagnet, BiFeO3, is reported. Structure analysis indicates that the crystal structure of film is monoclinic in contrast to bulk, which is rhombohedral. The films display a room-temperature spontaneous polarization (50 to 60 microcoulombs per square centimeter) almost an order of magnitude higher than that of the bulk (6.1 microcoulombs per square centimeter). The observed enhancement is corroborated by first-principles calculations and found to originate from a high sensitivity of the polarization to small changes in lattice parameters. The films also exhibit enhanced thickness-dependent magnetism compared with the bulk. These enhanced and combined functional responses in thin film form present an opportunity to create and implement thin film devices that actively couple the magnetic and ferroelectric order parameters.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Multiferroic magnetoelectric composites: Historical perspective, status, and future directions

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Multiferroic BaTiO3-CoFe2O4 Nanostructures.

              We report on the coupling between ferroelectric and magnetic order parameters in a nanostructured BaTiO3-CoFe2O4 ferroelectromagnet. This facilitates the interconversion of energies stored in electric and magnetic fields and plays an important role in many devices, including transducers, field sensors, etc. Such nanostructures were deposited on single-crystal SrTiO3 (001) substrates by pulsed laser deposition from a single Ba-Ti-Co-Fe-oxide target. The films are epitaxial in-plane as well as out-of-plane with self-assembled hexagonal arrays of CoFe2O4 nanopillars embedded in a BaTiO3 matrix. The CoFe2O4 nanopillars have uniform size and average spacing of 20 to 30 nanometers. Temperature-dependent magnetic measurements illustrate the coupling between the two order parameters, which is manifested as a change in magnetization at the ferroelectric Curie temperature. Thermodynamic analyses show that the magnetoelectric coupling in such a nanostructure can be understood on the basis of the strong elastic interactions between the two phases.
                Bookmark

                Author and article information

                Journal
                Journal of Applied Physics
                Journal of Applied Physics
                AIP Publishing
                0021-8979
                1089-7550
                August 21 2016
                August 21 2016
                : 120
                : 7
                : 074103
                Affiliations
                [1 ]Centro Atómico Bariloche, Comisión Nacional de Energía Atómica, CONICET and Instituto Balseiro, Universidad Nacional de Cuyo, 8400 San Carlos de Bariloche, RN, Argentina
                [2 ]INTEQUI, Universidad Nacional de San Luis, CONICET, Área de Química General e Inorgánica “Dr. G.F.Puelles”- Facultad de Química, Bioquímica y Farmacia, Chacabuco y Pedernera, 5700 San Luis, Argentina
                Article
                10.1063/1.4960697
                716b1e82-e689-499f-976c-86c734d49ff5
                © 2016
                History

                Comments

                Comment on this article