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      <dc:title>Multiferroism induced by spontaneous structural ordering in antiferromagnetic iron perovskites</dc:title>
      <dc:creator>Martínez de Irujo Labalde, Xabier</dc:creator>
      <dc:creator>Goto, Masato</dc:creator>
      <dc:creator>Urones-Garrote, Esteban</dc:creator>
      <dc:creator>Amador, Ulises</dc:creator>
      <dc:creator>Ritter, Clemens</dc:creator>
      <dc:creator>Amano Patino, Midori </dc:creator>
      <dc:creator>Koedtruad, Anucha</dc:creator>
      <dc:creator>Tan, Zhenhong</dc:creator>
      <dc:creator>Shimakawa, Yuichi</dc:creator>
      <dc:creator>García Martín, Susana</dc:creator>
      <dc:description>Room-temperature multiferroism in polycrystalline antiferromagnetic Fe perovskites is reported for the first time. In the perovskite-type oxides RE1.2Ba1.2Ca0.6Fe3O8 (RE = Gd, Tb), the interplay of layered ordering of Gd(Tb), Ba, and Ca atoms with the ordering of FeO4-tetrahedra (T) and FeO6-octahedra (O) results in a polar crystal structure. The layered structure consists of the stacking sequence of RE/Ca-RE/Ca-Ba-RE/Ca layers in combination with the TOOT sequence in a unit cell. A polar moment of 33.0 μC/cm2 for the Gd-oxide (23.2 μC/cm2 for the Tb one) is determined from the displacements of the cations, mainly Fe, and oxygen atoms along the b-axis. These oxides present antiferromagnetic ordering doubling the c-axis, and the magnetic structure in the Tb-compound remains up to 690 K, which is one of the highest transition temperatures reported in Fe perovskites.</dc:description>
      <dc:date>2024-01-10T10:45:14Z</dc:date>
      <dc:date>2024-01-10T10:45:14Z</dc:date>
      <dc:date>2019</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Martínez De Irujo-Labalde, Xabier, et al. «Multiferroism Induced by Spontaneous Structural Ordering in Antiferromagnetic Iron Perovskites». Chemistry of Materials, vol. 31, n.o 15, agosto de 2019, pp. 5993-6000. https://doi.org/10.1021/acs.chemmater.9b02716</dc:identifier>
      <dc:identifier>1520-5002</dc:identifier>
      <dc:identifier>10.1021/acs.chemmater.9b02716</dc:identifier>
      <dc:identifier>https://hdl.handle.net/20.500.14352/92201</dc:identifier>
      <dc:identifier>https://doi.org/10.1021/acs.chemmater.9b02716</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>restricted access</dc:rights>
      <dc:publisher>American Chemical Society</dc:publisher>
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