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Structural and Magnetic Properties of BaFeO2.667 Synthesized by Oxidizing BaFeO2.5 Obtained via Nebulized Spray Pyrolysis.
Wollstadt, Stephan; Ikeda, Yuji; Sarkar, Abhishek; Vasala, Sami; Fasel, Claudia; Alff, Lambert; Kruk, Robert; Grabowski, Blazej; Clemens, Oliver.
Afiliación
  • Wollstadt S; Institute for Materials Science, Materials Synthesis Group, University of Stuttgart, Heisenbergstraße 3, Stuttgart 70569, Germany.
  • Ikeda Y; Institut für Materialwissenschaft, Fachgebiet Materialdesign durch Synthese, Technical University of Darmstadt, Alarich-Weiss-Straße 2, Darmstadt 64287, Germany.
  • Sarkar A; Institute for Materials Science, Department of Materials Design, University of Stuttgart, Pfaffenwaldring 55, Stuttgart 70569, Germany.
  • Vasala S; Institut für Nanotechnologie, Karlsruher Institut für Technologie, Hermann-von-Helmholtz-Platz 1, Eggenstein Leopoldshafen 76344, Germany.
  • Fasel C; Institut für Materialwissenschaft, Gemeinschaftslabor Nanomaterialien, Technical University of Darmstadt, Alarich-Weiss-Straße 2, Darmstadt 64287, Germany.
  • Alff L; Institut für Materialwissenschaft, Fachgebiet Materialdesign durch Synthese, Technical University of Darmstadt, Alarich-Weiss-Straße 2, Darmstadt 64287, Germany.
  • Kruk R; Institut für Materialwissenschaft, Fachgebiet Disperse Feststoffe, Technical University of Darmstadt Alarich-Weiss-Straße 2, 64287 Darmstadt, Germany.
  • Grabowski B; Institut für Materialwissenschaft, Advanced Thin Film Technology, Technical University of Darmstadt Alarich-Weiss-Straße 2, 64287 Darmstadt, Germany.
  • Clemens O; Institut für Nanotechnologie, Karlsruher Institut für Technologie, Hermann-von-Helmholtz-Platz 1, Eggenstein Leopoldshafen 76344, Germany.
Inorg Chem ; 60(15): 10923-10933, 2021 Aug 02.
Article en En | MEDLINE | ID: mdl-34240868
A vacancy-ordered perovskite-type compound Ba3Fe3O8 (BaFeO2.667) was prepared by oxidizing BaFeO2.5 (P21/c) with the latter compound obtained by a spray pyrolysis technique. The structure of Ba3Fe3O8 was found to be isotypic to Ba3Fe3O7F (P21/m) and can be written as Ba3Fe3+2Fe4+1O8. Mössbauer spectroscopy and ab initio calculations were used to confirm mixed iron oxidation states, showing allocation of the tetravalent iron species on the tetrahedral site, and octahedral as well as square pyramidal coordination for the trivalent species within a G-type antiferromagnetic ordering. The uptake and release of oxygen were investigated over a broad temperature range from room temperature to 1100 °C under pure oxygen and ambient atmosphere via a combination of DTA/TG and variable temperature diffraction measurements. The compound exhibited a strong lattice enthalpy driven reduction to monoclinic and cubic BaFeO2.5 at elevated temperatures.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Inorg Chem Año: 2021 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Inorg Chem Año: 2021 Tipo del documento: Article País de afiliación: Alemania
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