Structural and magnetic characterization of BiFexMn2-xO5 oxides (x=0.5, 1.0) |
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Authors: | M. Retuerto,M.J. Martí nez-Lope,M.T. Ferná ndez-Dí az |
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Affiliation: | a Instituto de Ciencia de Materiales de Madrid, C.S.I.C., Cantoblanco, E-28049 Madrid, Spain b Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, 610 Taylor Road Piscataway, NJ 08854-808, USA c Institute for Nuclear Research and Nuclear Energy, Bulgarian Academy of Sciences, 72 Tsarigradsko Chaussee Boulevard, Sofia 1784, Bulgaria d Institut Laue-Langevin, BP156X, Grenoble F-38042, France |
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Abstract: | The title compounds have been synthesized by a citrate technique followed by thermal treatments in air (BiFe0.5Mn1.5O5) or under high oxygen pressure conditions (BiFeMnO5), and characterized by X-ray diffraction (XRD), neutron powder diffraction (NPD) and magnetization measurements. The crystal structures have been refined from NPD data in the space group Pbam at 295 K. These phases are isostructural with RMn2O5 oxides (R=rare earths) and contain infinite chains of Mn4+O6 octahedra sharing edges, linked together by (Fe,Mn)3+O5 pyramids and BiO8 units. These units are strongly distorted with respect to those observed in other RFeMnO5 compounds, due to the presence of the electronic lone pair on Bi3+. It is noteworthy the certain level of antisite disorder exhibited in both samples, where the octahedral positions are partially occupied by Fe cations, and vice versa. BiFexMn2−xO5 (x=0.5, 1.0) are short-range magnetically ordered below 20 K for x=0.5 and at 40 K for x=1.0. The main magnetic interactions seem to be antiferromagnetic (AFM); however, the presence of a small hysteresis in the magnetization cycles indicates the presence of some weak ferromagnetic (FM) interactions. |
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Keywords: | RMn2O5 BiMn2O5 Multiferroic oxides Magnetoelectric Ferromagnetic Neutron diffraction |
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