Phase transitions, dielectric, magnetic properties and valence of ions in AFe2/3W1/3O3±σ (A = Ba, Sr) multiferroic ceramics

The polycrystal multiferroic samples of BaFe2/3W1/3O3 (BFWO) and SrFe2/3W1/3O3 (SFWO) are synthesized by solid solution reaction route followed by sintering. The samples are analyzed using the methods of X-ray diffraction (XRD), dielectric, Mössbauer and X-ray photoelectron spectroscopy (XPS) and vi...

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Published inJournal of alloys and compounds Vol. 740; pp. 1037 - 1045
Main Authors Pavlenko, A.V., Kubrin, S.P., Kozakov, A.T., Shilkina, L.A., Reznichenko, L.A., Nikolskii, A.V., Stashenko, V.V., Rusalev, Y.V., Petrosyan, K.S.
Format Journal Article
LanguageEnglish
Published Elsevier B.V 05.04.2018
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Summary:The polycrystal multiferroic samples of BaFe2/3W1/3O3 (BFWO) and SrFe2/3W1/3O3 (SFWO) are synthesized by solid solution reaction route followed by sintering. The samples are analyzed using the methods of X-ray diffraction (XRD), dielectric, Mössbauer and X-ray photoelectron spectroscopy (XPS) and vibrating sample magnetometry (VSM). The XRD study reveals that BFWO possesses two crystal phases: cubic and hexagonal. SFWO is a single phase with a tetragonal symmetry. The VSM and Mössbauer spectroscopy show that both materials are ferrimagnets with magnetic phase transition temperatures TM ≈ 300 K for BFWO and TM ≈ 400 K for SFWO. The iron ions are in Fe3+ state. The XPS studies reveal the presence of the oxygen vacancies in the BFWO and SFWO samples which are responsible for the appearance of the tungsten ions with intermediate valences. BFWO is found to be paraelectric at room temperature. In the SFWO sample the phase transition from tetragonal (ferroelectric) to cubic (paraelectric) phase occurs in the range of 420 < T < 550 K. •The BFWO and SFWO samples have oxygen non-stoichiometry.•The iron ions are in Fe3+ state in the both samples.•The tungsten ions in the two states with formal valence values 6 and 5.5–5.6.•SrFe2/3W1/3O3 is found to be ferroelectric-relaxor.
ISSN:0925-8388
1873-4669
DOI:10.1016/j.jallcom.2018.01.060