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XRD controll of mechanical synthesis process of (BiFeO3)0.5(BaTiO3)0.5 multiferroic system

Wiktor Walerczyk 1Adam Pietraszko 1Bożena Hilczer 2Izabella Szafraniak-Wiza 3

1. Institue of Low Temperature and Structure Research, Polish Academy of Sciences (INTIBS-PAN), P.Nr 1410, Wrocław 50-950, Poland
2. Institute of Molecular Physics, Polish Academy of Sciences, Smoluchowskiego 17, Poznań 60-179, Poland
3. Institute of Materials Science and Engineering, Poznań University of Technology, Poznań 60-965, Poland

Abstract

The trend towards miniaturization of the devices resulted in a renaissance in the studies of materials exhibiting simultaneously ferroelectric and ferromagnetic properties. Among them BiFeO3remains still interestingas a single-phase multiferroic at room temperature (TC=1100 K [1], TN=420 K [2]). Bismuth ferrite is known to form solid solutions with ferroelectric perovskites [3, 4] in which one can expect an enhancement of the magneto-electric coupling due to the increase in the long-range electric order. The properties of (BiFeO3)1-x(BaTiO3)xsolution obtained by solid state reaction were studied by Kumar et al. [5] and Buscaglia et al. [6]. We used much simpler procedure to obtain of (BiFeO3)0.7(BaTiO3)0.3solid solution: a direct synthesis from respective oxides at room temperature via mechanically triggered chemical reaction.

High purity Aldrich bismuth oxides in stoichiometric ratios (Bi2O3+ Fe2O3)0.7(BaO + TiO2)0.3were mechanically activated in SPEX 8000 Mixer Mill in the air atmosphere at room temperature during various milling time tm. The batch contained 6 g of the oxides and the weight ratio of the stainless steel balls to the oxides was 2:1.

The mechanical synthesis of the powder after different times tmwas controlled by X-ray diffraction using a Stoe Diffraction System with Cu-K1radiation. Linear position sensitive detector was used to measure the diffracted radiation in the 2angle from 3 to 103 degrees of arc and standard DHN-PDS reduction procedure was applied to analyze the powder diffraction pattern. The mean grain size of the powder was assessed with Scherrer method from the half-width of the (h1 k1 l1) and (h2 k2 l2) profiles with Williamson-Hall analysis. We assumed a monodispersive grain size distribution an the Lorentzian profile of the reflections.

The powder after 75 h of mechanical synthesis was found to be a single-phase (BiFeO3)0.7(BaTiO3)0.3with rhombohedral symmetry and lattice parameters: a = 0.5608(5) nm, c = 1.3853(3) nm. The assessed mean grain size of the powder amounts to ~12 nm and the grains exhibit a core-shell type structure.


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[5] M. Kumar, A. Srinivas, S.V. Suryanarayana, J. Appl. Phys. 87, 855 (2000).

[6] MT. Buscaglia, L. Mitoseriu, V. Buscaglia, B. Pallecchi, M. Viviani, P. Nanni, A.S. Siri, J. Europ. Ceram. Soc. 26, 3027 (2006).

 

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Presentation: Poster at 11th European Powder Diffraction Conference, Poster session, by Wiktor Walerczyk
See On-line Journal of 11th European Powder Diffraction Conference

Submitted: 2008-06-12 14:31
Revised:   2009-06-07 00:48