Issue 40, 2025, Issue in Progress

Magnetoelectric properties of bulk 0-3 Fe/BaTiO3-composites

Abstract

Magnetoelectric 0-3 Fex/(BaTiO3)1−x composites (x = 0.1–0.8) were synthesized by reduction of Fe2O3/BaTiO3 pellets in forming gas. In a subsequent sintering step, dense composite ceramics were formed. Depending on the oxygen getter used in the sintering step (carbon or zirconium carbide) a partly iron-doped or undoped ferroelectric barium titanate matrix is obtained, which encloses micrometer-sized ferromagnetic Fe particles. The experimentally determined iron contents derived from Rietveld refinements and magnetic measurements are in good agreement with the nominal ones in the undoped composites. Field dependent magnetoelectric measurements revealed only small differences between the composites with doped and undoped BaTiO3 component when the magnetic field and the polarization are oriented parallel to each other. For samples with iron-doped BaTiO3, additional third extrema at low fields were found when the field was oriented perpendicular to the electric polarization whereas undoped samples exhibited only two extrema. The largest αME values were measured for the Fex/(BaTiO3)1−x composites with x = 0.4 (parallel) and x = 0.3 (perpendicular). Based on the integral of αME, the magnetostriction of iron and a phenomenological model describing the connection between magnetostriction and the magnetoelectric effect was derived. In temperature-dependent magnetoelectric investigations the low-temperature phase transitions of BaTiO3 (tetragonal → orthorhombic → rhombohedral) were detected.

Graphical abstract: Magnetoelectric properties of bulk 0-3 Fe/BaTiO3-composites

Supplementary files

Article information

Article type
Paper
Submitted
16 May 2025
Accepted
05 Sep 2025
First published
15 Sep 2025
This article is Open Access
Creative Commons BY license

RSC Adv., 2025,15, 33480-33493

Magnetoelectric properties of bulk 0-3 Fe/BaTiO3-composites

T. Buttlar, H. S. Leipner and S. G. Ebbinghaus, RSC Adv., 2025, 15, 33480 DOI: 10.1039/D5RA03466C

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