Exchange bias effect in bulk multiferroic BiFe0.5Sc0.5O3

abstract

Below the Neel temperature, T-N similar to 220 K, at least two nano-scale antiferromagnetic (AFM) phases coexist in the polar polymorph of the BiFe0.5Sc0.5O3 perovskite; one of these phases is a weak ferromagnetic. Non-uniform structure distortions induced by high-pressure synthesis lead to competing AFM orders and a nano-scale spontaneous magnetic phase separated state of the compound. Interface exchange coupling between the AFM domains and the weak ferromagnetic domains causes unidirectional anisotropy of magnetization, resulting in the exchange bias (EB) effect. The EB field, H-EB, and the coercive field strongly depend on temperature and the strength of the cooling magnetic field. H-EB increases with an increase in the cooling magnetic field and reaches a maximum value of about 1 kOe at 5 K. The exchange field vanishes above T-N with the disappearance of long-range magnetic ordering. The effect is promising for applications in electronics as it is large enough and as it is tunable by temperature and the magnetic field applied during cooling.

keywords

BEHAVIOR

subject category

Science & Technology - Other Topics; Materials Science; Physics

authors

Fertman, EL; Fedorchenko, AV; Desnenko, VA; Shvartsman, VV; Lupascu, DC; Salamon, S; Wende, H; Vaisburd, AI; Stanulis, A; Ramanauskas, R; Olekhnovich, NM; Pushkarev, AV; Radyush, YV; Khalyavin, DD; Salak, AN

our authors

acknowledgements

This work was supported by the TUMOCS project. This project has received funding from the European Union Horizon 2020 Research and Innovation Programme under Marie Sklodowska-Curie Grant Agreement No. 645660. The research done in University of Aveiro was supported by the project CICECO-Aveiro Institute of Materials, UIDB/50011/2020 & UIDP/50011/2020, financed by national funds through the Portuguese Foundation for Science and Technology/MCTES. Financial support by the DFG via FOR 1509 (WE2623/13), CRC 1242 (Project No. 278162697, sub-project A05) and CRC/TRR 247 (Project No. 388390466, sub-project B02) is gratefully acknowledged.

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