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Studies on Multiferroic Behavior of Y-Mn Co-Doped Bi0.9La0.1FeO3

To understand the multiferroic behavior of the Y and Mn co-doped Bi 0.9 La 0.1 FeO 3 system, we have synthesized Bi 0.9 La 0.1 FeO 3 with the co-doped composition of Bi (0.9−a) Y a La 0.1 Fe (1−b) Mn b O 3 ( a  = 0.05, b  = 0.05, 0.10, 0.15, 0.20, and a  = 0.10, b  = 0.10) using the solid-state reac...

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Bibliographic Details
Published in:Journal of electronic materials 2022-12, Vol.51 (12), p.6689-6698
Main Authors: Jose, P. Josely, Rathod, Urjitsinh, Savaliya, Chirag, Jethva, Sadaf, Panchasara, Akshay, Katba, Savan, Keshvani, Mukesh, Vagadia, Megha, Ravalia, Ashish
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Language:English
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Summary:To understand the multiferroic behavior of the Y and Mn co-doped Bi 0.9 La 0.1 FeO 3 system, we have synthesized Bi 0.9 La 0.1 FeO 3 with the co-doped composition of Bi (0.9−a) Y a La 0.1 Fe (1−b) Mn b O 3 ( a  = 0.05, b  = 0.05, 0.10, 0.15, 0.20, and a  = 0.10, b  = 0.10) using the solid-state reaction method. The role of Y and Mn co-doping on the structural, magnetic, ferroelectric, and dielectric properties were studied by various characterization techniques, such as x-ray diffraction, vibrating sample magnetometer (VSM), polarization–electric field (P–E) loop tracer, and dielectric measurements. X-ray diffraction studies show that a 5% doped sample is single phasic nature and crystallizes in rhombohedral (R3c) symmetry, whereas higher doped samples are dual-phase in nature with minor impurity Bi 2 Fe 4 O 9 and crystallize in rhombohedral (R3c) and cubic (Pm-3 m) modulation in structural parameters with Y and Mn doping. The modulation in magnetic behavior with Y and Mn doping has been investigated and studied in the context of modification in the different interactions. P–E loop behavior is observed for lower Y (5%) and Mn (5, 10, 15%) doped samples, whereas a lossy/leaky loop is found for higher doped samples (Y-5, 10%, and Mn-20%). Lastly, the real and imaginary parts of dielectric permittivity indicate doping-induced increases in the values of ε ′ and ε ″.
ISSN:0361-5235
1543-186X
DOI:10.1007/s11664-022-09972-2