Abstract
To understand the multiferroic behavior of the Y and Mn co-doped Bi0.9La0.1FeO3 system, we have synthesized Bi0.9La0.1FeO3 with the co-doped composition of Bi(0.9−a)YaLa0.1Fe (1−b)MnbO3 (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 Bi2Fe4O9 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″.
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Acknowledgments
The authors acknowledge Prof. D.G. Kuberkar, Saurashtra University, Rajkot for his guidance and motivation. The authors are thankful to the Department of Physics, Saurashtra University, Rajkot for providing the XRD and P–E loop facility. The authors thank Prof. A. K. Nigam, TIFR, for magnetization measurements. M.V. acknowledges DST, India for the INSPIRE faculty award (DST/INSPIRE/04/2017/003059). ABR is thankful to IUAC New Delhi for UFR-65319 and UGC-DAE, CSR, Indore for CSR-IC-ISUM-64/ CRS-347/2020-21/949 Project funding.
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Jose, P.J., Rathod, U., Savaliya, C. et al. Studies on Multiferroic Behavior of Y-Mn Co-Doped Bi0.9La0.1FeO3. J. Electron. Mater. 51, 6689–6698 (2022). https://doi.org/10.1007/s11664-022-09972-2
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DOI: https://doi.org/10.1007/s11664-022-09972-2