Journal
MATERIALS TODAY-PROCEEDINGS
Volume 25, Issue -, Pages 134-139Publisher
ELSEVIER
DOI: 10.1016/j.matpr.2019.12.186
Keywords
Multiferroics; Sol-gel chemistry; Eu3+-doping; Bismuth ferrite (BiFeO3); Phase transition; Dielectric and magnetic properties
Categories
Funding
- Department of Science and Technology, Government of India [DST -FIST] [SR/FST/College101/2012]
- Mahatma Gandhi University, Kottayam, Kerala [529/A6/2/J. R. F.2018-19]
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A systematic investigation into the enhanced dielectric and magnetic properties of europium - doped bismuth ferrite (Bi(1-x)EuxFeO3, x = 0.0-0.3) multiferroic nanoparticles highlights its usefulness for device miniaturization and high-density data storage systems in nanoelectronics. The samples were synthesized by sol-gel method and calcined at 873 K. Structural characterization by X-ray diffraction and transmission electron microscopy showed the distribution of nanocrystallites with narrow size distribution and further revealed a transformation of the crystalline structure from the initial rhombohedra (R3c) to an orthorhombic (Pn21a) one. This was also accompanied by significant lattice contraction and the elemental composition for each Eu-incorporation was examined through energy dispersive analysis of X- Rays (EDAX). The EDAX studies clearly confirmed the successful and accurate incorporation of Eu3+ in place of Bi3+ and the presence of oxygen vacancies in the samples. Sample with x = 0.2 showed the maximum value of dielectric constant (epsilon') and leakage (epsilon '') as well as a.c. conductivity (sigma). Magnetic response studies reflected the enhancement of spontaneous magnetization by Eu-doping. The maximum values of saturation magnetization (M-S), remnant magnetization (M-r), and coercivity (H-C) were again obtained for the sample with x = 0.2. The studies thus demonstrate a doping concentration at which the material properties can be optimized for the best performance through substitution and size-controlled crystallization to nanometer dimensions. (C) 2019 Elsevier Ltd. All rights reserved. Selection and peer-review under responsibility of the scientific committee of the International Conference on the Science and Technology of Advanced Materials.
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