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Kumar A and Varshney D*
The present study reports the structural aspects of BiFeO3, Bi0.9Ba0.1Fe0.9M0.1O3, (M=Co, Mn) and Bi0.80RE0.2FeO3 (RE=Nd, Gd and Dy) powders as prepared by solid state reaction route while Bi0.80Sr0.2FeO3 ceramic has been prepared using citrate sol-gel process. X-ray diffraction along with the Rietveld-refinement reveals the rhombohedral (R3c) structure for BiFeO3 and Bi0.9Ba0.1Fe0.9M0.13, (M=Co, Mn), whereas, tetragonal (P4/mmm) for Bi0.80Sr0.2FeO3 ceramic. In case of rare earth substitution there is an abrupt change in the crystal structure. Bi0.8Nd0.2FeO3 ceramic crystallizes in triclinic structure (P1), Bi0.8Gd0.2FeO3 compound shows a major contribution is related to orthorhombic (Pna21) symmetry and minor contributions are attributed to Pnma and R3c phase, whereas the X-ray diffraction of Bi0.8Dy0.2FeO3 confirms the biphasic (Pnma+R3c) nature of the compound. All the properties of the ceramics reflect their structure so, structural evolution is important for enhancing the physical properties at room temperature.