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Title: Crystal structure and magnetic properties of Bi{sub 0.8}A{sub 0.2}FeO{sub 3} (A = La, Ca, Sr, Ba) multiferroics using neutron diffraction and Mossbauer spectroscopy

Journal Article · · AIP Advances
DOI:https://doi.org/10.1063/1.4893241· OSTI ID:22299800
; ;  [1]; ; ;  [2]
  1. Department of Applied Physics, Guru Jambheshwar University of Science and Technology, Hisar-125001 (Haryana) India (India)
  2. Solid State Physics Division, Bhabha Atomic Research Centre, Mumbai-400 085 (India)

Bi{sub 0.8}A{sub 0.2}FeO{sub 3} (A = La, Ca, Sr, Ba) multiferroics were studied using x-ray, neutron diffraction and magnetization techniques. All the samples crystallized in rhombohedral structure with space group R3c. The compounds exhibit antiferromagnetic (AFM) ordering at 300 K and no evidence of further structural or magnetic transition was observed on lowering of temperature below it. The magnetic structure of these substituted compounds are found to be collinear G-type AFM structure as against the non collinear incommensurate magnetic structure reported in the case of parent compound. The moments on Fe at 6 K are aligned along the a-axis in the case of Ca-doped sample. With increase in the ionic radii of dopant, the moments are found to be aligned in the ac plane and the angle of tilt away from the a-axis increases. The observed change in the magnetic structure with substitution is attributed to the intrinsic structural distortion as evidenced by the change in the bond angle (Fe-O-Fe) and bond distances (Bi-O, Fe-O). It has been found that heterovalent substitution A{sup 2+} results in the formation of oxygen vacancies in the parent lattices as the possibility of Fe{sup 4+} ruled out by Mössbauer spectra recorded at room temperature. Higher value of remnant magnetization (0.4187 emu/g) and coercivity (4.7554kOe) is observed in Bi{sub 0.8}Ba{sub 0.2}FeO{sub 3} sample in comparison to other substituted samples revealing a strong correlation between ionic radii and magnetization.

OSTI ID:
22299800
Journal Information:
AIP Advances, Vol. 4, Issue 8; Other Information: (c) 2014 Author(s); Country of input: International Atomic Energy Agency (IAEA); ISSN 2158-3226
Country of Publication:
United States
Language:
English