Published March 25, 2013 | Version v1
Journal article

Observation of high coercivity in multiferroic lanthanum doped BiFeO3

  • 1. School of Physics, University of Hyderabad, Gachibowli, Hyderabad 500 046 (India)

Description

Highlights: ► Two phase model is used to refine the structure. ► The quantitative estimates of phases as a function of doping are presented. ► Effect of La doping on the dielectric, magnetic properties is reported. ► High coercivity ∼1.5 Tesla is observed for La doped BiFeO3 samples. ► TN increases with increase in La doping. -- Abstract: LaxBi1−xFeO3 (x = 0.0–0.4) ceramics are synthesized by solid state reaction method. An increase in La results systematic decrease in rhombohedral (∼92.4% to ∼ 58.39%) and increase in orthorhombic phase (∼7.59% to ∼41.60%). The structural transition is further confirmed by the changes observed in Raman vibrational modes. A significant enhancement in the dielectric constant by two to three times is observed with La doping. Upon the La doping, the canted anti-ferromagnetic behavior of BiFeO3 turns to weak ferromagnetic. A huge enhancement in remanent magnetization (Mr) and coercivity (HC) of the order of 1.21 T is observed even for a small doping of x = 0.05. The improvement in the magnetic properties of La doped ceramics over BiFeO3 is due to the destruction of spin cycloid with the substitution of La. A cusp at 50 K in the M–T curve reveals a spin glass nature of these samples. Anti-ferromagnetic Néel temperature (TN) increases with x. From the high temperature M–T curve, it is revealed that these ceramics exhibit a large magnetic irreversibility confirming the spin glass state

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jallcom.2012.11.129

Additional details

Identifiers

DOI
10.1016/j.jallcom.2012.11.129;
PII
S0925-8388(12)02124-X;

Publishing Information

Journal Title
Journal of Alloys and Compounds
Journal Volume
554
Journal Page Range
p. 271-276
ISSN
0925-8388
CODEN
JALCEU

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.