Abstract

The changes in crystal and magnetic structure of BiFeO3 produced by partial substitution of Bi ions by Ho ions has been studied with powder X-ray diffraction, neutron powder diffraction, dielectric and magnetization techniques. The present study demonstrates that Bi1-xHoxFeO3(x = 0.05, 0.10, 0.15, & 0.2) multiferroics shows change in crystal structure at x > 0.05. The sample with x = 0.05 exhibits rhombohedral structure (space group R3c), while the other three samples (x > 0.05) exhibit mixed phase with coexisting rhombohedral (R3c) and Orthorhombic (Pnma) structure. This change in the crystal structure is attributed to the distortion of FeO6 octahedra via substitution of Ho at phase boundaries. The magnetization studies indicate that doping of Ho in pristine BiFeO3 leads to enhancement in the ferromagnetic moment. We find that doping of Ho breaks the spin cycloid phase of BiFeO3 and creates a canted G-type antiferromagnetic structure in the hexagonal phase whereas the orthorhombic phase exhibits a collinear G-type AFM structure. The canting angle increases with increase in doping with Ho, leading to an enhancement in the ferromagnetic component in magnetization. Dielectric constant (ε′) and loss factor (tanδ) are measured in frequency range 1 kHz to 7 MHz and ε′ and tanδ show dispersion behaviour at low frequencies. The significant improvement in magnetization and dielectric properties is achieved by Ho substitution which in turn enhances the potential of BiFeO3 for multiferroics applications.

Highlights

  • Multiferroic compounds have been paid a lot of attention due to their attractive basic physics and industrial applications in magnetic/ferroelectric systems used as data storage devices, sensor devices, electromagnets, quantum and spintronics.1–3 BiFeO3 (BFO) is one of the most widely studied room temperature (RT) single phase multiferroic ceramic, because it has ferroelectric order below a high Curie temperature (TC ∼1103 K)4,5 and the G-type antiferromagnetic parameters ordering of the Fe magnetic moments below a high Néel temperature (TN = 643 K).5 The G-type magnetic structure has been modified by a long-wavelength (λ∼620 Å) spiral modulation associated with a canting of magnetic moments.6,7 In this compound, the ferroelectricity is induced by a stereo-chemically active 6s2 lone pair of the Bi3+ ions

  • The changes in crystal and magnetic structure of BiFeO3 produced by partial substitution of Bi ions by Ho ions has been studied with powder X-ray diffraction, neutron powder diffraction, dielectric and magnetization techniques

  • The analysis of the room temperature X-ray diffraction (XRD) patterns taking into account both the hexagonal and orthorhombic phases were carried out using FullProf software

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Summary

INTRODUCTION

Along with SMSS arrangement, existence of the secondary phases such as Bi2Fe4O9 and Bi25Fe2O39 in BFO which causes high current leakage and low resistivity are the hindrance in practical use of BFO.14,15 To overcome these problems many solutions have been tried by several groups but substitution method are found to be the best to change specific physical properties of a material. Similar structural phase transformation from rhombohedral to orthorhombic has been observed in the Bi1-xCaxFeO3 compound and enhancement in the magnetization with Y doping and La doping leading to change in multiferroics characteristics has been reported In this manuscript we investigate the changes in the chemical and magnetic structure using neutron diffraction and other techniques and show the appearance of canted antiferromagnetic structure with Ho doping. The results are compared with existing doping studies with trivalent ions and the effect of external pressure on BiFeO3

EXPERIMENTAL
X-ray diffraction
Neutron diffraction
Magnetic properties
Raman spectroscopy
Dielectric study
Impedance analysis
CONCLUSIONS
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