17 research outputs found
Interplay of 4f-3d Magnetism and Ferroelectricity in DyFeO3
DyFeO3 exhibits a weak ferromagnetism (TNFe ~ 645 K) that disappears below a
spin-reorientation (Morin) transition at TSRFe ~ 50 K. It is also known that
applied magnetic field induces ferroelectricity at the magnetic ordering
temperature of Dy-ions (TNDy ~ 4.5 K). Here, we show that the ferroelectricity
exists in the weak ferromagnetic state (TSRFe < T < TN,C) without applying
magnetic field, indicating the crucial role of weak ferromagnetism in inducing
ferroelectricity. 57Fe M\"ossbauer studies show that hyperfine field (Bhf)
deviates from mean field-like behaviour that is observed in the weak
ferromagnetic state and decreases below the onset of spin-reorientation
transition (80 K), implying that the Bhf above TSR had additional contribution
from Dy-ions due to induced magnetization by the weak ferromagnetic moment of
Fe-sublattice and below TSR, this contribution decreases due to collinear
ordering of Fe-sublattice. These results clearly demonstrate the presence of
magnetic interactions between Dy(4f) and Fe(3d) and their correlation with
ferroelectricity in the weak ferromagnetic state of DyFeO3.Comment: 5 pages, 6 figures, published in EP
Experimental observation of quantum corrections to electrical resistivity in nanocrystalline soft magnetic alloys
X-ray diffraction patterns of nanocrystalline Fe-Cu-Nb-Si-B (FINEMET) alloys reveal that bcc α-Fe/α -FeSi crystallites with the average grain size of 20(5) nm are dispersed in amorphous matrix. Enhanced electron-electron interaction (EEI) and quantum interference (QI) effects as well as electron-magnon (and/or electron-spin fluctuation) scattering turn out to be the main mechanisms that govern the temperature dependence of resistivity. Of all the inelastic scattering processes, inelastic electron-phonon scattering is the most effective mechanism to destroy phase coherence of electron wave functions. The diffusion constant, density of states at the Fermi level and the inelastic scattering time have been estimated, for the first time, for the alloys in question
Oxalate based non-aqueous sol-gel synthesis of phase pure sub-micron LiFePO<SUB>4</SUB>
We report on the synthesis and preliminary characterisation by X-ray diffraction (XRD),
scanning electron microscopy (SEM), Mossbauer spectroscopy and infrared spectroscopy (IR) of
C-LiFePO4. Homogeneous sub-micron sized particles of surface carbon coated phase pure
LiFePO4 are synthesised by a novel non-aqueous oxalate based sol-gel procedure. Our
synthetic route successfully overcomes the incidence of Fe3+, effectively controls
undesirable particle growth and has the potential for upscaling and application as Li-ion battery
cathodes
Investigation of structure and electrical transport in partially nanocrystallized amorphous soft magnetic alloys
X-ray diffraction patterns of melt-spun Fe-Cu-Nb-Si-B (FINEMET-type) alloys reveal that crystallites of Fe2Si
and Fe3B phases with average sizes of 15(5) and 20(2) nm are present in the surface layer of thickness ≈10 Å
and these nanocrystallites occupy 5-10% of the total volume. The results of an elaborate analysis of the high-resolution electrical resistivity data
taken in a temperature range from 13 K to 300 K and their discussion in the light of existing theories demonstrates that the enhanced
electron-electron interaction (EEI), quantum interference (QI) effects, inelastic electron-phonon scattering, coherent electron-magnon (and/or
electron-spin fluctuation) scattering are the main mechanisms that govern the temperature dependence of resistivity. Of all the inelastic scattering
processes, inelastic electron-phonon scattering is the most effective mechanism to destroy phase coherence of electron wavefunctions. The
physical quantities such as diffusion constant, density of states at the Fermi level and the phase-breaking time, determined for the first time for the
alloys in question, exhibit a systematic variation with the copper concentration
On the defect origin of the room-temperature magnetism universally exhibited by metal-oxide nanoparticles
The occurrence of ferromagnetism in nanoparticles of otherwise non-magnetic oxides seems to be well established. It is, however, necessary to understand the origin of ferromagnetism in these materials. Herein, we present a combined study of the magnetic properties and photoluminescence (PL) behavior of nanoparticles of ZnO, ZrO<SUB>2</SUB>, and MgO annealed at different temperatures (and therefore of different sizes). We find that the magnetization and the intensity of the bands due to defects vary parallel in all these materials. The adsorption of ethanol leads to a decrease in the magnetization and to a reduced intensity of the defect PL band of ZnO nanoparticles whereas UV irradiation has the opposite effect. We have also examined the effect of the morphology of the ZnO on the properties
Spin-reorientation, ferroelectricity and magnetodielectric effect in YFe<sub>1−x</sub> Mn<sub>x</sub>O<sub>3</sub> (0.1 ≤ x ≤ 0.40)
We report the observation of magnetoelectric and magnetodielectric effects at different temperatures in Mn-substituted yttrium orthoferrite, YFe<sub>1−x</sub> Mn<sub>x</sub>O<sub>3</sub> (0.1 ≤ x ≤ 0.40). Substitution of Mn in antiferromagnetic YFeO<sub>3</sub> (T<sub>N</sub> = 640  K) induces a first-order spin-reorientation transition at a temperature, T<sub>SR</sub>, which increases with x whereas the Neel temperature (T<sub>N</sub>) decreases. While the magnetodielectric effect occurs at T<sub>SR</sub> and T<sub>N</sub>, the ferroelectricity appears rather at low temperatures. The origin of magnetodielectric effect is attributed to spin-phonon coupling as evidenced from the temperature dependence of Raman phonon modes. The large magnetocapacitance (18% at 50 kOe) near T<sub>SR</sub> = 320  K and high ferroelectric transition temperature (∼115  K) observed for x = 0.4 suggest routes to enhance magnetoelectric effect near room temperature for practical applications
Structure and magnetic properties of the Al<SUB>1−x</SUB>Ga<SUB>x</SUB>FeO<SUB>3</SUB> family of oxides: a combined experimental and theoretical study
Magnetic properties of the Al1−xGaxFeO3 family of oxides crystallizing in a non-centrosymmetric space group have been investigated in detail along with structural aspects by employing X-ray and neutron diffraction, Mössbauer spectroscopy and other techniques. The study has revealed the occurrence of several interesting features related to unit cell parameters, site disorder and ionic size. Using first-principles density functional theory based calculations, we have attempted to understand how magnetic ordering and related properties in these oxides depend sensitively on disorder at the cation site. The origin and tendency of cations to disorder and the associated properties are traced to the local structure and ionic sizes