53 research outputs found
Neutron Diffraction, Mossbauer and Electron Paramagnetic Resonance Studies of Pb0.8Bi0.2Fe0.6Nb0.4O3 Multiferroic
The Pb0.8Bi0.2Fe0.6Nb0.4O3 (PFN-BFO) multiferroic solid solution was synthesized by single step solid state reaction method with low calcination (700 degrees C/2h) and sintering (800 degrees C/3h) temperatures. Single phase formation was confirmed through X Ray Diffraction (XRD) and Neutron Diffraction (ND) at room temperature (RT). The structural analysis was carried out by Rietveld refinement through the Fullprof program. Refined XRD and ND patterns confirms the monoclinic structure with Cm space group and obtained cell parameters from the ND data are a = 5.6449(8) angstrom, b = 5.6536(5) angstrom, c = 4.0017(6) beta = 30(4). ND data at RT exhibits G-type antiferromagnetic structure. The Mossbauer and Electron Paramagnetic Resonance (EPR) spectroscopy studies were carried out at RT. The isomer shift and the quadrupole splitting of the Mossbauer spectra confirm the Fe in +3 states. An EPR spectrum shows a single broad slight asymmetric line, is an evidence of Fe in +3 states. ND, Mssbauer and EPR studies are the clear evidence of existence of antiferromagnetic ordering near room temperature
Low-temperature neutron diffraction and magnetic studies on the magnetoelectric multiferroic Pb(Fe0.534Nb0.4W0.066)O3
Size Control and Magnetic Property Trends in Cobalt Ferrite Nanoparticles Synthesized Using an Aqueous Chemical Route
Cobalt ferrite (CoFe2O4) is an engineering material which is used for applications such as magnetic cores, magnetic switches, hyperthermia based tumor treatment, and as contrast agents for magnetic resonance imaging. Utility of ferrites nanoparticles hinges on its size, dispersibility in solutions, and synthetic control over its coercivity. In this work, we establish correlations between room temperature co-precipitation conditions, and these crucial materials parameters. Furthermore, post-synthesis annealing conditions are correlated with morphology, changes in crystal structure and magnetic properties. We disclose the synthesis and process conditions helpful in obtaining easily sinterable CoFe2O4 nanoparticles with coercive magnetic flux density (H-c) in the range 5.5-31.9 kA/m and M-s in the range 47.9-84.9 A.m(2)Kg(-1). At a grain size of similar to 54 +/- 2 nm (corresponding to 1073 K sintering temperature), multi-domain behavior sets in, which is indicated by a decrease in H-c. In addition, we observe an increase in lattice constant with respect to grain size, which is the inverse of what is expected of in ferrites. Our results suggest that oxygen deficiency plays a crucial role in explaining this inverse trend. We expect the method disclosed here to be a viable and scalable alternative to thermal decomposition based CoFe2O4 synthesis. The magnetic trends reported will aid in the optimization of functional CoFe2O4 nanoparticle
Origin of room temperature weak-ferromagnetism in antiferromagnetic Pb(Fe2/3W1/3)O-3 ceramic
We report the origin of room temperature weak ferromagnetic behavior of polycrystalline Pb(Fe2/3W1/3)O-3 (PFW) powder. The structure and magnetic properties of the ceramic powder prepared by a Columbite method were characterized by X-ray and neutron diffraction, Mossbauer spectroscopy and magnetization measurements. Rietveld analysis of diffraction data confirm the formation of single phase PFW, without traces of any parasitic pyrochlore phase. PFW was found to crystallize in the cubic structure at room temperature. The Rietveld refinement of neutron diffraction data measured at room temperature confirmed the G-type antiferromagnetic structure of PFW in our sample. However, along with the antiferromagnetic (AFM) ordering of the Fe spins, we have observed the existence of weak ferromagnetism at room temperature through: (i) a clear opening of hysteresis (M-H) loop, (ii) bifurcation of the field cooled and zero-field cooled susceptibility; supported by Mossbauer spectroscopy results. The P-E loop measurements showed a non-linear slim hysteresis loop at room temperature due to the electronic conduction through the local inhomogeneities in the PFW crystallites and the inter-particle regions. By corroborating all the magnetic measurements, especially the spin glass nature of the sample, with the conduction behavior of the sample, we report here that the observed ferromagnetism originates at these local inhomogeneous regions in the sample, where the Fe-spins are not perfectly aligned antiferromagnetically due to the compositional disordering. (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved
Neutron diffraction, Mossbauer effect and Electron Paramagnetic Resonance studies on multiferroic Pb(Fe2/3W1/3)O-3
Multiferroic Pb(Fe2/3W1/3)O-3 ceramics were synthesized via a modified two-stage Columbite method. Single phase formation was confirmed from the analysis of x-ray and neutron diffraction patterns recorded at room temperature. Structural analysis of the diffraction data reveals cubic phase (space group Pm-3m) for the title compound. Magnetic structure of the title compound at room temperature exhibits G-type antiferromagnetic structure. The Mossbauer spectroscopy and Electron Paramagnetic Resonance (EPR) studies were carried out at 300 K. The isomer shift and quadrupole splitting of the Mossbauer spectra confirms the trivalent state of iron (Fe3+). The Mossbauer spectra also suggest that the iron and tungsten are randomly distributed at the octahedral, B site. EPR spectra show a single broad line associated with Fe3+ ions. Both spectra clearly exhibit weak ferromagnetic behaviour of Pb(Fe2/3W1/3)O-3 ceramic at 300 K. Considering neutron diffraction, Mossbauer and EPR results together, it may be stated here that Pb(Fe2/3W1/3)O-3 exhibits antiferromagnetic behavior along with weak ferromagnetism at room temperature
Neutron diffraction, Mossbauer effect and electron paramagnetic resonance studies on multiferroic Pb(Fe2/3W1/3)O3
Multiferroic Pb(Fe2/3W1/3)O3 ceramics were synthesized via a modified two-stage Columbite method. Single phase formation was confirmed from the anal. of x-ray and neutron diffraction patterns recorded at room temp. Structural anal. of the diffraction data reveals cubic phase (space group Pm-3m) for the title compd. Magnetic structure of the title compd. at room temp. exhibits G-type antiferromagnetic structure. The Mossbauer spectroscopy and ESR (EPR) studies were carried out at 300 K. The isomer shift and quadrupole splitting of the Mossbauer spectra confirms the trivalent state of iron (Fe3+). The Mossbauer spectra also suggest that the iron and tungsten are randomly distributed at the octahedral, B site. EPR spectra show a single broad line assocd. with Fe3+ ions. Both spectra clearly exhibit weak ferromagnetic behavior of Pb(Fe2/3W1/3)O3 ceramic at 300 K. Considering neutron diffraction, Mossbauer and EPR results together, it may be stated here that Pb(Fe2/3W1/3)O3 exhibits antiferromagnetic behavior along with weak ferromagnetism at room temp. (c) 2015 American Institute of Physics
Low Temperature Dielectric and Conductivity Relaxation Studies on Magnetoelectric Pb(Fe2/3W1/3) O3
The single phase perovskite Pb(Fe2/3W1/3)O3 [PFW] was synthesized by modified low – temperature (sintering at 850°C) solid-state reaction. Rietveld refinement ofroom temperature (RT) X-ray diffraction (XRD) and neutron diffraction (ND) patterns of the samples confirm the single phase formation with cubic structure (Pm-3m). Surface morphology of the compounds was studied by Scanning electron microscope (SEM) and average grain size was estimated to be ∼2 µm. The RT dielectric properties of PFW ceramic are studied as a function of frequency from 100 - 1MHz. The temperature dependent (120 – 293K) dielectric properties were studied at few selected frequencies. We found the frequency dependent dielectric constant shows increasing trend with increase in temperature from 120 – 293K, with minimum dielectric loss. The frequency dependence of dielectric loss shows a maximum in between 10 Hz and 1 kHz, confirms the extrinsic phenomena like interfacial polarization due to space charge accumulation at grain boundaries. Impedance spectroscopy is used to study the electrical behaviour of PFW in the frequency range from 100 to 1MHz and in the temperature range from 120 - 293 K. The frequency-dependent electrical data are analysed by impedance formalisms and shows the relaxation (conduction) mechanism in the sample. We suggest this low temperature sintered PFW is a suitable candidate for the multilayer ceramic capacitorsandrelated negative temperature coefficient of resistance type (NTCR) behavior like that of semiconductors
On the Room Temperature Ferromagnetic and Ferroelectric Properties of Pb(Fe1/2Nb1/2)O-3
We report the origin of room temperature (RT) ferromagnetic and ferroelectric properties of Pb(Fe1/2Nb1/2)O-3 (PFN) ceramic sample prepared by modified solid-state reaction synthesis by a single-step method, based on X-ray diffraction (XRD), neutron diffraction (ND), Mossbauer spectroscopy and electron paramagnetic resonance (EPR) spectroscopy results. Formation of single-phase monoclinic PFN ceramic with Cm space group was confirmed by XRD and ND at RT. The morphology studied by scanning electron microscopy (SEM) confirmed uniform microstructure of the sample with average grain size of similar to 2 mu m. The ND, Mossbauer spectroscopy, M-H loop and EPR studies were carried out to confirm the existence of weak ferromagnetism at RT. A clear opening of hysteresis (M-H) loop is evidenced as the existence of weak ferromagnetism at RT. EPR spectrum clearly shows the ferromagnetism through a good resonance signal. The symmetric EPR line shape with g = 1.9895 observed in PFN sample was identified to be due to Fe3+ ions. Mossbauer spectroscopy at RT shows superparamagnetic behaviour with presence of Fe in 3+ valence state. Ferroelectric P-E loops on PFN at RT confirm the existing ferroelectric ordering. Our observation is in agreement with literature, and it supports that the origin of ferromagnetism and ferroelectricity is isolated, i.e. from different regions in the sample. Our results do not support the multiferroic nature of PFN at RT
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