Magnetic and magnetodielectric properties of Bi-substituted yttrium iron garnet ceramics

Effects of Bi substitution upon magnetic and magnetodielectric properties of Y₃Fe₅O₁₂ ceramics were investigated. It was found that the saturation magnetization decreases and the magnetic ordering temperature increases as the amount of Bi increases. The contribution of intrinsic and extrinsic effects to magnetodielectric effects decreases with increase of Bi, which results in the decrease of magnetodielectric coefficient of Y_3−xBi_xFe₅O₁₂ ceramics.     

Structure dependence of magnetic properties in yttrium iron garnet by metal-organic decomposition method

The yttrium iron garnet(YIG) samples are prepared at different temperatures from 900?C to 1300?C by the metalorganic decomposition(MOD) method. The chemical composition and crystal structure of the samples are studied by scanning electron microscope(SEM), XRD, and M ¨ossbauer spectrometer. It is shown that the ratio of ferric ions on two types of sites, the octahedral and the tetrahedral, is increased with the sintering temperature. At 1300?C, the pure garnet phase has been obtained, in which the ferric ions ratio is 2:3 leading to the minimum magnetic coercivity and maximum saturation magnetization. These results provide a route to synthesize pure YIG materials as the basic materials used in various spintronics applications.     

Preparation of nano-sized Al-substituted yttrium iron garnets by the mechanochemical method and investigation of their magnetic properties

The polycrystalline Y₃Fe_5−xAl_xO₁₂ compounds with x=0.5, 1.0, 1.5 and 2.0 were prepared by the mechanochemical method. The samples were milled for 40 h in a high-energy planetary mill and then calcined at different temperatures from 1300 to 1100 °C. The minimum calcination temperature to get a single phase garnet decreases by increasing Al concentration. X-ray diffraction patterns reveal that the structures of nano-powders are bcc and the garnet phase has been obtained after calcining. Also, the lattice constant of the samples decreases by increasing Al concentration ,which is discussed based on the substitution of smaller aluminum ions instead of iron ions. The average crystallite sizes are in the range 24-35 nm using Scherrer's formula. The Curie temperature of single phase samples was found to decrease by increasing Al concentration, which can be discussed upon the reduction of magnetic interactions per magnetic ion. When more Al³⁺ is added, the magnetization is reduced because of the reduction of superexchange interactions in crystal lattice.     

The electrodeposition behaviors and magnetic properties of Ni-Co films

Ni-Co films with different compositions and microstructures were produced on ITO glasses by electrodeposition from sulphate bath at 25 °C. Cyclic voltammograms give a result that the increase in the Co²⁺ concentration displaces Ni-Co alloy oxidation peaks to negative potential with high Co current distributions. It is observed that the content of cobalt in the films increases from 22.42% to 56.09% as the molar ratio of CoSO₄/NiSO₄ varying from 0.015/0.085 to 0.045/0.055 in electrolyte. XRD patterns reveal that the structure of the films strongly depends on the Co content in the deposited films. The saturation magnetization (M_s) moves up from 144.84 kA m⁻¹ to 342.35 kA m⁻¹ and coercivity (H_c) falls from 15.27 kA m⁻¹ to 7.27 kA m⁻¹ with the heat treatment temperature increasing from 25 °C to 450 °C. The saturation magnetization (M_s) and coercivity (H_c) move up from 340.97 kA m⁻¹ and 7.98 kA m⁻¹ to 971.58 kA m⁻¹ and 18.62 kA m⁻¹ with the Co content increasing from 22.42% to 56.09% after annealing at 450.     

Structural characterization and magnetic properties of superparamagnetic zinc ferrite nanoparticles synthesized by the coprecipitation method

Single phase zinc ferrite (ZnFe₂O₄) nanoparticles have been prepared by the coprecipitation method without any subsequent calcination. The effects of precipitation temperature in the range 20–80 °C on the structural and the magnetic properties of zinc ferrite nanoparticles were investigated. The crystallite size, microstructure and magnetic properties of the prepared nanoparticles were studied using X-ray diffraction (XRD), Fourier transmission infrared spectrum, transmission electron microscope (TEM), energy dispersive X-ray spectrometer and vibrating sample magnetometer. The XRD results showed that the coprecipitated nanoparticles were single phase zinc ferrite with mixture of normal and inverse spinel structures. Furthermore, ZnFe₂O₄ nanoparticles have the crystallite size in the range 5–10 nm, as confirmed by TEM. The magnetic measurements exhibited that the zinc ferrite nanoparticles synthesized at 40 °C were superparamagnetic with the maximum magnetization of 7.3 emu/g at 10 kOe.     

Heat treatment effects on microstructure and magnetic properties of Mn-Zn ferrite powders

Mn-Zn ferrite powders (Mn_0.5Zn_0.5Fe₂O₄) were prepared by the nitrate-citrate auto-combustion method and subsequently annealed in air or argon. The effects of heat treatment temperature on crystalline phases formation, microstructure and magnetic properties of Mn-Zn ferrite were investigated by X-ray diffraction, thermogravimetric and differential thermal analysis, scanning electron microscopy and vibrating sample magnetometer. Ferrites decomposed to Fe₂O₃ and Mn₂O₃ after annealing above 550 °C in air, and had poor magnetic properties. However, Fe₂O₃ and Mn₂O₃ were dissolved after ferrites annealing above 1100 °C. Moreover, the 1200 °C annealed sample showed pure ferrite phase, larger saturation magnetization (M_s=48.15 emu g⁻¹) and lower coercivity (H_c=51 Oe) compared with the auto-combusted ferrite powder (M_s=44.32 emu g⁻¹, H_c=70 Oe). The 600 °C air annealed sample had the largest saturation magnetization (M_s=56.37 emu g⁻¹) and the lowest coercivity (H_c=32 Oe) due to the presence of pure ferrite spinel phase, its microstructure and crystalline size.     

Composition dependence of microstructure,magnetic and microwave properties in ball-milled FeSiB nanocrystalline flakes

The soft magnetic nanocrystalline/amorphous FeSiB flakes were fabricated by the ball-milling method and evaluations were made of the composition, microstructure, magnetic and microwave properties in the milling process. An investigation of the relationship between microstructure and magnetic/microwave properties showed that the electromagnetic characteristics were attributed to the changes of nanograin size, crystal and amorphous content corresponding to the composition variation. The replacing of Fe atoms by Si in α-Fe crystal caused the decrease of grain size, saturation magnetization and coercivity, while B content devoted to amorphous phase and decreased the permittivity. Consequently, it was observed that the optimum composition for microwave performance is Fe₈₂Si₅B₁₃.     

Optical and magneto-optical properties of nanostructured yttrium iron garnet

Bulk dense samples of nanostructured yttrium iron garnet Y₃Fe₅O₁₂ with crystallite sizes of 20–40 nm are prepared by high-pressure torsion from a garnet powder with micron grains. The absorption and Faraday rotation spectra in the IR range and the transverse Kerr effect spectra in the visible spectral range for these samples are measured. The absorption and magneto-optical effect spectra are in agreement with the corresponding spectra of single crystals. The appearance of additional absorption bands at 2 and 3 μm is associated with the violation of the stoichiometry of the nanogarnet and the possible contamination of the initial material. The specific Faraday rotation in the transparency window is approximately 1.5 times smaller than the corresponding quantity for single crystals. The extrema in the Kerr effect spectra coincide with those for single crystals, are smaller in magnitude, and are smeared. On the whole, the prepared bulk samples are transparent in the IR spectral range and exhibit optical and magneto-optical characteristics comparable to the corresponding parameters for single crystals. The high density of point defects of the nanogarnet is primarily due to the violation of the stoichiometry and the valence state of iron ions.     

Structure and properties of deposited yttrium iron garnet films

Ferromagnetic resonance (FMR) and vibrating-sample magnetometer techniques were used to study the nature of the structural characteristics of yttrium iron garnet films deposited through either liquid phase epitaxy or laser evaporation on a (111)-oriented gallium gadolinium garnet substrate. It was proved that, based on the experimentally observed cubic magnetic anisotropy, deposited films should be considered to be single crystals. However, the absence of the FMR domain branch in a nonsaturated film and the shape of the magnetization curve indicate that a deposited film when demagnetized does not have a domain structure, as would be expected for a single-crystal film. According to the model proposed, a deposited film consists of close-packed single-crystal fragments with equal crystallographic orientation, the boundaries between which are in a partially atomically disordered state. As a result, such a film is both locally and macroscopically anisotropic, like a continuous single crystal. This film can split into domains only within a fragment (as is the case in a magnetic granular polycrystal); however, this does not happen, because the linear dimensions of a submicroscopic fragment are smaller than the equilibrium domain width.     

Dependence of developing magnetic hysteresis characteristics on stages of evolving microstructure in polycrystalline yttrium iron garnet

The microstructure evolution in several polycrystalline yttrium iron garnet samples as a result of a sintering scheme was studied in detail, in parallel with the changes in their magnetic properties. Samples with nanometer sized starting powder were synthesized by employing the High-Energy Ball Milling technique and then sintering toroidal compacts of the milled powder. Nine sintered samples were obtained, each corresponding to a particular sintering from 600 °C to 1400 °C. The samples were characterized for their evolution in crystalline phases, microstructure and magnetic hysteresis-loops parameters. The results showed an increasing tendency of the saturation magnetization and saturation induction with grain size, which is attributed to crystallinity increase and to reduction of demagnetizing fields in the grains. The variation in coercivity could be related to anisotropy field changes within the samples due to grain size changes. In particular, the starting appearance of room temperature ferromagnetic order suggested by the sigmoid-shaped B-H loops seems to be dependent on a sufficient number of large enough magnetic domain-containing grains having been formed in the microstructure. Viewed simultaneously, the hysteresis loops appear to belong to three groups with different magnetism-type dominance, respectively dependent on phase purity and three different groups of grain size distributions.     

The influence of NiO addition on the magnetic properties of polycrystalline yttrium iron garnet

The influence of NiO addition on the magnetic properties of polycrystalline Y₃Fe₅O₁₂ is studied for the saturation magnetization, Curie temperature, initial magnetic permeability and ferromagnetic resonance line width. Dependence of saturation magnetization on NiO addition suggest that Ni²⁺ ions enter octahedral sites of the garnet lattice. Real part of the complex initial permeability versus temperature curves reveal the single phase for samples with NiO content. The absence of any additional peak in these curves and the invariance of Curie temperature suggest that NiO addition cannot alter the magneto-crystalline anisotropy of the material. Variations of initial permeability with NiO content are due to change of saturation magnetization and grain size of the materials. The ferromagnetic resonance line width varies linearly with the porosity of samples with NiO showing no anisotropy contribution in it.     

Growth and magnetic behavior of bismuth substituted yttrium iron garnet nanoparticles

Crystal growth and the magnetic properties of bismuth substituted yttrium iron garnet (Bi-YIG) nanoparticles were studied with particular focus on the bismuth composition dependence of the magnetic properties of the particles and the effects of annealing on the garnet phase formation. The Bi-YIG nanoparticles of 47–67 nm in size can be chemically synthesized when they are annealed at 650–850 °C. Both the lattice constant and the magnetization of the garnet nanoparticles linearly increase when the bismuth composition in the Bi-YIG particles increases. We have found that chemically synthesized nanoparticles transform from the amorphous to the garnet phase when annealed at temperatures below 650 °C, while the onset of magnetic moment of iron in the garnet nanoparticles is observed slightly above 650 °C. According to Mössbauer effect measurements, the hyperfine fields of ⁵⁷Fe at the tetrahedral and octahedral sites in the garnet are 39 and 48 T, respectively.     

Structure and magnetic properties of nanocrystalline cobalt ferrite powders synthesized using organic acid precursor method

Nanocrystalline octahedra of cobalt ferrite CoFe₂O₄ powders were synthesized using the organic acid precursor route. The effect of the calcination temperature, Fe³⁺/Co²⁺ molar ratio, calcination time and type of organic acid (oxalic, benzoic and tartaric acids) on the formation, crystallite size, microstructure and magnetic properties was studied systematically. The Fe³⁺/Co²⁺ molar ratio was varied from 2 to 1.739 while the annealing temperature was controlled from 400 to 1000 °C for various periods from 0.5 to 2 h. The resulting powders were investigated using X-ray diffraction (XRD) analysis, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and vibrating sample magnetometer (VSM). XRD results indicate that a well crystallized, single spinel cobalt ferrite phase was formed for the precursors annealed at 600-800 °C for 2 h, using oxalic and tartaric acids as precursors for Fe³⁺/Co²⁺ molar ratio 1.818. The crystallite size of as-formed powders was in the range of 38.0-92.6 nm at different operating conditions. The calcination temperature and Fe³⁺/Co²⁺ molar ratio have a significant effect on the microstructure of the produced cobalt ferrite. The microstructure of the produced powders was found to be octahedra-shaped. The crystalline, pure cobalt ferrite powders with magnetic properties having a maximum saturation magnetization (76.1 emu/g) was achieved for the single phase at Fe³⁺/Co²⁺ molar ratio 1.818 and annealing temperature of 600 °C for 2 h using tartaric acid precursor.     

Growth, structural, and magnetic properties of iron nitride thin films deposited by dc magnetron sputtering

FeN thin films were deposited on glass substrates by dc magnetron sputtering at different Ar/N₂ discharges. The composition, structure and the surface morphology of the films were characterized using X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and atomic force microscopy (AFM). Films deposited at different nitrogen pressures exhibited different structures with different nitrogen contents, and the surface roughness depended on the mechanism of the film growth. Saturation magnetization and coercivity of all films were determined using superconducting quantum interference device, which showed that if N₂/(Ar+N₂) flow ratio was equal to or larger than 30% the nonmagnetic single-phase γ″-FeN appeared. If N₂/(Ar+N₂) flow ratio was less than 10%, the films consisted of the mixed phases of FeN_0.056 and γ′-Fe₁₆N₂, whose saturation magnetizations were larger than that of -Fe. If N₂/(Ar+N₂) flow ratio was 10%, the phases of γ′-Fe₄N and -Fe₃N appeared, whose saturation magnetizations were lower than that of -Fe.     

Magnetic properties of magnetite prepared by ball-milling of hematite with iron

Magnetic properties of magnetite powder prepared by ball-milling of stoichiometric mixture of hematite and iron in an inert atmosphere are reported. Hysteresis loops, isothermal remanence acquisition curves and temperature dependence of magnetic susceptibility measurements are used to characterise this material and to examine the effects of heating in air and in an argon atmosphere. Ball-milling of hematite with iron during periods ranging from 30 min up to almost 5 h yields magnetite which exhibits high magnetic hardness, characterised by coercive force three times higher than that typical for single-domain natural magnetites. However, the magnetite produced is unstable upon heating in air, reoxidising almost completely to hematite. Heating in an argon atmosphere causes enhancement of typical magnetic parameters, but decreases the magnetic hardness.     

Effects of excessive grain growth on the magnetic and mechanical properties of hot-deformed NdFeB magnets

The magnetic and mechanical properties of rare-earth magnets hot-deformed at temperature range 750-950 °C have been investigated. The grains tended to grow excessively from dozens of nanometers to several microns at the temperatures above 850 °C. The alignment of grains was disrupted by the hot deformation at the high temperatures. The Nd-rich phase was extruded at the temperatures which are higher than 850 °C. The Nd-rich phase extrusion resulted in the reduction of density by 1% and the reduction of remanence from 1.42 to 0.72 T. The reduction of grain boundaries caused by flat platelet-shaped grains changing to spherical grains and the weak binding strength among large grains of Nd₂Fe₁₄B phase may be the main reasons for the low mechanical strength of hot-deformed magnets.     

Synthesis and characterization of manganese ferrite nanoparticles by thermal treatment method

Cubic structured manganese ferrite nanoparticles were synthesized by a thermal treatment method followed by calcination at various temperatures from 723 to 873 K. In this investigation, we used polyvinyl pyrrolidon (PVP) as a capping agent to control the agglomeration of the nanoparticles. The characterization studies were conducted by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The average particle sizes of manganese ferrite nanoparticles were determined by TEM, which increased with the calcination temperature from 12 to 22 nm and they had good agreement with XRD results. Fourier transform infrared spectroscopy confirmed the presence of metal oxide bands at all temperatures and the absence of organic bands at 873 K. Magnetic properties were demonstrated by a vibrating sample magnetometer, which showed a super-paramagnetic behavior for all samples and also saturation magnetization (M_s) increases from 3.06 to 15.78 emu/g by increasing the calcination temperature. The magnetic properties were also confirmed by the use of electron paramagnetic resonance spectroscopy, which revealed the existence of unpaired electrons and also measured peak-to-peak line width, resonant magnetic field and the g-factor.     

Morphology and magnetic properties of FeCo nanocrystalline powder produced by modified mechanochemical procedure

Properties of FeCo nanocrystalline intermetallic powders prepared by salt-matrix hydrogen reduction of a milled Fe₂O₃-Co₃O₄ mixture were investigated. The product of 72 ks ball-milling at 350 rpm was CoFe₂O₄ nanopowder. Reduction of this powder for 3.6 ks by hydrogen at 750 °C resulted in the formation of Fe_0.67Co_0.33 stoichiometric compound. Scanning electron microscopy, electron dispersive spectrometry, X-ray diffraction and vibrating sample magnetometry were used to characterize the nanopowder. Using a salt-matrix (NaCl as a dispersion medium) resulted in the decrease of the reduction temperature and improvement of the morphology and magnetic properties of the nanopowder. Dispersion of the ball-milled product in Hexan resulted in further improvements of the magnetic properties.     

Structural and magnetic properties of holmium substituted cobalt ferrites synthesized by chemical co-precipitation method

CoHo_xFe_2−xO₄ ferrites (x=0.00–0.1) were prepared by the co-precipitation technique and the effect of holmium substitution on the magnetic properties was investigated. X-ray diffraction reveals that the substituted samples show a second phase of HoFeO₃ along with the spinel phase. The magnetic properties such as the saturation magnetization (M_s), coercivity (H_c) and remanence (M_r) are obtained from the hysteresis loops. It is observed that the M_s decreases while H_c increases with Ho³⁺ substitution. The decrease of saturation magnetization is attributed to the weakening of exchange interactions. The coercivity increases with increase of the Ho³⁺ concentration, which is attributed to the presence of an ultra-thin layer at the grain boundaries that impedes the domain wall motion. Low field AC susceptibility was also measured over the temperature range 300–600 K at the frequency of 200 Hz. It decreases with the increase of temperature following the Curie–Weiss law up to the Curie temperature. Above the Curie temperature it shows paramagnetic behavior. The increase in coercivity suggests that the material can be used for applications in perpendicular recording media.     

Hard magnetic properties of anisotropic Sm-Fe-N magnets produced by compression shearing method

Anisotropic Sm-Fe-N bulk magnets were produced by the compression shearing method using a hardened steel plate and a tungsten-carbide (WC) plate. It was found that the magnets retained the original Sm₂Fe₁₇N₃ phase structure without any appreciable decomposition of the Sm₂Fe₁₇N₃ phase. The anisotropic Sm-Fe-N bulk magnet produced using a WC plate had a higher density and higher crystallographic alignment of the Sm₂Fe₁₇N₃ phase than that produced using a hardened steel plate, and exhibited high maximum energy products of 228 kJ/m³ with a high coercivity of 0.88 MA/m.