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.     

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.     

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.     

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.     

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.     

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.     

Effect of Bi-substitution on the dielectric properties of polycrystalline yttrium iron garnet

The effect of Bi-substitution on the dielectric properties of yttrium iron garnet (YIG) was studied in this paper. The Bi-substituted YIG (YIG:Bi) polycrystalline samples, having composition of Y_3−xBi_xFe₅O₁₂, were prepared by the solid-state reaction method. x varied from 0 to 1.2. The phase formation and microstructure were performed by X-ray diffraction and scanning electron microscopy, respectively. Ions valency was identified by X-ray photoelectron spectroscopy. The impedance analyzers are used to measure the frequency dependence and the temperature dependence of relative dielectric constant (_r) and loss tangent (tan δ). The experimental results show that the Bi-substitution lowers the phase formation and sintering temperature. Electronic carrier concentration drops dramatically due to limitation of ferric valency variation. Hence, _r and tan δ decrease with addition of Bi. Dispersion characteristic indicates non-Debye-type dispersion. A maximum of _r appears as the temperature rises.     

Investigation of nanostructural,thermal and magnetic properties of yttrium iron garnet synthesized by mechanochemical method

This paper focuses on the magnetic, structural and thermal properties of mechanically alloyed Y₂O₃/α-Fe₂O₃ mixed powders and investigates the effects of the mechanical milling and heat treatment on the synthesis of yttrium iron garnet from the primary materials. The morphological and structural studies were carried out by scanning electron microscope and X-ray diffraction, respectively. The thermal activities were measured by differential thermal analysis. The magnetic properties were studied by vibrating sample magnetometer. The results showed that high-energy milling does not lead to the garnet formation and even does not decrease the temperature of the garnet formation. Furthermore, the orthoferrite phase can be achieved slightly during the milling process (up to 96 h) and completely by the heat treatment at lower temperatures (850 °C).     

The 50 nm-thick yttrium iron garnet films with perpendicular magnetic anisotropy

Yttrium iron garnet (YIG) films possessing both perpendicular magnetic anisotropy (PMA) and low damping would serve as ideal candidates for high-speed energy-efficient spintronic and magnonic devices. However, it is still challenging to achieve PMA in YIG films thicker than 20 nm, which is a major bottleneck for their development. In this work, we demonstrate that this problem can be solved by using substrates with moderate lattice mismatch with YIG so as to suppress the excessive strain-induced stress release as increasing the YIG thickness. After carefully optimizing the growth and annealing conditions, we have achieved out-of-plane spontaneous magnetization in YIG films grown on sGGG substrates, even when they are as thick as 50 nm. Furthermore, ferromagnetic resonance and spin pumping induced inverse spin Hall effect measurements further verify the good spin transparency at the surface of our YIG films.     

High-temperature electrical properties of yttrium iron garnet under varying oxygen pressures

The d.c. conductivity and Seebeck coefficient of Ca and Mg doped YIG have been measured at 1200–1700 K. A change of p-type to n-type conductivity was accomplished by varying the oxygen pressure between 1 and 10^-8 atm. From the position of the conductivity minimum as a function of temperature the band gap energy is estimated to be 2.85 eV.     

Element selective X-ray magnetic circular and linear dichroisms in ferrimagnetic yttrium iron garnet films

X-ray magnetic circular dichroism (XMCD) was used to probe the existence of induced magnetic moments in yttrium iron garnet (YIG) films in which yttrium is partly substituted with lanthanum, lutetium or bismuth. Spin polarization of the 4d states of yttrium and of the 5d states of lanthanum or lutetium was clearly demonstrated. Angular momentum resolved d-DOS of yttrium and lanthanun was shown to be split by the crystal field, the two resolved substructures having opposite magnetic polarization. The existence of a weak orbital moment involving the 6p states of bismuth was definitely established with the detection of a small XMCD signal at the Bi M₁-edge. Difference spectra also enhanced the visibility of subtle changes in the Fe K-edge XMCD spectra of YIG and {Y, Bi}IG films. Weak natural X-ray linear dichroism signatures were systematically observed with all iron garnet films and with a bulk YIG single crystal cut parallel to the (1 1 1) plane: this proved that, at room temperature, the crystal cannot satisfy all requirements of perfect cubic symmetry (space group: ), crystal distortions preserving at best trigonal symmetry ( or R3m). For the first time, a very weak X-ray magnetic linear dichroism (XMLD) was also measured in the iron K-edge pre-peak of YIG and revealed the presence of a tiny electric quadrupole moment in the ground-state charge distribution of iron atoms. Band-structure calculations carried out with fully relativistic LMTO-LSDA methods support our interpretation that ferrimagnetically coupled spins at the iron sites induce a spin polarization of the yttrium d-DOS and reproduce the observed crystal field splitting of the XMCD signal.     

Layered structure of epitaxial yttrium iron garnet films

The layered structure of yttrium iron garnet films, ranging in thickness from 0.7 to 4.1 μm, grown epitaxially on single-crystal gallium-gadolinium garnet substrates, was investigated by x-ray spectral microanalysis. The ferrite films were chemically etched layer by layer in a mixture of orthophosphoric and sulfuric acids at T=353–423 K. It was established that the chemical composition of the films varies over the thickness because of the nonuniform distribution of gadolinium, gallium, lead, and platinum ions; the film-substrate transitional layer and the surface layer of the film differ most greatly with respect to the composition and magnetic properties. It was shown that the thickness of the transitional layers and their negative effect on the magnetic characteristics of ferrite films decrease appreciably if at the time of immersion of the substrate and pulling of epitaxial structure out of the fluxed solution the substrate holder together with a special mixer rotate at a rate of 50 rpm and the pulling velocity is 20 cm/min. Zh. Tekh. Fiz. 69, 62–64 (December 1999)     

DCEMS of neon implantation in yttrium iron garnet

⁵⁷Fe-enriched, epitaxial Y₃Fe₅O₁₂ films have been implanted with 50 keV and 100 keV neon ions with a dose of 4·10¹⁴Ne⁺/cm². Depth-selective conversion electron Mössbauer spectroscopy has been performed at 300 K and 40 K. The results show that the 50 keV-implanted sample can be interpreted as an amorphous layer on top of an almost unperturbed YIG layer. In the 100 keV-implanted film a buried amorphous layer is observed.     

Effect of reversible adsorption on the magnetic properties of iron garnet films

The reversible change in the domain structure and the magnetic domain width in bismuth-containing iron garnet films with an easy magnetization axis oriented normal to their surface during adsorption caused by hydrogen bonds is studied by a magnetooptical method. The dependence of the domain width on the vapor pressure of methyl alcohol or water in a cell with a sample is determined, and the time dependence of the domain width induced by the adsorption-desorption processes occurring between methyl alcohol molecules or water molecules on the film surface is studied. A model is proposed to explain the detected effects.     

Influence of substitutions on the magnetic anisotropy of Gd-containing magnetooptic iron garnet films

The properties of magnetooptical films of the system (Bi,Gd,Ln)₃(Fe,M)₅O₁₂, where Ln = Lu or La and M = Ga or Al, grown by liquid-phase epitaxy on Nd₃Ga₃O₁₂ substrates oriented along (100), along (110), and close to (111), are investigated by x-ray and ferromagnetic resonance methods. Zh. Tekh. Fiz. 68, 113–116 (May 1998)     

Spin-lattice relaxation of Fe nuclei in yttrium iron garnet

Pulse measurements of T₁ for ⁵⁷Fe nuclei in very pure, single crystals of YIG are reported. The temperature was varied from 2° to 292°K, and the externally applied field ranged from 0 to 6000 Oe. The temperature variation of T₁ is quite strong, being three orders of magnitude in the range 2°–40°K. At constant temperature, T₁ changed approximately one order of magnitude between saturation field and 6000 Oe. The data are compared with the results of a calculation by Beeman and Pincus, in which a second-order Raman process and the three-magnon process are assumed to predominate below 50°K. Agreement is only qualitative, the experimental values of T₁ being larger than predicted. At 4.2°K in zero field, it is found that a polycrystalline sample containing particles of ≈ 5 × 10⁻⁴ cm dia. has a value of 1/T₁ which is some two orders of magnitude larger than for a macroscopic crystal. The presence of a relaxation mechanism associated with surface effects is suggested.     

Pr:YIG晶体抗磁性Faraday转动谱的研究

在单电子模型下，用量子理论研究了Pr:YIG晶体中Pr3+离子的抗磁性Faraday转动（FR）谱.分别在温度为77K和300K时，计算了Pr3+离子的λF-1/2θ-λ2的变化关系，计算结果与实验值符合较好.证实了晶场为单态的离子，其抗磁性FR比顺磁性FR对交换场（或外场）有更大的依赖性，且与温度有关.在强交换场环境中，两种转动对FR的贡献有相同的重要性. 关键词： Pr:YIG晶体 单离子模型 抗磁性Faraday转动     

Microstructure and spin wave scattering in polycrystalline yttrium iron garnet

Polycrystalline ceramic YIG has been synthesized with submicron microstructure. The log-log plot of FMR linewidth versus average grain size gives a power law dependence α^-1₀ where α₀ is the average grain size. The instability threshold h_crit for increasing magnetic field vector of the microwave parallel pump shows a linear log-log dependence with average grain size.