Investigation of the photothermally modulated ferromagnetic resonance signal from magnetostatic modes in yttrium iron garnet films

The conventional and photothermally modulated (PM) ferromagnetic resonance (FMR) of magnetostatic modes (MSM) in yttrium iron garnet (YIG) films have been investigated as a function of temperature. Approaching the ferrimagnetic transition at T _c=560 K a strong enhancement of the PM-FMR signal amplitude is observed which is accompanied by a change of the signal shape. The observations are discussed in the framework of a model that takes into account the temperature derivatives of those quantities that contribute to the high-frequency susceptibility. At temperatures still below T _c a paramagnetic line emerges. The MSM disappear in a state of finite magnetization which is explained on the basis of damping of the MSM being important in the vicinity of the magnetic phase transition. Additionally, frequency and power dependent measurements are presented and the imaging ability of PM-FMR is demonstrated.     

Four-magnon decay of magnetostatic surface waves in yttrium iron garnet films

The four-magnon instability of magnetostatic surface waves (MSSWs) in yttrium iron garnet epitaxial films is investigated experimentally. It is shown that four-magnon instability for MSSWs with wave numbers 30–600 cm⁻¹ is a decay instability and develops for values of the wave magnetization close to the threshold level for second-order parametric instability of a homogeneous transverse pump wave. When the supercriticality of the MSSW power is 15–20 dB, the generated parametric spin waves themselves become unstable with respect to the four-magnon interaction, so that kinetic instability develops in the film. It is shown that the pump signal transmitted through the signal and the length of the “nonlinear” part of the film, where a MSSW is capable of exciting parametric spin waves, increase as the pump power is increased. Fiz. Tverd. Tela (St. Petersburg) 38, 330–338 (February 1997)     

Possible identification of magnetostatic surface spin wave modes in ferromagnetic resonance on epitaxial yttrium—iron—garnet films

In ferromagnetic resonance experiments of yttrium—iron—garnet films, resonances have been observed whose characteristics are consistent with their interpretation as magnetostatic surface spin wave modes.     

Spin reorientation in silicon-substituted yttrium iron garnet

Mössbauer spectroscopy of a silicon substituted YIG containing 0.3 Si⁴⁺ per formula unit has shown that a spin reorientation, from [111] to [100], occurs between 265 and 80 K. The transitions occur by way of the magnetic space groups $\text{R}\text{3}\text{c}\text{′ →}\text{F}\text{2′}\text{d}\text{′}\text{→}\text{I}\text{4}{}_1\text{ac}\text{′}\text{d}\text{′}$. The broad spin reorientation is mainly a consequence of the persistence of a nonuniform distribution of Fe²⁺ ions over the octahedral sites.     

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.     

Tunable negative index metamaterial using yttrium iron garnet

A magnetic field tunable, broadband, low-loss, negative refractive index metamaterial is fabricated using yttrium iron garnet (YIG) and a periodic array of copper wires. The tunability is demonstrated from 18 to 23 GHz under an applied magnetic field with a figure of merit of 4.2 GHz/kOe. The tuning bandwidth is measured to be 5 GHz compared to 0.9 GHz for fixed field. We measure a minimum insertion loss of 4 dB (or 5.7 dB/cm) at 22.3 GHz. The measured negative refractive index bandwidth is 0.9 GHz compared to 0.5 GHz calculated by the transfer function matrix theory and 1 GHz calculated by finite element simulation.     

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.     

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.     

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.     

Exchange coupling in ultrathin epitaxial yttrium iron garnet films

Magnetic exchange coupling has been observed for ultrathin films of yttrium iron garnet (Y₃Fe₅O₁₂ or YIG). Single-crystalline YIG films were prepared on yttrium aluminium garnet (Y₃Al₅O₁₂ or YAG) substrates by pulsed laser deposition. (111) and (110) oriented substrates were used. Film thicknesses were varied from 180 ? to 4600 ?. Epitaxial growth of YIG on YAG was obtained in spite of the lattice mismatch of 3%. Magnetic hysteresis loops recorded for ultrathin YIG films have a “bee-waist” shape and show a coupling between two different magnetic phases. The first phase is magnetically soft YIG. A composition study by secondary ion mass spectroscopy shows the second phase to be Y₃Fe_5-xAl_xO₁₂ due to the interdiffusion of Fe and Al at the film/substrate interface. This compound is known to be magnetically harder and to have weaker magnetization than YIG. The coupling of the two phases leads to a hysteresis loop displacement at low temperatures. This displacement varies differently with film thickness for two substrate orientations. Assuming an interfacial coupling, the maximal interaction energy is estimated to be about 0.17 erg/cm² at 5 K for (111) oriented sample. Received 3 June 2002 / Received in final form 7 October 2002 Published online 27 January 2003 RID="a" ID="a"Presently at LPM, Université H. Poincaré, BP 239, 54506 Vandœuvre-lès-Nancy e-mail: popova@lpm.u-nancy.fr     

Magnetic triangular bubble lattices in bismuth-doped yttrium iron garnet

Magnetic bubbles have again become a subject of significant attention following the experimental observation of topologically nontrivial magnetic skyrmions. In recent work, tailoring the shape of the bubbles is considered a key factor for their dynamics in spintronic devices. In addition to the reported circular, elliptical, and square bubbles, here we observe triangular bubble domains in bismuth-doped yttrium iron garnet(Bi-YIG) using Kerr microscopy. The bubble domains evolve from discrete cir...     

Polarized neutron study of covalency effects in yttrium iron garnet

Magnetic structure amplitudes of 170 reflections up to sin $\text{θ}\text{λ}\text{= 1.0}\text{A}\text{?}{}^{\mathrm{?1}}$ were measured by polarized neutron diffraction at T = 295K on yttrium iron garnet. The data set was completed by model calculations and the magnetization density was determined. The magnetic moments obtained by integration and refinement are considerably reduced on both iron sites due to charge density transferred from intervening ligand ions. A residual moment of uncancelled spin of (0.032 ±0.004) μ_B is observed on the oxygen ion. Evidence for magnetization density on the oxygen atom and between oxygen and tetrahedral iron was found. A qualitative discussion in terms of a molecular orbital model is given. A further data set collected at 4.2K showed equally a magnetic moment lower than expected for the free ion.     

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.     

Optical constants of yttrium–iron garnet single-crystal film structures

Light-attenuation spectra of yttrium–iron garnet single-crystal film structures grown on a gallium–gadolinium garnet substrate by liquid-phase epitaxy from the undercooled solution in the melt have been studied and compared with those of bulk yttrium–iron garnet samples. The calculated optical constants are discussed taking into account the influence of crystal field on the splitting of the energy states of iron ions in the film samples. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 76, No. 2, pp. 218–224, March–April, 2009.     

Light scattering from thermal acoustic magnons in yttrium iron garnet

Brillouin scattering measurements on yttrium iron garnet (YIG) have revealed the scattering due to thermal acoustic magnons. The intensity and frequency shift of the magnon peaks as a function of applied magnetic field and incident light wavelength have been investigated and are discussed here within the framework of a simple light scattering theory.