Spin-dependent current and magnetization reversal in Tb22Co5Fe73/Pr6O11/Tb19Co5Fe76 nanofilms in laser radiation field

The results of investigation of magnetization reversal dynamics of ferrimagnetic amorphous nanolayers with transverse anisotropy is investigated for Al₂O₃/Tb₂₂Co₅Fe₇₃/Al₂O₃ and Al₂O₃/Tb₂₂Co₅Fe₇₃/Pr₆O₁₁/Tb₁₉Co₅Fe₇₆/Al₂O₃ multilayer films irradiated by laser pulses, as well as the effect of such irradiation on the resistance in a Tb₂₂Co₅Fe₇₃/Pr₆O₁₁/Tb₁₉Co₅Fe₇₆ tunnel microcontact. It is shown that magnetization reversal in magnetic nanolayers in the laser radiation field may occur not only because of heating and the action of the external magnetic field, but also under the action of the magnetic field induced by circularly polarized laser radiation, as well as owing to transfer of magnetic moments by polarized electrons. Laser radiation can be used to control (by changing the resistance by a factor of 1.5–2.0) the conductivity of the Tb₂₂Co₅Fe₇₃/Pr₆O₁₁/Tb₁₉Co₅Fe₇₆ tunnel microresistor. Original Russian Text ? N.N. Krupa, 2009, published in Zhurnal éksperimental’noĭ i Teoreticheskoĭ Fiziki, 2009, Vol. 108, No. 5, pp. 981–992.     

Structural,magnetic, and magnetothermal properties of the Tb<Subscript>0.3</Subscript>Dy<Subscript>0.7</Subscript>Co<Subscript>2</Subscript> compound

A complex investigation of the structural, magnetic, and magnetothermal properties of the Tb_0.3Dy_0.7Co₂ compound synthesized with the use of high-purity rare-earth metals has been performed. The phase composition has been controlled using the X-ray structural analysis, and the topology of the alloy surface has been investigated using atomic-force microscopy. It has been established that the Tb_0.3Dy_0.7Co₂ compound is single-phase, while the samples selected for measurements possess a clearly pronounced texture. The magnetization has been measured using a vibrating-sample magnetometer in the fields up to 100 kOe in a temperature range from 4.2 to 200 K. The Curie temperature of the compound is 170 K. The data on the temperature dependence of heat capacity of Tb_0.3Dy_0.7Co₂ have been obtained. The magnetocaloric effect ΔT has been measured by a direct method in the fields up to 18 kOe applied both along and perpendicularly to the texture axis. The anisotropic behavior of the magnitude ΔT for this compound, which possesses the cubic structure, has been found. The maximum value of the magnetocaloric effect ΔT = 2.3 K (ΔH = 18 kOe) has been observed upon applying the magnetic field along the texture axis.     

Low-field magnetization of ludwigites Co3O2BO3 and Co3 ? xFexO2BO3 (x ≈ 0.14)

Ludwigite single crystals of compositions Co₃O₂BO₃ and Co_{3 − x} Fe _x O₂BO₃ (x ≈ 0.14) have been synthesized. The crystal structure is investigated at room temperature, and the magnetization is studied in the temperature range T = 4.2–100 K in magnetic fields of up to 600 Oe. The orthorhombic symmetry is revealed, and the unit cell parameters are determined. A number of features are established for the temperature dependence of the magnetization. In unsubstituted Co₃O₂BO₃, two magnetic transitions are found at T _C1 = 43 K and T _C2 = 15 K. At temperatures below 40 K, spin-glass state is revealed. Substitution of iron ions for cobalt ions leads to a noticeable shift in the magnetic transitions toward the high-temperature range: T _C1 = 83 K and T _C2 = 74 K. A ferromagnetic ordering of the P type is found in the Co_{3 − x} Fe _x O₂BO₃ (x ≈ 0.14) compound. Original Russian Text ? N.V. Kazak, N.B. Ivanova, V.V. Rudenko, A.D. Vasil’ev, D.A. Velikanov, S.G. Ovchinnikov, 2009, published in Fizika Tverdogo Tela, 2009, Vol. 51, No. 5, pp. 916–919.     

Crystal structure and magnetic anisotropy of ludwigite Co<Subscript>2</Subscript>FeO<Subscript>2</Subscript>BO<Subscript>3</Subscript>

Co₃O₂BO₃ and Co₂FeO₂BO₃ single crystals with a ludwigite structure are fabricated, and their crystal structure and magnetic properties are studied in detail. Substituted ludwigite Co₂FeO₂BO₃ undergoes two-stage magnetic ordering at the temperatures characteristic of Fe₃O₂BO₃ (T _N1 ≈ 110 K, T _N2 ≈ 70 K) rather than Co₃O₂BO₃ (T _N = 42 K). This effect is explained in terms of preferred occupation of nonequivalent crystallographic positions by iron, which was detected by X-ray diffraction. Both materials exhibit a pronounced uniaxial magnetic anisotropy. Crystallographic direction b is an easy magnetization axis. Upon iron substitution, the cobalt ludwigite acquires a very high magnetic hardness.     

Technical magnetization of Tb3Fe5O12 garnet ferrite near the magnetic compensation point

The domain structure and technical magnetization of a single-crystalline Tb₃Fe₅O₁₂ garnet ferrite sheet near its magnetic compensation point (T _c ≈ 250 K) are studied. It is found that above this temperature the domain structure persists and considerably influences the field and temperature dependences of the Faraday effect. It is shown that the behavior of Tb₃Fe₅O₁₂ during technical magnetization near T _c is not fully described by the existing thermodynamic theory of the domain structure. The features of the domain structure and technical magnetization of Tb₃Fe₅O₁₂ are related to the transition of the magnetic structure to a non-collinear phase.     

Large magnetocaloric effect and magnetoresistance behavior in Gd4Co3

We report a large entropy change (ΔS) below 300 K, peaking near T _C = 220 K, due to isothermal change of magnetic field, for Gd₄Co₃, with a refrigeration capacity higher than that for, say, LaFe_11.4Si_1.6, ordering magnetically in the same temperature range. A noteworthy finding is that the isothermal magnetization is nonhysteretic — an important criterion for magnetic refrigeration without loss. ΔS behavior is also compared with that of magnetoresistance.     

Magnetic and transport properties of monocrystalline<Emphasis Type="Italic">Fe</Emphasis><Subscript>3</Subscript><Emphasis Type="Italic">O</Emphasis><Subscript>4</Subscript>

A monocrystal ofFe ₃ O ₄ is characterized by resistance, magnetoresistance and magnetic measurements in a temperature range from 4.2 K to 350 K and magnetic field-cycling from −9 T to 9 T. The resistance measurements revealed a metal-insulator Verwey transition (VT) atT _v =123.76 K with activation energy E=92.5 meV at T >T _v and temperature-substitute for the activation energy below the VT,T ₀=E/k _B ≈3800 K within 70 K–110K. The magnetotransport results independently verified the VT at 123.70 K, with discontinuous change in the magnetic moment ΔM≈0.21 ΔM≈0.21μ _B and resistance hysteresis, dependent on the magnetic field in a narrow temperature range of 0.4° around theT _v . The magnetic characterization established self consistentlyT _v as ≈123.67 K, the jump in the magnetization at the VT≈0.25μ _B and confirmed, that the magnetocrystalline anisotropy is the main microscopic mechanism responsible for the magnetization of the monocrystal (88%) with additional natural and imposed defects contributing as 12%.     

Magneto-optical properties of the iron garnet Tb3Fe5O12 near the magnetic compensation temperature

The magneto-optical susceptibility and magnetic hysteresis loops of the Faraday effect, which accompany the technical magnetization of the iron garnet Tb₃Fe₅O₁₂, have been investigated experimentally in the temperature region near the magnetic compensation point of this ferrimagnet T _c = 249 K. It has been found that, during the technical magnetization as the temperature approaches the magnetic compensation point T _c , the velocity of domain walls increases, whereas the magneto-optical susceptibility has local maxima to the right and to the left from T _c . Mentioned features of magneto-optical properties of the iron garnet Tb₃Fe₅O₁₂ are associated with the resonance natural frequency of the domain wall oscillations in the crystal with the frequency of the alternating magnetic field. It has been shown that the used theoretical model of the magnetic resonance of domain walls makes it possible to consistently describe (at the qualitative level) the revealed regularities of the variation of the Faraday effect in the iron garnet Tb₃Fe₅O₁₂ near T _c .     

Synthesis and magnetic properties of Pr(Fe 1-xCo x) 2 and Pr 1-yTb y(Fe 0.4Co 0.6) 2 alloys

Measurement of X-ray diffraction, magnetization and magnetostriction was made on the Pr(Fe_1-xCo_x)₂ (x=0.4, 0.5 and 0.6) and Pr_1-yTb_y(Fe_0.4Co_0.6)₂ (y=0, 0.1, 0.2 and 0.3) alloy series. It was found that a cubic phase with the MgCu₂ structure can be obtained in the Pr(Fe_1-xCo_x)₂ series only at x=0.6. The Pr_1-yTb_y(Fe_0.4Co_0.6)₂ system has the cubic MgCu₂ structure over the studied range for y. The lattice constant and magnetization decrease and the Curie temperature increases with increasing y. At 7 K, Pr_1-yTb_y(Fe_0.4Co_0.6)₂ samples are found to have huge intrinsic coercivities, which are associated with narrow domain walls. It is also found from X-ray measurement that in Pr_1-yTb_y(Fe_0.4Co_0.6)₂ the spontaneous magnetostriction ₁₁₁ increases due to Tb substitution, while the saturation magnetostriction _s is much lower than ₁₁₁. This can be attributed to the large value of ₁₀₀ with an opposite sign to ₁₁₁, which may be caused by the filling of the d band due to Co substitution. PACS 75.80.-g; 61.10.-i; 75.60.-d     

Photon pressure and magnetic moment transfer in multilayered nanosize films

The effect of nanosecond laser pulses with λ = 355 nm on the Kerr and Faraday angles in nanosize layered magnetic films Al₂O₃/TbFe/Al₂O₃/TbFe/Al₂O₃ and Al₂O₃/TbFe/Au/TbFe/Al₂O₃ is studied experimentally. The first ferrimagnetic TbFe layer in these films with transverse anisotropy is enriched by terbium, while the second Tb₂₂Fe₇₈ layer is enriched by iron relative to the composition at the compensation point. When the ferrimagnetic TbFe layers in the film are magnetized in the same direction, the magnetooptical characteristics of each TbFe layers and of the film as a whole depend on the laser radiation power, which is in good agreement with the temperature characteristics. When the TbFe layers are magnetized in opposite directions for a high power of nanosecond pulses, the values of the Faraday and Kerr angles for the output TbFe layer sharply change and even reverse their signs. These results are explained by the effect of electrons with a high spin polarization, which are injected by radiation due to the photon pressure. In the case of antiparallel magnetizations of the TbFe layers, a high concentration of such electrons not only changes the local magnetization of the output layer, but also causes its magnetization reversal due to magnetic moment transfer by such electrons.     

Magnetocaloric effect of Gd–Tb alloys: influence of the sample shape anisotropy

The magnetocaloric effect of Gd_1−x Tb _x alloys with x=0.00, 0.10, 0.20, 0.25, 0.30 and 0.40 was studied. The magnetic ordering temperatures were determined from the magnetization measurement. The data obtained from magnetization and specific-heat measurements as well as by the direct measurement are well comparable within their experimental errors. The values of ΔT _ad are in the proximity of 2.5 K for field change of 1 T and all studied concentrations. The dependence of magnetocaloric effect on the sample shape anisotropy was documented by the magnetization measurement as well as by the direct measurement.     

Temperature and magnetic field dependence of the elastic properties of rare earth-cobalt laves phase compounds

Ultrasonic sound velocity measurements have been carried out in order to determine the elastic moduli, adiabatic compressibility and the Debye temperature of polycrystalline rare earth-cobalt Laves phase compounds RCo₂(R = Pr, Nd, Sm, Gd, Tb, Dy, Ho, ErandLu) and YCo₂ between 4.2 and 300 K. DyCo₂ HoCo₂ and ErCo₂ exhibit a first-order transition at T_c. In SmCo₂ and TbCo₂ the phase transition is of the second-order accompanied by a large lattice softening. NdCo₂, GdCo₂ and HoCo₂ show spin reorientations from one easy direction of magnetization to another one, at low temperatures, below T_c.The influence of an external magnetic field (up to 25 kOe) on the elastic properties of these Laves phases, the so-called ΔE effect was determined. No saturation was reached in SmCo₂, TbCo₂ and DyCo₂ in magnetic fields up to 25 kOe. The behavior of the RCo₂ compounds was compared with that of RFe₂, published earlier.     

Magnetism of the Tb2Fe14−xCoxB system

The Tb₂Fe_14−xCo_xB materials were synthesized for the entire composition range (x = 0–14) and studied by X-ray and magnetometry methods. All materials have a tetragonal crystal structure with decreasing lattice parameters upon Co substitution. The Curie temperature markedly rises for alloys with low Co content. Saturation magnetization at 77 K reaches a slight maximum around x ≈ 1 and gradually decreases for higher Co concentrations. An antiparallel coupling of 3d and Tb magnetic moments is inferred from saturation magnetization data. Anisotropy fields exhibit a maximum at low Co contents, but they decrease rapidly for x > 5. A spin reorientation (axis-to-plane) occurs at high temperature in materials with x ⩾ 12.5 due to competing effects of the terbium sublattice anisotropy and the 3d sublattice anisotropy. The spin-reorientation temperature becomes lower for alloys with higher Co content. The observed magnetic behavior is discussed in terms of preferential Co substitution into 16 k₂ sites and changes in the 3d sublattice due to Co introduction. A magnetic phase diagram is constructed for the Tb₂Fe_14-xCo_xB system and compared with that of Pr₂Fe_14-xCo_xB and Nd₂Fe_{14 -x}Co_xB systems.     

Magnetic,electrical, magnetoelectrical,and magnetoelastic properties of La<Subscript>0.9</Subscript>Sr<Subscript>0.1</Subscript>MnO<Subscript>3 − <Emphasis Type="Italic">y</Emphasis></Subscript> manganites

This paper reports on a study of the influence of oxygen deficiency on the magnetization, paramagnetic susceptibility, electrical resistivity, magnetoresistance, and volume magnetostriction of the La_0.9Sr_0.1MnO_{3 − y} manganite with y = 0.03, 0.10, and 0.15. The magnetization M(T) behaves in a complex way with temperature; for T < 80 K, it only weakly depends on T, and at 80 ≤ T ≤ 300 K, the M(T) curve shows a falloff. Within the interval 240 K ≤ T ≤ 300 K, the long-range magnetic order breaks up into superparamagnetic clusters. For T < 80 K, the magnetic moment per formula unit is about one-fourth that which should be expected for complete ferromagnetic alignment of Mn ion moments. Although the composition with y = 0.03, in which part of acceptor centers is compensated by donors (oxygen vacancies), the negative magnetoresistance Δρ/ρ and volume magnetostriction ω are observed to pass through maxima near the Curie point, their values are one to two orders of magnitude smaller than those for the y = 0 composition. In compositions with y = 0.10 and 0.15 with electronic doping, the values of Δρ/ρ and ω are smaller by one to two orders of magnitude than those observed for the y = 0.03 composition. They do not display giant magnetoresistance and volume magnetostriction effects, which evidences the absence of ferrons near unionized oxygen vacancies. This allows the conclusion that the part played by both compensated and uncompensated doubly charged donors consists in forming dangling Mn-O-Mn bonds, which lead to a decrease in the Curie temperature with increasing y and to the formation above it of superparamagnetic clusters of the nonferron type.     

Phase transformations and magnetotransport properties of the Pr0.5Sr0.5Co1 ? xMnxO3 system

The structural, magnetic, and magnetotransport properties of Pr_0.5Sr_0.5Co_{1 − x} Mn _x O₃ (x < 0.65) perovskites are studied by magnetization and electrical conductivity measurements in magnetic fields up to 14 T and by neutron diffraction. In the manganese concentration range x < 0.5 and T = 300 K, the crystal structure is described by monoclinic space group I2/a; at x > 0.5, it is described by orthorhombic space group Imma. When the temperature decreases, a structural transformation without changing the symmetry takes place in all compounds. This transformation is caused by an active role of the inner shells of the praseodymium ion in chemical bond formation. The substitution of manganese for cobalt breaks a long-range ferromagnetic order near x ≈ 0.25, and a metal-dielectric transition occurs at x ≈ 0.15. The negative magnetoresistance is found to be maximal near a critical manganese concentration, where a long-range magnetic order is broken; it reaches 95% in a field of 14 T at T = 10 K for x = 0.2. An unusual dielectric magnetic state with a small spontaneous magnetic moment and a sharp transition into a paramagnetic state at T > 200 K is revealed in the concentration range 0.30 ≤ x ≤ 0.65 in spite of the absence of coherent magnetic neutron scattering. A model is proposed to explain the behavior of the magnetic properties in this phase.     

Antiferromagnetic resonance and dielectric properties of rare-earth ferroborates in the submillimeter frequency range

The magnetoresonance and dielectric properties of a number of crystals of a new family of multiferroics, namely, rare-earth ferroborates RFe₃(BO₃)₄ (R = Y, Eu, Pr, Tb, Tb_0.25Er_0.75), are studied in the sub-millimeter frequency range (ν = 3–20 cm⁻¹). Ferroborates with R = Y, Tb, and Eu exhibit permittivity jumps at temperatures of 375, 198, and 58 K, respectively, which are caused by the R32 → P3₁21 phase transition. Antiferromagnetic resonance (AFMR) modes in the subsystem of Fe³⁺ ions are detected in the range of anti-ferromagnetic ordering (T < T _N = 30–40 K) in all ferroborates that have either an easy-plane (Y, Eu) or easy-axis (Pr, Tb, Tb_0.25Er_0.75) magnetic structure. The AFMR frequencies are found to depend strongly on the magnetic anisotropy of a rare-earth ion and its exchange interaction with the Fe subsystem, which determine the type of magnetic structure and the sign and magnitude of an effective anisotropy constant. The basic parameters of the magnetic interactions in these ferroborates are found, and the magnetoelectric contribution to AFMR is analyzed.     

Structural, AC, and DC magnetic properties of Zn1−xCoxFe2O4

Structural, AC and DC magnetic properties of polycrystalline Zn_1−xCo_xFe₂O₄ (x=0.2, 0.4) samples sintered at various temperatures (1100-1300 °C), and various dwell times (0.2-15 h) have been investigated thoroughly. The bulk density of the Zn_0.60Co_0.40Fe₂O₄ samples increases as the sintering temperature (T_s) increases from 1100 to 1250 °C, and above 1250 °C the bulk density decreases slightly. The Zn_0.80Co_0.20Fe₂O₄ samples show similar behavior of changes to that of Zn_0.60Co_0.40Fe₂O₄ samples except that the bulk density is found to be highest at 1200 °C. The DC magnetization as a function of temperature curves show that the Zn_0.60Co_0.40Fe₂O₄ sample is ferrimagnetic at room temperature while the Zn_0.80Co_0.20Fe₂O₄ sample is paramagnetic at room temperature. The T_c of Zn_0.80Co_0.20Fe₂O₄ sample is found to be 170 K from DC magnetization measurement. Separate measurement (AC magnetization), initial permeability as a function of temperature shows that the T_c of the Zn_0.60Co_0.40Fe₂O₄ sample is 353 K. Slight variation of T_c is observed depending on sintering condition. The initial permeability for the Zn_0.60Co_0.40Fe₂O₄ composition sintered at 1250 °C is found to be maximum.     

Structure and impedance spectroscopy of Pr1? x Sr x Fe0.8Co0.2O3? δ ( x =0.1, 0.2, 0.3) thin films grown by laser ablation

Polycrystalline samples of Pr_1−x Sr _x Fe_0.8Co_0.2 O_3−δ (x=0.1, 0.2, 0.3) (PSFC) were prepared by the combustion synthesis route at 1200°C. The structure of the polycrystalline powders was analysed with X-ray powder diffraction data. The X-ray diffraction (XRD) patterns were indexed as the orthoferrite similar to that of PrFeO₃ having a single-phase orthorhombic perovskite structure (Pbnm). Pr_1−x Sr _x Fe_0.8Co_0.2O_3−δ (x=0.1, 0.2, 0.3) films have been deposited on yttria-stabilized zirconia (YSZ) single-crystal substrates at 700°C by pulsed laser deposition (PLD) for application to thin film solid oxide fuel cell cathodes. The structure of the films was analysed by XRD, scanning electron microscopy (SEM) and atomic force microscopy (AFM). All films are polycrystalline with a marked texture and present pyramidal grains in the surface with different size distributions. Electrochemical impedance spectroscopy (EIS) measurements of PSFC/YSZ single crystal/PSFC test cells were conducted. The Pr_0.7Sr_0.3Fe_0.8Co_0.2O_3−δ film at 850°C presents a lower area specific resistance (ASR) value, 1.65 Ω cm², followed by the Pr_0.8Sr_0.2Fe_0.8Co_0.2O_3−δ (2.29 Ω cm² at 850°C) and the Pr_0.9Sr_0.1Fe_0.8Co_0.2O_3−δ films (5.45 Ω cm² at 850°C).     

Heat capacity and the magnetocaloric effect in Pr0.6Sr0.4Mn1–x Fe x O3 manganite

The heat capacity and the magnetocaloric effect of Pr_0.6Sr_0.4Mn_1–xFe_xO₃(x = 0 and 0.1) manganite have been studied in the temperature range 80–350 K and magnetic fields to 18 kOe. The magnetocaloric effect is estimated using two independent methods: the method of magnetic field modulation (direct method) and from the data on the heat capacity in magnetic field and without magnetic field (indirect method). The substitution of Fe atoms for Mn atoms (x = 0.1) shifts T _C by 167 K to lower temperatures; in this case, the magnetocaloric effect (MCE) is changed insignificantly in magnetic field 18 kOe with ΔS _M = 2.05 and 2.31 J/kg K for x = 0 and 0.10, respectively.