Temperature dependence of the intrinsic Faraday rotation of ErFeO3

The Faraday rotation of ErFeO₃ as a function of temperature was measured from ambient down to the spin reorientation region (90 to 100°K) at a wavelength of 6070 Å. The intrinsic Faraday rotation increases gradually with decreasing temperature and then drops rapidly to zero in the spin reorientation region. It is concluded that the contribution of the polarized Er³⁺ magnetic moments to the measured rotation is negligible and that the Faraday effect is due almost entirely to the magnetic moments of the Fe³⁺ ions.     

Anisotropic behaviour of the faraday rotation in erbium iron garnet

Faraday rotation (FR) measurements performed on single crystals Erbium Iron Garnet (ErIG) at 1.15 μm wavelength are presented in a magnetic field up to 20 kOe applied along the three main crystallographic directions. Spontaneous FR and FR susceptibilities are found to be anisotropic. The results are discussed in terms of electric and magnetic dipole transitions and compared to the magnetic anisotropy. A strong anisotropy of the first order electric dipole coefficient of the Er³⁺ ion is evidenced at low temperature (below 30 K).     

Magnetic properties of the mixed spinel Co1+xSnxFe2−2xO4

The structural and magnetic properties of the mixed spinel Co_1+xSn_xFe_2?2xO₄ system for 0.1≤x≤0.5 have been studied by means of X‐ray diffraction, magnetization, a.c. susceptibility and Mössbauer effect measurements. X‐ray intensity calculations indicate that Sn⁴⁺ ions occupy only octahedral (B) sites replacing Fe³⁺ ions and the added Co²⁺ ions substitute for A‐site Fe³⁺ ions. The lattice constants are determined and the applicability of Vegard's law has been tested. The Mössbauer spectra at 300 K have been fitted with two sextets in the ferrimagnetic state corresponding to Fe³⁺ at tetrahedral (A) and octahedral (B) sites for x≤0.4. The Mössbauer intensity data show that Sn possesses a preference for the B‐site of the spinel. As expected, the hyperfine field and Curie temperature determined from a.c. susceptibility decreases with increasing Sn content. The variation of the saturation magnetic moment per formula unit measured at 77 and 300 K with Sn content is satisfactorily explained on the basis of Néel's collinear spin ordering model for x=0.1–0.4.     

Contribution of Co3+ ions to the high-temperature magnetic and electrical properties of GdCoO3

The temperature dependence of the static magnetization of polycrystalline rare-earth cobaltite GdCoO₃ is measured in the temperature range 2?C800 K. The magnetic behaviors of GdCoO₃ and Gd³⁺ are found to be different at temperatures above room temperature, which is caused by the appearance of a contribution from Co³⁺ ions at high temperatures. The temperature dependence of the magnetic susceptibility of GdCoO₃ is determined by the magnetization of rare-earth gadolinium ions and the additional paramagnetic contribution induced by the thermally excited magnetic terms of Co³⁺ ions. The LDA + GTB method is used to calculate the electronic structure of GdCoO₃ in the temperature range 0?C300 K with allowance for strong electron correlations. The energy spectrum of GdCoO₃ is found to have intragap states that decrease the dielectric gap width with increasing temperature.     

Phenomenological analysis of the linear magnetic birefringence in dysprosium iron garnet

Experimental data on linear magnetic birefringence (LMB), previously reported at 1.15 μm wavelength in the 4.2-300 K temperature range and with an applied field up to 20 kOe, in dysprosium iron garnet (DyIG) are analyzed in terms of electric dipole transition within the three magnetic sublattices. Assuming that the garnet symmetry is cubic and that the contribution of the Fe³⁺ ions to LMB is the same as yttrium iron garnet (YIG), the 2nd order magneto-optical (MO) coefficient (Γ₂) of the Dy³⁺ ions is deduced. In the spontaneous state, Γ₂ is linear temperature dependent as previously found for the 1st order (MO) coefficient. It is shown that Γ₂ must be field dependent to explain the evolution of the LMB.     

THE INFLUENCE OF THE ADMIXING OF DIFFERENT MULTIPLETS ON THE SPIN MAGNETIC MOMENT AND FARADAY EFFECT OF HARE EARTH IONS IN GARNETS

The influence of the admixing of the excited multiplets of the ground configuration with the ground multiplet on the spin magnetic moment of the crystal- field-and exchange-interaction-split ground state, the Faraday rotation and the magneto-optic coefficient induced by the rare earth ions in rare-earth-substituted garnets Y_3-xR_xFe₅O₁₂ (R=Ce and Pr) has been calculated in this paper. It is found that, in the case of Ce³⁺ ions, the admixing of the 4f^{1 2}F_7/2 multiplet with the ²F_5/2 multiplet makes the spin magnetic moment of the crystal-field- and exchange-interaction-split ground state increase by 140% and the Faraday rotation increase by 180% at 633nm wavelength, and 150% at 1150nm at 294 K. In the case of Pr³⁺ ions, the admixing of the 4f^{2 3}H₅ multiplet with the ³H₄ multiplet makes the spin magnetic moment of the crystal-field- and exchange-interaction-split ground state increase by 34% and the Faraday rotation increase by 59% at 294K. The admixing of different multiplets of the Ce³⁺ ions makes the ratio between the magneto-optic coefficients at 50 and 294K increase by 7% at 633nm wavelength and 15% at 1150nm.     

Faraday effect in Tb3Ga5O12 in a rapidly increasing ultrastrong magnetic field

The Faraday effect is measured in paramagnetic terbium gallate garnet Tb₃Ga₅O₁₂ at a wavelength λ=0.63 μm at 6 K in pulsed magnetic fields up to 75 T increasing at a rate of 10⁷ T/s for field orientation along the crystallographic direction 〈110〉. The experimental data are compared with the results of theoretical calculations taking into account the crystal fields acting on the Tb³⁺ ion and various contributions to the Faraday rotation. Since the measurements in pulsed fields are carried out in the adiabatic regime, the dependence of the sample temperature on the magnetic field acting during a current pulse is obtained from the comparison of the experimental dependence of Faraday rotation with the theoretically calculated dependences of the Faraday effect under isothermal conditions at various temperatures. __________ Translated from Fizika Tverdogo Tela, Vol. 44, No. 11, 2002, pp. 2013–2017. Original Russian Text Copyright ? 2002 by Levitin, Zvezdin, Ortenberg, Platonov, Plis, Popov, Puhlmann, Tatsenko.     

Magnetization studies of TbFeO3

The spontaneous magnetization and principal magnetic susceptibilities of TbFeO₃ were measured from 4.2 to 300 K. The weak ferromagnetic moment is along the c crystallographic axis in the entire temperature range. The field dependence of the magnetization at 4.2 K was also studied. The magnetic behavior is interpreted in terms of an interaction between the ordered Fe³⁺ spin system and the electrons occupying the lowest lying “accidental” doublet of the Tb³⁺ ions. The FeTb interaction and the Tb³⁺ Van Vl eck susceptibility along the c axis play significant roles in determining the magnetic configuration of the Fe³⁺ spin system. No indication was found that the TbTb interaction plays a significant role in the magnetic behavior of TbFeO₃ at temperature above 4.2 K.     

顺磁物质CeF3磁光Faraday效应及其温度特性的量子理论

本文计算了顺磁物质CeF₃因Ce³⁺离子从基态能级4f至5d的电偶极跃迁产生的Fara-day旋转。讨论晶场对Ce⁺³离子4f和5d能级的影响,通过唯象地引入一个与磁化强度M成正比的“附加磁场”H_m=λM,由此获得4f离子在外加磁场和“附加磁场”的共同作用下的一级Zeeman分裂。经劈裂后的两个子能级上各自产生左、右圆偏振光激发的电偶极跃迁,导致磁光Faraday效应。对于波长为0.6328μm的入射光,在60—300 关键词：     

Localization of conduction electrons and the magnetic properties of the molecular metals β″-(BEDT-TTF)4NH4[M(C2O4)3] · DMF (M = Cr3+, Fe3+)

Quasi-two-dimensional organic metals β″-(BEDT-TTF)₄NH₄[M(C₂O₄)₃] · DMF containing the oxalate complexes of Cr³⁺ or Fe³⁺ ions between the conducting organic layers of the BEDT-TTF molecules are studied by EPR spectroscopy, and the contributions of these metallic complexes, conduction electrons, and non-equilibrium lattice defects to the magnetic susceptibility are determined. An analysis of the temperature dependence of the magnetic susceptibility and the EPR line shape has revealed partial localization of conduction electrons at T < 20 K in the crystals with Cr³⁺ ions. The size of the localization region is close to the size of an individual BEDT-TTF molecule. The localization effect weakens as nonequilibrium defects disappear during long-term storage at room temperature. The localization of conduction electrons is found to be accompanied by the appearance of weak antiferromagnetic interaction between the Cr³⁺ ions at T < 20 K, which disappears when Fe³⁺ ions substitute for Cr³⁺ ions.     

Spin glass-like phenomena in antiferromagnetic (Fe0.77Mg0.23)0.92O

An investigation on magnesiumwüstite, (Fe_0.77Mg_0.23)_0.92O, has been carried out using neutron diffraction and susceptibility measurements. The diffraction patterns obtained both at room and liquid helium temperature are similar to the ones found on wüstite (Fe_yO). Plots of the susceptibility vs. temperature in the temperature range 5–300 K show evidence of spin glass-like phenomena in the long range antiferromagnetic order with a freezing temperature of 76 K and Néel temperature of 128 K. It is postulated that a similar defect structure with the one found in wüstite could also be expected here, with Mg²⁺ and Fe²⁺ ions, and vacancies found on octahedral sites of an fcc lattice, and Fe³⁺ ions on tetrahedral sites. It is thought that both Mg²⁺ substitutional defects and Fe³⁺ interstitial defects could play a role in the formation of a spin glass.     

Synthesis and properties of barium ferrigermanate Ba<Subscript>2</Subscript>Fe<Subscript>2</Subscript>GeO<Subscript>7</Subscript>

The magnetic susceptibility and specific heat of single crystals of the Ba₂Fe₂GeO₇ barium ferrigermanate are investigated. It is revealed that the temperature dependence of the magnetic susceptibility exhibits a kink at a temperature T = 8.5 K. The number of nonequivalent positions of Fe³⁺ ions and their occupancies are determined using Mössbauer spectroscopy. It is shown that the Fe³⁺ ions located in tetrahedral positions T2 are ordered incompletely, which is inconsistent with the results obtained previously. An assumption is made regarding the possible ground magnetic state of the Ba₂Fe₂GeO₇ compound.     

Field-induced magnetic transition in a mixed rare-earth aluminum garnet Er<Subscript>2</Subscript>HoAl<Subscript>5</Subscript>O<Subscript>12</Subscript>

The temperature dependence of the ac magnetic susceptibility of a single-crystal mixed rare-earth garnet Er₂HoAl₅O₁₂ has been investigated within the range from 1.8 to 300 K in a zero constant field and in applied bias fields of up to 9 T. In the absence of a constant magnetic field the magnetic susceptibility followed the Curie–Weiss law. The application of a constant magnetic field caused a magnetic phase transition, the temperature of which increased with increasing magnetic field. The temperature of the maximum of the ac magnetic susceptibility, which is a characteristic of the phase transition, did not show a noticeable dependence on the frequency of the alternating magnetic field.     

Mössbauer study of iron sodium borosilicate glasses

Mössbauer effect and susceptibility measurements have been performed from 1.4 K up to 300 K on Na Borosilicate glasses with 4, 8, 12, 20% by weight of Fe₂O₃ content. Besides some small isolated paramagnetic Fe²⁺ species, two Fe³⁺ particle distributions coexist with some isolated Fe³⁺ ions. Attempts have been made to give a chart of the particle size distribution in all samples.     

Quantum theory of the magneto-optical effect induced by Ni ions in barium ferrites

To reveal the physical origin of the giant magneto-optical enhancement of Ni²⁺ ions in barium ferrite, quantitative calculations of the contributions of both the intra-ionic electric dipole transition between the 3d⁸ and 3d^{7 4p} configurations of the Ni²⁺ ions and the intra-ionic electric dipole transition induced by odd-parity crystal field terms are presented. It is deduced that the transition is important in the origin of the considered magneto-optical enhancement. The most important factor is the Ni-Fe superexchange interaction; since it is strong enough, the Faraday rotation produced by the Ni²⁺ ions is large though the energy difference between the 3d⁸ and 3 d7 4 p configurations is large. It is demonstrated that though the intra-ionic electric dipole transition does produce Faraday rotation peaks in the visible range, their magnitude is too small to explain the observed Faraday rotation. The effect of the spin-orbit interaction on the Faraday rotation is analysed. The spin-orbit interaction of the ground configuration plays a very important role in the occurrence of Faraday effects, but the Faraday rotation does not increase linearly with the strength of the spin-orbit coupling. On the contrary, the spin-orbit interaction of the excited configuration has almost no effect on the Faraday rotation. It is shown that the mixing of the different multiplets of the ground term induced by the crystal field has a great influence on the magneto-optical properties. Received 7 January 1998     

Radiative and non-radiative decays from the excited state of Ti3+ ions in oxide crystals

The fluorescence spectra of Ti³⁺ in Y₃Al₅O₁₂ (YAG), Al₂O₃ (sapphire), YAlO₃ (YAP) observed at 10 K are composed of zero-phonon lines accompanied by the broad vibronic sidebands. The temperature dependence of the fluorescence lifetime and of the total intensity of the broadband measured in YAG and Al₂O₃ indicate that the radiative decay times from the excited states are nearly constant in the range 10–300 K. This demonstrates that the broadband radiative emissions in Ti³⁺:YAG and Ti³⁺:Al₂O₃ are due to magnetic dipole transitions or to electric dipole transitions induced by static odd-parity distortion, respectively. The decrease of the fluorescence lifetime with increasing temperature in Ti³⁺:YAG and Ti³⁺:Al₂O₃ is due to non-radiative decay from the excited state which occurs through phonon-assisted tunnelling between the excited and ground states. The radiative decay of Ti³⁺:YAP is enhanced with increasing temperature, indicating that radiative decay rate contains a term associated with odd-parity phonons. Nevertheless, a non-radiative decay rate of 3.6 × 10⁴ s^–1 observed in the temperature range 10–300 K is due to excited state absorption, which depopulates the excited state and quenches the fluorescence at the laser wavelength.     

Growth and characterization of cerium-substituted yttrium iron garnet single crystals for magneto-optical applications

This paper is concerned with the preparation and characterization of cerium-substituted yttrium iron garnets, which are known to be oxides having a large Faraday rotation effect. Using the improved flux method we successfully grew bulk single crystals of iron garnet doped with Ce³⁺ ions with maximum substitutions up to 0.349. Here we investigate different solution compositions for maximum Ce³⁺ substitution. The Faraday rotation and optical absorption spectra were measured in the near infrared region for different Ce³⁺ ion substituted iron garnets. The specific Faraday rotation of Ce_0.349Eu_0.195Y_2.456Fe₅O₁₂ was found to be 1430 deg/cm at a wavelength of 780 nm and –1280 deg/cm at 1150 nm. The Ce substitution prominently enhances the Faraday rotation effect, and Yb³⁺ and Eu³⁺ ions substituted for Y³⁺ in the dodecahedral sites of YIG can increase the concentration of Ce³⁺ ions, depressing the formation of nonmagnetic Ce⁴⁺ ions by charge compensation. Received: 24 January 2001 / Accepted: 2 March 2001 / Published online: 27 June 2001     

Quantum theory of the magneto-optical effect and magnetization of Nd-substituted yttrium iron garnet

The magneto-optical and magnetic properties of Nd ³⁺ ions in Y ₃Fe ₅O ₁₂ garnet are analyzed by using quantum theory. In the spontaneous state, the magneto-optical effects originate mainly from the intra-ionic electric dipole transitions between the 4 f ³ and 4 f ²5d states split by the spin-orbit, crystal field, and superexchange interactions. For the excited configuration, the coupling scheme of Yanase is extended to the Nd ³⁺ ion. The magneto-optical resonance frequencies are mainly determined by the splitting of the 5d states induced by the crystal field. The theoretical results of both Nd magnetization and Faraday rotation are in good agreement with experiments. The observed Faraday rotation is proved to be of the paramagnetic type. Although the value of the magneto-optical resonance frequency derived from a macroscopic analysis is approximately confirmed by our theoretical study, a new assignment about the transitions associated with this resonance is unambiguously determined. The spin-orbit coupling of the ground configuration has a great influence on both the Faraday rotation and magnetization, but, unlike the theoretical results obtained in some metals and alloys, the relation between the Faraday rotation and the spin-orbit coupling strength is more complex than a linear one. The magnitude of the magneto-optical coefficient increases as the spin-orbit interaction strength of the ground configuration decreases when the strength is not very weak. Finally, the temperature dependence of the magneto-optical coefficient and the effect of the mixing of different ground-term multiplets induced by the crystal field are analyzed. Received 8 November 2000     

Properties of clinopyroxene LiFeGe2O6

The polycrystalline compound LiFeGe₂O₆ has been synthesized by the solid-phase reaction. The X-ray diffraction, Mössbauer, calorimetric, and magnetic investigations have been carried out. The Mössbauer spectrum at 300 K represents a single quadrupole doublet. The isomer shift with respect to the metal iron α-Fe is 0.40 mm/s, which is characteristic of the Fe³⁺ high-spin ion in the octahedral coordination. The quadrupole splitting of 0.42 mm/s indicates a distortion of the oxygen octahedron around the iron cation. The results of the measurement of the temperature dependence of the heat capacity in the range 2–300 K have shown the presence of the only anomaly with a maximum at T _m ～ 20.5 K, which indicates the occurrence of a magnetic phase transition in this point. The data of the measurement of the temperature dependence of the magnetization have confirmed that the magnetic order with the dominant antiferromagnetic interaction of magnetically active ions exists in LiFeGe₂O₆ at a temperature below 20.5 K. The investigation of the temperature dependence of the heat capacity in the magnetic field H up to 9 T has demonstrated that the external factor insignificantly changes the order-disorder transition point (at H = 9 T, there occurs a shift of ～0.5 K toward the low-temperature range).

     

Magnetic,electrical transport and electron spin resonance studies of Fe-doped manganite LaMn0.7Fe0.3O3+δ

We have investigated the magnetic, electrical transport and electron spin resonance (ESR) properties of polycrystalline Fe-doped manganite LaMn_0.7Fe_0.3O_3+δ prepared by sol–gel method. A typical cluster-glass feature is presented by DC magnetization and AC susceptibility measurements and a sharp but shallow memory effect was observed. Symmetrical Lorentzian lines of the Mn/Fe spectra were detected above 120 K, where the sample is a paramagnetic (PM) insulator. When the temperature decreases from 120 K, magnetic clusters contributed from ferromagnetic (FM) interaction between Mn³⁺ and Mn³⁺/Fe³⁺ ions develop and coexist with PM phase. At lower temperature, these FM clusters compete with antiferromagnetic (AFM) ones between Fe³⁺ ions, which are associated with a distinct field-cooled (FC) effect in characteristic of cluster-glass state.