Helical magnetic structure in a quasi-one-dimensional LiCu<Subscript>2</Subscript>O<Subscript>2</Subscript> multiferroic crystal according to <Superscript>63,65</Superscript>Cu NMR studies

The NMR spectra of ⁶³Cu and ⁶⁵Cu natural copper isotopes in a LiCu₂O₂ multiferroic single crystal compound have been measured above and below the temperature of magnetic phase transition (T _c = 23 K) in zero magnetic field and in applied magnetic field H ₀ = 94 kOe parallel to the c axis of the crystal. In LiCu₂O₂ below T _c, a complicated helical magnetic structure with the magnetic moment of copper ions Cu²⁺ varying along the chain according to the harmonic law with the wave vector being incommensurate to the crystal lattice constants has been revealed. The experimental results have been successfully interpreted using the model based on the planar helical magnetic structure. It has been found that the plane of rotation for Cu²⁺ magnetic moments in LiCu₂O₂ does not coincide at H ₀ = 0 with the ab plane. The high magnetic field (H ₀ = 94 kOe) applied along the c axis of the single crystal does not affect the spatial orientation of the plane of rotation.     

Magnetic and ferroelectric properties of exchange-frustrated multiferroics (Ni1 ? xTx)3V2O8 (T = Co, Mn, Zn)

The effect of the substitution of Co²⁺, Mn²⁺, and Zn²⁺ ions for Ni²⁺ ions on the magnetic, dielectric, and ferroelectric properties of vanadate single crystals (Ni_{1 − x} T _x )₃V₂O₈ has been analyzed. It has been found that the low-level (x ≤ 0.1) substitution of both magnetic and nonmagnetic ions stabilizes the ferroelectric state with a cycloidal magnetic structure. The existence region of this state is expanded to low temperatures down to 3 K for Zn²⁺ and below 1.8 K for Co²⁺ and Mn²⁺ owing to the suppression of a low-temperature weak ferromagnetic phase. At the same time, the ferroelectric phase disappears completely at large concentrations of Co and Mn. The effect of magnetic fields on the magnetic and ferroelectric states has been analyzed. It has been shown that the magnetic field along the c axis suppresses the ferroelectric state, whereas the magnetization along the antiferromagnetism axis (a axis) induces the reentrant phase transition from a paraelectric weak ferromagnetic structure to a ferroelectric structure. The corresponding H-T phase diagrams have been drawn.     

NMR-ON measurements of123, 124, 131I in nickel

The magnetic hyperfine splitting frequencies of¹²³INi,¹²⁴INi and¹³¹INi in a zero external magnetic field have been determined by the NMR-ON method as 258.9(1), 165.9(1) and 179.5(2) MHz, respectively. With the known values of the magnetic moments, the magnetic hyperfine fields have been deduced:B _HF(¹²³INi)=30.17(5) T,B _HF(¹²⁴INi)=30.14(9) T,B _HF(¹³¹INi)=30.06(4) T; the weighted average isB _HF(INi)=30.11(4) T. The small difference of theB _HF(¹³¹INi) with those of¹²³INi and¹²⁴INi is discussed comparing with results of the hyperfine splitting frequency of iodine in iron host.     

Investigation of the impurity hyperfine field polarization in polycrystalline Rare Earth ferromagnets

Time differential perturbed angular correlation spectra of¹¹¹Cd in ferromagnetic polycrystalline Dy have been measured at 4.2 K in external magnetic fields up to 60 kG. The experimental data were well reproduced by a calculation which assumed that the angular distribution of the magnetic hyperfine fields is identical to that of the magnetic moments of the 4f-shells. The distribution of the 4f-moments was derived from magnetic anisotropy data. The results of this work seem to justify the application of the integral perturbed angular correlation technique for the determination of magnetic hyperfine fields in incompletely polarized ferromagnetic samples. The magnetic hyperfine fields of¹⁷⁷Hf:Gd and¹⁷⁷Hf:Dy have been measured by this method as:H _hf(Hf:Gd)=–375(60)kG andH _hf(Hf:Dy)=–225(45)kG.     

Mössbauer Studies of Dilute 119Sn and 57Fe in SrRuO3 and Sr2FeRuO6

Nuclear magnetic resonance on oriented ¹⁷⁵Hf in iron host has been measured. Samples of ¹⁷⁵HfFe were made by recoil implantation of the precursor ¹⁷⁵Ta isotope. The resonance frequency and the resonance line width have been determined to be 139.0 (1) MHz and FWHM = 2.7 (2) MHz, respectively, in an external magnetic field of 0.1 T. The resonance width was very narrow compared with the previously reported value of 11.0 (1.1) MHz. With the known value of the magnetic moment of μ(¹⁷⁵Hf) = −0.62 (3) μ_N, the hyperfine field has been deduced as B _HF = −73.6 (3.5) T.     

Nuclear magnetic resonance on oriented76,77,82Br in Fe

Nuclear magnetic resonance on oriented^76,77,82BrFe has been measured using recoil-implanted samples. The magnetic hyperfine splitting frequency of⁸²BrFe in a zero external magnetic field has been determined to be 201.90(3) MHz. The resonances of⁷⁶BrFe and⁷⁷BrFe were also observed in an external magnetic field of 0.2 T asv(⁷⁶BrFe)=340.9(3) MHz andv(⁷⁷BrFe)=403.5(2) MHz. With the known values of theg-factors, the hyperfine fields have been deduced:B _HF(⁸²BrFe)=81.397(27) T,B _HF(⁷⁶BrFe)=81.38(7) T. Theg-factor of⁷⁷Br was determined to be |0.6487(4)|.     

Magnetic Moment of the 3/2− Ground State of 185W

Nuclear magnetic resonance measurement have been performed for ¹⁸⁵W oriented at 8 mK in an Fe host. The magnetic hyperfine splitting frequency at an external magnetic field of 0.1 T was determined to be 196.6(2) MHz. With the known hyperfine field of B _hf = −71.4(18) T, the nuclear magnetic moment of ¹⁸⁵W is deduced as μ(¹⁸⁵W) = +0.543(14) μ_N.     

Influence of magnetic ordering on electronic structure of Tb<Superscript>3+</Superscript> ion in TbFe<Subscript>3</Subscript>(BO<Subscript>3</Subscript>)<Subscript>4</Subscript> crystal

Optical absorption spectra of trigonal crystal TbFe₃(BO₃)₄ have been studied in the region of ⁷F₆ → ⁵D₄ transition in Tb³⁺ ion depending on temperature (2–220 K) and on magnetic field (0–60 kOe). Splitting of the Tb³⁺ excited states, both under the influence of the external magnetic field and effective exchange field of the Fe-sublattice, have been determined. Landé factors of the excited states have been found. Stepwise splitting of one of the absorption lines has been discovered in the region of the Fe-sublattice magnetic ordering temperature. This is shown to be due to the abrupt change of equilibrium geometry of the local Tb³⁺ ion environment only in the excited state of the Tb³⁺ ion. In general, the magnetic ordering is accompanied by temperature variations of the Tb³⁺ local environment in the excited states. The crystal field splitting components have been identified. In particular, it has been shown that the ground state (in D ₃ symmetry approximation) consists of two close singlet states of A ₁ and A ₂ type, which are split and magnetized by effective exchange field of the Fe-sublattice. Orientations of magnetic moments of the excited electronic states relative to that of the ground state have been experimentally determined in the magnetically ordered state of the crystal. A pronounced shift of one of absorption lines has been observed in the vicinity of the TbFe₃(BO₃)₄ structural phase transition. The temperature interval of coexistence of the phases is about 3 K.     

Magnetically stabilized electron-hole liquid in indium antimonide

Luminescence spectra of sufficiently pure n-type indium antimonide crystals (N _D−N _A=(1–22)·10¹⁴ cm⁻³) in a magnetic field of up to 56 kOe, at temperatures of 1.8–2 K, and high optical pumping densities (more than 100 W/cm²) have been studied. More evidence of the existence of electron-hole liquid stabilized by magnetic field has been obtained, and its basic thermodynamic parameters as functions of magnetic field have been measured. When the magnetic field increases from 23 to 55.2 kOe, the liquid density increases from 3.2·10¹⁵ to 6.7·10¹⁵ cm⁻³, the binding energy per electron-hole pair rises from 3.0 to 5.2 meV, and the binding energy with respect to the ground exciton level (work function of an exciton in the liquid) rises from 0.43 to 1.2 meV. Zh. éksp. Teor. Fiz. 111, 737–758 (February 1997)     

Microstructural and magnetic properties of Ax:Zn1-xO (A=Mn,Gd and Mn/Gd) nanocrystals

We report the microstructural and magnetic properties of transition (3d) and rare earth (4f) metal substituted into the A_x:Zn_1?xO (A=Mn, Gd and Mn/Gd) nanocrystal samples synthesized by solgel method. The structural properties and morphology of all samples have been analysed using X-ray diffraction (XRD) method and scanning electron microscopy. The impurity phase in the XRD patterns for all samples is not seen, except (Mn/Gd):ZnO sample where a very weak secondary phase of Gd₂O₃ is observed. Due to the large mismatch of the ionic radii between Mn²⁺ and Gd³⁺ ions, the strain inside the matrix increases, unlike the crystallite size decreases with the substitution of Mn and Gd into ZnO system. A couple of additional vibration modes due to the dopant have been observed in Raman spectrum. The magnetic properties have been studied by vibrating sample magnetometer. The magnetic hysteresis shows that Mn:ZnO and Gd:ZnO have soft ferromagnetic (FM) behaviour, whereas (Mn/Gd):ZnO has strong FM behaviour at room temperature (RT). The enhancement of ferromagnetism (FM) in (Mn/Gd):ZnO sample might be related to short-range FM coupling between Mn²⁺ and Gd³⁺ ions via defects potential and/or strain-induced FM coupling due to the expansion lattice by doping. The experimental results indicate that RTFM can be achieved by co-substitution of 3d and 4f metals in ZnO which can be used in spintronics applications.     

Singlet—triplet oscillations of spin-correlated radical pairs due to the Larmor precession in low magnetic fields

Singlet—triplet oscillations in spin-correlated radical pairs have been studied at magnetic field strengths low for one radical and high for the other. Oscillations with frequencies close to the Larmor frequency ω₀ of electron spin precession have been predicted under these conditions. Both numerical and exact analytical solutions in arbitrary magnetic fields are presented for three cases of hyperfine couplings in wide-spectrum radical. For the case of unresolved spectrum, singlet—triplet evolution was found to contain a single oscillating term with frequency ω₀. In the case of one spin-I magnetic nucleus, there are two low frequency oscillating terms with frequencies ω_? = ω₀ ? ω₀/(2I + 1) and ω₊ = ω₀ + ω₀/(2I + 1), the amplitude of the first term being larger than that of the second. The case of a number of equivalent protons also has been analysed as a superposition of one-nucleus oscillations. The predicted oscillations were observed in a time resolved magnetic field effect for several radical ion pairs produced by X-ray irradiation of alkane solutions with charge acceptors. For pairs (p-terphenyl-d ₁₄)^?./(isooctane)^+. and (p-terphenyl-d ₁₄)^?./(2,4-dimethylpentane)^+. the oscillation frequency in a field B ₀ of 0.5–4mT is about 20% lower than ω₀. Oscillations were observed also in pairs with equivalent nuclei: (p-terphenyl-d ₁₄)^+./(C₆F₆)^?. and (p-terphenyl-d ₁₄)^?./(hexamethylethane)^+.     

Isotope effect in charge transport of LuB12

The galvanomagnetic properties of single-crystal samples with various isotopic boron compositions have been investigated for the first time for the normal state of superconductor LuB₁₂ (T c ≈ 0.44 K). Precision measurements of the resistivity, Hall coefficient, and magnetic susceptibility have been performed over a wide temperature range of 2–300 K in magnetic fields up to 80 kOe. A change of the charge transport regime in this nonmagnetic compound with metallic conduction is shown to occur near T* ≈ 50−70 K. As a result, a sharp peak with significantly different amplitudes for Lu¹⁰B₁₂ and Lu¹¹B₁₂ is recorded in the temperature dependences of the Hall coefficient R _H(T) near T*. A significant (about 10%) difference (in absolute value) of the Hall coefficients R _H for the Lu¹⁰B₁₂ and Lu¹¹B₁₂ compounds at helium and intermediate temperatures has been found and the patterns of behavior of the dependence R _H(H) for T < T* in an external magnetic field H ≤ 80 kOe for Lu¹⁰B₁₂ and Lu¹¹B₁₂ are shown to differ significantly. Analysis of the Curie-Weiss contribution to the magnetic susceptibility χ(T) leads to the conclusion about the formation of magnetic moments μ_eff ≈ (0.13−0.19)μ_B in each unit cell of the fcc structure of LuB₁₂ compounds with various isotopic compositions. The possibility of the realization of an electronic topological 2.5-order transition near T* and the influence of correlation effects in the 5d-band on the formation of a spin polarization near the rare-earth ions in LuB₁₂ is discussed.     

Crystal field effects on the saturation magnetic moment of Sm3+ ion in ferronagnetic samarium compounds

The effects of cubic crystal fields on the saturation magnetic moment of Sm³⁺ ion in ferromagnetic compounds have been investigated. In samarium compounds with magnetic elements, the exchange fieldH _ex acting on Sm³⁺ ion is taken to be proportional to the sublattice magnetization of the magnetic element, while in compounds with nonmagnetic elementsH _ex is taken to be proportional to the spin average of the Sm³⁺ ion and is determined self-consistently. In both types of compoundsH _ex is assumed to be along [001] direction. The saturation magnetic moment is calculated by taking into account the admixture of excited (J=7/2 andJ=9/2) levels into the ground (J=5/2) level of Sm³⁺ ion by crystal fields and exchange fields. It is shown that depending upon the strength, the crystal fields quench or enhance the magnetic moment from the free ion value, and in some cases force Sm³⁺ ion to behave effectively like an (L+S) ion rather than an (L−S)ion. The crystal fields may have important bearing on the performance of samarium compounds as permanent magnet materials.     

Weak-field magnetoresistance anomaly and Shubnikov–de Haas oscillations in Sn-doped InSb thin films on GaAs (100) substrates

Distinctive magnetoresistance (MR) effects in weak magnetic fields before the appearance of Shubnikov–de Haas (SdH) oscillations at low temperatures in Sn-doped (7×10¹⁶ cm⁻³) InSb films grown on GaAs(100) substrates by MBE have been investigated with decreasing film thickness d from 1 μm. The negative MR found in weak magnetic fields for d0.5 μm can be broadly divided into two regimes: T-sensitive negative MR below B_c observed with anisotropy between parallel and perpendicular magnetic field and a T-insensitive parabolic one above B_c observable only under in-plane magnetic fields. The latter is ascribable to the skipping orbit effect due to surface boundary scattering. In vanishing magnetic fields far below B_c, the negative MR reduces with decreasing d and the different positive MR overlaps with it below 0.5 μm, eventually dominating the positive MR at d0.2 μm. These results have been analyzed using a two-layer model for the films, where the composition of the upper layer under the surface and the lower one adjacent to the InSb/GaAs interface is assumed. The MR data in the extremely weak magnetic fields below 100 G for each layer have been successfully fitted to the two-dimensional (2D) weak localization (WL) theory. These results explain that the crossover from the 2D WL to the weak anti-localization (WAL) occurs when the interface is approached with the increase of SO interaction in the layers caused by the increased influence of the asymmetric potential at the hetero interface (Rashba term) and the SO rate in the intrinsic InSb film due to the crystal field of the zinc-blende structure (Dresselhaus term) is as small as τ_so⁻¹3×10⁸ s⁻¹.     

FMR and TEM Studies of Co and Ni Nanoparticles Implanted in the SiO<Subscript>2</Subscript> Matrix

Fused silica plates have been implanted with 40 keV Co⁺ or Ni⁺ ions to high doses in the range of (0.25–1.0) × 10¹⁷ ions/cm², and magnetic properties of the implanted samples have been studied with ferromagnetic resonance (FMR) technique supplemented by transmission electron microscopy, electron diffraction and energy dispersive X-ray spectroscopy. The high-dose implantation with 3d-ions results in the formation of cobalt and nickel metal nanoparticles in the irradiated subsurface layer of the SiO₂ matrix. Co and Ni nanocrystals with hexagonal close packing and face-centered cubic structures have a spherical shape and the sizes of 4–5 nm (for cobalt) and 6–14 nm (for nickel) in diameter. Room-temperature FMR signals from ensembles of Co and Ni nanoparticles implanted in the SiO₂ matrix exhibit an out-of-plane uniaxial magnetic anisotropy that is typical for thin magnetic films. The dose and temperature dependences of FMR spectra have been analyzed using the Kittel formalism, and the effective magnetization and g-factor values have been obtained for Co- and Ni-implanted samples. Nonsymmetric FMR line shapes have been fitted by a sum of two symmetrical curves. The dependences of the magnetic parameters of each curve on the implantation dose and temperature are presented.     

139La and63Cu-NQR of high-T c oxide superconductors

Nuclear quadrupole resonances (NQR) of¹³⁹La in La_2−xM_xCuO₄ (M=Ba, Sr) and⁶³Cu in YBa₂CU₃O₇ have been investigated with substitution of Cu by magnetic impurities. For La-system, the strong enhancement of the nuclear relaxation rate, 1/T ₁ atT _c ^*≈10 K (suggesting the occurrence of magnetic instability with hole-doping), is suppressed by 3D-antiferromagnetism induced by magnetic impurities. In the superconducting region, fluctuations of Cu moments at low temperatures remain extremely fast as at high temperatures. For Y-system, Fe-ions are substituted for both Cu(1) and Cu(2) sites, But Co-ions are preferentially substituted to Cu1 sites. The peaks in the relaxation rate of Cu indicate the appearance of magnetic ordering without destroying superconductivity for the 0.5%-Fe doped sample.     

Electronic topological transition in an <Emphasis Type="Italic">n</Emphasis>-BiSb semiconductor alloy in the quantum limit range of magnetic fields for H‖<Emphasis Type="Italic">C</Emphasis><Subscript>2</Subscript>

The galvanomagnetic properties of single-crystal samples of the Bi_0.93Sb_0.07 semiconductor alloy with the electron density n = 1.6 × 10¹⁷ cm⁻³ in magnetic fields up to 14 T at T = 1.6 K have been investigated. The resistivity ρ and Hall coefficient R have been measured as functions of the magnetic field directed along the binary axis of a crystal for a current flowing through a sample along the bisector axis; i.e., the components ρ₂₂ and R _{32, 1} have been measured. The strong anisotropy of the electron spectrum of the samples makes it possible to separately observe quantum oscillations of the magnetoresistance ρ₂₂(H) for H ‖ C ₂ in low magnetic fields for two equivalent ellipsoids with small extremal cross sections (secondary ellipsoids) and in high magnetic fields for electrons of the ellipsoid with a large extremal cross section (main ellipsoid). An increase in the energy of the electrons of secondary ellipsoids in the quantum limit magnetic fields is accompanied by the flow of electrons to the main ellipsoid; i.e., an electronic topological transition occurs from the three-valley electron spectrum to the single-valley one. After the flow stops, the Fermi energy E _F increases from 18 meV to 27.8 meV. With an increase in the quantizing magnetic field, the Fermi energy of the electrons decreases both in the region of quantum oscillations of the resistance that are attributed to the electrons of the secondary ellipsoids and in the region of oscillations associated with the electrons of the main ellipsoid. The Hall coefficient R _{32, 1} decreases in high magnetic fields; this behavior indicates the absence of the electron magnetic freezing effect.     

Role of Er<Superscript>3+</Superscript> ion in the formation of the ErFeO<Subscript>3</Subscript> magnetic properties in the region of spin-reorientation phase transition

The 90° reorientation of Er³⁺ spins in ErFeO₃ have been directly observed using optical spectroscopy. The peculiarities of the absorption spectrum of ErFeO₃ in the region of the ⁴ I _15/2 → ⁴ F _9/2 transition of the Er³⁺ ion in the temperature range of ac-spin reorientation have been studied. It is shown that the spin reorientation phase transition (SRPT) is accompanied by splitting of the ground and excited states into Kramers doublets in the iron exchange field. This fact is a direct evidence of purely magnetic origin of SRPT. The experimental results were used to analyze the magnetic properties of ErFeO₃. This analysis showed that the order of magnitude of the magnetic moment, its variation in the SRPT region, and the existence of T _comp can be interpreted in terms of the single-ion model, taking into account the influence of the crystal field and the molecular field produced by the iron subsystem ions.     

Magnetization measurements on some rare-earth iron garnets

The magnetic properties of Fe-based singlecrystal garnets have been studied. A magnetic field up to 55 kOe in the temperature range from 4.5 to 300 K has been used. The compensation temperature (T _comp) of the studied garnets has been determined. The compensation temperature increases with the increase of the rare-earth ions (Ho³⁺ or Gd³⁺) substituting Y³⁺ ions in thec sublattice of R₃Fe₅O₁₂. AboveT _comp, the magnetization was found to be linearly field dependent. The results are in good agreement with magnetization measurements performed on polycrystaline samples, and with calculations based on the crystal field parameters of the isostructural Holmium Gallium Garnet (HoGG).     

Study of the NMR spectra of hydrogen isotopic analogs and estimation of the magnetic moment of the triton

Nuclear magnetic resonance spectra of the hydrogen isotopic analogs TH and TD on the triton resonance and HT, HD, and H₂ on the proton resonance in the gas phase have been studied. The triton and proton spectra from a single sample have been recorded simultaneously by using the inductivity of a common receiver LC circuit. The energies of the interaction between the magnetic moments of the nuclei of the hydrogen isotopic analogs have been determined: J _tp = 299.3(1) Hz, J _td = 45.5(1) Hz, and J _pd = 43.3(1) Hz. The ratio of the resonance frequencies of the HT molecule nuclei: F _t (TH)/F _p (HT) = 1.066693898(2), which is equal to the ratio of the magnetic moments of the nuclei in the bound state, has been obtained. If the value Δσ(TH) = 2.04 × 10⁻⁸ calculated previously is used for the difference in the screening of nuclei in the HT molecule, then the ratio of the magnetic moment of the triton to the magnetic moment of the proton is μ _t /μ _p = 1.066693920(2), where the statistical standard deviation of the data is given in the parentheses in the units of the last digit.