Effect of intercalation by silver on the charge-density-wave state in TiSe2

The temperature dependence of electrical conductivity σ (77–300 K) and magnetic susceptibility χ (2–300 K) of Ag_xTiSe₂ in the Ag_1/4TiSe₂ phase has been studied in order to determine the possibility of preserving the charge-density-wave state in silver-intercalated TiSe₂. The behavior of χ and σ in this phase is compared with that of the starting compound TiSe₂. Fiz. Tverd. Tela (St. Petersburg) 40, 2165–2167 (December 1998)     

Frozen magnetic states in quasi-two-dimensional Cr1/3−x NixTaS2 compounds with competing exchange interactions

A study of the dynamic and static magnetic susceptibility of quasi-two-dimensional, doubly intercalated compounds Cr_1/3−x Ni_xTaS₂ (0.08⩽x⩽0.23) is reported. It is shown that cooling from paramagnetic phase in this concentration range produces a spin-glass-type frozen magnetic state. In contrast to the classical 3D spin glasses, however, this state sets in within a broad temperature range rather than at a phase transition. A magnetic phase diagram of the studied compounds has been constructed. Fiz. Tverd. Tela (St. Petersburg) 39, 1801–1805 (October 1997)     

Phase transitions and magnetic-transport phenomena in the system La2/3Ba1/3(Mn1−x Cox)O3

A study is performed of the crystalline structure, magnetization, and magnetotransport properties of the system La_2/3Ba_1/3(Mn_1−x Co_x)O₃ with perovskite structure. It is shown that cubic solid solutions exist over the entire range of cobalt concentrations 0⩽x⩽1. Compositions with x⩽0.2 are ferromagnets with maximum resistance near T _C . Compositions with 0.2<x<0.4 manifest properties of inhomogeneous ferromagnets. Measurements of magnetic properties indicate the absence of long-range magnetic order in compositions with 0.5⩽x⩽0.9, which are probably spin glasses. The spontaneous magnetization of cobaltate (2μ _B per formula unit) corresponds to ferromagnetic ordering of the moments of the Co³⁺ and Co⁴⁺ ions found in the intermediate spin state. It is conjectured that the magnetoresistance consists of an extrinsic and an intrinsic contribution. The first arises as a result of intergrain transport of spin-polarized charge carriers, and the second, as a result of magnetic ordering near T _C . The magnetoresistance is essentially independent of the spontaneous magnetization and decreases abruptly as the cobalt concentration is increased with a corresponding transition from long-range to short-range magnetic order. Zh. éksp. Teor. Fiz. 116, 604–610 (August 1999)     

Influence of structural deformations on the magnetic properties of Jahn-Teller complexes of divalent copper in CaxSr1−x F2 mixed crystals

Crystals of variable constituency Ca_xSr_1−x F₂:Cu (0⩽x⩽0.05, x≅0.5, 1.0⩾x⩾0.95) are investigated by EPR and x-ray structural analysis. The electron-Zeeman, intrinsic hyperfine, and ligand hyperfine interaction parameters are determined; they characterize the magnetic properties of the copper paramagnetic complexes formed in the crystals. Models of the molecular structures of these complexes are discussed, along with the influence of structural deformations and vibronic interactions on their magnetic properties. Fiz. Tverd. Tela (St. Petersburg) 40, 445–451 (March 1998)     

X-ray,electrical conductivity,magnetic and infrared studies of the system Co2−x Ge1−x Fe2x O4

X-ray, electrical conductivity, magnetic hysteresis and IR studies for the system Co_2−x Ge_1−x Fe_2x O₄ were carried out. All the compounds, 0⩽x⩽1, showed cubic symmetry. X-ray intensity calculations, magnetic hysteresis measurements and IR studies indicated the presence of Ge⁴⁺ at tetrahedral, Co²⁺ at octahedral and Fe³⁺ at both the sites. The activation energy and threshold frequency decreased with increasing value ofx. The compounds withx⩽0.5 arep-type and those withx⩾0.75 aren-type semiconductors. Magnetic hysteresis indicated that all the compounds are ferrimagnetic except forx=0 which is antiferromagnetic. The shapes of χ/χ _i vsT plots, highH _c values andJ _R/J_s ratios showed that all the compounds exceptx=0 exhibit single-domain behaviour. Curie temperature,T _c increased with increasing Fe³⁺ ions. The probable ionic configuration for the system is suggested as Ge _1−x ⁴⁺ Fe _x ³⁺ [co _2−x ²⁺ Fe _x ³⁺ ]O ₄ ²⁻ .     

Atomic structure and transport and magnetic properties of the Sm1−x SrxMnO3 system

This is the first study of the temperature dependences of the atomic structure by neutron diffraction, as well as of the resistivity, differential magnetic susceptibility, and magnetoresistance of the ceramic system ¹⁵⁴Sm_1−x Sr_xMnO₃ (x∼0.16–0.4). Samples (x⩾0.3) having an initially orthorhombic structure transfer upon cooling from the insulating to the metallic state and exhibit giant magnetoresistance, which at liquid-helium temperature reaches as high as 90% in magnetic fields up to 30 kOe. At lower doping levels (x⩽0.25), the compound has monoclinic structure. The resistivity of such compounds in zero magnetic field displays insulating behavior upon lowering the temperature to 77 K. Fiz. Tverd. Tela (St. Petersburg) 40, 1271–1276 (July 1998)     

Characteristics of magnetic order in perovskite manganites La1−x CaxMnO3

Solid solutions of the system La_1−x Ca_xMnO₃ are synthesized, and their magnetic and electrical properties are investigated. As x is increased, the crystal lattice changes symmetrically from an orthorhombic (x=0 and x=0.8) to a cubic structure (0<x⩽0.6 and x=1). Nonstoichiometric LaMnO₃ and compositions with a low Ca content (0<x<0.4) are collinear ferromagnets. A metal-insulator transition is observed in them near the Curie temperature. Compositions with 0.6⩽x⩽0.9 exhibit a semiconductor-type conductivity and an unusual temperature behavior of the magnetization and the susceptibility with very distinct Curie and Néel temperatures. The magnetic properties of the solid solutions are explained on the basis of the model of ferro-antiferromagnetic phase separation. Zh. éksp. Teor. Fiz. 116, 1664–1675 (November 1999)     

Magnetic properties of LaNi <Emphasis Type="Bold">1-</Emphasis><Emphasis Type="Bold">x</Emphasis>Mn <Emphasis Type="Bold">x</Emphasis>O <Emphasis Type="Bold">3+δ</Emphasis> perovskites

Magnetic measurements have been carried out in different LaNi_1-xMn_xO _{3 + δ} samples with 0.1 ⩽ x ⩽ 0.9. All these samples show two magnetic anomalies, one at relatively high temperature characteristic of a ferromagnetic ordering and the other at low temperature, typical of magnetic relaxation phenomena. Neutron diffraction patterns indicate that long-range ferromagnetic ordering is only achieved for x ≥ 0.5. Neutron patterns of LaNi_0.5Mn_0.5O _{3 + δ} samples show an ordered arrangement of Ni and Mn atoms in the perovskite lattice. LaNi_0.5Mn_0.5O _{3 + δ} is then, a double perovskite A₂BB'O₆ whereas Ni and Mn atoms are randomly distributed for the rest of the samples. X-ray magnetic circular dichroism experiments confirm the presence of collinear ferromagnetism in LaNi_0.5Mn_0.5O _{3 + δ} . The role of competitive magnetic interactions, structural disorder, magnetic anisotropy and magnetic disaccommodation is also discussed Received 19 July 2002 / Received in final form 23 October 2002 Published online 31 December 2002     

Structural and magnetic characterisation of the perovskite oxides La0.7Ca0.3−x Na x MnO3

X-ray powder diffraction (XRD) and magnetic measurements were performed in order to investigate the effect of Na⁺ ion substitution for Ca²⁺ ions on the crystallographic structure, the character of magnetic ordering, and the effect of transition temperature in La_0.7Ca_0.3−x Na _x MnO₃ manganites series (0 ⩽ × ⩽ 0.2). All samples crystallise in an orthorhombic structure with the Pnma space group. We have found a strong dependence of structural and magnetic properties on the cation-size disorder parameter σ ². The temperature dependence of magnetization of all samples obeys the Bloch T ^3/2 law. The values of the spin wave constant at low temperature B increase with the increase of x and the Curie temperature decreases. It is concluded that the substitution of Ca by Na⁺ ions causes a decrease in total exchange integral Aof the samples.      

Ferromagnetism and the metal-insulator transition in the magnetic semiconductor system FexMn1−x S

The results of investigations of the structure, electrical, and magnetic properties in the system of antiferromagnetic semiconductors Fe_xMn_1−x S (0<x⩽0.5) are described. It is established that metal-insulator transitions with respect to concentration and temperature are connected with changes in the magnetic properties of the system. Fiz. Tverd. Tela (St. Petersburg) 40, 276–277 (February 1998)     

Spin-glass and reentrant spin-glass states in iron sulfospinels having dilute A and B sublattices

The magnetic and electrical properties of new compounds having spinel structure Fe_1−x Cr_2(1−x)Sn_2x S₄ (0.1⩽x⩽0.33) (system 1), Fe_0.67 [Fe_0.165CrSn_0.835]S₄, and Fe_0.67 [Fe_0.33Cr_0.67Sn]S₄ has been studied. These compounds are p-type semiconductors with magnetic properties characteristic of the following magnetic-order types: ferrimagnetic (the x=0.1 composition of system 1), spin glass (the x=0.33 composition of system 1 and Fe_0.67 [Fe_0.165CrSn_0.835]S₄), and reentrant spin glass (the x=0.2 composition of system 1 and Fe_0.67 [Fe_0.33Cr_0.67Sn]S₄). For the spin-glass compositions, the dependence of the freezing temperature T _f defined as the temperature of the maximum of initial magnetic susceptibility, on temperature and magnetic field obeys the Almeida-Thouless relation, and the dependence of T _f on magnetic-field frequency is a power-law function. For the spin-glass and reentrant spin-glass compositions, a large peak in the absolute value of negative isotropic magnetoresistance was found near T _f , which becomes as high as 15% in spin glasses and 30% in reentrant spin-glass compositions. In compositions with reentrant behavior, the activation energy of conductivity in the region of T _f was found to change by about two orders of magnitude. This experimental evidence suggests that the spin-glass-paramagnet (in spin glasses) and spin-glass-long-range magnetic-order transformations are actually phase transitions, and that the spin-glass region contains ferron-type ferromagnetic clusters. These are the first spin-glasses among the chalcospinels with magnetically active ions on the tetrahedral and octahedral sublattices. Fiz. Tverd. Tela (St. Petersburg) 41, 84–90 (January 1999)     

Magnetic phases in Pr0.5Sr0.5Mn1 ? xCoxO3 (x ≤ 0.5) solid solutions

The magnetic and magnetotransport properties of Pr_0.5Sr_0.5Mn_{1 − x} Co _x O₃ (x ≤ 0.5) solid solutions have been investigated using neutron diffraction methods. The magnetization and electrical conductivity have been measured in magnetic fields up to 140 kOe. It has been established that, during cooling in the temperature range from 160 to 110 K, the compounds of compositions with a cobalt content x ≤ 0.07 undergo a structural phase transition from the high-temperature ferromagnetic phase to the antiferromagnetic phase. A further substitution of cobalt for manganese leads to a stabilization of the inhomogeneous dielectric ferromagnetic state, whereas a state of the cluster spin-glass type has been revealed in compositions with x = 0.15 and 0.20. At x ≥ 0.25, a new magnetic phase with a Curie temperature up to 210 K is formed as a result of the magnetic interaction between manganese and cobalt ions. A magnetic phase diagram of the system under investigation has been constructed.     

Magnetic, electrical, and crystallographic properties of thin La1−x SrxMnO3 films

A study is reported of the magnetic, electrical, and crystallographic properties of La_1−x Sr_xMnO₃ (0.15⩽x⩽0.23) epitaxial films grown on single-crystal substrates of (001)ZrO₂(Y₂O₃) having the fluorite structure and (001)LaAlO₃ having the perovskite structure. It was found that films with close compositions for x=0.15 and 0.16, grown on different substrates, have different properties, namely, the film on a fluorite substrate is semiconducting and has a coercive strength 30 times that of the film on a perovskite substrate; the temperature dependence of electrical resistance of the latter film has a maximum around the Curie point T _C and follows metallic behavior for T<T _C. These differences are explained as due to different structures of the films. The x=0.23 film on the perovskite substrate has been found to exhibit a combination of giant magnetoresistance at room temperature with a resistance of ≈300 Ω which is useful for applications. The maxima in resistance and absolute value of negative magnetoresistance are accounted for by the existence of two-phase magnetic states in these films. Fiz. Tverd. Tela (St. Petersburg) 40, 290–294 (February 1998)     

Non-fermi liquid transport in <Emphasis Type="Italic">R</Emphasis>Co<Subscript>2</Subscript>-based alloys

Results on the experimentally investigated dependence of the electrical resistivity of quasibinary alloys R _x Y_1−x Co₂, where R stands for magnetic rare earth elements, on temperature (2–300 K), composition (x = 0–1), and magnetic field (0–15 T) are presented. Non-Fermi liquid behavior of electrical resistivity in a magnetic field was observed in paramagnetic Gd _x Y_1−x Co₂ alloys. The relative magneto-thermopower of these alloys exhibits diverging behavior with decreasing temperature, indicating anomalous temperature variation of the thermopower in the non-Fermi liquid regime.     

Formation of bound magnetic polarons in Cd1−x MnxTe crystals. Contribution of the average exchange field and thermodynamic fluctuations of the magnetization to the binding energy

It is shown that the temperature dependence of the binding energy of exciton-impurity complexes in the semimagnetic semiconductors Cd_1−x Mn_xTe (x≈0.05) is described well in the donor-electron model with an effective characteristic magnetic-polaron energy. The contributions of the average exchange field and of thermodynamic fluctuations of the magnetization to the binding energy and their variation with temperature with and without a weak magnetic field (H⩽3.5 kOe) are determined. How doping with scandium, vanadium, and cobalt effects the appearance of the magnetic-polaron in the experimental crystals was studied. Fiz. Tverd. Tela (St. Petersburg) 39, 527–535 (March 1997)     

New line of thermodynamic phase transitions on the x-T diagram of a dilute Heisenberg system with short-range interactions Li0.5Fe2.5−x GaxO4

It is established on the basis of an investigation of the temperature dependences of the saturation magnetization σ_S(T) and the magnetic contribution to the specific heat C _m(T) that in the reentrant region of the x-T diagram (0.9⩽x⩽1.5) of dilute iron spinels Li_0.5Fe_{2.5− x} Ga_xO₄ there exists between the line of Curie points T _C(x) and the line of freezing temperatures T _f(x) another line of first-order phase transitions T ₁(x) to a noncollinear ferrimagnetic phase: T _C(x)⩽T ₁(x)⩽T _f(x). Pis’ma Zh. éksp. Teor. Fiz. 67, No. 5, 329–333 (10 March 1998)     

The antiferromagnetic-ferromagnetic transition in the system Zn1−x CuxCr2S4

The magnetization and paramagnetic susceptibility of the system of compounds Zn_1−x Cu_xCr₂S₄ (0<x⩽1) are investigated at low temperatures. It is shown that as the content of Cu increases the system exhibits a transition from an antiferromagnetic to a ferromagnetic state. Fiz. Tverd. Tela (St. Petersburg) 40, 278–279 (February 1998)     

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.     

Magnetic phases in Mn<Subscript>1</Subscript>_<Subscript>x</Subscript>Fe<Subscript>x</Subscript>WO<Subscript>4</Subscript> studied by neutron powder diffraction

The magnetic structures of Mn_1-xFe_xWO₄ with x = 0.0, 0.16, 0.21, 0.225, 0.232, 0.24, 0.27, 0.29, and 1.0 were refined from neutron powder diffraction data. The magnetic phase diagram could be completed in the coexistence range of different magnetic structures up to x = 0.29. For the magnetic state at 1.5 K a commensurate antiferromagnetic structure with a propagation vector = (±1/4, 1/2, 1/2) was found for x ⩽ 0.22 while the magnetic spins order with = (1/2, 0, 0) for x ≥ 0.22. In the latter phase, additionally, weak magnetic reflections indexed to an incommensurate ordering with = (- 0.214, 1/2, 0.457) occur in the diffraction pattern up to x = 0.29 indicating the occurence of a reentrant phase. For 0.12 ⩽ x ⩽ 0.29 the low temperature phases are separated from a magnetic high temperature phase showing only magnetic reflections indexed to a spin arrangement with = (1/2, 0, 0). The magnetic phase diagram is discussed qualitatively considering random superexchange between the statistically distributed Mn²⁺- and Fe²⁺-ions in the coexistence range 0.12 ⩽ x ⩽ 0.29 of different magnetic structures related to those of pure MnWO₄ and FeWO₄. Received 9 October 2002 Published online 14 March 2003