Structure and electromagnetic properties of hot-pressed La0.65Sr0.35Mn1 ? x Cr x O3 manganites under different synthesis conditions

The effect of hot pressing conditions on the characteristics of the crystalline and magnetic structures of Cr-doped lanthanum-strontium manganites has been investigated for the first time using X-ray diffraction, electron microscopy, magneto-optical visualization of magnetic flux, ferromagnetic resonance, and magnetic measurements. It is shown that application of pressure during sintering affects the concentration of differentvalence ions and structural vacancies and phase separation in the manganites studied. Original Russian Text ? N.A. Vybornov, F.D. Aliev, V.K. Karpasyuk, A.A. Pankratov, A.V. Saitov, V.V. Senin, S.G. Titova, L.S. Uspenskaya, 2008, published in Izvestiya Rossiiskoi Akademii Nauk. Seriya Fizicheskaya, 2008, Vol. 72, No. 10, pp. 1506–1509.     

Electrical conductivity and magnetic properties of La1 ? xCaxMn1 ? yFeyO3 ceramic samples (x = 0.67, y = 0, 0.05)

The temperature dependences of the magnetic susceptibility χ(T) and the electrical resistivity ρ(T) of ceramic samples of La_{1 − x} Ca _x MnO₃ with x = 0.67 (LCMO) and La_{1 − x} Ca _x Mn_{1 − y} Fe _y O₃ with x = 0.67 and y = 0.05 (LCMFO) are investigated in magnetic fields B = 50–10⁵ G and the temperature range T = 4.2–400 K. Both samples undergo a transition from the paramagnetic state to a state with charge (orbital) ordering (CO) at temperatures T _CO ≈ 272 K for LCMO and T _CO ≈ 222 K for LCMFO. The behavior of the paramagnetic phase in the temperature range 320–400 K for LCMO and 260–400 K for LCMFO is described by the Curie-Weiss law with effective Bohr magneton numbers p _eff = 4.83 μ_B (LCMO) and 4.77 μ_B (LCMFO), respectively. The disagreement between the observed positive Weiss temperatures (θ ≈ 175 K (LCMO) and θ ≈ 134 K (LCMFO)) and negative Weiss temperatures required for the antiferromagnetic ground state can be explained by the phase separation and transition to the charge-ordered state. The magnetic irreversibility for T < T _CO is accounted for by the existence of a mixture of the ferromagnetic and antiferromagnetic phases, as well as the cluster glass phase. At low temperatures, doping with iron enhances the frustration of the system, which manifests itself in a more regular behavior of the decay rate of the remanent magnetization with time. The temperature dependence of the electrical resistivity in the range of the charge-ordered phase conforms to the variable-range hopping model. The behavior of the electrical resistivity is governed by the complex structure of the density of localized states near the Fermi level, which includes a soft Coulomb gap Δ = 0.464 eV for LCMO and 0.446 eV for LCMFO. It is established that the ratio between the localization radii of charge carriers a for LCMFO and a _und for LCMO is a/a _und = 0.88. Original Russian Text ? V.S. Zakhvalinskiĭ, R. Laiho, T.S. Orlova, A.V. Khokhulin, 2008, published in Fizika Tverdogo Tela, 2008, Vol. 50, No. 1, pp. 61–68.     

Effect of oxygen deficiency on the magnetic, electrical, magnetoelectric, and magnetoelastic properties of La1 ? x Sr x MnO3 ? δ manganites

This paper reports on a study of the effect of oxygen deficiency on the magnetic and electrical properties of the La_{1 − x} Sr _x MnO_{3 − δ} manganites (x = 0, 0.2, 0.4; δ = 0, 0.13, 0.2). In compositions with x = 0 and δ = 0.13 and 0.2, the temperature dependence of the magnetization M (T) can be approximated by the Langevin function with the moment of superparamagnetic clusters μ = 77μ_B (δ = 0.13) and 86μ_B (δ = 0.2) at temperatures of 25 K ≤ T ≤ 250 K, with the exception of a small temperature range near 132 K in which a maximum characteristic of the LaMnO₃ antiferromagnet is seen. These compositions, as well as Sr-doped compositions with δ ≠ 0, reveal a difference between the magnetizations of the sample cooled in a weak magnetic field and in zero field. At T = 6 K in a magnetic field of 16 kOe, the compositions with x = 0.2 and 0.4, δ = 0.13 possess a magnetic moment per formula unit lower than that with δ = 0, as well as reveal an anomalous relation between the Curie temperature T _C and the Curie paramagnetic point gJ, namely, T _C > gJ. The magnetization of compositions with x = 0.2 and 0.4, δ = 0.2 follows the Langevin function with μ = 40μ_B and 130μ_B, respectively. The electrical resistivity of samples with x = 0.4 and δ = 0.13 and 0.2 is one to two orders of magnitude larger than that of the composition with x = 0.4, δ = 0, which evidences partial or complete compensation of acceptor defects (Sr²⁺ ions) by donor defects (doubly charged O²⁻ vacancies). The above properties of oxygen-deficient compositions suggest that they contain an insulating ferro-antiferromagnetic magnetically double-phase state. The magnetoresistance and volume magnetostriction in samples with x = 0.4 and δ = 0, 0.13, and 0.2 are small; indeed, in a magnetic field of 8 kOe, they do not exceed 1.4% and 6 × 10⁻⁶, respectively. On this basis, it is concluded that the unbalanced doubly charged donors (O vacancies) are in the state with antiparallel spins and, thus, do not initiate the formation of ferron-type ferromagnetic clusters. The significance of both compensated and unbalanced doubly charged donors consists in that they give rise to the formation of fractured Mn-O-Mn bonds, which bring about lowering of the magnetic moment per formula unit in compositions with x = 0.2 and 0.4 and δ = 0.13 and the transition to superparamagnetism in compositions with x = 0.2 and 0.4, δ = 0.2. Original Russian Text ? L.I. Koroleva, D.M. Zashchirinskiĭ, T.M. Khapaeva, L.I. Gurskiĭ, N.A. Kalanda, V.M. Trukhan, R. Szymczak, B. Krzumanska, 2008, published in Fizika Tverdogo Tela, 2008, Vol. 50, No. 12, pp. 2201–2205.     

M?ssbauer and X-ray studies of the structural phase transformations and suppression of polymorphism in La1 ? xSrxMn0.98Fe0.02O3 + δ (x = 0.05?0.30)

The specific features of the structural transformations in La_{1 − x} Sr _x Mn_0.98Fe_0.02O_{3 + δ} (x = 0.05−0.30) as functions of the Sr content have been investigated using M?ssbauer spectroscopy and X-ray diffraction. It has been shown that, when the Sr content is lower than 10%, three phases are formed: PnmaII, PnmaI, and R-3c. In the Sr concentration range from 10 to 20%, the PnmaI and R-3c phases are formed. At a strontium content of 20%, the rhombohedral phase is formed. When the strontium content increases to 30%, the presumably monoclinic (distorted cubic) phase is formed in addition to the rhombohedral phase. The specific features of the formation and suppression of the phases in the LaMn_0.98Fe_0.02O_{3 + δ} compound are compared with those observed in the strontium-doped La_{1 − x} Sr _x Mn_0.98Fe_0.02O_{3 + δ} compound. The general regularities of the structural transformations and substantial differences between them have been revealed.     

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.     

Influence of cobalt on the structural and magnetic Inhomogeneities, phase transitions, and magnetoresistive properties of La0.6Sr0.2Mn1.2 ? x Co x O3 ± δ

The structure and properties of magnetoresistive ceramics La_0.6Sr_0.2Mn_{1.2 − x} Co _x O3 ± δ (x = 0−0.3) sintered at a temperature of 1200°C are investigated using x-ray diffraction, resistance, and magnetic (χ _ac , M, ⁵⁵Mn NMR) measurements. It is shown that the samples contain the rhombohedral (R c) perovskite (90%) and tetragonal (I4₁/amd) hausmannite (10%) phases. The lattice parameters of these phases decrease with an increase in the cobalt content x. The real perovskite structure involves point defects (anion and cation vacancies) and nanostructured defects of the cluster type. An analysis of the asymmetrically broadened ⁵⁵Mn NMR spectra confirms the high-frequency electron-hole exchange between Mn³⁺ and Mn⁴⁺ ions and a local inhomogeneity of their environment by other ions and defects of the point and cluster types. An increase in the Co content leads to an increase in the electrical resistivity, an enhancement of the magnetoresistance (MR) effect, and a decrease in the magnetic susceptibility and the temperatures of the metal-semiconductor (T _ms ) and ferromagnetic-paramagnetic (T _C) phase transitions due to the suppression of the exchange interaction between Mn³⁺ and Mn⁴⁺ ions by vacancies and clusters. The introduction of cobalt results in a decrease in the ferromagnetic component and the activation energy. The magnetoresistance effect in the vicinity of the phase transition temperatures T _ms and T _C is associated with the scattering of charge carriers from intracrystallite inhomogeneities of the lattice, and the low-temperature magnetoresistance effect is governed by the tunneling at the intercrystalline boundaries. Original Russian Text ? A.V. Pashchenko, V.P. Pashchenko, A.A. Shemyakov, N.G. Kisel’, V.K. Prokopenko, Yu.F. Revenko, A.G. Sil’cheva, V.P. Dyakonov, H. Szymczak, 2008, published in Fizika Tverdogo Tela, 2008, Vol. 50, No. 7, pp. 1257–1262.     

Low-temperature properties of magnetic Ni50 + x Mn25 ? x + y Ga25 ? y shape memory alloys

The effect of atomic disordering and deviation from the Ni₂MnGa stoichiometric composition on the low-temperature properties of alloys with magnetically controlled shape memory effect is studied. The specific features of the magnetic, galvanomagnetic, and electrical properties of alloys with magnetically controlled shape memory effect are discussed. The specific features of the magnetic, galvanomagnetic, and electrical properties of alloys Ni₅₀Mn₂₅Ga₂₅, Ni₅₄Mn₂₁Ga₂₅, and Ni₅₀Mn_28.5Ga_21.5 in the temperature range 2 ≤ T ≤ 80 K under magnetic fields H ≤ 12 MA/m are studied. Original Russian Text ? N.I. Kourov, V.V. Marchenkov, V.G. Pushin, A.V. Korolev, E.B. Marchenkova, H.W. Weber, 2008, published in Fizika Tverdogo Tela, 2008, Vol. 50, No. 11, pp. 2037–2042.     

Structure, phase transitions, 55Mn NMR, and magnetoresistive properties of La0.6Sr0.2Mn1.2 ? yCryO3 ± δ

The structure and properties of lanthanum strontium manganite perovskites La_0.6Sr_0.2Mn_{1.2 − y} Cr _y O_{3 ± δ} (y = 0–0.3) sintered at 1430°C have been studied by X-ray, resistive, and magnetic (χ_ac and ⁵⁵Mn NMR) methods. The parameter of the rhombohedrally distorted (R $ \bar 3 $ \bar 3 c) perovskite structure decreases with increasing y. The real perovskite structure contains point (anion and cation vacancies) and cluster-type nanostructure defects. The analysis of asymmetrically broadened ⁵⁵Mn NMR spectra has confirmed the high-frequency electron-hole exchange Mn³⁺ ↔ Mn⁴⁺ and local inhomogeneity of their surrounding by other ions and point and cluster-type defects. An increase in the Cr content leads to an increase in the resistivity and the magnetoresistive effect and a decrease in the metal-semiconductor and ferromagnetic-paramagnetic phase transition temperatures (T _ms and T _c ) due to the distortion of the exchange interactions Mn³⁺ ↔ Mn⁴⁺ by chromium ions, vacancies, and clusters. Introduction of Cr decreases the ferromagnetic component and increases the activation energy. The magnetoresistive effect near T _ms and T _c is caused by scattering of charge carriers from intercrystallite nanostructure inhomogeneities of the lattice, and the low-temperature effect is associated with the tunneling on mesostructural intercrystallite boundaries.     

Anomalies of the pyroelectric and dielectric properties of ferroelectric ceramics of the PbZr1- x Ti x O3 system with 0.06 ≤ x ≤ 0.35 at the R3 c ? R 3 m phase transition

The temperature dependences of the pyroelectric and dielectric properties of ferroelectric ceramics of the PbZr_{1 − x} Ti _x O₃ binary system with x = 0.06, 0.07, 0.08, 0.1, 0.15, 0.2, 0.25, 0.3, and 0.35 have been obtained synchronously for each sample in the range of the structural phase transition between the states with the symmetry space groups R3c ↔ R3m. It is established that the temperatures of this phase transition for unpolarized and polarized samples coincide in the range 0.06 ≤ x ≤ 0.15. In this case, the x−T phase diagram, constructed on the basis of the pyroelectric and dielectric data, is in excellent agreement with the X-ray diffraction data on single crystals in this concentration range. The effect of dc electric fields from 5 × 10⁵ V m⁻¹ did not lead to any temperature shifts of the R3c ↔ R3m phase transition for the compositions with 0.06 ≤ x ≤ 0.25. Original Russian Text ? Yu.N. Zakharov, A.G. Lutokhin, N.A. Korchagina, V.G. Kuznetsov, 2008, published in Izvestiya Rossiiskoi Akademii Nauk. Seriya Fizicheskaya, 2008, Vol. 72, No. 4, pp. 589–591.     

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 transformations in the Sr0.78Y0.22Co1 ? xFexO3 ? γ system with a perovskite structure

The Sr_0.78Y_0.22Co_{1 − x} Fe _x O_{3 − γ} cobaltite system is studied by neutron and X-ray diffraction and by measuring the magnetization and elastic properties. The crystal structure of the composition with x = 0 is described in terms of the monoclinic space group A2/m with the unit cell 2 a _p × 4a _p × 2 a _p , and the crystal structure of the composition with x = 0.12 is orthorhombic (space group Imma). The crystal structure of these compounds is characterized by alternating CoO₆ and CoO_4.5 layers. The magnetic structure is a G-type antiferromagnetic structure. The magnetic moments in the CoO₆ layers are significantly higher than those in the CoO_4.5 layers. In the compound with x = 0, magnetic measurements reveal a small ferromagnetic component (0.2 μ_B/Co) below T _N ≈ 350 K. Near T _N, a phase transformation occurs and lowers the crystallographic symmetry. Doping with iron ions suppresses the ferromagnetic component and sharply increases the average magnetic moments in both layers. The spontaneous magnetization is assumed to result from noncollinear magnetic moments, which can be caused by the competition of exchange interactions of different signs and magnetic anisotropy. The compounds with x = 0.5 and 1.0 are cubic (space group Pm3m) and are characterized by a G-type collinear antiferromagnetic structure. Original Russian Text ? I.O. Troyanchuk, D.V. Karpinsky, V.M. Dobryanskiĭ, A.N. Chobot, G.M. Chobot, A.P. Sazonov, 2009, published in Zhurnal éksperimental’noĭ i Teoreticheskoĭ Fiziki, 2009, Vol. 135, No. 3, pp. 490–497.     

Study of high-temperature oxygen permeability in Sr1 ? xLaxCo0.8 ? yNbyFe0.2O3 ? z perovskites

The oxygen permeability of ceramic SrCo_{0.8 − y} Fe_0.2Nb _y O_{3 − z} (0 ≤ y ≤ 0.2) and La_0.3Sr_0.7Co_0.6Fe_0.2Nb_0.2O_{3 − z} disc membranes as a function of temperature and oxygen partial pressure was studied. Kinetic analysis was performed based on the experimental data on oxygen permeability as a function of oxygen partial pressure.     

Mechanism of NdSr2 ? xCaxMn2O7 (0 ≤ x ≤ 2.0) solid solution formation

The mechanisms of formation of NdSr_{2− x} Ca _x Mn₂O₇ (0 ≤ x ≤ 2.0) solid solution have been studied. The dependence of its volume magnetic susceptibility on the calcium concentration is obtained. The stability of this solid solution is compared with that of similar solid solutions in lanthanum-containing systems.     

Phase formation in near-morphotropic region of the PbZr1 ? xTixO3 system, structural defects, and electromechanical properties of the solid solutions

Ceramics of PbZr_{1 − x} Ti _x O₃ solid solutions were systematically studied in the range 0.37 ≤ x ≤ 0.57. The x-T phase diagram (T = 25°C) is constructed containing in single-phase regions isosymmetric states characterized by different concentration dependences of the structural and electrophysical parameters. There are also regions where these states coexist, with their unit cell volume remaining unchanged. The existence of these states is interpreted in terms of the real (defect) structure of the ceramics. Several reasons are indicated that are responsible for the appearance of the phase states and related to the crystallochemical peculiarities of the solid solutions: the alternate valence of titanium ions; the infinitely adaptive structure of titanium dioxide; and the formation, ordering, and rotation of the planes of crystallographic shear. It is shown that the transition from the rhombohedral to tetragonal phase occurs indirectly, through two intermediate phases with lower symmetry whose appearance is favored by the defects in the solid solutions. Original Russian Text ? L.A. Reznichenko, L.A. Shilkina, O.N. Razumovskaya, E.A. Yaroslavtseva, S.I. Dudkina, O.A. Demchenko, Yu.I. Yurasov, A.A. Esis, I.N. Andryushina, 2009, published in Fizika Tverdogo Tela, 2009, Vol. 51, No. 5, pp. 958–965.     

层状钙钛矿La1.3Sr1.7Mn2-xCuxO7的磁性及电特性

通过固相反应烧结法成功制备了层状钙钛矿La_1.3Sr_1.7Mn_2-xCu_xO₇多晶，主要研究了其磁电特性.结果表明，样品为Sr₃Ti₂O₇型钙钛矿结构.随着温度的降低，其磁性经历了一个很复杂的转变过程.当x=0时，在T^*=231K出现二维短程铁磁有序，在<     

层状钙钛矿La1.3Sr1.7Mn2-xCuxO7的磁性及电特性

通过固相反应烧结法成功制备了层状钙钛矿La_1.3Sr_1.7Mn_2-xCu_xO₇多晶,主要研究了其磁电特性.结果表明,样品为Sr₃Ti₂O₇型钙钛矿结构.随着温度的降低,其磁性经历了一个很复杂的转变过程.当x=0时,在T^*=231K出现二维短程铁磁有序,在< 关键词： 层状钙钛矿 磁性 电特性     

Cu掺杂La0.67Sr0.33CuxMn1-xO3薄膜的光诱导效应研究

分别采用溶胶-凝胶和射频磁控溅射的方法制备了La_0.67Sr_0.33Cu_xMn_1-xO₃（x=0.05, 0.10和0.15）系列块材和薄膜,研究了Cu部分替代对薄膜光诱导特性的影响.实验结果表明随着Cu掺杂量的增加,薄膜的金属-绝缘转变温度向低温方向移动,且导电性降低.在金属相激光作用诱导电阻增大.光致电阻相对变化极大值随着Cu含量的增加而增大,当 关键词： 锰氧化物 光诱导 Cu掺杂 晶格效应     

Effect of excess oxygen on the electrical and magnetic properties of La1 ? xAgxMnO3 (x = 0.05, 0.1, 0.2) at 77 K < T < 300 K

A study has been made of the magnetic and electrical properties of oxygen-enriched La_{1 − x} Ag _x MnO_3.1 manganites at 77 K < T < 300 K. The samples have been produced by the sol-gel technique. The study has revealed an increase of the Curie temperature and a shift of the maximum in magnetoresistance toward high temperatures.     

Irreversible increase in the temperature range of existence of the orthorhombic antiferroelectric phase in PbZr1 ? xTixO3 ceramics (0.02 ≤ x ≤ 0.05)

The influence of thermostating at 450°C on the dielectric and pyroelectric properties of PbZr_{1 − x} Ti _x O₃ polarized ferroelectric specimens the range 0.02 ≤ x ≤ 0.05 has been investigated. An irreversible increase in the temperature of the ferroelectric-antiferroelectric phase transition was observed in all specimens upon their cooling after exposure to an elevated temperature for more than 1 h. The original position of the phase-transition point on the temperature scale was not recovered as a result of afterpoling upon cooling through the Curie temperature. Heating of the same specimens in the bridged mode up to 650°C with subsequent abrupt immersion in silicone oil at room temperature (hardening) is accompanied by an additional increase in the range of existence of the antiferroelectric phase from 3 to 15°C with an increase in the x concentration.