Crystal Structures and Magnetic Properties of the Co2Mn1−x V x Sb (0 ≤ x ≤ 1) Heusler Compounds

Crystal structure and magnetic properties of the Co₂Mn_1?x V _x Sb (0 ≤ x ≤ 1) Heusler compounds have been studied by X-ray powder diffraction (XRD), magnetometric measurements, and full-potential linearized augmented plane wave (FP–LAPW) method. All compounds crystallize in a cubic Cu₂MnAl-type crystal structure with the space group Fm–3m. The samples for x<0.8 have the Curie temperatures above room temperature, while the Curie temperature is observed at 68 K for the sample with x = 0.8. The saturation magnetization at 5 K decreases linearly with increasing vanadium concentration x. The values of the saturation magnetization obtained by FP–LAPW–local density approximation (LDA) calculations are in better agreement with the experimental results compared with the results obtained by FP–LAPW–generalized gradient approximation (GGA) calculations.     

Effect of Fe-doping on Magnetocaloric Properties of AMn1?x Fe x O3 Compounds (0≤x≤0.2)

We have investigated the effect of iron substitution on the magnetocaloric properties of manganites with La_0.75Ca_0.08Sr_0.17Mn_1?x Fe _x O₃ (x=0, 0.075, 0.15, 0.175, and 0.2) nominal composition. The magnetocaloric effect (MCE) was estimated, in terms of isothermal magnetic entropy change (???S _M ), using the M(T,?? ₀ H) data and employing the thermodynamic Maxwell equation. The large magnetic entropy in AMn_1?x Fe _x O₃ is attributed to the field-induced suppression of short-range charge-orbital ordering and antiferromagnetic fluctuations present above T _C . The increase of the Fe concentration x is accompanied by a decrease of (???S _M ), from 5.205 to 0.95?J/kg?K for x=0 and 0.20, respectively, with ?? ₀ H=5?T. For all samples, we find quite large values of (???S _M ), which are very close to that provided for Gd, the prototypical magnetocaloric material.     

Structural and Magnetic Properties of Pr0.6Sr0.4Mn1−x Fe x O3 (0≤x≤0.3) Manganites Oxide Prepared by the Ball Milling Method

We present the structural and magnetic properties of Pr_0.6Sr_0.4Mn_1?x Fe _x O₃ (x=0, 0.1, 0.2, and 0.3) compounds. Samples have been prepared by the ball milling method. Rietveld refinements of the X-ray powder diffraction data show that all our synthesized samples are single phase and crystallize in the orthorhombic symmetry with the Pnma space group. The unit cell volume increases with increasing the Fe content. The infrared spectrum shows two active bands, which can be ascribed to the internal stretching and bending modes. The magnetization measurements versus temperature showed that Fe doping leads to a weakening of the ferromagnetic ordering at low temperature, the Curie temperature T _C decreases from 300 K for x=0.0 to 88 K for x=0.2. The magnetization versus applied magnetic measurements at low temperature lead to conclude that the substitution of Mn³⁺ ions by Fe³⁺ ions triggers antiferromagnetic interactions between the Fe³⁺ and Mn⁴⁺ spins, and also the magnetization versus applied magnetic measurements at room temperature shows a small hysteresis loop and a low coercive field, which indicates that the samples are superparamagnetic.     

The Magnetic Properties of Mn x Fe1−x NiSi (x=0,0.25,0.5,0.75,1) Alloys

The magnetic properties of Mn _x Fe_1?x NiSi (x=0,0.25,0.5,0.75,1) alloys are studied using density functional theory and the WIEN2k package. The exchange correlation potential is treated by generalized gradient approximation (GGA). The total energy calculations of these alloys confirm the stability of the ferromagnetic phase as compared to a nonmagnetic phase. The total magnetic moment is not a linear function of x. By increasing x, it increases and then decreases. The peak position of the magnetic moment is near x=0.75.     

Structural and Magnetic Properties of the Gd2−x Ho x Ru2O7 Pyrochlore Solid Solution (0≤x≤2)

In this paper, we investigate the structural and magnetic properties of the Gd_2?x Ho _x Ru₂O₇ (0≤x≤2) pyrochlores. X-ray diffractograms of all samples studied presented a cubic pyrochlore type crystal structure with lattice parameters varying linearly in accordance to Vegard’s law. It is shown that by substituting Gd by Ho one can tune the magnetic order of this system moving from antiferromagnetic (in the absence of Ho) to ferromagnetic (in the absence of Gd).     

Structural, Raman Spectroscopy, and Magnetic Ordering in New Delafossite-Type Oxide CuCr1−x Ti x O2 (0≤x≤0.1)

We investigated in this paper a new mixture +3/+2 B cations delafossites by the doping at Cr³⁺ sites in CuCrO₂ by nonmagnetic cation Ti²⁺. Ceramics of CuCr_1?x Ti _x O₂ (0≤x≤0.1) were prepared via solid state synthesis techniques in a controlled atmosphere of O₂. The compound crystallized into the 3R delafossite phase with hexagonal structure. The slightly different size in B cations induced a slightly variation in unit cell parameters. We modulate the spin chirality by the effect of spin dilution for Ti²⁺ on the structural and magnetic properties of delafossite CuCrO₂ having a S=3/2 antiferromagnetic triangular lattice (ATL).     

Structural Magnetic and Electrical Properties in Nd-Doped Manganites (La0.70−x Nd x )Sr0.30Mn0.70Ti0.30O3 with 0 ≤ x ≤ 0.30

The structural, magnetic and electrical properties of (La_0.70?xNd_x)Sr_0.30Mn_0.70Ti_0.30 O ₃ perovskites (0 ≤ x ≤ 0.30) prepared by the usual ceramic procedure were investigated. Structural Rietveld refinements of the X-ray powder diffraction revealed that for x = 0 the compound crystallizes in a rhombohedral (R \(\bar {{3}}\) c) perovskite structure, while for x = 0.10, 0.20 and 0.30 the structure becomes orthorhombic (Pbnm). The field-cooled, zero-field-cooled and M(H) measurements lead to conclude that the samples with x≥0.10 behave like spin-glass systems. The temperature dependence of the resistivity exhibits two transitions at two temperatures T _p1 and T _p2, with the same width for the two peaks. T _P1 results from the competition between double-exchange and super-exchange mechanisms inside the grain (intrinsic effects) whereas T _P2 arises due to the grain boundary effects (extrinsic effect). The resistivity of this system seems to be related to the competition between antiferromagnetic insulating (AFI) phases, ferromagnetic insulating (FMI) phases and ferromagnetic metal (FMM) phases, which is induced by Nd doping effect.     

Appearance of Griffiths Phase in La0.7−x Pr x Ba0.3MnO3 (0 ≤x≤ 0.2)

Polycrystalline La_0.7?x Pr _x Ba_0.3MnO₃ (0 ≤x≤ 0.2) samples were prepared using solid-state reaction and checked by X-ray diffraction. Magnetization measurements versus temperature and applied magnetic field were used to investigate their magnetic properties. For samples with x= 0.2, the Griffiths phase is observed when the inverse of susceptibility (1/ χ vs. T) is analyzed.     

Photoconductivity in single crystals of (TlGaSe2)1−x(TlInS2)x alloys (0−0.45 ≤ x ≤0.55-1)

The spectral distribution of the photoconductivity in (TlGaSe₂)_1−x(TlInS₂)_x single crystals has been studied at 77 K and 300 K. At O ≤ x ≤ 4, Eg is observed to vary linearly with x. Eg(x) deviates from linearity at x = 0.6. This deviation is attributed to the effect of disorder in the composition. Over the range 0.6 to 2.2 eV pronounced impurity photoconductivity is detected at 77 K and 300 K. Deep impurity levels and their neighbourhood in this alloy are established to preserve their positions with the variation in the composition. The analysis of the obtained results indicates that the impurity centres are mainly connected with the cation neighbourhood.     

Influence of KClO3 Addition on the Magnetic Properties and Microstructural Morphology of Y(1−0.2x)Ba(2−0.2x)KxCu3Oy (x = 0 ÷ 0.40) Polycrystalline HTSC

The influence of KclO ₃ addition on the AC complex susceptibility (ac) and microstructural morphology of YBCO HTSC with nominal composition Y _(1–0.2x) Ba _(2–0.2x) K _x Cu ₃ O _y (x = 0 ÷ 0.40) were investigated. Xac was recorded as a function of temperature and of the concentration of KClO ₃ in various AC magnetic fields up to 19 Oe. The data were analyzed using the relation h = a(1 – T _m /T _c ) ⁿ . The results obtained showed that the presence of K- and Cl-containing impurities on the grain boundaries change the intergranular coupling and, within certain concentration limits, improves the superconducting parameters.     

Magnetic Moments in SmCo5 and SmCo5?x Cu x Films

SmCo₅ is an emerging perpendicular magnetic material for super-high density magnetic recording, due to its large magnetic anisotropy energy. In this paper, the magnetic moments of SmCo_5?x Cu _x have been studied using first principles calculation based on density-functional theory (DFT). Calculations are performed using the pseudopotential plane wave DFT code Vienna ab initio simulation package (VASP) with the projector augmented wave (PAW) method. The local density approximation LDA+U method is used for the calculation of the exchange correlation energy of Sm. The calculation results show that the average Co magnetic moment of SmCo_5?x Cu _x decreases with the increase of Cu doping concentrations, and the influence of the Cu doping on the spin state of Co is greater than that of Sm. The magnetic anisotropy energy of SmCo₅ is analyzed. The electronic density of states and the differential in spin densities of atoms show that the spatial distribution of 4f electron and the 4f?C3d coupling are the controlling factors of the magnetic anisotropy energy of SmCo₅.     

Oxidation Resistance and Magnetic Properties of SmCo7?x Si x Permanent Magnetic Alloys

The crystal structure, oxidation resistance, and magnetic properties of SmCo_7−x Si _x (x=0, 0.4, 0.6, and 0.9) permanent magnetic alloys were investigated systematically. It is found that the addition of silicon in the as-cast SmCo₇ ingot plays an important role in stabilizing TbCu₇ phase and improving inherent oxidation resistance. For the bulk nanocrystalline SmCo_7−x Si _x magnets, the oxidation resistance remarkably enhances but the corresponding Curie temperature T _c and maximum energy product (BH)_max exhibit a decreasing trend with the increase in Si content x. For the typical SmCo_6.4Si_0.6 nanocrystalline magnet, its final mass gain was about 1.71 mg/cm² after oxidation at 500 °C for 100 h, indicating the enhanced inherent oxidation resistance. Its T _c and (BH)_max were about 708 °C and 35.4 kJ/m³, respectively.