


Vol 52, No 9 (2016)
- Year: 2016
- Articles: 18
- URL: https://journals.rcsi.science/0020-1685/issue/view/9584
Article
Topographic analysis of the surface of the GaSb〈Mn〉 magnetic semiconductor
Abstract
We have studied the formation of magnetic properties on the impurity–dislocation magnetism principle in a sample of a manganese-doped gallium antimonide compound semiconductor prepared by melt quenching. It has been shown using X-ray diffraction, optical microscopy, and scanning electron microscopy that the generation of dislocations and their motion during quenching play a key role in determining the microstructure of the GaSb〈Mn〉 magnetic semiconductor.



Fabrication and spectral characteristics of a laser diode for remote sensing of methane
Abstract
This paper presents a technological study aimed at producing buried heterostructures for single-mode semiconductor lasers operating in the wavelength range 1651–1662 nm. We have fabricated laser diodes operating at a wavelength corresponding to an absorption band of methane. The effect of temperature on the optical emission spectrum of the laser diodes has been examined. The results demonstrate the possibility of tuning their emission spectrum in the range from 1651 to 1662 nm and producing smart fiber-optic systems for the remote monitoring of the methane concentration.



Composition- and temperature-dependent thermodynamic properties of the Cd, Ge‖Se, Te system, containing CdSe1–хTeх solid solutions
Abstract
The 298-K isothermal section through the phase diagram of the Cd, Ge‖Se, Te system is mapped out and the direction of the stable diagonal CdSe–CdTe is determined using thermodynamic analysis and data for the constituent binary systems CdSe–GeSe2, CdSe–CdTe, and CdTe–GeTe, in combination with X-ray diffraction and emf measurements. Data are presented on the thermodynamic properties of CdSe1–хTeх solid solutions as functions of composition and temperature. The Gibbs free energy of formation of the CdSe1–хTeх solid solutions is evaluated as a function of composition in the temperature range 300–1400 K using thermodynamic calculations. The composition dependence of the energy of mixing for CdSe1–хTeх is shown to have a negative deviation from ideality in the range x ≈ 0.2–0.6 at temperatures from 1000 to 1400 K. The contributions of each component of the CdSe1–хTeх solid solutions to their partial excess thermodynamic functions of mixing are estimated and the interaction parameter of their components in the solid and liquid states has been evaluated. The band gap of alloys in the CdSe–CdTe system is calculated as a function of composition and temperature.



Growth of epitaxial Cd1–xMnxTe films
Abstract
We have studied the growth and structure of epitaxial films of Cd1–xMnx (x = 0.03) diluted magnetic solid solutions grown on mica substrates by molecular beam epitaxy and identified conditions for producing n- and p-type epitaxial films. Using an additional Te vapor source and optimizing the substrate temperature in the growth process, we were able to obtain structurally perfect p-type Cd1–xMnxTe (x = 0.03) films with clean, smooth surfaces. The growth plane of the films on the mica substrates is (111) of a face-centered cubic lattice and their unit-cell parameter is а = 6.477 Å.



Effect of cadmium chloride on the photosensitivity of Cd1–xMgxTe (0 ⩽ x < 0.10) films grown in a quasi-closed system
Abstract
Films of Cd1–xMgxTe solid solutions have been grown by thermal evaporation of powders of CdTe-based MgTe–CdTe solid solutions in a quasi-closed system. The magnesium content of the films has been found to be lower than that of the source material used for film growth. It has been shown that the photocurrent amplitude in the Cd1–xMgxTe films as a function of incorporated CdCl2 concentration has a maximum at a particular cadmium chloride concentration, which is due to the doping of the solid solutions with chloride ions. The cadmium chloride-activated Cd1–xMgxTe films are n-type.



Mechanochemical synthesis of chromium-based alloys
Abstract
This paper presents a detailed study of the formation of chromium-based alloys, Cr–Ta–W + plasticizing additives (Nb and Zr) and Cr–Ta–Si, during milling of powder mixtures in a Fritsch (P-7) planetary mill under an Ar atmosphere. It is shown that, after milling for 18 h, all the components of the starting mixtures convert into a Cr-based BCC solid solution. The powders of chromium alloys obtained in this study are readily compacted by hot isostatic pressing (HIP) under conditions typical of the processing of powders of high-temperature nickel alloys. Heating of the powders and compacts leads to the decomposition of the supersaturated solid solution and the formation of two forms of the Cr2M Laves phase with cubic crystal lattices. The formation of a mixed-phase fine microstructure in the chromium alloys after HIP suggests that the materials studied here are potentially attractive as a base of next-generation chromium-based high-temperature alloys.



V3.047O7, a new high-pressure oxide with the simpsonite structure
Abstract
Reaction between α-V2O5 and NaN3 has been studied at pressures from 5.0 to 6.0 GPa and temperatures from 600 to 800°C using Toroid high-pressure chambers. A new oxide, V3.047O7 (VO2.297), isostructural with simpsonite, Al4Ta3O13(OH), has been detected in samples with the initial composition 0.2NaN3 · V2O5 after high-temperature, high-pressure processing at p = 5.0 GPa and t = 800°C for 2 min. The crystal structure of the oxide has been refined by the Rietveld method using X-ray powder diffraction data: a = 7.35136(2) Å, c = 4.51462(2) Å, V = 211.294(1) Å3, Z = 2, sp. gr. P3. Each vanadium atom in this structure is coordinated by six oxygens in the form of a [VO6] octahedron. The synthesized oxide is a second compound with the simpsonite structure. We have measured the infrared transmission and Raman spectra of V3.047O7. Electrical measurements have demonstrated that the material is a semiconductor.



Preparation and magnetic characteristics of mesoporous nickel oxide–silica composites
Abstract
Mesoporous NiO–SiO2 (MCM-41) silica-matrix composites with various nickel oxide concentrations (NiO : SiO2 = 0.025 : 1 to 0.2 : 1) have been produced by oxide cocondensation under hydrothermal synthesis conditions in the presence of cetyltrimethylammonium bromide as a template and (2-cyanoethyl) triethoxysilane as an organosubstituted trialkoxysilane additive. X-ray diffraction data have been used to evaluate the maximum nickel(II) oxide concentration (NiO : SiO2 = 0.1 : 1) that allows the ordered mesopore structure of MCM-41 to persist in the silica-matrix composites. We have studied the magnetic properties of this material as functions of temperature and magnetic field. The results demonstrate that the magnetic properties of the nanocomposite with NiO : SiO2 = 0.1 : 1 at low temperatures (T < 20 K) are determined by incomplete spin compensation in the matrix and on the surface of the NiO nanoparticles.



Filtration combustion of silicon tetrafluoride and calcium hydride for the preparation of monosilane
Abstract
We have studied reaction between silicon tetrafluoride and calcium hydride in a vertical flow reactor, which proceeds as combustion in filtration mode. The principal kinetic characteristics of the reaction between SiF4 and CaH2 in a counterpropagating wave have been determined: reaction order n = 1, rate constant k = 0.38 ± 0.05 s–1, and activation energy Ea = 17 ± 2 kJ/mol.



Kinetics of germanium tetrachloride reduction with hydrogen in the presence of pyrolytic tungsten
Abstract
Pyrolytic tungsten coatings have been produced on the surface of ash microspheres under steady-state conditions using tungsten hexacarbonyl as a precursor. The nanostructured composites thus obtained were characterized by X-ray diffraction and scanning electron microscopy. We have studied the kinetics of the catalytic reduction of germanium tetrachloride with hydrogen in the temperature range 423–973 K in the presence of the composites as catalysts and determined the reaction order and activation energy for the catalytic reduction of germanium tetrachloride with hydrogen.



Phase formation and dielectric properties of ceramics in the BiFeO3–BaTiO3–Bi(Mg0.5Ti0.5)O3 system
Abstract
We have studied the effect of Bi(Mg0.5Ti0.5)O3 additions on the phase formation, structural parameters, microstructure, and dielectric properties of solid solutions in the region of a morphotropic phase boundary in the BiFeO3–BaTiO3 system. Single-phase samples with the perovskite structure have been obtained and the addition of Bi(Mg0.5Ti0.5)O3 has been shown to raise the Curie temperature of the ceramics and improve their dielectric properties.



Synthesis, structure, and magnetic properties of rare-earth-doped Ni0.75Zn0.25Fe2O4 nickel zinc ferrite
Abstract
We have developed processes for the synthesis of Ni0.75Zn0.25Fe2–xLnxO4 ferrite solid solutions with the spinel structure and investigated the effect of the rare-earth elements Nd, Gd, Yb, and Lu on the chemical composition, extent, lattice parameters, and magnetic properties of the solid solutions. The results demonstrate that rare-earth solubility in the parent spinel reaches ≈2.5 at %, which leads to changes in the magnetic characteristics of the material, in particular in its saturation magnetization Ms, TC, and coercive force Hc.



Composition and structure of coatings based on rare-earth zirconates
Abstract
Coatings based on lanthanum, neodymium, samarium, and gadolinium zirconates have been grown by atmospheric plasma spraying of powders, and their composition and structure have been investigated by scanning electron microscopy, chemical analysis, and X-ray diffraction. The results demonstrate that the chemical composition of the coatings differs from the compositions of the powders they were prepared from. During plasma spraying of Ln2Zr2O7-based powders, the rare-earth oxide vaporizes more rapidly than zirconia. The difference in composition between the powders and coatings decreases as the atomic number of the rare earths increases in going from La to Gd. We have studied the processes that take place in the coatings during heat treatment at a temperature of 1250°C. It has been shown that the major phase in the La2Zr2O7-, Nd2Zr2O7-, and Sm2Zr2O7-based coatings undergoes a defect fluorite–pyrochlore structural phase transition. The La2Zr2O7-based coatings have been found to contain ∼5 wt % t-ZrO2 in addition to the major phase. The Gd2Zr2O7-based coating retained a defect fluorite structure.



Structure and phase composition of thin TiO2 films grown on the surface of metallized track-etched polyethylene terephthalate membranes by reactive magnetron sputtering
Abstract
We have studied TiO2, Ag, Ag/TiO2, and Cu/TiO2 coatings grown on track-etched polyethylene terephthalate membranes. The metals and oxides were deposited by reactive vacuum sputtering using a planar magnetron. The microstructure of the samples were examined by scanning and transmission electron microscopy techniques. The elemental composition of the coatings were determined by energy dispersive X-ray microanalysis, and their phase composition was determined by X-ray diffraction at different temperatures and by transmission electron diffraction. Titanium dioxide can be present on the surface of track-etched membranes (TMs) in three forms: nanocrystals of tetragonal anatase with orthorhombic brookite and amorphous TiO2 impurities. The copper-metallized TM has been shown to contain cubic Cu2O. The optical properties of the composite membranes and films have been studied by absorption spectroscopy. The energies of direct and indirect allowed optical transitions have been evaluated from measured absorption spectra of the TiO2, Ag/TiO2, and Cu/TiO2 coatings.



Synthesis of a two-phase nanopowder from prototype human synovial fluid and the use of the nanopowder for the preparation of coatings on titanium plates
Abstract
Using prototype human synovial fluid, we have synthesized a calcium phosphate nanopowder consisting of two crystalline phases (whitlockite and carbonate-containing hydroxyapatite). The nanopowder was used to produce calcium phosphate (monetite) coatings on titanium substrates by microarc oxidation. It has been shown that, with increasing microarc oxidation voltage (from 200 to 300 V), the mass, thickness, roughness parameter, and Ca : P ratio of the coatings increase linearly. Increasing the voltage to 300 V and the calcium phosphate coating growth time to 10 min allows a single-phase coating up to 100 μm in thickness, consisting of monetite nanocrystals, to be produced on a metallic surface and its adhesion strength to be improved.



Growth of optically active multilayer metal oxide films on a plastic substrate
Abstract
An optically active ITO/Au/ITO multilayer coating (where ITO stands for an indium tin oxide with the composition 90% In2O3 + 10% SnO2 and Au is nanoparticulate gold on a thin-film poly(ethylene terephthalate) substrate) has been prepared by a solution-phase process using an ITO nanopowder dispersion in isopropanol and a solution of chloroauric acid, which was converted to colloidal gold by photolysis. A sol–gel process has been proposed for the synthesis of tin-doped indium oxide nanopowder. The properties and composition of the powder were assessed by IR spectroscopy, thermal analysis, electron microscopy, and X-ray diffraction. The phase composition of the ITO nanopowder and the optical properties of the films grown using the nanopowder have been shown to depend on the thermal annealing conditions during synthesis. Layer-by-layer growth of metal oxide films in ITO/Au/ITO coatings influences the absorption in the composite in the IR spectral region.



Effect of the Brij 30 porogen on the properties of sol–gel derived thin polymethylsilsesquioxane films
Abstract
Thin polymethylsilsesquioxane films with Brij 30 porogen concentrations in the range ωsurf = 15.5–52.5 wt % have been produced by a sol–gel process. Their dielectric permittivity, refractive index, relative porosity, and shrinkage have been measured as functions of heat treatment temperature and porogen concentration.



Effect of barium hydrosilicates on the early hydration rate of Portland cement
Abstract
We have studied the effect of a barium hydrosilicate-based modifier on the phase composition of Portland cement hydration products. The results demonstrate that the addition of a modifier containing barium hydrosilicates, silicic acid, and calcium carbonate makes it possible to reduce the nucleation rate of crystals of new phases during the induction period of the hydration process, increase alite (3СaO · SiO2) hydration, and reduce the rate of aluminate phase (3CaO · Al2O3) hydration. The use of such a modifier increases the degree of cement hydration and the amount of calcium hydrosilicates and reduces the amount of forming portlandite and ettringite, thereby improving the mechanical properties and durability of the set cement.


