


Vol 54, No 3 (2018)
- Year: 2018
- Articles: 16
- URL: https://journals.rcsi.science/0020-1685/issue/view/9613
Article
Effect of Ascorbic Acid Additions on the Mechanism Underlying the Growth of Nanostructured PbSe Films via Hydrochemical Deposition
Abstract
The effect of ascorbic acid additions on the growth mechanism of thin PbSe films produced by hydrochemical deposition has been studied by atomic force microscopy (AFM). A fractal analysis of AFM images of the lead selenide films has shown that their formation follows the “cluster–particle” aggregation mechanism. The fractal dimension assessed by the box-counting method is 2.26 at an average grain size of ~150 nm. From the transmission spectra of the films grown at deposition times from 20 to 120 min, we have evaluated their optical band gap, which has been shown to decrease from 0.595 to 0.53 eV with increasing deposition time. These values are attributable to the manifestation of quantum size effects in the grown PbSe films.



One-Step Synthesis of a Hybrid of Graphene Films and Ribbons
Abstract
Hybrid structures composed of graphene films and (0001) graphene ribbons perpendicular to the surface of a graphene-like film have been produced through the catalytic decomposition of a carbon-containing gas on an Al-coated SiO2/Si substrate having Ni catalyst islands on its surface. A hybrid structure has been grown by a one-step chemical vapor deposition process, by admitting acetylene into a chamber for a short time. The hybrid structures thus produced have been used to fabricate Hall sensors with a sensitivity of 3000 Ω/T. The synthesized hybrid structures are potential candidates for use in nanoelectronic devices, energy storage systems, etc. The technique proposed for the growth of such films is compatible with technologies that are employed in the electronics industry.



Synthesis of Hybrid Materials Based on Iron Nanoparticle-Decorated Multiwalled Carbon Nanotubes
Abstract
Fe-containing nanoparticles have been grown for the first time on the surface of multiwalled carbon nanotubes by metalorganic chemical vapor deposition using iron acetylacetonate, Fe(acac)3, as a precursor. The resultant hybrid nanomaterial has been characterized by X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, and thermogravimetric analysis. The results demonstrate that the synthesized material consists of multiwalled carbon nanotubes whose surface is decorated with iron nanoparticles.



Thermal Conductivity of Tetragonal Cadmium Diphosphide Crystals
Abstract
Tetragonal cadmium diphosphide (β-CdP2) single crystals with high structural perfection have been grown and their thermal conductivity has been measured. The results indicate that the higher thermal conductivity across the c axis corresponds to the smaller unit-cell parameter of the crystals (a = 5.08 ± 0.01 Å and c = 18.59 ± 0.05 Å). The observed thermal conductivity anisotropy is tentatively attributed to the fact that structural basis of β-CdP2 is made up of spectral phosphorus chains running in the [100] and [010] directions.



Formation of Compounds in the Ag2O–Sb2O3–MoO3 System on Heating
Abstract
This paper presents a detailed study of phase formation processes in the AgNO3–Sb2O3–MoO3 system during heating in air. The compositions of the solid-state reaction products have been determined using thermogravimetry and qualitative X-ray diffraction. The results demonstrate that, at a final heat treatment temperature of 1023 K, synthesis yields a range of Ag2–xSb2–xMoxO6 compounds with the pyrochlore structure and 0.0 ≤ x ≤ 2.0. The structural parameters of the synthesized phases have been refined by the Rietveld method in space group Fd3̅m and their electrical conductivity has been measured.



Order–Disorder Structural Transformations in Nanocrystalline Highly Imperfect Gd2MO5 (M = Zr and Hf) Fluorite Derivatives
Abstract
Order–disorder phenomena in nanocrystalline Gd2ZrO5 and Gd2HfO5 with highly imperfect fluorite- derived structures in the range 1000–1600°C have been studied using monochromatic synchrotron X-ray diffraction and Raman spectroscopy. The results demonstrate that the synthesis process leads to the formation of two coherent phases identical in composition: a nanocrystalline disordered fluorite-like (F) phase (Fm3m) and a nanoparticulate ordered fluorite derivative (C1) (Ia3). Their lattice parameters have been determined. In the range 1000–1600°C, the Raman spectra of the Gd2ZrO5 and Gd2HfO5 materials contain broad bands in low- and high-frequency regions, at ~118 (108), 362 (353), and 670 (665) cm–1, which characterize the C1 and F phases, respectively.



Structure–Composition Relationship of Skeletal and Dendritic Ferrospheres Isolated from Calcium-Rich Power Plant Ash
Abstract
This paper presents a systematic SEM–EDS study of polished sections of individual skeletal and dendritic ferrospheres in the–0.04 + 0.032 mm size fraction, isolated from fly ash from the combustion of brown coal from the Berezovskoe field. The ferrospheres are characterized by a wide range of variations in the macrocomponent composition of local areas. We have identified groups of globules whose overall composition as well as the composition of local areas on their polished sections can be represented by general equations for component concentrations: SiO2 = f(FeO), SiO2 = f(Al2O3), and CaO = f(SiO2). Such equations make it possible to identify the nature of the mineral precursors involved in the formation of the globules. FeO-rich skeletal ferrospheres with low CaO concentration originate from the thermochemical transformation of pyrite and illite associates. Skeletal and dendritic ferrospheres with monotonically increasing CaO and SiO2 concentrations are formed from pyrite and montmorillonite associates, with the participation of a melt containing quartz and decomposition products of Ca-humates of the initial coal. Skeletal and dendritic spinel ferrite crystallization is due to a magnesium aluminate spinel “seed,” resulting from the thermal transformation of illite and montmorillonite from the parent coal. The observed increase in glass phase concentration and the change from the skeletal type of crystallization to a dendritic in the ferrospheres containing ≤64 wt % FeO and ≥6.5 wt % CaO are due to the low concentration of the spinel-forming cations Fe2+ and Fe3+ in the melt and the increase in the percentage of [Fe3+O2]− and [Fe23+ O5]4− ferrite complexes with an increase in the degree of oxidation of the melt.



Vibrational Relaxation in the Solid NaNO3–NaClO4, NaNO3–NaNO2, and Na2CO3–Na2SO4 Binary Systems
Abstract
Molecular relaxation processes in the solid binary systems NaNO3–NaClO4, Na2CO3–Na2SO4, and NaNO3–NaNO2 have been studied by Raman spectroscopy. It has been shown that the relaxation time of the ν1(A) vibrational mode of the NO3- and CO32- anions in the binary systems is shorter than that in individual (nitrate or carbonate) crystals. The increase in the relaxation rate can be accounted for by an additional mechanism for the relaxation of excited vibrational states of the anions in the binary systems. The mechanism involves the excitation of vibrations in a different anion (ClO4-, SO42- or NO2-) and the “generation” of a lattice phonon. This relaxation mechanism is possible when the difference in frequency between the vibrational modes involved corresponds to a region with a sufficiently high density of states in the phonon spectrum.



Correlation between the Molecular Refractions of Crystals and the Ionic Radii of the Cations in the Rare-Earth Trifluoride Homologous Series
Abstract
We have identified linear correlations between the molecular refractions Rmol (cm3/mol) of crystals and the ionic radii ri (Å) of the cations in the RF3 rare-earth trifluoride homologous series: Rmol = 8.33ri + 0.102 for R = La–Nd and Rmol = 13.03ri–4.42 for R = Sm–Lu. The fact that the RF3 rare-earth trifluorides can be divided into two groups is related to the morphotropic transition from the LaF3 (tysonite) structure to the β-YF3 structure. The correlation found here for RF3 crystals with the β-YF3 structure because the electronic structure of Y (4d15s2) differs from that of Sm–Lu (4f6–145d0–16s2) in that it has no 4f electrons.



Fabrication of Active Fluoroaluminosilicate Fibers for High-Power Fiber Lasers
Abstract
An all-vapor phase modified chemical vapor deposition (MCVD) process has been proposed for the fabrication of active-fiber preforms with a fluorine-rich F–Yb2O3–GeO2–Al2O3–SiO2 glass core. The composition of the glass has been shown to differ significantly from that of the vapor–gas mixture because of the formation of GeF4, AlF3, and YbF3, which are volatile at typical MCVD temperatures. We have identified F–Yb2O3–GeO2–Al2O3–SiO2 glass deposition conditions that ensure uniform distributions of the dopants along the length of the preform.



Fabrication of Yb2O3–Al2O3–P2O5–SiO2 Optical Fibers with a Perfect Step-Index Profile by the MCVD Process
Abstract
An all-vapor phase MCVD process has been proposed for the fabrication of fiber preforms with a Yb2O3–Al2O3–P2O5–SiO2 multicomponent glass core. We have investigated the tubular preform collapse into a rod and demonstrated approaches capable of preventing P2O5 losses in the central part of the core during the collapse process. Preforms with a flat, perfect step-index profile have been fabricated.



Local Environment of Fe Ions in a 40ZnO · 60B2O3 Glass Matrix
Abstract
The valence state and coordination environment of the Fe ions in a number of Fe-containing zinc borate glasses with the general formula xFe2O3–(100–x)[40ZnO · 60B2O3] (x = 2.5–10 mol %) have been studied by Mössbauer spectroscopy. The results indicate that all of the glasses contain both Fe2+ and Fe3+ ions. The percentage of trivalent ions considerably exceeds that of Fe2+ ions and the relationship between the Fe2+ and Fe3+ concentrations is essentially independent of the Fe2O3 content in the zinc borate matrix. Most of the Fe3+ ions are in tetrahedral coordination, but raising the Fe2O3 content to above 5 mol % leads to a gradual increase in the percentage of Fe ions in octahedral coordination.



Synthesis, X-ray Diffraction Characterization, Mössbauer Spectroscopy, and Dielectric Properties of Solid Solutions in the PbFe2/3W1/3O3–PbSc2/3W1/3O3 System
Abstract
Ceramic Pb(Fe1–xScx)2/3W1/3O3 samples with 0 ≤ x ≤ 1 have been prepared and characterized by X-ray diffraction, Mössbauer spectroscopy, and dielectric and pyroelectric measurements. The stoichiometry ranges of the perovskite solid solutions in this system have been identified, their structural parameters have been determined, and their dielectric permittivity, dielectric loss tangent, resistivity, and thermally stimulated depolarization current have been measured as functions of temperature. The composition dependences of the dielectric properties for the solid solutions have been obtained. The solid solutions have been shown to exhibit ferroelectric relaxor properties, with a well-defined maximum in their permittivity in the range 180–250 K.



Structure and Hardness of Ceramics Produced through High-Temperature Nitridation of Titanium Foil
Abstract
We have studied the variation in the phase composition, elemental composition, and microstructure of rolled titanium samples during thermal annealing in a nitrogen atmosphere at 1300, 1500, 1700, and 2000°C. The results demonstrate that the nitridation process can yield compact titanium nitride-based ceramics or TiN/TiNx/α-Ti〈N〉 heterostructures. X-ray diffraction data for the near-surface region of the samples before and after nitridation and those for cross-sectional fracture surfaces of heterostructures are used to infer orientation relationships between the TiN phase and α-Ti〈N〉 solid solution. Scanning electron microscopy results for cross-sectional fracture surfaces indicate that complete nitridation of the samples leads to the formation of a three-layer microstructure.



Effect of Laser Irradiation on the PTCR Behavior of Semiconducting Barium Strontium Titanate Ceramics
Abstract
This paper examines the effect of pulsed laser irradiation on the electrical properties of n-type semiconductor ferroelectric ceramics (based on a (Ba,Sr)TiO3 solid solution) with a planar contact configuration. The elemental compositions and surface morphologies of the material before and after laser irradiation are compared using scanning electron microscopy data. In the framework of the well-known Heywang model for the positive temperature coefficient of resistance effect, we calculate the resistance of the material as a function of temperature for the paraelectric phase and determine parameters of grain boundaries that ensure good agreement between the experimental data and theoretical curves.



Structural, Morphological, and Resorption Properties of Carbonate Hydroxyapatite Prepared in the Presence of Glycine
Abstract
Carbonate-containing hydroxyapatite has been synthesized from prototype human synovial fluid in the presence of glycine. The resultant powders have been shown to contain 75 to 80 wt % the amino acid. If the model solution contains less than 0.08 mol/L of glycine, the latter influences neither the composition of the solid phase nor the size of the forming crystallites, but changes the degree of their crystallinity and the specific surface area of the material. At high amino acid concentrations, we observe the formation of poorly crystallized composites consisting of smaller nanocrystallites. The dissolution of the samples in a 0.9% NaCl solution has been shown to be a two-step process. The highest solubility under weakly acidic conditions has been demonstrated by the precipitates containing the largest amount of the amino acid.


