Reaction of tantalum oxide with calcium chloride–calcium oxide melts

Tantalum oxide is a suitable precursor for electro-deoxidation, where a cathodic potential is applied to the oxide, immersed in a molten salt, to remove oxygen from the oxide leaving tantalum metal. The electro-deoxidation reactions take place in a melt of CaCl₂–CaO and, unlike the reduction of other metal oxides where little or no reaction occurs between the melt and oxide until the application of a cathodic potential, tantalum oxide readily reacts with the calcium oxide to form CaTa₄O₁₁, CaTa₂O₆ and Ca₂Ta₂O₇. These phases have completely different morphologies which convert a robust pellet into a collection of poorly connected particles.     

Reduced graphene oxide–nickel oxide composites with high electrochemical capacitive performance

Reduced graphene oxide (RGO)–NiO composites have been fabricated by a simple solvothermal route starting with graphite oxide (GO). The morphology, composition and microstructure of the as-obtained samples are systematically characterized by thermogravimetric (TG) analysis, X-ray diffraction (XRD), and field emission scanning electron microscopy (FESEM). Moreover, the electrochemical performances of composites were evaluated by cyclic voltammogram (CV) and galvanostatic charge–discharge. Interestingly, it was found that the electrochemical performance of the composites could be affected by the mass ratio between RGO and NiO. The composite with the mass ratio up to 79:21 (NiO:RGO) exhibits the highest specific capacitance of 576 F g⁻¹ at 1 A g⁻¹, which is much higher than that of pure NiO (240 F g⁻¹) and pure RGO (98 F g⁻¹). In addition, the cycling measurements showed that RGO–NiO composite exhibited excellent cycling stability with no decay in the available capacity over 1100 cycles. The enhancement in specific capacitance and cycling stability may be attributed to the increased electrode conductivity owing to RGO network, the increased effective interfacial area between NiO and the electrolyte, as well as the contact area between NiO and RGO.     

Synthesis, characterization and oxide ionic conductivity of β-type solid solution in bismuth oxide doped with ytterbium oxide binary system

In this study, after doping Yb₂O₃ substance to α -Bi₂O₃ substance in the range of 1% ≤ n ≤ 8% in a series of different mole ratios, heat treatment was performed by applying a cascade temperature rise in the range of 700–790 °C for 48 and 120 h and new phases were obtained in the (Bi₂O₃)_1???x (Yb₂O₃) _x system. After 48 h of heat treatment at 750 °C and 120 h of heat treatment at 790 °C, mixtures containing 1–8% mole Yb₂O₃ formed a tetragonal phase. With the help of XRD, crystal systems and lattice parameters of the solid solutions were obtained and their characterization was carried out. Thermal measurements were made by using a simultaneous DTA/TG system. The total conductivity (σ _T) in the β-Bi₂O₃ doped with Yb₂O₃ system was measured using four-probe d.c. method.     

Effect of gadolinia addition on varistor characteristics of vanadium oxide–doped zinc oxide ceramics

The effect of gadolinia addition on microstructure, electrical and dielectric characteristics, and aging behavior of vanadium oxide–doped zinc oxide varistor ceramics was systematically investigated. The average grain size decreased from 5.6 to 5.2 μm with an increase in the amount of Gd₂O₃ up to 0.1 mol%, whereas a further increase caused it to increase to 5.7 μm at 0.25 mol%. The sintered densities decreased from 5.51 to 5.44 g/cm³ with an increase in the amount of Gd₂O₃. With increasing the amount of Gd₂O₃, the breakdown field increased from 4,800 to 5,365 V/cm up to 0.05 mol%, whereas a further increase decreased it to 4,781 V/cm at 0.25 mol%. The varistor ceramics modified with 0.05 mol% Gd₂O₃ exhibited excellent nonlinear properties, with 66.1 in the nonlinear coefficient, whereas a further increase caused it to decrease to 17.6 at 0.25 mol%. The gadolinium acted like a donor, based on the electron concentration increasing from 4.20 × 10¹⁷/cm³ to 7.38 × 10¹⁷/cm³ with an increase in the amount of Gd₂O₃.     

The photo-electrochemical studies of Eu doped yttrium orthovanadate–zinc oxide–reduced graphene oxide nanohybrid

A new class of nanostructured photo-electrocatalyst Eu³⁺ doped yttrium orthovanadate–zinc oxide–reduced graphene oxide (YVO₄:Eu³⁺–ZnO–RGO) nanohybrid was developed by a simple electrostatic self-assembly at room temperature, using ZnO, YVO₄:Eu³⁺ and RGO as building blocks. Interaction among YVO₄:Eu³⁺, ZnO and RGO is indicated by variation in hydrodynamic diameter (H_D) and zeta potentials of the products as compared to their individual components, thus suggesting that YVO₄:Eu³⁺–ZnO–RGO is a nanohybrid and not a physical mixture. Electrochemical response of this nanohybrid towards the redox couple of Fe(CN)₆^3−/4− was investigated before and after UV irradiation. Apart from quenching of the green emission of ZnO in photoluminescence spectrum, which serves as a probe to monitor the interfacial electron transfer from excited ZnO to RGO, degradation in electrochemical redox process provides an additional path to monitor interfacial electron transfer.     

Magnetic properties and Mössbauer spectra of gamma ferric oxide and doped gamma ferric oxide

Magnetic hysteresis, Mössbauer spectra and temperature variation of initial magnetic susceptibility of thirteen samples of doped -Fe₂O₃ containing cobalt or gadolinium are determined. The samples containing more than 1.0% cobalt are found to have a multi-domain configuration, and undoped -Fe₂O₃, gadolinium-doped -Fe₂O₃ and doped -Fe₂O₃ containing less than 1.0% (except 0.3%) cobalt have a single domain configuration. Mössbauer spectra of gadoliniumdoped samples suggest that gadolinium occupies A and B sites. In cobalt-doped samples, the effective magnetic fields at A and B sites are different at room temperature and liquid nitrogen temperature. The samples which have a multi-domain configuration display an additional central doublet in Mössbauer spectra indicating that these samples contain multi-domain clusters. The saturation magnetization of gadolinium-doped -Fe₂0₃ is much lower, and the coercive force of cobalt-doped samples is much higher than of gadolinium-doped and undoped samples.     

Nanoscale epitaxial growth control of oxide thin films by laser molecular beam epitaxy—towards oxide nanoelectronics

The nanoscale growth control of oxide thin films, such as ferroelectric and magnetic materials, were explored by a novel technique based on nanoscale substrate engineering as well as atomic layer control via laser molecular beam epitaxy (laser-MBE). Atomic-scale analysis of the terminating layer of perovskite oxide films was performed by in situ coaxial impact-collision ion scattering spectroscopy. The novel heteroepitaxies that could be attained were: (1) the termination-regulated molecular layer-by-layer epitaxy of BaTiO₃ and La_0.7Sr_0.3MnO₃ thin films and (2) the step-decoration epitaxy resulting in the nanowire or nanodot structures of magnetic oxides such as (Mn, Zn) ferrite on ultrasmooth sapphire substrates with straight atomic steps.     

SrTiO3 glass–ceramics as oxide thermoelectrics

Glass-ceramics obtained via a true bulk glassy phase offer a possibility to obtain high-temperature stable nanostructured materials in a cost efficient way which is suitable for mass production. We apply the method of glass-ceramic manufacturing to a crystalline phase which is known for its good thermoelectric properties as an n-doped material. Nb-doped SrTiO₃ with grain sizes of several nanometers is obtained as the main crystalline phase from transparent bulk glass after applying a well-defined time–temperature profile for ceramization. The glass-ceramics show a low thermal conductivity of around 1.6 W/mK and a Seebeck coefficient around ?480 μV/K together with electronic conductivity. Thermal cycling of these glass-ceramics without degradation of the thermoelectric properties for temperatures up to 650 °C (923 K) is shown as well.     

Effects of environment on creep behavior of two oxide/oxide ceramic–matrix composites at 1200 °C

The tensile creep behavior of two oxide/oxide ceramic–matrix composites (CMCs) was investigated at 1200 °C in laboratory air, in steam, and in argon. The composites consist of a porous oxide matrix reinforced with laminated, woven mullite/alumina (Nextel™720) fibers, have no interface between the fiber and matrix, and rely on the porous matrix for flaw tolerance. The matrix materials were alumina and aluminosilicate. The tensile stress–strain behavior was investigated and the tensile properties were measured at 1200 °C. Tensile creep behavior of both CMCs was examined for creep stresses in the 80–150 MPa range. Creep run-out defined as 100 h at creep stress was achieved in air and in argon for stress levels ≤100 MPa for both composites. The retained strength and modulus of all specimens that achieved run-out were evaluated. The presence of steam accelerated creep rates and reduced creep life of both CMCs. In the case of the composite with the aluminosilicate matrix, no-load exposure in steam at 1200 °C caused severe degradation of tensile strength. Composite microstructure, as well as damage and failure mechanisms were investigated. Poor creep performance of both composites in steam is attributed to the degradation of the fibers and densification of the matrix. Results indicate that the aluminosilicate matrix is considerably more susceptible to densification and coarsening of the porosity than the alumina matrix. The views expressed are those of the authors and do not reflect the official policy or position of the United States Air Force, Department of Defense or the U.S. Government.     

Enhanced capacitance of composite anodic ZrO₂ films comprising high permittivity oxide nanocrystals and highly resistive amorphous oxide matrix

Anodic oxide films with nanocrystalline tetragonal ZrO(2) precipitated in an amorphous oxide matrix were formed on Zr-Si and Zr-Al alloys and had significantly enhanced capacitance in comparison with those formed on zirconium metal. The capacitance enhancement was associated with the formation of a high-temperature stable tetragonal ZrO(2) phase with high relative permittivity as well as increased ionic resistivity, which reduces the thickness of anodic oxide films at a certain formation voltage. However, there is a general empirical trend that single-phase materials with higher permittivity have lower ionic resistivity. This study presents a novel material design based on a nanocrystalline-amorphous composite anodic oxide film for capacitor applications.     

The influence of zinc oxide–cerium oxide nanoparticles on the structural characteristics and electrical properties of polyvinyl alcohol films

With the objective to investigate the influence of zinc oxide–cerium oxide (ZnO–Ce₂O₃) nanoparticles on the electrical properties of polyvinyl alcohol (PVA), PVA/ZnO–Ce₂O₃ nanocomposite films were prepared by solution intercalation method with different weight percentage viz., 0.5, 1.0, and 2.0?wt% of ZnO–Ce₂O₃ nanoparticles. The fabricated nanocomposites were characterized by Fourier transform-infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and differential scanning calorimetry (DSC). The effect of ZnO–Ce₂O₃ nanoparticles on the dielectric constant (ε′), dielectric loss (ε″), electric modulus (M′ and M″), ac conductivity (σ _ac), and dielectric loss tangent (tan δ) over a range of frequencies at room temperature of PVA nanocomposites have been studied. FT-IR, XRD, and DSC analysis indicates the nature of ZnO–Ce₂O₃ nanoparticles interaction with the PVA matrix. The morphological behavior of the nanocomposites has been performed using scanning electron microscopy (SEM). The dielectric behaviors such as dielectric constant (ε′) and dielectric loss (ε″) increases with increase in nanoparticle concentration, but decreases with increase in frequency. But, the electric modulus (M′) increases with increase in frequency. Dielectric loss tangent (tan δ) decreases with increase in filler content at lower frequency, but at higher frequencies the tan δ increases with increase in nanoparticles content. AC conductivity (σ _ac) of PVA/ZnO–Ce₂O₃ nanocomposites increases with increasing frequency following the universal dielectric response law.     

Cyclic and sustained loading behaviors of oxide/oxide Nextel™720/alumina composite with double edge sharp notch

This study investigated an oxide/oxide CMC consisting of Nextel?720 (meta-stable mullite) fibers in alumina matrix, N720/A, with 0°/90° fiber orientation having double edge sharp notch under sustained and cyclic loading conditions at 1200 °C in laboratory air environment. Monotonic tensile tests at 1200 °C were also conducted. Fracture surfaces were examined to analyze failure and damage mechanisms. Comparisons with counterparts from unnotched geometry showed N720/A is mildly sensitive to the sharp notch under monotonic tensile, creep and fatigue loading conditions. The ultimate tensile strength of the composite was reduced by about 15% in the presence of the sharp notch. The rupture strength of the sharp notched geometry was reduced by about 15% of unnotched geometry for a given rupture time. The fatigue strength was reduced by about 20% of unnotched geometry for a given number of cycles to failure. Deformation under cyclic loading condition had contributions both from fatigue and creep. Damage mechanisms were identical under cyclic and sustained loading conditions.     

Ruthenium oxide–niobium hydroxide composites for pseudocapacitor electrodes

A simple solution-based method has been developed to vary the composition of redox active ruthenium oxide with highly proton-conducting niobium hydroxide to create stable, high capacitance electrodes at elevated temperatures. This method presents a dramatic departure from most other ruthenium oxide systems, which are prepared through annealing of hydrous ruthenium oxide. Typically RuO₂ processed at high temperature only exhibits high electrical conductivity and suffers from poor proton conduction, giving low overall capacitances. Here, the optimized Ru/Nb oxide composition can be used to achieve high power densities, high capacitances, and stabilized electrodes while significantly reducing ruthenium content. Extensive materials characterization including high-resolution cross-sectional TEM, elemental mapping, XRD, electrochemical impedance spectroscopy, and proton NMR were used to evaluate the structure of the material system. The electrochemically inert niobium oxide serves as a network former enhancing accessibility to redox active ruthenium oxide. The dispersion of RuO₂ in the NbO(OH)_x matrix results in reduced RuO₂ particle size, as observed via TEM and XRD, while also increasing the proton concentration in the material. Interconnected RuO₂ particles provide electrically conducting pathways, even at low Ru contents, where percolation networks remain intact. Ruthenium is more efficiently utilized in the Ru/Nb composites and ruthenium content can be significantly reduced without decreasing capacitive performance. In addition, the composite electrodes, with the fine mixing of Ru and Nb, give higher power performance than for RuO₂ alone.     

A glycerol–water-based nanofluid containing graphene oxide nanosheets

Nanofluids are simply the dispersion of nanometer-sized particles in different fluids. Graphene oxide nanosheets (GONs) were prepared by exfoliating the graphite oxide. The GONs were investigated using Fourier transform-infrared spectroscopy, Raman spectroscopy, XRD analysis, high-resolution emission electron microscopy, transmission electron microscopy, and UV–visible spectroscopy. GONs/glycerol–water-based nanofluid was prepared by the two-step method. The stability of the nanofluid was investigated with respect to time. Thermal and electrical conductivity of the prepared nanofluid was examined with different temperatures (25–45 °C) and weight fractions (0.02–0.1 wt%). The nanofluid is found to be stable for more than 5 months. The results showed an enhancement in thermal conductivity of about 4.5 % at 25 °C with a weight fraction of 0.02 %. The improvement was up to 11.7 % with a weight fraction of 0.1 wt% at 45 °C. The electrical conductivity was increased with increasing the weight fraction and temperature. The improvement in electrical conductivity was about 5890 % at 25 °C and 0.1 wt%.     

The effect of strontium oxide in glass–ionomer cements

The reaction of strontium oxide powder with poly(acrylic acid) has been studied both alone and within glass–ionomer cements. Reaction was found to be slow and the strontium-carboxylate structure was found to be partially covalent in character, as determined by Fourier transform infrared spectroscopy (FTIR). These are similar to the structures formed by calcium in glass–ionomer cements, but are different from typical monomeric strontium carboxylates, which tend to be purely ionic. Strontium oxide powder introduced in two types of glass–ionomer cements, slowed down the setting reaction at both 21 °C and 37 °C, but at low levels (5 wt %), increased the compressive strength in both cement formulations studied. However, at higher levels, it was found to decrease the compressive strength. This study confirms the view that strontium is a cement-forming ion; but concludes that, except at very low levels, strontium oxide powder does not improve the properties of glass–ionomer cements.     

Fine-tuning of stannic oxide anodes’ material properties through calcination

Journal of Materials Science: Materials in Electronics - Phase pure stannic oxide (SnO2) is an efficient and reliable anode material for Li ion batteries. Understanding of pure SnO2 phase formation...     

Temperature dependent transport properties in molybdenum oxide doped α-NPD

The temperature dependent transport properties of molybdenum oxide (MoO₃) doped N,N′-di(1-naphthyl)-N,N′-diphenylbenzidin (α-NPD) were studied over a frequency range of 100 Hz to 1 MHz. The value of trap density and mobility calculated by detailed analysis of current–voltage (I–V) characteristics are 9.43 × 10²⁶ m^?3 and 1.23 × 10^?6 cm² V^?1 s^?1, respectively. The relaxation time for the carriers in the bulk and in the interface region decreases with temperature. The Cole–Cole plot indicates the device can be modeled as the combination of two parallel resistor–capacitor (R–C) circuits with a series resistance of around 70 Ω. The dc conductivity shows two different regions in the studied temperature range with activation energy of E_a ～ 0.107 eV (region I) and E_a ～ 52 meV (region II), respectively. The ac conductivity follows the universal power law and the onset frequency increases with increase of temperature. The temperature dependent conduction mechanism can be explained by correlated hopping barrier (CBH) model.     

Preparation and characterization of epoxy/γ-aluminum oxide nanocomposites

Epoxy/γ-Al₂O₃ nanocomposites were prepared with a homogenizer and followed by a stepwise thermal curing process in this study. The dispersion of γ-Al₂O₃ nanoparticles was examined with a transmission electron microscopy (TEM). Meanwhile, the effects of γ-Al₂O₃ nanoparticles on thermal, dynamic mechanical and tensile properties of epoxy/γ-Al₂O₃ nanocomposites were also investigated and discussed. When the γ-Al₂O₃ content was increased from 1phr to 5phr, results revealed that γ-Al₂O₃ nanoparticles were effective to enhance both the stiffness and toughness of epoxy resin. Meanwhile, the maximum properties of glass transition temperature (T_g), T_d5%, storage modulus, tensile modulus, and elongation at break were observed in the epoxy/5phr γ-Al₂O₃ nanocomposite.     

Low-temperature synthesis of manganese oxide–carbon nanotube-enhanced microwave-absorbing nanocomposites

Noting that the dielectric properties of manganese oxide make it a promising microwave-absorbing material, a low-temperature method to deposit crystalline MnO₂ over carbon nanotubes (CNTs) is developed. Adjusting the pH of the precursor solution allows control over the phases and morphologies of the synthesized manganese oxides MnO₂ and Mn₃O₄ that have minimum reflection losses of ??11 dB and ??6 dB, respectively. The synthesized CNT–MnO₂ and CNT–Mn₃O₄ nanocomposites are superior microwave absorbers than simpler physical mixtures of CNTs and manganese oxides, with reflection losses as high as ??19 dB at 9.5 GHz and ??34 dB at 4 GHz, and have wider absorption bands than pure manganese oxides. Coating CNTs with manganese oxide not only increases dielectric and magnetic losses, but also improves the impedance match between free space and the absorber. The addition of CNTs to pure MnO₂ and Mn₃O₄ improves impedance matching by enhancing the relaxation polarization and conductivity losses, magnetic loss, including contributions form eddy current and natural resonance. This facile, low-cost, scalable, high-yield method produces an enhanced microwave-absorbing nanocomposite.