Electrical properties of TiO<Subscript>2</Subscript>: equilibrium vs dynamic electrical conductivity

The present work reports semiconducting properties of high purity TiO₂ determined in the gas/solid equilibrium, as well as during controlled heating and cooling in the range 300–1,273 K. The activation energy of the electrical conductivity is considered in terms of the activation enthalpy of the formation of ionic defects and the activation enthalpy of the mobility of electronic defects. These data, determined from the dynamic electrical conductivity experiments, are compared to the electrical conductivity data determined in equilibrium. It is shown that only the equilibrium electrical conductivity data for high-purity TiO₂ are well defined. It is shown that the activation energy of the electrical conductivity determined in equilibrium differs substantially from that for the dynamic electrical conductivity data during cooling and heating. It is concluded that the formation enthalpy term determined from the dynamic conductivity data is determined by the heating/cooling rate rather than materials’ properties.     

Ionic conduction in Li<Subscript>2</Subscript>Ge<Subscript>7</Subscript>O<Subscript>15</Subscript> crystals doped with Cr and Mn ions

The electrical conductivity σ of crystals of lithium heptagermanate Li₂Ge₇O₁₅ doped with Cr and Mn is measured in an alternating-current field with a frequency of 1 kHz in the temperature range 300–700 K. It is found that doping strongly affects the electrical conductivity. It is established that the addition of 0.1 wt % Cr leads to an increase in the electrical conductivity σ by almost one order of magnitude, whereas the introduction of 0.03 wt % Mn substantially reduces the electrical conductivity along particular crystallographic directions. Data available on the incorporation of Cr and Mn impurity atoms into the lattice suggests that the electrical conductivity is determined by lithium ions hopping over interstitial positions along the structural channels.     

The transport and thermal properties of glassy LiPO<Subscript>3</Subscript>/crystalline Al<Subscript>2</Subscript>O<Subscript>3</Subscript> (ZrO<Subscript>2</Subscript>) composite electrolytes

Glassy LiPO₃/crystalline Al₂O₃ and glassy LiPO₃/crystalline ZrO₂ (0–12.5 vol.% of oxide fillers) composite solid electrolytes have been prepared by glass matrix softening. Their thermal and transport properties have been investigated by differential scanning calorimetry (DSC) and impedance spectroscopy methods. The addition of ZrO₂ leads to a decrease in the crystallization temperature of LiPO₃ glass. It was found that the conductivity behavior depends on the nature of the dispersed addition. In the case of the Al₂O₃ addition, the increase in the electrical conductivity is observed. The ionic conductivity of the LiPO₃/10% Al₂O₃ composite reaches 5.8 × 10^?8 S/cm at room temperature. In contrast, the conductivity in the LiPO₃/ZrO₂ composite system decreases.     

Photoelectric characteristics of nanostructured hydrochemically deposited films of the Pb<Subscript>0.975</Subscript>Sn<Subscript>0.025</Subscript>Se substitutional solid solution

The photoelectric characteristics of Pb_0.975Sn_0.025Se solid solution films prepared by the hydrochemical codeposition of PbSe and SnSe with the subsequent heat treatment in air at 573–700 K have been investigated. The thermal and optical band gaps, the temperature coefficient of the optical band gap, the dark resistance, the volt-watt sensitivity, and the range of spectral sensitivity have been determined in the temperature range of 220–300 K. It has been found that, after heat treatment below 573 K, the films of the Pb_0.975Sn_0.025Se solid solutions possess metallic conductivity, while being heat treated at elevated temperatures, they become semiconductors with p-type conductivity. The composition of the solid solution is independent of the heat treatment temperature; it is formed during deposition.     

Magnetic,thermal, and electrical properties of an Ni<Subscript>45.37</Subscript>Mn<Subscript>40.91</Subscript>In<Subscript>13.72</Subscript> Heusler alloy

The magnetization, the electrical resistivity, the specific heat, the thermal conductivity, and the thermal diffusion of a polycrystalline Heusler alloy Ni_45.37Mn_40.91In_13.72 sample are studied. Anomalies, which are related to the coexistence of martensite and austenite phases and the change in their ratio induced by a magnetic field and temperature, are revealed and interpreted. The behavior of the properties of the alloy near Curie temperature T_C also demonstrates signs of a structural transition, which suggests that the detected transition is a first-order magnetostructural phase transition. The nontrivial behavior of specific heat detected near the martensite transformation temperatures is partly related to a change in the electron density of states near the Fermi level. The peculiar peak of phonon thermal conductivity near the martensitic transformation is interpreted as a consequence of the appearance of additional soft phonon modes, which contribute to the specific heat and the thermal conductivity.     

Tellurium Solubility in TlGaTe<Subscript>2</Subscript> and TlInTe<Subscript>2</Subscript> and the Electrophysical Properties of Solid Solutions

The complex methods of the physicochemical analysis are used to study TlGaTe₂–Te and TlInTe₂–Te alloys in which the tellurium solubility region up to 5.0 at % is observed. The temperature dependences of the lattice parameters and the electrical conductivity of TlGaTe_{2 + x} and TlInTe_{2 + x} have been studied in different crystallographic directions. The TlGaTe_{2 + x} and TlInTe_{2 + x} solid solutions undergo a phase transition at a temperature of 498 K. The transition nature is interpreted.     

Mn-doped Bi<Subscript>26</Subscript>Mo<Subscript>10</Subscript>O<Subscript>69-d</Subscript>: synthesis and characterization

In this work, we research two series of Mn-substituted bismuth molybdates: Bi_26-2xMn_2xMo₁₀O_69-d and Bi₂₆Mo_10-2yMn_2yO_69-d. The synthesis of powder samples is performed by the conventional solid state technology. Samples are characterized by X-ray diffraction, scanning electron microscopy, and chemical analysis methods, and it is shown that single phase Bi_26-2xMn_2xMo₁₀O_69-d and Bi₂₆Mo_10-2yMn_2yO_69-d complex oxides form up to x = 0.8 and y = 0. We use densitometry, grain size measurements and scanning electron microscopy to study the morphology of ceramic pellets and powders. This issue reveals formation of dense ceramic samples with low porosity (≤3%). High-temperature X-ray diffraction is used to define small deviation of unit cell parameters from their linear dependence on temperature. Measurement of electrical conductivity is made using a.c. impedance spectroscopy method. We observe the decrease of electrical conductivity in Bi_26-2xMn_2xMo₁₀O_69-d series depending on dopant concentration.     

Ion transfer in solid solutions of Cu<Subscript>2</Subscript>Se and Ag<Subscript>2</Subscript>Se superionic conductors

The cationic conductivities of Cu₂Se and Ag₂Se superionic conductor solid solutions in the composition region from Cu₂Se to Cu_0.7Ag_1.3Se are measured. It is demonstrated that the activation energy of ionic conduction depends only slightly on the chemical composition, varies from 0.14 to 0.17 eV, and exhibits a weakly pronounced maximum for the Ag_0.44Cu_1.56Se solid solution. The ionic Seebeck coefficients are measured for the Ag_0.23Cu_1.757Se solid solution. The heat of cation transfer in this solution is found to be equal to 0.144±0.014 eV from the Seebeck coefficients.     

NMR study and electrical properties investigation of Zn<Subscript>2</Subscript>P<Subscript>2</Subscript>O<Subscript>7</Subscript>

The α-Zn₂P₂O₇ compound was obtained by conventional solid-state reaction. The sample was characterized by X-ray powder diffraction, solid state ³¹P NMR MAS, and electrical impedance spectroscopy. The solid state ³¹P MAS NMR, performed at 121.49 MHz, shows three isotropic resonances at −21.1, −18.8, and −15.8 ppm, confirming the non-equivalency of the three PO₄ groups in the α-Zn₂P₂O₇ form. They are characterized by different chemical shift tensor parameters with the local geometrical features of the tetrahedra. Electrical impedance measurements of β-Zn₂P₂O₇, form stable for temperature greater than 403 K, were performed as a function of both temperature and frequency. The electrical conduction and dielectric relaxation have been studied. The AC conductivity obeys the universal power law. The approximation type correlated barrier hopping model explains the universal behavior of the n exponent. The impedance plane plot shows semicircle arcs at different temperatures, and an electrical equivalent circuit has been proposed to explain the impedance results. The circuits consist of the parallel combination of bulk resistance R _p and constant phase elements CPE. The simulated spectra show a good correlation with the experimental data.     

Investigation of ion transport in Li<Subscript>8</Subscript>ZrO<Subscript>6</Subscript> and Li<Subscript>6</Subscript>Zr<Subscript>2</Subscript>O<Subscript>7</Subscript> solid electrolytes

Lithium ionic conductivity and spin-lattice relaxation rates were measured in Li₈ZrO₆ and Li₆Zr₂O₇ solid electrolytes. It was found that the Li₈ZrO₆ solid electrolyte undergoes a transition to the superionic state in the temperature range 673–703 K. It was shown that Li⁺ ions are mobile in particular lattice positions of the Li₆Zr₂O₇ phase, and that ionic conductivity is monotonic at an activation energy of 79.4 kJ/mol.     

Studies on Al<Subscript>2</Subscript>O<Subscript>3</Subscript>, CuO,and TiO<Subscript>2</Subscript> water-based nanofluids: A comparative approach in laminar and turbulent flow

The Prandtl number, Reynolds number and Nusselt number are functions of thermophysical properties of nanofluids, and these numbers strongly influence the convective heat transfer coefficient. The thermophysical properties vary with volumetric concentration of nanofluids. Therefore, a comprehensive analysis was performed to evaluate the effects on the performance of nanofluids due to variations of density, specific heat, thermal conductivity and viscosity, which are functions of nanoparticle volume concentration. Three metallic oxides, aluminum oxide (Al₂O₃), copper oxide (CuO), and titanium dioxide (TiO₂), dispersed in water as the base fluid were studied. A convenient figure of merit, known as the Mouromtseff number, is used as a base of comparisonfor laminar and turbulent flows. The results indicated that the considered nanofluids can successfully replace water in specific applications for a single-phase forced convection flow in a tube.     

Structural and electrical properties of pure and H<Subscript>2</Subscript>SO<Subscript>4</Subscript> doped (PVA)<Subscript>0.7</Subscript>(NaI)<Subscript>0.3</Subscript> solid polymer electrolyte

Solid polymer electrolytes (SPE) based on poly-(vinyl alcohol) (PVA)_0.7 and sodium iodide (NaI)_0.3 complexed with sulfuric acid (SA) at different concentrations were prepared using solution casting technique. The structural properties of these electrolyte films were examined by X-ray diffraction (XRD) studies. The XRD data revealed that sulfuric acid disrupt the semi-crystalline nature of (PVA)_0.7(NaI)_0.3 and convert it into an amorphous phase. The proton conductivity and impedance of the electrolyte were studied with changing sulfuric acid concentration from 0 to 5.1 mol/liter (M). The highest conductivity of (PVA)_0.7(NaI)_0.3 matrix at room temperature was 10⁻⁵ S cm⁻¹ and this increased to 10⁻³ S cm⁻¹ with doping by 5.1 M sulfuric acid. The electrical conductivity (σ) and dielectric permittivity (ε′) of the solid polymer electrolyte in frequency range (500 Hz–1 MHz) and temperature range (300–400) K were carried out. The electrolyte with the highest electrical conductivity was used in the fabrication of a sodium battery with the configuration Na/SPE/MnO₂. The fabricated cells give open circuit voltage of 3.34 V and have an internal resistance of 4.5 kΩ.     

Electrical Properties of Intercalated Ag<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>MoSe<Subscript>2</Subscript> Compounds in Constant and Alternating Fields

On intercalated Ag_xMoSe₂ samples, in addition to temperature measurements of the direct current electrical resistivity, measurements of the alternating current resistivity using the impedance spectroscopy technique are carried out in a wide frequency range and at different temperatures. The activation behavior of the d.c. conductivity, which increases with increasing silver content in the samples, is shown. The a.c. conductivity undergoes frequency dispersion, described by a “universal dynamic response” (UDR). It is shown that the relaxation processes during charge transfer in a variable field are accelerated with increasing silver content in the samples and with increasing temperature. The data obtained are analyzed using the models of the band and hopping conduction.     

Infralow-frequency dielectric response of Pb<Subscript>3</Subscript>O<Subscript>4</Subscript> polycrystalline layers

This paper reports on the results of the investigation into the frequency dispersion of the capacitance and dielectric loss in capacitor structures based on red lead Pb₃O₄. It is established that, in the range of frequencies f = 1.50 × 10^?3?0.25 Hz, the capacitance decreases and the dielectric loss tangent increases with increasing frequency. The frequency dependence of the electrical conductivity in an alternating-current electric field indicates the applicability of the hopping model of charge transfer under normal conditions. The role of a lone electron pair of Pb²⁺ cations in dielectric polarization is discussed.     

Phase transition and electrical investigation in lithium copper pyrophosphate compound Li<Subscript>2</Subscript>CuP<Subscript>2</Subscript>O<Subscript>7</Subscript> using impedance spectroscopy

Lithium pyrophosphate compound Li₂CuP₂O₇ has been synthesized through solid state reaction method. FTIR and XRD results, realized at room temperature, indicate respectively the dominant feature of pyrophosphate anion (P₂O₇)^4? and a pure monoclinic phase with I2/a space group. Electrical and dielectric properties have been studied using impedance spectroscopy complex over a wide temperature (576–710 K) and frequency (209 Hz–1 MHz) range. From the direct and alternative conductivities (DC and AC), electrical conduction is found to be thermally activated process. The frequency-dependent AC conductivity obeys Jonscher’s universal power law σ_AC~Aω^s. The differential scanning calorimetry spectrum discloses phase transition at 622 K.     

Effect of Y-site and Ba-site substitution on thermal properties of YBa<Subscript>2</Subscript>Cu<Subscript>3</Subscript>O<Subscript>7−δ</Subscript>

The effect of partial replacement of Y site with Ca or Ba site with Sr on the thermal and electrical properties of YBa₂Cu₃O_7?δ superconductors was investigated. For Y(Ba_1?XSr_X)₂Cu₃O_7?δ system, the characteristic enhancement of the thermal conductivity κ(T) below the transition temperature T_c was decreased more slowly by substitution than that for (Y_1?XCa_X)Ba₂Cu₃O_7?δ system. Electron-phonon interaction in these systems were discussed based on the phonon heat conduction model under the weak coupling d-wave energy gap.     

Thermal conductivity and heat capacity of LuMgCu<Subscript>4</Subscript>

This paper reports on the measurements of the thermal conductivity κ and electrical resistivity ρ in the temperature range 5–300 K and the heat capacity at constant pressure C _p in the range 80–300 K for the metallic nonmagnetic compound LuMgCu₄. The experimental values of κ and C _p for the LuMgCu₄ compound are compared with the corresponding data available in the literature for the light heavy-fermion compound YbMgCu₄. It is shown that, in the low-temperature range (5–20 K), the phonon thermal conductivity κ_ph of YbMgCu₄ is lower than κ_ph of LuMgCu₄ as a result of phonon scattering from magnetic moment fluctuations of the Yb 4f electrons and, conversely, the heat capacity of LuMgCu₄ in the range 80–300 K is lower than that of YbMgCu₄ because the heat capacity of the latter compound has an additional magnetic component.     

Electrical properties,equivalent circuit,and dielectric relaxation studies on [(C<Subscript>3</Subscript>H<Subscript>7</Subscript>)<Subscript>4</Subscript>N]<Subscript>2</Subscript>Cd<Subscript>2</Subscript>Cl<Subscript>6</Subscript> polycrystalline

The Ac electrical conductivity and the dielectric relaxation properties of the [(C₃H₇)₄N]₂Cd₂Cl₆ polycrystalline sample have been investigated by means of impedance spectroscopy measurements over a wide range of frequencies and temperatures, 209 Hz–5 MHz and 361–418 K, respectively. The purpose is to make a difference between the electrical and dielectric properties of the polycrystalline sample and single crystal. Besides, a detailed analysis of the impedance spectrum suggests that the electrical properties of the material are strongly temperature-dependent. Plots of (Z" versus Z') are well fitted to an equivalent circuit model consisting of a series combination of grains and grains boundary elements. Moreover, the temperature dependence of the electrical conductivity in the different phases follows the Arrhenius law and the frequency dependence of σ (ω) follows the Jonscher’s universal dynamic law. Furthermore, the modulus plots can be characterized by full width at half height or in terms of a nonexperiential decay function φ(t) = exp(t/t)^β. Finally, the imaginary part of the permittivity constant is analyzed with the Cole–Cole formalism.     

Thermal expansion and thermal conductivity of CuGa<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>In<Subscript>x</Subscript>Te<Subscript>2</Subscript> solid solutions

The thermal expansion coefficients and the thermal conductivity of Bridgman-grown crystals of CuGa_1−x In_xTe₂ solid solutions are investigated. It is found that the thermal expansion coefficient varies with x linearly, while the thermal conductivity is minimal when x=0.5. The Debye temperature and the rms dynamic atomic displacements are calculated from experimental data. It is shown that the Debye temperature decreases and the rms displacements in the crystal lattice sharply increase as the In content in the solid solutions grows.     

Electrical characterization of the [N(CH<Subscript>3</Subscript>)<Subscript>4</Subscript>][N(C<Subscript>2</Subscript>H<Subscript>5</Subscript>)<Subscript>4</Subscript>]ZnCl<Subscript>4</Subscript> compound

The [N(CH₃)₄][N(C₂H₅)₄]ZnCl₄ compound has been synthesized by a solution-based chemical method. The X-ray diffraction study at room temperature revealed an orthorhombic system with P2₁2₁2 space group. The complex impedance has been investigated in the temperature and frequency ranges 420–520 K and 200 Hz–5 MHz, respectively. The grain interior and grain boundary contribution to the electrical response in the material have been identified. Dielectric data were analyzed using the complex electrical modulus M ^* for the sample at various temperature. The modulus plots can be characterized by full width at half height or in terms of a non-exponential decay function ϕ(t) = exp[(−t/τ) ^β ]. The detailed conductivity study indicated that the electrical conduction in the material is a thermally activated process. The variation of the AC conductivity with frequency at different temperatures obeys the Almond and West universal law.