Activation Energy Of Electrical Conductivity Research Articles

Dissipation of Current Carriers in Lead Telluride Films

The mechanisms of current carrier scattering in polycrystalline lead telluride (PbTe) films deposited on glass substrates in the temperature range 77-300 K have been studied. The main attention is paid to scattering at the grain-to-grain limits, which is the dominant mechanism affecting the mobility of current carriers. In this work, a mathematical expression is obtained for calculating the mobility of current carriers in thin films, considering scattering on the surface and intergrain limits, which makes it possible to evaluate the influence of these mechanisms on the mobility of current carriers. The dependence of current carrier mobility in PbTe films on thickness and temperature has been studied. It has been established that the dominant scattering mechanism is scattering at grain boundaries. The activation energy of electrical conductivity was estimated, which is approximately 0.04-0.07 eV.

Facile Interfacial Reduction Suppresses Redox Chemical Expansion and Promotes the Polaronic to Ionic Transition in Mixed Conducting (Pr,Ce)O2-δ Nanoparticles.

Mixed ionic/electronic conductors (MIECs) are essential components of solid-state electrochemical devices, such as solid oxide fuel/electrolysis cells. For efficient performance, MIECs are typically nanostructured, to enhance the reaction kinetics. However, the effect of nanostructuring on MIEC chemo-mechanical coupling and transport properties, which also impact cell durability and efficiency, has not yet been well understood. In this work, Pr0.2Ce0.8O2-δ (PCO20) nanopowders were prepared by coprecipitation, then sintered in a modified dilatometer at three different temperatures (600, 725, and 850 °C) for microstructure evolution, resulting in three samples with different average particle sizes (23, 30, and 53 nm). The chemical strain and electronic/ionic conductivity were then measured simultaneously on stable nanostructures in four isotherms from 550 to 400 °C with steps in pO2 (1 to 10-4 atm O2). A microcrystalline bar was prepared and measured for comparison. Particle size reduction led to a monotonically decreasing isothermal redox chemical strain, confirmed by in situ high-temperature, controlled-atmosphere XRD measurements. The corresponding conductivity measurements provided defect chemical insight into the particle size-dependent chemical expansion behavior. The significant weakening of the pO2 dependence and decreased activation energy for electrical conduction with decreasing particle size indicated a decrease in the reduction enthalpy of PCO, shifting the transition from (Pr) polaronic to ionic behavior to higher pO2. STEM-EELS measurements confirmed the majority of Pr was reduced to 3+ in the nanoparticles, while Ce remained 4+. These results demonstrate suppression of deleterious chemical expansion and tailoring of the dominant charge carrier simply through controlling the particle size, providing insights for MIEC microstructural design.

Melting Behavior and Ionic Conduction of Multicomponent Carbonates Coexisting with Porous Oxides

Multicomponent systems of alkali carbonates indicate high electrical conductivity, high chemical and thermal conductivity, and low viscosity in the medium temperature range around 500°C, and are used as high temperature reaction media, thermocouples, and sensing materials for CO However, in electrochemical reactions, the high reactivity of carbonates is accompanied by the problem of corrosion of electrodes and reaction systems. We have studied ceria-based oxides and zirconia, which have high reactivity through surface treatment of CO2 absorbing media, and have examined the electrical and thermal properties of the composite materials with molten carbonate. Ceria-based oxides have been considered for application in solid oxide fuel cells as solid electrolytes, whereas γ-LiAlO2 has insulating properties and is used as an electrolyte in molten carbonate fuel cells. In this study, lithium carbonate, sodium carbonate, and potassium carbonate are used as the liquid phase, and mono-, binary-, and ternary complex carbonates or carbonates with eutectic compositions are used. The results are summarized on the effect of salt complexation on the improvement of electrical conductivity at low temperature ranges and the lowering of melting points.The solid phase was obtained by drying three types of γ-LiAlO2 (24.0 m2/g, 10.3 m2/g, 5.4 m2/g) and other various oxides such as α-Al2O3, MgO, ZrO2 etc. at 500°C for 2 hours under nitrogen. Li2CO3, Na2CO3, and K2CO3 were used for the carbonate phase and dried at 200°C for 48 hours under a carbon dioxide atmosphere. Eutectic carbonates were prepared by mixing them to form a eutectic composition. Each oxide powder was mixed thoroughly in a mortar to form carbonate at a given volume ratio. The sample was formed by pressurization and sintered at 500°C for 1 hour to obtain a tablet for the measurements of ionic conduction and thermal analysis.As shown in Figure 1, the activation energy of electrical conductivity increased near the solid phase in all cases. The range of influence from the solid phase decreased significantly with increasing carbonate polymorphism: 40 nm for the mono-salt system, 10 nm for the binary system, and about 2 nm for the ternary system. These melting point drops are also affected by the solid phase, but the effect of the distance from the solid phase is not so great. In the vicinity of the solid phase, the effect of the solid phase on ionic conduction is not as strong as that on the phase change, and the more numerous ions move, the less affected by the solid phase the system is. In this presentation, we will discuss the influence of the solid phase from a viewpoint of thermodynamics.Fig.1 Variation of ΔE a with apparent average thickness for various carbonates /inorganic powders coexisting systems. Carbonates: (a)Li2CO3, (b) (Li0.52Na0.48)2CO3, and (c) (Li0.435Na0.315K0.25)2CO3. Figure 1

Multi-scale structural regulation of negative temperature coefficient effect and electrical conduction mechanism of xSm2O3-(1-x) CaCu3Ti4O12 ceramics

Multi-scale structural regulation of negative temperature coefficient effect and electrical conduction mechanism of xSm2O3-(1-x) CaCu3Ti4O12 ceramics

Manganese dioxide nanoparticles and nanocomposites with carbon black. Synthesis, physical-chemical and electrical properties

In this study, α- and β-MnO2 and composites with carbon black (CB) were chemically synthesized and prepared through mechanical mixing respectively. The samples’ crystal structure, morphology, and electrical properties have been investigated herein. It is found that average particle sizes of 12–15 nm and 18–24 nm for α- and β-MnO2, respectively. The surface area and average pore volume of obtained samples of α- and β-MnO2 are 200 and 70 m2/g, and 3.2 and 5.3 nm, respectively. The electrical conductivity performances and activation energy behavior of samples have been analyzed. The correlation between the CB content in the composites and their electrical conductivity was established based on experimental data. The electrical conductivity of the α-MnO2/C monotonic increase from 1.31 to 18.6 S/m. There was a 7.5-fold increase of conductivity for α-MnO2 with 15 wt.% CB and almost a 30-fold increase for β-MnO2 with the corresponding CB content compared to the pure samples. In composite samples, the activation energy decreases from 0.069 to 0.041 eV and from 0.154 to 0.074 eV for α- and β- MnO2/C, respectively.

DISCUSSION OF THE MECHANISM OF THE ELECTRICAL CONDUCTIVITY OF PURE WATER IN THE FRAMEWORK OF THE BJERRUM MODEL

An alternative mechanism of electrical conductivity and ionization of molecules in pure water is considered. Calculation of the temperature dependence for the activation energy of ionization of water molecules was carried out using data on the value of its ionic product. The calculated activation energies for the ionization and flow processes show the presence of a certain proportionality between them. This suggests that the ionization of water is caused by intermolecular forces rather than intramolecular forces. Accordingly, the electrical conductivity of water is associated with the appearance and movement in it of L and D defects of hydrogen bonds between water molecules, which have significant electrical pseudo charges and are considered in the Bjerrum model for ice. This work proposes a new interpretation of the mechanism of ionization (pseudoionization) of molecules and generation of L and D defects in water. Rotation is considered not for one, but for two of its molecules in opposite directions with partial compensation of their angular momentum, and the breaking of not three bonds for one molecule, but four bonds with neighbors for two molecules. Moreover, these four neighbors do not include molecules from water clusters that have stronger bonds, since neighboring molecules with weaker bonds can be found for the process of rotation activation. Accordingly, the exponential contribution made by molecules from water clusters is absent or small in the ionization activation energy. In this way, the activation energy for the flow, which occurs throughout the entire volume of the liquid and automatically includes molecules from clusters, differs from the activation energy of electrical conductivity, which occurs for individual molecules in chains of bonds. The presence of a maximum in the ionic product of water near 250 ⁰C can be explained by the rapid decrease in the lifetime of L and D defects with heating, which prevents the use of the standard equation for accurate calculation of the ionization activation energy above 100...200 ⁰C. However, the presence of this maximum contradicts the generally accepted model of proton hopping between neighboring hydronium and water molecules in the mechanism of its electrical conductivity.

ОЦІНКА СТРУКТУРИ ШЛАКОВИХ РОЗПЛАВІВ НА ПІДСТАВІ АНАЛІЗУ ТЕМПЕРАТУРНИХ ЗАЛЕЖНОСТЕЙ В’ЯЗКОСТІ ТА ЕЛЕКТРОПРОВІДНОСТІ З ВИКОРИСТАННЯМ АДАПТИВНОЇ СЕГМЕНТНОЇ РЕГРЕСІЙНОЇ МОДЕЛІ

The expediency of using an adaptive segmented regression model for the analysis of logarithmic dependences of viscosity and electrical conductivity on temperature to assess the structure of slag melts is shown. Calculated values of the activation energies of viscosity ( ) and electrical conductivity ( ) in different temperature ranges. The obtained calculation results confirm that the viscosity and electrical conductivity of slag melts characterize the interaction of various structural particles (ions and/or their groups) and can be used in the study of the structure of slag melts. It was established that the activation energy of viscosity and electrical conductivity decreases as the temperature of slag melts increases. The performed calculations of the indicator n=En/Ex indicate that it can be a criterion for evaluating the structure of the slag melt, when n >1, the slag melt is a heterogeneous system, and when n < 1, it is a homogeneous system. Viscosity and electrical conductivity are interdependent properties and can be predicted if there is data on one of the properties, provided the value of n is known.

Физико-химические свойства растворов перхлората и тетрафторбората лития в смеси сульфолана и сернистого ангидрида

The temperature dependencies of physical and chemical properties (viscosity, density, electrical conductivity) and the melting temperature of 1M solutions of lithium salts (LiClO4 and LiBF4) in the mixture of sulfolane and sulfurous anhydride (∼1M) were studied. It was shown that the introduction of 1M (5% wt.) of sulfurous anhydride into 1M solutions of LiClO4 and LiBF4 in sulfolane increased the specific and corrected electrical conductivity, densities, activation energy of electrical conductivity and viscous flow of electrolyte solutions; and reduced viscosity and melting temperatures.

Non-isothermal crystallization kinetics and memory switching properties of Tl-Se-Ge-Sb chalcogenide semiconductor alloy for thermally stable phase change memory applications

Quaternary (Tl20Se70Ge10)0.85Sb0.15 chalcogenide glass was synthesized using melt-quenching and thermal evaporation techniques for bulk and thin film samples, and its amorphous character was confirmed by XRD. Based on different models of non-isothermal crystallization kinetics, the average values of the glass transition and the crystallization activation energies are 121.33 and 82.94 kJ mol−1, respectively. The crystallization mechanism in the examined composition is 2D nucleation growth, according to Avrami exponent Thermal parameters of the studied quaternary glass, like fragility fluctuation free volume reduced glass transition temperature thermal stability and glass formation ability were investigated and indicated that the (Tl20Se70Ge10)0.85Sb0.15 ChG exhibits a good ability of glass formation and thermal stability. The obtained results of the dc electrical conductivity are found to increase with temperature and decrease with film thickness. The electrical conduction activation energy (0.583 ± 0.004 eV) is thickness independent and the predominant conduction mechanism is the hopping of charge carriers in the band tail localized states. The () curves of (Tl20Se70Ge10)0.85Sb0.15 chalcogenide glass film samples were analyzed and shown to be appropriate for a memory switch. The mean value of the threshold voltage decreases exponentially as temperature increases, whereas it increases linearly as film thickness increases. The values of threshold voltage and threshold resistance activation energies are 0.282 ± 0.003 and 0.521 ± 0.004 eV, respectively. The obtained switching characteristics data were discussed in view of the electrothermal model motivated by current channel Joule heating. These findings highlight the suitability of the investigated composition for various optoelectronic applications, such as memory switching devices, optical data storage, phase-change memories and optical fibres sensing devices.

Structural, micro-structural, morphological, electrical spectroscopy and optical analysis of lithium-titanium oxide electronic material

Structural, micro-structural, morphological, electrical spectroscopy and optical analysis of lithium-titanium oxide electronic material

ELECTROCONDUCTIVITY OF MOLTEN FLiNaK AND FLiNaK–CeF<sub>3</sub>

The eutectic mixture LiF–NaF–KF (FLiNaK) is promising as a carrier salt for molten-salt reactors. Cerium fluoride CeF3 can be considered as a simulant of plutonium fluoride PuF3. In this work, the temperature dependence of the electrical conductivity of the molten ternary eutectic LiF–KF–NaF containing from 0 to 25 mol % cerium fluoride in the temperature range 480–777°C. FliNaK–CeF3 mixtures containing up to 25 mol. % of cerium fluoride were prepared directly in the experimental cell, dropping the required amount of CeF3 into the melt and keeping mixtures of a given composition for 12 h at temperatures exceeding the liquidus temperatures of the studied compositions. The electrolyte resistance was determined from impedance hodographs, which were taken using the Z-1500J impedance meter. A two-electrode cell with Pt electrodes was used. Analysis of the experimental values of the electrical conductivity of double and triple fluoride melts KF–LiF available in the literature; KF–NaF; LiF–NaF–KF shows that our data on the electrical conductivity of the LiF–NaF–KF (FLiNaK) eutectic mixture are consistent with the general trend in electrical conductivity with increasing KF concentration in the melt. A significant decrease in the specific electrical conductivity of the molten system and a slight increase in the activation energy of electrical conductivity with an increase in the concentration of cerium fluoride are shown. The temperature dependences of the electrical conductivity of the molten system were approximated by second-order polynomials. The formation of the \({\text{CeF}}_{6}^{{3 - }}\) complex ion in the melt was confirmed by spectral studies. The Raman spectra of molten FLiNaK and FliNaK–CeF3 mixtures containing 8 and 15 mol. % of cerium fluoride were recorded. With an increase in the concentration of CeF3 in the melt, the amount of \({\text{CeF}}_{6}^{{3 - }}\) complex ions increases, which leads to an increase in the intensity of the observed vibrational bands.

INVESTIGATION OF THE SPECIFIC ELECTRICAL CONDUCTIVITY OF RHENIUM-CONTAINING SOLUTIONS OF AMMONIUM CARBONATE AND CALCULATION OF ITS ACTIVATION ENERGY

The specific electrical conductivity dependence of aqueous solutions of ammonium carbonate and solutions of the ammonium carbonate—ammonium perrenate system on the reagents content in the range of their concentration of 0.1—1.8 mol/l for (NH4)2CO3, 0.01—0.1 mol/l for NH4ReO4 and solution temperatures in the range of 20-50 °C were investigated by the conductometric method. A linear increase in electrical conductivity with an increase in the temperature of electrolytes and a nonlinear increase with an increase in the concentration of reagents was revealed. The temperature coefficients values of electrical conductivity and the activation energy values of electrical conductivity in the studied range of concentrations and temperatures are calculated. A decrease in the activation energy of electrical conductivity with an increase in the temperature of the solution was noted. The calculated value of the activation energy of electrical conductivity indicates the diffusive nature of charge transfer.

Electrical performance and conductive mechanism of xLaCoO3-(1-x)Ba0.98Ca0.02Ti0.96Sn0.04O3 ceramics with NTC effect via chemical modification

Electrical performance and conductive mechanism of xLaCoO3-(1-x)Ba0.98Ca0.02Ti0.96Sn0.04O3 ceramics with NTC effect via chemical modification

Temperature-dependent electrical resistivity of tungsten oxide thin films

Temperature-dependent electrical resistivity of tungsten oxide thin films

High temperature dielectric properties of calcium zirconate

AbstractThe electrical properties of dense, high purity CaZrO3 discs, sintered at 1380°C with and without added ZrO2, were investigated up to 950°C. Dielectric constant, loss tangent, and electrical conductivity were measured from 25 to 725°C, and the real and imaginary impedances were measured between 800 and 950°C by impedance spectroscopy techniques. Dielectric constant increased by 8% above 300°C and loss tangent increased from .1% at 25°C to ∼2% above 300°C. Activation energy of electrical conductivity determined between 300°C and 950°C by alternative current (AC) and direct current (DC) measurements. These results indicate that CaZrO3 could be a useful dielectric material for capacitor applications up to 500°C. A reported decrease in conductivity due to addition of excess ZrO2 into stoichiometric CaZrO3 could not be confirmed.

Study of the Resistive Properties of Lead Silicate Glasses after Chemical Impact

The change in the resistive characteristics of lead silicate glasses (LSGs) after treatment in alkaline and acid solutions is studied. It is established that the chemical treatment of glasses and, accordingly, blanks of microchannel plates (MCPs) affects the high-temperature ionic conductivity at a constant activation energy of electrical conductivity. It is shown that the treatment of glasses in NaOH and HF solutions can significantly change the electrical resistance.

ELECTRICAL CHARACTERISTICS OF BISMUTH-CONTAINING CERIUM OXIDE

Ceramics Ce0.9Bi0.1O2 – ? was obtained by solid-phase synthesis. It is shown that the obtained samples have a cubic fluorite structure with the space symmetry group Fm3m. The electrical properties of the Ce0.9Bi0.1O2 – ? solid solution were studied by ac impedance spectrometry. It has been established that the activation energy of electrical conductivity has two sections 0.51 eV (400 – 680 ?С) and 1.6 eV (680 – 800 ?С), the activation energy of the dielectric relaxation process was 0.88 eV.

Chemical bottom-up approach for inorganic single-atomic layers aiming beyond graphene.

A chemical bottom-up approach for single-atomic-layered materials like graphene is attractive due to the possibility of introducing functions. This article includes the synthesis and properties of borophene-oxide and metalladithiolene layers, which are reported as inorganic materials. They have graphene-like two-dimensional networks that enable conjugated structures. Their atomically thin layers are also available by dissolution or synthetic methods. Their two-dimensional electronic features are evaluated from the activation energies for electrical conduction, focusing on the anisotropic features of borophene-oxide layers and the switching abilities of metalladithiolene layers.

Physical insights into the grain size effect on the electrical properties of nanocrystalline La2Zr2O7 pyrochlores

Physical insights into the grain size effect on the electrical properties of nanocrystalline La2Zr2O7 pyrochlores

Optical and electrical properties of copper alumina nanoparticles reinforced chlorinated polyethylene composites for optoelectronic devices

The incorporation of transition metal oxide fillers into the polymer matrix through solution mixing polymerization imparts enhanced electrical and thermal properties. The present work focused on the optical properties, crystallinity, thermal stability, temperature-dependent conductivity, dielectric constant and modulus of chlorinated polyethylene/copper alumina (CPE/Cu–Al 2 O 3 ) nanocomposites. Optical absorption measured using an ultraviolet–visible (UV–visible) spectrometer shows enhanced intensity and a blue shift for CPE/Cu–Al 2 O 3 nanocomposites. The bandgap energy of CPE/Cu–Al 2 O 3 nanocomposites was lower than pure CPE and minimum bandgap energy was recorded for a 7 wt% composites. The X-ray diffraction demonstrates that Cu–Al 2 O 3 nanoparticles were uniformly introduced into the CPE matrix. Thermogravimetric analysis (TGA) manifests improved thermal stability of nanocomposites. Dielectric properties decrease with frequency, whereas AC conductivity increases with frequency, and both AC conductivity and dielectric properties increase with temperature. The maximum AC conductivity and dielectric constant were obtained for 7 wt % nanofiller loaded sample. For all systems, the activation energy for electrical conductivity decreases with rising temperatures. The experimental dielectric constant values of CPE nanocomposites were correlated with different theoretical models. The Bruggeman model was in good agreement with the experimental permittivity. The impedance experiments showed a decreasing trend with temperature, indicating the semiconducting nature of prepared nanocomposites. • CPE loaded with different contents of Cu–Al2O3 nanoparticles were synthesized by a simple solution mixing method. • The nanocomposites were characterized for their optical, thermal, and dielectric properties. • Temperature and frequency had a pivotal role in the dielectric parameters, conductivity and modulus properties. • The experimental dielectric constant values were in good agreement with Bruggeman's model.