Search Results (69)

In this article, the mechanism of relaxation polarization currents occurring at a constant temperature (isothermal process) in crystals with ionic-molecular chemical bonds (CIMBs) in an alternating electric field was investigated. Methods of the quasi-classical kinetic theory of dielectric relaxation, based on solutions of the nonlinear system of Fokker–Planck and Poisson equations (for the blocking electrode model) and perturbation theory (by expanding into an infinite series in powers of a dimensionless small parameter) were used. Generalized nonlinear mathematical expressions for calculating the complex amplitudes of relaxation modes of the volume-charge distribution of the main charge carriers (ions, protons, water molecules, etc.) were obtained. On this basis, formulas for the current density of relaxation polarization (for transient processes in a dielectric) in the k-th approximation of perturbation theory were constructed. The isothermal polarization currents are investigated in detail in the first four approximations (k = 1, 2, 3, 4) of perturbation theory. These expressions will be applied in the future to compare the results of theory and experiment, in analytical studies of the kinetics of isothermal ion-relaxation (in crystals with hydrogen bonds (HBC), proton-relaxation) polarization and in calculating the parameters of relaxers (molecular characteristics of charge carriers and crystal lattice parameters) in a wide range of field parameters (0.1–1000 MV/m) and temperatures (1–1550 K). Asymptotic (far from transient processes) recurrent formulas are constructed for complex amplitudes of relaxation modes and for the polarization current density in an arbitrary approximation k of perturbation theory with a multiplicity r by the polarizing field (a multiple of the fundamental frequency of the field). The high degree of reliability of the theoretical results obtained is justified by the complete agreement of the equations of the mathematical model for transient and stationary processes in the system with a harmonic external disturbance. This work is of a theoretical nature and is focused on the construction and analysis of nonlinear properties of a physical and mathematical model of isothermal ion-relaxation polarization in CIMB crystals under various parameters of electrical and temperature effects. The theoretical foundations for research (construction of equations and working formulas, algorithms, and computer programs for numerical calculations) of nonlinear kinetic phenomena during thermally stimulated relaxation polarization have been laid. This allows, with a higher degree of resolution of measuring instruments, to reveal the physical mechanisms of dielectric relaxation and conductivity and to calculate the parameters of a wide class of relaxators in dielectrics in a wide experimental temperature range (25–550 K). Full article

Temperature homeostasis is controlled by the vagus nerve. Thermal information is collected by thermoreceptors present in the viscera and driven across sensory neurons of the nodose ganglia (NG), which in turn send it to the hypothalamus. While transient receptor potential channels (TRPs) are traditionally considered for thermal transduction, TREK channels belonging to the two-pore domain K⁺ channels family are emerging as thermosensors, but their role in the NG remains understudied. Patch-clamp recordings revealed that increasing the temperature to physiological levels causes a hyperpolarization of the membrane potential followed by a depolarization and, despite physiological temperature increased the firing rate, we have demonstrated that TREK channels might be taking part in the excitability control by counteracting TRPs’ effects. In fact, single-channel experiments revealed an increase in TREK channel open probability and a subsequent rise in their activity in NG neurons. All this indicates that TREK channels, mainly TREK1, may be responsible along with TRPs for the maintenance of the membrane potential at physiological temperature in NG neurons. Full article

Power cable dielectrics must be tested to ascertain their insulation integrity after their design and manufacture. In Southern Africa, power cables must undergo testing in accordance with the South African National Standard (SANS) 1339. The SANS 1339 provides a destructive diagnostic method to evaluate voltage breakdown strength and water tree growth. The shortfall is that there is no provision for the non-destructive determination of the residual strength and assessment of the condition of the power cables. It is possible that non-destructive tests are available. However, a question arises as to how they compare in effectiveness, which is the intention of this study. Accelerated aging at 500 Hz was conducted on the water-retardant cross-linked polyethene (TR-XLPE) power cable sample specimens, each 10 m long, according to SANS 1339. Non-destructive diagnostic tests (Tan δ, IRC, and RVM) were conducted on accelerated-aged and unaged cable samples. The comparative results of the accelerated-aged and unaged XPLE power cable samples, when applying non-destructive diagnostic techniques, show consistency and reveal the extent of degradation in the tested cable samples. This study demonstrates that non-destructive diagnostic methods can be used to assess the extent of XLPE power cable insulation aging. Full article

Cross-linked polyethylene (XLPE) cables will gradually experience aging under various stresses during long-term operation, which may lead to faults and seriously affect the safe and stable operation of the power system. This article prepares aged cable samples by accelerating the thermal aging of XLPE cables, and combines frequency-domain dielectric spectroscopy (FDS) and the polarization–depolarization current method (PDC) for detection and analysis. By measuring the dielectric loss of aged cables using frequency-domain dielectric spectroscopy, it was found that the dielectric loss value in the low-frequency region significantly increases with aging time, indicating that aging leads to an increase in polarity groups and polarization loss. The high-frequency dielectric loss also significantly increases with the strengthening of dipole polarization. At the same time, using the polarization–depolarization current method to measure the polarization current and depolarization current of cables, it was found that the stable value of polarization current increases with aging time, further verifying the changes in the conductivity and polarization characteristics of insulation materials. Combining the broadband dielectric response characteristics of FDS (0.001 Hz–1 kHz) with the time-domain charge transfer analysis of PDC, the molecular structure degradation (dipole polarization enhancement) and interface defect accumulation (space charge effect) of cable aging are revealed from both frequency- and time-domain perspectives. The experimental results show that the integral value of the low-frequency region of the frequency-domain dielectric spectrum and the stable value of the polarization depolarization current are positively correlated with the aging time, and can make use of effective indicators to evaluate the aging state of XLPE cables. Full article

The synergistic combination of outstanding electrical properties and exceptional thermal stability holds significant implications for advancing piezoelectric ceramic applications. In this work, lead-free ((1−x)(0.94Bi_0.5Na_0.5TiO₃-0.06BaTiO₃)-xBiFeO₃ (x = 0.08, 0.10, 0.12)) ceramics were synthesized using a conventional solid-state method, with systematic investigation of phase evolution, microstructural characteristics, and their coupled effects on electromechanical performance and thermal stability. Rietveld refinement analysis revealed a rhombohedral–tetragonal (R–T) phase coexistence, where the tetragonal phase fraction maximized at x = 0.10. This structural optimization enabled the simultaneous enhancement of piezoelectricity and thermal resilience. The x = 0.10 composition achieved recorded values of d₃₃ = 132 pC/N, g₃₃ = 26.11 × 10⁻³ Vm/N, and a depolarization temperature T_d = 105 °C. These findings establish BiFeO₃ doping as a dual-functional strategy for developing high-performance lead-free ceramics. Full article

A cable accessory is a critical component in constructing high-voltage direct current (HVDC) power grids, and it is typically composed of multiple materials. Due to the discontinuity of the insulation medium, it is prone to failure. This study focuses on a two-layered composite insulation medium simplified from HVDC cable accessories, and its surface potential decay (SPD) characteristics are related to the space charge transport characteristics. Previous studies on surface charge migration have been limited and primarily focused on single-layered insulation materials. However, the actual insulation structure is mostly composite. Therefore, it is of great practical significance to explore the surface charge migration characteristics of two-layered structures. This study presents a bipolar charge transport model after pre-depositing surface charges to investigate the surface charge migration characteristics of an ethylene–propylene–diene monomer (EPDM)/polyethylene (PE) two-layered polymer film. The effects of charge injection and trap related to nano-doping, local defects, and thermal aging on the surface potential decay (SPD) and space charge distribution in EPDM/PE were analyzed. The results show that the increase in the electron injection barrier slows surface charge dissipation and inhibits charge accumulation at the interface. An increase in the trapping coefficient leads to a higher surface potential in the stable state and a greater space charge density. During the early depolarization stage, the SPD rate is weakly dependent on the trap depth, with charge migration primarily governed by the external electric field. Full article

Aceclofenac (ACF), a non-steroidal anti-inflammatory drug, was obtained in its amorphous state by cooling from melt. The glass transition was investigated using dielectric and calorimetric techniques, namely, dielectric relaxation spectroscopy (DRS), thermally stimulated depolarization currents (TSDC), and conventional and temperature-modulated differential scanning calorimetry (DSC and TM-DSC). The dynamic behavior in both the glassy and supercooled liquid states revealed multiple relaxation processes. Well below the glass transition, DRS was able to resolve two secondary relaxations, γ and β, the latter of which was also detectable by TSDC. The kinetic parameters indicated that both processes are associated with localized motions within the molecule. The main (α) relaxation was clearly observed by DRS and TSDC, and results from both techniques confirmed a non-Arrhenian temperature dependence of the relaxation times. However, the glass transition temperature (T_g) extrapolated from DRS data significantly differed from that obtained via TSDC, which in turn showed reasonable agreement with the calorimetric T_g (T_g-DSC = 9.2 °C). The values of the fragility index calculated by the three experimental techniques converged in attributing the character of a moderately fragile glass former to ACF. Above the α relaxation, TSDC showed a well-defined peak. In DRS, after “removing” the high-conductivity contribution using ε’ derivative analysis, a peak with shape parameters α_HN = β_HN = 1 was also detected. The origin of these peaks, found in the full supercooled liquid state, has been discussed in the context of structural and dynamic heterogeneity. This is supported by significant differences observed between the FTIR spectra of the amorphous and crystalline samples, which are likely related to aggregation differences resulting from variations in the hydrogen bonds between the two phases. Additionally, the pronounced decoupling between translational and relaxational motions, as deduced from the low value of the fractional exponent x = 0.72, derived from the fractional Debye–Stokes–Einstein (FDSE) relationship, further supports this interpretation. Full article

The influence of processing procedures and microstructural features on the functional properties of relaxor ferroelectric ceramics are of fundamental interest and directly relevant to their applications in dielectric capacitors and electromechanical sensors/actuators. In the present work, solid solutions of 0.65(K_0.5Bi_0.5)TiO₃-0.35(Ba_0.94Ca_0.06)(Ti_0.93Zr_0.07)O₃ (0.65KBT-0.35BCZT) were processed by solid-state reaction using two different procedures, distinguished in terms of mixed or separate calcination of the KBT and BCZT components and leading to homogeneous or core-shell-type relaxor ferroelectric ceramics, respectively. Systematic research was conducted on the impact of the processing techniques and air-quenching procedures on the structure and ferroelectric and electromechanical properties. Higher remanent polarization of the separately calcined materials was ascribed to the ferroelectric nature of the core regions, along with the non-ergodic relaxor ferroelectric response in the shell, which was enhanced by the quenching process. It was also demonstrated that the thermal depolarization temperature increased significantly after quenching, from ~100 to ~160 °C for the separately calcined ceramic, and from ~50 to ~130 °C for the mixed material; moreover, these effects are linked to notable improvements in the ferroelectric tetragonal phase content by air-quenching. Full article

This paper addresses the author’s current understanding of the physics of interactions in polymers under a voltage field excitation. The effect of a voltage field coupled with temperature to induce space charges and dipolar activity in dielectric materials can be measured by very sensitive electrometers. The resulting characterization methods, thermally stimulated depolarization (TSD) and thermal-windowing deconvolution (TWD), provide a powerful way to study local and cooperative relaxations in the amorphous state of matter that are, arguably, essential to understanding the glass transition, molecular motions in the rubbery and molten states and even the processes leading to crystallization. Specifically, this paper describes and tries to explain ‘interactive coupling’ between molecular motions in polymers by their dielectric relaxation characteristics when polymeric samples have been submitted to thermally induced polarization by a voltage field followed by depolarization at a constant heating rate. Interactive coupling results from the modulation of the local interactions by the collective aspect of those interactions, a recursive process pursuant to the dynamics of the interplay between the free volume and the conformation of dual-conformers, two fundamental basic units of the macromolecules introduced by this author in the “dual-phase” model of interactions. This model reconsiders the fundamentals of the TSD and TWD results in a different way: the origin of the dipoles formation, induced or permanent dipoles; the origin of the Wagner space charges and the T_g,ρ transition; the origin of the T_LL manifestation; the origin of the Debye elementary relaxations’ compensation or parallelism in a relaxation map; and finally, the dual-phase origin of their super-compensations. In other words, this paper is an attempt to link the fundamentals of TSD and TWD activation and deactivation of dipoles that produce a current signal with the statistical parameters of the “dual-phase” model of interactions underlying the Grain-Field Statistics. Full article

β-tricalcium phosphate (β-TCP) is a widely utilized resorbable bone graft material, whose surface charge can be modified by electrical polarization. However, the specific effects of such a charge modification on osteoblast and osteoclast functions remain insufficiently studied. In this work, electrically polarized β-TCP with a high surface charge density was synthesized and evaluated in vitro in terms of its physicochemical properties and biological activity. Polarization was performed to achieve a high surface charge density, which was quantified using a thermally stimulated depolarization current. The proliferation and differentiation of MC3T3-E1 osteoblast-like cells were assessed via WST-8 and alkaline phosphatase assays. Tartrate-resistant acid phosphatase (TRAP) activity and a resorption pit assay were used to evaluate the impact of surface charge on RAW264.7 osteoclast-like cell activity. Polarized β-TCP exhibited a surface charge of 1.3 mC cm⁻². Electrically polarized surfaces significantly enhanced osteoblast proliferation and differentiation. TRAP activity assays demonstrated effective osteoclast differentiation of RAW264.7 cells, with enhanced activity observed on charged surfaces. Resorption pit assays further revealed improved osteoclast resorption capacity on β-TCP surfaces with a polarized charge. These findings indicate that β-TCP with a highly dense surface charge promotes osteoblast proliferation and differentiation, as well as osteoclast activity and resorption capacity. Full article

In this study, we investigate the dielectric, electric, and pyroelectric properties of Ba_1−xCa_xTiO₃ (BCT) ceramics with compositions of x = 0.2, 0.25, and 0.3. The ceramics were synthesized using the solid-state reaction method. A microstructural analysis was performed using scanning electron microscopy (SEM), revealing that calcium concentration influences grain size and morphology, with BCT20 showing larger, hexagonal grains, while BCT25 and BCT30 exhibited smaller, irregular grains. Phase composition and crystalline structure were characterized via X-ray diffraction (XRD), which confirmed the absence of secondary phases and a predominantly tetragonal P4mm structure for BCT20 and BCT25. However, BCT30 showed an additional orthorhombic (Pbam) phase at 5.9 wt. % alongside the dominant tetragonal phase. Dielectric measurements revealed that increasing the calcium concentration shifts the temperature of dielectric permittivity maximum to lower values, correlating with a shift in the ferroelectric–paraelectric phase transition. Pyroelectric measurements indicated the highest pyroelectric current for BCT25, while BCT30 showed the maximum thermally stimulated depolarization current. Full article

Ba_0.75Ca_0.25TiO₃ ceramics were successfully synthesized by a simple solid-state reaction method. This study examined the influence of sintering temperature on the structure, microstructure, dielectric properties and electrical behavior of the material. The XRD analysis reveals that the tetragonal phase (P4mm) is dominant in all the synthesized materials, with those sintered at T = 1400 °C and T = 1450 °C being single-phase, while others exhibit a minor orthorhombic phase (Pbnm). Higher sintering temperatures promoted better grain boundary formation and larger grain sizes. The electric permittivity increased with temperature up to T = 1400 °C, followed by a sharp decline at T = 1450 °C. Additionally, the Curie temperature decreased with increasing sintering temperature, indicating changes in phase transition characteristics. Thermal analysis showed that higher sintering temperatures led to sharper heat capacity peaks, while pyroelectric and thermally stimulated depolarization currents were maximized at T = 1400 °C due to oxygen vacancies. These findings highlight the significant impact of sintering temperature on the material’s structural and functional properties. Full article

This paper studies the structural parameters and electrophysical properties (dielectric and piezo electric, as well as currents of thermostimulated depolarization) of samples of composition 0.20BiScO₃·0.45PbTiO₃·0.35PbMg_1/3Nb_2/3O₃ (or in short 0.20BS·0.45PT·0.35PMN) obtained by ceramic and melt-hardening methods of synthesis. In the ceramic method, the samples were obtained from the starting oxides by two-stage firing. In the melt method, amorphous precursors were first obtained from heat-treated and non-heat-treated starting oxide mixtures by melting and subsequent quenching under sharply gradient temperature conditions. Samples were obtained after grinding, pressing, and thermal annealing of the synthesized precursors, and four types of samples differing in size and shape of the intermediate precursor particles (crystallites) were obtained. The X-ray phase analysis showed that the predominant phase in the studied samples is the perovskite phase; in both types of samples, up to 5 wt.% of impurity phase with pyrochlore structure was also present. The samples of 0.20BS·0.45PT·0.35PMN exhibit dielectric properties characteristic of relaxor ferroelectrics, and the polarized samples exhibit a pronounced piezo effect with a piezo modulus value of d₃₃~200 pC/N. A comparative analysis of the properties of the samples obtained by different methods has been carried out. The essential advantage of the melt method is that its use allows obtaining varieties of four kinds of ferroelectric relaxors and reduces the time of synthesis of samples by 2–3 times. Full article

A novel method was proposed for the experimental investigation of wavefront distortion introduced to amplified radiation by pumped active elements in high-power laser amplifiers. The method is based on the simultaneous measurement of temperature distribution and the distribution of population density of the excited laser level in active elements. The underlying theory of the technique was presented; various factors affecting the accuracy of wavefront distortion determination were analyzed. The method was tested to study the wavefront distortion and the depolarization of radiation introduced by the Yb:YAG active element of a cryogenically cooled laser amplifier with high-power diode pumping. The focal length of the thermal lens was 0.40 ± 0.03 and 0.47 ± 0.05 m for the horizontal and vertical planes, respectively. The focal length of the electron lens was two orders of magnitude larger. The maximum value of losses induced by depolarization was 8.5%. Full article

The single crystals of CsI-Yb²⁺ were grown, and their spectroscopic studies were conducted. The observed luminescence in CsI-Yb²⁺ is due to 5d–4f transitions in Yb²⁺ ions. Using time-resolved spectroscopy, spin-allowed and spin-forbidden radiative transitions of ytterbium ions at room temperature were found. The excitation spectra of Yb²⁺ luminescence bands were obtained in the range of 3–45 eV. The mechanism of charge compensation of Yb²⁺ ions in a CsI crystal was also studied, the spectrum of the thermally stimulated depolarization current was measured, and the activation energies of the two observed peaks were calculated. These peaks belong to impurity–vacancy complexes in two different positions. The charge compensation of Yb²⁺ occurs via cation vacancies in the nearest-neighbor and next-nearest-neighbor positions.The Yb²⁺ ions are promising dopants for CsI scintillators and X-ray phosphors in combination with SiPM photodetectors. Full article