Permittivity Research Articles

TOPO-decanoic acid based DES – Structural insights using DFT, physico-chemical investigations and extraction efficiency of DES diluted with chloroform

Deep eutectic solvents (DESs) are recently regarded as evolving candidates in the field of separation science in order to achieve sustainability. In the present work, hydrophobic TOPO-Decanoic acid DES has been synthesized and scrutinized by FTIR and 1HNMR studies. The structures of TOPO (Tri-octyl phosphine oxide), decanoic acid, chloroform, DES and DES + chloroform have been optimized employing B3LYP functional using DFT-D3 of Grimme’s method. The HOMO-LUMO (Eg) energy gap, bond lengths, mulliken charges,dipole moment and interaction energy has been evaluated using DFT. The geometry optimization provides the bond parameters which explain about the existence of non-bonded interactions. DES and DES + chloroform show more reactiveness as compared to its constituents evident from the chemical potential value. Physico-chemical properties such as density, volumetric (V), dielectric constant (ε), refractive index (nD) and ultrasonic velocity (U) of the hydrophobic TOPO-Decanoic acid DES diluted with polar cosolvent chloroform have been determined over a wide range of mole fraction of DES at 298.15 K. The excess properties such as VE, εE, nDE and UE have been calculated to predict the type of inter-molecular interaction existing within the components of the DES diluted chloroform mixture. Different mixing rules have been used to estimate properties such as dielectric permittivity, refractive index and ultrasonic velocity. Various acoustic parameters such as Z, βs, and (Lf)mix of binary mixtures are evaluated to predict about the presence of inter molecular interactions within the mixture components. The prepared hydrophobic eutectic mixture in chloroform has been further used for extraction of Y (III) and Eu (III). The solvent extraction of Eu (III) showed better performance as compared to that of Y (III).

Investigating the dielectric characteristics, electrical conduction mechanisms, morphology, and structural features of mullite via sol-gel synthesis at low temperatures

This research explores the fabrication of mullite precursor powder utilizing the sol-gel process at low temperatures. Silicon tetraethoxide (Si(C2H5O)4) and aluminum nitrate nonahydrate (Al(NO3)3.9H2O) were employed as the sources of SiO2 and Al2O3 oxides, respectively. Various analytical techniques, such as Fourier transform infrared spectroscopy (FTIR), thermogravimetry (TG), dilatometry, differential thermal analysis (DTA), and X-ray powder diffractometer (XRD), were utilized to investigate the formation and crystallization of the amorphous powder. The microstructure of specimens sintered at 1600 °C for 1 h was examined utilizing scanning electron microscopy (SEM). Measurements of hardness (HV) and coefficient of thermal expansion (CTE) were conducted on mullite samples heated to 1600 °C and then cooled, revealing an increase in HV from 888 to 1000 HV as the sintering temperature rose from 1500 to 1600 °C. The CTE of mullite within the temperature range of 50–1300 °C was determined as 5.23 × 10−6/°C. Additionally, the dielectric and electrical characterization of mullite was analyzed utilizing complex impedance spectroscopy at a frequency of 0.1–106 Hz and conductivity measurements over a temperature range of 40–400 °C. The real and imaginary parts of the dielectric permittivity exhibited frequency-dependent and temperature-dependent behaviors. Significantly, the observed variations in the imaginary component of the modulus and impedance maximum frequency point to a relaxation process that is not Debye-type, with calculated activation energies (Ea) consistent across different methods.

Outstanding dielectric permittivity and humidity sensitivity in (Y/Sb) co[sbnd]doped TiO2 ceramics with rapid response/recovery time

The synthesized (Y0.5Sb0.5)xTi1-xO2 (YSTO) ceramics (x=0.005 and 0.05) were investigated for their potential application in humidity sensors. The rutile phase of TiO2 for YSTO ceramics was confirmed. SEM images revealed dense microstructures, with relative densities and average grain sizes decreasing with doping concentrations. YSTO ceramics exhibited outstanding dielectric constants (ε′∼ 6.617.31×104) and low loss tangents (tanδ∼0.0190.067) at 25°C and 1 kHz. Capacitive humidity sensing properties demonstrated significant increases in capacitance with rising relative humidity (%RH) levels, with sensitivities of 165 and 386 pF/%RH. Hysteresis analysis showed narrow loops with low hysteresis error (γH∼1.4 and 2.0 %). Rapid response (∼9 s) and recovery (∼7 and 4 s) times, with stable repeatability, were observed. The presence of VO•• and SbTi• was confirmed, enhancing humidity sensing through chemical absorption reactions. This analysis underscores the potential of YSTO ceramics for humidity sensors, emphasizing the role of microstructural characteristics and induced defects in sensor performance, which is vital for the development of advanced sensing technology.

Efficient determination of Born-effective charges, LO-TO splitting, and Raman tensors of solids with a real-space atom-centered deep learning approach

We introduce a deep neural network (DNN) framework called the Real-space Atomic Decomposition NETwork (radnet), which is capable of making accurate predictions of polarization and of electronic dielectric permittivity tensors in solids and aims to address limitations of previously available machine learning models for Raman predictions in periodic systems. This framework builds on previous, atom-centered approaches while utilizing deep convolutional neural networks. We report excellent accuracies on direct predictions for two prototypical examples: GaAs and BN. We then use automatic differentiation to efficiently calculate the Born-effective charges, longitudinal optical-transverse optical (LO-TO) splitting frequencies, and Raman tensors of these materials. We compute the Raman spectra, and find agreement with ab initio results. Lastly, we explore ways to generalize the predictions of polarization while taking into account periodic boundary conditions and symmetries.

Enhanced dielectric and electrical properties of Ba(1−x)Nd2x∕3Zr0.1Ti0.9O3 (0.00 ≤ x ≤ 0.04) electroceramics for high temperature-based energy storage devices

The demand for high-temperature endurable dielectric materials with higher thermal stability in electronic systems operating under extreme temperatures sets a significant channel for the electronic industry. This work focuses on the dielectric and impedance behavior for lead-free Ba1−xNd2x∕3Zr0.1Ti0.9O3 (BNZT); (0.00 ≤x≤ 0.04) between 300 ∘C – 400 ∘C and synthesized by conventional solid-state reaction method at optimum temperatures. Structural characterizations confirmed the tetragonal (P4mm symmetry) structure formations for the BNZT ceramics. XPS analysis confirmed the Nd-substitution at the Ba-site in the BNZT ceramics. FE-SEM study showed grain growth reduction with enhanced grain boundaries. The dielectric study showed lower dielectric loss with enhanced dielectric permittivity at high temperatures. Impedance analysis confirmed the negative temperature coefficient of resistance (NTCR) and non-Debye type behavior with higher thermal stability. Singly-ionized oxygen vacancies mainly govern the conduction process in BNZT ceramics. Enhanced dielectric and impedance properties suggest that Nd-substituted BNZT electroceramics are promising materials for applications in high-temperature-based energy storage systems.

Droplet Electrophoresis with Internal Free Ions: Effect of Permittivity Changes in the Electric Double Layer.

Droplet electrophoresis (EP) is of interest in biological systems, microfluidics, and separation techniques. We investigate EP of an oil droplet that contains free ions and is stabilized in an electrolyte solution through an amphoteric surfactant. The presence of mobile ions within the droplet leads to the creation of a distinct nonzero space charge density inside the droplet and consequently, formation of an inner EDL inside the droplet in addition to the traditionally considered outside EDL. While we assume the permittivity inside the inner EDL to remain constant, we consider both the case of constant and variable permittivity in the outer EDL. Our findings demonstrate a change in the droplet direction of motion in the electric field when transitioning from acidic to alkaline pH, regardless of permittivity and ionic strength in both oil and electrolyte. We further find a significant reduction in the magnitude of droplet velocity in the case of a variable permittivity due to reduction of the local space charge density within the EDL surrounding the droplet. When decreasing the viscosity ratio of the oil to the electrolyte, in all cases we find a reduction in droplet velocity. This decline is attributed mostly to the formation and strength of a vortex around the droplet. We finally demonstrate that with constant permittivity in the outer EDL, the variation in κaouter has a more significant effect on the droplet's EP velocity than altering κainner. However, in cases where the body forces inside of the droplet dominate, minor changes in the outer electrolyte concentration have no influence on the droplet motion, which is relevant for biological colloids that can contain significant free internal charges. Our results are important for the manipulation of biological colloids, water and waste treatment such as lubricant removal from processing streams.

How Molecular Orientation Affects the Static Permittivity Profile of the Polar and Nonpolar Liquid-Liquid Interface.

The dielectric permittivity across the liquid-liquid interface presents an intrinsic response, with respect to the instantaneous interface reference. We hypothesize that dielectric responses across the nonpolar and polar liquid-liquid interfaces have different behaviors and underlying mechanisms. Molecular dynamics simulations were used to compare and contrast the dielectric response of a nonpolar (1,2-dichloroethane/water) and a polar (1-octanol/water) liquid-liquid interface system. We found that the enhanced dielectric permittivity at the nonpolar interface is attributed to the increased water dipole orientation and polarization density. In the case of the polar interface, strong association of the immiscible solvents inhibits the molecular dipole orientation, counteracting the effect from the enhanced surface water polarization density and resulting in a standard dielectric response. Detailed knowledge of the hydrogen bond networks and molecular dipole orientation with respect to the specific instantaneous interfacial and bulk regions reveals the effect of molecular proximity and the interaction with the opposing interfacial molecules on the mechanism of the dielectric permittivity response across the liquid-liquid interface phase boundary.

Innovative enhancements in polymer nanocomposites: Integrating ZnO nanorods into Hydroxypropyl methylcellulose/Polyvinyl pyrrolidone blend for advanced energy storage devices

Polymer nanocomposites are promising for various industrial and scientific applications due to their flexibility, diverse functionalities, and unique properties. In this study, zinc oxide nanorods (ZnO NRs) were incorporated into a blend of polymers (Hydroxypropyl methylcellulose - HPMC and Polyvinyl pyrrolidone - PVP) using a solution-casting technique, with concentrations varying from 2 % to 8 % by weight. Transmission electron microscopy (TEM) revealed that the ZnO NRs had an average diameter of 140 nm and a length of 3.22 μm. X-ray diffraction (XRD) analysis showed reduced crystallinity in the samples as the ZnO NR content increased. Fourier-transform infrared spectroscopy (FTIR) indicated changes in vibrational peaks due to interactions between functional groups in the blend and the nanorods. The addition of ZnO NRs significantly influenced the optical bandgap energies and UV/visible light absorption spectra of the samples. The bandgap of the nanocomposites significantly decreased upon ZnO NR incorporation, with direct and indirect bandgaps ranging from 5.19 to 4.70 eV and 4.74–3.66 eV, respectively. Electrical conductivity and dielectric characteristics were assessed across frequencies ranging from 0.1 to 10 MHz, revealing increasing AC conductivity, dielectric permittivity, and dielectric loss with higher ZnO NR content. Notably, at 10 Hz, the electrical conductivity increased from 3.5 × 10⁻12 S/m to 3.62 × 10⁻10 S/m upon loading with ZnO NR. The combination of adjustable optical bandgaps, frequency-dependent AC conductivity, and a wide range of tunable permittivity highlights the potential of these HPMC/PVP-ZnO NR nanocomposites for developing flexible optoelectronic and energy storage devices.

Innovative Nanostructuring of Li–Zn ferrite/graphene composites with tunable properties

The Li-ferrite and graphene oxide (GO) nanocomposites, denoted as (Li0.5-x/2ZnₓFe2.5-x/2O4: x = 0.25), were produced through ultrasonication. The wet method generated Li-ferrite, while the Hummers' method synthesized the GO. X-ray diffraction (XRD) was used to validate the development of Li-ferrite and GO in the nanocomposites. The dimensions of the crystal were determined between 41 and 52 nm, and the porosity of the composites increased with the higher quantity of GO. The scanning electron micrographs (SEM) of ferrites illustrated the formation of uniform and well-defined grains with consistent shapes, exhibiting properties well-suited for effective microwave absorption. The electrical resistance of spinel ferrite was measured at approximately 3.34 × 1011 Ω-cm and significantly lowered as the fraction of GO increased at ambient temperature. As per Maxwell Wagner's model, the electrical permittivity exhibited interfacial polarization with distinct real and imaginary components. The AC conductivity exhibited a positive correlation with the GO content due to the conductive properties of GO and the improved charge hopping mechanism. The frequency exponent parameter's value falls from 0.36 to 0.95 b y the Jonscher's Power law. The magnetic susceptibility of all the samples exhibited a progressive decrease as the temperature increased. The choice of using lithium-based ferrite as filler is made to strengthen the ferrite/GO composites and improve their magnetic and electrical properties. This is undertaken to harness these composites for high-frequency applications, such as their use as microwave absorbers in microwave devices.

Effect of BaTiO3 Filler Modification with Multiwalled Carbon Nanotubes on Electric Properties of Polymer Nanocomposites.

Two ranges of dielectric permittivity (k) increase in polymer composites upon the modification of BaTiO3 filler with multiwalled carbon nanotubes (MWCNTs) are shown for the first time. The first increase in permittivity is observed at low MWCNT content in the composite (approximately 0.07 vol.%) without a considerable increase in dielectric loss tangent and electrical conductivity. This effect is determined by the intensification of filler-polymer interactions caused by the nanotubes, which introduce Brønsted acidic centers on the modified filler surface and thus promote interactions with the cyanoethyl ester of polyvinyl alcohol (CEPVA) polymer binder. Consequently, the structure of the composites becomes more uniform: the permittivity increase is accompanied by a decrease in the lacunarity (nonuniformity) of the structure and an increase in scale invariance, which characterizes the self-similarity of the composite structure. The permittivity of the composites in the first range follows a modified Lichtenecker equation, including the content of Brønsted acidic centers as a parameter. The second permittivity growth range features a drastic increase in the dielectric loss tangent and conductivity corresponding to the percolation effect with the threshold at 0.3 vol.% of MWCNTs.

New Series of Hydrogen-Bonded Liquid Crystal with High Birefringence and Conductivity.

Liquid crystals with high dielectric anisotropy, low operational thresholds, and significant birefringence (Δn) represent a key focus in soft matter research. This work introduces a novel series of hydrogen-bonded liquid crystals (HBLCs) derived from 4-n-alkoxybenzoic, 4-alkoxy-3-fluorobenzoic derivatives (nOBAF), 4-alkoxy-2,3-fluorobenzoic derivatives (nOBAFF), and 2-fluoro-4-nitrobenzoic acid. The HBLCs were characterized using Fourier transform infrared spectroscopy, and their thermal behavior was evaluated via differential scanning calorimetry. Optical observations were conducted using polarized optical microscopy. The results indicate that mixtures containing benzoic acid with a bilateral fluorine substituent exhibit both SmA and SmC phases, while those with a unilateral fluorine substituent exhibit nematic and SmA phases. Moreover, an increase in the length of the alkoxy chain results in an expanded mesophase temperature range. This study demonstrates that the presence of a fluorine substituent and the incorporation of an NO2 group in the molecular structure result in an increase in dielectric permittivity, DC conductivity, dielectric anisotropy, and birefringence.

A novel method to fabricate curved piezoelectric composites with high piezoelectric phase volume fraction

Underwater acoustic transducer based on high piezoelectric phase volume fraction, large thickness, large area and curved piezoelectric composites (PC) possess wider beam width, higher source level and better directivity. However, the curved PC with large size is difficult to fabricate. The preparation of curved PC with large size and high piezoelectric phase volume fraction is even more tricky. The reported methods have risks of depolarization, deformation and poor periodicity and are not suitable for preparing PC with high piezoelectric phase volume fraction and large thickness. In this work, we proposed a novel fabrication method of the shaped-mold-assisted dice and fill technology. The 1–3 PC with high piezoelectric ceramic volume fraction of 80 %, thickness of 4.3 mm and area of 340 mm × 77 mm and the 2-2 PC with high piezoelectric ceramic volume fraction of 89.5 %, thickness of 5 mm and area of 262 mm × 20 mm were fabricated. The piezoelectric coefficient d33 and relative constant stress permittivity ε33T/ε0 of 1–3 and 2-2 PCs were comparable to piezoelectric phase itself. In addition, both 1–3 and 2-2 PCs exhibited a favorable performance consistency. This method solved the problem of limited cutting depth of thin blade, realizing PC with the structure of high piezoelectric phase volume fraction (＞ 70 %) and large thickness (＞ 3 mm) and eliminates the risk of depolarization, deformation and poor periodicity. This work enabled the potential for achieving large area, high piezoelectric phase volume and special-shaped PCs, which offers new ideas for designing innovative acoustic transducers and facilitates the progress of acoustic sensing technology.

Effect of NiO and Al2O3 on the Curie temperature, microstructure, and dielectric properties of Ba0.5Sr0.5TiO3 ceramics

AbstractA series of new x(yNiO/zAl2O3)‐(1–x)Ba0.5Sr0.5TiO3 (x = 10, 30, and 50 wt.%, y = 1, 1.3, 1.5, z = 1, 1.3, and 1.5 mol) ceramics were prepared using the solid‐phase method. The effects of the spinel oxides on the microstructure, lattice vibrations, and dielectric properties of Ba0.5Sr0.5TiO3 were assessed. When NiO and Al2O3 were present in equal quantities, they reacted to form NiAl2O4. Under the recombination effect, the dielectric permittivity of Ba0.5Sr0.5TiO3 was effectively reduced, the Curie temperature (Tc) was increased, and tunability gradually increased. The Tc value was not significantly altered when NiO was in excess. Impurity phases were generated, and the Tc value decreased when Al2O3 was in excess. This study elucidated the unique role of the spinel structure. The 50 wt.%(NiO/Al2O3)‐50 wt.%Ba0.5Sr0.5TiO3 had excellent microwave dielectric properties, with dielectric permittivity, tunability, and Q values of 300, 18.7%, and 357, respectively.

Understanding of the correlation of structural and microwave dielectric performance of (1-x)MgTiO3 - xCaTiO3 ceramics for dielectric resonator antenna applications

In this article, the effect of CaTiO3 on the structural and microwave dielectric characteristics of MgTiO3 has been discussed. The (1-x)MgTiO3 - xCaTiO3 (abbreviated as (1-x)MT- xCT) for x = 0.025, 0.05, 0.075, 0.1 ceramics have been developed using a solid-state reaction route. The structural as well as morphological characteristics of specimens have been observed by employing X-ray diffraction and scanning electron microscope methods. The Rietveld refinement technique of X-ray diffraction data have been conducted for the refinement of structural phases. It suggests that two crystallographic phases have been present in all materials. The SEM images display dense well-identified grains of (1-x)MT - xCT (for x = 0.025–0.1) ceramics. The Raman spectroscopy method has been employed to detect the symmetry of ceramics and modes of vibration of the materials. The microwave dielectric characteristics like dielectric permittivity (εr), loss (tanδ), quality factor (Q×f), and temperature coefficient at resonant frequency (τf) of (1-x)MT - xCT (for x = 0.025–0.1) ceramics have been thoroughly investigated. The bond strength, bond valency, bond energy, and tolerance factor of (1-x)MT - xCT (for x = 0.025–0.1) materials have been evaluated and their relation with microwave dielectric characteristics has been discussed. The (1-x)MT - xCT (for x = 0.025–0.1) ceramics show excellent dielectric properties with near to zero τf. In addition, DRAs have been designed with (1-x)MT - xCT (for x = 0.025–0.1) materials as dielectric resonators and various antenna properties have been studied with the help of HFSS software. This work suggests that (1-x)MT - xCT for (x=0.05) material can be a promising candidate for DRA applications working in the C band.

Rietveld refined structural, optical and temperature dependent impedance spectroscopy of NiO–ZnO heterostructure composite: Synthesized through solid state method for high-frequency devices

Multifunctional NiO–ZnO heterostructure composite powder is economically synthesized through a solid-state route having a crystallite size of 23 (±2) nm. Chemical composition is identified through FTIR, the peak associated with Zn–O is detected at 1049 cm−1. However, the peaks detected at 870 cm−1 and 590 cm−1 show Ni–O stretching vibrations. UV-DRS technique is employed to estimate the energy band gap (Eg) around 3.18 eV. The impedance studies confirmed the presence of a non-Debye-type relaxation mechanism, electrical parameters confirm the contribution of electroactive regions i.e. grains and interfaces. An equivalent circuit model (R-CPE) is employed to measure various electrical parameters. Adiabatic small polaron hopping model is applied to estimate activation energies for Ni+2 (0.30 eV), Zn+2 (0.35 eV), and bulk (0.32 eV) respectively. The hopping length at the interface is estimated at around 0.8 Å by employing Mott's variable range hopping model. Jonscher's power law (JPL) is used to fit ac conductivity data, and conclude activation energy around 0.3 eV. The conduction mechanism through the whole frequency range (1–107 Hz) is governed by correlated barrier hopping. Various physical parameters i.e. binding energy (Wm), hopping length, and barrier height compared throughout the whole temperature range (313–393 K). The rate of increase in real permittivity at low frequency is related to the disorder of the cation at sublattices. These results deduced potential for NiO–ZnO heterostructure composite for high dielectric permittivity with low tangent loss for high energy storage applications.

Investigation of an absorption plasmonic electro-optical modulator based on the free carrier dispersion effect in the aluminum doped zinc oxide layer

A plasmonic electro-optical modulator, which is based on the free carrier dispersion effect, has been introduced here. The structure of the proposed modulator is a substrate of fused silica/gold/aluminum doped zinc oxide/hafnium dioxide/gold/air. The free carrier dispersion effect occurs in the aluminum doped zinc oxide (AZO) layer. As the electrical permittivity of the AZO layer is near zero (the epsilon near zero effect) at a wavelength of 1.55 μm, the amplitude of an electrical field is high in this layer, therefore, the modulator is highly sensitive to the varying refractive index of this layer. By applying a voltage to two gold layers, the electrical charge density changes in the AZO layer. Therefore, the real and imaginary parts of the refractive index have been changed, which led to a change in the absorption of the modulator. In order to obtain the charge density distribution in the AZO layer, the Poisson equation is solved by using the finite difference method. To investigate modulator absorption, the Nelder-Mead method is implemented in order to solve the dispersion equation numerically. Finally, the magnetic field, the electric field, and the time average of the Poynting vector have been given by using the least squares approximation method.

Structural elucidation, morphological properties, dielectric properties and their physical interpretation of cerium-substituted cobalt and barium-based M-type hexagonal nano ferrites

This research uses the sol–gel method to look into how adding Co2+ and Ce3+ dopant cations changes the structure, shape, and electrical properties of M-type Ba hexagonal ferrites that have been synthesized. x-ray diffraction (XRD) analysis confirms the successful formation of the targeted hexagonal M-type crystal structure. We observed a reduction in unit cell volume and lattice parameters as the dopant concentration increased, indicating the effective incorporation of dopant ions into the crystal lattice. When the doping process happened, needle-like grain shapes appeared, which could be seen with a field emission scanning electron microscope (FESEM). As the concentration of the dopant increased, the dielectric spectroscopic measurements revealed an increase in the loss tangent (tan δ) from 0.05 to 3.68, and a decrease in the dielectric constant (ε′) from 283 to 3.41. This suggests a reduction in polarization and dielectric permittivity, as well as increased energy dissipation within the material. The electric modulus spectra showed relaxation behaviour that was non-Debye-type, which is another sign that there are complex and multifaceted ways for charges to move. The measurements of relaxation time and AC conductivity showed that the relaxation intervals were not regular and that the conductivity dropped from 2.22*10–4 Ω−1m−1 to 1.4*10–7 Ω−1m−1 as the doping concentration increased. Based on these findings, it seems that the processes of conductivity and dielectric relaxation play a big role in how charges move around in the doped ferrites. We validated complex impedance data obtained through electrochemical impedance spectroscopy (EIS) software against calculated impedance values. The derived grain and grain boundary characteristics also agreed with the observed grain distribution and boundaries from the micrographs, further corroborating the analysis.

Electric and dielectric responses of Au/n-Si structure by Mn doped PVC interfacial layers

This paper has investigated and compared the impact of polyvinyl chloride (PVC) without/with manganese (Mn) metallic nanoparticles interfacial layer on the electric and impedance characteristics of Schottky diode (SD) with a structure of Au/n-Si (MS). The structures of these two metal-polymer-semiconductor (MPS) SDs are Au/PVC/n-Si and Au/PVC:Mn/n-Si. A detailed description of the SDs manufacturing process is given. The x-ray diffraction (XRD) analysis, Scanning Electron Microscope (FE-SEM) images, and Electron Dispersive x-ray (EDX) spectroscopy are three methods that have been utilized to examine mean size of crystallite, morphology of surface, purity specification. The fundamental electronic variables of these devices are ascertained and contrasted with one another using the I-V characteristic measurement at ±6 V. Ohm’s law, Thermionic Emission (TE) theory, modified Norde, and Cheung functions are used to calculate the SDs’ leakage current (I0), ideality coefficient (n), potential barrier height (BH), shunt (Rsh), and series (Rs) resistances. Investigations are conducted on the energy dependence of surface states density (Nss) and the current conduction mechanisms (CCMs) for both reverse and forward biases. These interfacial layers are known to decrease the n, Rs, and Nss. The PVC polymer interlayer leads to improve the efficiency of the MS-type SD, but it does not when doped by Mn nanoparticles. Additionally, by measuring impedance at a bias of 1.5 V and 100 Hz-1 MHz frequency range, the frequency dependence of dielectric properties of the prepared SDs is studied. The dielectric permittivity, dielectric loss tangent, electronic modulus, and ac electronic conductivity of these SDs are all studied.

Improvement in dielectric properties of polyacrylate copolymers by engineering the interphase region with polymer-grafted reduced graphene oxide

In this study, an innovative interfacial design strategy aimed to investigate the effects of interfacial interactions between the matrix and reduced graphene oxide (rGO) on the dielectric properties of nanocomposites. The polymer matrices with varying comonomer ratios of butyl acrylate and methyl methacrylate were synthesized to deliberately engineer diverse interfacial interactions with polymer-grafted reduced graphene oxide. Through this approach, fine-tuned interfacial interactions between the polymer matrix and polymer-grafted rGO were achieved, which was verified by FE-SEM, DSC, and DMTA analysis. Subsequently, the dielectric properties of the nanocomposites were investigated to elucidate the relationship between interfacial strength and dielectric efficiency. It was found that polymer nanocomposites with enhanced interfacial interactions exhibit higher dielectric permittivity compared to the neat matrix. This enhancement was attributed to the increased charge storage in the interfacial area and improved alignment of polarizable polymer chains in the interphase between the polymer matrix and polymer-grafted rGO.

Effect of soil compaction on the measurements of complex dielectric permittivity spectrum with an open-ended antenna probe and the coaxial cell system

The paper proposes the use of dielectric spectroscopy to measure changes in dielectric permittivity for soil subjected to compression. Density-dependent dielectric permittivity characteristics of soils for the entire range of obtained density, and thus for a significant parameter of soil properties corresponding with ideal conditions for plant growth as well as those inhibiting their growth were presented. Measurements were carried out for three soil types with different moisture content using an open-ended antenna probe (OE-A), operating in the frequency range of 20 MHz–1.2 GHz and a coaxial cell system in frequency range of 20 MHz–3 GHz. Experimental results showed that an increase in bulk density and volumetric water content of soil affects the complex dielectric permittivity spectrum – a model for this relationship was proposed. Soil dielectric permittivity as a parameter reflecting soil moisture and density can be useful in assessing soil quality.