Dielectric Strength Research Articles

Bi3+/Zr4+] induced ferroelectric to relaxor phase transition of BaTiO3 ceramic for significant enhancement of energy storage properties and dielectric breakdown strength

Bi3+/Zr4+] induced ferroelectric to relaxor phase transition of BaTiO3 ceramic for significant enhancement of energy storage properties and dielectric breakdown strength

Utility of argon as a static charge and wall fouling suppressant in atmospheric gas-solid fluidized beds

This work aimed to study the usability of argon to mitigate electrostatic charging and fouling of polyethylene resin fluidized in a stainless-steel column. Nitrogen, argon, and their binary mixtures of various concentrations were utilized to fluidize polyethylene. Successive and intermittent fluidizations with argon and nitrogen were also carried out to explore the feasibility of using argon in commercial reactors. Fluidization with pure argon resulted in the lowest specific charge and substantially reduced the fouling by 90% relative to pure nitrogen. The results for the mixture trials showed a decreasing non-linear trend as the concentration of argon increased. Even presence of 10 vol% argon in the mixture reduced the wall fouling by 50%. Successive and intermittent fluidization also yielded fouling and specific charge values comparable to pure argon. The results are attributed to argon's relatively low dielectric strength and subsequent localized gas discharge within the particle-dense section of the bed.

Segmental mobility in linear polylactides of various molecular weights

In this work we synthesized and studied a series of linear polylactides (PLA) with a fixed L/d -lactide stereoisomer ratio, covering together the wide range of molecular weights, Mn, from ∼6 to ∼80 kg/mol. The basic aims are the segmental mobility mapping, in terms of time scale and fragility, the recording of the Mn dependences of the glass transition temperature and fragility, and, finally, the comparison with corresponding findings from the literature. Obviously, the direct Mn effects on Tg are assessed by preserving PLA at the amorphous state, i.e., via melting and relatively fast cooling. The segmental mobility is studied by conventional and temperature modulated calorimetry, whereas the molecular dynamics is assessed employing the technique of broadband dielectric spectroscopy in combination with proper critical analysis and evaluation routes. The calorimetric and dielectric Tg(Mn) trends were found consistent between each other as well as with previous findings in similar systems, both with respect to experimental findings and theoretic predictions for PLAs of similar L/D ratio. The Mn threshold of entanglements seems to lay between 13 and 28 kg/mol. The fragility index of the α relaxation, i.e., the dielectric analogue of the glass transition, exhibits a similar dependence to that of Tg(Mn). When decreasing Mn to very low values, the high fragility (∼150) drops down to 0 (Mñ6 kg/mol), denoting the vanishing of the polymer chains’ cooperativity. Qualitatively interesting alternations are recorded in the dielectric strength of the α relaxation and the relaxation times width. The effects are discussed in terms of the various parameters co-affecting the polymer dynamics, namely, chain lengths, free volume and dynamical heterogeneities.

Tailoring amorphous boron nitride for high-performance two-dimensional electronics

Two-dimensional (2D) materials have garnered significant attention in recent years due to their atomically thin structure and unique electronic and optoelectronic properties. To harness their full potential for applications in next-generation electronics and photonics, precise control over the dielectric environment surrounding the 2D material is critical. The lack of nucleation sites on 2D surfaces to form thin, uniform dielectric layers often leads to interfacial defects that degrade the device performance, posing a major roadblock in the realization of 2D-based devices. Here, we demonstrate a wafer-scale, low-temperature process (<250 °C) using atomic layer deposition (ALD) for the synthesis of uniform, conformal amorphous boron nitride (aBN) thin films. ALD deposition temperatures between 125 and 250 °C result in stoichiometric films with high oxidative stability, yielding a dielectric strength of 8.2 MV/cm. Utilizing a seed-free ALD approach, we form uniform aBN dielectric layers on 2D surfaces and fabricate multiple quantum well structures of aBN/MoS2 and aBN-encapsulated double-gated monolayer (ML) MoS2 field-effect transistors to evaluate the impact of aBN dielectric environment on MoS2 optoelectronic and electronic properties. Our work in scalable aBN dielectric integration paves a way towards realizing the theoretical performance of 2D materials for next-generation electronics.

Experimental and Simulation Studies on Stable Polarity Reversal in Aged HVDC Mass-Impregnated Cables

Mass-impregnated (MI) cables have been used for many years as cables in high-voltage direct current (HVDC) systems. In line commutated converter (LCC) HVDC systems, polarity reversal for power flow control can induce significant electrical stress on MI cables. Furthermore, the mass oil and kraft paper comprising the impregnated insulation have significantly different coefficients of thermal expansion. Load fluctuations in the cable lead to expansion and contraction of the mass, creating pressure within the insulation and causing redistribution of the impregnant. During this process, shrinkage cavities can form within the butt gaps. Since the dielectric strength of the cavities is lower than that of the surrounding impregnation, cavitation phenomena in impregnated paper insulation are considered a factor in degrading insulation performance. Consequently, this study analyzes the electrical conductivity of thermally aged materials and investigates the transient electric field characteristics within the cable. Additionally, it closely analyzes the formation and dissolution of cavities in MI cables during polarity reversal based on a numerical model of pressure behavior in porous media. The conductivity of the impregnated paper indicates that it has excellent resistance to thermal degradation. Simulation results for various load conditions highlight that the interval of load-off time and the magnitude of internal pressure significantly influence the cavitation phenomenon. Lastly, the study proposes stable system operation methods to prevent cavitation in MI cables.

Realizing Outstanding Energy Storage Performance in KBT-Based Lead-Free Ceramics via Suppressing Space Charge Accumulation.

The great potential of K1/2Bi1/2TiO3 (KBT) for dielectric energy storage ceramics is impeded by its low dielectric breakdown strength, thereby limiting its utilization of high polarization. This study develops a novel composition, 0.83KBT-0.095Na1/2Bi1/2ZrO3-0.075 Bi0.85Nd0.15FeO3 (KNBNTF) ceramics, demonstrating outstanding energy storage performance under high electric fields up to 425kVcm-1: a remarkable recoverable energy density of 7.03Jcm-3, and a high efficiency of 86.0%. The analysis reveals that the superior dielectric breakdown resistance arises from effective mitigation of space charge accumulation at the interface, influenced by differential dielectric and conductance behaviors between grains and grain boundaries. Electric impedance spectra confirm the significant suppression of space charge accumulation in KNBNTF, attributable to the co-introduction of Na1/2Bi1/2ZrO3 and Bi0.85Nd0.15FeO3. Phase-field simulations reveal the emergence of a trans-granular breakdown mode in KNBNTF resulting from the mitigated interfacial polarization, impeding breakdown propagation and increasing dielectric breakdown resistance. Furthermore, KNBNTF exhibits a complex local polarization and enhances the relaxor features, facilitating high field-induced polarization and establishing favorable conditions for exceptional energy storage performance. Therefore, the proposed strategy is a promising design pathway for tailoring dielectric ceramics in energy storage applications.

Voltage-assisted 3D printing of polymer composite dielectric films with low energy loss and high energy storage density

PVDF-based polymers have garnered significant attention in the field of high-power density electrostatic capacitors due to their exceptional dielectric strength. However, their practical applications are constrained by low charge-discharge efficiency (η) and energy storage density (Ue), which stem from high ferroelectric relaxation and low breakdown strength (Eb). Here, a hydrogenated glassy polymer poly(styrene-methyl methacrylate-methylallyl alcohol) (PSMA) is designed and synthesized to be homogeneously distributed in PVDF through voltage-assisted 3D printing-hot pressing, resulting in a flexible composite film. The findings demonstrate that PSMA, rich in hydrogen bonds and high modulus strength, effectively mitigates the ferroelectric phase transition of PVDF to enhance η. Additionally, the voltage-assisted 3D printing process induces an entropy gain mechanism, facilitating the uniform distribution of the two phases and enhancing the interfacial properties for enhancing Eb. Remarkably, the study achieves prominent growth in energy storage performance, with Ue and η reaching 18.1 J/cm3 and 80 % at 525 MV/m, respectively. These remarkable results highlight the potential of 3D printing technology in enhancing the energy storage performance of PVDF-based dielectrics.

Multilaminate Energy Storage Films from Entropy-Driven Self-Assembled Supramolecular Nanocomposites.

Composite materials comprising polymers and inorganic nanoparticles (NPs) are promising for energy storage applications, though challenges in controlling NP dispersion often result in performance bottlenecks. Realizing nanocomposites with controlled NP locations and distributions within polymer microdomains is highly desirable for improving energy storage capabilities but is a persistent challenge, impeding the in-depth understanding of the structure-performance relationship. In this study, a facile entropy-driven self-assembly approach is employed to fabricate block copolymer-based supramolecular nanocomposite films with highly ordered lamellar structures, which are then used in electrostatic film capacitors. The oriented interfacial barriers and well-distributed inorganic NPs within the self-assembled multilaminate nanocomposites effectively suppress leakage current and mitigate the risk of breakdown, showing superior dielectric strength compared to their disordered counterparts. Consequently, the lamellar nanocomposite films with optimized composition exhibit high energy efficiency (>90% at 650MVm-1), along with remarkable energy density and power density. Moreover, finite element simulations and statistical modeling have provided theoretical insights into the impact of the lamellar structure on electrical conduction, electric field distribution, and electrical tree propagation. This work marks a significant advancement in the design of organic-inorganic hybrids for energy storage, establishing a well-defined correlation between microstructure and performance.

Advancements and challenges in BaTiO3-Based materials for enhanced energy storage

Numerous researchers worldwide have been motivated to develop highly effective, environmentally acceptable green energy sources as a result of the recent sharp increase in energy use and the need for low emission levels. The energy generated from various renewable sources can be stored efficiently with a system that has a high energy density and high energy efficiency. Due to their enhanced dielectric, ferroelectric, and breakdown strength characteristics, BaTiO3 based dielectric/ferroelectric ceramic materials have received a lot of interest for energy storage applications in the past tw decades. In the present work, a thorough analysis of recent advancements in composites and single-phase BaTiO3 materials with enhanced energy storage performance. This review's main focus is on the crucial tactics and theoretical frameworks for improving the energy efficiency and recovered energy storage density of various BaTiO3-based materials. A thorough summary has been provided with the most recent developments in BaTiO3 based materials for multi-layered ceramic capacitors (MLCCs), pulse power capacitors, piezoelectric transducers, energy harvesting, electric vehicle batteries, and high-power electronic devices in order to confirm the commercial applications of BaTiO3 based single phase as well as multi-phase layered structures and composites.

Molybdenum disulfide modified silicon carbide ceramic nanofiber: Phase engineering for tuning microwave absorption properties of absorbers

Molybdenum disulfide (MoS2) is an important two-dimension multifunction material, which is widely used in semiconductor devices due to its special electrical properties. However, the electromagnetic wave absorption performance of MoS2 is severely limited as a result of the impedance mismatch between the material and free space. To address this issue, effective strategies of phase engineering and in situ growth techniques are employed to synthesize 2 H MoS2, 1 T/2 H MoS2, SiC@2 H MoS2, and SiC@1 T/2 H MoS2 composites. The electromagnetic absorbing property data reveal that the minimum reflection loss can reach 58.04 dB at 11.16 GHz in a 2.5 mm thick SiC@1 T/2 H MoS2 nanofiber coating; the effective absorbing bandwidth is up to 5.04 GHz (9.16–14.2 GHz). From the detailed analysis, it can be seen that the dielectric loss strength and the degree of impedance matching are the critical factors impacting the microwave absorption properties. The attenuation mechanisms underlying the excellent microwave absorption performance and related phenomena are explored, opening new directions for synthesizing MoS2-based electromagnetic wave absorbing materials with efficient and broadband.

Tungsten-bronze-type BaNd2Ti4O12 ceramics with high permittivity and ultra-low dielectric loss under low frequency

High dielectric constant and ultra-low dielectric loss are important for electronic device applications of dielectrics. In this work, the novel ceramic BaNd2Ti4O12, synthesized via solid-state reaction, exhibits remarkable dielectric stability, with excellent dielectric properties (ε′ = 117 and tanδ = 6.27 × 10−4, at 1 kHz) and high dielectric strength (Eb = 260 kV/cm). By exploring its polarization behavior and loss mechanisms at low frequencies for the first time, we found that the sustained high dielectric constant is attributed to the synergy of defect dipole polarization and interface polarization, while the observed exponential increase of dielectric loss is primarily caused by the conduction loss, with a minor contribution from the anelastic relaxation loss. In the low-temperature range of 50∼350 °C, the relaxation behavior is governed by the aggregation and subsequent thermal ionization of the oxygen vacancies, whereas at temperatures above 350 °C, it is predominated by the long-range motion of the doubly ionized oxygen vacancies. These findings provide valuable insights for the potential electronic device applications of BaNd2Ti4O12.

The effect of thermal ageing on electrical and mechanical properties of thermoplastic nanocomposite insulation of power high-voltage cables

This research explores the thermal ageing influence on the Low Density Polyethylene (LDPE) dielectric properties, which is utilised as electrical insulation in high-voltage cables. An accelerated thermal ageing test was done at four temperature ranges ranging from 25 °C to 120 °C to define the degree of material deterioration under thermal ageing and to prevent its failure. LDPE composite samples were made by adding aluminium oxide (Al2O3) inorganic filler in two different grain sizes (nano and micro) with various concentrations. The effect of adding inorganic filler on the acceleration of the thermal ageing of the polymer was studied by heating the samples for different periods of time and measuring the dielectric strength of the samples. The obtained results show that thermal ageing considerably affects the electrical properties of the material. The LDPE/Al2O3 nanofiller sample has the highest dielectric strength value at different temperatures. Thermogravimetric analysis was used to investigate the thermal characteristics of materials. The mechanical characteristics of LDPE polymer are studied using tensile strength and elongation at break tests. References 27, table 4, figures 6.

Microwave Dielectric Response of Bovine Milk as Pregnancy Detection Tool in Dairy Cows.

The most reliable methods for pregnancy diagnosis in dairy herds include rectal palpation, ultrasound examination, and evaluation of plasma progesterone concentrations. However, these methods are expensive, labor-intensive, and invasive. Thus, there is a need to develop a practical, non-invasive, cost-effective method that can be implemented on the farm to detect pregnancy. This study suggests employing microwave dielectric spectroscopy (MDS, 0.5-40 GHz) as a method to evaluate reproduction events in dairy cows. The approach involves the integration of MDS data with information on milk solids to detect pregnancy and identify early embryonic loss in dairy cows. To test the ability to predict pregnancy according to these measurements, milk samples were collected from (i) pregnant and non-pregnant randomly selected cows, (ii) weekly from selected cows (n = 12) before insemination until a positive pregnancy test, and (iii) daily from selected cows (n = 10) prior to insemination until a positive pregnancy test. The results indicated that the dielectric strength of Δε and the relaxation time, τ, exhibited reduced variability in the case of a positive pregnancy diagnosis. Using principal component analysis (PCA), a clear distinction between pregnancy and nonpregnancy status was observed, with improved differentiation upon a higher sampling frequency. Additionally, a neural network machine learning technique was employed to develop a prediction algorithm with an accuracy of 73%. These findings demonstrate that MDS can be used to detect changes in milk upon pregnancy. The developed machine learning provides a broad classification that could be further enhanced with additional data.

Leakage current as a probe into the mechanics of carrier transport in insulating composite polymers

Amorphous composite polymers are widely used as insulators in microelectronics due to their high dielectric strength, mechanical robustness, and thermal stability. However, organic–inorganic composite systems suffer from undesirable performance and accelerated degradation due to leakage current (JTot). Unfortunately, the underlying mechanism of JTot and its components (e.g., ionic and electronic constituents) are inadequately understood, particularly in extreme use conditions (e.g., high humidity and temperature). In this study, we use numerical simulation and experimental JTot data (in amorphous epoxy polymer with silica fillers) to (i) unify the electrostatic model for JTot in composite polymers, (ii) illustrate that the early part of JTot (i.e., external current) is primarily due to the image charge associated with ion transport/ localization (Jion) near the metallic contacts, (iii) demonstrate that the accumulated counter-ions reduce the barrier for electronic charge injection (by band bending) and facilitate electronic injection from the metals (Jelec), and (iv) provide an algorithm for the in situ ion transport characterization of composite insulators by exploiting Jion. This work provides new insights regarding the leakage current mechanism and how it can be used as a probe into the complex transport mechanisms of the composite material.

Analysis of Deterioration Characteristics of Service-Aged XLPE Cables According to Installation Location of Combined Heat and Power Plant

The number of XLPE cables being used near or beyond their design life is increasing. The importance of timely cable replacement is necessary. Therefore, research is actively being conducted using VLF Tan δ diagnostic technology to assess the insulation condition of cables. Present studies lack in measuring and analyzing the VLF Tan δ of service-aged XLPE cables. Additionally, there is a research gap considering the operating environment. Therefore, it is needed to diagnose and analyze the insulation condition of the same service-aged cable when it is operated in a different environment. This paper assesses and analyzes the insulation condition of cables installed in the BFP, cooling tower, and deaerator booster pump of a combined heat and power plant. Each cable was evaluated by measuring the VLF Tan δ, the dielectric breakdown test of the cable, and the tensile strength, elongation at break, crystallinity, and dielectric strength of the XLPE specimens. Additionally, the correlation between the VLF Tan δ and other characteristics was also analyzed. It was found that degradation progressed in the order of the BFP, the cooling tower, and the deaerator booster pump. Therefore, it was confirmed that even for the same cable, deterioration varies depending on the installation location.

Selection of performance indicators on dielectric strength and viscosity for chlorinated polyvinyl chloride with N-Methyl-2-pyrrolidone: Optimization using central composite design-response surface methodology

N-methyl-2-pyrrolidone is a highly polar aprotic solvent that is frequently utilized across a broad range of applications in industry. The composition of chlorinated polyvinyl chloride is commonly flame-resistant and mechanically strong. In this research, the central composite design technique uses response surface methodology to perform a parametric study. The effect of the input variables wt.% (16%, 20%, 24%), stirring speed (300, 600, 900 r/min), and stirring time (20 min, 30 min, 40 min) on the output responses (dielectric strength kV/mm, and viscosity Pascal) were examined. The output responses were recorded during the experiments according to the experimental design. The factors impacting the response were identified through analysis of variance. According to the predicted vs. actual diagram, the confirmed experiments fit well with the predictions. Based on the response surface, the parameter interaction profile was analyzed. According to the contour plots related to each interaction, the maximum value can be achieved within different stirring parameters. Based on the result of optimization, the optimum values of dielectric strength and viscosity were found in (wt.% of chlorinated polyvinyl chloride—18.101%), (stirring speed—664 r/min), (stirring time—21.860 min). The output response obtained from the response surface methodology is the dielectric strength (18.5 kV/mm) and viscosity (37.67 Pa).

Nano and micro co‐filled aluminum nitride/magnesium dihydrate—Silicone rubber composites for high voltage insulation

AbstractCo‐filled composites of micro magnesium dihydrate (MDH) and hydrophobically treated nano aluminum nitride (nH‐AlN) fillers in high temperature vulcanizing silicone gum are studied for thermal and dielectric characteristics for use as an insulating material in high voltage applications. The study begins with description of the compounding protocol adopted, followed by spectroscopic and optical characterization. Fourier transform infrared spectroscopy (FTIR) and energy dispersive X‐ray spectroscopy (EDX) analysis are used to verify the presence of nH‐AlN and MDH in the composites. Thermal analysis through thermogravimetric analysis revealed a stark enhancement in the onset of polymer degradation temperature, with an improvement of 208 °C achieved at 30 phr by weight loading level of MDH. Volume resistivity of 9.71 E14 Ω‐cm is obtained at 30 phr weight loading of MDH and 5 phr of nH‐AlN. AC, +DC, and −DC dielectric strength improved by 1.09, 2.06, and 1.08 times for co‐filled composites at 30 phr MDH and 5 phr nH‐AlN loading levels over unitary filled composite. Effect of dielectric polarization on dielectric constant and dissipation factor is studied at various frequencies. Limitations while conducting dry arc resistance test at standard voltage of 12.50 kV is discussed, with modification in dry arc resistance test voltage to 16.95 kV. The results are presented and discussed here.

Selective and Controlled Grafting from PVDF-Based Materials by Oxygen-Tolerant Green-Light-Mediated ATRP.

Poly(vinylidene fluoride) (PVDF) shows excellent chemical and thermal resistance and displays high dielectric strength and unique piezoelectricity, which are enabling for applications in membranes, electric insulators, sensors, or power generators. However, its low polarity and lack of functional groups limit wider applications. While inert, PVDF has been modified by grafting polymer chains by atom transfer radical polymerization (ATRP), albeit via an unclear mechanism, given the strong C-F bonds. Herein, we applied eosin Y and green-light-mediated ATRP to modify PVDF-based materials. The method gave nearly quantitative (meth)acrylate monomer conversions within 2 h without deoxygenation and without the formation of unattached homopolymers, as confirmed by control experiments and DOSY NMR measurements. The gamma distribution model that accounts for broadly dispersed polymers in DOSY experiments was essential and serves as a powerful tool for the analysis of PVDF. The NMR analysis of poly(methyl acrylate) graft chain-ends on PVDF-CTFE (statistical copolymer with chlorotrifluoroethylene) was carried out successfully for the first time and showed up to 23 grafts per PVDF-CTFE chain. The grafting density was tunable depending on the solvent composition and light intensity during the grafting. The initiation proceeded either from the C-Cl sites of PVDF-CTFE or via unsaturations in the PVDF backbones. The dehydrofluorinated PVDF was 20 times more active than saturated PVDF during the grafting. The method was successfully applied to modify PVDF, PVDF-HFP, and Viton A401C. The obtained PVDF-CTFE-g-PnBMA materials were investigated in more detail. They featured slightly lower crystallinity than PVDF-CTFE (12-18 vs 24.3%) and had greatly improved mechanical performance: Young's moduli of up to 488 MPa, ductility of 316%, and toughness of 46 × 106 J/m3.

Role of powder morphology on α-phase content in plasma sprayed alumina coatings

Despite various studies addressing the retention of α phase in thermal sprayed alumina coatings, a noticeable research gap persists regarding the impact of feedstock morphology on phase retention and properties. In this work, we explored this simple way to enhance the retention of the α phase and studied its impact on mechanical and dielectric properties. To achieve this, we deposited alumina powders with two different morphologies (such as angular and spherical) with similar particle size using plasma spraying. After deposition, we quantified the retention of α phase present in the coatings using the Rietveld refinement method. From this analysis, we noticed that spherical morphology (SM) powder exhibited the highest percentage of α phase retention (82.81 %) as compared to angular morphology (AM) powder (48.8 %). In turn, SM-coating demonstrated superior mechanical properties, with improvements in hardness, elastic modulus and fracture toughness of 21.9 % 13.7 % and 25 % respectively, compared to AM-coating. This improved mechanical properties in SM-coating is attributed to high α phase retention, synergistic effect of both fully melted (FM) and partial melted (PM) regions of coating microstructure which hindered the crack propagation. Furthermore, the SM-coating exhibited superior dielectric properties, with a dielectric strength 9.9 % higher than the AM-coating. This dielectric performance is ascribed to high retained α phase and generation of discontinuous crack due to presence of PM regions in the SM-coating. These findings suggest the impact of feedstock powder morphology on coating performance and offer avenues for optimizing coating processes in diverse technological fields.

Determination of Highly Transient Electric Field in Water Using the Kerr Effect with Picosecond Resolution

This study utilizes the Kerr effect in the analysis of a pulsed electric field (intensity ~108 V/m, limited by the liquid dielectric strength) in deionized water at the sub-nanosecond time scale. The results provide information about voltage waveforms at the field-producing anode (160 kV peak, du/dt &gt; 70 kV/ns). The analysis is based on detecting the phase shifts between measured and reference pulsed laser beams (pulse width, 35 ps; wavelength, 532 nm) using a Mach–Zehnder interferometer. The signal-to-noise ratio of the detected phase shift is maximized by an appropriate geometry of the field-producing anode, which creates a correctly oriented strong electric field along the interaction path and simultaneously does not electrically load the feeding transmission line. The described method has a spatial resolution of ~1 μm, and its time resolution is determined by the laser pulse duration.