Optimizing the Interdomain Spacing in Alicyclic Polythiourea toward High-Energy-Storable Dielectric Material.

Organic dielectric materials have been widely developed and investigated for energy storage capacitors. However, challenges remain in terms of the relatively low dielectric constant and energy density. Enhancing the dipolar polarization to increase the dielectric constant is considered to be an effective way to improve the energy density of polymer dielectrics. Herein, enlightened by the chain-packing structure that affects the dipolar relaxation behavior, a simple and low-cost approach is proposed to tailor the interdomain spacing in an alicyclic polythiourea (PTU) by changing quenching temperatures and further facilitate the dipolar polarization. It is found that the large interdomain spacing is beneficial to promote the localized motion of segmental chains in amorphous regions, but at the same time inevitably reduces the dipole density. Therefore, in order to achieve the highest dielectric constant in the PTU, there is an optimal value for the interdomain spacing. It is worth noting that the dielectric constant of PTU increases from 5.7 to 10, and thus the energy density increases by 53% to 16.3 J cm-3 . It proposes a simple and feasible strategy to further improve the energy density through optimizing the interdomain spacing toward high-energy-storable dielectric material.

Surface Modification-Dominated Space-Charge Behaviors of LDPE Films: A Role of Charge Injection Barriers.

Gradually increasing power transmission voltage requires an improved high-voltage capability of polymeric insulating materials. Surface modification emerges as an easily accessible approach in enhancing breakdown and flashover performances due to the widely acknowledged modification of space-charge behaviors. However, as oxidation and fluorination essentially react within a limited depth of 2 µm underneath polymer surfaces, the nature of such bulk space-charge modulation remains a controversial issue, and further investigation is needed to realize enhancement of insulating performance. In this work, the surface oxidation-dependent space-charge accumulation in LDPE film was found to be dominated by an electrode/polymer interfacial barrier, but not by the generation of bulk charge traps. Through quantitative investigation of space-charge distributions along with induced electric field distortion, the functions of surface oxidation on the interfacial barrier of a typical dielectric polymer, LDPE, is discussed and linked to space-charge behaviors. As the mechanism of surface modification on space-charge behaviors is herein proposed, space-charge accumulation can be effectively modified by selecting an appropriate surface modification method, which consequentially benefits breakdown and flashover performances of polymeric insulating films for high-voltage applications.

Improvement of DC Breakdown Strength of the Epoxy/POSS Nanocomposite by Tailoring Interfacial Electron Trap Characteristics.

To date, breakdown voltage is an underlying risk to the epoxy-based electrical high voltage (HV) equipment. To improve the breakdown strength of epoxy resin and to explore the formation of charge traps, in this study, two types of polyhedral oligomeric silsesquioxane (POSS) fillers are doped into epoxy resin. The breakdown voltage test is performed to investigate the breakdown strength of neat epoxy and epoxy/POSS composites. Electron traps that play an important role in breakdown strength are characterized by thermally stimulated depolarized current (TSDC) measurement. A quantum chemical calculation tool identifies the source of traps. It is found that adding octa-glycidyl POSS (OG-POSS) to epoxy enhances the breakdown strength than that of neat epoxy and epoxycyclohexyl POSS (ECH-POSS) incorporated epoxy. Moreover, side groups of OG-POSS possess higher electron affinity (EA) and large electronegativity that introduces deep-level traps into epoxy resin and restrain the electron transport. In this work, the origin of traps has been investigated by the simulation method. It is revealed that the functional properties of POSS side group can tailor an extensive network of deep traps in the interfacial region with epoxy and enhance the breakdown strength of the epoxy/POSS nanocomposite.

Substantial Improvement of the Dielectric Strength of Cellulose-Liquid Composites: Effects of Traps at the Nanoscale Interface.

The dielectric strength of cellulose-liquid composites is always about several times higher than that of the cellulose paper and insulating liquids. However, this experimental phenomenon has not yet been demonstrated theoretically. Herein, the spectra characterization, molecular simulation, and wave function analysis method provide a new insight that the role of nanoscale interfacial adsorption of cellulose-liquid is exclusive for composites affecting the charge separation and producing the deep-level traps to seriously hinder electromigration under an electric field, which is responsible for the difference in dielectric strength. Meanwhile, the π conjugation and σ-π hyperconjugation effects enhance the electrical stability of aromatic hydrocarbon insulating liquids. In conclusion, interfacial trap theory can be used to explain the correlation of dielectric strength between cellulose-liquid composites and cellulose paper or dielectric liquids. It can be expected that materials with high dielectric strength can be manufactured according to the fundamental study of interfacial trap theory.

Synergic effect of adsorbed gas and charging on surface flashover.

Flashover is a crucial issue in both high-voltage engineering and surface physics. It not only challenges the existing theories about its dynamic evolution, but also inhibits the clean energy revolution by limiting the accessible voltage rating of power equipment. It is of significance to elucidate the microscopic process along the interface to improve the flashover performance. In the present study, the synergic effect of adsorbed gas and surface charging is investigated, which reveals a long ignored factor for determining the flashover voltage. Depending on the relative amount of adsorbed gas, the flashover voltage varies, which exhibit different behavior from the bulk breakdown of the same gas. The amount of N2 gas adsorbed on epoxy resin (EP) surface is much larger than that on Al2O3 ceramic surface, corresponding to the observed higher flashover voltage on EP. It is proposed that the adsorbed gas molecules not only modify the local surface charging state via their interaction with the trapped charges, but also capture free electrons due to the distortion of their electronic distribution. Both effects suppress the free path length of electrons in the gas-solid interface. This work explores another possibility to improve the surface flashover performance.