Uniform Electric Field Research Articles

Mxene and GaIn Alloy Nanostructures Regulate Zn Surface Ion Deposition for High-Performance Zinc-Ion Battery.

Zinc is an ideal energy storage material because of its low toxicity, nonflammability, and good biocompatibility. However, the commercial application is seriously hindered due to problems such as dendrite growth, hydrogen evolution, and interface passivation caused by "dead zinc" in the process of cyclic deposition. Herein, a nanoscale deposition dispersion model is designed in order to achieve directional deposition and uniform distribution of zinc ions for the growth of interfacial dendrites. Liquid metal GaIn was combined with Mxene for this nanostructure, which provides a rapid ion transfer channel to achieve lower overpotentials, a more uniform electric field distribution, and stronger corrosion resistance in a core-shell structure to achieve interface reaction suppression. The material was coated on the surface of the zinc metal as an artificial protective layer. It has a better cycle life at 1 mA·cm-2 compared with the bare Zn metal anode, achieving a long cycle time of 1100 h and an ultralow voltage lag (28.1 mV). It maintains the stability for 1000 cycles at 1 mA·cm-2 after assembling the complete battery. This provides a way to improve the performance of zinc-ion secondary batteries and paves the way for the next generation of energy storage devices.

Aspects of a novel nonlinear electrodynamics in flat spacetime and in a gravity-coupled scenario

A novel nonlinear electrodynamics (NLE) model with two dimensionful parameters is introduced and investigated. Our model obeys the Maxwellian limit and exhibits behaviour similar to the Born–Infeld Lagrangian in the weak field limit. It is shown that the electric field of a point charge in this model has a definite maximum value. Thus, the self-energy of the point charge is finite. The phenomenon of vacuum birefringence is found to occur in the presence of an external uniform electric field. Causality and unitarity conditions for all background electric fields hold, whereas, for magnetic fields, a restricted domain of validity is found. Moreover, a minimal coupling of Einstein’s General Relativity (GR) with this NLE results in solutions of regular black holes or naked singularities, depending on whether the source is a nonlinear magnetic monopole or an electric charge, respectively.

Regulating chiral nematic liquid crystal of hydroxypropyl methylcellulose coating on separator for High-Safety Lithium-Ion batteries

The conventional commercial polypropylene separator (PP) struggles to inhibit the thermal runaway triggered by dendrite short circuits, and its safety cannot meet the needs of the development of high-energy–density batteries. Herein, an easily commercializable design strategy was employed to induce the aqueous solution of natural polymer hydroxypropylmethylcellulose (HPMC) to self-assemble on the surface of the PP separator by Na2SO4, MnSO4, and Al2(SO4)3 to form the chiral nematic liquid crystal (CLC) with excellent performance, and finally the thermally stable separators (H-Na@PP, H-Mn@PP, and H-Al@PP) were obtained. Theoretical calculations and experiments demonstrate that the CLC induced by Na+, Mn2+, and Al3+ can interact with the electrolyte solvent to form a desolvation structure of Li+, which reduces the migration barrier of Li+ through the separator and accelerate the Li+ transport. Furthermore, the ordered CLC structure can ensure uniform electric field and Li+ flux. Hence, Li//LFP, Li (50 μm)//LFP, and Li//NCM811cells are assembled using these modified separators, featuring remarkable cycling stability and high Coulombic efficiency. As the result, H-Na@PP, H-Mn@PP, and H-Al@PP separators in Li//LFP cell display a high initial capacity of 141.2 mAh/g, 146.7 mAh/g and 130.7 mAh/g at 1C, respectively and stable cycling performance over 1000 cycles. Notably, the capacity retention rate remains high at 87 %, 69 %, and 59 % even after 700 cycles, respectively, which are higher than the 21 % capacity retention rate of PP separator. Meanwhile, the pouch cells equipped with these separators deliver exceptional electrochemical performance and show a lower temperature distribution without thermal runaway behavior under the Φ3 mm nail penetration test, indicating its feasibility for high-safety energy storage systems.

Dense integration of chlorocatechols crosslinked polyphenylene sulfide solid-state separator for Li Metal-Free Batteries

Dry electrode film fabrication technology, known for its environmental friendliness and low energy consumption, is recognized as an effective industrial approach for producing highly dense solid-state electrolytes and pore-free separators. It holds promise for applying thin lithium metal and Li metal-free anodes in ultra-high energy density Li-ions batteries. However, the films produced by this method suffer from issues such as poor toughness, low strength, uneven thickness, and difficulties in rewinding, which limit its widespread adoption in the large-scale manufacturing of lithium batteries. In this study, we propose a hydrothermal process to introduce a chlorocatechol-based cross-linker onto the surface of highly crystalline polyphenylene sulfide (PPS) powder. By employing the dry electrode process, a PPS-based solid-state separator (PPS-SSS) is fabricated, featuring a thin profile (18±2 μm), a smoother surface, and a denser structure, significantly enhancing its mechanical properties. Moreover, the dense integration structure and chlorocatechol groups contribute to a higher Li+ transference number and more effectively inhibit the growth of Li dendrites. Li metal-free batteries, constructed with this separator, a Sn-plated Cu 10 μm foil anode, and a thick high-nickel cathode dry electrode, exhibit high discharge areal and specific capacities (5 mAh cm−2 and 200 mAh g−1, respectively) and pouch battery device energy density exceeding 440 Wh kg−1. Impressively, even in the presence of Cu or Fe powder contamination on the CuSn foil anode or cathode, this separator can still achieve uniform electric field distribution and lithium deposition, demonstrating good cycle stability.

The influence of water polarization on slip friction at charged interfaces.

The present study employs equilibrium molecular dynamics simulations to explore the potential mechanism for controlling friction by applying electrostatic fields in nanoconfined aqueous electrolytes. The slip friction coefficient demonstrates a gradual increase corresponding to the surface charge density for pure water and aqueous electrolytes, exhibiting a similar trend across both nanochannel walls. An expression is formulated to rationalize the observed slip friction behavior, describing the effect of the electric field on the slip friction coefficient. According to this formulation, the slip friction coefficient increases proportionally to the square of the uniform electric field emanating from the charged electrode. This increase in slip friction results from the energy change due to the orientation polarization of interfacial water dipoles. The minimal variations in the empirically determined proportionality constant for pure water and aqueous electrolytes indicate that water polarization primarily governs slip friction at charged interfaces. These findings offer insights into the electrical effects on nanoscale lubrication of aqueous electrolytes, highlighting the significant role of water polarization in determining slip.

Electroabsorption in InGaAs and GaAsSb p-i-n photodiodes

The application of an electric field to a semiconductor can alter its absorption properties. This electroabsorption effect can have a significant impact on the quantum efficiency of detector structures. The photocurrents in bulk InGaAs and GaAsSb p-i-n photodiodes with intrinsic absorber layer thicknesses ranging from 1 to 4.8 μm have been investigated. By using phase-sensitive photocurrent measurements as a function of wavelength, the absorption coefficients as low as 1 cm−1 were extracted for electric fields up to 200 kV/cm. Our findings show that while the absorption coefficients reduce between 1500 and 1650 nm for both materials when subject to an increasing electric field, an absorption coefficient of 100 cm−1 can be obtained at a wavelength of 2 μm, well beyond the bandgap energy when they are subject to a high electric field. The results are shown to be in good agreement with theoretical models that use Airy functions to solve the absorption coefficients in a uniform electric field.

Electrohydrodynamic flow about a colloidal particle suspended in a non-polar fluid

Nonlinear electrokinetic phenomena, where electrically driven fluid flows depend nonlinearly on the applied voltage, are commonly encountered in aqueous suspensions of colloidal particles. A prime example is the induced-charge electro-osmosis, driven by an electric field acting on diffuse charge induced near a polarizable surface. Nonlinear electrohydrodynamic flows also occur in non-polar fluids, driven by the electric field acting on space charge induced by conductivity gradients. Here, we analyse the flows about a charge-neutral spherical solid particle in an applied uniform electric field that arise from conductivity dependence on local field intensity. The flow pattern varies with particle conductivity: while the flow about a conducting particle has a quadrupolar pattern similar to induced-charge electro-osmosis, albeit with opposite direction, the flow about an insulating particle has a more complex structure. We find that this flow induces a force on a particle near an electrode that varies non-trivially with particle conductivity: while it is repulsive for perfectly insulating particles and particles more conductive than the suspending medium, there exists a range of particle conductivities where the force is attractive. The force decays as the inverse square of the distance to the electrode and thus can dominate the dielectrophoretic attraction due to the image dipole, which falls off with the fourth power with the distance. This electrohydrodynamic lift opens new possibilities for colloidal manipulation and driven assembly by electric fields.

High-voltage FinFET with floating poly and high-k material for enhanced intrinsic gain and safe operating area

We propose a new drain-extended FinFET (DeFinFET) that can improve the intrinsic gain (gm/gds) and the electrical safe operating area (SOA). This structure features a novel utilization of the drain potential by using a floating poly (FP) and split high-k material (HK) on the drain and drift regions. This method effectively controls the potential drop profile within the drift region, which makes a uniform electric field distribution in the gate-on state. The evenly distributed electric field significantly increases the on-state breakdown voltage (7.33 V) compared to a conventional structure (5.89 V). In addition, it prevents the device from operating in an undesirable quasi-saturation mode, even after space charge modulation. This operation distinguishes our results from other studies, showing a notable improvement in gm/gds. Moreover, electron accumulation is induced in the drift region, leading to a significant decrease in the on-resistance. As a result, the proposed device demonstrates clear advantages in high-voltage applications with a 45% expanded electrical SOA over conventional DeFinFET.

Polyethylene Glycol-Protected Zinc Microwall Arrays for Stable Zinc Anodes.

Aqueous zinc-ion batteries promise good commercial application prospects due to their environmental benignity and easy assembly under atmospheric conditions, positioning them as a viable alternative to lithium-ion batteries. However, some inherent issues, such as chaotic zinc dendrite growth and inevitable side reactions, challenge the commercialization progress. In this work, we imprint highly ordered zinc microwall arrays to regulate the electric field toward uniform Zn deposition. Afterward, coating a polyethylene glycol protection layer on the zinc microwalls aims to passivate the surface defects that rise unintentionally by mechanical imprinting. Polyethylene glycol can also boost oriented Zn deposition along the (002) plane and inhibit hydrogen gas production, further enhancing the stability of such three-dimensional (3D) hybrid anodes. Compared to the messy electric field near the polyethylene glycol-protected Zn foil, the uniform electric field provided by these 3D hybrid anodes can regulate the Zn deposition behaviors, enabling a longer lifespan and thus certifying the necessity of adding 3D microstructures. Additionally, 3D microstructures can offer a larger surface area than that of the planar Zn foil, providing more reaction sites and higher specific capacity. In this case, the 3D hybrid electrode exhibits a good initial capacity of approximately 120 mA h/g at a current density of 5 A/g and a nice retention of more than 80% after 800 cycles. The proposed scheme paves the way for a long-term stable 3D zinc anode solution with promising application prospects.

Optimal design configuration of grading ring for polymeric insulator under different environmental conditions

Polymeric insulators play a crucial role in power transmission lines. To ensure safe and reliable operation at High Voltage (HV), they are often equipped with single or double grading rings to uniformly distribute the electric field and voltage along the creepage distance. This study investigates the impact of optimal grading ring configurations on electric field distribution using the Finite Element Method (FEM). In addition, an adaptable method for achieving optimal grading ring design is proposed. Numerical results demonstrate that employing the Nelder-Mead (NM) optimization algorithm helps determine the ideal configuration for grading ring material, dimensions, and location to achieve uniform electric field distribution compared to insulators without grading rings or with original designs. This method has also been adapted for different environmental conditions, including pollution, water droplets, and icing conditions.

Uniform electric-field optimal design method using machine learning

The demand for uniform electric fields (UEFs) in engineering is very high, particularly in high-voltage devices. The existing methods encounter limitations in terms of optimization region and universality. Herein, we propose a method for designing UEFs based on finite element calculations of electromagnetic fields and machine learning. First, the electric-field distribution of the plate-to-plate electrode structure determined using three electrode-shape parameters (ESPs) is calculated using finite element software and is drawn. Thereafter, a dataset of 2000 images is created with different electric-field strength distributions using various ESPs. Net, we employ image-processing techniques to extract nine statistical features from the gray-level information in the images. Models are trained through machine learning to predict ESPs based on the gray-level features (GLFs). Finally, the electric-field strength distribution image of the expected ideal uniform field is artificially selected. In addition, the ESPs from which the uniform electric-field is produced are predicted by the models. The proposed method provides an accurate solution for optimizing the design of a uniform electric-field and a new approach for solving inverse problems of electric-field. This involves drawing the required electric-field strength distribution image for high-voltage engineering and obtaining the required ESPs.

Exact solvable family of discrete Schrödinger operators with long-range hoppings

It is shown that one-dimensional discrete Schrödinger operators, with a uniform electric field and long-range hoppings, form an isospectral family with discrete and simple spectrum (and isospectral operators with eigenfunctions having different decay properties). Explicit relations between hopping decay rates and eigenvectors decay rates are obtained. Small perturbations of exponentially decay hopping operators preserve dynamical localization.

Surface flashover in 50 years: II. Material modification, structure optimisation, and characteristics enhancement

AbstractSurface flashover is a gas–solid interface insulation failure that significantly jeopardises the secure operation of advanced electronic, electrical, and spacecraft applications. Despite the widespread application of numerous material modification and structure optimisation technologies aimed at enhancing surface flashover performance, the influence mechanisms of the present technologies have yet to be systematically discussed and summarised. This review aims to introduce various material modification technologies while demonstrating their influence mechanisms on flashover performances by establishing relationships among ‘microscopic structure‐mesoscopic charge transport‐macroscopic insulation failure’. Moreover, it elucidates the effects of chemical structure on surface trap parameters and surface charge transport concerning flashover performance. The review categorises and presents structure optimisation technologies that govern electric field distribution. All identified technologies highlight that achieving a uniform tangential electric field and reducing the normal electric field can effectively enhance flashover performance. Finally, this review proposes recommendations encompassing mathematical, chemical, evaluation, and manufacturing technologies. This systematic summary of current technologies, their influence mechanisms, and associated advantages and disadvantages in improving surface insulation performance is anticipated to be a pivotal component in flashover and future dielectric theory.

Bi-Functional Agarose-Filled Porous Polysulfone Protective Layer for Dendrite-Free Zn Anode.

The uneven electric field and slow Zn2+ desolvation lead to rapid dendrite growth during Zn plating and stripping, which severely deteriorates the performance of Zn metal anodes (ZMAs) in Zn-ion batteries (ZIBs). Although polymer-based artificial protective (PBAP) layers are widely applied to homogenize the electric field of ZMAs, they often fail to promote the desolvation process that eventually induces Zn dendrite growth. Herein, a bi-functional protective layer, comprising a finger-like porous matrix of polysulfone (PSF) and a hydroxyl-rich filler of agarose (AG), is constructed to suppress Zn dendrite growth. COMSOL simulation demonstrates the ZMAs with bi-functional protective layers (Zn@PSF/AG) exhibit uniform electric field and Zn2+ distribution. Besides, the Zn@PSF/AG has both low desolvation energy and nucleation overpotential, effectively promoting the desolvation of Zn2+. Therefore, the Zn@PSF/AG symmetric cell exhibits excellent cycling performance, achieving 4200h at 1mA cm-2/1 mAh cm-2 and 1000h at 5mA cm-2/5 mAh cm-2. When coupling with ZnxV2O5 (ZnVO) cathode, the ZnVO‖Zn@PSF/AG full cell shows similarly high cycling stability, maintaining 72% of its capacity after 7000 cycles at 10 A g-1. This research highlights the positive roles of PBAP layer with multi-functional matrix-filler structure in developing long-life ZIBs.

Design and Optimization of High Performance Multi-Step Separated Trench 4H-SiC JBS Diode

In this paper, a novel 3300 V/40 A 4H-SiC junction barrier Schottky diode (JBS) with a multi-step separated trench (MST) structure is proposed and thoroughly investigated using TCAD simulations. The results show that the introduction of MST expands the Schottky contact area, resulting in a decrease in the forward voltage drop. Furthermore, the combination of the deep P+ shielded region and the central P+ region effectively reduces the leakage current, leading to a 43.7% increase in the blocking voltage compared to conventional 4H-SiC JBS. The effects of the step depth (ds) and the width of the central P+ region (wm) on the device performance are analyzed in depth. In addition, a multi-step trenched linearly graded field-limiting rings (MTLG-FLR) termination ensures a more uniform electric field distribution, and the terminal protection efficiency reaches up to 90%, which further enhances the reliability of the terminal structure.

Zincophilic host with lattice plane matching enables stable zinc anodes in aqueous zinc-ion batteries

The practical application of aqueous zinc-ion batteries (AZBs) as attractive energy storage devices is severely hampered by the uncontrollable zinc dendrite growth on the metal anode. Here, a lightweight and flexible free-standing membrane of MXene/Ag nanowires (AgNWs) was synthesized via vacuum filtration to support the zinc anode. The 3D cross-linked network structure provides ample space for densely packed zinc electrodeposition. Zincophilic AgNWs that exhibit a low lattice plane mismatch with zinc lower the nucleation barrier for zinc, inducing uniform nucleation and lateral growth of zinc on the substrate. In addition, the 3D network framework effectively reduces the local current density and area capacity of the anode, creating a uniform electric field that is not conducive to zinc dendrite formation. Consequently, the highly reversible Zn@MXene/AgNWs composite anode exhibits long cycle stability of 1000 h at 2.0 mA cm−2, 1.0 mAh cm−2 in the symmetrical battery. The full battery assembled with a sodium vanadate (NVO) cathode demonstrates excellent rate performance and long cycle life (2000 cycles at 5.0 A/g). The design of zincophilic hosts with high lattice plane matching provides a promising strategy for realizing dendrite-free zinc anodes for AZBs.

Multiscale Defective Interfaces for Realizing Na-CO2 Batteries With Ultralong Lifespan.

Despite their favorable high energy density and potential for CO2 recycling, Na-CO2 batteries have been held back by limitations in cycling capability, stemming from the sluggish CO2 reduction/evolution reaction (CO2RR/CO2ER) kinetics at CO2 cathode and unmanageable deposition/stripping of metallic Na at the anode upon cycling. Herein, a "two-in-one" electrode with multiscale defective FeCu interfaces (CP@FeCu) is presented, which is capable of improving the CO2RR/CO2ER kinetics of CO2-breathing cathode, while modulating sodium deposition behavior. Experimental and theoretical investigations reveal multiscale defective FeCu interfaces are responsible for the enhancement of sodiophilicity and catalytic properties. The defect and valence oscillation effects originate in multiscale defective FeCu interfaces, effectively facilitating the adsorption of reactants and decomposition of Na2CO3 during CO2RR/CO2ER processes, along with exceptional cycling stability of 2400 cycles (4800h) at 5µAcm-2. Meanwhile, the CP@FeCu with sodium affinity creates a uniform electric field and robust adsorption for Na, making initial nucleation sites more conducive to Na deposition and achieving dendrite-resistant and durable anodes. This work offers a scientific insight into the functionalization design of "two-in-one" electrodes, which is essential for a unified solution to the challenges in sodium anodes and CO2 cathodes.

Kinetic theory of vacuum pair production in uniform electric fields revisited

We investigate the phenomenon of electron-positron pair production from vacuum in the presence of a uniform time-dependent electric field of arbitrary polarization. Taking into account the interaction with the external classical background in a nonperturbative manner, we quantize the electron-positron field and derive a system of ten quantum kinetic equations (QKEs) showing that the previously-used QKEs are incorrect once the external field rotates in space. We employ then the Wigner-function formalism of the field quantization and establish a direct connection between the Dirac-Heisenberg-Wigner (DHW) approach to investigating the vacuum pair-production process and the QKEs. We provide a self-contained description of the two theoretical frameworks rigorously proving their equivalence and present an exact one-to-one correspondence between the kinetic functions involved within the two techniques. Special focus is placed on the analysis of the spin effects in the final particle distributions. Published by the American Physical Society 2024

High-Entropy-Inspired Multicomponent Electrical Double Layer Structure Design for Stable Zinc Metal Anodes.

Regulating the electrical double layer (EDL) structure can enhance the cycling stability of Zn metal anodes, however, the effectiveness of this strategy is significantly limited by individual additives. Inspired by the high-entropy (HE) concept, we developed a multicomponent (MC) EDL structure composed of La3+, Cl-, and BBI anions by adding dibenzenesulfonimide (BBI) and LaCl3 additives into ZnSO4 electrolytes (BBI/LaCl3/ZnSO4). Specifically, La3+ ions accumulate within EDL to shield the net charges on the Zn surface, allowing more BBI anions and Cl- ions to enter this region. Consequently, this unique MC EDL enables Zn anodes to simultaneously achieve uniform electric field, robust SEI layer, and balanced reaction kinetics. Moreover, the synergistic parameter - a novel descriptor for quantifying collaborative improvement - was first proposed to demonstrates the synergistic effect between BBI and LaCl3 additives. Benefitting from these advantages, Zn metal anodes achieved a high reversibility of 99.5 % at a depth of discharge (DoD) of 51.3 %, and Zn|MnO2 pouch cells exhibited a stable cycle life of 100 cycles at a low N/P ratio of 2.9.

High‐Entropy‐Inspired Multicomponent Electrical Double Layer Structure Design for Stable Zinc Metal Anodes

AbstractRegulating the electrical double layer (EDL) structure can enhance the cycling stability of Zn metal anodes, however, the effectiveness of this strategy is significantly limited by individual additives. Inspired by the high‐entropy (HE) concept, we developed a multicomponent (MC) EDL structure composed of La3+, Cl−, and BBI anions by adding dibenzenesulfonimide (BBI) and LaCl3 additives into ZnSO4 electrolytes (BBI/LaCl3/ZnSO4). Specifically, La3+ ions accumulate within EDL to shield the net charges on the Zn surface, allowing more BBI anions and Cl− ions to enter this region. Consequently, this unique MC EDL enables Zn anodes to simultaneously achieve uniform electric field, robust SEI layer, and balanced reaction kinetics. Moreover, the synergistic parameter – a novel descriptor for quantifying collaborative improvement – was first proposed to demonstrates the synergistic effect between BBI and LaCl3 additives. Benefitting from these advantages, Zn metal anodes achieved a high reversibility of 99.5 % at a depth of discharge (DoD) of 51.3 %, and Zn|MnO2 pouch cells exhibited a stable cycle life of 100 cycles at a low N/P ratio of 2.9.