Electric Field Force Research Articles

Electrohydrodynamic effects on the viscoelastic droplet deformation in shear flows

Droplet deformation under shear flows is widely observed in many practical applications, including droplet-based microfluidics and emulsion processing, whereby the droplet usually exhibits viscoelastic characteristics. It has been shown that the performance of these applications is significantly influenced by the size and shape of the resulting droplets. Therefore, the underlying performance is directly tied to the precision and efficiency of viscoelastic droplet control. Previous studies demonstrate that the electric field is a straightforward and efficient way of manipulating fluid flows. However, the effects of an electric field on the viscoelastic droplet deformation remain unexplored. To this aim, this work investigates the electrohydrodynamic (EHD) control of viscoelastic droplets under shear flows using a hybrid numerical framework coupling the lattice Boltzmann method and finite difference method. Extensive simulations are conducted under various electrical properties, such as conductivity ratio R, permittivity ratio S, and electric field strength CaE. Focus is placed on the quantitative analysis of the viscoelastic droplet morphological metrics including deformation D and inclination angle θ. Phase diagrams of D, θ, and combined D and θ in the plane of R–S are developed, where four regions can be identified based on different droplet behaviors under an electric field. The mechanism of this phenomenon is presented by analyzing the distribution of the electric field, electric charge, and electrical force at different regions. It is further observed that the electric field strength CaE amplifies these effects, either suppressing or promoting the droplet deformation and rotation. While viscoelastic effects are considered, they are found to play a subdominant role compared to EHD forces in controlling or modifying droplet morphology. This study provides insights into the electrohydrodynamic (EHD) effects on the dynamics of viscoelastic droplets in shear flow, contributing to the development of active control strategies for viscoelastic droplets in microfluidic applications, including drug delivery and food processing.

Modeling of Electric Field and Dielectrophoretic Force in a Parallel-Plate Cell Separation Device with an Electrode Lid and Analytical Formulation Using Fourier Series.

Dielectrophoresis (DEP) cell separation technology is an effective means of separating target cells which are only marginally present in a wide variety of cells. To develop highly efficient cell separation devices, detailed analysis of the nonuniform electric field's intensity distribution within the device is needed, as it affects separation performance. Here we analytically expressed the distributions of the electric field and DEP force in a parallel-plate cell separation DEP device by employing electrostatic analysis through the Fourier series method. The solution was approximated by extrapolating a novel approximate equation as a boundary condition for the potential between adjacent fingers of interdigitated electrodes and changing the underlying differential equation into a solvable form. The distributions of the potential and electric fields obtained by the analytical solution were compared with those from numerical simulations using finite element method software to verify their accuracy. As a result, it was found that the two agreed well, and the analytical solution was obtained with good accuracy. Three-dimensional fluorescence imaging analysis was performed using live non-tumorigenic human mammary (MCF10A) cells. The distribution of cell clusters adsorbed on the interdigitated electrodes was compared with the analytically obtained distribution of the DEP force, and the mechanism underlying cell adsorption on the electrode surface was discussed. Furthermore, parametric analysis using the width and spacing of these electrodes as variables revealed that spacing is crucial for determining DEP force. The results suggested that for cell separation devices using interdigitated electrodes, optimization by adjusting electrode spacing could significantly enhance device performance.

The Effect of Metal Shielding Layer on Electrostatic Attraction Issue in Glass-Silicon Anodic Bonding.

Silicon-glass anode bonding is the key technology in the process of wafer-level packaging for MEMS sensors. During the anodic bonding process, the device may experience adhesion failure due to the influence of electric field forces. A common solution is to add a metal shielding layer between the glass substrate and the device. In order to solve the problem of device failure caused by the electrostatic attraction phenomenon, this paper designed a double-ended solidly supported cantilever beam parallel plate capacitor structure, focusing on the study of the critical size of the window opening in the metal layer for the electric field shielding effect. The metal shield consists of 400 Å of Cr and 3400 Å of Au. Based on theoretical calculations, simulation analysis, and experimental testing, it was determined that the critical size for an individual opening in the metal layer is 180 μm × 180 μm, with the movable part positioned 5 μm from the bottom, which does not lead to failure caused by stiction due to electrostatic pull-in of the detection structure. It was proven that the metal shielding layer is effective in avoiding suction problems in secondary anode bonding.

Effect of the cation-to-anion mass ratio of ionic liquid on plume neutralization characteristics for novel electrospray thruster

Abstract The ionic liquid electrospray thruster (ILET), a promising technology for space electric propulsion, has been gaining attention due to its theoretical capability to operate without an external neutralizer, which is a key component for traditional ion thrusters. Some experiments have shown that the cation-to-anion mass ratio significantly affects the self-neutralization of thruster plumes, but further depth research is still needed. Therefore, numerical simulations of ion emission process both in uni-thruster and bi-thruster modes of ILETs are conducted using particle-in-cell method, to investigate the effect of the cation-to-anion mass ratio in ionic liquid on plume neutralization characteristics. In bi-thruster mode, the anions and cations are emitted simultaneously, while in uni-thruster mode, only anions or cations are emitted under the action of electric field force. Plume neutralization characteristics of four ionic liquid propellants, with different cation-to-anion mass ratio, in bi-thruster mode are obtained and compared to the uni-thruster mode. The results show that the plume profile morphology is significantly dependent on operating mode of the thruster and the cation-to-anion mass ratio of ionic liquid. Unlike the circular profile in uni-thruster mode, the plume in bi-thruster mode exhibit distortion with vertical stratification. The contours of the high-potential region in bi-thruster mode also distort, showing stratification and a V-shape, respectively, influenced by the mass ratio. Ion beam neutralization in bi-thruster mode is primarily achieved through the horizontal displacement of anion and cation beams, as well as their interactions. The cation-to-anion mass ratio influences the oscillation effects of the mass center in anion and cation clouds during neutralization, which in turn affects the neutralization effect. Ionic liquids with a significant mass ratio difference between cations and anions necessitate a longer time and greater distance for neutralization under identical conditions. These findings are instrumental for understanding the plume neutralization process and advancing the design of ILETs.

Mesoscopic Simulation on Centrifugal Melt Electrospinning of Polyetherimide and Polyarylethernitrile

Polyetherimide (PEI) and polyarylethernitrile (PEN) are high–performance materials for various applications. By optimizing their fiber morphology, their performance can be further enhanced, leading to an expanded range of applications in carbon fiber composites. However, developing processes for stable and efficient fiber production remains challenging. This research aims to simulate the preparation of high–performance ultrafine PEI or PEN fibers using electrospinning. A mesoscopic simulation model for centrifugal melt electrospinning was constructed to compare and analyze the changes in molecular chain orientation, unfolding, fiber diameter, and fiber yield under high-voltage electrostatic fields. The simulation results showed that temperature and electric field force had a particular impact on the diameter and yield of PEI and PEN fibers. Changes in rotational speed had negligible effects on both PEI and PEN fibers. Additionally, due to their different molecular structures, PEI and PEN, which have different chain lengths, exhibit varied spinning trends. This study established a mesoscopic dynamic foundation for producing high-performance ultrafine fibers and provided theoretical guidance for future electrospinning experiments.

Membrane piezoelectric MDS-actuator with a flat double spiral of interacting electrodes

A schematic diagram and mathematical model of functioning of a new piezoelectric membrane (MDS) actuator with double spiral (DS) electrodes on the upper and/or lower surfaces of a thin piezoelectric layer with axisymmetric and periodic (with a small period) in radial coordinate mutual reversed electric polarization are presented. The polarization of the layer was realized as a result of connecting the polarizing electric voltage of the appropriate value to the outputs of the double spirals of the electrodes. The electrodes of each (upper and lower) double spiral of the MDS-actuator are made in the form of electrodeposited ribbon coatings on the surfaces of the piezoelectric layer in close proximity to each other (due to the small spiral pitch) to create high values of electric field strength along the lines of force in localized areas of the piezoelectric layer between them when an alternating or constant control electric voltage is connected to the electrodes, in particular, with positive and negative values of the electrical potentials. Importantly, the electric field force lines and, as a consequence, the polarization of the piezoelectric layer of the MDS actuator are oriented mainly along (i.e. towards or against) the radial coordinate of the membrane, in contrast to many conventional actuator schemes. The results of numerical modeling for a circular elastic membrane with piezoelectric actuators installed on its upper and lower surfaces confirmed the effectiveness of the proposed piezoelectric MDS-actuator when it functions according to the “bimorph” scheme, including the use of the proposed new structural element (section) – a piezoelectric “compression ring” MDS at various geometric and control parameters. The effect of a significant increase in the membrane deflection with installed piezoelectric MDS-actuators compared to the use of traditional homogeneous plate piezoelectric actuators of bimorph type for different conditions of the membrane fixation, in particular, stationary (rigid) fixation of its center is revealed. For a hybrid piezoelectric MDS-actuator including independent concentric round and circular (i.e. “compression ring”) sections, the non-monotonic nature and numerical analysis of the nonlinear dependence of the largest deflection at the center of a hinge-immobile membrane fixed at the edge on the ratio of the radii of its round and circular MDS sections were revealed. The cases in which the effect of the “compression ring” is manifested, i.e. when the maximum deflection of a membrane with the “compression ring” exceeds the best possible value of the deflection of this membrane without its use in the traditional “bimorph” scheme, are identified. The new piezoelectric MDS-actuator can be used in micromechanics, controlled optics, sensor technology, acoustics, in particular, in the manufacture of piezoelectric acoustic or sensor elements of membrane type, electromechanical transducers for vibration energy collection.

Effects of Ion Valence States and Radii on the Performance of Solid-State PEDOT:PSS Electrochromic Devices.

Ion transport is a critical factor influencing the performance of electrochromic devices (ECDs). In this work, the effects of the valence state and ionic radius of six cations, Li+, Na+, K+, Mg2+, Zn2+, and Al3+, on the performance of poly(3,4-ethylenedioxythiophene)-polystyrene sulfonic acid (PEDOT:PSS)-based ECDs are investigated. Both ion migration and diffusion are discussed as processes that were analyzed, with results indicating that the primary contributor to the response of ECDs is ion migration. The response time decreases with increasing ionic valence and ionic radius, with the valence state having the predominant effect on response speed. Multivalent ions, due to strong electric field forces, migrate more rapidly and intercalate fewer ions at equivalent reaction charges, thereby facilitating a faster response. ECDs with larger-radius ions, which exhibit slower diffusion rates, also achieve faster response speeds. Among the tested ECDs with various electrolytes, the Al3+-based ECD demonstrates the fastest colored/bleached response time of 0.36/0.4 s. In addition, ions with larger radii introduce greater steric hindrance and structural damage during insertion and extraction, leading to ion retention issues and reduced cycling stability. After 500 cycles (2025 s) under a square wave voltage of ±1.5 V, the peak current of ECDs with Li+ (0.60 Å) electrolyte decreased by only 5.07/5.66%, whereas for K+ (1.33 Å) electrolyte, the decrease was 11.55/12.37%. ECDs utilizing small-radius, higher-valence ions, such as Al3+, achieved both fast response and high cycling stability, with peak current reductions of only 6.98/5.01%. Additionally, the charge storage dynamics were examined by analyzing the contributions from surface-controlled and diffusion-controlled charges, further confirming that ion migration dominates in ECDs. The high contribution of surface-controlled charges (80%) supports the fast response of ECDs and contributes to the high coloration efficiency (592.6 cm2/C for Al3+-based devices).

Electrohydrodynamic effect within CFRP laminates by bipolar nsPDC electric field during the curing process

In this paper, a new method based on bipolar nanosecond pulsed superimposed direct current (nsPDC) electric field assisted curing technique was developed to fabricate modified fiber-reinforced composites to enhance their mechanical properties. It was found that the mode I interlaminar fracture toughness of the electric field-modified CFRP laminates reached 1014.2 MPa, which increased by 80.4 %. The average tensile strength and tensile modulus were 2180 MPa and 100780 MPa, respectively, which were 20.7 % and 3.5 % higher than the blank control group. The enhancement mechanism was explored by COMSOL simulation, curing temperature inspection, and microscopic characterization by electron microscopy. The results show that the presence of electric field and electric field force inside the laminate, which affects the flow of resin and the weak migration of fibers, enables the elimination of larger air bubbles present in the material, the reduction of resin-rich zones in the interlayer as well as the improvement of the fiber-resin wettability without significantly altering the curing temperature. The proposed simple, convenient, and environmentally friendly strategy can effectively regulate some of the deficiencies in the conventional manufacturing methods and thus is suitable for the optimal design of fiber-reinforced composites.

Performance of a novel annular electric field membrane bioreactor and its membrane fouling control in treating catering wastewater

This study aimed to investigate the effects of different voltage and aeration conditions on catering wastewater treatment and membrane fouling in a novel annular electric field membrane bioreactor (AEMBR). The results indicated that the synergistic effect of annular electric field and aeration promoted the degradation of wastewater and the alleviation of membrane fouling. The treatment effect was optimal under a micro electric field of 0.5 V, with removal rates for COD, NH4+-N, TP, and oil ranging from 96.85% to 99.36%, 80.43%–83.01%, 95.46%–97.79%, and 98.83%–99.15%, respectively. Additionally, the fluorescence intensity of macromolecular proteins and small molecular acids decreased. Simultaneously, the average growth rate of transmembrane pressure (TMP) reduced by approximately 0.4 kPa/d. The species abundance and diversity of activated sludge increased, promoting the growth of dominant bacteria, all while maintaining low energy consumption. The aeration intensity had relatively little impact on system operation, and the force of the annular electric field was greater than the force of aeration. This study verified the optimal benefits under micro electric field conditions and provided a basis for the optimization of future process design to achieve a more efficient and economical wastewater treatment system.

Desolvation Effect Triggered by TiS2‐TiO2 Heterostructure for Ultrahigh‐Rate Aqueous Zinc‐Ion Batteries

AbstractAqueous Zn ion batteries (AZIBs) represent a promising candidate for the next‐generation energy storage and conversion systems due to their high safety and cost‐effectiveness. However, sluggish kinetics arising from interface desolvation processes pose challenges in achieving high‐power density and long cycle life for AZIBs. Here, it is discovered for the first time that heterostructures utilize built‐in electric field forces to promote the desolvation process at the electrode‐electrolyte interface. Density functional theory (DFT) calculations and structural characterization demonstrate that heterogeneous structures simultaneously accelerate the desolvation process and enhance ion diffusion, resulting in the outstanding rate performance (160.9 mA h g−1 at 5 A g−1) of TiS2‐TiO2 heterostructures, far exceeding that of a conventional TiS2 electrode with 14.2% capacity retention. Meanwhile, the insertion/extraction of the desolvated charge carriers reduced the volume change of TiS2‐TiO2 material during the charging/discharging processes, enabling the long‐lasting cycling stability (108.6 mA h g−1 after 2000 cycles at 0.5 A g−1). This study provides instructive electrode design strategies for the construction of fast‐charging electrochemical energy storage systems.

Multifunctional Interface Layer Constructed by Trace Zwitterions for Highly Reversible Zinc Anodes

AbstractThe inhomogeneous plating/stripping of Zn anode, attributed to dendrite growth and parasitic reactions at the electrode/electrolyte interface, severely restricts its cycling life‐span. Here, trace zwitterions (trifluoroacetate pyridine, TFAPD) are introduced into the aqueous electrolyte to construct a multifunctional interface that enhances the reversibility of Zn anode. The TFA− anions with strong specific adsorption adhere onto the Zn surface to reconstruct the inner Helmholtz plane (IHP), preventing the hydrogen evolution and corrosion side reactions caused by free H2O. The Py+ cations accumulate on the outer Helmholtz plane (OHP) of Zn anode with the force of electric field during Zn2+ plating, forming a shielding layer to uniformize the deposition of Zn2+. Besides, the adsorbed TFA− and Py+ promote the desolvation process of Zn2+ resulting in fast reaction kinetics. Thus, the Zn||Zn cells present an outstanding cycling performance of more than 10000 hours. And even at 85 % utilization rate of Zn, it can stably cycle for over 200 hours at 10 mA cm−2 and 10 mAh cm−2. The Zn||I2 full cell exhibits a capacity retention of over 95 % even after 30000 cycles. Remarkably, the Zn||I2 pouch cells (95 mAh) deliver a high‐capacity retention of 99 % after 750 cycles.

Multifunctional Interface Layer Constructed by Trace Zwitterions for Highly Reversible Zinc Anodes.

The inhomogeneous plating/stripping of Zn anode, attributed to dendrite growth and parasitic reactions at the electrode/electrolyte interface, severely restricts its cycling life-span. Here, trace zwitterions (trifluoroacetate pyridine, TFAPD) are introduced into the aqueous electrolyte to construct a multifunctional interface that enhances the reversibility of Zn anode. The TFA- anions with strong specific adsorption adhere onto the Zn surface to reconstruct the inner Helmholtz plane (IHP), preventing the hydrogen evolution and corrosion side reactions caused by free H2O. The Py+ cations accumulate on the outer Helmholtz plane (OHP) of Zn anode with the force of electric field during Zn2+ plating, forming a shielding layer to uniformize the deposition of Zn2+. Besides, the adsorbed TFA- and Py+ promote the desolvation process of Zn2+ resulting in fast reaction kinetics. Thus, the Zn||Zn cells present an outstanding cycling performance of more than 10000 hours. And even at 85 % utilization rate of Zn, it can stably cycle for over 200 hours at 10 mA cm-2 and 10 mAh cm-2. The Zn||I2 full cell exhibits a capacity retention of over 95 % even after 30000 cycles. Remarkably, the Zn||I2 pouch cells (95 mAh) deliver a high-capacity retention of 99 % after 750 cycles.

Molecular dynamics insights into electric Field-Induced heterogeneous ice nucleation

In this study, molecular dynamics simulations on the LAMMPS platform were used to investigate heterogeneous ice nucleation of water molecules based on the TIP4P/Ice-Water molecular model. We have developed a method for calculating electric field force for the TIP4P model, revealing distinct outcomes in the absence and presence of an electric field. In the absence of the electric field, both single and mixed ice structures are observed as final states. In contrast, the introduction of an electric field exclusively leads to the formation of a single ice structure, effectively reducing the energy barrier associated with heterogeneous nucleation. Importantly, this study highlights the significant impact of the electric field, resulting in the controlled formation of a specific ice structure and a pronounced reduction in the energy barrier for non-homogeneous nucleation. These findings provide valuable insights for the freezing industry, offering theoretical guidance for optimizing the freezing process. The developed method for electric field force calculation, specifically tailored to the TIP4P water molecule model, contributes to advancing our understanding of the complex dynamics in ice nucleation and holds promise for practical applications in controlled freezing environments.

Eliminating interface shielding effect endowed by piezoelectric polarization in S-scheme heterojunction for high-efficiency H2 evolution

Eliminating the interface shielding effect within step-scheme (S-scheme) heterojunctions which can attenuate the separation driving force of built-in electric field plays a vital role in enhancing the photocatalytic performance. Herein, an extra driving force induced by piezoelectric field is introduced to mitigate such predicament in S-scheme, thereby facilitating the charge separation. Specifically, the piezoelectric CuInS2-BiFeO3 S-scheme heterojunction which with powerful piezoelectric field endowed by the piezoelectric BiFeO3 is constructed via a facile electrostatic self-assembly strategy and served as the touchstone to verify that hypothesis. The direction of built-in field between the heterojunction interface that is orienting from CuInS2 to BiFeO3 has been confirmed by in-situ X-ray photoelectron spectroscopy and electron paramagnetic resonance. Furthermore, the obviously piezo-field at the interface of CuInS2-BiFeO3 which can tilt energy band to enhance the built-in field under external force is also revealed by piezoresponse force microscopy. Consequently, benefiting from the highly-efficient charge separation offered by the synergy of piezoelectric field and S-scheme built-in electric field, a remarkably H2 production rate of 1465.1 µmol/g is achieved under simultaneous visible light and ultrasonic vibration irradiation. This work sheds light on the role of external field in enhancing the efficient separation of carriers in S-scheme heterojunctions.

Corrosion resistance and forming mechanism of phytic acid conversion film on copper foil prepared by electrolysis

In this paper, the phytic acid conversion film was prepared on copper foil by electrolysis for the first time. Its morphology and chemical composition were characterized by SEM, EDS, FTIR and XPS, and its corrosion resistance was evaluated using electrochemistry. Finally, the formation mechanism of the phytic acid conversion film on the surface of copper foil and its corrosion resistance mechanism were revealed by quantum chemical calculations and molecular dynamics simulations. The results show that the phytic acid conversion film on the surface of copper foil prepared by electrolysis is uniform and dense. The electrochemical impedance value of copper foil in 3.5 wt% NaCl solution increased from 3956 Ω·cm2 to 24828 Ω·cm2 after the preparation of phytic acid conversion film, and the protection efficiency reached 91 %. During the electrolysis process, copper atoms are oxidized into copper ions, which can be coordinated with phytate ions to form negatively charged complexes. Under the action of electric field force, these complexes move toward the anode copper foil, and finally adsorbed on the surface of the anode copper foil to form phytic acid conversion film. The molecular dynamics show that the adsorption configuration of the phytic acid molecule on Cu(111) surface changed from perpendicular to parallel, and the binding energy increased from 234.87 kJ/mol to 354.23 kJ/mol after applying an electric field, Therefore, the phytic acid conversion film prepared on the surface of copper foil by electrolysis has good corrosion resistance. This study provides a new method for the rapid preparation of phytic acid conversion film with excellent performance on metal surface.

Analysis of the motion and deformation of water-in-oil emulsion droplets under the action of an electric field

Molecular dynamics simulations are used to study the aggregation dynamics of water-in-oil emulsion droplets under an electric field, and to analyze the effects of electric field strength, type, droplet position, and ionic concentration on their kinematic properties. The best droplet aggregation is observed at E = 0.03V/Å for DC field condition, and E = 0.045V/Å - 80ps for rectangular AC field condition. The rectangular alternating current (AC) field is able to merge the droplets farther away from the center of mass, but the two fields are not able to merge when the angle between the center of mass of the droplets and the electric field force is ≥ 35.54°. For different ion concentrations, t40N < t20N < t60N < t0N in the DC field and t20N < t40N < t0N < t60N in the rectangular AC field, and for the same ion concentration, the rectangular AC field takes longer time to merge.

Quantitative Investigation of Parallel Interactions Between Charged Particles

On the premise that the charged particle is a normal geometry model, an expression of the migration current, displacement current and magnetic induction intensity generated by the charged particle motion is deduced according to the microscopic definition of current intensity, the total current law and the Biot-Savart law. Further calculate the electric field force between two charged particles in vacuum, give the velocity constraint relationship and velocity value criterion of the electric and magnetic field forces, and compare the consistency with the correlation results obtained considering the relativistic effect. It is pointed out that the magnetic field force is comparable to the electric field force only when the charged particle moves near the speed of light.

Characteristics of soil pore structure response to electric field strength and their effects on Cr(VI) removal from a historically chromium-contaminated soil

The characteristics of soil pore structure response to electric field strength and their effects on the migration of hexavalent chromium during electrokinetic remediation remain unclear. This paper investigates the effects of soil actual voltage and pore redistribution on hexavalent chromium removal under various voltage gradients during electrokinetic remediation. The electric field across the soil was the dominant factor that affected the soil properties, pore structure, and transportation of hexavalent chromium. The removal efficiency of dissolved hexavalent chromium was significantly enhanced from 36.1 % to 80.5 % as the theoretical voltage gradients increased from 0.5 V·cm−1 to 3 V·cm−1 due to the highest voltage proportion (52.7 %) of the soil chamber at 3 V·cm−1, while it only increased to 82.0 % at 4 V·cm−1. The optimal actual electric field strength of 1.00–1.50 V·cm−1 across the soil matrix facilitated the efficient electromigration of hexavalent chromium. The electric field force exerted a direct (0.70) or indirect action intensity (1.55) on soil pore structure by altering soil chemical properties. Soil mesopores and ultra-micropores transformed into micropores through collapsing, shrinking, ion migration, weakening electrostatic repulsion, and enhancing adhesive bonding among particles with increasing electric field. The distribution and structure of soil pores were more homogenous under optimal electric field conditions, thereby improving the migration path of hexavalent chromium. Soil mesopores facilitated hexavalent chromium removal and the formed micropores were opposite. These findings have significant scientific and practical implications for applying the in-situ electrokinetic techniques in the remediation of metal-contaminated soils.

Numerical simulation of He atmospheric pressure plasma jet impinging on the tilted dielectric surface

The target surface to be treated in reality is often not smooth and horizontal and may also be in different tilting angles. The treatment of the tilted dielectric surface by the atmospheric pressure plasma jet (APPJ) undoubtedly increases the complexity of surface modification. Therefore, a two-dimensional fluid model is established to reveal the internal mechanism of the interaction between the He APPJ and the tilted dielectric surface by means of numerical simulation. The distribution of the gas flow in a small angular range (0°, 3°, 5°, 8°, 10°, and 15°) is studied. In addition, the effects of the tilt angle on the jet morphology, discharge dynamic properties, and species distribution of the He APPJ are emphatically discussed. It is found that the jet morphology and parameters are no longer symmetrical under the tilted surface. With the increase in the tilt angle, the enhanced electric field in the upper surface region leads to the increase in the ionization rate and electron density here, and also accelerates the propagation speed of the jet to the dielectric surface in the atmospheric environment. Driven by the electric field force, the jet is closer to the dielectric surface, resulting in a decrease in the thickness of the cathode sheath and an increase in the surface charge density in the area to the right of the central axis. The influence of the gas flow structure leads to the shortening of the jet development distance and a decrease in the jet velocity on the upper surface. N and O also form higher fluxes on the upper surface due to the increase in the electron density.

Steric hindrance and orientation polarization by a zwitterionic additive to stabilize zinc metal anodes

AbstractZinc metal stands out as a promising anode material due to its exceptional theoretical capacity, impressive energy density, and low redox potential. However, challenges such as zinc dendrite growth, anode corrosion, and side reactions in aqueous electrolytes significantly impede the practical application of zinc metal anodes. Herein, 3‐(1‐pyridinio)‐1‐propanesulfonate (PPS) is introduced as a zwitterionic additive to achieve long‐term and highly reversible Zn plating/stripping. Due to the orientation polarization with the force of electric field, PPS additive with π–π conjugated pyridinio cations and strong coordination ability of sulfonate anion tends to generate a dynamic adsorption layer and build a unique water–poor interface. PPS with steric hindrance effect and strong coordination ability can attract solvated Zn2+, thereby promoting the desolvation process. Moreover, by providing a large number of nucleation sites and inducing zinc ion flow, the preferred orientation of the (002) crystal plane can be achieved. Therefore, the interfacial electrochemical reduction kinetics is regulated and uniform zinc deposition is ensured. Owing to these advantages, the Zn//Zn symmetrical cell with PPS additive exhibits remarkable cycling stability exceeding 2340 h (1 mA cm−2 and 1 mA h cm−2). The Zn//V2O5 full cell also delivers stable cycling for up to 6000 cycles.