Surface Charge Density Research Articles

Recent advances in high charge density triboelectric nanogenerators

Abstract Triboelectric materials with high charge density are the building-block for the commercial application of triboelectric nanogenerators (TENGs). Unstable dynamic processes influence the change of the charge density on the surface and inside of triboelectric materials. The charge density of triboelectric materials depends on the surface and the internal charge transfer processes. The focus of this review is on recent advances in high charge density triboelectric materials and advances in the fabrication of TENGs. We summarize the existing strategies for achieving high charge density in triboelectric materials as well as their fundamental properties. We then review current optimization methods for regulating dynamic charge transfer processes to increase the output charge density: first, increasing charge injection and limiting charge dissipation to achieve a high average surface charge density, and second, regulating the internal charge transfer process and storing charge in triboelectric materials to increase the output charge density. Finally, we present the challenges and prospects in developing high-performance triboelectric materials.

Stability of charged anisotropic thin shell gravastars admitting conformal motion in [formula omitted] gravity

This paper investigates the interesting features of gravastar configuration under charged anisotropic fluid distribution considering geometry-matter coupling theory. In the context of f(R,T) gravity, we derive exact solutions of the Einstein field equations using the linear form of the function f(R,T)=R+2γT, where R is the Ricci scalar and T is the trace of the energy–momentum tensor with conformal motion. We consider three different regions of gravastar, the interior region having a definite radius r, the intermediate layer of matter with the thickness ϵ, and the outer region with the radius r+ϵ. For the viability of our developed solution, we examine the metric potentials, energy density, and pressure components inside the thin shell for different values of theory parameter γ, and charge Q. Using the well-known matching conditions, we interpret the dynamical properties of gravastar such as surface charge density, surface pressure, proper length, equation of state parameter, entropy, and evolution of shell energy under the allowed range of parameters. Moreover, we analyze the presence of realistic matter inside the thin shell through energy conditions. The dynamical stability of the gravastar is checked through the equilibrium profile and speed of sound parameter, which shows the stable configuration of the gravastar in our theoretical studies.

Fully‐Recyclable Green and Fire‐Resistant Triboelectric Elastomer via Geometrical Synergistic Fillers and Its Applications for Smart Firefighting Boots

AbstractWearable sensors for high temperatures (WSHT) applications pose a significant challenge in the electronics field due to the inherent inability of most electronics to function in harsh environments. Triboelectric nanogenerators (TENG) present a substantial potential for applications in such challenging conditions. Herein, a fully‐recyclable flame‐retardant triboelectric elastomer is developed, which exhibits superior charge stability under high temperature conditions and proposes the specially designed synergistic fillers that play a dual role by trapping more charges into the interface and stabilizing the char layers via layer‐ball‐layer structure. An efficient flame‐retardant system is presented, which exhibits a 31% lower fire growth index than the individual components. The maximum surface charge density of this triboelectric elastomer can reach 361 µC m−2, while this surface charge density can be preserved to 70.9% after 16 s of combustion (≈520 °C) and to 37.9% by continuously working at 130 °C. At last, utilizing this flame‐retardant triboelectric elastomer, smart firemen's boots featuring gait analysis for identification and second level early warning systems have been developed. This work paves the way for the development of triboelectric materials and intelligent wearable devices suitable for applications in harsh environments.

The underlying mechanism between emulsification stability and in vitro digestion in golden pompano (Trachinotus ovatus) myofibrillar protein-fish oil oleogel emulsion under ultrasonic treatments

Fish oil contains rich EPA and DHA, but their low absorption rate and bioavailability in the gastrointestinal tract limit their physiological activity. Ultrasonic treatments can modify the spatial structure of myofibrillar proteins and influence their function. The microstructure, viscoelastic properties, spatial conformation, size and charge, interfacial characteristics were investigated in the emulsions with fish oil oleogels to clarify the mechanism between emulsification stability and lipid digestion by ultrasonic treatment. The results showed that ultrasonic-treated (120 s or 150 W) fish myofibrillar protein had higher interfacial protein concentration and formed the more stable interfacial adsorption layer to wrap the fish oil oleogel with higher viscoelastic properties. The surface charge density was affected by adsorbed proteins, and higher interfacial adsorption capacity enhanced electrostatic repulsion and reduced the size. CLSM images also indicated that the droplet distribution was more uniform with smaller particle size. The increase in β-sheets facilitated interfacial adsorption and emulsion stability, and hydrophobic force and disulfide bonds promoted the interactions between myofibrillar protein and fish oil oleogel. In the stomach, the demulsification and flocculation occurred, and β-sheets increased along with hydrophobic forces and disulfide bonds, facilitating flocculation and aggregation as well as the increase in particle size. The electrostatic repulsion and spatial conformation altered the molecular interaction. In the intestine, the decreasing β-sheets, hydrophobic force and disulfide bonds were conducive to the adsorption of bile salts and lipase/colipase. Hence, ultrasonic treatments simultaneously enhanced emulsion stability and lipid digestion.

Bridging Ionic Current Rectification and Resistive-Pulse Sensing for Reliable Wide-Linearity Detection.

As two mainstream ionic detection techniques, ionic current rectification (ICR) suffers from large fluctuations in trace level detection, while resistive-pulse sensing (RPS) encounters easy clogs in high-concentration detection. By rationally matching the nanopore size with the DNA tetrahedron (TDN), this work bridges the two techniques to achieve reliable detection with wide linearity. As a representative analyte, miRNA-10b could specifically combine with and release TDN from the interior wall, which thus induced the simultaneous generation of distinct ICR and RPS signals. The ICR signals could be attributed to the balance between the effective orifice and surface charge density of the inner wall, while the RPS signals were induced by the complex of miRNA-10b and TDN passing through the nanopore. Such an operation contributed to a wide detection range of 1 fM-1 nM with a good linearity. The feasibility of this method is also validated in single-cell and real plasma detection.

Method for Measuring Surface Charge on Insulating Materials Based on the Vibrating Capacitor Method

The phenomenon of surface charging, known as contact electrification or tribocharging, has wide-ranging applications but also notable hazards. Precisely measuring surface charge density in insulating materials is crucial for optimizing tribocharging and mitigating adverse effects. Although the vibrating capacitor method is commonly used for this purpose, its principle, designed for conductive materials, limits direct application to insulating surfaces, leaving the relationship between measured surface potential and surface charge density unclear. To address this issue, this study simulated the process of measuring the surface potential of insulating materials using Comsol simulations. It analyzed the effects of charged area size, probe height, and probe position, and utilized the spatial distribution of potential measurement values of surface point charges to derive an integral relationship between the distribution of measured surface potential values and the distribution of surface charge density. The integral relationship of surface potential distribution under different forms of surface charge density distributions calculated from this formula largely matches the numerical simulation results. Based on this, a relationship between the distribution of surface charge density and surface potential measurement values was further derived. This relationship can be used for measuring the surface charge density of insulating materials.

All Wood‐Based Water Evaporation‐Induced Electricity Generator

AbstractWater evaporation‐induced electricity generators (WEIGs) are promising as self‐powered electronic devices, as they can harvest green, small‐grade, and ubiquitous hydrovoltaic energy in ambient environment to electricity. Here, biodegradable wood‐based WEIGs with high performance are reported by removing lignin and hemicellulose from balsa wood (BW) with more exposed cellulose nanofibrils. Delignified BW (DBW) and cellulosic BW (CBW) display significant enhance in open circuit potential (Voc) and short circuit current (Isc) due to increased specific surface area, hydrophilicity, and surface charge density. The electricity‐generating performance of CBW‐based WEIG (CBWG) is not stable due to its structural collapse. DBW‐based WEIG (DBWG) shows a steady electricity output and fast responsivity to ambient environments, such as humidity, temperature, light, and wind. Therefore, DBWGs can be employed as self‐powered environmental sensors. The effects of different kinds of electrolytes with varied concentrations on the performance of DBWG are also studied. The DBWG (40 mm × 40 mm × 2 mm) displays a Voc of 0.77 V and Isc of 148 µA in 1.2 m CaCl2 solution. In this study, all wood‐based sustainable WEIGs with high electricity generating performance are facilely prepared and are promising for remote self‐powered environmental sensors and power sources.

All porous Ecoflex and SEBS-based stretchable high-performance triboelectric nanogenerator for self-powered human activity monitoring

Achieving a high output performance by expanding the surface area of triboelectric materials is key to developing triboelectric nanogenerators (TENGs) for future versatile applications. Herein, highly porous Ecoflex and styrene-ethylene-butylene-styrene (SEBS) using chloroform are introduced to improve TENG performance. The triboelectric output increases significantly with increasing porosity, which can be attributed to the increase in the contact area, dielectric constant, and electrostatic induction in the porous structure, thereby resulting in additional surface charges on the porous surface and increased surface charge density of the friction materials. The TENG can stretch by up to 550 % with the designed fabric electrode configuration. Facilitated by the increased contact area of 3D printed microstructure and porous Ecoflex substrate, the fabricated TENG demonstrates a high voltage of 2280 V, corresponding to a power density of 18.8 W m−2, which is enough to power 460 light-emitting diodes and stopwatches. Demonstration of monitoring the walking steps of patients with Parkinson’s and blind people was also performed, which revealed outstanding sensing capabilities. In addition, the TENG-based self-powered sensor demonstrated an identification accuracy of 99.3 % and a motion detection accuracy of 98.2 % based on a deep learning model. Furthermore, by exploiting the outstanding ultrahigh sensitivity, the TENG was demonstrated for low-frequency football player motion monitoring. Therefore, the results of this study provide new insights into investigating porous materials and an efficient method to construct high-performance TENGs that can promote their practical application in the fields of smart healthcare and sports.

Secondary roughness effect of surface microstructures on secondary electron emission and multipactor threshold for PTFE-filled and PI-filled single ridge waveguides

Secondary electron yield (SEY) is a dominant factor in determining the multipactor threshold. In this study, we analyzed the secondary roughness effect of surface microstructures for plastic dielectric on SEY reduction and multipactor mitigation. A single ridge waveguide (SRW) operating in Ku-band, filled with polytetrafluoroethylene (PTFE) or polyimide (PI), was designed with a dielectric–metal multipactor gap. By employing a femtosecond laser, periodic microstructures were fabricated on PTFE and PI surfaces to suppress SEY. The SEY peak values of PTFE and PI decreased from 2.05 to 1.40 and 1.37 to 1.07 by the porous surface. The surface morphologies and cross-sectional images of the porous PTFE and PI demonstrated the existence of secondary roughness structures. Via simulation, we obtained multipactor thresholds of 8496 W, 12 374 W, and 9397 W for the SRWs filled with untreated PTFE surface, ideal porous surface (without secondary roughness), and real porous surface (with secondary roughness). Similar works were implemented for the PI-filled SRWs, resulting in simulated multipactor thresholds of 7640 W, 11 327 W, and 9433 W. The results indicate that the multipactor effect may not be effectively suppressed under the influence of secondary roughness structures such as plastic velvet and foam. Besides, simulation works indicated that the radio frequency electric field could extract secondary electrons from the microstructures, weakening the mitigation effect of microstructures on multipactor. The impact of surface charging on electron motion was also analyzed by considering energy distribution. It was suggested that the surface microstructures of plastic dielectrics lead to a decrease in the surface charge density and the electrostatic field strength, weakening the self-extinguishing effect and lowering the multipactor threshold. This study provides an in-depth analysis of the effect of secondary roughness on SEY and multipactor for organic dielectrics, which makes significant sense for the further investigation of dielectric multipactor.

Spontaneous Wetting Induced by Contact-Electrification at Liquid-Solid Interface.

Wettability significantly influences various surface interactions and applications at the liquid-solid interface. However, the understanding is complicated by the intricate charge exchange occurring through contact electrification (CE) during this process. The understanding of the influence of triboelectric charge on wettability remains challenging, especially due to the complexities involved in concurrently measuring contact angles and interfacial electrical signals. Here, the relationship is investigated between surface charge density and change of contact angle of dielectric films after contact with water droplets. It is observed that the charge exchange when water spared lead to a spontaneous wetting phenomenon, which is termed as the contact electrification induced wetting (CEW). Notably, these results demonstrate a linear dependence between the change of contact angle (CA) of the materials and the density of surface charge on the solid surface. Continuous CEW tests show that not only the static CA but also the dynamics of wetting are influenced by the accumulation charges at the interface. The mechanism behind CEW involves the redistribution of surface charges on a solid surface and polar water molecules within liquid. This interaction results in a decrease in interface energy, leading to a reduction in the CA. Ab initio calculations suggest that the reduction in interface energy may stem from the enhanced surface charge on the substrate, which strengthens the hydrogen bond interaction between water and the substrate. These findings have the potential to advance the understanding of CE and wetting phenomena, with applications in energy harvesting, catalysis, and droplet manipulation at liquid-solid interfaces.

Effective parameters on polydimethylsiloxane/graphene composite-based triboelectric nanogenerator performance

ABSTRACT This paper systematically investigates the effective parameter on the performance of polydimethylsiloxane/graphene (PDMS@Gr)-based triboelectric nanogenerators (TENGs) as well as their applications. PDMS@Gr films containing 0, 0.05, 0.5, 1, and 1.5 wt.% graphene are synthesized, and their surface characteristics, mechanical behavior, and electrical properties are characterized. Vertical contact-separation mode TENGs are fabricated, and their performance is evaluated. The results demonstrate that the surface roughness and surface charge density are the most critical parameters for the performance of PDMS@Gr-based TENGs compared to the electrical and mechanical properties of the friction layers. The PDMS@Gr-based TENG with 1 wt.% graphene shows the highest power output of 2.6 W/m2 at an optimized working condition (5 Hz and 15 N). It also exhibits stable power output until 15,000 working cycles and displays battery-free applications by powering a light-emitting diode (LED) array, a calculator, a digital watch, and a digital thermometer.

Ion Transport in Multi-Nanochannels Regulated by pH and Ion Concentration.

Nanochannels are a powerful technique for detecting a wide range of biomolecules without labeling. The ion transport phenomena in nanochannel arrays differ from those in single nanochannels and are caused by interchannel communication. This study uses a fully coupled Poisson-Nernst-Planck (PNP) and Navier-Stokes model to investigate ion transport in nanochannel arrays. Instead of being set at a constant value, the surface charge density used in this study is established by the protonation and deprotonation of the silanol groups that are present on the walls of the silicon-based nanochannels. The surface charge density of the nanochannel walls varies with the number of nanochannels, the channel lateral distance, and the background solution properties, which consequently influence the ionic concentration distribution, flow velocity, and electric field strength. For example, in different numbers of nanochannel systems, the ion concentration in nanochannels is not much different, but it is different in reservoirs, especially near the openings of nanochannels. The number of nanochannels and the distance between nanochannels can also affect the formation of electro-convective vortex zones under certain conditions. These findings can aid in optimizing the nanochannel array design by regulating the number and distance of nanochannels and facilitating the construction of solid-state nanochannel arrays with any desired nanochannel dimensions.

Unveiling the non-innocence of vanadium dopant in TiO2 nanocrystals for advanced energy storage and smart windows

Vanadium doped TiO2 NCs stand out as a promising candidate for energy storage applications due to its high electrical conductivity and redox properties. However, the thermodynamical behavior of the material under working conditions has not been explored and the reasons for its superior performance remain unlocked. This study explores the use of a combination of advanced in situ spectroscopy techniques, including x-ray absorption spectroscopy (XAS), spectro-electrochemistry (SEC), and electrochemical impedance spectroscopy (EIS) to provide unprecedented insights into the intricate electrochemical reaction mechanisms within these nanocrystals. Density functional theory calculations and EIS reveal the active role of substitutional V ions in the TiO2 anatase network as electron donors, enhancing surface charge and carrier density and improving pseudocapacitive properties. Cyclic voltammetry and in situ SEC reveal that V-doped TiO2 NCs exhibit significantly improved charge storage capacities, particularly in the pseudo-capacitance storage mechanism. In situ SEC and XAS analyses indicate that a more effective reduction of Ti4+ ions occurs during the electrochemical process in doped NCs, leading to higher charge capacitance and faster processes. Furthermore, in situ XAS measurements of the V K-edge revealed that the vanadium ions, beyond improving the redox behavior of the host, also actively participate in the reduction process. The significant changes in the V K-edge XANES and extended x-ray absorption fine structure spectra observed under reduction conditions can be ascribed to a change in the structure and oxidation state of the vanadium ions during the electrochemical reaction.

Enhancing ion transport in pressure-driven nanofluidic systems for energy harvesting

In this work, we propose a new design to enhance ion transport in pressure-driven nanofluidic systems for energy harvesting. The proposed system uses two counter-charged nanochannels, i.e., one of the channels is negatively charged while the other one is positively charged. Under a pressure gradient, cations and anions move through negatively and positively charged channels, respectively, in different directions and contribute to the streaming current. Molecular dynamics simulations are employed to study the effects of surface charge density, channel height, and pressure gradient on the streaming current. Compared with the traditional system, where the nanochannel is negatively charged, the streaming current in the proposed system can be enhanced by a factor up to 6.6. In addition to the involvement of both cations and anions, the enhanced current in the proposed system is caused by the strengthened ionic fluxes due to relatively low-energy barriers for ions entering the channels.

Zeta potential of Z-DNA: A new signature to study B-Z transition in linear and branched DNA

Zeta potential is commonly referred as surface charge density and is a key factor in modulating the structural and functional properties of nucleic acids. Although the negative charge density of B-DNA is well understood, there is no prior description of the zeta potential measurement of Z-DNA. In this study, for the first time we discover the zeta potential difference between B-DNA and lanthanum chloride-induced Z-DNA. A series of linear repeat i.e. (CG)n and (GC)n DNA as well as branched DNA (bDNA) structures was used for the B-to-Z DNA transition. Herein, the positive zeta potential of Z-DNA has been demonstrated as a powerful tool to discriminate between B-form and Z-form of DNA. The generality of the approach has been validated both in linear and bDNA nanostructures. Thus, we suggest zeta potential can be used as an ideal signature for the left-handed Z-DNA.

Photoinduced charge generation of nanostructured carbon derived from human hair biowaste for performance enhancement in polyvinylidene fluoride based triboelectric nanogenerator

Carbon nanostructures derived from human hair biowaste are incorporated into polyvinylidene fluoride (PVDF) polymer to enhance the energy conversion performance of a triboelectric nanogenerator (TENG). The PVDF filled with activated carbon nanomaterial from human hair (AC-HH) exhibits improved surface charge density and photoinduced charge generation. These remarkable properties are attributed to the presence of graphene-like nanostructures in AC-HH, contributing to the augmented performance of PVDF@AC-HH TENG. The correlation of surface morphologies, surface charge potential, charge capacitance properties, and TENG electrical output of the PVDF composites at various AC-HH loading is studied and discussed. Applications of the PVDF@AC-HH TENG as a power source for micro/nanoelectronics and a movement sensor for detecting finger gestures are also demonstrated. The photoresponse property of the fabricated TENG is demonstrated and analyzed in-depth. The analysis indicates that the photoinduced charge carriers originate from the conductive reduced graphene oxide (rGO), contributing to the enhanced surface charge density of the PVDF composite film. This research introduces a novel approach to enhancing TENG performance through the utilization of carbon nanostructures derived from human biowaste. The findings of this work are crucial for the development of innovative energy-harvesting technology with multifunctionality, including power generation, motion detection, and photoresponse capabilities.

High-rate aqueous magnesium ion battery enabled by Li/Mg hybrid superconcentrated electrolyte

Rechargeable aqueous magnesium ion batteries (AMIBs) are considered a promising energy storage system due to the relatively high energy density, excellent rate performance and reversibility, and absence of dendrite formation during cycling. However, the high surface charge density of Mg2+ ions results in slow diffusion kinetics, and high voltage leads to excessive electrolyte decomposition at the electrode/aqueous electrolyte interface, thereby limiting the development of high-energy–density MIBs. In this work, we extend the electrochemical stability window of the aqueous electrolyte to 2.1 V by using a hybrid ion superconcentrated electrolyte at concentrations not achievable with Mg2+ electrolytes alone. The AMIB with a water-in-salt (WIS) electrolyte delivers discharge capacities of up to 200.6 and 84.4 mAh g−1, and energy densities of 170.1 and 68.1 Wh Kg−1 at 0.5 and 20 A g−1, respectively, representing excellent rate performance, while retaining 85 % of the specific capacity after 2000 cycles. Additionally, we explore the corresponding electrochemical reaction mechanism, revealing the synergistic effect of Mg2+ and Li+ ions in the charge/discharge process, which supports the excellent electrochemical performance of AMIB.

Electrostatic conductive disc singularity resolved

The conventional electrostatic solutions for two-dimensional (2D) electrodes possess edge singularities for the surface charge density σ and the normal component of the electric field En. These singularities are generally non-physical because they admit infinite gradients of the concentration of free charge carriers. In particular, they are unacceptable in the studies of the local field sensitive effects, such as the electric breakdown and the ferroelectric domain reversal. We claim that account for diffusion of free charge carriers leads to the disappearance of the edge singularities. This generalization occurs consistently within the same basic concept of conduction. Specifically, we consider the case of U-biased circular disc electrode of radius a. Account for diffusion leads here to a strongly nonlinear integral 2D equation for the electrostatic potential φ(r). Numerical solution of this equation shows that the law σ(a)∝U2/a takes place. Outside a close vicinity of the disc edge, we stay close to the conventional electrostatic solution for φ and σ.

The Effect of Lysozyme on the Aggregation and Charging of Oxidized Carbon Nanohorn (CNHox) in Aqueous Solution

To clarify the effect of proteins on the charging and aggregation–dispersion characteristics of oxidized carbon nanohorn (CNHox), we measured the electrophoretic mobility and stability ratios as a function of concentrations of a model protein, lysozyme (LSZ), and KCl. The zeta potential from the electrophoretic mobility of CNHox was neutralized and reversed by the addition of oppositely charged LSZ. Electrical and hydrophobic interactions between CNHox and LSZ can be attributed to the adsorption and charge reversal of CNHox. The stability ratio of CNHox in the presence or absence of LSZ showed Derjaguin–Landau and Verwey–Overbeek (DLVO) theory-like behavior. That is, the slow aggregation regime, fast aggregation regime, and critical coagulation concentration (CCC) were identified. At the isoelectric point, only the fast aggregation regime was shown. The existence of patch-charge attraction due to the charge heterogeneity on the surface was inferred to have happened due to the enhanced aggregation of CNHox at high LSZ dosage and low electrolyte concentration. The relationship between critical coagulation ionic strength and surface charge density at low LSZ dosage showed that the aggregation of CNHox is in line with the DLVO theory. An obvious decrement in the Hamaker constant at high LSZ dosage can probably be found due to an increased interaction of LSZ-covered parts.

Heat and mass transfer of molten carbonates at charged electrode interface and its anisotropic behavior: A molecular dynamics study

Molten carbonates are broadly used in fuel cells with potential applications in reducing CO2 emission, while their heat and mass transfer properties near a charged electrode surface are less well understood. Using molecular dynamics (MD) simulations, the heat and mass transfer properties of molten Na2CO3-K2CO3 salts at charged nickel surfaces are revealed in this study. Simulation results indicates that when surface charge density increases, molten salt’s thermal transport exhibit anisotropic behavior: the interfacial thermal resistance show strong dependence on the surface charge while heat transfer parallel to surface is not sensitive to the surface charge. As for interfacial mass transfers, the shear viscosity of the carbonate tends to rise with external electric field, while the corresponding ion diffusion does not vary very much and exhibit position-dependent behavior. To further explore this, we find that the anisotropy of this heat and mass transfer properties is primarily attributed to the nonuniform ion distribution in the direction perpendicular to nickel surface with the increasing of charge, while the interatomic correlation does not vary much as surface charge increases. These results have suggested that the anisotropy of heat and mass transport properties of molten salt near electrode, which should be taken care of when modelling the macroscopic heat and mass transport of molten carbonate fuel cells in particular.