Surface Charge Distribution Research Articles

In Situ Transformation of Hybrid Bismuth Halide into Rhombohedral Bismuth for Electrochemical CO2 Reduction to Formate

AbstractBi‐based electrocatalysts have attracted high attention due to their high selectivity for formate, low cost, and high biocompatibility. Surface modification with halides can adjust the surface charge distribution of metal catalysts, thereby regulating the binding force of the intermediate. Organic‐inorganic hybrid bismuth halides provide an alternative, especially low dimensional structures. Herein, zero‐dimensional hybrid bismuth halides containing Bi4I16 units (denoted as Bi4I16) was recommended as pre‐catalyst due to the Bi ⋅ ⋅ ⋅ Bi spacing in Bi4I16 is 4.760 Å, nearly equaling to the Bi ⋅ ⋅ ⋅ Bi spacing in rhombohedral Bi (4.750 Å). The equal spacing may be more beneficial for the electricity‐driven in situ conversion and rearrangement of Bi atoms in the catalytic process. As a contrast, zero‐dimensional bismuth halide containing Bi2I9 units (denoted as Bi2I9) with shorter Bi ⋅ ⋅ ⋅ Bi spacing (4.2415 Å) was prepared. The working electrode prepared by Bi4I16 ink was measured for CO2RR, and the partial formate current density can reach 8.2 mA cm−2 at −1.1 V vs RHE. The Bi4I16 catalyst delivers a maximum Faradaic Efficiency (FE, ~80 %) for formate at −0.86 V vs RHE and maintain a FE higher than 78.5 % after 16 h.

Nitrogen-doped carbon nanosheet confined PtNi alloy for efficient acidic electrocatalytic hydrogen evolution reaction

Low intrinsic electrocatalytic activity and inferior conductivity limit the application of Ni/NC in acidic electrocatalytic hydrogen evolution reaction (HER). Herein, we prepared nitrogen-doped carbon nanosheet confined PtNi alloy electrocatalysts (PtNi/NC-10) using PtCl62− electrostatic adsorption coupling melamine pyrolysis nitriding strategy. PtNi alloying was confirmed by the crystallinity decrease and lattice expansion of Ni/NC. The alloying and confinement effect of Metal-Organic Frameworks (MOFs) suppresses the oxidation and agglomeration of metal nanoparticles during pyrolysis, thus significantly reducing particle size, increasing specific surface area, and promoting the exposure of active sites. The strong electronic interaction between Pt and Ni optimizeds the surface charge distribution, enhancing the adsorption of H species on electron-rich Pt sites, thereby improving reaction kinetics. In addition, PtNi alloying improves the conductivity of the material, accelerating charge transfer and proton transport. Consequently, the prepared PtNi/NC-10 exhibits superior HER performance than Ni/NC in 0.5 M H2SO4 solution, even comparable to commercial 20 wt% Pt/C, with the overpotentials of 35 mV at 0.01 A cm−2. Furthermore, the electrocatalysts assembled PtNi/NC-10-CP‖RuO2-TFF proton exchange membrane (PEM) electrolyzer only requires 2.32 V cell voltage to achieve 1 A cm−2, presenting practical application prospects. Our work provides a novel idea for designing efficient and stable MOFs confined to alloy-based HER electrocatalysts.

Efficient remediation of cadmium and lead contaminated soil in coal mining areas by MICP application in hydrothermal carbon-based bacterial agents: Nucleation pathways and mineralization mechanisms

The development of industrial mining has resulted in a large amount of Cd and Pb polluting the soil in mining areas, and leads to adverse health effects on the life of both plants and animals. Here, a soft template method was conducted to prepare hydrothermal carbon (HC) with regular morphology, which assisted with Bacillus pasteurii to induce calcite precipitation for decontamination of mining soil. Soil remediation experiments over 30 days of remediation with an HC microbial agent (HCMA) resulted in 89.4% and 87.8% decrease in the amount of leached Cd and Pb, respectively. The content of exchangeable Cd and Pb decreased by 76.1% and 81.0%, respectively. At the same time, soil fertility significantly improved. The electrostatic potential and surface charge distribution of extracellular polymeric substances (EPS) and sodium citrate (NaCit) were analyzed using DFT simulations, their nucleophilic and electrophilic regions were determined, and the nucleation mechanism was determined. The DFT results indicated that the oxygen-containing groups of EPS and NaCit had strong negative electrostatic potential and electronegativity, which could cause Cd2+, Pb2+, and Ca2+ to aggregate on their surfaces. They also combined with CO32− produced by urease during the decomposition of urea, resulting in Cd2+ and Pb2+ being encapsulated by calcium carbonate to form a coprecipitate. X-ray diffraction analyses revealed that the precipitate was mainly calcite calcium carbonate, which is more stable and less prone to secondary leaching of HMs. The gathered data prove the significant role of HCMA in remediation of mining soil contaminated with Cd and Pb.

Mechanically activated and deactivated ion transport across nanopores with heterogeneous surface charge distributions

To mimic the intricate and adaptive functionalities of biological ion channels, electrohydrodynamic ion transport has been studied extensively, albeit mostly, across uniformly charged nanochannels. Here, we analyze the ion transport under coupled electric field and pressure across heterogeneously charged nanopores with oppositely charged sections on their lateral surface. We only consider such pores with symmetric hourglass-like and cylindrical shapes to focus on the effects of the non-uniform surface charge distribution. Finite-element simulations of a continuum model demonstrate that a pressure applied in either direction of the pore-axis equally suppresses or amplifies the ionic conductance, depending on the electric field polarity, by distorting the quasi-static distribution of ions in the pore. The resulting anomalous mechanical deactivation and activation of ionic current under opposite voltage biases exhibit the functional modularity of our setup, while their intensities are highly tunable, substantially greater than those of analogous behaviors in other nanochannels, and fundamentally correlated to ionic current rectification (ICR) in our pores. A detailed study of ICR subsequently reveals its counterintuitive non-monotonous variations, in the pores, with the magnitude of applied voltage and the pore length, that can help optimize their diode-like behavior. We further illustrate that while the hourglass-shaped nanopores yield the more efficient mechanical suppressors of ion transport, their cylindrical analogs are the superior rectifiers and mechanical amplifiers of ion conduction. Therefore, this article provides a blueprint for the strategic design of nanofluidic circuits to attain a robust, modular, and tunable control of ion transport under external electrical and mechanical stimuli.

Tuning Pyrrolo[3,2-b] pyrrole Core-based hole transport materials properties via Addition of fluorine for highly efficient and Stable planar perovskite solar cells

Hole-transport materials (HTM) play a crucial role in functioning perovskite solar cells (PSCs). In this research, we develop and synthesize two pyrrolo[3,2-b] pyrrole core (PP) based small molecular HTMs, FPPY and BPPY with/without (w/wo) fluorine (F) substitution on PP core that connected to the carbazole diphenylamine peripheral end groups, respectively. The F-substituted fused electron-rich pyrrole ring core greatly impacts FPPY molecular surface charge distribution, which contributes to higher hole extraction properties and excellent band alignment. Finally, FPPY-based PSCs obtain a best power conversion efficiency (PCE) of 24.3 %, significantly higher than BPPY (20.1 %). After aging 2000 h at ambient condition (25 °C, 30–50 % RH), the FPPY-based device still keeps over 87 % of its initial PCE.

Phase Dependence of Surface Charge Measurement on Epoxy Insulator in C4F7N/CO2 under AC Voltage.

The application of binary gas mixtures consisting of heptafluorobutyronitrile (C4F7N) and carbon dioxide (CO2) in AC GIS is currently attracting much attention. Therefore, the evaluation of the gas-solid interface charge distribution characteristics of epoxy resin is indispensable. Additionally, the phase-dependency of the charging behavior remains not fully understood. We simulated coaxial electrode structure in GIS and investigated the surface charge distribution on a down-scaled epoxy insulator. The influence of the truncated phase angle and duration of AC voltage on charge behavior were analyzed, and the charge transport mechanism under AC voltage was theoretically analyzed. The results showed that there was a noticeable negative charge speckle with the presence of the metal particle and the accumulated negative charge on the insulator surface far exceeded that of the positive charge. The maximum surface charge density and the amount of surface charge accumulated first increased and then decreased over time. It was found that the phase angle has a negligible influence on the surface charge distribution at the cut-off moment.

Torque about electrostatically charged spheres makes them more attractive.

The strength of interparticle interactions in a granular system controls how a collection of insulating particles flow, cohere and fragment. Forces due to electrostatic charging, particularly in free-fall or low gravity environments, can dominate the static and dynamic interactions with important implications for understanding natural and industrial processes. Here we show that shaking of homogeneous, spherical particles can result in a non-uniform surface charge distribution. The measured dipole moment and torque for each particle are found to be strongly correlated. However, our model shows that to predict the torque and force requires one to consider the full surface charge distribution. This overlooked torque is not only significant, but would amplify attractive interactions through particle reorientation.

Dependence of Protein Immobilization and Photocurrent Generation in PSI-FTO Electrodes on the Electrodeposition Parameters.

This study investigates the immobilization of cyanobacterial photosystem I (PSI) from Synechocystis sp. PCC 6803 onto fluorine-doped tin oxide (FTO) conducting glass plates to create photoelectrodes for biohybrid solar cells. The fabrication of these PSI-FTO photoelectrodes is based on two immobilization processes: rapid electrodeposition driven by an external electric field and slower adsorption during solvent evaporation, both influenced by gravitational sedimentation. Deposition and performance of photoelectrodes was investigated by UV-Vis absorption spectroscopy and photocurrent measurements. We investigated the efficiency of PSI immobilization under varying conditions, including solution pH, applied electric field intensity and duration, and electrode polarization, with the goals to control (1) the direction of migration and (2) the orientation of the PSI particles on the substrate surface. Variation in the pH value of the PSI solution alters the surface charge distribution, affecting the net charge and the electric dipole moment of these proteins. Results showed PSI migration to the positively charged electrode at pH 6, 7, and 8, and to the negatively charged electrode at pH 4.4 and 5, suggesting an isoelectric point of PSI between 5 and 6. At acidic pH, the electrophoretic migration was largely hindered by protein aggregation. Notably, photocurrent generation was consistently cathodic and correlated with PSI layer thickness, and no conclusions can be drawn on the orientation of the immobilized proteins. Overall, these findings suggest mediated electron transfer from FTO to PSI by the used electrolyte containing 10 mM sodium ascorbate and 200 μM dichlorophenolindophenol.

Heterogeneous atoms mediated formation MnCo2S4/PNG heterostructures for high-performance supercapacitors

Transition metal sulfides are considered as potential electrode materials for high performance energy storage devices. However, structural instability during electrochemical reactions has seriously hindered their wide applications. In this study, we demonstrate that MnCo2S4/PNG (N- and P-doped graphene) composite constructed with hetero-atomic induction exhibits excellent morphological stability. Heterogeneous atoms doping on graphene can change its surface charge distribution. Under the induced effect of surface charge, the crystal growth and assembly process of MnCo2S4 nanostructure are changed as well, which leads to MnCo2S4 nanoparticles (NPs) uniformly anchored on the curled and folded PNG layer. In this case, it avoids the agglomeration of MnCo2S4 NPs, and thus increasing the specific surface area and pore volume of the composite, which is conducive to the full contact between the electrode and the electrolyte and therefore the rapid diffusion rate of the electrolyte ions at the interfaces. The obtained 1.4MnCo2S4/PNG material has a specific capacitance of 2465 F g−1 at 1 A g−1. In addition, the electrode possesses high conductivity, excellent rate performance and cyclic stability. The assembled 1.4MnCo2S4/PNG//PNG asymmetric supercapacitor yields an energy density of up to 65.1 Wh kg−1 under the power density of 800 W kg−1, showing excellent energy storage characteristics.

Investigation of Partial Discharge Transformation Characteristics in Polyimide (PI) Insulations under High-Frequency Electric Stress.

This research delves into the primary issue of polyimide (PI) insulation failures in high-frequency power transformers (HFPTs) by scrutinizing partial discharge development under high-frequency electrical stress. This study employs an experimental approach coupled with a plasma simulation model for a ball-sphere electrode structure. The simulation model integrates the particle transport equation, Poisson equation, and complex chemical reactions to ascertain microscopic parameters, including plasma distribution, electric field, electron density, electron temperature, surface, and space charge distribution. The effect of the voltage polarity and electrical energy on the PD process is also discussed. The contact point plays a pivotal role in triggering partial discharges and culminating in the breakdown of PI insulation. Asymmetry phenomena were found between positive and negative half-cycles by analyzing the PD data stage by stage. A significant number of PDs increased at every stage and the PD amplitude was higher during the negative cycle at the initial stage, but in later stages, the PD amplitude was found to be higher in the positive half-cycle, and scanning electron microscopy (SEM) revealed that the maximum damage occurred near the contact point junction. The simulation results show that the plasma initially accumulates the electron density near the contact point junction. Under the action of the electric field, plasma starts traveling at the PI surface outward from the contact point. Before the PD activity, all parameters have higher values in the plasma head. The microscopic parameters reveal maximum values near the contact point junction, during PD activities where significant damage takes place. These parameter distributions exhibit a decreasing trend over time as when the PD activity ends. The model's predictions are consistent with the experimental data. The paper lays the foundation for future research in polymer insulation design under high-frequency electrical stress.

Overexpression of a Designed Mutant Oxyanion Binding Protein ModA/WtpA in Acidithiobacillus ferrooxidans for the Low pH Recovery of Molybdenum and Rhenium.

Molybdenum and rhenium are critically important metals for a number of emerging technologies. We identified and characterized a molybdenum/tungsten transport protein (ModA/WtpA) of Acidithiobacillus ferrooxidans and demonstrated the binding of tungstate, molybdate, and chromate. We used computational design to expand the binding capabilities of the protein to include perrhenate. A disulfide bond was engineered into the binding pocket of ModA/WtpA to introduce a more favorable geometric coordination and surface charge distribution for oxyanion binding. The mutant protein experimentally demonstrated a 2-fold higher binding affinity for molybdate and 6-fold higher affinity for perrhenate. The overexpression of the wild-type and mutant ModA/WtpA proteins in A. ferrooxidans cells enhanced the innate tungstate, molybdate, and chromate binding capacities of the cells to up to 2-fold higher. In addition, the engineered cells expressing the mutant protein exhibited enhanced perrhenate binding, showing 5-fold and 2-fold higher binding capacities compared to the wild-type and ModA/WtpA-overexpressing cells, respectively. Furthermore, the engineered cell lines enhanced biocorrosion of stainless steel as well as the recovered valuable metals from an acidic wastewater generated from molybdenite processing. The improved binding efficiency for the oxyanion metals, along with the high selectivity over nontargeted metals under mixed metal environments, highlights the potential value of the engineered strains for practical microbial metal reclamation under low pH conditions.

Evaluation of cold plasma treatment technology in biosynthesized silver nanoparticles encapsulated with chitosan by Aliinostoc persicum SA14 against HepG-2

Hepatocellular carcinoma (HCC) is the commonest cancer and the third most common cause of cancer-related mortality. The combination of cold atmospheric plasma (CAP) and nanoparticles is a promising treatment for hepatocellular carcinoma cancers. In the present study, activated water was prepared using the cold atmospheric plasma technique (JET and PAW), and then the biosynthesis ability of silver nanoparticles by the cyanobacterium Aliinostoc persicum SA14 was measured after cultivation in the culture medium containing activated water at 5, 15, and 20 min. After the encapsulation of nanoparticles with chitosan and UV–visible spectroscopy analysis, the characterization of AgNPs, including FTIR analysis. X-ray diffraction, particle size and zeta potential, SEM, TEM, as well as cytotoxicity assays against HepG-2 cell lines, were performed. The comparison of the absorption spectra of silver oxide nanoparticles prepared by the boiling-dender method at concentrations and different times showed that the production of silver nanoparticles was confirmed for all three samples based on the amount of absorption obtained. The outcomes of field emission scanning electron microscopy at all magnifications exhibited that spherical nanoparticles are scattered on the surface of the polymer matrix. Furthermore, the FT-IR spectrum and XRD crystallography confirmed the success of chitosan's production of microcoated silver nanoparticles. The results of the cytotoxicity test against HepG-2 cell lines showed that with increasing concentrations of silver nanoparticles, the survival frequency of cancer cells declined significantly. In conclusion, the tests confirmed that the silver nanoparticles produced by cyanobacteria act as both a stabilizing and reducing agent. The results indicated that CAP decreases nanoparticle size, decreases surface charge distribution of AgNP, and induces uptake, aggregation, and enhanced cytotoxicity against HepG-2 in vitro. The chitosan-AgNPs with cold plasma could have potential applications in the food, agricultural, and pharmaceutical industries.

Circulating extracellular vesicles in Systemic Lupus Erythematosus: physicochemical properties and phenotype

ObjectiveThis study aimed to identify the physicochemical and phenotypic characteristics of circulating Extracellular Vesicles (EVs) in the plasma of patients with SLE, with or without Lupus Nephritis (LN), and their...

Impact of nanosilver surface electronic distributions on serum protein interaction and hemocompatibility.

Translation of silver-based nanotechnology "from bench to bedside" requires a deep understanding of the molecular aspects of its biological action, which remains controversial at low concentrations and non-spherical morphologies. Here, we present a hemocompatibility approach based on the effect of the distinctive electronic charge distribution in silver nanoparticles (nanosilver) on blood components. On basis of spectroscopic, volumetric, microscopic, dynamic light scattering measurements, pro-coagulant activity tests and cellular inspection we determine that, at extremely low nanosilver concentrations (0.125 - 2.5 μg mL-1) there is a relevant interaction effect on serum albumin and on red blood cells. The explanation has its origin in the surface charge distribution of nanosilver and their electron-mediated energy transfer mechanism. Prism-shaped nanoparticles, with anisotropic charge distributions, act at the surface level generating a compaction of the native protein molecule, while the spherical nanosilver, by exhibiting isotropic surface charge, generates a polar environment comparable to the solvent. Both morphologies induce aggregation at NPs / BSA ≅ 0.044 molar ratio values without altering the coagulation cascade tests, although the spherical-shaped nanosilver has a negative impact on red blood cells. Overall, our results suggest that the electron distributions of nanosilver, even at extremely low concentrations, are a critical factor influencing the molecular structure of blood proteins and red blood cells' membranes. Isotropic forms of nanosilver should be considered with caution, as they are not always the least harmful.

Effects of Surface Charge Distribution and Electrolyte Ions on the Nonlinear Spectra of Model Solid-Water Interfaces.

Molecular dynamics simulations of model charged solid/water interfaces were carried out to provide insight about the relationship between the second-order nonlinear susceptibility χ(2) and the structure of the interfacial water layer. The results of the calculations reveal that the density fluctuations of water extend to about 12 Å from the surface regardless of the system, while the orientational ordering of molecules is long-ranged and is sensitive to the presence of electrolytes. The charge localization on the surface was found to affect only the high-frequency part of the Im[χ(2)] spectrum, and the addition of salt has very little effect on the spectrum of the first water layer. For solid/neat water interfaces, the spectroscopically active part of the liquid phase has a thickness largely exceeding the region of density fluctuations, and this long-ranged nonlinear activity is mediated by the electric field of the molecules. The electrolyte ions and their hydration shells act in a destructive way on the molecular field. This effect, combined with the screening of the surface charge by ions, drastically reduces the thickness of the spectroscopic diffuse layer. There is an electrolyte concentration at which the nonlinear response of the diffuse layer is suppressed and the χ(2) spectrum of the interface essentially coincides with that of the first water layer.

Non-uniform surface charge distribution of tribodielectric material by edge effect

The surface effect of dielectric material is one of the important cornerstones for the performance parameters. Here, an “edge effect” model of the surface charge of tribodielectric material in the natural environment based on the semiconductor interface and surface theory is established for the first time, and a theoretical exploration of the surface charge distribution is carried out as well. The result indicates that the surface charge density at the center of the tribodielectric material is higher and gradually decreases towards the edges. By exploring the functional relationship between the surface charge density and the edge distance, the interrelation between the inner edge width, outer edge width, and nick distance and the output charge on the tribodielectric material can be achieved. Meanwhile, the output performance is a nearly 3-fold higher between the fully covered triboelectric nanogenerator (FC-TENG) and non-fully covered triboelectric nanogenerator (NFC-TENG) due to the “edge effect” of the tribodielectric material. Finally, the distribution of surface charge is intuitively demonstrated by the visual experiment. This work provides a deeper understanding of the charge distribution on the surface of tribodielectric materials, holding significant implications for enhancing the fabrication process of TENG and its commercialization and mass production.

Regulating band structure, charge transfer and separation, oxygen adsorption and activation by surface ion modification.

As a most promising environmental technology, the substantial enhancement of photocatalytic efficiency is still a big challenge for practical applications. In this work, the surface of Bi2O2CO3 (BOC) nanotubes are modified by Cl and I. The as-obtained samples at different hydrothermal temperatures (T) are designated as T-X-BOC (X = Cl, I). X-ray diffraction (XRD), energy dispersive X-ray (EDX) spectroscopy and X-ray photoelectron spectroscopy (XPS) prove that Cl and I merely chemically adsorb on the BOC surface, rather than dope into the crystal lattice. The surface modification of Cl and I slightly increases light absorption range, while significantly promotes the photoelectron migration from bulk to the surface that greatly enhances the carrier separation efficiency. Density functional theory (DFT) calculations further prove that surface Cl and I have adjusted band structure and surface charge distribution. Besides, the surface Cl and I favor the O2 adsorption and trap the surface photoelectrons, thus promoting the formation of •O2-; while the surface Cl and I impede the surface adsorption of H2O, thus refraining the generation of •OH. In the degradation of rhodamine B (RhB), holes and •O2- radicals play the crucial role. Under ultraviolet light irradiation (λ < 420nm) for 45min, the RhB degradation ratios over 150-Cl-BOC (94%) and 150-I-BOC (85%) are 4.2 and 3.7 times higher than that of original BOC (18%), respectively. This work demonstrates that the simple surface halogenation modification greatly improves the photocatalytic activity.

Ion current rectification coupled with asymmetric temperature and surface charge in ultrashort conical nanopores

Ion current rectification (ICR) is one of the electrodynamic properties in asymmetric nanochannels, which has been utilized to develop biosensors, heavy metal ion detection, and ion diodes. Previous studies on ICR mainly focused on long nanopores (length >500 nm), and relatively few studies on ion rectification performance in short nanopores. Here, we use a finite element numerical solution to simulate the effect of coupling asymmetric temperature and surface charge distribution on the ion rectification performance of ultrashort conical nanopores (length = 100 nm). The results show that the ion rectification performance is significantly improved when the inner and outer surfaces of the nanopore are charged non-uniformly, which is more than three times that when the inner surface of the nanopore is charged non-uniformly or the outer surface is charged non-uniformly. In addition, the positive temperature difference enhances the ion enrichment and dissipation and improves the ion rectification performance of nanopores. On the contrary, negative temperature difference inhibits ion enrichment and dissipation in pores, which is not conducive to improving ion rectification performance. Abnormal behavior is observed for nanopores non-uniform charged only on the outer wall surface, where the negative temperature gradient enhances the accumulation and dissipation of ions within the pores, thereby increasing the rectification ratio. In addition, in order to more clearly understand the ion transport behavior in the ultrashort nanopore under asymmetric temperature conditions, we further investigated the influence of the tip radius of the nanopore, the solution volume concentration, and the charge type of each surface charge distribution on the ion current rectification performance. The results reveal the ion transport mechanism of ultrashort conical nanopores and provide practical guidance for designing and optimizing nanofluidic devices.

Modulating the Water Contact Angle Using Surface Roughness: Interfacial Properties of Hexagonal Boron Nitride Surfaces.

Hexagonal boron nitride (hBN) exhibits immense potential in H2O-related technologies, but its interaction with H2O, especially on rough surfaces, remains unclear. This study unravels the influence of surface roughness and force field selection on hBN wettability using molecular dynamics (MD) simulations. We leverage quantum mechanical calculations to accurately capture the hBN surface charge distribution and combine it with free energy calculations via MD simulations for the hBN-H2O interfaces. Incorporating surface roughness into the model yields results in close agreement with the experimental contact angle of 66° for H2O using FF-3 force fields, validating the simulation approach. However, this approach can yield an unrealistic water contact angle (WCA) of 0° for FF-2 force fields, highlighting the crucial role of force field selection and realistic surface representations. We further dissect the impact of roughness on the WCA, identifying the individual contributions of electrostatic and Lennard-Jones interactions to the work of adhesion. This research investigates the combined impact of surface roughness and force fields on interfacial properties, providing new possibilities for the advancement and optimization of desalination.

Efficiently solving large-scale electrostatic lightning problems by integrating characteristic basis functions into boundary element method

The evaluation of the electric field near objects of complex geometries is critical in the pre-bridging regime of lightning strikes in high-voltage transmission systems, which is subject to an open domain problem and can be computationally expensive. In this paper, the characteristic basis function method (CBFM) is incorporated into the conventional boundary element method (BEM) to efficiently handle large-scale electrostatic problems. Within the CBFM, low-level basis functions have been replaced by high-level macro characteristic basis functions, resulting in a significant reduction in the number of degrees of freedom. This reduction in unknowns allows iteration-free direct solvers to approximate the matrices, further reducing the computational complexity of the problem. Numerical examples of the surface charge distribution of an actual 500 kV tower-transmission-line system and a three MW wind turbine in the lightning environment demonstrate the accuracy of the proposed CBFM, while requiring considerably much fewer computational resources compared with conventional BEM. Furthermore, CBFM is highly parallelizable, implying the feasibility of handling large electrostatic lightning problems with complex geometries.