Space Charge Research Articles

Impact of La doping on the optoelectronic and structural properties of CsPbIBr2 perovskite solar cell

Inorganic lead halide perovskite solar cells (IPSC) have high power conversion efficiency (PCE). Currently, heteroatom substitution is a promising method for enhancing the properties of perovskite materials and the performance of associated devices. This study outlines the production process of a perovskite solar cell made from inorganic CsPbIBr2 with a 4 % La doping. The cubic crystal structure with large grain size and small band gap energy is observed at 4 % La–CsPbIBr2. The optoelectronic and structural characteristics of CsPbIBr2 perovskite solar cells have been substantiated through various methodologies, such as the determination of space charge restricted current, examination of the photoluminescence decay profile, assessment of charge transfer resistance, and utilization of Mott Schottky analysis. The incorporation of lanthanum-doped cesium lead iodide bromide (La-doped CsPbIBr2) resulted in a notable enhancement in both the open circuit voltage (Voc), and the short circuit current density (Jsc), leading to a much higher overall efficiency of 9.89 % compared to the pristine counterpart, which exhibited an efficiency of 8.62 %.

Realizing Outstanding Energy Storage Performance in KBT-Based Lead-Free Ceramics via Suppressing Space Charge Accumulation.

The great potential of K1/2Bi1/2TiO3 (KBT) for dielectric energy storage ceramics is impeded by its low dielectric breakdown strength, thereby limiting its utilization of high polarization. This study develops a novel composition, 0.83KBT-0.095Na1/2Bi1/2ZrO3-0.075 Bi0.85Nd0.15FeO3 (KNBNTF) ceramics, demonstrating outstanding energy storage performance under high electric fields up to 425kVcm-1: a remarkable recoverable energy density of 7.03Jcm-3, and a high efficiency of 86.0%. The analysis reveals that the superior dielectric breakdown resistance arises from effective mitigation of space charge accumulation at the interface, influenced by differential dielectric and conductance behaviors between grains and grain boundaries. Electric impedance spectra confirm the significant suppression of space charge accumulation in KNBNTF, attributable to the co-introduction of Na1/2Bi1/2ZrO3 and Bi0.85Nd0.15FeO3. Phase-field simulations reveal the emergence of a trans-granular breakdown mode in KNBNTF resulting from the mitigated interfacial polarization, impeding breakdown propagation and increasing dielectric breakdown resistance. Furthermore, KNBNTF exhibits a complex local polarization and enhances the relaxor features, facilitating high field-induced polarization and establishing favorable conditions for exceptional energy storage performance. Therefore, the proposed strategy is a promising design pathway for tailoring dielectric ceramics in energy storage applications.

Electronic properties of polyethylene naphthalate as derived from photo-stimulated discharge, luminescence experiments and quantum chemical calculation

The electronic properties of thin films of poly(ethylene 2,6-naphthalate)—PEN, are investigated based on their photo-physical (optical absorption, photoluminescence) and electrical (space charge distribution, photo-stimulated discharge) behavior. Photo-stimulated currents are associated with optical absorption of the material leading to space charge dissipation as demonstrated by space charge distribution measurement. Based on this set of experimental results and quantum chemical calculation performed on PEN macromolecular system, we propose a new scheme for the electronic levels of PEN. This scheme allows understanding the mechanisms at play in photo-stimulated discharge. One of the main conclusions of our work is that photo-stimulated current measurements do not probe the energy level of traps. Detrapping of charges results from a two-step process where the photon energy is absorbed by chromophores that restitute a part of this energy to trapped charges through various mechanisms. Moreover, the new scheme allows discussing the components of the luminescence excited under different stresses, being electric field, electronic and UV irradiation, charge recombination and thermal activation.

Model Parameters and Degradation Mechanism Analysis of Indium Phosphide Hetero-Junction Bipolar Transistors Exposed to Proton Irradiation

The degradation properties of Indium phosphide hetero-junction bipolar transistors (InP HBTs) under proton irradiation are studied and modelled using a compact model for pre-irradiation, post-irradiation, and post-annealing. The variation rates of the model parameters, such as the base–emitter saturation current (ISE) and ideality factor in the ideal region (NE) in the forward Gummel characteristics, the zero-biased capacitance (Cje) and the grading factor (Mjer) in the BE junction capacitance, and the transit time parameter in the base region (Tfb), are analysed to delve into the degradation mechanism induced by proton irradiation. The displacement damage, induced by proton irradiation in the space charge region of the base–emitter junction and in the quasi-neutral bulk base region, is found to be responsible for the decrease in current gain and cut-off frequency. After annealing, the variation rates of the parameters decrease significantly compared to post-irradiation. This suggests that the recombination of unstable defects leads to a slight recovery in the degradation characteristics of InP HBTs after a period of annealing.

Propagation of nanosecond discharge in an air gap containing a water droplet: modelling and comparison with time-resolved images

The plasma-water interface is a complex medium characterized by interesting physical and chemical phenomena useful for many applications such as water processing or material synthesis. In this context, optimizing the transport of reactive species from plasma to water is crucial, and it may be achieved by increasing the surface-to-volume ratio of the processed object. Herein, we study the characteristics of a streamer produced by nanosecond discharge in air gap with a droplet of deionized water. The discharge is characterized experimentally by electrical measurements as well as by 1 ns-intergated ICCD images. To report plasma properties that are not accessible through experiment, such as the spatio-temporal evolution of electron density, electric field, and space charge density, a 2D fluid model is developed and adapted to the experimental geometry. Due to the fast propagation of the ionization front, the droplet is considered as a solid dielectric. The model solves Poisson’s equation as well as the drift-diffusion equation for electrons, positive ions, and negative ions. The utilized transport coefficients are tabulated as a function of the reduced electric field. Helmholtz equations are also included in the model to account for photoionization. The electron impact ionization source obtained from the model is compared to experimental 1 ns-integrated ICCD images, and a good agreement is observed. Finally, the model is used to investigate the influence of droplet dielectric permittivity and wetting angle (the angle between a liquid surface and a solid surface) on the properties of the discharge. Overall, the data reported herein demonstrate that the model can be used to investigate plasma properties under different conditions.

Interfacial Engineering of MoS2@CoS2 Heterostructure Electrocatalysts for Effective pH-Universal Hydrogen Evolution Reaction.

The practical utilization of the hydrogen evolution reaction (HER) necessitates the creation of electrocatalysts that are both efficient and abundant in earth elements, capable of operating effectively within a wide pH range. However, this objective continues to present itself as an arduous obstacle. In this research, we propose the incorporation of sulfur vacancies in a novel heterojunction formed by MoS2@CoS2, designed to exhibit remarkable catalytic performances. This efficacy is attributed to the advantageous combination of the low work function and space charge zone at the interface between MoS2 and CoS2 in the heterojunction. The MoS2@CoS2 heterojunction manifests outstanding hydrogen evolution activity over an extensive pH range. Remarkably, achieving a current density of 10 mA cm-2 in aqueous solutions 1.0 M KOH, 0.5 M H2SO4, and 1.0 M phosphate-buffered saline (PBS), respectively, requires only an overpotential of 48, 62, and 164 mV. The Tafel slopes for each case are 43, 32, and 62 mV dec-1, respectively. In this study, the synergistic effect of MoS2 and CoS2 is conducive to electron transfer, making the MoS2@CoS2 heterojunction show excellent electrocatalytic performance. The synergistic effects arising from the heterojunction and sulfur vacancy not only contribute to the observed catalytic prowess but also provide a valuable model and reference for the exploration of other efficient electrocatalysts. This research marks a significant stride toward overcoming the challenges associated with developing electrocatalysts for practical hydrogen evolution applications.

Induced Diffusion Effect Realizes Heterogeneous Separation/Aggregation for In Situ Fabrication of Heterostructure with Enhanced Catalytic Activity

AbstractSpace charge transfer, which can be provided by heterogeneous structure, is the key to efficient electrocatalytic processes. However, difficulty in controlling the relative atomic diffusion rates due to different atomic radii and affinity makes heterogeneous nanostructures difficult to be accurately designed. Herein, an induced diffusion strategy based on affinity differences between elements is proposed to direct the separation/aggregation of different components in the precursor. The key to strategy in this study is the different affinity of Cu and Co to S/P in the precursor of CuCo Prussian blue analogue (PBA). By controlling the molar ratio of S and P during the phosphorization/vulcanization process, induced diffusion can be achieved and leads to directional separation/aggregation of Cu and Co species. As a result, a heterogeneous yolk‐shell Cu2S@CoP2‐C‐N‐S structure is successfully synthesized with a reticular CoP2‐C‐N‐Cu‐S as the shell and a Cu2S nanocrystal as the core. The space charge effect of the semiconductor heterojunction resulting from component separation/aggregation significantly promotes oxygen evolution reaction, resulting in an ultralow overpotential of 180 mV at 10 mA·cm−2. This work not only provides a simple method for efficient separation of key components in gas‐solid systems but also provides a method for fine‐tuning the active site in an active‐site‐engineering approach.

A fast-charging/discharging and long-term stable artificial electrode enabled by space charge storage mechanism

Lithium‐ion batteries with fast-charging/discharging properties are urgently needed for the mass adoption of electric vehicles. Here, we show that fast charging/discharging, long-term stable and high energy charge-storage properties can be realized in an artificial electrode made from a mixed electronic/ionic conductor material (Fe/LixM, where M = O, F, S, N) enabled by a space charge principle. Particularly, the Fe/Li2O electrode is able to be charged/discharged to 126 mAh g−1 in 6 s at a high current density of up to 50 A g−1, and it also shows stable cycling performance for 30,000 cycles at a current density of 10 A g−1, with a mass-loading of ~2.5 mg cm−2 of the electrode materials. This study demonstrates the critical role of the space charge storage mechanism in advancing electrochemical energy storage and provides an unconventional perspective for designing high-performance anode materials for lithium-ion batteries.

Simulation comparison of the positive and negative surface discharges induced by metal particles in a plate–surface–plate structure under DC excitation in atmospheric air

Surface discharge induced by metal particles is a common insulation failure in many high-voltage equipment. In order to further understand the mechanisms of this surface discharge, a 2D simulation model of a plate–surface–plate structure with a pin is established and verified by experiments in this paper to simulate the actual discharge configurations, and the evolution characteristics of the positive and negative surface discharges are compared. The evolutions of both positive and negative discharges could be divided into two phases: the bridging phase and the expansion phase. As the electric field in the gap between the streamer and the dielectric surface is strengthened by the effect of the space charge, the ionization sources and the secondary electrons excited on the dielectric surface, the dielectric surface presents attraction to the streamer, and subsequently the two streamer routes first touch the dielectric surface and then arrive at the grounding electrode. However, the channel branching is the most distinctive characteristic of the positive and negative discharges. In the positive discharge, the channel first branches, then merges, and finally expands, and the gaps of pin to dielectric surface and pin to grounding electrode are broken down by two slender positive branches, respectively. The negative discharge presents a stout channel without branching, which develops and expands simultaneously. This is ascribed to the thinner space charge layer, the weaker shielding effect of the internal electric field and the more active movement of the internal charges in the positive discharge. Another important factor for the discharge branching is the appropriate matching of the sheath thickness and the curvature radius of the channel’s head.

Electric field measurement in DC corona discharge in atmospheric pressure air using E-FISHG and laser-triggering methods

Abstract Electric field measurement using electric-field-induced second-harmonic generation (E-FISHG) draws attention because of its non-invasiveness and is
increasingly being applied to various discharge plasmas. However, measurement accuracy of previous studies is unclear since approximations in calibration are
inadequate. Therefore, we have developed a measurement and analysis method that does not require approximations and can furthermore obtain the distribution
of the electric field. To demonstrate the applicability of the proposed method to discharge plasmas, in this paper, we measure the electric field as a result of the space
charge generated by DC corona discharge in atmospheric pressure air and validate the results by comparing them with those obtained using the laser-triggering method.
We demonstrate that the electrostatic field and electric field resulting from the space charge can be measured with a difference of about 10% between the results obtained
from the laser triggering method and E-FISHG method. The proposed method holds potential for applications in discharge plasmas.

Electrostatic discharge mechanisms and dynamic characteristics of different polarity powders in the Silo

Electrostatic discharge in powder silos poses a significant safety hazard due to the risk of fire or explosion. However, the underlying discharge mechanisms are not fully understood. This study aims to improve the comprehension of electrostatic discharge dynamics and mechanisms by introducing a fluid discharge model for charged powder silos. The model validation is carried out by examining discharge patterns and electric field variations. The investigation of the electrostatic field and potential distribution prior to discharge helps to comprehend the discharge conditions. The discharge modes and evolution laws of different polarity powders are explored to reveal disparities in discharge phenomena. These disparities are further scrutinized in relation to electron density, space charge, electric field, and potential. To elucidate the discharge mechanism, the electric field distortion caused by space charge, electron existence time, and migration law are analyzed. The electrostatic and diffusion effects are the main reasons for the discharge differences.

Electrical properties of MAH-g-PP modified PP/SEBS matrix semi-conductive composite materials

Polypropylene (PP) becomes a superior candidate material for new environmental-friendly cable insulation layer with its excellent heat resistance, electrical properties and degradability. At present, most of studies focus on the insulation layer of PP cable. However, there are few studies on semi-conductive shielding layer of PP cable which match its insulation layer. In this paper, polypropylene (PP)/ styrene ethylene butylene styrene (SEBS) is adopted as matrix of PP cable semi-conductive layer to matching its insulation layer. Meanwhile, Maleic anhydride grafted polypropylene (MAH-g-PP) is used to cooperatively improve the compatibility between PP and SEBS. The physicochemical properties, space charge injection properties and compatibility of semi-conductive composites with different CB and MAH-g-PP contents is studied by combining experiment and simulation methods. The experimental results show that the surface roughness of the semi-conductive layer and the space charge inside the insulation layer decrease first and then increase with the increase of CB addition. Among them, the two parameters of 25phr CB semi-conductive layer is the lowest, respectively 13.98 nm and 2.25×10-8C. These two parameters are significantly reduced after the addition of compatibilizer MAH-g-PP, which decreased by 29.47% and 62.22%, respectively. The simulation results show that the Flory-Huggins interaction parameters (χ) of MAH-g-PP with PP and SEBS are -73.3 and -45.2, respectively, which are 236.24% and 107.34% lower than those of PP/SEBS. The χ value of MAH-g-PP/CB is 8.20, which is 33.27% and 9.59% lower than CB/PP and CB/SEBS, respectively. It shows that MAH-g-PP can effectively improve the compatibility of matrix and filler. This work has important guiding significance for the research of semi-conductive layer formulation of PP cable.

Precise synthesis of three-arm star polymethacrylates with high emission efficiency both in solution and in the solid state

Organic/polymeric fluorescent materials with bright emission both in solution and in the solid state have garnered growing interest in biological and optoelectronic fields. Herein, triphenylamine-derived boron ketoimine (TPA-BKI-3Br) was utilized as the initiator for atom transfer radical polymerization (ATRP) to prepare dual-state emission three-arm star polymethacrylates. Due to the intramolecular charge transfer (ICT) effect and highly distorted structure of the TPA-BKI unit, as well as the polymer arms constraining intramolecular motions, the resultant polymers displayed significant emission in solution. In the aggregated and solid states, the photophysical characteristics of the resultant polymethacrylates were notably impacted by the space charge transfer between the TPA-BKI unit and polymer chains. In addition, the TPA-BKI-based poly(2-(dimethylamino)ethyl methacrylate) (TPA-BKI-(PDMAEMA)3) exhibited fluorescence responses to temperature variations owing to the presence of dimethylamino group. This study presents an approach for the advancement of dual-state emission polymeric materials.

Effect of sintering temperature on microstructure and electrical properties of Na0.5Bi0.47Sr0.02TiO3-δ ceramics

In this investigation, a series of Na0.5Bi0.47Sr0.02TiO3-δ samples, sintered from 1000 to 1100 °C, were synthesized utilizing the solid-state method. The XRD results indicate that all samples exhibit a perovskite phase, with the exception of those sintered at 1100 °C, which display no discernible impurity peaks. The SEM results indicate that the average grain size exhibits an increase proportionate to the sintering temperature, which attributes to the variations in the actual Na/Bi ratio. From the study of grain conductivity we can obtain that the dominant factor affecting grain conductivity is the activation energy. At 1100 °C, the oxygen vacancy concentration emerges as the primary determinant of grain conductivity. It should be noticed that the phase transition temperature of the sample increases (350 °C→400 °C) with the increase of sintering temperature, which is due to the local A-site disorder aggravated by high temperature sintering. Therefore, reducing the sintering temperature is beneficial to improve the grain conductivity. The grain boundary conductivity initially rises, then diminishes with increasing sintering temperature. It is evident that the enhanced macroscopic grain boundary conductivity stems from a marked reduction in space charge potential within the 1000–1025 °C temperature range. Within the 1050 °C−1100 °C temperature range, the space charge potential barely changed, the significant decrease of intrinsic grain boundary conductivity can be attributed to the surge in the coverage ratio of grain boundary impurities and the number of grain boundary impurities increased caused by the rapid reduction of grain boundary area and thermal evaporation. The research on electrical performance of NBT-based oxygen-ion conductors will promote the application of NBT-based oxygen ion conductors in solid oxide fuel cells, oxygen sensors and other fields.

Effect of doping and preparation parameter on AC conductivity and dielectric modulus formalism of Al doped DLC thin films

Here, we report the composite effect of aluminum doping on the dielectric response of Diamond-Like Carbon (DLC) thin films. In addition, the contribution from preparation parameters like acetylene flow rate is also considered to understand sample behavior. AC conductivity study shows the existence of a nonlinear increase of conductivity with frequency leading toward the Jump Relaxation Model (JRM). The transition frequency (ft) is observed, which increases with conductivity. The study reveals that dielectric response is influenced by space charge conductivity, prompting us to adopt the modified Debye law. Deviation from ideal Debye behavior is also confirmed in dielectric modulus analysis. The deviation is frequency-dependent, and a higher deviation is observed in the high-frequency region. Plotting of the Master curve shows the presence of different relaxation dynamics in different samples. A current-voltage (I-V) study of different samples is also undertaken, showing higher values (greater than unity) of the ideality factor.

Structural, Microstructural, and Electrical Properties Study of Pb(Sn0.45Ti0.55)O3 Ceramics

We undertook a comprehensive investigation of the the structural, dielectric, and electrical characteristics of Pb(Sn0.45Ti0.55)O3 ceramics prepared using the conventional solid-state route. A meticulous preparation protocol, involving solvating various precursors, was followed by extensive characterization employing X-ray diffraction, scanning electron microscopy, and dielectric studies. The synthesized sample features a single-phase tetragonal structure with P4mm symmetry. Using impedance spectroscopy, electrical transport properties of the polycrystalline Pb(Sn0.45Ti0.55)O3(PST) ceramic were studied in detail. Relaxation and conduction mechanisms of the material were inferred using complex impedance, complex electric modulus, and frequency dependent ac conductivity analysis. Impedance spectroscopy results reveal the range of frequencies in which the grain, grain boundary, and electrode effects are dominant. Above certain temperatures, the imaginary component of impedance (Z//) exhibits some resonant type peaks at different frequencies indicating relaxor nature of the sample. The activation energy obtained for both the relaxation and conduction process indicates the role of doubly-ionized oxygen vacancy in the conduction mechanism of the sample. The dielectric relaxation occurring at low frequency and high temperatures is related to the space charges associated with the ionized oxygen vacancies being trapped at the grain boundaries. The Cole-Cole plots confirm the poly-dispersive nature of dielectric relaxation in the sample.

Interfacial space charge design with desired electron density to enhance sodium storage of MoS2@Nb2O5 anode

Interfacial space charge design with desired electron density to enhance sodium storage of MoS2@Nb2O5 anode

Influence of the Capillary Design and Conditions upon the Transmission Efficiency of a Portable Ion Trap Mass Spectrometer

The capillary is a widely used atmospheric pressure interface in mass spectrometers that may be heated to enhance the desolvation of ions. In this study, the ion transmission efficiency of a portable ion trap mass spectrometer was investigated using capillaries with different inner diameters and temperatures, different vacuum pressures, and different ion optics designs. Due to the incomplete desolvation and the space charge effect inside the miniature ion funnel, the increase of ion intensities with the inner diameter of the capillary leveled off when the inner diameter of the capillary was larger than 0.37 mm. With the increase of capillary temperature, the ion intensities first increase due to better desolvation and then decrease due to greater diffusion loss. The optimal temperature of the capillary increases with the inner diameter of the capillary and the mass-to-charge ratio of ion. In addition, the pressures of different vacuum stages also exerted remarkable effects on the sensitivity of the portable mass spectrometer. From the perspective of instrument miniaturization, optimal transmission efficiency can be obtained when the first-stage vacuum pressure is maintained from 4 to 6 mbar. For a capillary with an inner diameter of 0.37 mm, the background of mass spectrum can be significantly reduced by replacing the pinhole behind the ion funnel with an off-axis skimmer.

Molecular Dynamics Simulations on Epoxy Resin Composite via Grafting Acryloyl-chloride to Inhibit Electron Transport and Improve Thermal-mechanical Properties

Abstract Electrical, thermal, and mechanical properties of cross-linked epoxy resin (EP) modified by the chemical grafting of acryloyl chloride (AC) were studied to explore the trapping mechanism of charge transport inhibition. The bound state traps deriving from grafted molecules were analyzed by first-principles calculations combined with electron transmission spectra to study the underlying mechanism of the electrical properties. In contrast to pure EP, the EP-graft-AC (EP-g-AC) represents significantly depressed conductivity due to the electron scattering from polar-groups of the grafted AC molecule. The substantial deep traps are generated in EP-g-AC molecules by the polar group of grafted AC and accordingly decrease charge mobility and raise the charge injection barrier, consequently suppressing space charge accumulation and charge carrier transport. EP-g-AC polymer acquires a significant amelioration in thermal and mechanical properties, as indicated by the higher cohesive energy density, glass transition temperature, and decomposition temperature in consistence with the lower thermal vibrations compared with pure EP polymer, except that the resulting higher fractional free volume is not preferable, which is attributed to the mixing incompatibility of the grafted AC molecules with EP molecular-chains.

Charge interaction behaviors at interfacial domains in DC GIL insulators

Long-term operation of high voltage direct current at elevated temperatures can result in the accumulation of surface charges in DC gas-insulated transmission line (GIL) insulators. Such a phenomenon leads to localized electric field distortion, increasing the risk of surface discharge. The analysis of interaction behaviors between surface charge and space charge at interfacial domains of GIL insulators is a complex task, which requires a comprehensive understanding of physical mechanisms of the gas–solid interface charging. In this work, a two-dimensional bipolar charge transport and interaction (2D BCTI) model is established, with the consideration of both surface and space charge dynamics. Pulsed electroacoustic tests and surface potential measurements are conducted on DC GIL insulator materials under different electrical-thermal coupling conditions. Experimental results exhibit great consistency with the predictions from the 2D BCTI model. The local accumulation of space charge near interfaces has certain effects on surface potential distribution, which in turn influences charge injection behavior from electrodes. In comparison to traditional surface charge simulation models, the consideration of space charge–surface charge interaction behaviors proves to be essential for estimating the polarity and amplitude of surface potential distribution. This model holds promise for assessing charge characteristics in electrical equipment where direct measurement is challenging.