Search

Due to the excellent quantum conversion and spectral response characteristics of the AlGaN photocathode, it has become the most promising III-V group semiconductor photocathode in solar-blind signal photoconversion devices in the ultraviolet band. Herein, the influence factors of the time-resolved characteristics of the AlGaN photocathode are researched by solving the photoelectron continuity equation and photoelectron flow density equation, such as the AlN/AlGaN interface recombination rate, AlGaN electron diffusion coefficient, and AlGaN activation layer thickness. The results show that the response time of the AlGaN photocathode decreases gradually with the increase in AlGaN photoelectron diffusion coefficient and AlN/AlGaN interface recombination rate, but the response time of the AlGaN photocathode gradually becomes saturated with the further increase in AlN/AlGaN interface recombination rate. When the thickness of the AlGaN photocathode is reduced from 250 nm to 50 nm, the response time of the AlGaN photocathode decreases from 63.28 ps to 9.91 ps, and the response time of AlGaN photocathode greatly improves. This study provides theoretical guidance for the development of a fast response UV detector. [ABSTRACT FROM AUTHOR]

Photocatalytic H2 evolution has been regarded as a promising technology to alleviate the energy crisis. Designing graphitic carbon nitride materials with a large surface area, short diffusion paths for electrons, and more exposed reactive sites are beneficial for hydrogen evolution. In this study, a facile method was proposed to dope P into a graphitic carbon nitride framework by calcining melamine with 2-aminoethylphosphonic acid. Meanwhile, PCN nanosheets (PCNSs) were obtained through a thermal exfoliation strategy. Under visible light, the PCNS sample displayed a hydrogen evolution rate of 700 μmol·g−1·h−1, which was 43.8-fold higher than that of pure g-C3N4. In addition, the PCNS photocatalyst also displayed good photostability for four consecutive cycles, with a total reaction time of 12 h. Its outstanding photocatalytic performance was attributed to the higher surface area exposing more reactive sites and the enlarged band edge for photoreduction potentials. This work provides a facile strategy to regulate catalytic structures, which may attract great research interest in the field of catalysis. [ABSTRACT FROM AUTHOR]

Sodium-ion batteries (SIBs) have received considerable attention in recent years. Anode material is one of the key factors that determine SIBs' electrochemical performance. Current commercial hard carbon anode shows poor rate performance, which greatly limits applications of SIBs. In this study, a novel vanadium-based material, SrV4O9, was proposed as an anode for SIBs, and its Na+ storage properties were studied for the first time. To enhance the electrical conductivity of SrV4O9 material, a microflower structure was designed and reduced graphene oxide (rGO) was introduced as a host to support SrV4O9 microflowers. The microflower structure effectively reduced electron diffusion distance, thus enhancing the electrical conductivity of the SrV4O9 material. The rGO showed excellent flexibility and electrical conductivity, which effectively improved the cycling life and rate performance of the SrV4O9 composite material. As a result, the SrV4O9@rGO composite showed excellent electrochemical performance (a stable capacity of 273.4 mAh g−1 after 200 cycles at 0.2 A g−1 and a high capacity of 120.4 mAh g−1 at 10.0 A g−1), indicating that SrV4O9@rGO composite can be an ideal anode material for SIBs. [ABSTRACT FROM AUTHOR]

The integration of heterostructures within electrode materials is pivotal for enhancing electron and Li-ion diffusion kinetics. In this study, we synthesized CoO/MnO heterostructures to enhance the electrochemical performance of MnO using a straightforward electrostatic spinning technique followed by a meticulously controlled carbonization process, which results in embedding heterostructured CoO/MnO nanoparticles within porous nitrogen-doped carbon nanofibers (CoO/MnO/NC). As confirmed by density functional theory calculations and experimental results, CoO/MnO heterostructures play a significant role in promoting Li+ ion and charge transfer, improving electronic conductivity, and reducing the adsorption energy. The accelerated electron and Li-ion diffusion kinetics, coupled with the porous nitrogen-doped carbon nanofiber structure, contribute to the exceptional electrochemical performance of the CoO/MnO/NC electrode. Specifically, the as-prepared CoO/MnO/NC exhibits a high reversible specific capacity of 936 mA h g−1 at 0.1 A g−1 after 200 cycles and an excellent high-rate capacity of 560 mA h g−1 at 5 A g−1, positioning it as a competitive anode material for lithium-ion batteries. This study underscores the critical role of electronic and Li-ion regulation facilitated by heterostructures, offering a promising pathway for designing transition metal oxide-based anode materials with high performances for lithium-ion batteries. [ABSTRACT FROM AUTHOR]

Diamonds produced using chemical vapor deposition (CVD) have found many applications in various fields of science and technology. Many applications involve polycrystalline CVD diamond films of micron thicknesses. However, a variety of optical, thermal, mechanical, and radiation sensing applications require more bulky CVD diamond samples. We report the results of a magnetic resonance and structural study of a thick, sizable polycrystalline CVD diamond disc, both as-prepared and treated with e-beam irradiation/high-temperature annealing, as well as gamma irradiation. The combination of various magnetic resonance techniques reveals and enables the attribution of a plentiful collection of paramagnetic defects of doublet and triplet spin origin. Analysis of spectra, electron, and nuclear spin relaxation, as well as nuclear spin diffusion, supports the conclusion of significant macro- and micro-inhomogeneities in the distribution of nitrogen-related defects. [ABSTRACT FROM AUTHOR]

Metal–oxide–semiconductor field-effect transistors (MOSFETs) have proven to be effective devices for rectifying electromagnetic radiation at extremely high frequencies, approximately 1 THz. This paper presents a new interpretation of the THz rectification process in the structure of an MOS transistor. The rectification depends on the nonlinear effect of the carrier dynamics. The paper shows that the so-called self-mixing effect occurs within the interface region between the source and the channel. The basic tool used numerical TCAD simulations, which offer a direct interpretation of different aspects of this interaction. The complex, 2D effect is examined in terms of its basic aspects by comparing the MOS structure with a simplified case study structure. We demonstrate that a contribution to the output-rectified voltage detectable at the drain arises from the charging of the drain well capacitance due to the diffusion of excess electrons from the self-mixing interaction occurring at the source barrier. In addition, the paper provides a quantitative description of the rectification process through the definition of the output equivalent circuit, offering a new perspective for the design of detection systems. [ABSTRACT FROM AUTHOR]

The influence of various energetic particles and electron injection on the transport of minority carriers and non-equilibrium carrier recombination in Ga2O3 is summarized in this review. In Ga2O3 semiconductors, if robust p-type material and bipolar structures become available, the diffusion lengths of minority carriers will be of critical significance. The diffusion length of minority carriers dictates the functionality of electronic devices such as diodes, transistors, and detectors. One of the problems in ultrawide-bandgap materials technology is the short carrier diffusion length caused by the scattering on extended defects. Electron injection in n- and p-type gallium oxide results in a significant increase in the diffusion length, even after its deterioration, due to exposure to alpha and proton irradiation. Furthermore, post electron injection, the diffusion length of an irradiated material exceeds that of Ga2O3 prior to irradiation and injection. The root cause of the electron injection-induced effect is attributed to the increase in the minority carrier lifetime in the material due to the trapping of non-equilibrium electrons on native point defects. It is therefore concluded that electron injection is capable of "healing" the adverse impact of radiation in Ga2O3 and can be used for the control of minority carrier transport and, therefore, device performance. [ABSTRACT FROM AUTHOR]

This study aims to investigate in situ the three-dimensional (3D) morphology and distribution of primary carbides (PCs) in electro-slag remelting (ESR) forged 30Cr3Ni3Mo2V steel. A facile non-aqueous electrolytic etching method was applied to prepare 3D PCs on the matrix. The morphology, composition, and element concentrations of PCs were characterized using a combination of optical microscopy (OM), scanning electron microscopy (SEM) with energy dispersive spectroscopy (EDS), and electron back-scattered diffusion (EBSD). The precipitation, type, and composition of PCs in the same steel were also simulated using Thermo-Calc software Version 2015a. The results indicate that PC is rich in Nb, which is a potential heterogeneous nucleating agent. Both the size and number of PCs increase from the edge to the center of the ingot. The large-sized PCs present three dominant types of morphology, which vary in different regions, i.e., a bulky type dominates in the edge region, a lamellar type dominates in the middle region, and a stripy type dominates in the core region. The results of EBSD analysis show that the orientation of PCs with different morphologies is different and that more nanosized V-rich type carbides are precipitated on the matrix. The thermodynamic calculations show that MC precipitates from the liquid phase when the solid phase fraction is greater than 0.985 and that the MC-type carbides are rich in Nb, which agrees well with the experimental results. [ABSTRACT FROM AUTHOR]

The high power density and long cyclic stability of N-doped carbon make it an attractive material for supercapacitor electrodes. Nevertheless, its low energy density limits its practical application. To solve the above issues, Fe2O3 embedded in N-doped porous carbon (Fe2O3/N-PC) was designed by pyrolyzing Hemin/activated carbon (Hemin/AC) composites. A porous structure allows rapid diffusion of electrons and ions during charge–discharge due to its large surface area and conductive channels. The redox reactions of Fe2O3 particles and N heteroatoms contribute to pseudocapacitance, which greatly enhances the supercapacitive performance. Fe2O3/N-PC showed a superior capacitance of 290.3 F g−1 at 1 A g−1 with 93.1% capacity retention after 10,000 charge–discharge cycles. Eventually, a high energy density of 37.6 Wh kg−1 at a power density of 1.6 kW kg−1 could be delivered with a solid symmetric device. [ABSTRACT FROM AUTHOR]

This paper presents the development, analysis, and performance evaluation of a novel transversal-feed Electron Cyclotron Resonance Plasma Thruster (ECRPT). The ECRPT operates based on the transversal-feed principle and incorporates optimized structural design. Through extensive simulation of the S-parameters of the antenna, optimal antenna sizes are determined for both coaxial and transversal-feed configurations. Additionally, the electric field intensity of the antenna is simulated for both feed structures, revealing higher electric field intensity in the transversal structure, thereby promoting discharge. We employ the drift-diffusion model to calculate the number density of electrons in the discharge chamber and ascertain that the number density can reach an order of magnitude of 1018 m−3. Experimental discharge tests are conducted under various microwave power conditions, demonstrating that the thruster can initiate and cease operation with an incident power as low as 5 W, significantly lower than that of traditional coaxial feed structures. At a power level of 20 W, the ion current density can attain 3 A/m2. Moreover, the transversal-feed thruster exhibits exceptional performance when the power exceeds 10 W, and the propellant flow rate ranges from 0.5 SCCM to 5 SCCM. The superior performance characteristics of the proposed thruster configuration make it a promising candidate for applications demanding efficient and low-power plasma propulsion systems. [ABSTRACT FROM AUTHOR]

We study the low-temperature (T = 4.7 K) emission dynamics of a thin film of methylammonium lead bromide (MAPbBr 3 ), prepared via the anti-solvent method. Using intensity-dependent (over 5 decades) hyperspectral microscopy under quasi-resonant (532 nm) continuous wave excitation, we revealed spatial inhomogeneities in the thin film emission. This was drastically different at the band-edge (∼550 nm, sharp peaks) than in the emission tail (∼568 nm, continuum of emission). We are able to observe regions of the film at the micrometer scale where emission is dominated by excitons, in between regions of trap emission. Varying the density of absorbed photons by the MAPbBr 3 thin films, two-color fluorescence lifetime imaging microscopy unraveled the emission dynamics: a fast, resolution-limited (∼200 ps) monoexponential tangled with a stretched exponential decay. We associate the first to the relaxation of excitons and the latter to trap emission dynamics. The obtained stretching exponents can be interpreted as the result of a two-dimensional electron diffusion process: Förster resonant transfer mechanism. Furthermore, the non-vanishing fast monoexponential component even in the tail of the MAPbBr 3 emission indicates the subsistence of localized excitons. Finally, we estimate the density of traps in MAPbBr 3 thin films prepared using the anti-solvent method at n∼10 17 cm − 3 . [ABSTRACT FROM AUTHOR]

The response of plasmonic metal particles to an electromagnetic wave produces significant features at the nanoscale level. Different properties of the internal composition of a metal, such as its ionic background and the free electron gas, begin to manifest more prominently. As the dimensions of the nanostructures decrease, the classical local theory gradually becomes inadequate. Therefore, Maxwell's equations need to be supplemented with a relationship determining the dynamics of current density which is the essence of nonlocal plasmonic models. In this field of physics, the standard (linearized) hydrodynamic model (HDM) has been widely adopted with great success, serving as the basis for a variety of simulation methods. However, ongoing efforts are also being made to expand and refine it. Recently, the GNOR (general nonlocal optical response) modification of the HDM has been used, with the intention of incorporating the influence of electron gas diffusion. Clearly, from the classical description of fluid dynamics, a close relationship between viscosive damping and diffusion arises. This offers a relevant motivation for introducing the GNOR modification in an alternative manner. The standard HDM and its existing GNOR modification also do not include the influence of interband electron transitions in the conduction band and other phenomena that are part of many refining modifications of the Drude–Lorentz and other models of metal permittivity. In this article, we present a modified version of GNOR-HDM that incorporates the viscosive damping of the electron gas and a generalized Drude–Lorentz term. In the selected simulations, we also introduce Landau damping, which corrects the magnitude of the standard damping constant of the electron gas based on the size of the nanoparticle. We have chosen a spherical particle as a suitable object for testing and comparing HD models and their modifications because it allows the calculation of precise analytical solutions for the interactions and, simultaneously, it is a relatively easily fabricated nanostructure in practice. Our contribution also includes our own analytical method for solving the HDM interaction of a plane wave with a spherical particle. This method forms the core of calculations of the characteristic quantities, such as the extinction cross-sections and the corresponding components of electric fields and current densities. [ABSTRACT FROM AUTHOR]

This study presents the disorderedness effects on the subthreshold characteristics of atomically deposited ZnO thin-film transistors (TFTs). Bottom-gate ZnO TFTs show n-type enhancement-mode transfer characteristics but a gate-voltage-dependent, degradable subthreshold swing. The charge-transport characteristics of the disordered semiconductor TFTs are severely affected by the localized trap states. Thus, we posit that the disorderedness factors, which are the interface trap capacitance and the diffusion coefficient of electrons, would result in the degradation. Considering the factors as gate-dependent power laws, we derive the subthreshold current–voltage relationship for disordered semiconductors. Notably, the gate-dependent disorderedness parameters are successfully deduced and consistent with those obtained by the gm/Ids method, which was for the FinFETs. In addition, temperature-dependent current–voltage analyses reveal that the gate-dependent interface traps limit the subthreshold conduction, leading to the diffusion current. Thus, we conclude that the disorderedness factors of the ZnO films lead to the indefinable subthreshold swing of the ZnO TFTs. [ABSTRACT FROM AUTHOR]

The Jeffreys-type heat conduction equation with flux precedence describes the temperature of diffusive hot electrons during the electron–phonon interaction process in metals. In this paper, the deformation resulting from ultrafast surface heating on a "nanoscale" plate is considered. The focus is on the anomalous heat transfer mechanisms that result from anomalous diffusion of hot electrons and are characterized by retarded thermal conduction, accelerated thermal conduction, or transition from super-thermal conductivity in the short-time response to sub-thermal conductivity in the long-time response and described by the fractional Jeffreys equation with three fractional parameters. The recent double-strip problem, Awad et al., Eur. Phy. J. Plus 2022, allowing the overlap between two propagating thermal waves, is generalized from the semi-infinite heat conductor case to thermoelastic case in the finite domain. The elastic response in the material is not simultaneous (i.e., not Hookean), rather it is assumed to be of the Kelvin–Voigt type, i.e., σ = E ε + τ ε ε ˙ , where σ refers to the stress, ε is the strain, E is the Young modulus, and τ ε refers to the strain relaxation time. The delayed strain response of the Kelvin–Voigt model eliminates the discontinuity of stresses, a hallmark of the Hookean solid. The immobilization of thermal conduction described by the ordinary Jeffreys equation of heat conduction is salient in metals when the heat flux precedence is considered. The absence of the finite speed thermal waves in the Kelvin–Voigt model results in a smooth stress surface during the heating process. The temperature contours and the displacement vector chart show that the anomalous heat transfer characterized by retardation or crossover from super- to sub-thermal conduction may disrupt the ultrafast laser heating of metals. [ABSTRACT FROM AUTHOR]

Dispersed silver nanoparticles (NPs) are synthesized on a silicone oil substrate under varied substrate temperature T by thermal vaporization method. Scanning electron microscopic investigation demonstrates that the mean size of the NPs are around 7.8 nm with a standard deviation of 1.0 nm. The NPs are transferred to a strontium titanate (STO) crystal as co-catalyst for water splitting efficiency test. The photoelectrochmical (PEC) measurement reveals the photocatalytic activity of NP co-catalyst sensitively relies on T during deposition process: the relative current density j r increases from 4.8 μ A/cm 2 to 25.4 μ A/cm 2 as T goes up from 253 K to 333 K. However, a slight decrease of j r from 25.4 μ A/cm 2 to 22.8 μ A/cm 2 is found as T further increases to 353 K. The dependent behavior of j r on T is explained in term of a competition mechanism between microstructure evolution and growth model of the NPs under different T: for T ranging from 253 K to 333 K, the effect of a higher crystalline structure for NPs fabricated under higher T improves the electron transfer rate from STO to NPs is dominant. As T increases to 353 K, the overlapping of NPs become a factor for photocatalytic activity of NP/STO system: the diffusion distance of electrons becomes larger and the apparent contact area between NPs and STO is reduced which in turn reduce the photocatalytic activity of NP/STO. The experimental method to synthesize NPs in this report may open up a way to further apply fine NPs in enhancing photocatalytic water splitting efficiency. [ABSTRACT FROM AUTHOR]

This study focuses on time-resolved surface modifications of a single-phase Ti25Zr25Nb15V15Ta20 high-entropy alloy (HEA) when immersed in 0.9 wt% NaCl and phosphate-buffer solutions (PBS) at 37 °C. A remarkable transition from high ionic diffusion to electron conduction was observed in PBS, whereas the existing conductivity in NaCl solution was further enhanced after 3 h of exposure. During in-situ testing, NaCl improved passivation conceived by the decrease in passivation-current density and increase in Tafel slope. Heterogeneously dispersed oxide particles with NaCl could have accounted for the moderate increase in conductivity while not affecting the capacitive behavior. The Tafel slope decreased after 2 h of immersion in PBS linked to K+ and P−3 accumulation on the surface. The pronounced change in the post-PBS treated sample was also revealed by a four-fold increase in HEA-electrolyte resistance. A visible decrease in the constant-phase-element parameter of the HEA-electrolyte interface after long-term PBS immersion indicated a rise in electrode conductivity and ionic build-up on the surface. The findings suggest that compared to PBS, the selected HEA has a faster passive-layer formation in NaCl with smaller changes in interface resistivity upon long-term immersion, which is promising for enhanced protein-adsorption rates and loading amount. [ABSTRACT FROM AUTHOR]

Electron beam melting (EBM) is a promising technique for processing γ-TiAl alloys that are susceptible to cracking. TiAl alloys are usually built on stainless steel platforms to reduce overall costs. The interface between the samples and the platform is generally brittle due to the strong diffusion of elements between the two components, making them easily separable just by applying impulsive bending stress. In this work, Ti-48Al-2Cr-2Nb samples were processed via EBM and separated from the platform without altering the interface layer. The interface was studied in four different conditions (as-built, hot isostatic pressed, and solution annealed at 1320 °C and 1360 °C) by using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), and hardness measurement. The results revealed that due to the diffusion of elements such as Fe Cr, and Ni, some hard intermetallics and phases were formed close to the interface of the platform and the first deposited layers, which was confirmed by SEM and XRD. According to the results among all diffusing elements, only Fe could diffuse significantly past the interface. More specifically, the diffusion range in the as-built condition was limited to about 350 μm. However, when the sample was heat treated at 1360 °C, Fe amounts of about 0.7 wt.% was still traced at distances as far as 500 μm. Additionally, annealing at higher temperatures led to more homogeneous and relatively higher hardness values within the matrix. According to the results obtained, removing the samples from the building platform with Electro Discharge Machining (EDM) above the contaminated layer before performing any heat treatment is advised to avoid the removal of thick material layers in order to get back to the nominal alloying composition. [ABSTRACT FROM AUTHOR]

TiO2 is a promising anode material for lithium-ion batteries (LIBs) due to its low cost, suitable operating voltage, and excellent structural stability. The inherent poor electron conductivity and low ion diffusion coefficient, however, severely limit its application in lithium storage. Here, Co-doped TiO2 is synthesized by a hydrothermal method as an anode material since Co@TiO2 possesses a large specific surface area and high electronic conductivity. Thanks to the Co dopants, the ion diffusion and electron transport are both greatly improved, which is very beneficial for cycle stability, coulombic efficiency (CE), reversible capacity, and rate performance. As a result, Co@TiO2 shows a high reversible capacity of 227 mAh g−1 at 3 C, excellent rate performance, and cycling stability with a capacity of about 125 mAh g−1 at 10C after 600 cycles (1 C = 170 mA g−1). [ABSTRACT FROM AUTHOR]

In this study, a high-performance H2S sensor that operates at RT was successfully fabricated using biodegradable electroactive polymer-polyurethane-urea (PUU) and PUU-activated-carbon (AC) composites as sensitive material. The PUU was synthesized through the copolymerization of biodegradable polycaprolactone diol and an electroactive amine-capped aniline trimer. AC, with a large surface area of 1620 m2/g and a pore diameter of 2 nm, was derived from coconut-shell waste. The composites, labeled PUU-AC1 and PUU-AC3, were prepared using a physical mixing method. The H2S-gas-sensing performance of PUU-AC0, PUU-AC1, and PUU-AC3 was evaluated. It was found that the PUU sensor demonstrated good H2S-sensing performance, with a sensitivity of 0.1269 ppm−1 H2S. The H2S-gas-sensing results indicated that the PUU-AC composites showed a higher response, compared with PUU-AC0. The enhanced H2S-response of the PUU-AC composites was speculated to be due to the high surface-area and abounding reaction-sites, which accelerated gas diffusion and adsorption and electron transfer. When detecting trace levels of H2S gas at 20 ppm, the sensitivity of the sensors based on PUU-AC1 and PUU-AC3 increased significantly. An observed 1.66 and 2.42 times' enhancement, respectively, in the sensors' sensitivity was evident, compared with PUU-AC0 alone. Moreover, the as-prepared sensors exhibited significantly high selectivity toward H2S, with minimal to almost negligible responses toward other gases, such as SO2, NO2, NH3, CO, and CO2. [ABSTRACT FROM AUTHOR]

An easy and scalable synthetic route was proposed for synthesis of a high-energy stable anode material composed of carbon-coated Si nanoparticles (NPs, 80 nm) confined in a three-dimensional (3D) network-structured conductive carbon nanotube (CNT) matrix (Si/CNT@C). The Si/CNT@C composite was fabricated via in situ polymerization of resorcinol formaldehyde (RF) resin in the co-existence of Si NPs and CNTs, followed by carbonization at 700 °C. The RF resin-derived carbon shell (~10 nm) was wrapped on the Si NPs and CNTs surface, welding the Si NPs to the sidewall of the interconnected CNTs matrix to avoid Si NP agglomeration. The unique 3D architecture provides a highway for Li+ ion diffusion and electron transportation to allow the fast lithiation/delithiation of the Si NPs; buffers the volume fluctuation of Si NPs; and stabilizes solid–electrolyte interphase film. As expected, the obtained Si/CNT@C hybrid exhibited excellent lithium storage performances. An initial discharge capacity of 1925 mAh g−1 was achieved at 0.1 A g−1 and retained as 1106 mAh g−1 after 200 cycles at 0.1 A g−1. The reversible capacity was retained at 827 mAh g−1 when the current density was increased to 1 A g−1. The Si/CNT@C possessed a high Si content of 62.8 wt%, facilitating its commercial application. Accordingly, this work provides a promising exploration of Si-based anode materials for high-energy stable lithium-ion batteries. [ABSTRACT FROM AUTHOR]

Photocatalytic systems for CO2 reduction operate via complicated multi-electron transfer (ET) processes. A complete understanding of these ET dynamics can be challenging but is key to improving the efficiency of CO2 conversion. Here, we report the ET dynamics of a series of zinc porphyrin derivatives (ZnPs) in the photosensitization reactions where sequential ET reactions of ZnPs occur with a sacrificial electron donor (SED) and then with TiO2. We employed picosecond time-resolved fluorescence spectroscopy and femtosecond transient absorption (TA) measurement to investigate the fast ET dynamics concealed in the steady-state or slow time-resolved measurements. As a result, Stern-Volmer analysis of fluorescence lifetimes evidenced that the reaction of photoexcited ZnPs with SED involves static and dynamic quenching. The global fits to the TA spectra identified much faster ET dynamics on a few nanosecond-time scales in the reactions of one-electron reduced species (ZnPs•–) with TiO2 compared to previously measured minute-scale quenching dynamics and even diffusion rates. We propose that these dynamics report the ET dynamics of ZnPs•– formed at adjacent TiO2 without involving diffusion. This study highlights the importance of ultrafast time-resolved spectroscopy for elucidating the detailed ET dynamics in photosensitization reactions. [ABSTRACT FROM AUTHOR]

Infrared detection technology has important applications in laser ranging, imaging, night vision, and other fields. Furthermore, recent studies have proven that hot carriers which are generated by surface plasmon decay can be exploited for photodetection to get beyond semiconductors' bandgap restriction. In this study, silicon nanopillars (NPs) and gold film at the top and bottom of silicon nanopillars were designed to generate surface plasmon resonance and Fabry–Perot resonance to achieve perfect absorption. The absorption was calculated using the Finite Difference Time Domain (FDTD) method, and factors' effects on resonance wavelength and absorption were examined. Here we demonstrate how this perfect absorber can be used to achieve near-unity optical absorption using ultrathin plasmonic nanostructures with thicknesses of 15 nm, smaller than the hot electron diffusion length. Further study revealed that the resonance wavelength can be redshifted to the mid-infrared band (e.g., 3.75 μm) by increasing the value of the structure parameters. These results demonstrate a success in the study of polarization insensitivity, detection band adjustable, and efficient perfect absorption infrared photodetectors. [ABSTRACT FROM AUTHOR]

The FTO/ITO transparent conductive films currently used in photoelectrochemical devices limit performance improvement due to their low conductivity, poor flexibility, and inability to transmit UV light. Ag nanowire-based films are a very promising alternative to address these problems, and are considered to be the next generation in transparent conductive film. Here, we prepared a cross-linked nano-network composed of ultra-long Ag nanowires by a special physical template method. The obtained Ag nanowire transparent conductive film has a transmittance of over 80% in a wide range of 200 nm–900 nm, a sheet resistance as small as 5.2 Ω/sq, and can be easily transferred to various substrates without damage. These results have obvious advantages over Ag nanowire films obtained by traditional chemical methods. Considering the special requirements of photoelectrochemical devices, we have multifunctionally enhanced the film by a TiO2 layer. The heat-resistant temperature of transparent conductive film was increased from 375 °C to 485 °C, and the mechanical stability was also significantly improved. The presence of the multifunctional layer is expected to suppress the carrier recombination in self-powered photoelectrochemical devices and improve the electron diffusion in the longitudinal direction of the electrode, while serving as a seed layer to grow active materials. The high-quality Ag nanowire network and functional layer synergize to obtain a UV–Visible transparent conductive film with good light transmittance, conductivity, and stability. We believe that it can play an important role in improving the performance of photoelectrochemical devices, especially the UV devices. [ABSTRACT FROM AUTHOR]

Pulsar wind nebula (PWN) Boomerang and the associated supernova remnant (SNR) G106.3+2.7 are among candidates for the ultra-high-energy (UHE) gamma-ray counterparts published by LHAASO. Although the centroid of the extended source, LHAASO J2226+6057, deviates from the pulsar's position by about 0.3 ∘ , the source partially covers the PWN. Therefore, we cannot totally exclude the possibility that part of the UHE emission comes from the PWN. Previous studies mainly focus on whether the SNR is a PeVatron, while neglecting the energetic PWN. Here, we explore the possibility of the Boomerang Nebula being a PeVatron candidate by studying its X-ray radiation. By modeling the diffusion of relativistic electrons injected in the PWN, we fit the radial profiles of X-ray surface brightness and photon index. The solution with a magnetic field B = 140 μ G can well reproduce the observed profiles and implies a severe suppression of IC scattering of electrons. Hence, if future observations reveal part of the UHE emission originating from the PWN, we propose to introduce a proton component to account for the UHE emission in light of the recent LHAASO measurement on Crab Nebula. In this sense, Boomerang Nebula would be a hadronic PeVatron. [ABSTRACT FROM AUTHOR]

A nanocomposite electrode of graphene (Gr) and zinc oxide (ZnO) nanoparticles was fabricated to study the electrochemical oxidation behavior of an anti-inflammatory drug, i.e., cetirizine (CET). The voltametric response of CET for bare CPE, Gr/CPE, ZnO/CPE, and the ZnO-Gr nanocomposite electrode was studied. The modifier materials were characterized using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray powder diffraction (XRD) to comprehend the surface morphology of the utilized modifiers. The influence of pH, scan rate, and accumulation time on the electrooxidation of CET was examined. It was found that the electrochemical oxidation of CET was diffusion-controlled, in which two protons and two electrons participated. The detection limit was found to be 2.8 × 10−8 M in a linearity range of 0.05–4.0 µM. Study of excipients was also performed, and it was found that they had negligible interference with the peak potential of CET. The validation and utility of the fabricated nanocomposite sensor material were examined by analyzing clinical and biological samples. Stability testing of the nanocomposite electrode was conducted to assess the reproducibility, determining that the developed biosensor has good stability and high efficiency in producing reproducible results. [ABSTRACT FROM AUTHOR]

Abnormal protein phosphorylation may relate to diseases such as Alzheimer's, schizophrenia, and Parkinson's. Therefore, the real-time detection of phosphoproteins in sweat was of great significance for the early knowledge, detection, and treatment of neurological diseases. In this work, anatase/rutile TiO2 was in situ grown on the MXene surface to constructing the intercalation structure MXene@anatase/rutile TiO2 ternary heterostructure as a sensing platform for detecting phosphoprotein in sweat. Here, the intercalation structure of MXene acted as electron and diffusion channels for phosphoproteins. The in situ grown anatase/rutile TiO2 with n-n-type heterostructure provided specific adsorption sites for the phosphoproteins. The determination of phosphoprotein covered concentrations in sweat, with linear range from 0.01 to 1 mg/mL, along with a low LOD of 1.52 μM. It is worth noting that, since the macromolecular phosphoprotein was adsorbed on the surface of the material, the electrochemical signal gradually decreased with the increase of phosphoprotein concentration. In addition, the active sites in the MXene@anatase/rutile TiO2 ternary heterojunction and synergistic effect of the heterojunction were verified by first-principle calculations to further realize the response to phosphoproteins. Additionally, the effective diffusion capacity and mobility of phosphoprotein molecules in the ternary heterojunction structure were studied by molecular dynamics simulation. Furthermore, the constructed sensing platform showed high selectivity, repeatability, reproducibility, and stability, and this newly developed sensor can detect for phosphoprotein in actual sweat samples. This satisfactory sensing strategy could be promoted to realize the noninvasive and continuous detection of sweat. [ABSTRACT FROM AUTHOR]

Transport of energetic electrons in the heliosphere is governed by resonant interaction with plasma waves, for electrons with sub-GeV kinetic energies specifically with dispersive modes in the whistler regime. In this paper, particle-in-cell simulations of kinetic turbulence with test-particle electrons are performed. The pitch-angle diffusion coefficients of these test particles are analyzed and compared to an analytical model for left-handed and right-handed polarized wave modes. [ABSTRACT FROM AUTHOR]

Featured Application: An optical readout GEM-based detector based on a matrix of organic photodiodes with an active area of 60 × 80 mm2, called the LaGEMPix, was assembled and characterized, using low energy X-rays as a preliminary step toward the development of a 200 × 200 mm2 detector for use in Quality Assurance in hadron therapy. Quality Assurance (QA) in hadron therapy is crucial to ensure safe and accurate dose delivery to patients. This can be achieved with fast, reliable and high-resolution detectors. In this paper, we present a novel solution that combines a triple Gas Electron Multiplier (GEM) and a highly pixelated readout based on a matrix of organic photodiodes fabricated on top of an oxide-based thin-film transistor backplane. The first LaGEMPix prototype with an active area of 60 × 80 mm2 was developed and characterized using low energy X-rays. The detector comprises a drift gap of 3.5 mm, a triple-GEM stack for electron amplification, and a readout featuring 480 × 640 pixels at a 126 µm pitch. Here, we describe the measurements and results in terms of spatial resolution for various experimental configurations. A comparison with GAFCHROMIC® films and the GEMPix detector used in the charge readout mode was performed to better understand the contribution to the spatial resolution from both the electron diffusion and the isotropic emission of photons. The measurements were compared to Monte Carlo simulations, using the FLUKA code. The simulation predictions are in good agreement with the GEMPix results. Future plans with respect to applications in hadron therapy are discussed. [ABSTRACT FROM AUTHOR]

In this work, a new type of Co2VO4 hollow nanocube (CoVO-HNC) was synthesized through an ion exchange process using ZIF-67 nanocubes as a template. The hollow nanocubic structure of the CoVO-HNC provides an abundance of redox sites and shortens the ion/electron diffusion path. As the electrode material of supercapacitors, the specific capacitance of CoVO-HNC is 427.64 F g−1 at 1.0 A g−1. Furthermore, an asymmetric supercapacitor (ASC) was assembled using CoVO-HNC and activated carbon (AC) as electrodes. The ASC device attains an energy density of 25.28 Wh kg−1 at a high-power density of 801.24 W kg−1, with 78% capacitance retention after 10,000 cycles at 10 A g−1. [ABSTRACT FROM AUTHOR]

This study investigated the application of an advanced electrooxidation process with three-dimensional tin oxide deposited onto a titanium plate anode, named 3-D Ti/SnO2, for the degradation and mineralization of one of the most important emerging contaminants with cytostatic properties, doxorubicin (DOX). The anode was synthesized using a commercial Ti plate, with corrosion control in acidic medium, used as a substrate for SnO2 deposition by the spin-coating method. X-ray diffraction (XRD) and scanning electron microscopy (SEM) analyses revealed that porous SnO2 was obtained, and the rutile phase of TiO2 was identified as an intermediary substrate onto the Ti plate. The results of CV analysis allowed us to determine the optimal operating conditions for the electrooxidation process conducted under a constant potential regime, controlled by the electron transfer or the diffusion mechanisms, involving hydroxyl radicals. The determination of UV–VIS spectra, total organic carbon (TOC), and chemical oxygen demand (COD) allowed us to identify the degradation mechanism and pathway of DOX onto the 3-D Ti/SnO2 anode. The effective degradation and mineralization of DOX contained in water by the electrooxidation process with this new 3-D dimensionally stable anode (DSA) was demonstrated in this study. [ABSTRACT FROM AUTHOR]

The Vogel-Fulcher-Tammann (VFT) equation has been used extensively in the analysis of the experimental data of temperature dependence of the viscosity or of the relaxation time in various types of supercooled liquids including metallic glass forming materials. In this article, it is shown that our model of viscosity, the Bond Strength—Coordination Number Fluctuation (BSCNF) model, can be used as an alternative model for the VFT equation. Using the BSCNF model, it was found that when the normalized bond strength and coordination number fluctuations of the structural units are equal, the viscosity behaviors described by both become identical. From this finding, an analytical expression that connects the parameters of the BSCNF model to the ideal glass transition temperature T0 of the VFT equation is obtained. The physical picture of the Kohlrausch-Williams-Watts relaxation function in the glass forming liquids is also discussed in terms of the cooperativity of the structural units that form the melt. An example of the application of the model is shown for metallic glass forming liquids. [ABSTRACT FROM AUTHOR]

Topological crystalline insulators form a class of semiconductors for which surface electron states with the Dirac dispersion relation are formed on surfaces with a certain crystallographic orientation. Pb1−xSnxTe alloys belong to the topological crystalline phase when the SnTe content x exceeds 0.35, while they are in the trivial phase at x < 0.35. For the surface crystallographic orientation (111), the appearance of topologically nontrivial surface states is expected. We studied the photoelectromagnetic (PEM) effect induced by laser terahertz radiation in Pb1−xSnxTe films in the composition range x = (0.11–0.44), with the (111) surface crystallographic orientation. It was found that in the trivial phase, the amplitude of the PEM effect is determined by the power of the incident radiation, while in the topological phase, the amplitude is proportional to the flux of laser radiation quanta. A possible mechanism responsible for the effect observed presumes damping of the thermalization rate of photoexcited electrons in the topological phase and, consequently, prevailing of electron diffusion, compared with energy relaxation. [ABSTRACT FROM AUTHOR]

Transition metal dichalcogenides (TMDs) are the auspicious inexpensive electrocatalysts for the hydrogen evolution reaction (HER) which has been broadly studied owing to their remarkable enactment, however the drought of factors understanding were highly influenced to hinder their electrocatalytic behavior. Recently, transition metal carbide (TMC) has also emerged as an attractive electrode material due to their excellent ionic and electronic transport behavior. In this work, Mo2C@WS2 hybrids have been fabricated through a simple chemical reaction method. Constructed heterostructure electrocatalyts presented the small Tafel slope of 59 and 95 mV per decade and low overpotential of 93 mV and 98 @10 mA·cm−2 for HER in acidic and alkaline solution, respectively. In addition, 24-h robust stability with the improved interfacial interaction demonstrated the suitability of hybrid electrocatalyst for HER than their pure form of Mo2C and WS2 structures. The derived outcomes describe the generated abundant active sites and conductivity enhancement in TMC/TMD heterostructure along with the weaken ion/electron diffusion resistance for efficient energy generation applications. [ABSTRACT FROM AUTHOR]

Electrochemical decomposition of spent catalyst dissolved in molten salts is a promising approach for the extraction of precious metals from them. This article reports the results of the study of aluminum electrowinning from the xLiF–(1-x)AlF3 melt (x = 0.64; 0.85) containing 0–5 wt.% of spent petroleum Pt/γ-Al2O3 catalyst on a tungsten electrode at 740–800 °C through cyclic voltammetry and chronoamperometry. The results evidence that the aluminum reduction in the LiF–AlF3 melts is a diffusion-controlled two-step process. Both one-electron and two-electron steps occur simultaneously at close (or same) potentials, which affect the cyclic voltammograms. The diffusion coefficients of electroactive species for the one-electron process were (2.20–6.50)∙10−6 cm2·s–1, and for the two-electron process, they were (0.15–2.20)−6 cm2·s−1. The numbers of electrons found from the chronoamperometry data were in the range from 1.06 to 1.90, indicating the variations of the partial current densities of the one- and two-electron processes. The 64LiF–36AlF3 melt with about 2.5 wt.% of the spent catalysts seems a better electrolyte for the catalyst treatment in terms of cathodic process and alumina solubility, and the range of temperatures from 780 to 800 °C is applicable. The mechanism of aluminum reduction from the studied melts seems complicated and deserves further study to find the optimal process parameters for aluminum reduction during the spent catalyst treatment and the primary metal production as well. [ABSTRACT FROM AUTHOR]

The effects of different I2 concentrations and different ionic liquids (ILs) in the electrolyte on the performances of dye-sensitized solar cells (DSCs) containing an iron(II) N-heterocyclic carbene dye and containing the I–/I3– redox shuttle have been investigated. Either no I2 was added to the electrolyte, or the initial I2 concentrations were 0.02, 0.05, 0.10, and 0.20 M. The short-circuit current density (JSC), open-circuit voltage (VOC), and the fill factor (ff) were influenced by changes in the I2 concentration for all the ILs. For 1-hexyl-3-methylimidazole iodide (HMII), low VOC and low ff values led to poor DSC performances. Electrochemical impedance spectroscopy (EIS) showed the causes to be increased electrolyte diffusion resistance and charge transfer resistance at the counter electrode. DSCs containing 1,3-dimethylimidazole iodide (DMII) and 1-ethyl-3-methylimidazole iodide (EMII) showed the highest JSC values when 0.10 M I2 was present initially. Short alkyl substituents (Me and Et) were more beneficial than longer chains. The lowest values of the transport resistance in the photoanode semiconductor were found for DMII, EMII, and 1-propyl-2,3-dimethylimidazole iodide (PDMII) when no I2 was added to the initial electrolyte, or when [I2] was less than 0.05 M. Higher [I2] led to decreases in the diffusion resistance in the electrolyte and the counter electrode resistance. The electron lifetime and diffusion length depended upon the [I2]. Overall, DMII was the most beneficial IL. A combination of DMII and 0.1 M I2 in the electrolyte produced the best performing DSCs with an average maximum photoconversion efficiency of 0.65% for a series of fully-masked cells. [ABSTRACT FROM AUTHOR]

The cathode, a crucial constituent part of Li-ion batteries, determines the output voltage and integral energy density of batteries to a great extent. Among them, Ni-rich LiNixCoyMnzO2 (x + y + z = 1, x ≥ 0.6) layered transition metal oxides possess a higher capacity and lower cost as compared to LiCoO2, which have stimulated widespread interests. However, the wide application of Ni-rich cathodes is seriously hampered by their poor diffusion dynamics and severe voltage drops. To moderate these problems, a nanobrick Ni-rich layered LiNi0.6Co0.2Mn0.2O2 cathode with a preferred orientation (110) facet was designed and successfully synthesized via a modified co-precipitation route. The galvanostatic intermittent titration technique (GITT) and electrochemical impedance spectroscopy (EIS) analysis of LiNi0.6Co0.2Mn0.2O2 reveal its superior kinetic performance endowing outstanding rate performance and long-term cycle stability, especially the voltage drop being as small as 67.7 mV at a current density of 0.5 C for 200 cycles. Due to its unique architecture, dramatically shortened ion/electron diffusion distance, and more unimpeded Li-ion transmission pathways, the current nanostructured LiNi0.6Co0.2Mn0.2O2 cathode enhances the Li-ion diffusion dynamics and suppresses the voltage drop, thus resulting in superior electrochemical performance. [ABSTRACT FROM AUTHOR]

The microstructure of carbide-free bainitic steel has been widely reported because of its excellent mechanical properties. However, no work has explored the deformation behavior of each phase in the microstructure, namely, retained austenite (RA) and bainitic ferrite (BF). In this paper, the deformation behavior of RA and BF during tension was investigated through the in situ electron backscatter diffusion method. The results showed that the RA surrounded by BF with a high Schmid factor (SF) was accelerated towards being transformed into martensite, but the surrounding BF with low SF value retarded the transformation. The kernel average misorientation (KAM) findings revealed that the strain of the RA and BF rapidly increased initially, slowed down after the critical points of 0.25 and 0.54, respectively, and then increased again. The calculated result for the KAM fraction indicated that the contribution of RA to the total plastic deformation gradually decreased throughout the total tensile process, whereas that of BF increased in the presence of RA. [ABSTRACT FROM AUTHOR]

At present, lithium-ion batteries (LIBs) have received widespread attention as substantial energy storage devices; thus, their electrochemical performances must be continuously researched and improved. In this paper, we demonstrate a simple self-template solvothermal method combined with annealing for the synthesis of NiFe2O4 yolk-shell (NFO-YS) and NiFe2O4 solid (NFO-S) nanospheres by controlling the heating rate and coating them with a carbon layer on the surface via high-temperature carbonization of resorcinol and formaldehyde resin. Among them, NFO-YS@C has an obvious yolk-shell structure, with a core-shell spacing of about 60 nm, and the thicknesses of the NiFe2O4 shell and carbon shell are approximately 15 and 30 nm, respectively. The yolk-shell structure can alleviate volume changes and shorten the ion/electron diffusion path, while the carbon shell can improve conductivity. Therefore, NFO-YS@C nanospheres as the anode materials of LIBs show a high initial capacity of 1087.1 mA h g−1 at 100 mA g−1, and the capacity of NFO-YS@C nanospheres impressively remains at 1023.5 mA h g−1 after 200 cycles at 200 mA g−1. The electrochemical performance of NFO-YS@C is significantly beyond NFO-S@C, which proves that the carbon coating and yolk-shell structure have good stability and excellent electron transport ability. [ABSTRACT FROM AUTHOR]

The advanced electrochemical properties, such as high energy density, fast charge–discharge rates, excellent cyclic stability, and specific capacitance, make supercapacitor a fascinating electronic device. During recent decades, a significant amount of research has been dedicated to enhancing the electrochemical performance of the supercapacitors through the development of novel electrode materials. In addition to highlighting the charge storage mechanism of the three main categories of supercapacitors, including the electric double-layer capacitors (EDLCs), pseudocapacitors, and the hybrid supercapacitors, this review describes the insights of the recent electrode materials (including, carbon-based materials, metal oxide/hydroxide-based materials, and conducting polymer-based materials, 2D materials). The nanocomposites offer larger SSA, shorter ion/electron diffusion paths, thus improving the specific capacitance of supercapacitors (SCs). Besides, the incorporation of the redox-active small molecules and bio-derived functional groups displayed a significant effect on the electrochemical properties of electrode materials. These advanced properties provide a vast range of potential for the electrode materials to be utilized in different applications such as in wearable/portable/electronic devices such as all-solid-state supercapacitors, transparent/flexible supercapacitors, and asymmetric hybrid supercapacitors. [ABSTRACT FROM AUTHOR]

In this work, the hierarchical porous Ni1.5Co1.5S4/g-C3N4 composite was prepared by growing Ni1.5Co1.5S4 nanoparticles on graphitic carbon nitride (g-C3N4) nanosheets via a hydrothermal route. Due to the self-assembly of larger size g-C3N4 nanosheets as a skeleton, the prepared nanocomposite possesses a unique hierarchical porous structure that can provide short ions diffusion and fast electron transport. As a result, the Ni1.5Co1.5S4/g-C3N4 composite exhibits a high specific capacitance of 1827 F g−1 at a current density of 1 A g−1, which is 1.53 times that of pure Ni1.5Co1.5S4 (1191 F g−1). In particular, the Ni1.5Co1.5S4/g-C3N4//activated carbon (AC) asymmetric supercapacitor delivers a high energy density of 49.0 Wh kg−1 at a power density of 799.0 W kg−1. Moreover, the assembled device shows outstanding cycle stability with 95.5% capacitance retention after 8000 cycles at a high current density of 10 A g−1. The attractive performance indicates that the easily synthesized and low-cost Ni1.5Co1.5S4/g-C3N4 composite would be a promising electrode material for supercapacitor application. [ABSTRACT FROM AUTHOR]

Recent years have witnessed an incredibly high interest in perovskite-based materials. Among this class, metal halide perovskites (MHPs) have attracted a lot of attention due to their easy preparation and excellent opto-electronic properties, showing a remarkably fast development in a few decades, particularly in solar light-driven applications. The high extinction coefficients, the optimal band gaps, the high photoluminescence quantum yields and the long electron–hole diffusion lengths make MHPs promising candidates in several technologies. Currently, the researchers have been focusing their attention on MHPs-based solar cells, light-emitting diodes, photodetectors, lasers, X-ray detectors and luminescent solar concentrators. In our review, we firstly present a brief introduction on the recent discoveries and on the remarkable properties of metal halide perovskites, followed by a summary of some of their more traditional and representative applications. In particular, the core of this work was to examine the recent progresses of MHPs-based materials in photocatalytic applications. We summarize some recent developments of hybrid organic–inorganic and all-inorganic MHPs, recently used as photocatalysts for hydrogen evolution, carbon dioxide reduction, organic contaminant degradation and organic synthesis. Finally, the main limitations and the future potential of this new generation of materials have been discussed. [ABSTRACT FROM AUTHOR]

In this work, we propose poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) material to form a hybrid heterojunction with amorphous silicon-based materials for high charge carrier collection at the frontal interface of solar cells. The nanostructural characteristics of PEDOT:PSS layers were modified using post-treatment techniques via isopropyl alcohol (IPA). Atomic force microscopy (AFM), Fourier-transform infrared (FTIR), and Raman spectroscopy demonstrated conformational changes and nanostructural reorganization in the surface of the polymer in order to tailor hybrid interface to be used in the heterojunctions of inorganic solar cells. To prove this concept, hybrid polymer/amorphous silicon solar cells were fabricated. The hybrid PEDOT:PSS/buffer/a-Si:H heterojunction demonstrated high transmittance, reduction of electron diffusion, and enhancement of the internal electric field. Although the structure was a planar superstrate-type configuration and the PEDOT:PSS layer was exposed to glow discharge, the hybrid solar cell reached high efficiency compared to that in similar hybrid solar cells with substrate-type configuration and that in textured well-optimized amorphous silicon solar cells fabricated at low temperature. Thus, we demonstrate that PEDOT:PSS is fully tailored and compatible material with plasma processes and can be a substitute for inorganic p-type layers in inorganic solar cells and related devices with improvement of performance and simplification of fabrication process. [ABSTRACT FROM AUTHOR]

An explicit mapping is given from the space of general complex meromorphic functions to a space of special time-dependent solutions of the 1 + 2-dimensional nonlinear diffusion equation with diffusivity depending on concentration as D = 1 / u . These solutions have constant-flux boundary conditions. Some simple examples are constructed, including that of a line source enclosed by a cylindrical barrier. This has direct application to electron diffusion in a laser-heated plasma. [ABSTRACT FROM AUTHOR]

The VIolation of Pauli (VIP) experiment (and its upgraded version, VIP-2) uses the Ramberg and Snow (RS) method (Phys. Lett. B 1990, 238, 438) to search for violations of the Pauli exclusion principle in the Gran Sasso underground laboratory. The RS method consists of feeding a copper conductor with a high direct current, so that the large number of newly-injected conduction electrons can interact with the copper atoms and possibly cascade electromagnetically to an already occupied atomic ground state if their wavefunction has the wrong symmetry with respect to the atomic electrons, emitting characteristic X-rays as they do so. In their original data analysis, RS considered a very simple path for each electron, which is sure to return a bound, albeit a very weak one, because it ignores the meandering random walks of the electrons as they move from the entrance to the exit of the copper sample. These complex walks bring the electrons close to many more atoms than in the RS calculation. Here, we consider the full description of these walks and show that this leads to a nontrivial and nonlinear X-ray emission rate. Finally, we obtain an improved bound, which sets much tighter constraints on the violation of the Pauli exclusion principle for electrons. [ABSTRACT FROM AUTHOR]