Search Results (183)

Volcanic super-eruptions can perturb atmospheric composition and climate-relevant radiative properties in ways that are not captured by simple scaling from Pinatubo-like events. This study presents a reduced-order regime theory for the coupled evolution of stratospheric sulfur, sulfate aerosol burden, reactive halogens, ozone loss, stratospheric thermal adjustment, and aerosol residence time. The analysis is intended as an interpretive tool for organizing sulfur-rich volcanic scenarios, comparing literature-based benchmark classes, and designing chemistry–climate model experiments, rather than as an event-specific calibration or a substitute for three-dimensional models. Four control parameters structure the response: sulfur loading relative to microphysical saturation, effective halogen strength, ash-uptake efficiency, and dynamical lifetime sensitivity, with hemispheric asymmetry treated diagnostically. An external consistency check against published Pinatubo-like, idealized 10–40 teragrams of sulfur (Tg S), Toba-like, and Los Chocoyos-like responses is used to evaluate whether the reduced theory reproduces the expected rank ordering of aerosol saturation, forcing-efficiency decline, ozone-loss amplification, ash-driven sulfur suppression, and residence-time sensitivity. This comparison does not assign pointwise error margins against three-dimensional model output; it evaluates regime membership, sign of response, rank ordering, and broad magnitude behavior. The main conclusion is that volcanic super-eruption impacts are governed by interacting regime transitions rather than by sulfur mass alone. Microphysical saturation can limit forcing efficiency, halogens can shift the system toward chemically amplified ozone depletion, ash uptake can reduce the effective sulfur burden during the early phase, and dynamical state can control persistence and hemispheric expression. By separating these mechanisms, the study provides a compact basis for interpreting large volcanic perturbations to atmospheric chemistry and for designing targeted model experiments on extreme eruption scenarios. Full article

AlGaN-based deep ultraviolet light-emitting diodes (DUV LEDs) have been widely deployed in water treatment, sterilization, and optical communication owing to their intrinsic merits of mercury-free operation, compact footprint, and fast turn-on capability. However, poor reliability and short operating lifetime, mainly caused by electrical degradation and poor heat dissipation, have severely limited their commercial applications. In this work, the degradation mechanism of 270 nm DUV LEDs was systematically studied via multi-condition accelerated aging tests. Results confirm that electrical stress is the dominant factor inducing device degradation, while thermal stress plays a secondary role. Electrical stress generates internal defects, increases leakage current and thermal resistance, enhances non-radiative recombination, and causes a sharp drop in light output power. Based on test data, the L70 lifetimes predicted by the inverse power law and the Arrhenius models are 5832 h and 5724 h, with relative errors of 8.59% and 10.28% compared with the measured 6380 h. This work provides reliable experimental support for the performance evaluation and lifetime prediction of DUV LEDs. Full article

We present a detailed study of the atomic structure and radiative properties of highly charged neon-like selenium (Se XXV), motivated by its importance in plasma diagnostics, fusion research, and astrophysical spectroscopy. We calculated excitation energies and radiative parameters for the 50 lowest levels of fine structure using a fully relativistic multiconfiguration Dirac–Fock approach. We calculated transition wavelengths, radiative transition rates, oscillator strengths, and line strengths for electric dipole, magnetic dipole, electric quadrupole, and magnetic quadrupole transitions among the specified levels. We also evaluated Einstein coefficients for spontaneous and stimulated emission, transition dipole moments, and radiative lifetimes of the low-lying states. To validate the results, we performed independent relativistic calculations using an alternative theoretical method and compared the datasets to examine internal consistency. The calculated excitation energies and radiative parameters agree well with values reported in the National Institute of Standards and Technology database (NIST) and other published theoretical results. The agreement between the independent approaches confirms the consistency of the present dataset. These results provide reliable atomic data for spectral line identification and quantitative plasma modeling in laboratory and astrophysical environments and support ongoing experimental and diagnostic studies of highly charged ions. Full article

In this study, the PV performance of Au/BSF/CTS/CdS/i-ZnO/ITO thin-film solar cell (TFC) structure was systematically investigated using SCAPS-1D software. The effects of several critical parameters, including interface defect density, recombination mechanisms, absorber defect density, operating temperature, parasitic resistances, and different back surface field (BSF) layers, were comprehensively analyzed. The SCAPS-1D software results reveal that the photovoltaic performance is highly sensitive to the defect density at the absorber layer interface. When the interface defect density increased from 10¹² cm⁻³ to 10¹⁶ cm⁻³, the open-circuit voltage ($V_{OC}$) decreased from approximately 0.68 V to 0.45 V, while the power conversion efficiency (PCE) declined from nearly 19% to about 7%. Similarly, an increase in absorber defect density enhanced the Shockley–Read–Hall recombination rate, thereby reducing carrier lifetime and significantly deteriorating PV parameters. The influence of radiative and Auger recombination ($B_{Auger}$) processes was also examined, revealing that higher recombination coefficients lead to substantial reductions in current density and efficiency due to increased carrier losses. Furthermore, the impact of parasitic resistances was evaluated, demonstrating that decrease the series resistance from 9.5 Ω·cm² to 0.5 Ω·cm² increased the fill factor ($FF$) from about 48% to nearly 78%, while the device efficiency improved to approximately 32%. In addition to these parameters, particular emphasis was placed on the investigation of different BSF materials to enhance back contact performance. Various BSF layers, including SnS, PbS, V₂O₅, and Sb₂S₃, were examined to improve band alignment and suppress minority carrier recombination at the rear interface. Among these materials, the SnS BSF layer provided the most favorable band alignment with the CTS absorber, leading to a notable improvement in PV parameters and increasing the efficiency to approximately 25%. Overall, the results demonstrate that optimizing defect densities, recombination mechanisms, parasitic resistances, and especially the selection of appropriate BSF materials plays a crucial role in improving the performance of CTS-based TFCs. Full article

Organic–inorganic hybrid halide perovskites have attracted extensive attention due to their excellent optoelectronic properties and potential applications in field-effect transistors (FET), light-emitting diodes (LEDs), and photodetectors. However, conventional three-dimensional (3D) perovskites are limited by intrinsic instability and ion migration. Two-dimensional Ruddlesden-Popper (2D RP) perovskites offer improved structural stability, but many systems still suffer from modest photoluminescence efficiency and limited charge-transport performance. In this work, a novel 2D RP perovskite, (C₆H₅NH₃)₂CsPb₂Cl₇, was designed and synthesized, where the anilinium ion (C₆H₅NH₃⁺) serves as the organic spacer. Structural characterization indicates that the material possesses high crystallinity and a smooth surface morphology. Optical measurements reveal a violet emission peak at 411 nm with a single-peak feature and a full width at half maximum (FWHM) of 10 nm. The bandgap is determined to be 3.1 eV. Time-resolved photoluminescence (TRPL) measurements show an average lifetime of 4 ns, and the photoluminescence quantum yield (PLQY) is 29.8%. Based on the measured PLQY and lifetime, the radiative and non-radiative recombination rates were estimated to be K_r ≈ 7.45 × 10⁷ s⁻¹ and K_nr ≈ 1.76 × 10⁸ s⁻¹, respectively, suggesting that radiative recombination is appreciable although non-radiative pathways remain present. FET measurements demonstrate an on/off current ratio of 10⁴ and a carrier mobility of 1.1 cm² V⁻¹ s⁻¹. Without any systematic optimization, (C₆H₅NH₃)₂CsPb₂Cl₇ exhibits relatively favorable emissive behavior and measurable field-effect charge transport performance when compared with structurally similar 2D RP perovskites reported under comparable, non-optimized conditions. This study expands the family of chloride-based 2D perovskites and provides a basis for future improvements in their recombination and field-effect transport properties. Full article

This paper examines whether a compact electron–proton configuration (“small hydrogen”) with a characteristic radius of a few femtometers is excluded by basic relativistic kinematics and simple stationarity constraints. Motivated by earlier discussions of formally deep relativistic energy scales in Dirac-based treatments, a phenomenological, virial-inspired energy-balance framework that incorporates relativistic kinetic energy, finite-size regularization of the central field, and order-of-magnitude spin–magnetic and spin–orbit contributions is developed in this paper. Within this framework, self-consistent characteristic scales associated is obtained with a hypothetical compact configuration without invoking Dirac or quantum-electrodynamics (QED) bound-state eigenvalues. The resulting scales—namely, a central energy scale of about 260 keV and a characteristic spin-dependent scale of order ΔE_spin ≈ 100 ± 20 keV—define concrete experimental and observational energy ranges of interest. The present study does not establish the existence, formation probability, lifetime, or dynamical stability of such states. Rather, it shows that relativistic kinematics, finite-size effects, and virial-inspired stationarity constraints do not, by themselves, rule out compact stationary electron–proton configurations within the assumptions of the model. If such states were realized in nature and possessed radiative or interaction channels, those states may have implications for astrophysics, fusion concepts, and dark-matter phenomenology. Full article

This study evaluates mission-long inter-sensor radiometric calibration biases in Sensor Data Record (SDR) and/or Temperature Data Record (TDR) radiances from NOAA microwave sounders, including Advanced Technology Microwave Sounder (ATMS) (Suomi National Polar-orbiting Partnership or SNPP, NOAA-20, NOAA-21) and Advanced Microwave Sounding Unit-A (AMSU-A) (NOAA-19). Using four complementary validation techniques within the Inter-Sensor Radiometric Bias Assessment (iSensor-RCBA) system—32-day averaging, Community Radiative Transfer Model (CRTM) Double Difference (DD), Simultaneously Nadir Overpass (SNO), and sensor-DD via SNO—we characterize long-term performance. Results indicate that the SDR/TDR radiance quality remains stable and generally meets scientific requirements throughout their operational lifetimes with minimal anomalies; observed anomalies were infrequent and primarily correlated with calibration-table updates or spacecraft events or instrument degradation. Moreover, this research examines how radiometric calibration biases for the three ATMS instruments vary with Earth scene radiance or temperatures using the CRTM and SNO methods, as well as the radiance-dependency of inter-sensor calibration biases across the three instruments. Notably, due to its exceptional stability over 14 years, despite an approximate two-month data gap, the SNPP ATMS TDR and SDR datasets are recommended as the ideal reference to link legacy AMSU-A and Microwave Humidity Sounder (MHS) with Joint Polar Satellite System (JPSS), QuickSounder, and MetOp-Second Generation (MetOp-SG) microwave instruments. Beyond quantifying data quality, our multi-method framework with iSensor-RCBA effectively diagnosed critical issues, including a simulation error for CRTM ATMS radiance related to the CRTM spectral-response approximation and a NOAA-19 AMSU-A channel-8 performance anomaly. These findings confirm the long-term integrity of NOAA microwave sounder records and reinforce the value of integrated cross-sensor calibration assessments. Full article

Organic dye-, pharmaceutical-, and heavy metal-contaminated water are emerging environmental issues, and thus there is a requirement for the development of efficient and sustainable purification methods. Semiconductor (SmC) material-based photocatalysis using TiO₂ and Fe₂O₃ nanostructures is considered a promising field for pollutant degradation due to its chemical stability, nontoxicity, and ability to perform photocatalytic degradation using light irradiation. Understanding the thermal, optical, and charge transport properties governing their photocatalytic activity requires advanced characterisation methods. In this context, photothermal (PT) techniques provide powerful tools for probing non-radiative processes and energy transport in photocatalytic materials. The photocatalytic activity of these materials strongly depends on their structural, optical, thermal, and electronic properties. These properties can be enhanced through several modification strategies, including metal and non-metal doping (e.g., C, N, Cu, Ag, Au), surface modification, forming a complex with SiO₂, and the formation of Fe₂O₃–TiO₂ heterostructure nanocomposites. In this review, a comprehensive overview is provided of TiO₂ and Fe₂O₃-based nanocomposites with a specific focus on characterisation techniques for photothermal characterisation techniques, including thermal lens spectroscopy (TLS), beam deflection spectrometry (BDS), and photoacoustic spectroscopy (PAS), for determining thermal diffusivity, thermal conductivity, bandgap energy, carrier lifetime, surface roughness, porosity, etc., which are related to photocatalytic activity. The properties of these nanocomposites are correlated with photocatalytic activity for pollutant degradation using these nanocomposites. The challenges faced while using these nanocomposites for pollutant degradation are also discussed, along with future prospects for designing efficient photocatalysts for water purification applications. Full article

Lead borophosphate zinc barium glass systems doped with different concentrations of Dy₂O₃ (0.5–2.0 mol%) were fabricated using the traditional melt-quenching method. The non-crystalline nature of the synthesized glass samples was verified through X-ray diffraction (XRD) analysis, which exhibited the characteristic absence of sharp diffraction peaks. Morphological, structural, and vibrational properties were analyzed using scanning electron microscopy (SEM) and Fourier infrared transmission (FTIR) spectroscopy. Optical absorption, emission, and decay lifetime observations were recorded to evaluate the luminescence behavior of Dy³⁺ ions. Judd–Ofelt parameters (Ω₂, Ω₄, and Ω₆) were evaluated from the optical absorption spectra of all the prepared glass samples. The emission spectra revealed three dominant transitions in the visible region corresponding to the ⁴F_9/2 ⟶ ⁶H_15/2 (blue ~ 484 nm), ⁴F_9/2 ⟶ ⁶H_13/2 (yellow ~ 574 nm), and ⁴F_9/2 ⟶ ⁶H_11/2 (~663 nm) transitions. Radiative characteristics, including radiative transition probability (A_R), radiative lifetime (τ_R), and branching ratio (β_R), were calculated from the emission spectra. Among the investigated compositions, the host glass embedded with 1.0 mol% Dy₂O₃ demonstrated the maximum emission intensity was observed along with superior quantum efficiency (η = 91.68%). The chromaticity coordinates for this composition (x = 0.33, y = 0.41) are positioned close to the white-light region in the CIE 1931 chromaticity diagram. These findings suggest that incorporating 1.0 mol% of Dy₂O₃ yields the highest luminescence efficiency, making the present glass system a promising candidate for white-light-emitting and photonic device applications. Full article

Tb³⁺-doped CaF₂ single crystals are attractive materials for green photonic applications due to their low phonon energy, high optical transparency, and efficient Tb³⁺ emission. In this work, CaF₂ single crystals doped with different TbF₃ concentrations (1, 5, and 10 mol%) were grown and systematically investigated in order to clarify the concentration-dependent spectroscopic behavior of Tb³⁺ ions in a fluorite host. Optical absorption spectroscopy, Judd–Ofelt analysis, steady-state and time-resolved photoluminescence, colorimetric evaluation, and emission cross-section and gain calculations were employed. Judd–Ofelt intensity parameters typical of fluoride hosts were obtained, enabling the calculation of radiative transition probabilities and lifetimes. The emission spectra are dominated by intense green luminescence from the ⁵D₄ → ⁷F₅ transition, while the absence of ⁵D₃ emission is attributed to efficient cross-relaxation processes. Fluorescence lifetimes in the millisecond range show slight changes with Tb³⁺ concentration. Quantum efficiency increases from low to intermediate concentrations and tends to saturate at higher doping levels. CIE 1931 chromaticity coordinates confirm stable green emission, while emission cross-sections and gain parameters reveal a highest value for orange emission of 10 mol% TbF₃-doped CaF₂ crystal. These results indicate that CaF₂:Tb³⁺ single crystals are promising materials for photonic applications. Full article

Air transport, acknowledged as the safest and most efficient mode for long-haul travel, is confronted with diverse challenges aimed at improving its environmental performance. A notable aspect of this effort involves the formation of contrails, arising from the emission of water vapor and condensation nuclei in a cold, ice-supersaturated atmosphere, which represents one of the most difficult-to-predict yet physically quantifiable environmental impacts of air traffic. Adopting the bottom-up principle to evaluate individual contrails for trajectory optimization introduces uncertainties in calculating the radiative forcing of contrails and modeling their life cycle. Former studies for modeling the microphysical life cycle of individual contrails based on a 2D Gaussian plume model could be validated with a photographic contrail tracking method in the mid-latitudes. However, contrails rarely form individually over Central Europe; rather, they form as an accumulation behind many aircraft flying through an ice-supersaturated region. For this reason, the 3D Gaussian plume model has been extended for the co-existence of several contrails. The greater the overlap of the contrails, the greater the competition in ice supersaturation between the contrails and therefore the greater the reduction in lifetime compared to single contrails. Furthermore, with increasing overlap, the number density of ice crystals increases, resulting in smaller ice crystals with shorter lifetimes. The overlap effect is also reflected in the angle between non-parallel contrails. The results can be used for further studies on the optical properties of real co-existing contrails. Full article

To investigate drug delivery in cancer therapy, we integrate fluorescence lifetime measurements, microspectrometry, and confocal laser scanning microscopy to track the uptake of inorganic–organic hybrid nanoparticles (IOH-NPs) by breast cancer cells over incubation periods ranging from 2 to 24 h. Non-radiative energy transfer (FRET) from the LysoTracker Green to the IOH-NPs confirms their lysosomal localization and possibly improves their optical excitation. Beyond the resolution limits of light and electron microscopy, fluorescence lifetime kinetics—including FRET—can thus reveal the nanoscale cellular localization of IOH-NPs and guide the optimization of fluorescence excitation. Here, we extend optical microscopy into a fifth dimension—picosecond fluorescence decay times—complementing 3D spatial and spectral information, establishing lifetime measurements as a versatile tool to study nanoparticle uptake in cancer therapy. Full article

The rate constant k_OH for the reaction of 1,1,1,3,3,3-hexafluoroprop-2-imine with OH radicals was measured relative to two reference compounds, CH₃F and CH₃CHF₂, to be k_OH = (4.2 ± 1.1) × 10⁻¹⁴ cm³ molecule⁻¹ s⁻¹ at 295 K. This implies an atmospheric lifetime with respect to consumption by OH of 0.75 years. Reaction with Cl atoms yielded k_Cl = (7.9 ± 1.7) × 10⁻¹⁶ cm³ molecule⁻¹ s⁻¹ at 295 K, and reaction with O₃ has an upper limit of k_O3 < 4 × 10⁻²³ cm³ molecule⁻¹ s⁻¹, so that the atmospheric consumption by Cl and O₃ is negligibly slow. Absolute infrared cross sections of the imine yield a radiative efficiency of 0.34 W m⁻² ppb⁻¹, which is corrected to 0.23 W m⁻² ppb⁻¹ for the effects of atmospheric lifetime. The imine’s corresponding 100-year global warming potential is 64 ± 19. This value is an upper limit, given that heterogenous atmospheric removal paths, such as hydrolysis in water droplets, are not included. Full article

Perovskite quantum dots (PQDs) based on CsPbX₃ (X = Cl, Br, I) have attracted extensive attention due to their outstanding optoelectronic properties; however, their practical applications are hindered by poor environmental stability. In this work, a sequential surface-modification strategy is developed to address these limitations. First, CsPbBr₃ PQDs are passivated with (3-aminopropyl) triethoxysilane (APTES), which reduces surface defects and enhances the photoluminescence quantum yield (PLQY) from 38.5% to 74.4%. Subsequently, a dense silica shell is constructed via in situ hydrolysis of tetramethyl orthosilicate (TMOS), further improving the PLQY to 95.6% and significantly boosting environmental stability. Structural and optical characterizations confirm effective defect passivation and suppress non-radiative recombination, with carrier lifetimes extended from 2.5 ns to 36.9 ns. Remarkably, the silica-coated PQDs retain over 50% of their initial emission intensity after 100 min of water immersion, far exceeding the stability of uncoated counterparts. Furthermore, when integrated with a commercial K₂SiF₆: Mn⁴⁺ red phosphor and a blue light-emitting diode (LED) chip, the resulting white LED (WLED) exhibits a wide color gamut covering 104% of the National Television System Committee (NTSC) standard and Commission Internationale de l’Éclairage (CIE) coordinates of (0.323, 0.331), closely matching standard white light. Importantly, only the silica-coated PQDs maintain a stable electrically driven device emission spectrum after water exposure. Full article

Boro-antimonite glasses doped with Eu³⁺ and having the general composition (90-x) Sb₂O₃–xB₂O₃–10Li₂O-0.5Eu₂O₃ (x = 0 to 60 in 10 mol. % increment) were prepared using the melt quenching method. The influence of B₂O₃/Sb₂O₃ substitution on the spectroscopy and photoluminescence of Eu³⁺ ions was analyzed by studying the measured and calculated properties of these glasses. The relative value of a given property was shown to increase or decrease by up to 26% with the addition of up to 60 mol. % B₂O₃, while the number of Eu³⁺ ions per unit volume increased by approximately 32%. Strong emissions were obtained in association with the transitions of Eu³⁺ (⁵D₀→⁷F_j, j = 1–4). A weak, broad emission centered at 450 nm was also detected. This emission is clearly linked to the glass composition. It originates from a potential presence of Eu²⁺ ions. This enhances ⁵D₀ level emission via charge transfer. The radiative and experimental lifetimes of the ⁵D₀ level increase linearly with B₂O₃ content. This results in high quantum efficiency (η) ranging from 74 to nearly 84%. Tunable chromaticity, as defined by the CIE 1931 standard, was achieved, resulting in a warm orange-red color with high brightness. These new glasses have a variety of potential laser-related applications. Full article