Search Results (814)

TiO₂ nanoparticles were synthesized by a simple sol–gel route followed by high-temperature calcination at 800 °C, aiming to obtain an anatase-dominant reference photocatalyst with enhanced structural stability after severe thermal treatment. Raman spectroscopy and X-ray diffraction confirmed that anatase is the major crystalline phase, with only a minor rutile contribution after calcination at 800 °C. Nitrogen adsorption–desorption measurements revealed a narrow mesoporous contribution arising from interparticle voids and a relatively high specific surface area (108 m² g⁻¹) despite the severe thermal treatment, while electron microscopy showed nanometric primary particles assembled into compact agglomerates. Surface hydroxyl groups were identified by Fourier-transform infrared spectroscopy, consistent with sol–gel-derived TiO₂ systems. Diffuse reflectance UV–Vis spectroscopy combined with Kubelka–Munk and Tauc analysis yielded an optical band gap of 3.12 eV, typical of anatase TiO₂. Methylene blue (MB) was used as a probe molecule to evaluate photocatalytic activity under ultraviolet and visible light irradiation. Under UV illumination, degradation kinetics were governed by band-gap excitation and reactive oxygen species generation, whereas a slower but reproducible reference behavior under visible light was predominantly associated with surface-related effects and dye sensitization rather than intrinsic visible-light absorption. Overall, the results establish this anatase-dominant TiO₂ as a reliable high-temperature reference photocatalyst, retaining measurable activity after calcination at 800 °C and exhibiting UV-driven behavior as the dominant contribution. Full article

Emerging landslides and severe floods highlight the urgent need to analyse and support predictive models and early warning systems. Soil moisture is a crucial parameter and it can now be determined from space with a resolution of a few tens of meters, potentially leading to the continuous global monitoring of landslide risk. We address this issue by determining the volumetric water content (VWC) of a testbed in Southern Italy (bare soil with significant flood and landslide hazard) through the comparison of two different satellite observations on the same day. In the first observation (Sentinel-1 mission of the European Space Agency, C-band Synthetic Aperture Radar (SAR)), the back-scattered radar signal is used to determine the VWC from the dielectric constant in the microwave range, using a time-series approach to calibrate the algorithm. In the second observation (hyperspectral PRISMA mission of the Italian Space Agency), the short-wave infrared (SWIR) reflectance spectra are used to calculate the VWC from the spectral weight of a vibrational absorption line of liquid water (wavelengths 1800–1950 nm). As the main result, we obtained a Pearson’s correlation coefficient of $0.4$ between the VWC values measured with the two techniques and a separate ground-truth confirmation of absolute VWC values in the range of 0.10–0.30 within $\pm 0.05$. This overlap validates that both SAR and hyperspectral data can be well calibrated and mapped with 30 m ground resolution, given the absence of artifacts or anomalies in this particular testbed (e.g., vegetation canopy or cloud presence). If hyperspectral data in the SWIR range become more broadly available in the future, our systematic procedure to synchronise these two technologies in both space and time can be further adapted to cross-validate the global high-resolution soil moisture dataset. Ultimately, multi-mission data integration could lead to quasi-real-time hydrogeological risk monitoring from space. Full article

The mineral-mapping capability of three spaceborne sensors with different spatial and spectral resolutions, the Environmental Mapping and Analysis Program (EnMap), Sentinel-2, and World View-3 (WV3), is assessed regarding bauxite mining wastes in Amphissa, Greece, with validation based on ground samples. We applied the well-established Linear Spectral Unmixing (LSU) and Spectral Angle Mapping (SAM) classification techniques utilizing endmembers of two established spectral libraries and incorporated ground data through geochemical and mineralogical analyses, X-ray fluorescence (XRF), Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS), and X-ray Diffraction (XRD), to assess classification performance. The main lithologies in this area are bauxites and limestones; therefore, aluminum oxyhydroxides, calcite, and iron oxide minerals were the dominant phases as indicated by the XRF/XRD results. Almost all target minerals were mapped with the three sensors and both methods. The performance of EnMap is affected by its coarser spatial resolution despite its higher spectral resolution using these methods. Sentinel-2 is most effective for mapping iron-bearing minerals, particularly hematite, due to its higher spatial resolution and the presence of diagnostic iron oxide absorption features in the VNIR. World View 3 Shortwave Infrared (WV3-SWIR) performs better when mapping calcite, benefiting from its eight SWIR spectral bands and very high spatial resolution (3.7 m). Hematite and calcite yield the highest accuracy, especially with SAM, indicating 0.80 for Sentinel-2 (10 m) for hematite and 0.87 for WV3-SWIR (3.7 m) for calcite. AlOOH shows higher accuracy with SAM, ranging from 0.57 to 0.80 across the sensors, while LSU shows lower accuracy, ranging from 0.20 to 0.73 across the sensors. This study showcases each sensor’s ability to map minerals while also demonstrating that spectral coverage and the spatial and spectral resolution, as well as the characteristics of the selected endmembers, exert a critical influence on the accuracy of mineral mapping in mine waste. Full article

In this paper, a nano-layered transmission GaAs photocathode structure is proposed. The near-infrared absorption of the photocathode is enhanced by inserting a “sandwich” structure of nano-SiO₂ layer + Si₃N₄ nanopillar array + nano-SiO₂ layer between the cathode optical window and the photocathode. Compared with the flat film structure GaAs photocathode used in the current third-generations image intensifiers, the optical absorption of the optimized “sandwich” structure GaAs photocathode in the near-infrared band has been significantly improved: when the wavelength λ is 868 nm and 896 nm, the optical absorption is increased by 41.69%, 55.08%, respectively. The effects of structural parameters including film thickness and grating filling medium on the light absorption of photocathode are investigated. The results show that the near-infrared light absorption enhancement is the most obvious when Si₃N₄ is selected as the grating filling medium for the current design, and the deposition of SiO₂ film with 10 nm thickness could effectively prevent the damage of Si₃N₄ during bonding with the photocathode. The theoretical analyses offer important guidance in material selection and structural optimization in the grating cathode optical window used in the third-generation image intensifier for improving performance. Full article

Organic optoelectronic devices receive appreciable attention due to their low cost, ecology, mechanical flexibility, band-gap engineering, brightness, and solution process ability over a broad area. In this study, we designed and studied organic light-emitting diodes (OLEDs) consisting of an assembly of natural dyes, extracted from noble fir leaves (evergreen) and blue hydrangea flowers mixed with poly-methyl methacrylate (PMMA) as light emitters. We experimentally demonstrate the effective conversion of blue light emitted by an inorganic laser/photodiode into longer-wavelength red and green tunable photoluminescence due to the excitation of natural dye–PMMA nanostructures. UV-visible absorption and photoluminescence spectroscopy, ellipsometry, and Fourier transform infrared methods, together with optical microscopy, were performed for confirming and characterizing the properties of light-emitting diodes based on natural dyes. We highlighted the optical and physical properties of two different natural dyes and demonstrated how such characteristics can be exploited to make efficient LED devices. A strong pure red emission with a narrow full-width at half maximum (FWHM) of 23 nm in the noble fir dye–PMMA layer and a green emission with a FWHM of 45 nm in blue hydrangea dye–PMMA layer were observed. It was revealed that adding monolayer MoS₂ to the nanostructures can significantly enhance the photoluminescence of the natural dye due to a strong correlation between the emission bands of the inorganic–organic emitters and back mirror reflection of the excitation blue light from the monolayer. Based on the investigation of two natural dyes, we demonstrated viable pathways for scalable manufacturing of efficient hybrid OLEDs consisting of assembly of natural-dye polymers through low-cost, purely ecological, and convenient processes. Full article

New alternatives in the construction industry are essential for economic, sustainable, and environmental progress. In this context, this work investigated three sets of sustainable mortars incorporating industrial lamination waste, assessing their chemical, physical, microstructural, and mechanical properties to inform their development. Cylindrical and prismatic specimens were produced using the following incorporation methods: a reference mortar, mortars with mill scale addition, partial cement replacement with mill scale, and partial sand replacement with mill scale, at proportions of 10%, 20%, 30%, 40%, and 50%. Additionally, analyses including X-ray fluorescence (XRF), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy with energy-dispersive spectroscopy (SEM/EDS) were performed. Physical and mechanical tests, including bulk density, consistency index, capillary water absorption, axial compressive strength, and flexural tensile strength, were also conducted. XRF results indicated an increase in iron oxide content and a decrease in calcium oxide with the addition of mill scale. XRD confirmed the presence of compounds, such as alite and portlandite, which are common in cementitious mortars. FTIR spectra exhibited characteristic functional groups through absorption bands related to Si–O stretching. SEM micrographs revealed slight morphological changes in the composites as the quantity of industrial lamination waste increased, and EDS data supported the XRF findings. The addition of industrial lamination waste affected the spread index and density of the mixtures, while capillary water absorption decreased in some formulations with mill scale. The strength of the mortars increased with the incorporation of industrial lamination waste. In conclusion, using industrial lamination waste in mortars is a technically and environmentally feasible alternative that aligns with the principles of sustainable development and the circular economy in the construction industry. Full article

The Sar-e-Sang lapis lazuli deposit has a mining history exceeding 5000 years, producing the world’s finest lapis lazuli. Recently, gem-quality forsterite has been discovered in the marble containing spinel, dolomite, and phlogopite at the periphery of the lapis lazuli ore body at the Pitawak mine, located east of the Sar-e-Sang deposit. The mineral assemblage indicates that the protolith of this marble is dolomite with aluminous and siliceous components. These forsterite crystals occur as colorless, transparent anhedral grains, exhibiting distinct red fluorescence under 365 nm ultraviolet light. To investigate the gemological and spectroscopic characteristics of the Pitawak mine forsterite, this study conducted and analyzed data from basic gemological analysis, electron probe microanalysis (EPMA), Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), ultraviolet–visible absorption spectroscopy (UV-VIS), Fourier-transform infrared spectroscopy (FTIR), laser Raman spectroscopy (RAMAN), and photoluminescence spectroscopy (PL) on four forsterite samples from the Pitawak mine. The analysis results reveal that the samples indicate a composition close to ideal forsterite with a crystal chemical formula of (Mg_2.00Fe_0.02)_Σ2.02Si_0.99O₄. The trace elements present include Fe, Mn, Ca, and minor amounts of Cr and Ni. The UV-VIS spectroscopy results show that the samples possess high transmittance across the visible light range with very weak absorption bands, contributing to the colorless and transparent appearance of Pitawak mine forsterite. This phenomenon is attributed to the extremely low content of chromophoric elements, which have a negligible effect on the forsterite’s color. PL spectroscopy indicates that the red fluorescence of the samples is caused by an emission peak near 642 nm. This emission peak arises from the spin-forbidden ⁴T₁ → ⁶A₁ transition of Mn²⁺ ions situated in octahedral sites within the forsterite structure. Full article

In this present study, sodium- and strontium-modified bismuth titanate—Bi_0.5Na_0.5TiO₃ (BNT) and Bi_0.5Sr_0.5TiO₃ (BST)—were synthesized using the auto-combustion technique with citric acid (C₆H₈O₇) and glycine (C₂H₅NO₂) as fuels in an optimized ratio of 1.5:1. The resulting powders were characterized using X-ray diffraction (XRD), energy-dispersive X-ray (EDX) spectroscopy, UV–Visible diffuse reflectance spectroscopy (DRS), and Fourier-transform infrared (FT-IR) spectroscopy. The electrical behavior of the samples was studied using an LCR meter. XRD analysis confirmed the formation of a single-phase perovskite structure with average crystallite sizes of 18.60 nm for BNT and 22.03 nm for BST, attributed to the difference in ionic radii between Na⁺ and Sr²⁺. An increase in crystallite size was accompanied by a corresponding increase in lattice parameters and unit-cell volume. The Williamson–Hall analysis further validated the strain-size contributions. EDX (Energy-Dispersive X-ray analysis) results confirmed successful incorporation of Na⁺ and Sr²⁺ without detectable impurity phases. Optical studies revealed distinct absorption peaks at 341 nm for BNT and 374 nm for BST, and the optical bandgap (E_g), calculated using Tauc’s relation, was found to be 2.6 eV and 2.0 eV, respectively. FT-IR spectra exhibited characteristic Ti-O vibrational bands in the range of 420–720 cm⁻¹, consistent with the perovskite structure. For electrical characterization, the powders were pelletized under 3-ton pressure and sintered at 1000 °C for 3 h. The dielectric constant (ε_r), dielectric loss (tan δ), and ac conductivity (σ) of both samples increased with frequency. The combined structural, optical, and electrical results indicate that the optimized compositions of BNT and BST possess properties suitable for use in capacitors and other energy-storage applications. Full article

A new family of highly uniform, cubic-shaped Cu₃VS_xSe_4−x (CVSSe; 0 ≤ x ≤ 4) nanocrystals based on earth-abundant materials with intermediate bandgaps (IB) in the visible range is reported, synthesized via a hot-injection method. The IB transitions and optical band gap of the novel CVSSe nanocrystals are investigated using ultraviolet-visible spectroscopy, revealing tunable band gaps that span the visible and near-infrared regimes. The composition-dependent relationships among the crystal phase, optical band gap, and photoluminescence properties of the novel IB semiconductors with progressive substitution of Se by S are examined in detail. High-resolution transmission electron microscopy and scanning electron microscopy characterization confirm the high crystallinity and uniform size (~19.7 nm × 17.2 nm for Cu₃VS₄) of the cubic-shaped nanocrystals. Density functional theory (DFT) calculations based on virtual crystal approximation support the experimental findings, showing good agreement in lattice parameters and band gaps across the CVSSe series and lending confidence that the targeted phases and compositions have been successfully realized. A current conversion efficiency, i.e., incident photon-to-current efficiency, of 14.7% was achieved with the p-type IB semiconductor Cu₃VS₄. These novel p-type IB semiconductor nanocrystals hold promise for enabling thin film solar cells with efficiencies beyond the Shockley–Queisser limit by allowing sub-band-gap photon absorption through intermediate-band transitions, in addition to the conventional direct-band-gap transition. Full article

In this study, hydroxyapatite was synthesized using a microwave-assisted hydrothermal method. Calcium nitrate tetrahydrate (Ca(NO₃)₂·4H₂O) and ammonium phosphate ((NH₄)₂HPO₄) served as precursors in a pH 10 ammonium hydroxide (NH₄OH) solution. Polyvinylpyrrolidone (PVP) was employed as a surfactant at varying concentrations of 0 (M0), 0.1% (M1), 0.2% (M2), and 0.3%wt (M3) to control particle size and morphology. The synthesized samples were characterized using Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), X-ray Diffraction (XRD) and Fourier Transform Infrared Spectroscopy (FTIR). The addition of PVP during synthesis resulted in Ca/P ratios ranging from 0.93 to 1.37, and promoted predominantly rod-like morphologies. Samples M1 and M3 exhibited average diameters of 11.23–104.24 nm and lengths of 47.21–222.32 nm. XRD analysis confirmed the presence of both hexagonal and monoclinic phases, with crystallite sizes varying from 18.66 to 22.49 nm. FTIR spectra of sample M1 revealed an elongation at 3432 cm⁻¹ corresponding to OH⁻ groups, indicative of water absorption within the material structure. Vibrational bands at 2950–2300, 1090, and 975 cm⁻¹, attributed to C–H bonds in PVP were also identified. These findings highlight the influence of PVP concentration on the structural and morphological properties of hydroxyapatite, providing insights into its potential applications in various fields. Full article

Tin selenide (SnSe) is a sustainable, lead-free IV–VI semiconductor whose layered orthorhombic crystal structure induces pronounced electronic and phononic anisotropy, enabling diverse energy-related functionalities. This review systematically summarizes recent progress in understanding the structure–property–processing relationships that govern SnSe performance in thermoelectric and optoelectronic applications. Key crystallographic characteristics are first discussed, including the temperature-driven Pnma–Cmcm phase transition, anisotropic band and valley structures, and phonon transport mechanisms that lead to intrinsically low lattice thermal conductivity below 0.5 W m⁻¹ K⁻¹ and tunable carrier transport. Subsequently, major synthesis strategies are critically compared, spanning Bridgman and vertical-gradient single-crystal growth, spark plasma sintering and hot pressing of polycrystals, as well as vapor- and solution-based thin-film fabrication, with emphasis on process windows, stoichiometry control, defect chemistry, and microstructure engineering. For thermoelectric applications, directional and temperature-dependent transport behaviors are analyzed, highlighting record thermoelectric performance in single-crystal SnSe at hi. We analyze directional and temperature-dependent transport, highlighting record thermoelectric figure of merit values exceeding 2.6 along the b-axis in single-crystal SnSe at ~900 K, as well as recent progress in polycrystalline and thin-film systems through alkali/coinage-metal doping (Ag, Na, Cu), isovalent and heterovalent substitution (Zn, S), and hierarchical microstructural design. For optoelectronic applications, optical properties, carrier dynamics, and photoresponse characteristics are summarized, underscoring high absorption coefficients exceeding 10⁴ cm⁻¹ and bandgap tunability across the visible to near-infrared range, together with interface engineering strategies for thin-film photovoltaics and broadband photodetectors. Emerging applications beyond energy conversion, including phase-change memory and electrochemical energy storage, are also reviewed. Finally, key challenges related to selenium volatility, performance reproducibility, long-term stability, and scalable manufacturing are identified. Overall, this review provides a process-oriented and application-driven framework to guide the rational design, synthesis optimization, and device integration of SnSe-based materials. Full article

In this study, the authors wish to introduce an unsupervised procedure designed for real-time generation of maps depicting advected aerosols, specifically focusing on desert dust and smoke originating from biomass combustion. This innovative approach leverages the high-resolution capabilities provided by Sentinel-2 imagery, operating at a 10 m scale, which is particularly advantageous for urban settings. Concurrently, it takes advantage of the near-daily revisit frequency afforded by Sentinel-3. The methodology involves generating aerosol maps at a 10 m resolution using bands 2, 3, 4, and 5 of Sentinel-2, available in L1C and L2A formats, conducted every five days, contingent upon the absence of cloud cover. Subsequently, this map is enhanced every two days through spatial modulation, utilizing a similar map derived from the visible and near-infrared observations (VNIR) captured by the OLCI instrument aboard Sentinel-3, which is accessible at a 300 m scale. Data from the two satellites undergo independent processing, with integration at the feature level. This process combines Sentinel-3 and Sentinel-2 maps to update aerosol concentrations in each 300 m × 300 m grid every two days or more frequently. For the dates when Sentinel-2 data is unavailable, the spatial texture or the aerosol distribution within these grid cells is extrapolated. This spatial index represents an advancement over prior studies that focused on differentiating between dust and smoke based on their scattering and absorption characteristics. The entire process is rigorously validated by comparing it with point measurements of fine- and coarse-mode Aerosol Optical Depth (AOD) obtained from AERONET stations situated at the test sites, ensuring the reliability and accuracy of the generated maps. Full article

Background and Objectives: Elastodontic appliances made of medical-grade silicone are increasingly used in interceptive orthodontics, but prolonged intraoral exposure may affect their stability. This study evaluated structural changes in LM-Activator^TM 2 appliances after clinical use, using Fourier-transform infrared (FTIR) spectroscopy. Materials and Methods: Eight appliances (one unused control and seven worn for 3–24 months) were analyzed by FTIR-ATR in the 4000–650 cm⁻¹ range. Absorption bands characteristic of polydimethylsiloxane (PDMS) were quantified, and indices reflecting backbone crosslinking, side-group retention, hydrophilicity, and relative reduction in methyl-related spectral contributions were calculated. Results: The PDMS backbone remained chemically intact across all samples. However, progressive molecular reorganization was detected with wear duration. The Backbone Dominance Index increased significantly from control to 24 months, while side-group indices decreased, confirming apparent depletion of methyl-related FTIR bands. Hydrophilicity and crosslinking indices rose over time, particularly after 12 months, indicating increased surface polarity and network densification. Conclusions: LM-Activator^TM 2 appliances undergo gradual intraoral aging, marked by backbone crosslinking and apparent reduction in methyl-associated vibrational contributions inferred from FTIR ratio side-groups. These changes, while not compromising the polymer identity, may influence surface properties, biofilm retention, and long-term mechanical behavior. Periodic replacement is recommended to ensure optimal clinical performance. Full article

In this paper, the design of a mid-infrared four-band ultra-narrowband wave-absorbing sensor based on the localized equi-excited exciton resonance of graphene metamaterials is presented. The designed super-surface unit has a geometrically symmetric structure and is insensitive to incident light sources with different polarization directions. The absorbing sensor has four resonant wavelengths located at λ₁ = 3.172 μm, λ₂ = 3.525 μm, λ₃ = 3.906 μm, and λ₄ = 4.588 μm, with absorption efficiencies of 99.94%, 99.46%, 99.55%, and 98.16%, respectively. In addition, the dynamic tuning of the resonant wavelength and absorption efficiency can be realized by changing the gate voltage or through chemical doping of graphene. Moreover, the wave-absorbing performance can maintain stable absorption over a wide range of incidence angles from 0 to 50°. Finally, the wave-absorbing sensor was subjected to different ambient refractive indices, and the refractive index sensitivities corresponding to the four resonant wavelengths were obtained as 587.5 nm/RIU, 700.0 nm/RIU, 850.0 nm/RIU, and 900.0 nm/RIU, with FOM values of 48.96 RIU⁻¹, 58.34 RIU⁻¹, 53.13 RIU⁻¹, and 28.13 RIU⁻¹, respectively, all of which have superior sensing characteristics. Therefore, this paper enriches the variety of mid-infrared absorber sensors and has a broad application prospect in the fields of wave absorption, sensing, and detection. Full article

The osmium(II) polypyridyl complex [Os(tpy)(pydppn)]²⁺ (tpy = 2,2′:6′,2″-terpyridine; pydppn = 3-(pyrid-2′-yl)-4,5,9,16-tetraaza-dibenzo[a,c]naphthacene) was synthesized and characterized to evaluate the effect of an extended planar π-system on photophysical properties and DNA interactions. This complex represents the π-expanded analog of the previously studied [Os(tpy)(pydppz)]²⁺ system. Electrochemical studies revealed a reversible Os(II)/Os(III) oxidation at +0.99 V vs. SCE and five ligand-centered reductions, generally less negative than those of the smaller pydppz analog, consistent with enhanced electron-accepting ability. In acetonitrile, the complex exhibits UV absorption bands at 328 and 473 nm and near-infrared emission at 840 nm, assigned to a long-lived ³MLCT state (τ = 110 ns, Φ = 0.02). Upon titration with calf-thymus DNA, [Os(tpy)(pydppn)]²⁺ shows a pronounced light-switch effect, hypochromism, red-shifted MLCT bands, induced circular dichroism, and an increase in DNA melting temperature (ΔT_m = 8.9 ± 0.5 °C), consistent with intercalative binding. Viscometric titrations further support intercalation, with a binding constant K_B ≈ 1.2 × 10⁶ M⁻¹. Transient absorption spectroscopy indicates that DNA binding prolongs the excited-state lifetime and modifies vibrational relaxation pathways. These results highlight how π-system extension in Os(II) complexes modulates photophysical behavior and DNA affinity, offering insights for the rational design of NIR-emitting, DNA-targeted luminescent probes and potential phototherapeutic agents. Full article