Search Results (1,306)

SrTiO₃/Nb₂O₅ composite materials with 1 and 10 wt.% Nb₂O₅ were prepared by a sol–gel route and characterized by XRD, Raman spectroscopy, SEM, BET, UV-Vis DRS, photoluminescence, and dielectric spectroscopy. The photocatalytic activity was evaluated via degradation of rhodamine B and tetracycline under UV and visible light. The addition of Nb₂O₅ resulted in a significant reduction in specific surface area (from 22.7 to 3.1 m²/g), a narrowing of the optical band gap (from 3.22 to 2.49 eV), and a decrease in photoluminescence intensity. Despite these changes, the photocatalytic performance decreased with increasing Nb₂O₅ content. For rhodamine B degradation, the UV rate constant fell from 0.0136 min⁻¹ for pristine SrTiO₃ to 0.0035 min⁻¹ for SrTiO₃/10% Nb₂O₅. The lower activity is mainly ascribed to the loss of active sites, surface carbonate formation, and enhanced non-radiative recombination at interface defects, which suppress charge transfer to the surface. The results demonstrate that careful control of the composite microstructure is essential for achieving efficient photocatalysis, even when heterojunction formation is thermodynamically favorable. Full article

In this work, a comprehensive analysis of the relationship between photoluminescent, thermo-oxidative, and photocatalytic (upon simulated sunlight exposure) properties of ZnO powders is performed. The correlation between the X-ray diffraction and microscopic data is studied. ZnO powders of various sizes and morphologies were used: pseudo-spherical nanoparticles (30–50 nm), submicron faceted crystallites (100–500 nm), and plate- and rod-like microstructures (up to 20 μm). The mean specific surface area values were 32 m²/g, 3.8 m²/g, and 2.6 m²/g for pseudo-spherical nanoparticles, submicron faceted crystallites, and plate- and rod-like microstructures, respectively. According to the XRD data, microstresses and carbon-based impurities were present in ZnO nanoparticles, which is characteristic of nanomaterials synthesized at low temperatures. According to the photoluminescence spectroscopy data, the emission in ZnO was reduced due to high defectiveness, and characteristic emission bands indicated the presence of organic impurities. Upon long signal registration times, an intensive luminescence band with an effective maximum at 579 nm occurred, which indicated the presence of long-term components exhibiting decay times τ ~300 μs. According to the XRD data, the crystal structure parameters of ZnO submicro- and microparticles were close, with no impurities present. In their photoluminescence spectra, pronounced UV and defect-related bands were present with intensity ratios of 11.6 and 6.88, respectively. The decrease in the UV and defect-related luminescence band intensity ratios indicates deviation from the stoichiometry toward an increased Zn over oxygen content. At long signal registration times, in submicron ZnO particles, a luminescence band with maxima at 425 and 490 nm is present, which decays rapidly. An emission band in the 530 nm region is also present, which decays for ≤80 μs, and a weak long-wavelength emission decaying for ~100 μs. At long delay and strobe times (up to milliseconds), only an emission in the 460 nm region is observed, which we connect to the triplet–singlet transition of a defect center (F*, F⁺*). At lower intensities, an emission connected to the surface contamination by organic impurities is observed. In photoluminescence spectra of ZnO microparticles, no long-wavelength emission components are observed. However, upon immersing into methylene blue solution, a modification of the surface and UV region of the spectra is observed with signs of charge carrier recombination rate acceleration. It is shown that the catalytic action of ZnO powders in polyethylene thermo-oxidation processes is determined by a combination of factors. In addition to dispersity and concentration, which are the key parameters, the morphology of ZnO particles, the presence of impurities, the surface state, and the distribution of active sites have a significant influence on catalysis. It has been experimentally demonstrated that these secondary factors can markedly affect the rate of radical formation in polyethylene films and alter their resistance to oxidation. ZnO nanoparticles exhibited low catalytic activity in both photocatalysis (rate constant 0.146 min⁻¹) and thermocatalysis due to the high defect density of the crystallites and the presence of carbon-containing impurities. Submicron ZnO particles, owing to a high carrier generation rate and suppressed recombination (via trapping), demonstrated the highest photoactivity (rate constant 0.729 min⁻¹). Submicron ZnO particles exhibit a catalytic effect on the thermo-oxidation of polyethylene (PE films); however, at concentrations above 8 wt.% a transition to an inhibiting effect is observed. ZnO microparticles catalyzed the oxidation of PE films over a broader concentration range (1–12 wt.%), with oxidation inhibition observed only at 18 wt.%. At the same time, they demonstrated moderate photocatalytic activity (rate constant 0.256 min⁻¹). These characteristics of the samples correlate with data obtained by microscopy, photoluminescence spectroscopy, and X-ray diffraction analysis. Full article

Zinc oxide (ZnO) is a wide-bandgap semiconductor with important optoelectronic, photonic, and radiation-related applications. In this work, hydrothermally grown ZnO bulk single crystals were irradiated with fast neutrons and characterized using low-temperature photoluminescence (PL) spectroscopy to investigate irradiation-induced changes in the Ga-related donor-bound exciton (I₈). The Zn-polar surfaces were exposed to fast neutrons for irradiation durations of 2 and 5 min. The PL measurements showed a reproducible enhancement of the Ga-related I₈ emission intensity, with increases of approximately 33% after 2 min and 82% after 5 min relative to the unirradiated reference crystal. The selective enhancement of the I₈ emission is consistent with increased Ga-related donor activity associated with the proposed Zn-to-Ga neutron transmutation mechanism, although irradiation-induced defect formation and redistribution may also contribute to the observed optical response. Under the irradiation conditions investigated, fast-neutron exposure produced substantial enhancement of the I₈ emission within only a few minutes. However, direct quantitative comparison with previously reported slow-neutron irradiation should be interpreted with caution because the two studies employed different neutron energies, fluences, and irradiation conditions. These findings demonstrate the potential of fast-neutron irradiation for modifying the low-temperature optical response of hydrothermally grown ZnO and provide a foundation for future investigations of neutron-induced defect and donor engineering in wide-bandgap oxide semiconductors. Full article

Natural blue calcite is relatively rare, and its coloration and luminescence mechanisms have not been systematically established. In this study, four natural blue calcite samples from China were comprehensively characterized using mineralogical testing, X-ray diffraction (XRD), electron probe microanalysis (EPMA), scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, ultraviolet–visible spectroscopy (UV-Vis), photoluminescence (PL), and electron paramagnetic resonance (EPR). XRD confirms single-phase trigonal calcite (space group R-3c). EPMA detects minor Mg, Fe, Cu, and Sr, with smaller-radius Mg²⁺, Fe²⁺, and Cu²⁺ being the main contributors to the contraction through isomorphous substitution for Ca²⁺. UV-Vis spectra show characteristic absorptions at 270 nm and 340 nm related to lattice defects with a broad emission band centered at 480 nm in the PL spectra. EPR detects a CO₂⁻ radical center (g = 2.003), and the same signal is also observed in the colorless sample. The colorless sample also contains the same CO₂⁻ radicals, indicating that these radicals alone do not account for the blue coloration. A broad 480 nm blue-violet fluorescence band is observed in the four blue samples under 405 nm excitation. These findings provide a spectroscopic and crystallographic basis for distinguishing natural blue calcite from analogous materials and for understanding the origin of its color and luminescence. Full article

This study investigated twelve gem-quality color-change fluorite specimens exhibiting a purple–blue gradient from Nova Era, Brazil, using colorimetry, Raman spectroscopy, UV-Vis spectroscopy, photoluminescence spectroscopy, EDXRF, and DiamondView imaging to explore the relationship between color depth and coloration mechanism. Raman spectroscopy further revealed enhanced defect-related peaks in dark samples, indicating cumulative irradiation-induced lattice damage. EDXRF analysis revealed that the radioactive element Th was detected exclusively in dark samples, with the darkest specimen reaching 0.184 wt.% Th, confirming that long-term Th-induced irradiation is the primary driver of color deepening. In UV-Vis spectra, the ~583 nm plasmon resonance absorption band of calcium colloids progressively red-shifted and broadened with increasing color depth, indicating elevated colloid concentrations and enhanced aggregation that directly intensify body color. DiamondView fluorescence weakened with deepening color, attributed to the quenching effect of calcium colloids. Photoluminescence spectra showed that the Eu²⁺ emission peak intensified in dark samples, while the broad 700–900 nm emission band systematically blue-shifted, reflecting differential responses of luminescence centers to radiation damage. This study provides non-destructive spectroscopic criteria for the fluorite color-change mechanism without relying on micro-area compositional analysis, establishing an analytical paradigm linking color gradients with spectral characteristics. Full article

High-entropy oxide (HEO) nanoceramics based on (Y_0.2La_0.2Gd_0.2Eu_0.2Er_0.2)₂O₃ were synthesized at 600 °C for 10 min under pressures of 2, 4, 6, and 8 GPa using High-Pressure–Low-Temperature (HPLT) technology, and the resulting structural, phase, and optical changes were studied as a function of synthesis pressure. X-ray diffraction with Rietveld refinement showed that the initial single-phase cubic nanopowder decomposes under pressure into a mixture of cubic, monoclinic, and orthorhombic high-entropy phases: the cubic fraction falls from 67.3% at 2 GPa to 46.8% at 4 GPa, 42.9% at 6 GPa, and 31.1% at 8 GPa, while low-symmetry monoclinic and orthorhombic inclusions become correspondingly more abundant. Raman spectroscopy validated this evolution, with the 2 GPa sample showing a resolvable doublet near 364 and 353 cm⁻¹ attributable to two coexisting cubic phases, while samples synthesized at 4–8 GPa converge on a single narrow band at 353 cm⁻¹ that broadens with increasing pressure. Photoluminescence measurements revealed that the sample synthesized at 2 GPa exhibits the highest Eu³⁺ and Er³⁺ luminescence intensity, with emission and excitation intensities decreasing systematically as synthesis pressure increases. We attribute this decline to the growing fraction of low-symmetry monoclinic phase, whose C2h point-group sites impose parity-forbidden selection rules on the ⁵D₀ → ⁷F_J transitions of Eu³⁺, combined with an increased probability of nonradiative relaxation at structural defects introduced by pressure. These results establish synthesis pressure as a practical lever for tuning the phase composition and luminescent efficiency of multi-lanthanide HEO nanoceramics and indicate that low pressures (~2 GPa) are preferable for optical applications requiring high luminescence intensity. Full article

In this work, we report the synthesis of a photocatalytic system based on impregnating g-C₃N₄ quantum dots (CNQDs) onto the surface of exfoliated graphitic carbon nitride (CN). The CNQDs were prepared using a top-down strategy via a hydrothermal route and then grafted onto exfoliated g-C₃N₄ under solvothermal conditions. The prepared CNQDs/CN composites were characterized using several techniques, including X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS), photoluminescence spectroscopy (PL), and nitrogen physisorption. According to XPS analysis, a slight increase in the O 1s signal in the 1-CNQDs/CN sample could indicate a higher amount of adsorbed hydroxyl groups, which would favor the dispersion of the powder material in the aqueous medium. The photocatalytic degradation of the antibiotic levofloxacin (LEVO) was assessed using the CNQDs/CN samples, with the sample impregnated with 1 wt.% of CNQDs demonstrating the highest photocatalytic performance under UV-vis radiation conditions. Likewise, the 1-CNQDs/CN sample also exhibited the lowest photoluminescence emission (λ_exc = 315 nm), indicating that the presence of g- C₃N₄ quantum dots contributed to the decrease in the recombination rate of the photogenerated electron–hole pairs in the photoexcited graphitic carbon nitride. The stability tests revealed a modest performance reduction of 21% over three cycles. From the photocatalytic tests using scavenger agents, it was determined that hydroxyl (·OH) and superoxide (·O₂⁻) radicals are the reactive species that govern the levofloxacin photodegradation under experimental conditions. Consequently, we determined a photocatalytic mechanism consistent with the results. Full article

We investigate BA₂MAPb₂I₇ (BAMA) quasi-2D Ruddlesden–Popper perovskite thin films prepared through single-crystal-derived and conventional polycrystalline routes. Morphological and X-ray diffraction analyses reveal significant differences in film texture, crystallinity, and phase distribution. Steady-state and time-resolved optical spectroscopies show that polycrystalline films are mainly composed of n = 2 and n = 3 phases and exhibit limited interphase energy transfer. In contrast, single-crystal-derived films display a richer excitonic landscape characterized by the presence of higher-(n) domains. Transient photoluminescence and pump–probe measurements demonstrate that the n = 2 exciton acts as the primary donor state and, uniquely in the single-crystal-derived films, undergoes two distinct transfer processes on the same timescale. The correlation between the decay of the n = 2 exciton and the population of lower-energy excitonic states provides direct evidence of hierarchical exciton funneling. These findings highlight the crucial role of phase distribution and crystallinity in governing exciton migration and energy-transfer pathways in low-dimensional perovskite heterostructures. Full article

The tunable structural and chemical properties of graphitic carbon nitride (gCN) provide a promising route toward tailored activity in photocatalytic applications. A primary challenge in optimizing gCN toward this end is its intrinsically heterogeneous structure, due in part to the many parameters employed in its synthesis. Variability in type and density of chemical and structural defects simultaneously change the electronic, photocatalytic, and optical properties of gCN. Here, we elucidate the complicated structure–function relationship in a series of three related gCN samples by correlating photochemical activity to a host of structural, chemical, and spectroscopic characterization techniques. Of the 22 physical properties measured, we find that transient absorption spectroscopy lifetimes are the only observable that trends with photochemical activity across the series. These results show that a key challenge to photocatalytic material optimization stems from covariant material properties that have competitive influences on photocatalytic activity, making the determination of a robust structure–function relationship challenging. Full article

This study addresses the urgent issue of nitrate-contaminated water by investigating Ni-Pt and Co-Pt catalysts supported on TiO₂, with the aim of improving both photocatalytic efficiency and reaction selectivity. The influence of adding non-noble metal co-catalysts to TiO₂, in addition to Pt, was explored. The synthesized samples were characterized by scanning electron microscopy (SEM), powder X-ray diffraction (XRD), hydrogen temperature-programmed reduction (H₂-TPR), diffuse reflectance UV–Vis spectroscopy, photoluminescence (PL), and X-ray photoelectron spectroscopy (XPS). The assessment of catalytic performance was conducted during the catalytic hydrogenation of nitrate, followed by an evaluation of the photocatalytic performance achieved when the aqueous nitrate solution was irradiated with UV light. The focus is on assessing the synergistic effects of the catalysts supported on TiO₂ in nitrate reduction, as well as their selectivity towards benign reaction products during the photocatalytic process, in contrast to the reactions occurring in the absence of light. Despite the selectivity for nitrite being preserved, the photocatalytic experiments indicated that the selectivity for N₂ reached around 68%, which is about 1.5 times higher than the values observed during the dark catalytic reaction. In contrast, the selectivity for ammonium saw a notable reduction. The findings were discussed in relation to the characteristics of the synthesized materials. Full article

Relatively low-cost titanium carbide (TiC) materials and metal matrix composites (MMC) are proposed for waste-to-hydrogen conversion. Two types of steels are used as bases prepared from EN 10088 flat products, namely X2CrTi12 (1.4512, AISI 409) and X5CrNi18-10 (1.4301, AISI 304). TiC is mixed with TRIBALOY^® T-800 alloy in powder form and applied via laser-directed energy deposition (DED-LB) over the substrates. For the powder mixture, Fourier transform infrared spectroscopy (FT-IR) and differential scanning calorimetry (DSC) are performed. The raw materials are investigated for the processes that occur in them under heating. After the solidification of the molten mixture, grinding and polishing are performed to achieve a thin layer. The studies of the obtained MMC include interface zone assessment, hardness and Young’s modulus distribution, microstructural analysis, and visual defect evaluation. Advanced sensors for acoustic emission (AE) and Electrical Contact Resistance (ECR) provided characterization together with micro-scratch testing. The use of photoluminescence spectroscopy is proposed for the new composite materials. The electron transfer pathway can be studied with time-resolved spectroscopy. Renewable energy production by breaking down waste into hydrogen-rich syngas can be achieved through pyrolysis, followed by steam reforming and purification. The obtained novel materials show promising application solutions with increased durability, corrosion, and wear resistance. Full article

Van der Waals indium selenide is a promising material for next-generation optoelectronics due to its thickness-dependent band structure and high carrier mobility. Here, we investigate the optical properties of size-selected liquid-phase exfoliated γ-InSe nanosheets. The dispersions, composed of flakes with lateral dimensions below 100 nm, exhibit pronounced structural disorder and size-dependent optical behavior. Absorbance spectroscopy reveals systematic changes across size-selected fractions, enabling the extraction of quantitative metrics for estimating nanosheet lateral size and layers number. In addition, stability studies demonstrate significant degradation under ambient conditions, which is accelerated at elevated temperatures. Photoluminescence measurements on nanosheets exfoliated under inert conditions show broad, asymmetric emission with a clear blue-shift for smaller flakes, reflecting quantum confinement and dielectric screening effects. The emission characteristics further indicate a dominant contribution from localized states associated with disorder. These findings provide insight into the structure–property relationships in liquid-phase exfoliated γ-InSe and highlight its potential for solution-processed optoelectronic applications. Full article

Phloroglucinol is an oxygen-rich aromatic precursor whose thermal evolution can yield emissive carbonaceous materials with excitation-dependent photoluminescence. However, the influence of the reaction atmosphere on its low-temperature transformation remains insufficiently understood. In this work, phloroglucinol was thermally treated at 200 °C under air or static vacuum for 5 and 10 h. The resulting materials were investigated by electron microscopy, energy-dispersive X-ray spectroscopy, Raman spectroscopy, steady-state and time-resolved photoluminescence, transient absorption spectroscopy, and density functional theory calculations. The reaction atmosphere mainly affected the early stages of structural evolution. Air-treated samples formed irregular networks of filamentous substructures, whereas vacuum-treated samples displayed more compact quasi-spherical aggregates with a fibrous internal organization. Raman spectra indicated the progressive transformation of crystalline phloroglucinol into a disordered carbonaceous network containing small sp²-rich domains. Optical measurements revealed violet/deep-blue and cyan emissive centers whose relative contributions depended on atmosphere and treatment time. Transient absorption supported a multi-center photophysical picture involving ultrafast relaxation, intermediate trapping or interconversion, and longer-lived decay. Calculations on representative molecular motifs identified furan-containing conjugated domains as plausible candidates for the violet/deep-blue centers and compact triangular phloroglucinol-derived structures for the cyan center. Overall, oxygen availability and treatment duration modulate the morphology and emissive-center distribution of phloroglucinol-derived carbonaceous materials. Full article

This study analyzes a low-cost potassium feldspar mineral from Chihuahua, Mexico, for removing cationic dyes (methylene blue and rhodamine 6G) from water. The raw mineral, characterized by Rietveld refinement as a polymineralic composite of sanidine (49 vol%), muscovite (27 vol%), calcite (16 vol%), and anorthoclase (7 vol%), demonstrated significant dual functionality. In darkness, it acted as an effective adsorbent, achieving 98% and 76% removal of MB and R6G, respectively, after 120 min, with adsorption behavior fitting the Langmuir isotherm. Under solar irradiation, the mineral facilitated photocatalytic degradation, evidenced by a faster intensity decrease and a shift in the absorption bands, and the near-complete decolorization of the dyes. The degradation kinetics were significantly accelerated in a synergistic advanced oxidation process (AOP) with added hydrogen peroxide (H₂O₂), achieving 98% degradation for MB and 93% degradation for R6G within 15 min, compared with 97% for MB and 65% for R6G under sunlight irradiation alone. Kinetic analysis revealed that the process consistently followed a pseudo-second-order model, indicating a surface-controlled mechanism dependent on dye concentration and the availability of active sites. Additional fitting with the Elovich and Avrami models suggested heterogeneous surface behavior and multistep degradation pathways, implying that the overall process involved concurrent adsorption, surface-mediated catalytic reactions, and oxidative degradation driven by photogenerated reactive species. Additionally, the scavenger tests revealed that the dominant reactive species depended on the presence of ${\mathrm{H}}_2{\mathrm{O}}_2$: ${\mathrm{O}}_2^{•-}$ radicals prevailed in the peroxide-free system, whereas $•\mathrm{OH}$ radicals dominated under ${\mathrm{H}}_2{\mathrm{O}}_2$- assisted conditions. Photoluminescence spectroscopy analysis provided mechanistic insights, tracking the evolution of dye monomers, dimers, and aggregates, confirming structural degradation of the dyes and revealing the formation of specific fluorescent intermediates. Together, these findings highlight the mineral’s potential as an abundant, eco-friendly material for solar-driven wastewater treatment. Full article

Three new isomeric pyridone fluorenone hydrazone-based boron complexes, 3-BrN to 5-BrN, with bromination at the 3-, 4-, or 5-position of the pyridone ring and their corresponding σ-platinum complexes trans-Pt(PEt₃)₂(n-N)X (n = 3, 4, or 5; X = Cl, Br, I) resulting from oxidative addition of the aryl-Br bond of n-BrN to Pt(PEt₃)₂ and, for X = Cl, I, subsequent substitution of the halogenide ligand, were synthesized and characterized by NMR, UV–Vis absorption, and photoluminescence spectroscopy. The molecular structures of dyes 3-BrN to 5-BrN and of seven complexes, including the cis-isomer of the bromo complex resulting from 3-BrN, were established by single X-ray diffraction. The nearly orthogonal orientation of the Pt coordination plane with respect to the plane of the dye ligand limits intermolecular π-stacking interactions in the crystalline state while giving rise to extensive C-H···halogen and C-H···π interactions, resulting in intricate packing patterns. Electronic absorption spectra of dyes 3-BrN to 5-BrN show a prominent HOMO-LUMO absorption band at ca. 520 nm, which is red-shifted and intensifies on platination. All compounds are dual fluorescence and phosphorescence emitters in the range of 520 to 670 nm, or at ca. 1000 nm, both at room temperature and at 77 K. The population of an excited triplet state and their photostability even towards continuous light irradiation renders these compounds efficient sensitizers for singlet oxygen generation and catalysts for the photo-oxidation of triphenylphosphine. Full article