Search Results (1,357)

Herein, we propose a simple and cost-effective method for fabricating moderate-sensitivity surface-enhanced Raman scattering (SERS) substrates using Cu-plasma polymer fluorocarbon (Cu-PPFC) nanocomposite films fabricated through RF sputtering. The use of a composite target composed of carbon nanotube (CNT), Cu, and polytetrafluoroethylene (PTFE) powders (5:60–80:35–15 wt%) offers the advantage of the simple fabrication of moderate-sensitivity SERS substrates with a single cathode compared to co-sputtering. X-ray photoelectron spectroscopy (XPS) revealed that the film surface was partially composed of metallic Cu with Cu-F bonds and Cu–O bonds, confirming the coexistence of the conducting and plasmon-active domains. UV-VIS spectroscopy revealed a distinct absorption peak at approximately 680 nm, indicating the excitation of localized surface plasmon resonances in the Cu nanoclusters embedded in the plasma polymer fluorocarbon (PPFC) matrix. Atomic force microscopy and grazing incidence small-angle X-ray scattering analyses confirmed that the Cu nanoparticles were uniformly distributed with interparticle distances of 20–35 nm. The Cu-PPFC nanocomposite film with the highest Cu content (80 wt%) exhibited a Raman enhancement factor of 2.18 × 10⁴ for rhodamine 6G, demonstrating its potential as a moderate-sensitivity SERS substrate. Finite-difference time-domain (FDTD) simulations confirmed the strong electromagnetic field localization at the Cu-Cu nanogaps separated by the PPFC matrix, corroborating the experimentally observed SERS enhancement. These results suggest that a Cu-PPFC nanocomposite film, easily fabricated using a composite target, provides an efficient and scalable route for fabricating reproducible, inexpensive, and moderate-sensitivity SERS substrates suitable for practical sensing applications. Full article

Zn_1−xFe_xO nanocomposites (NCs) with varying Fe concentrations (x = 0, 0.1, 0.2, 0.3, and 0.4) were effectively prepared using the hydrothermal approach, and their morphology, structural, optical, and magnetic properties were systematically analyzed. XRD analysis confirmed Fe doping reduced crystallinity and crystallite size. TEM images of Zn_1−xFe_xO NCs exhibited smaller and more agglomerated nanostructures compared to the pure ZnO NPs. Raman and XPS analyses indicated increased lattice disorder, oxygen vacancies, and the coexistence of Fe²⁺/Fe³⁺ species. UV–Vis spectra showed enhanced visible light absorption and a tunable band gap, while PL results reflected defect-induced emission shifts and quenching, associated with zinc vacancies, interstitials, and oxygen-related defects. Magnetic measurements revealed a transition from diamagnetism to ferromagnetic-like behavior at room temperature for Fe content x ≥ 0.2, with magnetization strongly dependent on doping level. These results highlight Zn_1−xFe_xO for advanced optoelectronic and spintronic applications. 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

The coexistence of plastics and metal-based materials in aquatic systems introduces complex interfacial processes that influence pollutant speciation and mobility. This study investigates the role of polystyrene (PS) in promoting UV-induced dissolution of ZnO and Cu₂O in aqueous media, revealing a plastic-mediated pathway for metal ion mobilization. Post-use expanded PS fragments were co-dispersed with the oxides and irradiated at 254 nm for 24 h. Ion concentrations were quantified by ICP-MS, while PS morphology and chemistry were characterized by SEM, EDX, FTIR, Raman, and DSC. The presence of PS markedly enhanced metal release, bringing Zn²⁺ from 29.9 to 50.6 ppm and Cu²⁺ from 1.1 to 26.5 ppm under irradiation, compared to minimal dissolution in the dark. Spectroscopic analyses indicated negligible polymer degradation, suggesting that enhanced dissolution arises from interfacial photooxidation and associated redox/pH microgradients at the polymer–oxide boundary. These findings demonstrate that PS may serve as a catalytic interface that accelerates UV-driven dissolution of otherwise poorly soluble metal oxides. This mechanism expands current understanding of plastic–pollutant interactions and has implications for predicting metal bioavailability and designing strategies to mitigate pollutant release in sunlit marine and coastal environments. Full article

Resistance to conventional antibiotics remains a global health challenge. The search for more effective antimicrobial agents has led to the consideration of nanoparticles due to their potential biocidal activities. This study synthesized, characterized, and evaluated the antimicrobial behavior of cadmium sulfide nanoparticles (CdS NPs) during incubations at 37 °C and at room temperature (rt; 23 to 27 °C). XRD results showed that the synthesized nanoparticles had a cubic zinc blende structure, while microscopic investigations confirmed the particle size to be 7.236 nm on average. UV-Vis spectroscopy showed that the nanoparticles are active in the visible light region. Raman spectroscopy results showed peaks at 302.3 cm⁻¹ and 601 cm⁻¹, which represent the first- and second-order longitudinal optical phonon. Agar well diffusion, minimum inhibitory concentration (MIC), and minimum bactericidal concentration (MBC) assays were conducted to investigate the antimicrobial activity of CdS NPs (50 mg/mL, 25 mg/mL, and 10 mg/mL) against Escherichia coli and Staphylococcus aureus. CdS NPs were effective against both test organisms. However, they were more effective against Gram-negative E. coli. The higher the concentration of CdS NPs, the more effective they were against the test organisms. Furthermore, MBC results showed greater bactericidal activity of CdS NPs at 37 °C. With increasing incidences of antimicrobial resistance against conventional antimicrobial agents, especially in wastewater treatment, nanoparticles are considered promising alternatives and the next generation of antimicrobial agents. Full article

Composite materials based on polymethylmethacrylate (PMMA) and carbon nanoparticles are used in aviation, construction, medical and other fields of activity. Carbon nanotubes and carbon nano-dots are mainly used as carbon nanoparticles. Both carbon nanotube and carbon nano-dots are difficult to obtain materials with considerable cost. Amorphous carbon nanoparticles, on the contrary, are easy to obtain and have a low cost. The purpose of this work is to study the physico-chemical and biological characteristics of polymethylmethacrylate modified with amorphous carbon nanoparticles. Laser ablation was used to obtain the nanoparticles. Dynamic light scattering, measurement of the electrokinetic potential, TEM, AFM, and Raman microscopy are used to characterize nanoparticles. FTIR, MIM, AFM, UV-visual diagnostics, ROS tests, and biopolymer regeneration tests were used to analyze the combined sensors. The bacteriostatic effect was evaluated using turbodimetry, and the antibacterial effect was evaluated using precision cytofluorometry. Mammalian cells were examined using fluorescence microscopy. Carbon nanoparticles (CNPs) have been obtained and characterized. A protocol has been developed for the introduction of CNPs into photolithographic resin. Printed samples of complex geometry. It is shown that the printed samples are amenable to polishing, have pro-oxidant properties, and are able to prevent damage to biopolymers. Printed samples inhibit the development of bacteria and cause loss of viability. At the same time, the printed samples do not affect the development of mammalian cells. The obtained resins based on PMMA with CNPs can potentially serve as the basis for the creation of non-toxic materials in biomedicine and pharmacology. Full article

This study investigates the effect of laser power, focal length, and number of passes on the fabrication of graphene-based strain sensors using a 450 nm diode laser at the upper limit of the UV spectrum. Polyimide substrates were irradiated to produce laser-induced graphene, and the resulting sensors were evaluated under three-point bending tests. The main requirements for deformation sensors—adequate conductivity, mechanical stability under bending, and high sensitivity (gauge factor)—were assessed through morphological analysis by SEM, Raman spectroscopy, and electrical characterization using the Van der Pauw method. The results indicate that laser power is the critical factor influencing graphene quality and sensor performance, while focal length has a negligible effect and additional passes reduce material quality and sensitivity. Overall, this work demonstrates the feasibility of producing functional, low-cost graphene strain sensors with a commercial diode laser, offering a scalable and affordable alternative for sensor fabrication. Full article

A review of studies has shown that aromatic azo and hydrazo derivatives are used in a wide spectrum of fields, including food, pharmaceutical, and cosmetic products, as well as in technical and electronic technologies, which has contributed to the development of new such compounds. In this work, the structures of newly obtained 4-methyl-3,5-dinitro-2-(2-phenylhydrazinyl)pyridine (4MDNPHP) and its azo derivative, 4-methyl-3,5-dinitro-2-[(E)-phenyldiazenyl]pyridine (4MDNPAP), were established by spectroscopic (NMR, IR, Raman, and UV-Vis) and emission studies. Single-crystal X-ray diffraction analysis was used to determine the molecular structure of the studied compounds, and the results were compared with DFT calculations (B3LYP/6-311G(2d,2p)). The collected X-ray data revealed that the crystal of the hydrazo compound (4MDNPHP) belongs to the triclinic space group P$\overline{1}$ (Z = 2), whereas the crystal of the azo compound (4MDNPAP) follows the symmetry of the monoclinic space group P2₁/n (Z = 4). Both presented derivatives crystallized with one molecule in the asymmetric unit. Specific properties of the hydrazo bridge C_ϕ-NH-NH-C_θ moiety and its azo counterpart C_ϕ-N=N-C_θ were considered in detail. Full article

Laser slicing has emerged as a promising low-kerf and low-damage technique for SiC wafer fabrication; however, its effects on the crystal integrity, near-surface modification, and charge-transport properties require further clarification. Here, a heavily N-doped 4° off-axis 4H-SiC wafer was sliced using an ultraviolet (UV) picosecond laser, and both laser-irradiated and laser-sliced surfaces were comprehensively characterized. X-ray diffraction and pole figure measurements confirmed that the 4H stacking sequence and macroscopic crystal orientation were preserved after slicing. Raman spectroscopy, including analysis of the folded transverse-optical and longitudinal-optical phonon–plasmon coupled modes, enabled dielectric function fitting and determination of the plasmon frequency, yielding a free-carrier concentration of ~3.1 × 10¹⁸ cm⁻³. Hall measurements provided consistent carrier density, mobility, and resistivity, demonstrating that the laser slicing process did not degrade bulk electrical properties. Multi-scale Atomic Force Microscopy (AFM), Angle-Resolved X-Ray Photoelectron Spectroscopy (ARXPS), Secondary Ion Mass Spectrometry (SIMS), and Transmission Electron Microscopy (TEM)/Selected Area Electron Diffraction (SAED) analyses revealed the formation of a near-surface thin amorphous/polycrystalline modified layer and an oxygen-rich region, with significantly increased roughness and thicker modified layers on the hilly regions of the sliced surface. These results indicate that UV laser slicing maintains the intrinsic crystalline and electrical properties of 4H-SiC while introducing localized nanoscale surface damage that must be minimized by optimizing the slicing parameters and the subsequent surface-finishing processes. Full article

Understanding the molecular mechanisms of protein–nanoparticle interactions is crucial for enabling the development of new applications in biomedicine and nanotechnology. Ubiquitin, an important and structurally small functional protein, plays a central role in numerous cellular processes. Therefore, in the current study, we focused on the few-layer graphene (FLG)–Ubiquitin complexes formed by exfoliating FLG structures using only water. Optical spectroscopic techniques (Raman, FT-IR, UV-Vis and circular dichroism) were employed to investigate these complexes on the molecular level. Overall, both CD and FT-IR data reveal that the formation of the FLG–Ubiquitin complexes occurred without inducing disordered structures in the protein. Based on the existence of a blue shift (hypsochromic shift) in the UV-Vis data, the presence of a single tyrosine and two phenylalanine residues in ubiquitin enables the detection of FLG-induced micro-environmental changes, particularly influencing the protein’s β-sheet and α-helix structures. The CD spectral results and CDPro quantitative estimations are in line with ATR FT-IR results, confirming the absence of disordered structure formation while altering the protein’s chirality. UV-Vis and CD spectroscopy results revealed concentration-dependent trends consistent with FLG–protein interactions that preserve the overall protein structure. This study has potential applications in both academic research and practical usage, particularly in biomedicine and nanotechnology specifically for FLG. Full article

The optimization of BiVO₄-based structures significantly contributes to the development of a global system towards clean, renewable, and sustainable energies. Enhanced photocatalytic performance has been reported for numerous doped BiVO₄ materials. Bi³⁺-based compounds can be easily doped with rare earth (RE³⁺) ions due to their equal valence and similar ionic radius. This means that RE³⁺ ions could be regarded as active co-catalysts and dopants to enhance the photocatalytic activity of BiVO₄. In this study, a simple microwave-assisted approach was used for preparing nanostructured Bi_1−xEu_xVO₄ (x = 0, 0.03, 0.06, 0.09, and 0.12) samples. Microwave heating at 170 °C yields a bright yellow powder after 10 min of radiation. The materials are characterized through X-ray diffraction (XRD), transmission electron microscopy (TEM), ultraviolet–visible–near-infrared diffuse reflectance spectroscopy (UV-Vis-NIR DRS), photoluminescence spectroscopy (PL), and micro-Raman techniques. The effects of the different Eu³⁺ ion concentrations incorporated into the BiVO₄ matrix on the formation of the monoclinic scheelite (ms-) or tetragonal zircon-type (tz-) BiVO₄ structure, on the photoluminescent intensity, on the decay dynamics of europium emission, and on photocatalytic efficiency in the degradation of Rhodamine B (RhB) were studied in detail. Additionally, microwave chemistry proved to be beneficial in the synthesis of the tz-BiVO₄ nanostructure and Eu³⁺ ion doping, leading to an enhanced luminescent and photocatalytic performance. Full article

The extensive application of synthetic dyes in various industries and potential accidental uncontrolled discharge into natural water bodies have led to significant environmental challenges and a need for effective treatment. In this study, UiO-66 metal–organic framework/activated carbon (MOF/AC) composites were used to evaluate the photocatalytic degradation of Congo Red dye (CR) in aqueous solution under natural solar irradiation. The degradation efficiency of CR was determined using UV-Vis spectroscopy, while material characterization and additional insight into the reaction mechanism were obtained by XRD, FTIR, and Raman analysis. For a 50 ppm CR solution, within a 2 h reaction time, pure MOF achieved 57.2% and 26.3% degradation under solar irradiation and dark conditions, respectively, while the 75/25 MOF/AC composite reached 74% and 38.3% under the same conditions. These results confirm the synergistic interaction between MOF and AC, where AC acts as an electron sink, preventing charge recombination and enhancing photocatalytic activity. Chemisorption occurred simultaneously with photocatalytic degradation on the MOF surface. Reusability tests showed that pure MOF retained the highest stability over repeated cycles. Overall, the combination of MOF and AC enhances catalytic performance, which represents a sustainable approach for treating dye-contaminated wastewater under natural solar conditions. Full article

Two folding screens by futurist artist Giacomo Balla (1871–1958) in the collection of the Kröller-Müller Museum (the Netherlands) were investigated: Paravento con linea di velocità (1916–1917) and Paravento (1916/1917–1958). The screens are painted on both sides, the first on four canvases, stretched onto two wooden strainers and framed with painted wooden strips, and the second on wooden panels set into four painted stiles. In the past, damages on Paravento con linea di velocità were restored by conservators, while Paravento was probably first reworked by the artist himself and later restored by conservators. Yellowed varnish and discolored retouches on both screens led to a wish for treatment. The aim of this research was to gain insight into the painting techniques, layer buildup, pigments, binders, and varnishes of the two artworks. This information supported the decision making for treatment, and it broadens the knowledge on the materials used by Balla. Up to now, only a few published studies deal with the technical examination of paintings by this artist. Both folding screens were subjected to technical photography (UV, IR photography, and X-ray) and were examined with portable point X-ray fluorescence (pXRF) and Raman spectroscopy. Moreover, samples were taken. Cross-sections were studied with optical microscopy, scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX), attenuated total reflection Fourier-transform infrared (ATR-FTIR) imaging, and micro-Raman spectroscopy. Loose samples were examined with SEM-EDX, FTIR and micro-Raman spectroscopy, and pyrolysis gas chromatography mass spectrometry (Py-GC/MS). For Paravento con linea di velocità, all pigments and fillers of the painted canvases are compatible with the dating of the screen (1916–1917), but they differ from those on the frame. Here, rutile, in combination with various pigments, among which are blue copper phthalocyanine (PB15) and other synthetic organic pigments, was found. This indicates that the frame has been painted later, likely after the Second World War. The composition of the binders differs as well. Drying oil and pine resin have been used on the canvases, explaining the smooth and glossy appearance and solvent-sensitivity of the paint. On the frame, oil with some alkyd resin was identified. The provenance of the screen before 1972 is not clear, nor when the frame was made and painted and by whom. The results for Paravento indicate that the palettes of the two sides—painted in different styles—are comparable. Mainly inorganic pigments were found, except for the dark red areas, where toluidine red (PR3) is present. pXRF showed high amounts of zinc; cross-sections revealed that zinc white is present in the lower layers. These pigments are compatible with the dating of the screen (1916–1917). In many of the upper paint layers though, except for some green, dark red, and black areas, rutile has been identified. This indicates that these layers were applied later, likely after the Second World War. Since this folding screen was used by the artist and his family until his death in 1958, it seems likely that Balla himself reworked the screen. Full article

Yuanjiang County is one of the most important gem-producing areas in China. The authors of this study discovered and collected gem-quality andradite Garnsts in the epidote amphibolite from the periphery of the ruby deposit in Shaku Village, Yuanjiang County. After careful observation of the collected andradite, it was found that these andradite samples appear green when the thickness is less than 2 mm and reddish-brown when the thickness is greater than 2 mm, exhibiting the typical Usambara effect. To investigate the gemological and spectroscopic characteristics of Yuanjiang andradite, this study conducted basic gemological tests, microscopic observation, electron probe microanalysis (EPMA), ultraviolet–visible (UV-Vis) absorption spectroscopy, Fourier transform infrared (FTIR) spectroscopy, and laser Raman spectroscopy on the collected samples. Tests show that Yuanjiang andradite has a lower specific gravity than typical andradite, which is due to the presence of epidote inclusions inside. EPMA results indicate that the samples contain a certain amount of Cr element. The crystal chemical formula of the samples calculated from the EPMA results is (Ca_2.89–2.93, Mn_0.01–0.02, Fe_0.15–0.10)(Fe_1.69–1.95, Al_0.00–0.23, Cr_0.00–0.23, Si_0.05–0.08)(SiO₄)₃. UV-Vis tests show that the samples have transmission windows in both the green- and red-light regions, with Fe³⁺ and Cr³⁺ acting as the main chromogenic ions, among which Cr³⁺ is crucial for the occurrence of the Usambara effect. The FTIR and Raman test results are basically the same as previous research results, but some peak positions related to metal cations differ from the theoretical values, which may be caused by the presence of a certain amount of Cr³⁺ in the samples. Full article

This study presents the synthesis and comprehensive characterization of tin dioxide nanoparticles (SnO₂NPs). SnO₂NPs were obtained using a conventional wet-chemistry route and an environmentally friendly green-chemistry approach employing plant extracts from rooibos leaves (Aspalathus linearis), pomegranate seeds (Punica granatum), and kiwifruit peels (family Actinidiaceae). The thermal stability and decomposition profiles were analyzed by thermogravimetric analysis (TGA), while their structural and physicochemical properties were investigated using X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), ultraviolet–visible (UV–Vis) spectroscopy, dynamic light scattering (DLS), Raman spectroscopy, and attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopy. Transmission electron microscopy (TEM) confirmed the nanoscale morphology and uniformity of the obtained particles. The photocatalytic activity of SnO₂NPs was evaluated via the degradation of methyl orange (MeO) under UV irradiation, revealing that nanoparticles synthesized using rooibos extract exhibited the highest efficiency (68% degradation within 180 min). Furthermore, surface-enhanced Raman scattering (SERS) spectroscopy was employed to study the adsorption behavior of L-phenylalanine (L-Phe) on the SnO₂NP surface. To the best of our knowledge, this is the first report demonstrating the use of pure SnO₂ nanoparticles as SERS substrates for biologically active, low-symmetry molecules. The calculated enhancement factor (EF) reached up to two orders of magnitude (10²), comparable to other transition metal-based nanostructures. These findings highlight the potential of SnO₂NPs as multifunctional materials for biomedical and sensing applications, bridging nanotechnology and regenerative medicine. Full article