Search Results (8,525)

In this work, Ce-doped ZnO thin films at various contents of cerium were deposited on glass substrates by thermal vacuum evaporation to study the influence of Ce concentration on their optical, structural, morphological, and photocatalytic behavior. Pure ZnO and Ce-doped ZnO films doped with 2% and 5% Ce were characterized by SEM, XRD, AFM, UV–VIS spectroscopy, and ellipsometry. The XRD analysis confirmed that all the films retained the hexagonal wurtzite structure, while Ce incorporation induced lattice strain and reduced crystallite size, particularly at higher doping levels. SEM and AFM studies showed that films with 2% Ce exhibited smaller grain size and lower roughness, whereas 5% Ce-doped films showed grain growth and increased roughness. Pure ZnO films displayed high transparency (>90%), whereas Ce incorporation caused a red shift in the absorption edge and narrowing of the optical band gap due to defect-related states and lattice distortion. Photocatalytic experiments revealed that Ce doping improved charge carrier separation and increased the number of oxygen vacancies. Among all samples, the 2% Ce-doped ZnO film demonstrated the highest photocatalytic efficiency. These findings highlight the importance of controlled Ce doping in tuning the microstructure, optical properties, and photocatalytic performance of ZnO thin films, making them suitable for environmental remediation and optoelectronic applications. Full article

Two metallacyclic tetranuclear Fe(III) complexes, [{Fe₂(μ-O)(μ-RCOO)₂(tpon)}₂](BPh₄)₄ [R = Me (1), Ph (2)], where the flexible ditopic ligand tpon (N,N,N′,N′-tetrakis(2-pyridylmethyl)octane-1,8-diamine) links two μ-oxo-bis(μ-carboxylato) triple-bridged dinuclear units, have been prepared. Single-crystal X-ray diffraction establishes that both complexes adopt a 26-membered macrocyclic framework featuring an internal cavity capable of guest inclusion. Notably, incorporation of a monoatomic μ-oxo bridge enforces an outward orientation of the ligand alkyl chains, thereby suppressing the “zipper effect” observed in the previously reported Mn(II) analogue and facilitating the encapsulation of an acetone molecule. UV–vis absorption and diffuse-reflectance spectra confirm that the tetranuclear scaffold remains intact in both the solid state and in solution. These results demonstrate that modulating local coordination directionality via μ-oxo bridging is an effective strategy for controlling the global conformation and host–guest properties of large metallasupramolecular architectures. Full article

With the rapid advancement of autonomous driving in modern society, dense pedestrian detection technology has encountered performance bottlenecks. To address this, we propose a robust and lightweight pedestrian detection algorithm, RMP-YOLO, designed to efficiently detect small, occluded, and low-light objects. Firstly, RFAConv is utilized as the core component of the backbone network, combining standard convolution with attention mechanisms and using group convolution to extract features from the spatial receptive field. Secondly, MobileViTv3 is introduced into the backbone to combine CNNs with Transformers. The model is further enhanced by adjusting feature fusion, introducing residual connections, and optimizing local representation with deep convolutional layers. Finally, the PIoUv2 loss function is employed for bounding-box regression, significantly reducing detection errors for small-scale pedestrians in crowded environments. Experimental results demonstrate that RMP-YOLO improves mAP@0.5 by 1.3% on a custom dataset and 0.91% on the WiderPerson dataset. Crucially, it maintains high efficiency with only 3.71 million parameters and 6.29 GFLOPs, meeting the deployment requirements for low computational power and high precision. Full article

The Middle Triassic Bulz Dolomite Formation in the Apuseni Mountains (Romania) lacks detailed microfacies documentation and paleoenvironmental reconstruction, leaving its regional correlation unresolved. This study aims to describe the microfacies and fossil assemblages of the Bulz Dolomite to reconstruct the Anisian depositional environment and establish regional stratigraphic links. More than twenty outcrop samples were analyzed using conventional microfacies analysis, UV/VIS-fluorescence, and cathodoluminescence microscopy. Results reveal that early, fabric-retentive dolomitization preserved microbial boundstones, dasycladalean algae (Teutloporella peniculiformis, Physoporella pauciforata), and benthic foraminifers (Hoyenella sinensis), indicating shallow-marine, peritidal, and restricted lagoonal environments. The multiphase diagenetic history involves early reflux dolomitization from hypersaline brines, burial recrystallization forming nonplanar and saddle dolomites, and late-stage meteoric calcite cementation. The diagnostic fossil assemblage firmly constrains the formation to the Anisian age. Consequently, the Bulz Dolomite shares compelling lithological, diagenetic, and biostratigraphic affinities with the Szeged Dolomite Formation in the basement of the southeastern Pannonian Basin, demonstrating the presence of a unified, expansive evaporitic carbonate shelf extending across the Tisza Megaunit along the Neotethyan passive margin. Full article

A Ce-doped photocatalytic composite with easy solid–liquid separation capability was prepared and a heterojunction was constructed between BiVO₄ and Fe₃O₄ via a co-precipitation method. A variety of characterization techniques were employed, such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), ultraviolet–visible spectroscopy (UV-vis), transmission electron microscopy (TEM) and energy-dispersive X-ray spectroscopy (EDS), as well as other related methods. Its photocatalytic performance for the degradation of Rhodamine B (RhB) was also studied. The results indicate that the photocatalytic efficiency of BiVO₄/Fe₃O₄ is 1.4 times that of the pure BiVO₄ matrix. In particular, the photocatalytic efficiency of Ce_1.5%-BiVO₄/Fe₃O₄ was 2.2 times higher than that of the pure BiVO₄ matrix, and a 100% degradation rate of RhB was achieved within 30 min. The introduction of Fe₃O₄ not only forms a heterojunction with BiVO₄, increasing the active sites and surface oxygen vacancies of the material and effectively suppressing the recombination of photogenerated electron (e^-)-hole (h⁺) pairs, but it also enables the rapid separation of the material from the wastewater solution by the magnetic properties of Fe₃O₄. Additionally, the partial substitution of Ce for Bi in the BiVO₄ lattice reduces the bandgap energy, which enhances the utilization efficiency of visible light and improves the photocatalytic performance of the composite material. The mechanism of RhB degradation by Ce_1.5%-BiVO₄/Fe₃O₄ composite materials is also analyzed in this study. Quenching experiments and EPR tests revealed that h⁺ and ${·\mathrm{O}}_2^{-}$ were the primary reactive species in the degradation process. Full article

Licania tomentosa leaf extract was used to synthesize zinc oxide nanoparticles (ZnO NPs) which were systematically analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-Visible (UV-Vis) and Fourier transform infrared (FT-IR) spectroscopies and energy-dispersion X-ray spectroscopy (EDS) methods. Based on XRD scans, the green NPs have an average crystallite size of 15.9 nm as estimated using the Scherrer equation and have a roughly spherical shape with an average diameter of 25.15 ± 1.2 nm as calculated from SEM data. As estimated from the Tauc plot based on UV-Vis absorption spectra, ZnO NPs have a small band gap of 3.0 eV. The biosynthesized ZnO NPs were effectively utilized for the photodegradation of methylene blue (MB) and crystal violet (CV) dyes under UV illumination with resulting MB and CV degradation efficiencies of ~94% and ~81% after 60 min and 70 min, with pH = 12 and pH = 10, respectively. Different experimental parameters such as NPs quantity, experimental pH, light intensity and initial concentration of dyes were varied to test the performance of the catalyst. Furthermore, efficient recycling of the catalyst was demonstrated. We also undertook antimicrobial studies of the green ZnO NPs. The ZnO NPs demonstrated broad-spectrum antimicrobial efficacy against Escherichia coli ATCC 35218, Enterococcus faecalis ATCC 29737, Klebsiella pneumoniae ATCC 700603, Pseudomonas aeruginosa ATCC 27853, P. aeruginosa B3, Staphylococcus aureus ATCC 29213, and S. aureus SA01, with the minimum inhibitory concentration (MIC) and the inhibitory concentrations associated with 50% effect (IC50) values ranging from 250 to 2000 µg/mL and 7.74 to 283.14 µg/mL, respectively. The nanoparticles also significantly inhibited biofilm formation by E. faecalis ATCC 29737, P. aeruginosa ATCC 27856, and S. aureus SA03. The antimicrobial efficiency of the ZnO NPs against Escherichia coli ATCC 25922 and Staphylococcus aureus SA03 isolates was also assessed using the disk diffusion assays. Taken together, our results reveal that the biosynthesized ZnO NPs are promising multifunctional materials with potential applications in antimicrobial treatments, biofilm control, and photocatalytic remediation. Full article

A zinc complex of chelidonic acid (4-oxo-4H-pyran-2,6-dicarboxylic acid) was obtained by reaction with zinc oxide under isothermal conditions. Its composition was confirmed by elemental and thermogravimetric analyses, and its molecular structure was characterized using NMR and IR spectroscopy. Single-crystal X-ray diffraction revealed that the complex crystallizes as a one-dimensional coordination polymer, [ZnChel(H₂O)₄]_n, in the triclinic space group P-1, featuring a distorted octahedral Zn(II) center coordinated by two chelidonate ligands and four water molecules. This six-coordinate arrangement contrasts with previously described tetra-coordinated Zn–chelidonate complexes. Quantum-chemical calculations and molecular dynamics simulations indicated that, in aqueous solution, Zn(II) preferentially forms a monodentate ZnChel(H₂O)₅ species, consistent with the solid-state coordination environment. The interaction of the complex with bovine serum albumin (BSA) was examined by fluorescence, UV–Vis absorption, and circular dichroism spectroscopy, revealing a mixed static–dynamic quenching mechanism, moderate binding affinity, and hydrogen-bonding/van der Waals contributions accompanied by alterations in BSA secondary structure. These results expand the structural chemistry of chelidonic acid and provide biophysical insight into the protein-binding behavior of zinc chelidonate, supporting its potential relevance as a zinc-based bioactive compound. Full article

The phytochemical variability in Cannabis sativa L. chemovars represents an underexplored factor in environmentally sustainable nanomaterial production. In this study, three distinct chemovars, (i) High-Δ⁹-Tetrahydrocannabinol (THC) (89% THC), (ii) Balanced (60% Cannabidiol (CBD)), and (iii) High-CBD (89% CBD), were comparatively evaluated to determine their suitability for the green synthesis of silver nanoparticles (AgNPs). Ethanolic inflorescence extracts were used to recover bioactive secondary metabolites; among them, the High-CBD extract exhibited the highest total phenolic (3.34 mg gallic acid equivalent/g) and flavonoid (29.49 mg quercetine equivalent/g) contents, together with superior antioxidant capacity (53.16% 2,2-diphenyl-1-picrylhydrazyl free radical (DPPH) inhibition), indicating enhanced redox potential for nanoparticle formation. The terpene profile of High-CBD showed a dominance of myrcene (21.4%), contributing to the stabilization of the system. Using the High-CBD extract, predominantly spherical nanoparticles of 5 ± 0.9 nm were synthesized and confirmed by UV–vis, EDS, and TEM. The biogenic AgNPs demonstrated significant dose-dependent antibacterial activity, with minimum bactericidal concentration (MBC) of 1.0 mg/mL against Staphylococcus aureus and 4.5 mg/mL against Escherichia coli. These findings highlight the critical role of chemovar-dependent phytochemical composition and support a phytochemistry-guided approach for developing silver nanoparticles with potential biomedical applications. Full article

Phenol derivatives display a prominent role in many biologically active molecules. Boron-containing molecules are considered valuable precursors for their synthesis. Therefore, the rise of photochemistry has led many researchers to develop novel, sustainable protocols that exploit the advantages offered by different irradiation sources. For this reason, the application of novel photocatalysts that promote challenging organic transformations is highly valued. Graphitic carbon nitride (g-C₃N₄) is a semiconductor photocatalyst widely used in organic chemistry for promoting complex organic transformations. Herein, we report a green and efficient methodology for the hydroxylation of boronic acids to the corresponding hydroxyl derivatives, using g-C₃N₄ as the photocatalyst. The heterogeneous photocatalyst (g-C₃N₄) was prepared by thermal polycondensation of melamine and characterized by XRD, FESEM/EDS, and UV–Vis diffuse reflectance spectroscopy. Green LED irradiation was employed as the energy source and air as the active oxidant. A variety of substrates were tested, showcasing excellent functional group tolerance in the aerobic photochemical protocol. Mechanistic studies were conducted to investigate the reaction pathway and to identify the oxygen species generated. Full article

The world’s growing need for energy, fueled by industrial expansion and a rising population, continues to be a challenge for the scientific community. The heavy reliance on fossil fuels that contribute to environmental degradation and public health concerns, is shifting toward sustainable alternatives, with hydrogen production via advanced catalysts as an energy source emerging as a promising solution. This transition addresses the challenges posed by harmful combustion emissions. In this study, we developed an innovative PANI@Cu-NA-MOF nanocomposite catalyst through a sol–gel synthesis approach that strategically integrates conducting polymers with metal–organic frameworks. The catalyst was characterized using different sets of techniques. Surface morphology and elemental composition were investigated using SEM-EDX, while structural analysis was carried out with FTIR that helped to identify the chemical bonds and functional groups, and UV-Vis spectroscopy provided information on its light absorption properties. In addition, TGA was used to evaluate thermal behavior, and XPS offered detailed surface chemical analysis. It was observed by morphology that PANI@Cu-NA-MOF is a noncapsular-like structure. It is thermally highly stable; a TGA study showed that up to 550 °C, almost 2.5% of weight was lost. The single peak in UV-Vis is the preparation of a successful composite. XPS and FTIR reveal the required peaks of functional groups and elements. The PANI@Cu-NA-MOF composite turned out to be quite effective for water electrolysis, requiring an overpotential of just 0.47 V to drive the reaction. When tested against the reversible hydrogen electrode, we observed onset potentials of 1.6 V/RHE for the oxygen evolution reaction and 0.2 V/RHE for the hydrogen evolution reaction. What makes this particularly interesting is that such performance significantly cuts down on the energy needed for electrolysis, which could make hydrogen production much more practical. Since hydrogen burns cleanly and offers a real alternative to fossil fuels, having an efficient catalyst like this brings us one step closer to sustainable energy. Full article

Welders constitute an occupational group that is particularly exposed to high-risk hazards arising from harmful radiation emitted during welding, including ultraviolet (UV) and infrared (IR) radiation, as well as visible (VIS) radiation, whose high intensity causes glare. Effective protection of the eyes and face is provided by welding shields equipped with automatic welding filters (AWFs), which activate automatically upon arc ignition. Their switching time is the most important protective parameter, as it has a direct impact on the user’s visual health. The objective of the work is to present a novel test stand for determining AWFs switching and holding times, which provides advanced possibilities for evaluating all types of AWFs. Until now, performance and safety levels have been determined based on numerical values: switching time and hold time. For the first time, it is possible to analyze the darkening and clearing phenomena over time with an interpretation of graphical results. Importantly, it is possible to analyze the symmetry of filter properties, using two measurement channels, which is crucial for binocular and curved (panoramic) AWFs. The results obtained for two types of AWFs mounted in goggles with a one-piece and a binocular visor differ from each other. Switching time differences between the left and right measurement channels were about 6–7% for the one-piece visor goggles (G1) and about 3–4% for the binocular goggles (G2). The dispersion of results confirmed the importance of the two measurement channels, which was not previously practiced. The test stand, designed in accordance with the requirements of the new European standards (EN ISO 18526-2:2020, EN ISO 16321-2:2021), can be used for prototyping and for AWF certification purposes. Full article

The excessive accumulation of biogenic amines (BAs) in aquatic products poses serious health risks, necessitating the development of rapid and sensitive detection methods. This study reports the synthesis of a novel fluorescent nanocomposite, carbon-dot-embedded covalent organic frameworks (CDs@COFs). Comprehensive characterization (TEM, XPS, FTIR, UV–Vis, and fluorescence spectroscopy) confirmed the successful fabrication of the nanocomposites, which exhibited excellent thermal and optical stability. A significantly enhanced quantum yield of 36.22% (compared with 12.92% for pure carbon dots) was obtained. As a fluorescent probe, the composite enabled the detection of nine BAs based on a fluorescence quenching mechanism. The proposed method demonstrated good linearity (1~100 ng/mL) and low detection limits of 0.58~0.98 ng/mL. The method was successfully applied to analyze tyramine in large yellow croaker, showing accurate spike recoveries ranging from 91.93% to 101.43% and excellent reproducibility (RSD < 3%). These results highlight the great potential of the developed method as a powerful tool for the rapid screening of BAs in aquatic products. Full article

In this study, nanolubricants based on SAE 5W-30 mineral oil were formulated using oleic acid-functionalized graphene nanoplatelets (GNPs), and their colloidal stability, rheological behaviour, thermal stability, and tribological performance under cold rolling conditions were systematically investigated. The nanolubricants were prepared at GNP concentrations of 0.05, 0.1, 0.2, 0.4, and 0.6 wt%. FT-IR analysis confirmed successful functionalization, evidenced by the characteristic C=O band at approximately 1710 cm⁻¹ and changes in CH₂ stretching vibrations in the 2850–3000 cm⁻¹ range. UV–VIS results indicated initially homogeneous dispersions; however, after three days, relative concentrations decreased to 95%, 90%, and 75% for 0.05, 0.2, and 0.6 wt% GNPs, respectively. Viscosity measurements showed minimal variation at low concentrations, with only a 0.64% increase at 0.2 wt% compared to the base oil. TGA revealed enhanced oxidative stability at low GNP contents, with the oxidation onset temperature increasing from 205.3 °C to 207.2 °C at 0.05 wt%, while a marked decline was observed at higher concentrations (176.8 °C at 0.6 wt%). In cold rolling experiments at a 3% reduction ratio, the rolling force was measured at 1341 N/mm with the neat lubricant, decreasing to 1210 N/mm with a lubricant containing 0.1 wt% GNPs, corresponding to an approximate 10% reduction. Compared with dry conditions, this reduction was approximately 21%. Surface roughness and 3D topography analyses further showed that GNPs-containing lubricants reduced asperities and promoted the formation of a more uniform tribofilm. At low concentrations, the improved lubrication performance of oleic acid-functionalized graphene nanoplatelets is attributed to their homogeneous dispersion in mineral oil, where physically adsorbed oleic acid improves colloidal stability by reducing agglomeration and promotes the formation of a stable tribofilm, facilitating interlayer sliding under boundary lubrication conditions. Overall, the findings demonstrate that oleic acid-functionalized GNPs, when used at optimal concentrations, significantly enhance both lubricant stability and cold rolling performance. Full article

This work proposes the doping of bi-electron transport layers consisting of TiO₂/SnO₂ with iron to facilitate electron movement and recombination reduction, which results in increases in power conversion efficiency and stability enhancement. Two different PSC structures are used: device 1—FTO/TiO₂/SnO₂/MAPbI₃/Spiro-OMETAD/Ag; device 2, a modified device—FTO/TiO₂/SnO₂ + Fe/MAPbI₃/Spiro-OMETAD/Ag. Characterization analysis revealed an improvement in perovskite crystallinity in the modified device; this leads to reductions in trap state density and the recombination of charges that enhance charge extraction. UV-vis absorbance enhancement in the modified device revealed an enhancement in the perovskite layer morphology and good coverage. As a result, PSCs with a short circuit current of 23.35 mA/cm², open circuit voltage of 1.07 V, fill factor of 0.73, and high PCE of 18.17% are obtained from device 2, compared to PSCs with only 22.13 mA/cm², 1.03 V, 0.7, and 16.053% for device 1 without Fe doping, respectively. The results reveal that the device based on Fe doping is more stable than the pristine one under stability tests with regard to aging, thermal, stress and prolonged light. Full article

Polyaniline-cadmium sulfide-gold (PANI-CdS-Au) nanocomposites were synthesized with varying Au loadings (0.023, 0.046, 0.092 wt%) to enhance antibacterial performance. Structural (FTIR, XRD) and morphological (FESEM) analyses confirmed successful formation, with nearly homogeneous nanoparticle distribution (27–53 nm) and slight XRD peak shifts indicating interfacial interactions between PANI, CdS, and Au. UV–Vis spectra revealed gold surface plasmon resonance and polaronic transitions consistent with PANI emeraldine base. XRD results showed the expected wurtzite CdS and fcc Au phases. Agar well diffusion tests against Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) demonstrated that the 0.092 wt% of Au composite produced the largest inhibition zones at 100 µg mL⁻¹ (E. coli: 36 mm; S. aureus: 24 mm), with the same trend at 25 µg mL⁻¹. The results indicate that PANI–CdS/Au nanocomposites are promising antibacterial materials; however, the presence of CdS necessitates additional cytotoxicity assays to confirm their suitability for medical applications. Full article