Search Results (1,136)

BaTi₅O₁₁ nanocrystals were synthesized via a sol–gel method employing different organic solvents. The influence of solvent choice on microstructure and photocatalytic performance was investigated through methylene blue (MB) degradation under UV light irradiation. The monoclinic BaTi₅O₁₁ nanocrystals were successfully synthesized, where solvent selection significantly affected their grain size and Brunauer–Emmett–Teller (BET) surface area. The BaTi₅O₁₁ nanocrystals synthesized using polyethylene glycol-200 (PEG-200) exhibited the highest BET surface area (9.78 m²/g) and smallest average pore size (17.8 nm). The BaTi₅O₁₁ nanocrystals also displayed a larger optical bandgap (3.61 eV), attributed to pronounced quantum confinement and surface effects. Consequently, the PEG-200-derived BaTi₅O₁₁ photocatalyst achieved complete MB degradation within 30 min under UV light irradiation. This enhanced performance was attributed to the high BET surface area providing abundant active sites. Furthermore, the BaTi₅O₁₁ nanocrystal photocatalyst maintained excellent reusability and stability over four consecutive cycles. Full article

This work reports a low-cost, microwave-assisted wet chemistry synthesis of zinc antimonate (ZnSb₂O₆) powders with a trirutile structure, yielding highly homogeneous, nanometric particles. X-ray diffraction (XRD) confirmed the formation of the trirutile phase with lattice parameters of a = 4.664 Å and c = 9.263 Å, and an estimated crystallite size of 42 nm. UV–vis spectroscopy revealed a bandgap of 3.35 eV. Scanning electron microscopy (SEM) showed that ethylenediamine, as a chelating agent, formed porous microstructures of microrods and cuboids, ideal for enhanced gas adsorption. Brunauer–Emmett–Teller (BET) analysis revealed a specific surface area of 6 m²/g and a total pore volume of 0.0831 cm³/g, indicating a predominantly mesoporous structure. The gas sensing properties of ZnSb₂O₆ pellets were evaluated in CO and C₃H₈ atmospheres at 100, 200, and 300 °C. The material exhibited high sensitivity at 300 °C, where the maximum responses were 5.86 for CO at 300 ppm and 1.04 for C₃H₈ at 500 ppm. The enhanced sensitivity at elevated temperatures was corroborated by a corresponding decrease in electrical resistivity. Furthermore, the material demonstrated effective photocatalytic activity, achieving up to 60% degradation of methylene blue and 50% of malachite green after 300 min of UV irradiation, with the process following first-order reaction kinetics. These results highlight that ZnSb₂O₆ synthesized by this method is a promising bifunctional material for gas sensing and photocatalytic applications. Full article

We fabricated TiO₂ thin films using the sol–gel method, incorporating TiO₂ nanoparticle sizes of 25 nm on the fluorine-doped tin oxide (FTO) substrates by spin coating and annelation at 600 °C. The influence of incorporating TiO₂ particles on the surface morphology, optical properties, and photovoltaic performance of TiO₂ thin-film dye-sensitized solar cells (DSSC) was examined. Structural characterization was analyzed using X-ray diffraction (XRD), while the morphologies were analyzed using scanning electron microscopy (SEM). The transmittance and absorbance of films were measured using an ultraviolet (UV)–visible (VIS)–near-infrared (NIR) spectrophotometer. The current–voltage (I-V) property was evaluated under simulated solar irradiation. The results demonstrated that the incorporation of TiO₂ particles enhanced the efficiency of DSSCs. The photovoltaic performance of DSSCs was improved with TiO₂ nanoparticle incorporation. The optimized DSSC incorporated TiO₂ films (TIFNA). TIFNA achieved a Jsc of 14.49 mA/cm², Voc of 0.69 V, fill factor of 60.5%, and efficiency of 6.05%, compared to 4.23% for the DSSC with unincorporated TiO₂ thin film. The improved performance was attributed to increased dye adsorption, better crystallinity, and enhanced electron transport. Full article

This study presents a comprehensive investigation of a novel graphene oxide/zinc oxide/lignin (GO/ZnO/lignin) nanocomposite for the photocatalytic degradation of methylene blue (MB) and gentian violet (also known as crystal violet, CV) dyes in aqueous solutions. The nanocomposite was synthesized through a hydrothermal method and thoroughly characterized using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX). FTIR spectra confirmed the successful incorporation of functional groups from all components, while XRD patterns revealed a well-crystallized structure with characteristic peaks. SEM micrographs showed a uniform, hierarchical morphology and EDX analysis verified the elemental composition and distribution. Under ultraviolet (UV) irradiation, the nanocomposite exhibited remarkable photocatalytic degradation efficiency (~97%) for both MB and CV. Key operational parameters were systematically evaluated, including pH (2–10), catalyst dosage (0.005–0.04 g/20 mL), and initial dye concentration (10–20 ppm). Optimal performance was achieved at pH 10, with a catalyst dosage of 0.03–0.04 g/20 mL and lower dye concentrations. The enhanced photocatalytic activity can be attributed to the synergistic effects coming from GO’s electron transport capabilities, ZnO’s strong photocatalytic activity and lignin’s additional degradation sites. Furthermore, the nanocomposite demonstrated excellent reusability, retaining nearly 60% of its degradation capacity after four cycles, outperforming its individual components. These results highlight the potential of this composite material for sustainable wastewater treatment applications. Full article

This study investigates the chemical and sensory effects of UV-C disinfection on black, white, green, and pink peppercorns using a scalable mechanical drum reactor. While previous research has demonstrated the efficacy of UV-C radiation in microbial disinfection, there is a lack of deep, quality-focused research on food products. Nevertheless, for spices, this is just as important, if not more so, than food safety. Different analyses were conducted to assess changes in volatile compounds, organic acids, fatty acids, tocopherols, and colour following UV-C exposure. Additionally, sensory evaluations were performed using triangular tests to determine whether these chemical changes were perceptible to consumers. Results revealed that many of the measured chemical components were affected by the UV treatment, with some volatile compounds decreasing by up to 90%, while certain organic acids increased by more than 150%. Despite these changes, no significant differences in colour, aroma, or flavour were detected by the sensory panel across all pepper types. These findings suggest that UV-C irradiation, when applied under the tested conditions, preserves the sensory quality of peppercorns, supporting its potential as a non-thermal processing method for spice treatment. Full article

The persistence of pharmaceutical pollutants such as ciprofloxacin (CIP) in aquatic environments represents a critical environmental threat due to their potential to induce antimicrobial resistance. Photocatalysis using TiO₂-based materials offers a promising solution for their mineralization; however, the limited visible-light response of TiO₂ and charge carrier recombination restricts its overall efficiency. In this study, Nb-doped TiO₂ nanoparticles were synthesized via the sol–gel method, incorporating Nb⁵⁺, ions into the TiO₂ lattice to modulate the structural and electronic properties of TiO₂ to enhance its photocatalytic performance for CIP degradation under UV and visible irradiation. Comprehensive structural, morphological, and optical analyses revealed that Nb incorporation stabilizes the anatase phase, reduces particle size (from 21.42 nm to 10.29 nm), and induces a slight band gap widening (from 2.85 to 2.87 eV) due to the Burstein–Moss effect. Despite this blue shift, Nb-TiO₂ exhibited significantly improved photocatalytic activity under visible light, achieving 86% CIP degradation with a reaction rate 16 times higher than that of undoped TiO₂. This enhancement was attributed to improved charge separation and higher hydroxyl radical (^•OH) generation, driven by excess conduction band electrons introduced by Nb doping. Density Functional Theory (DFT) calculations further elucidated the electronic structure modifications responsible for this behavior, offering molecular-level insights into Nb dopant-induced property tuning. These findings demonstrate how targeted doping strategies can engineer multifunctional nanomaterials with superior photocatalytic efficiencies, especially under visible light, highlighting the synergy between experimental design and theoretical modeling for environmental applications. Full article

Background/Objectives: This study reports the synthesis of TiO₂ nanoparticles, their functionalization with folic acid (FA), and the subsequent loading with zinc phthalocyanine (ZnPc) to develop photosensitizers for photodynamic therapy (PDT) targeting glioma cells. Methods: TiO₂, TiO₂-FA, and TiO₂-FA-ZnPc nanoparticles were synthesized via a sol–gel process involving the hydrolysis and condensation of titanium (IV) isopropoxide. FA and ZnPc were incorporated in vitro during the synthesis. The resulting materials were characterized by transmission and scanning electron microscopy (TEM and SEM), X-ray diffraction (XRD), Raman and UV–Vis spectroscopy, thermogravimetric analysis (TGA), and nitrogen adsorption–desorption measurements. Reactive oxygen species (ROS) generation was evaluated in vitro using the 1,3-diphenylisobenzofuran (DPBF) probe. A 40 ppm solution of each TiO₂ system was irradiated with UV light, and the degradation of DPBF was monitored. Biological assays were conducted to assess the viability of human glioblastoma cells (LN18 and U251) incubated with the TiO₂-based materials, with and without UV exposure. Human fibroblast cells (BJ) were used to evaluate biocompatibility. Results: All TiO₂-based materials retained key characteristics, including high surface area (~600–700 m²/g), mesoporous structure (pore diameter ~4–5 nm), mixed anatase–amorphous morphology, and a bandgap of approximately 3.46 eV. The UV–Vis spectrum of TiO₂-FA-ZnPc displayed additional absorption bands in the visible region (600–700 nm), consistent with ZnPc incorporation. Upon UV irradiation, the DPBF absorbance at 410 nm decreased over time, indicating ROS generation and resulting in complete degradation within 10 min (TiO₂), 12 min (TiO₂-FA), and 14 min (TiO₂-FA-ZnPc). BJ cells exhibited good biocompatibility at all concentrations. LN18 and U251 cells showed no cytotoxicity below 100 μg/mL unless exposed to UV light. Conclusions: The synthesized TiO₂-based systems demonstrate good biocompatibility and significant phototoxicity under UV irradiation, highlighting their strong potential for application in photodynamic therapy. Full article

The search for a simple, scalable, and eco-friendly method for synthesizing micro-sized photocatalysts is an urgent task. Plasma technologies are highly effective and have wide possibilities for targeted synthesis of novel materials. The mass-average temperature of plasma treatment is higher than the stability temperature of anatase and brookite, the most photoactive polymorphs of titanium dioxide. In this work, by optimizing the plasma treatment conditions and selecting source materials, a method for synthesizing micro-sized photocatalyst based on heterocomposite TiO₂/ZnO particles with high anatase content is proposed. The synthesis method involves treating a powder mixture of titanium and zinc by low-temperature argon plasma under atmospheric conditions. The relationship between the structural-phase composition, morphology, and photocatalytic properties of the microparticles was investigated. A model for the synthesis of composite microparticles containing anatase, rutile, and heterostructural contact with zinc oxide is proposed. The photocatalytic degradation of methylene blue and metronidazole was studied to evaluate both sensitized and true photocatalytic processes. The metronidazole degradation confirmed the intrinsic photocatalytic activity of the synthesized composites. Additionally, the features of photocatalysis under UV and solar irradiation were studied, and a photocatalysis mechanism is proposed. The synthesized micro-sized heterocomposite photocatalyst based on TiO₂/ZnO contained anatase (36%), rutile (60), and brookite (4%) and showed a photocatalytic activity during the methylene blue degradation process under UV irradiation (high-pressure mercury lamp, 250 W): 99% in 30 min. Full article

As a common semiconductor material, BiOBr has a unique layered structure and a suitable bandgap. However, the slow electron–hole separation efficiency leads to poor photocatalytic performance. To solve this problem, BiOBr/BNQDs heterojunctions were constructed. BiOBr/BNQDs composite photocatalysts were prepared by the solvothermal method, and the cocatalyst BNQDs were loaded onto BiOBr via electrostatic adsorption to enhance the photocatalytic degradation activity towards Rhodamine B (RhB). The photocatalysts were characterized by FT-IR, XRD, XPS, SEM-EDS, UV-Vis, PL, EIS, etc. Compared with pure BiOBr, the construction of heterojunctions BiOBr/BNQDs realized the rapid elimination of weak carriers and the effective separation and enrichment of high-energy carriers, which improved the efficiency of photocatalytic degradation of RhB. Among them, BiOBr/BNQDs-8.3% demonstrated the highest photocatalytic activity. The degradation rate of RhB under visible light irradiation for 60 min was up to 98.56%, and the reaction rate constant was 0.0696 min⁻¹, which was 2.80 times that of pure BiOBr. Moreover, after five photocatalytic cycles, the degradation rate was still 87.58%, demonstrating good cycling stability. Full article

Photocatalytic composite materials (TiO₂/SiO₂/BFSF) were first fabricated using the sol–gel method of loading SiO₂ and TiO₂ on blast furnace slag fibers (BFSFs) in sequence and using them as a new carrier. Then, TG-DTA, XRD, BET, SEM-EDS, and UV-Vis absorption spectra, as well as spectrophotometric measurements, were employed to analyze the physicochemical properties of TiO₂. The influence of SiO₂ coating, the number of impregnations in TiO₂ sol, the calcination temperature, and the number of repeated usages on the activity of TiO₂/SiO₂/BFSF was researched by analyzing the degradation of methylene blue (MB) aqueous solution. The results show that SiO₂ could increase the load of TiO₂, impede the growth of TiO₂ grains, and inhibit the recombination of electron–hole pairs, ultimately enhancing the photocatalytic activity of samples. The activity of TiO₂/SiO₂/BFSF first quickly increased and then slowly decreased with an increase in the loading times of TiO₂ sol and calcination temperature. After three impregnations in TiO₂ sol and calcining at 450 °C for 2.5 h, a uniform and compact anatase TiO₂ thin film was deposited on the surface of TiO₂/SiO₂/BFSF, showing the strongest activity. When this sample was used to degrade MB aqueous solution for 180 min under ultraviolet light irradiation, the degradation proportion reached a maximum of 96%. After four reuses, the degradation ratio could still reach 67%. In addition, three potential photocatalytic mechanisms were proposed. Finally, the high-value-added application of blast furnace slag for preparing photocatalytic composite materials was achieved, successfully turning solid waste into “treasure”. Full article

Background: The emergence and spread of antimicrobial-resistant bacteria (ARB) has become an urgent global concern as a silent pandemic. When taking measures to reduce the impact of antimicrobial resistance (AMR) on the environment, it is important to consider appropriate treatment of wastewater from medical facilities. Methods: In this study, a continuous-flow wastewater treatment system using ozone and ultraviolet light, which has excellent inactivation effects, was implemented in a hospital in an urban area of Japan. Results: The results showed that 99% (2 log₁₀) of Gram-negative rods and more than 99.99% (>99.99%) of ARB comprising ESBL-producing Enterobacterales were reduced by ozone treatment from the first day after treatment, and ultraviolet light-emitting diode (UV-LED) irradiation after ozone treatment; UV-LED irradiation after ozonation further inactivated the bacteria to below the detection limit. Inactivation effects were maintained throughout the treatment period in this study. Metagenomic analysis showed that the removal of these microorganisms at the DNA level tended to be gradual in ozone treatment; however, the treated water after ozone/UV-LED treatment showed a 2 log₁₀ (>99%) removal rate at the end of the treatment. The residual antimicrobials in the effluent were benzylpenicillin, cefpodoxime, ciprofloxacin, levofloxacin, azithromycin, clarithromycin, doxycycline, minocycline, and vancomycin, which were removed by ozone treatment on day 1. In contrast, the removal of ampicillin and cefdinir ranged from 19% to 64% even when combined with UV-LED treatment. Conclusions: Our findings will help to reduce the discharge of ARB and antimicrobials into rivers and maintain the safety of aquatic environments. Full article

Persistent reactive azo dyes released from textile finishing are a serious threat to water systems, but effective methods using sunlight to break them down are still limited. Everzol Yellow 3RS (EY-3RS) is particularly recalcitrant: past studies have relied almost exclusively on physical adsorption onto natural or modified clays and zeolites, and no photocatalytic pathway employing engineered nanomaterials has been documented to date. This study reports the synthesis, characterization, and performance of a visible-active ternary nanocomposite, Cu₄O₃/ZrO₂/TiO₂, prepared hydrothermally alongside its binary (Cu₄O₃/ZrO₂) and rutile TiO₂ counterparts. XRD, FT-IR, SEM-EDX, UV-Vis, and PL analyses confirm a heterostructured architecture with a narrowed optical bandgap of 2.91 eV, efficient charge separation, and a mesoporous nanosphere-in-matrix morphology. Photocatalytic tests conducted under midsummer sunlight reveal that the ternary catalyst removes 91.41% of 40 ppm EY-3RS within 100 min, markedly surpassing the binary catalyst (86.65%) and TiO₂ (81.48%). Activity trends persist across a wide range of operational variables, including dye concentrations (20–100 ppm), catalyst dosages (10–40 mg), pH levels (3–11), and irradiation times (up to 100 min). The material retains ≈ 93% of its initial efficiency after four consecutive cycles, evidencing good reusability. This work introduces the first nanophotocatalytic strategy for EY-3RS degradation and underscores the promise of multi-oxide heterojunctions for solar-driven remediation of colored effluents. Full article

Background/Objectives: The rapid emergence of multidrug-resistant bacterial infections demands innovative non-antibiotic therapeutic strategies. Dual-modal photoresponse therapy integrating photodynamic (PDT) and photothermal (PTT) effects offers a promising rapid antibacterial approach, yet designing single-material systems with synergistic enhancement remains challenging. This study aims to develop uniform Cu-based metal–organic framework micrometer cubes (Cu-BN) for efficient PDT/PTT synergy. Methods: Cu-BN cubes were synthesized via a one-step hydrothermal method using Cu(NO₃)₂ and 2-amino-p-benzoic acid. The material’s dual-mode responsiveness to visible light (420 nm) and near-infrared light (808 nm) was characterized through UV–Vis spectroscopy, photothermal profiling, and reactive oxygen species (ROS) generation assays. Antibacterial efficacy against multidrug-resistant Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) was quantified via colony counting under dual-light irradiation. Results: Under synergistic 420 + 808 nm irradiation for 15 min, Cu-BN (200 μg/mL) achieved rapid eradication of multidrug-resistant E. coli (99.94%) and S. aureus (99.83%). The material reached 58.6 °C under dual-light exposure, significantly exceeding single-light performance. Photodynamic analysis confirmed a 78.7% singlet oxygen (¹O₂) conversion rate. This enhancement stems from PTT-induced membrane permeabilization accelerating ROS diffusion, while PDT-generated ROS sensitized bacteria to thermal damage. Conclusions: This integrated design enables spatiotemporal PDT/PTT synergy within a single Cu-BN system, establishing a new paradigm for rapid-acting, broad-spectrum non-antibiotic antimicrobials. The work provides critical insights for developing light-responsive biomaterials against drug-resistant infections. Full article

Cobalt and Nickel (Co, Ni) co-doped magnesium oxide (MgO) nanoparticles (NPs) have been synthesized using the coprecipitation method. The structural, chemical, and optical properties of the as-synthesized NPs are systematically investigated using X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), and UV-visible spectroscopy. It is found that the optical bandgap of co-doped MgO NPs reduces from 2.30 to 1.98 eV (14%) with increasing Ni dopant concentrations up to 7%. The Co_0.05Ni_0.07Mg_0.88O NPs exhibit a high photocatalytic degradation efficiency of 93% for methylene blue dye (MB) under natural sunlight irradiation for 240 min. Our findings indicate that the Co_0.05Ni_xMg_0.95−xO NPs have strong potential for use as photocatalysts in industrial wastewater treatment. Full article

A facile and versatile strategy to obtain NPs@ZnAlO nanocomposite materials, comprising controlled-size nanoparticles (NPs) within a ZnAlO matrix is reported. The mono-(Au, Ni) and bimetallic (Ni-Au) NPs serving as an active phase were prepared by the polyol-alkaline method, while the ZnAlO support was obtained via the thermal decomposition of its corresponding layered double hydroxide (LDH) precursors. X-ray diffraction (XRD) patterns confirmed the successful fabrication of the nanocomposites, including the synthesis of the metallic NPs, the formation of LDH-like structure, and the subsequent transformation to ZnO phase upon LDH calcination. The obtained nanostructures confirmed the nanoplate-like morphology inherited from the original LDH precursors, which tended to aggregate after the addition of gold NPs. According to the UV-Vis spectroscopy, loading NPs onto the ZnAlO support enhanced the light absorption and reduced the band gap energy. ATR-DRIFT spectroscopy, H₂-TPR measurements, and XPS analysis provided information about the functional groups, surface composition, and reducibility of the materials. The catalytic performance of the developed nanostructures was evaluated by the photodegradation of bisphenol A (BPA), under simulated solar irradiation. The conversion of BPA over the bimetallic Ni-Au@ZnAlO reached up to 95% after 180 min of irradiation, exceeding the monometallic Ni@ZnAlO and Au@ZnAlO catalysts. Its enhanced activity was correlated with good dispersion of the bimetals, narrower band gap, and efficient charge carrier separation of the photo-induced e⁻/h⁺ pairs. Full article