Search Results (2,732)

TiO₂ nanotubes were synthesized using the anodization method on Ti foils and decorated with PbS nanoparticles by the SILAR method at different cycle numbers (10, 15, 20, 25, and 30). These samples were characterized using SEM, TEM, XRD, and microhardness tests. Morphologically, the PbS nanoparticles were evenly dispersed on TiO₂ nanotubes in the shape of small spheres. With an increase in the number of cycles, the size and shape of the nanoparticles increased. This also affected the structure and crystallinity of the PbS NPs, as the crystallite size of PbS increased. The in-depth analysis of the tribological characteristics of the coatings conducted using the scratch test allowed us to evaluate the adhesion of the coatings, a crucial aspect in determining their effectiveness and durability. Furthermore, we found that the wear resistance of the coatings increased with the number of PbS cycles up to 15 cycles. However, for the samples with higher size distribution and crystallite size, such as those with more than 15 cycles, the microhardness continued to decrease. This indicates that the addition of PbS can improve the durability of TiO₂ coatings, making them a potential candidate for advanced surface coatings in demanding engineering applications. Electrochemical measurements were conducted to assess the corrosion resistance of the samples. The electrochemical impedance spectra (EIS) results revealed that the PbS/TiO₂ coatings with 15 deposition cycles exhibited the most effective corrosion resistance, with a dense and uniform distribution of PbS nanoparticles forming a compact barrier that effectively protects against corrosion. The charge transfer resistance (R_ct) and the absorption capacitance (Q_ab) values were higher for the 15-cycle sample (4.49 Ω·cm² and 0.9 Fsⁿ⁻¹cm⁻², respectively). Full article

In this study, TiO₂ nanoparticles (NPs), CdS NPs and TiO₂/CdS nanocomposite were synthesized via the sol–gel, hydrothermal and ex situ method, respectively. The synthesized materials were characterized using XRD, UV–vis DRS, FTIR, SEM, and EDX analysis. XRD analysis confirmed the crystalline structure of the as-prepared samples, while the bandgap energy of TiO₂ NPs, CdS NPs, and TiO₂/CdS nanocomposite were determined to be 2.98, 1.94, and 2.27 eV, respectively. Photocatalytic efficiency of TiO₂ NPs, CdS NPs, and TiO₂/CdS nanocomposite was systematically evaluated by photocatalytic degradation of crystal violet (CV) dye under visible-light irradiation. Under optimized reaction conditions of [CV concentration] = 20 mg/L, [catalyst dosage] = 0.25 g/L, and pH = 6, TiO₂/CdS nanocomposite achieved 86.3% removal of CV within 180 min, outperforming pure TiO₂ NPs (16.4%) and CdS NPs (66.9%). The enhanced performance of TiO₂/CdS nanocomposite as compared to CdS NPs is attributed to improved charge separation via heterojunction formation, while significantly superior performance over TiO₂ demonstrates successful visible-light activation. Further optimization study revealed that maximum removal efficiency of CV (97.1%) was achieved at lower dye concentration (10 mg/L). Photocatalytic degradation of CV followed pseudo-first-order kinetics. Moreover, scavenger experiments confirmed hydroxyl radicals (^•OH) as dominant reactive species. Furthermore, the TiO₂/CdS nanocomposite demonstrated good reusability with minimal activity loss after five runs. Additionally, the as-prepared nanocomposites showed significant antibacterial activity against Pseudomonas aeruginosa (P. aeruginosa). The present study indicated that TiO₂/CdS nanocomposite could be simultaneously used for degradation of organic pollutants as well as for removal of microorganisms while targeting environmental sustainability and water purification. Full article

This study focused on elucidating the effects of chitosan (Ch), hyaluronic acid (HA), and titanium dioxide nanoparticles (nano-TiO₂) on the physicochemical characteristics of a model bacterial membrane (layer) composed of the phospholipid DPPG (1,2-dipalmitoyl-sn-glycero-3-phospho-rac-(1-glycerol) sodium salt). The membrane was prepared on mica using the Langmuir–Blodgett (LB) technique from an aqueous subphase containing Ch, HA and/or TiO₂. Its surface properties were subsequently characterized by optical profilometry and surface free energy estimation. The nanoscale topography of the DPPG layer provided a biomimetic platform that reflects the organization of bacterial membranes, enabling a precise evaluation of how external agents, such as Ch, HA, and nano-TiO₂, modify the surface’s structural and energetic properties. The results showed that the LB films exhibit mildly heterogeneous topography, which can be attributed to lipid domains with distinct molecular packing densities. Depending on the type of biopolymer employed with TiO₂, distinct topographic architectures of the DPPG monolayers were obtained. Furthermore, the presence of nano-TiO₂ was clearly manifested as a topographic irregularity, while the analysis of hydrophilic–hydrophobic properties revealed a structurally perturbed lipid film. The results provide detailed insight into how these specific molecules (Ch, HA, nano-TiO₂) interact at the molecular level with model bacterial membranes, offering a comprehensive picture of cell–microenvironment interactions. Full article

In this work, we report the fabrication of SnO₂-based composite nanostructures in view of their application as a sensor element toward N₂O gas exposure. The samples were produced by laser ablation of a composite SnO₂-TiO₂ target performed in air at atmospheric pressure (in open air). We examined how the structure, morphology, composition, and physical properties of the samples change with the TiO₂ content being introduced into the SnO₂ target. The laser ablation of SnO₂-based targets in open air produced samples with a structure in which SnO₂ and SnO crystal phases co-existed, as the crystal phases were distinguished in separate nanoparticles. The nanoparticles formed a complex porous structure with oxygen-related defects. We investigated the gas-sensing properties of composite SnO₂-based sensor elements working under UV irradiation. The highest response to N₂O exposure and the fastest response/recovery times were demonstrated by the sensor element produced by the laser ablation of a composite target prepared by 10 wt% TiO₂ in SnO₂. Additionally, we found that a small amount (below 0.1 wt%) of noble metal (Pt) added to the sensor element substantially improved the gas sensor performance without inducing significant structural and/or morphological changes. Further, we explored how simultaneous irradiation of the sensor surface with UV and visible light changes the sensor properties. The best sensor performance toward N₂O exposure was achieved by irradiating the Pt-doped SnO₂-TiO₂ sensor surface simultaneously with UV and red lights. Full article

MXene, as a suitable and alternative 2D nanofiller incorporated into a proton exchange membrane (PEM), has recently received considerable attention because of desired mechanical stability, promising conductivity, and active surface functional groups. However, agglomeration or sedimentation in PEMs, as well as the water retention capacity under low humidity of MXene, are limiting factors in the field of PEMs. In this paper, modified MXene and TiO₂ nanoparticles used as functional nanofillers were incorporated into sulfonated poly (ether ether ketone) (SPEEK) to prepare novel SPEEK-based composite PEMs. The effects of the nanofiller contents on self-humidifying and protonic conductivity of the composite PEMs were also investigated under different temperatures. When the contents of functionalized MXene and modified TiO₂ are 5 wt.%, proton conductivity, water uptake and methanol permeability of the composite PEMs can be up to 0.143 S/cm, 60% and 2.27 × 10⁻⁷ cm²/s, respectively, which represent increases of about 192%, about 38% and a decrease of 47%, respectively, compared with that of primary SPEEK PEM. Under the synergistic action of functionalized MXene providing a higher number of exchangeable proton sites, modified TiO₂ with inherent hydrophilicity enhancing water retention and Pt providing catalytic sites for the H₂/O₂ reaction to generate water in situ, the self-humidifying capability and proton conductivity of the composite PEMs were improved significantly. Full article

Various metal-modified titanium dioxide (TiO₂) nanotubes have been widely investigated for water purification due to their large surface area, stability, and photocatalytic activity. In this context, this study investigates the deposition of vanadium-based nanoparticles (V NPs) on TiO₂ nanotubes via immersion in aqueous dispersions of V NPs synthesized by picosecond and nanosecond pulsed laser ablation in liquid at four different output energies (picosecond: 15 and 30 mJ; nanosecond: 120 and 250 mJ), with the aim of improving their photocatalytic performance. By optimizing the concentration of V NPs in the dispersions and the immersion time, the degradation efficiency of Acid Yellow 23 under photocatalytic conditions was enhanced for TiO₂ modified with V NPs synthesized at output energies of 30 and 250 mJ, whereas no improvement was observed for TiO₂ modified with V NPs synthesized at 15 and 120 mJ. A series of V-TiO₂ photocatalysts was fabricated by depositing laser-synthesized V NPs of various sizes on TiO₂ nanotubes prepared by electrochemical anodization of a titanium mesh. Full article

Developing environmentally friendly, multifunctional waterproof and breathable membranes (WBMs) has attracted extensive attention and is of great significance but remains challenging. Herein, an environmentally friendly and multifunctional waterborne polyurethane WBM with self-healing and self-cleaning properties is developed in two steps. Firstly, by using polydimethylsiloxane (PDMS) as a hydrophobicity giver and tannic acid (TA) as a crosslinker, a dual-modified waterborne polyurethane (PTWPU) is prepared, which has high surface hydrophobicity due to the surface enrichment of siloxane segments and self-healing performance from the formation of a dynamic phenolic carbamate network. Secondly, by incorporating titanium dioxide (TiO₂) photocatalyst nanoparticles to increase internal porosity and establish hydrophilic pathways, a multifunctional waterborne polyurethane WBM (TPTWPU) is developed. This membrane features further enhanced surface hydrophobicity from generated micro-roughness and effective self-cleaning performance, because TA acts as an electron trap to promote the photocatalytic activity of TiO₂. The TPTWPU membrane shows good hydrophobicity (water contact angle of 115.3°) and satisfactory moisture permeability of 135.0 g/(m²·24 h), which is 61.2% higher than unmodified membranes. Furthermore, it exhibits efficient self-healing, with a recovery rate exceeding 80% within 2 h. This feasible strategy will provide guidance for materials design in multifunctional coatings for textiles and leather. Full article

Pesticides are a major cause of water contamination, making this issue a major environmental and public health concern. In this context, the development of advanced and effective remediation materials is needed. In this study, a titanium-functionalized magnetic silica aerogel (AG-Ti@Fe₃O₄-SA) was successfully prepared via microfluidics and evaluated for water decontamination. The structural and compositional features of the aerogel were determined using XRD, FT-IR, RAMAN, SEM, TEM, BET, and DLS, confirming the formation of the aerogel with dispersed Fe₃O₄-SA nanoparticles and the successful incorporation of titanium within the aerogel matrix. Regarding decontamination potential, the aerogel was tested against a pesticide mixture, yielding pesticide-dependent removal efficiencies (16–100%). Notably, the aerogel exhibited a high affinity for organophosphorus pesticides and a moderate affinity for polar compounds, whereas bulky hydrophobic pesticides showed lower adsorption. In vitro, the aerogel induced a moderate decrease in HaCaT cell viability after 48 h of exposure, accompanied by a slight increase in lactate dehydrogenase release, while HEK293 cells remained largely unaffected, indicating a cell-type-dependent biological response. Overall, the findings from this screening-level study recommend AG-Ti@Fe₃O₄-SA aerogel as a promising selective adsorbent for pesticide removal. Full article

Defect engineering and metal–support coupling provide an effective route to tune interfacial charge dynamics for selective photocatalytic CO₂ reduction. Here, Ti-vacancy-rich Bi₄Ti₃O₁₂ (BTvO) nanosheets were prepared and decorated with Au nanoparticles (Au NPs) to build Au-BTvO junctions that favor multi-electron/proton transfer toward deep hydrogenation. The optimized 3%Au-BTvO achieved high hydrocarbon productivity under visible light (λ > 420 nm), delivering CH₄ and C₂H₆ formation rates of 92.66 and 17.96 μmol g⁻¹ h⁻¹, respectively, with stable performance over 25 h. Spectroscopic analyses reveal higher CO₂ uptake and more effective surface activation, increased water adsorption with a more favorable interfacial hydration environment, and time-dependent formation of key C₁ and C₂ intermediates. In situ light-irradiation XPS, PL mapping, and KPFM collectively demonstrate directional electron transfer from Bi₄Ti₃O₁₂ to Au and amplified surface band bending, enabling efficient charge separation and accelerated surface reduction. This work highlights defect–metal synergy as a general strategy to boost activity, selectivity, and durability in visible-light CO₂-to-methane conversion. Full article

The photoelectrochemical water-splitting process for hydrogen production is limited by the large bandgap of semiconductor titanium dioxide (TiO₂) and by interfacial recombination at particle interfaces. The technique used in this paper is that of electrochemical anodization to produce robust, ordered TiO₂ nanotube arrays (TiO₂ nanorod arrays denoted as TNTAs). Using the immersion-annealing method, Nd₂O₃ nanoparticles can be immobilized in situ, and Nd₂O₃/TNTAs composite photoanodes are fabricated. The heterointerface caused between the Nd₂O₃ nanoparticles and TiO₂ results in the alignment of the Fermi levels and the formation of band bending and an internal electric field at the interface. It allows rapid photo-generated electron-hole (e⁻/h⁺) separation at the interface and, simultaneously, introduces novel localized electron states of Nd³⁺ within the TiO₂ bandgap. This triggers hybridisation between the 3d orbitals of Ti and the 2p orbitals of O, thereby altering the band structure of TiO₂. The best-performing Nd₂O₃/TNTAs photoelectrode outperforms pure TNTAs, with a photocurrent density of 1.59 mA·cm⁻² at 1.23 V vs. RHE. It produces 162.6 μmol·cm⁻² of hydrogen in a 3 h photocatalytic hydrogen production experiment, which is about 12.2 times that of pure TNTAs. This approach highlights the unique benefits and creative opportunities of applying rare-earth elements to address the critical issues of photocatalysts, such as significant band gaps and rapid recombination. Full article

Reductive deuteration of N-heterocycles provides an efficient route to deuterated scaffolds, yet achieving controlled deuterium incorporation in quinoline remains challenging. Herein, we report a high-temperature H₂-treated Rh/TiO₂ catalyst (Rh/TiO₂–H500) that enables efficient reductive deuteration of quinoline using D₂O as a deuterium source. Structural characterization reveals that reduction at 500 °C induces a pronounced strong metal–support interaction (SMSI), leading to partial TiO_x encapsulation of Rh nanoparticles and interfacial electron transfer that generates electron-rich Rh⁰ species. This optimized interfacial structure promotes cooperative C–H activation and effective H/D transfer across the reduced quinoline framework, affording high deuterium incorporation at multiple positions of 1,2,3,4-tetrahydroquinoline (THQ). These results highlight the importance of SMSI-driven electronic and interfacial modulation in regulating reductive H/D exchange over heterogeneous catalysts. Full article

Background: Viral infections represent a major challenge in modern medicine, including diseases caused by human papillomavirus (HPV), cytomegalovirus (CMV), and rotavirus, which are among the most prevalent viral pathogens. The rapid transmission and high mutation rates of these viruses contribute to substantial health burdens and socio economic consequences. Silver nanoparticles (Ag NPs) and titanium dioxide nanoparticles (TiO₂-NPs) are effective antiviral agents. The major objective of this investigation was to measure the antiviral activity of titanium dioxide nanoparticles (TiO₂-NPs) and green-produced silver nanoparticles (Ag NPs) against rotavirus, HPV, and CMV. Methods: UV-Vis spectroscopy, transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy, and X-ray diffraction (XRD) were used to characterize the nanoparticles. Cytotoxicity and antiviral activity were evaluated using a crystal violet assay in infected cell cultures. Results: The main findings indicate that both Ag NPs and TiO₂-NPs exhibited pronounced antiviral activity against HPV, CMV, and rotavirus. Ag NPs exhibited strong antiviral activity, with lower IC₅₀ values against HPV and CMV; however, this effect was associated with lower cytotoxic concentration (CC₅₀) and selectivity index (SI) values, indicating higher cytotoxicity. In contrast, TiO₂-NPs demonstrated a favorable safety profile, as indicated by higher CC₅₀ value particularly against CMV (863.90 µg/mL) and rotavirus (386.84 µg/mL)—and low cytotoxicity toward host cells—highlighting their strong antiviral selectivity and therapeutic potential. Conclusions: Overall, these findings suggest that, while Ag-NPs possess strong antiviral efficacy, TiO₂ NPs offer a more balanced combination of antiviral effectiveness and biosafety and may therefore be more promising candidates for antiviral applications. Full article

Hybrid nanomaterials integrating magnetic and semiconductor phases offer promising multifunctional platforms for wastewater remediation; however, their stabilization and recovery remain challenging. In this study, Fe₃O₄ and ZnTiO₃/TiO₂ nanoparticles were incorporated into a rice husk ash-based geopolymer matrix to develop hybrid nanocomposites for synergistic adsorption–photodegradation of methylene blue (MB) and methyl orange (MO). The materials were synthesized via alkaline activation followed by nanoparticle incorporation, and characterized by XRD, XRF, FTIR, SEM, EDX, BET surface area analysis, and pHPZC determination. XRD confirmed the presence of nanocrystalline Fe₃O₄ and ZnTiO₃/TiO₂ phases while preserving the amorphous aluminosilicate framework. Modified powders exhibited higher specific surface areas (up to 198 m² g⁻¹) compared to the unmodified geopolymer. Adsorption followed the Langmuir isotherm and pseudo-second-order kinetics, with spontaneous and exothermic behavior. Under UV irradiation, the ZnTiO₃/TiO₂-modified composite achieved photodegradation efficiencies up to 94% for MB and 92% for MO, whereas the Fe₃O₄-modified material combined adsorption capacity with magnetic recoverability. These results demonstrate that nanoparticle incorporation enables multifunctional performance while maintaining structural integrity of the geopolymeric matrix. Full article

This research investigates the optimization of surface integrity in powder-mixed electrical discharge machining (PMEDM) through the innovative use of Jatropha biodielectric fluid enhanced with titanium dioxide (TiO₂) nanoparticles. A comprehensive experimental framework was developed using design expert software (DOE) with Response Surface Methodology (RSM) to systematically analyze the machining of AISI D2 tool steel using copper electrodes. The study examined five critical process parameters, gap current (Ip), pulse-on duration (Ton), pulse-off time (Toff), gap voltage (V), and powder concentration, evaluating their combined effects on surface roughness (SR), surface crack density (SCD), and residual stress characteristics. Advanced characterization techniques including scanning electron microscopy (SEM) were employed to analyze surface topography and subsurface microstructural changes. The optimization process successfully identified optimal machining conditions of current = 9 A, Ton = 100 µs, Toff = 10 µs, and gap voltage = 65 V, achieving exceptional surface quality with a minimum surface roughness of 3.22 µm. Remarkably, these optimized parameters resulted in crack-free surfaces with zero surface crack density and minimal residual stress values across the 2θ range of 90° to 180°. To enhance predictive capabilities, supervised machine learning algorithms were implemented to model surface roughness behavior. Comparative analysis of classification algorithms demonstrated that Support Vector Machine (SVM), k-Nearest Neighbors (kNNs), and Gaussian Naïve Bayes achieved superior performance with F1-scores of 0.88 and prediction accuracies of 90%. The integration of sustainable Jatropha biodielectric with TiO₂ nanoparticles represents a significant advancement in environmentally conscious precision machining, while the machine learning approach establishes a robust framework for intelligent process optimization and quality prediction in advanced manufacturing applications. Full article

Polarized side-scattering techniques are widely used in aerosol detection, oceanographic optics, and biomedical sensing due to their high sensitivity to weak optical signals in low-scattering coefficient media. Conventional polarized Monte Carlo methods face significant challenges in such regimes due to geometric mismatch, where photon exit positions deviate substantially from the detector plane. This study addresses the geometric mismatch issue in polarized Monte Carlo simulations for side scattering in low-scattering media (scattering coefficient ${\mu }_s=$ 1 cm⁻¹), where photon exit positions often deviate from the detector plane. We propose a novel algorithm incorporating backward ray tracing with geometric projection correction to enhance simulation accuracy. Experimental validation was conducted using 532 nm laser illumination on both 500 nm polystyrene microspheres (${\mu }_s=$ 0.21 cm⁻¹) and 5 nm TiO₂ nanoparticles (${\mu }_s=$ 1.06 × 10⁻⁶–1.06 × 10⁻⁵ cm⁻¹). The results demonstrate excellent agreement between simulations and experiments, confirming the algorithm’s capability to accurately capture the polarization characteristics of side-scattered light. This work provides a high-fidelity simulation tool for designing optical sensors in low-scattering media and holds direct applicability in nanoparticle concentration sensing and aerosol monitoring. Full article