Search Results (158)

The anodic oxidation technique was used for surface modification, resulting in the creation of a titanium-based nanotube oxide layer on a coarse-grained and ultrafine-grained Ti-13Nb-13Zr alloy. The modified surface morphology was analyzed using scanning electron microscopy (SEM), atomic force microscopy (AFM), and X-ray diffraction (XRD). The electrochemical impedance spectroscopy (EIS) method was employed to evaluate the corrosion stability of the Ti-13Nb-13Zr alloy before and after anodic oxidation. Corrosion stability was determined by exposing the examined alloy to a solution that simulates environment in the human organism (Ringer’s solution). To examine the titanium-based nanotube oxide layer adhesion on the Ti-13Nb-13Zr alloy’s surface, a scratch test was performed. The hydrophilicity of the modified surface was measured using the contact angle between a drop of Ringer’s solution and the modified surface. The anodic oxidation led to the creation of a nanotube oxide layer on the surface of the Ti-13Nb-13Zr (wt.%) alloy. The impact of the ultrafine-grained structure on the homogeneity of the nanotube oxide layer obtained using anodic oxidation was observed. The ultrafine-grained structure contributed to the increased diameter of the nanotubes, while the combined effect of anodic oxidation and high-pressure torsion significantly increased the roughness of the Ti-13Nb-13Zr alloy’s surface, which is expected to enhance biomechanical compatibility by reducing cytotoxicity, providing a more adaptable modulus of elasticity for human body conditions and ensuring adequate corrosion resistance and hydrophilicity. In this study, it was established that the examined alloy had suitable corrosion resistance for utilization in medicine as a metallic implant in the human body. The scratch test showed acceptable adhesion from the titanium-based nanotube oxide layer created using anodic oxidation. Also, the determination of the surface contact angle showed that the surface after anodic oxidation was more hydrophilic than the surface before anodic oxidation. Full article

Endocytic uptake and lysosomal localization are suggested to be the key mechanisms underlying the toxicity of metal oxide nanoparticles (MONPs), with dissolution in the acidic milieu driving the response. In this study, we aimed to investigate if MONPs of varying solubility are similarly sequestered intracellularly, including in lysosomes and the role of the acidic lysosomal milieu on toxicity induced by copper oxide (CuO) nanoparticles (NPs), nickel oxide (NiO) NPs, aluminum oxide (Al₂O₃) NPs, and titanium dioxide (TiO₂) NPs of varying solubility in FE1 lung epithelial cells. Mitsui-7 multi-walled carbon nanotubes (MWCNTs) served as contrasts against particles. Enhanced darkfield hyperspectral imaging (EDF-HSI) with fluorescence microscopy was used to determine their potential association with lysosomes. The v-ATPase inhibitor Bafilomycin A1 (BaFA1) was used to assess the role of lysosomal acidification on toxicity. The results showed co-localization of all MONPs with lysosomes, with insoluble TiO₂ NPs showing the greatest co-localization. However, only acute toxicity induced by soluble CuO NPs was affected by the presence of BaFA1, showing a 14% improvement in relative survival. In addition, all MONPs were found to be associated with large actin aggregates; however, treatment with insoluble TiO₂ NPs, but not soluble CuO NPs, impaired the organization of F-actin and α-tubulin. These results indicate that MONPs are sequestered similarly intracellularly; however, the nature or magnitude of their toxicity is not similarly impacted by it. Future studies involving a broader variety of NPs are needed to fully understand the role of differential sequestration of NPs on cellular toxicity. Full article

Uncooled microbolometers play a pivotal role in infrared detection owing to their compactness, low power consumption, and cost-effectiveness. This review comprehensively summarizes recent progress in thermistor materials and focal plane arrays (FPAs), highlighting improvements in sensitivity and integration. Vanadium oxide (VO_x) remains predominant, with Al-doped films via atomic layer deposition (ALD) achieving a temperature coefficient of resistance (TCR) of −4.2%/K and significant 1/f noise reduction when combined with single-walled carbon nanotubes (SWCNTs). Silicon-based materials, such as phosphorus-doped hydrogenated amorphous silicon (α-Si:H), exhibit a TCR exceeding −5%/K, while titanium oxide (TiO_x) attains TCR values up to −7.2%/K through ALD and annealing. Emerging materials including GeSn alloys and semiconducting SWCNT networks show promise, with SWCNTs achieving a TCR of −6.5%/K and noise equivalent power (NEP) as low as 1.2 mW/√Hz. Advances in FPA technology feature pixel pitches reduced to 6 μm enabled by vertical nanotube thermal isolation, alongside the 3D heterogeneous integration of single-crystalline Si-based materials with readout circuits, yielding improved fill factors and responsivity. State-of-the-art VO_x-based FPAs demonstrate noise equivalent temperature differences (NETD) below 30 mK and specific detectivity (D*) near 2 × 10¹⁰ cm⋅Hz ^1/2/W. Future advancements will leverage materials-driven innovation (e.g., GeSn/SWCNT composites) and process optimization (e.g., plasma-enhanced ALD) to enable ultra-high-resolution imaging in both civil and military applications. This review underscores the central role of material innovation and system optimization in propelling microbolometer technology toward ultra-high resolution, high sensitivity, high reliability, and broad applicability. Full article

Anodised metal matrices represent a versatile and multifunctional platform for the development of advanced materials with tunable physicochemical properties. Through electrochemical oxidation processes—commonly referred to as anodisation—metals such as aluminium, titanium, niobium, zinc and tantalum can be transformed into structured oxide layers with defined porosity, thickness and surface morphology. These methods enable the fabrication of ordered nanoporous arrays, nanotubes and nanowires, depending on the process parameters and the type of metal. The review introduces and outlines the various anodisation techniques and parameters. This is crucial, since each individual metal requires specified optimal conditions to obtain a stable anodised oxide layer. This review provides an overview of recent advances in the design and application of anodised metal substrates, with the focus on their role as functional platforms in catalysis, sensing, energy storage and biomedical engineering. Special attention is given to post-anodisation surface modification strategies, such as chemical functionalisation, thin-film deposition and molecular-level integration, which significantly expand the utility of these materials. The review also highlights the challenges, limitations and future perspectives of anodising technologies, aiming to guide the rational design of next-generation devices based on engineered oxide architectures. Full article

In this work, we have used both plain titania nanotubes, TNTs, and their reduced black analogues, bTNTs, that bear metallic conductivity (prepared by solid state reaction of TNTs with CaH₂ at 500 °C for 2 h), as catalyst supports for the oxygen evolution reaction (OER). Ir was subsequently been deposited on them by the galvanic replacement of electrodeposited Ni by Ir(IV) chloro-complexes; this was followed by Ir electrochemical anodization to IrO₂. By carrying out the preparation of the TNTs in either two or one anodization steps, we were able to produce close-packed or open-structure nanotubes, respectively. In the former case, larger than 100 nm Ir aggregates were finally formed on the top face of the nanotubes (leading to partial or full surface coverage); in the latter case, Ir nanoparticles smaller than 100 nm were obtained, with some of them located inside the pores of the nanotubes, which retained a porous surface structure. The electrocatalytic activity of IrO₂ supported on open-structure bTNTs towards OER is superior to that supported on close-packed bTNTs and TNTs, and its performance is comparable or better than that of similar electrodes reported in the literature (overpotential of η = 240 mV at 10 mA cm⁻²; current density of 70 mA cm⁻² and mass specific current density of 258 mA mg_Ir⁻¹ at η = 300 mV). Furthermore, these electrodes demonstrated good medium-term stability, maintaining stable performance for 72 h at 10 mA cm⁻² in acid. Full article

Developments of nanostructured materials have a significant impact in various areas, such as energy technology and biomedical use. Examples include solar cells, energy management, environmental control, bioprobes, tissue engineering, biological marking, cancer diagnosis, therapy, and drug delivery. Currently, researchers are designing multifunctional nanodrugs that combine in vivo imaging (using fluorescent nanomaterials) with targeted drug delivery, aiming to maximize therapeutic efficacy while minimizing toxicity. These fascinating nanoscale “magic bullets” should be available in the near future. Inorganic nanovehicles are flexible carriers to deliver drugs to their biological targets. Most commonly, mesoporous nanostructured silica, carbon nanotubes, gold, and iron oxide nanoparticles have been thoroughly studied in recent years. Opposite to polymeric and lipid nanostructured materials, inorganic nanomaterial drug carriers are unique because they have shown astonishing theranostic (therapy and diagnostics) effects, expressing an undeniable part of future use in medicine. This review summarizes research from development to the most recent discoveries in the field of nanostructured materials and their applications in drug delivery, including promising metal-based complexes, platinum, palladium, ruthenium, titanium, and tin, to tumor cells and possible use in theranostics. Full article

Catalytic methane decomposition offers an attractive and sustainable pathway for producing CO_x-free hydrogen and valuable carbon nanotubes. This work investigates the innovative use of liquid metals, particularly gallium and indium, as promoters for iron catalysts based on a titanium dioxide and alumina composite to improve this process even more. In a fixed-bed reactor operating at 800 °C and atmospheric pressure, all catalyst activities for methane decomposition were thoroughly assessed while keeping the gas hourly space velocity at 6 L/g h. Surface area and porosity, H₂-temperature programmed reduction/oxidation, X-ray diffraction, Raman spectroscopy, scanning transmission electron microscopy, and thermogravimetry analysis were utilized to investigate the physicochemical properties of the catalyst. The result showed that iron supported on a titanium-alumina catalyst exhibited higher activity, stability, and reproducibility with a methane conversion of 90% and hydrogen production of 81% after three cycles, with 240 min for each cycle and stability for 480 min. In contrast, the liquid metal-promoted catalysts improved the metal-support interaction and textural properties, such as surface area, pore volume, and particle dispersion of the catalysts. Still, the catalytic efficiency significantly improved. However, the gallium-promoted catalyst displayed excellent reusability. The characterization of the spent catalyst proved that both the iron supported on a titanium-alumina and its gallium-promoted derivative produced graphitic carbon; on the contrary, the indium-promoted catalyst produced amorphous carbon. These results demonstrate how liquid metal promoters can be used to adjust the characteristics of catalysts, providing opportunities for improved reusability and regulated production of carbon byproducts during methane decomposition. Full article

The surface modification of dental implants with nanostructured films enables the development of the next generation of biomaterials that promote osseointegration. In this study, a uniform layer of titanium oxide nanotubes (TNTs) was successfully formed on a Ti-6Al-4V dental implant screw through anodic oxidation. TNTs were morphologically characterized by Scanning Electron Microscopy (SEM), obtaining dimensions of 64.88 ± 10 nm in diameter and 5.34 ± 5 µm in length. Additionally, a crystal size of 23.45 nm was determined by X-ray diffraction (XRD) analysis. The TNT layer on the dental implant screw was evaluated in an in vitro system in direct contact with human osteoblast cells (hFOB) for 24 h and 48 h, finding cell growth near to the screw threads. Further, the biocompatibility of the dental screw coated with TNTs was evaluated using a flow cytometric assay with 7-AAD, demonstrating that cell viability was not affected at 24 h and 48 h. This study opens the perspective of the study of inflammation and osseointegration induced by implants coated with TNTs. Full article

The advancement of optical materials has garnered significant interest from the global scientific community in the pursuit of efficient photocatalysts for the purification of water using light. This challenge, which cannot be addressed using traditional methods, is tackled in the present study utilizing unconventional approaches. This study presents the fabrication of an effective photocatalyst using an unconventional approach that employs explosive reactions. This method successfully produces 3D nanostructures composed of carbon nanotubes (CNTs), carbon nanofibers (CNFs), and silica–alumina nanoparticles at temperatures below 270 °C. Gold-supported silica–alumina–CNT–CNF nanostructures were synthesized and characterized using XRD, TEM, SEM, and EDX, in addition to mapping images. To study and determine the photoactivity of these produced nanostructures, two well-known photocatalysts—titanium dioxide and zinc oxide—were synthesized at the nanoscale for comparison. The results showed that the presence of CNTs and CNFs significantly reduced the band gap energy from 5.5 eV to 1.65 eV and 3.65 eV, respectively, after modifying the silica–alumina structure. In addition, complete degradation of green dye was achieved after 35 min of light exposure using the modified silica–alumina structure. Additionally, the surface properties of the modified silica–alumina had a positive role in accelerating the photocatalytic decomposition of the green dye NGB. A kinetic study confirmed that the modified silica–alumina functions as a promising additive for optical applications, accelerating the photocatalytic degradation of NGB to a rate three times faster than that of the prepared titanium dioxide and six times that of the prepared zinc oxide. Full article

Machining processes often face challenges such as elevated temperatures and wear, which traditional cutting fluids are insufficient to address. As a result, solutions involving nanoparticle additives are being explored to enhance cooling and lubrication performance. This study investigates the effect of thermal conductivity, an important property influenced by the densities of mono and hybrid nanofluids. To this end, various nanofluids were prepared by incorporating hexagonal boron nitride (hBN), zinc oxide (ZnO), multi-walled carbon nanotubes (MWCNTs), titanium dioxide (TiO₂), and aluminum oxide (Al₂O₃) nanoparticles into sunflower oil as the base fluid. Hybrid nanofluids were created by combining two nanoparticles, including ZnO + MWCNT, hBN + MWCNT, hBN + ZnO, hBN + TiO₂, hBN + Al₂O₃, and TiO₂ + Al₂O₃. A dataset consisting of 180 data points was generated by measuring the thermal conductivity and density of the prepared nanofluids at various temperatures (30–70 °C) in a laboratory setting. Conducting thermal conductivity measurements across different temperature ranges presents significant challenges, requiring considerable time and resources, and often resulting in high costs and potential inaccuracies. To address these issues, a feedforward artificial neural network (FFANN) method was proposed to predict thermal conductivity. Our multilayer FFANN model takes as input the temperature of the experimental environment where the measurement is made, the measured thermal conductivity of the relevant nanoparticle, and the relative density of the nanoparticle. The FFANN model predicts the thermal conductivity value linearly as output. The model demonstrated high predictive accuracy, with a reliability of R = 0.99628 and a coefficient of determination (R²) of 0.9999. The average mean absolute error (MAE) for all hybrid nanofluids was 0.001, and the mean squared error (MSE) was 1.76 × 10⁻⁶. The proposed FFANN model provides a State-of-the-Art approach for predicting thermal conductivity, offering valuable insights into selecting optimal hybrid nanofluids based on thermal conductivity values and nanoparticle density. Full article

This research investigates the enhanced photocatalytic activity of cuprous oxide (Cu₂O) nanoparticles (NPs)-titanium dioxide (TiO₂) nanotube (NT) composites for air purification, focusing on the removal of volatile organic compounds (VOCs) and Escherichia coli (E. coli) bacteria under simulated sunny light. Cu₂O-NPs were successfully deposited onto TiO₂-NTs via the successive ionic layer adsorption and reaction method. The resulting p- and n-type semiconductor heterojunction nanocomposites were characterized using various techniques, including scanning electron microscopy, transmission electron microscopy, ultraviolet–visible-light spectroscopy, and chlorinated radicals. The photocatalytic activity was evaluated for different VOCs present in indoor air (butadione, chloroform, and butyraldehyde) in the presence of E. coli bacteria. The results showed that the Cu₂O-NPs/TiO₂-NTs composites exhibited enhanced photocatalytic activity compared to pure TiO₂-NTs. The Langmuir–Hinshelwood model was used to describe the degradation kinetics, revealing that Cu₂O loading and the nature of the target pollutant influence the photocatalytic efficiency. This study has also highlighted the role of chlorinated radicals in the degradation process, especially for chloroform. The degradation process of chloroform generated chlorine radicals, which not only contributed to the degradation of other VOCs, but also enhanced the overall oxidative capacity of the system. This synergistic effect was observed to accelerate pollutant removal and improve the antibacterial efficacy against E. coli. The Cu₂O-NPs/TiO₂-NTs composites demonstrated significant reusability and antibacterial properties, highlighting their potential for sustainable indoor air purification applications. Full article

The nano-architecture of titanium oxide is a key element of a wide range of applications, mainly optical and catalytic activities. Therefore, the current study focuses on engineering and designing three interesting nanostructures of titanium oxides: nanoplates, nanotubes, and nanoparticle-supported nanolayers. The nanoplates of titanium oxides were prepared and confirmed by TEM images, X-ray diffraction, and EDX analysis. These nanoplates have an anatase phase, with the distance across the corners in the range of 15 nm. These nanoplates were modified and developed through a rolling process with sodium doping to generate the Na-doped TiO₂ nanotubes. These nanotubes were observed by TEM images and X-ray diffraction. In addition, the doping process of titanium oxides with sodium was confirmed by EDX analysis. A novel nano-architecture of titanium oxide was designed by supporting titanium oxide nanoparticles over Zn/Al nanolayers. The optical properties and activity of titanium oxides with the different morphologies indicated that titanium oxides became a highly photo-active photocatalyst after conversion to nanotubes. This finding was observed through the reduction in the band gap energy to 2.7 eV. Additionally, after 37 min of exposure to UV light, the titanium oxide nanotubes totally broke down and transformed the green dye of NGB into carbon dioxide and water. Furthermore, the kinetic analysis verified that the green dyes’ degradation was expedited by the high activity of nanotubes. Ultimately, based on these findings, it was possible to design an efficient photocatalyst for water purification by converting nanoplates into nanotubes, doping titanium sites with sodium ions, and creating new active sites for titanium oxides through defect-induced super radical formation. Full article

Due to the bio-inert nature of titanium (Ti) and subsequent accompanying chronic inflammatory response, an implant’s stability and function can be significantly affected, which is why various surface modifications have been employed, including the deposition of titanium oxide (TiO₂) nanotubes (TNTs) onto the native surface through the anodic oxidation method. While the influence of nanotube diameter on cell behaviour and osteogenesis is very well documented, information regarding the effects of nanotube lateral spacing on the in vivo new bone formation process is insufficient and hard to find. Considering this, the present study’s aim was to evaluate the mechanical properties and the osteogenic ability of two types of TNTs-based pins with different lateral spacing, e.g., 25 nm (TNTs) and 92 nm (spTNTs). The mechanical properties of the TNT-coated implants were characterised from a morphological point of view (tube diameter, spacing, and tube length) using scanning electron microscopy (SEM). In addition, the chemical composition of the implants was evaluated using X-ray photoelectron spectroscopy, while surface roughness and topography were characterised using atomic force microscopy (AFM). Finally, the implants’ hardness and elastic modulus were investigated using nanoindentation measurements. The in vivo new bone formation was histologically evaluated (haematoxylin and eosin—HE staining) at 6 and 30 days post-implantation in a rat model. Mechanical characterisation revealed that the two morphologies presented a similar chemical composition and mechanical strength, but, in terms of surface roughness, the spTNTs exhibited a higher average roughness. The microscopic examination at 1 month post-implantation revealed that spTNTs pins (57.21 ± 34.93) were capable of promoting early new bone tissue formation to a greater extent than the TNTs-coated implants (24.37 ± 6.5), with a difference in the average thickness of the newly formed bone tissue of ~32.84 µm, thus highlighting the importance of this parameter when designing future dental/orthopaedic implants. Full article

Propofol is one of the most widely used intravenous drugs for anaesthesia and sedation and is one of the most commonly used drugs in intensive care units for the sedation of mechanically ventilated patients. The correct dosage of propofol is of high importance, but there is currently a lack of suitable point-of-care techniques for determining blood propofol concentrations. Here, we present a cytochrome P450 2B6/carbon nanotube/graphene oxide/metal oxide nanocomposite sensor for discrete measurement of propofol concentration. Propofol is converted into a quinol/quinone redox couple by the enzyme and the nanocomposite enables sensitive and rapid detection. The metal oxide nanoparticles are synthesised via green synthesis and a variety of metal oxides and mixed metal oxides are investigated to determine the optimal nanocatalyst. Converting propofol into the redox couple allows for the measurement to take place over different potential ranges, enabling interference from common sources such as paracetamol and uric acid to be avoided. It was found that nanocomposites containing copper titanium oxide nanoparticles offered the best overall performance and electrodes functionalised with such nanocomposites demonstrated a limit of detection in bovine serum of 0.5 µg/mL and demonstrated a linear response over the therapeutic range of propofol with a sensitivity of 4.58 nA/μg/mL/mm². Full article

Antimicrobial polymeric coatings rely not only on their surface functionalities but also on nanoparticles (NPs). Antimicrobial coatings gain their properties from the addition of NPs into a polymeric matrix. NPs that have been used include metal-based NPs, metal oxide NPs, carbon-based nanomaterials, and organic NPs. Copper NPs and silver NPs exhibit antibacterial and antifungal properties. So, when present in coatings, they will release metal ions with the combined effect of having bacteriostatic/bactericidal properties, preventing the growth of pathogens on surfaces covered by these nano-enhanced films. In addition, metal oxide NPs such as titanium dioxide NPs (TiO₂ NPs) and zinc oxide NPs (ZnONPs) are used as NPs in antimicrobial polymeric coatings. Under UV irradiation, these NPs show photocatalytic properties that lead to the production of reactive oxygen species (ROS) when exposed to UV radiation. After various forms of nano-carbon materials were successfully developed over the past decade, they and their derivatives from graphite/nanotubes, and composite sheets have been receiving more attention because they share an extremely large surface area, excellent mechanical strength, etc. These NPs not only show the ability to cause oxidative stress but also have the ability to release antimicrobial chemicals under control, resulting in long-lasting antibacterial action. The effectiveness and life spans of the antifouling performance of a variety of polymeric materials have been improved by adding nano-sized particles to those coatings. Full article