Search Results (21)

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

Ir-based catalysts are the best in terms of activity and stability for oxygen evolution reactions (OERs) in proton exchange water electrolysis. Due to their cost, efforts have been made to decrease their load without a loss of activity. In this paper, Ir nanoparticles measuring 2–3 nm were loaded on TiO₂ anatase supports of submicrometric size in different amounts using the microwave polyol method to optimize their mass activity. Using anatase particles with a diameter of about 100 nm and titania nanotubes (TNTs), Ir/TiO₂ catalysts with Ir contents of 5, 10, 20, and 40 wt.% were synthesized and characterized via structural and electrochemical techniques. It was shown that the amount of Ir must be regulated to obtain continuous coverage on titania with strong Ir–TiO₂ interactions which, for the 100 nm diameter anatase, is limited to about 20 wt.%. A higher percentage of Ir over 40 wt.% can be dispersed over the TNTs. Exceeding one layer of coverage leads to a decrease in the catalyst’s utilization. Ir/TiO₂(10:90), Ir/TiO₂(20:80), and Ir/TiO₂(40:60) presented the highest pseudocapacitive currents per unit of Ir mass. The electrochemical active areas and mass activities for these later catalysts were also the highest compared to Ir/TiO₂(05:95), Ir/TNT(40:60), and the unsupported catalysts and increased from 40 to 10 wt.% Ir. They also presented the lowest overpotentials of about 300 mV at 10 mA cm⁻² for the OER, with Ir/TiO₂(10:90) presenting the best specific activities and surface turnover frequencies, thus showing that the size of the support can be regulated to decrease the Ir content of the catalyst without a loss of activity. Full article

Recently, titania nanotubes (TNTs) have been extensively studied because both their functional properties and highly controllable morphology make them important building blocks for understanding nanoscale phenomena and realizing nanoscale devices. Compared with sol–gel and template-assisted methods, electrochemical anodization is a simple, cost-effective, and low-temperature technique offering additional advantages such as straightforward processing and ease of scale-up. This review focuses on the process modalities and underlying mechanism of electrochemical anodization to achieve a different set of TNTs for a variety of applications. Finally, important applications of TNTs are highlighted including biomedical devices, water purification, and solar cells. Full article

This paper presents a comprehensive study of the performance of a newly developed titania nanotube incorporated RO membrane for endocrine-disrupting compound (EDC) removal at a low concentration. EDCs are known as an emerging contaminant, and if these pollutants are not properly removed, they can enter the water cycle and reach the water supply for residential use, causing harm to human health. Reverse osmosis (RO) has been known as a promising technology to remove EDCs. However, there is a lack of consensus on their performance, especially on the feed concentrations of EDC that vary from one source to another. In this study, polyamide thin-film composite (PA TFC) membrane was incorporated with one-dimensional titania nanotube (TNT) to mitigate trade-off between water permeability and solute rejection of EDC. The characterization indicated that the membrane surface hydrophilicity has been greatly increased with the presence of TNT. Using bisphenol A (BPA) and caffeine as model EDC, the removal efficiencies of the pristine TFC and thin-film nanocomposite (TFN) membranes were evaluated. Compared to TFC membrane, the membrane modified with 0.01% of TNT exhibited improved permeability of 50% and 49% for BPA and caffeine, respectively. A satisfactory BPA rejection of 89.05% and a caffeine rejection of 97.89% were achieved by the TNT incorporated TFN membranes. Furthermore, the greater hydrophilicity and smoother surface of 0.01 TFN membrane led to lower membrane fouling tendency under long-term filtration. Full article

Optimized Pt-based methanol oxidation reaction (MOR) anodes are essential for commercial direct methanol fuel cells (DMFCs) and methanol electrolyzers for hydrogen production. High surface area Ti supports are known to increase Pt catalytic activity and utilization. Pt has been deposited on black titania nanotubes (bTNTs), Ti felts and, for comparison, Ti foils by a galvanic deposition process, whereby Pt(IV) from a chloroplatinate solution is spontaneously reduced to metallic Pt (at 65 °C) onto chemically reduced (by CaH₂) TNTs (resulting in bTNTs), chemically etched (HCl + NaF) Ti felts and grinded Ti foils. All Pt/Ti-based electrodes prepared by this method showed enhanced intrinsic catalytic activity towards MOR when compared to Pt and other Pt/Ti-based catalysts. The very high/high mass specific activity of Pt/bTNTs (ca 700 mA mg_Pt⁻¹ at the voltammetric peak of 5 mV s⁻¹ in 0.5 M MeOH) and of Pt/Ti-felt (ca 60 mA mg_Pt⁻¹, accordingly) make these electrodes good candidates for MOR anodes and/or reactive Gas Diffusion Layer Electrodes (GDLEs) in DMFCs and/or methanol electrolysis cells. Full article

Photoanodes consisting of titania nanotubes (TNTs) grown on transparent conductive oxides (TCO) by anodic oxidation are being widely investigated as a low-cost alternative to silicon-based materials, e.g., in solar light-harvesting applications. Intending to enhance the optical properties of those photoanodes, the modification of the surface chemistry or control of the geometrical characteristics of developed TNTs has been explored. In this review, the recent advancement in light-harvesting properties of transparent anodic TNTs formed onto TCO is summarized. The physical deposition methods such as magnetron sputtering, pulsed laser deposition and electron beam evaporation are the most reported for the deposition of Ti film onto TCO, which are subsequently anodized. A concise description of methods utilized to improve the adhesion of the deposited film and achieve TNT layers without cracks and delamination after the anodization is outlined. Then, the different models describing the formation mechanism of anodic TNTs are discussed with particular focus on the impact of the deposited Ti film thickness on the adhesion of TNTs. Finally, the effects of the modifications of both the surface chemistry and morphological features of materials on their photocatalyst and photovoltaic performances are discussed. For each section, experimental results obtained by different research groups are evoked. Full article

The aim of this study is to synthesize Titania nanotubes (TNTs) on the 3D-printed Ti-6Al-4V surface and investigate the loading of antibacterial vancomycin drug dose of 200 ppm for local drug treatment application for 24 h. The antibacterial drug release from synthesized nanotubes evaluated via the chemical surface measurement and the linear fitting of Korsmeyer–Peppas model was also assessed. The TNTs were synthesized on the Ti-6Al-4V surface through the anodization process at different anodization time. The TNTs morphology was characterized using field emission scanning electron microscope (FESEM). The wettability and the chemical composition of the Ti-6Al-4V surface and the TNTs were assessed using the contact angle meter, Fourier transform infrared spectrophotometer (FTIR) and the X-ray photoelectron spectroscopy (XPS). The vancomycin of 200 ppm release behavior under controlled atmosphere was measured by the high-performance liquid chromatography (HPLC) and hence, the position for retention time at 2.5 min was ascertained. The FESEM analysis confirmed the formation of nanostructured TNTs with vertically oriented, closely packed, smooth and unperforated walls. The maximum cumulative vancomycin release of 34.7% (69.5 ppm) was recorded at 24 h. The wetting angle of both Ti-6Al-4V implant and the TNTs were found below 90 degrees. This confirmed their excellent wettability. Full article

Titania nanotubes (TNTs) impregnated with Pd and Pt nanoparticles are evaluated as heterogeneous catalysts in different conditions in two reactions: catalytic CO oxidation (gas phase, up to 500 °C) and H₂O₂ direct synthesis (liquid phase, 30 °C). The TNTs are obtained via oxidation of titanium metal and the intermediate layer-type sodium titanate Na₂Ti₃O₇. Thereafter, the titanate layers are exfoliated and show self-rolling to TNTs, which, finally, are impregnated with Pd or Pt nanoparticles at room temperature by using Pd(ac)₂ and Pt(ac)₂. The resulting crystalline Pd/TNTs and Pt/TNTs are realized with different lengths (long TNTs: 2.0–2.5 µm, short TNTs: 0.23–0.27 µm) and a specific surface area up to 390 m²/g. The deposited Pd and Pt particles are 2–5 nm in diameter. The TNT-derived catalysts show good thermal (up to 500 °C) and chemical stability (in liquid-phase and gas-phase reactions). The catalytic evaluation results in a low CO oxidation light-out temperature of 150 °C for Pt/TNTs (1 wt-%) and promising H₂O₂ generation with a productivity of 3240 mol_H2O2 kg_Pd⁻¹ h⁻¹ (Pd/TNTs, 5 wt-%, 30 °C). Despite their smaller surface area, long TNTs outperform short TNTs with regard to both CO oxidation and H₂O₂ formation. Full article

The goal of the present investigation was to find a solution to crucial engineering aspects related to the elaboration of multi-layered tissue-biomimicking composites. 3D printing technology was used to manufacture single-layered and gradient multi-layered 3D porous scaffolds made of poly-lactic acid (PLA). The scaffolds manufacturing process was optimized after adjusting key printing parameters. The scaffolds with 60 μm side length (square-shaped pores) showed increased stiffness values comparing to the other specimens. A silicone adhesive has been further used to join biomedical titanium plates, and the PLA scaffolds; in addition, titania nanotubes (TNTs were produced on the titanium for improved adhesion. The titanium-PLA scaffold single lap joints were evaluated in micro-tensile testing. The electrochemical processing of the titanium surface resulted in a 248% increase of the ultimate strength in the overlap area for dry specimens and 40% increase for specimens immersed in simulated body fluid. Finally, the biocompatibility of the produced scaffolds was evaluated with primary cell populations obtained after isolation from bone residual tissue. The manufactured scaffolds present promising features for applications in orthopedic implantology and are worth further. Full article

Titania nanotube was prepared from sludge generated TiO₂ (S-TNT) through a modified hydrothermal route and successfully composited with graphitic carbon nitride (g-CN) through a simple calcination step. Advanced characterization techniques such as X-ray diffraction, scanning and transmission electron microscopy, infrared spectroscopy, X-ray photoelectron spectroscopy, UV/visible diffuse reflectance spectroscopy, and photoluminescence analysis were utilized to characterize the prepared samples. A significant improvement in morphological and optical bandgap was observed. The effective surface area of the prepared composite increased threefold compared with sludge generated TiO₂. The optical bandgap was narrowed to 3.00 eV from 3.18 in the pristine sludge generated TiO₂ nanotubes. The extent of photoactivity of the prepared composites was investigated through photooxidation of NO_x in a continuous flow reactor. Because of extended light absorption of the as-prepared composite, under visible light, 19.62% of NO removal was observed. On the other hand, under UV irradiation, owing to bandgap narrowing, although the light absorption was compromised, the impact on photoactivity was compensated by the increased effective surface area of 153.61 m²/g. Hence, under UV irradiance, the maximum NO removal was attained as 32.44% after 1 h of light irradiation. The proposed facile method in this study for the heterojunction of S-TNT and g-CN could significantly contribute to resource recovery from water treatment plants and photocatalytic atmospheric pollutant removal. Full article

The nanotubular surface of titanium implants is known to have superior osteogenic activity but is also vulnerable to failure because of induced bacterial attachment and consequent secondary infection. Here, the problem was attempted to be solved by depositing nanosized tetracycline (TC)-loaded particles in poly(lactic-co-glycolic acid) on titania nanotubes (TNTs) using the electrospray deposition method. The antibacterial effect of the newly formed TNT surface was considered using the common pathogen Staphylococcus aureus. Maintenance of the biocompatibility and osteogenic characteristics of TNTs has been tested through cytotoxicity tests and osteogenic gene expression/extra-cellular matrix mineralization, respectively. The results showed that TNTs were successfully formed by anodization, and the characterization of TC deposited on the TNTs was controlled by varying the spraying parameters such as particle size and coating time. The TC nanoparticle-coated TNTs showed antibacterial activity against Staphylococcus aureus and biocompatibility with MC3T3-E1 pre-osteoblasts, while the osteogenic activity of the TNT structure was preserved, as demonstrated by osteocalcin and osteopontin gene expression, as well as Alizarin red staining. Hence, this study concluded that the electrosprayed TC coating of TNTs is a simple and effective method for the formation of bactericidal implants that can maintain osteogenic activity. Full article

In this paper the synthesis of self-organized Titania nanotubes (TNTs) by a facile potentiostatic anodization in a glycerol-based electrolyte is reported. The optimized TNTs were subsequently reduced through a cathodic reduction process to enhance its capacitive performance. FESEM and XRD were used to characterize the morphology and crystal structure of the synthesized samples. XPS analysis confirmed the reduction of Ti⁴⁺ to Ti³⁺ ions in the reduced Titania nanotubes (R-TNTs). The tube diameter and separation between the tubes were greatly influenced by the applied voltage. TNTs synthesized at voltage of 30 V for 60 min exhibited 86 nm and 1.1 µm of tube diameter and length, respectively and showed high specific capacitance of 0.33 mF cm⁻² at current density of 0.02 mA cm⁻². After reduction at 5 V for 30 s, the specific capacitance increased by about seven times (2.28 mF cm⁻²) at 0.5 mA cm⁻² and recorded about 86% capacitance retention after 1000 continuous cycling at 0.2 mA cm⁻², as compared to TNTs, retained about 61% at 0.01 mA cm⁻². The charge transfer resistance drastically reduced from 6.2 Ω for TNTs to 0.55 Ω for R-TNTs, indicating an improvement in the transfer of electrons and ions across the electrode–electrolyte interface. Full article

Three different Ti6Al4V surface oxidation methods have been applied to obtain three types of titania materials of different nanoarchitecture. Electrochemical oxidation of titanium alloy allowed for obtaining titania nanotubes (TNT), chemical oxidation led to obtain titania nanofibers (TNF), and thermal oxidation gave titania nanowires (TNW). My earlier investigations of these nanomaterials were focused mainly on the estimation of their bioactivity and potential application in modern implantology. In this article, the comparative analysis of the photocatalytic activity of produced systems, as well as the impact of their structure and morphology on this activity, are discussed. The activity of studied nanomaterials was estimated basis of UV-induced degradation of methylene blue and also acetone, and it was determined quantitatively according to the Langmuir–Hinshelwood reaction mechanism. The obtained results were compared to the activity of Pilkington Glass Activ^TM (reference sample). Among analyzed systems, titania nanofibers obtained at 140 and 120 °C, possessing anatase and anatase/amorphous structure, as well as titania nanowires obtained at 475 and 500 °C, possessing anatase and anatase/rutile structure, were better photocatalyst than the reference sample. Completely amorphous titania nanotubes, turned out to be an interesting alternative for photocatalytic materials in the form of thin films, however, their photocatalytic activity is lower than for Pilkington Glass Activ^TM. Full article

Titanium dioxide nanotubes/hydroxyapatite nanocomposites were produced on a titanium alloy (Ti6Al4V/TNT/HA) and studied as a biocompatible coating for an implant surface modification. As a novel approach for this type of nanocomposite fabrication, the atomic layer deposition (ALD) method with an extremely low number of cycles was used to enrich titania nanotubes (TNT) with a very thin hydroxyapatite coating. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were used for determination of the structure and the surface morphology of the fabricated nanocoatings. The biointegration activity of the layers was estimated based on fibroblasts’ proliferation on the TNT/HA surface. The antibacterial activity was determined by analyzing the ability of the layers to inhibit bacterial colonization and biofilm formation. Mechanical properties of the Ti6Al4V/TNT/HA samples were estimated by measuring the hardness, Young’s module, and susceptibility to scratching. The results revealed that the nanoporous titanium alloy coatings enriched with a very thin hydroxyapatite layer may be a promising way to achieve the desired balance between biofunctional and biomechanical properties of modern implants. Full article

Dispersed silver nanoparticles (AgNPs) on the surface of titanium alloy (Ti6Al4V) and titanium alloy modified by titania nanotube layer (Ti6Al4V/TNT) substrates were produced by the chemical vapor deposition method (CVD) using a novel precursor of the formula [Ag₅(O₂CC₂F₅)₅(H₂O)₃]. The structure and volatile properties of this compound were determined using single crystal X-ray diffractometry, variable temperature IR spectrophotometry (VT IR), and electron inducted mass spectrometry (EI MS). The morphology and the structure of the produced Ti6Al4V/AgNPs and Ti6Al4V/TNT/AgNPs composites were characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM). Moreover, measurements of hardness, Young’s modulus, adhesion, wettability, and surface free energy have been carried out. The ability to release silver ions from the surface of produced nanocomposite materials immersed in phosphate-buffered saline (PBS) solution has been estimated using inductively coupled plasma mass spectrometry (ICP-MS). The results of our studies proved the usefulness of the CVD method to enrich of the Ti6Al4V/TNT system with silver nanoparticles. Among the studied surface-modified titanium alloy implants, the better nano-mechanical properties were noticed for the Ti6Al4V/TNT/AgNPs composite in comparison to systems non-enriched by AgNPs. The location of silver nanoparticles inside of titania nanotubes caused their lowest release rate, which may indicate suitable properties on the above-mentioned type of the composite for the construction of implants with a long term antimicrobial activity. Full article