Photocatalytic degradation of methylene blue by Au-deposited TiO<Subscript>2</Subscript> film under UV irradiation

A TiO₂ photocatalytic film was prepared by the sol–gel and dip-coating methods. Au-loaded TiO₂ photocatalytic films were produced by the photodeposition method. The photocatalytic activity of the films under UV irradiation was evaluated by measuring the degradation of absorbance for a methylene blue (MB) aqueous solution. Au particles deposited on the TiO₂ film improved the photocatalytic activity under the O₂ bubbling condition. On the other hand, under N₂ or Ar bubbling, the doubly reduced form of MB, leuco-methylene blue (LMB), was formed at the beginning of UV irradiation, and then both MB and LMB were decomposed gradually by the photocatalytic reaction. In this process, Au particles on the TiO₂ film behave as electron traps.     

Photodeposition of Pt nanoparticles on TiO2-carbon xerogel composites

Carbon xerogels synthesized from polycondensation of resorcinol with formaldehyde, having specific surface areas in the range 650 to 990 m² g⁻¹ and variable degrees of surface oxidation, are used to prepare TiO₂-carbon xerogel composites by sol-gel methods. These composite materials are used to support Pt nanoparticles (5 wt.%) by the photodeposition technique. After a high temperature reduction treatment at 773 K, the obtained materials were characterized in order to assess the interactions between the phases Pt, TiO₂ and carbon xerogel. It is observed that the carbon xerogel acts as an adhesive agent of the TiO₂ and Pt particles, enhancing the interaction between the metal and the composite support.     

Preparation, characterization and photocatalytic activity of TiO2/polyaniline core-shell nanocomposite

Polyaniline (PANI) as a promising conducting polymer has been used to prepare polyaniline/TiO₂ (PANI/TiO₂) nanocomposite with core-shell structure as photocatalyst. Titanium dioxide (TiO₂) nanoparticles with an average crystal size of 21?nm were encapsulated by PANI via the in situ polymerization of aniline on the surface of TiO₂ nanoparticles. FT?CIR, UV-Vis-NIR, XRD, SEM and TEM techniques were used to characterize the PANI/TiO₂ core-shell nanocomposite. Photocatalytic activity of PANI/TiO₂ nanocomposite was investigated under both UV and visible light irradiations and compared with unmodified TiO₂ nanoparticles. Results indicated deposition of PANI on the surface of TiO₂ nanoparticles which improved the photocatalytic activity of pristine TiO₂ nanoparticles.     

Investigation of photocatalytic removal and photonic efficiency of maxilon blue dye GRL in the presence of TiO2 nanoparticles

TiO₂ nanoparticles have been synthesized by solvent-free hydrothermal process. TiO₂ nanoparticles were annealed at 500°C for enhancing the characterization and the photocatalytic activity. The synthesized TiO₂ was characterized by x-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), atomic force microscopy (AFM), BET, and diffuse reflectance spectroscopy (UV-DR) techniques to study the morphology and structural configuration. The effects of different parameters such as the initial dye concentration, catalyst concentration, pH of the solution, light intensity, and reactive oxygen species (ROS) on relative photonic efficiencies and photocatalytic degradation kinetics of GRL were investigated, and the degradation of GRL follows pseudo-first order kinetics according to the Langmuir–Hinshelwood model. The ROS studies indicate that hydroxyl radicals and holes are the predominant reactive species within the same step, contributing up to 92.64%, hydroxyl radicals participate for about 55%, and holes share for about 37.64% in the photocatalytic degradation of GRL.     

Synthesis of iron-doped TiO2 nanoparticles by ball-milling process: the influence of process parameters on the structural,optical, magnetic,and photocatalytic properties

Titanium dioxide (TiO₂) absorbs only a small fraction of incoming sunlight in the visible region thus limiting its photocatalytic efficiency and concomitant photocatalytic ability. The large-scale application of TiO₂ nanoparticles has been limited due to the need of using an ultraviolet excitation source to achieve high photocatalytic activity. The inclusion of foreign chemical elements in the TiO₂ lattice can tune its band gap resulting in an absorption edge red-shifted to lower energies enhancing the photocatalytic performance in the visible region of the electromagnetic spectrum. In this research work, TiO₂ nanoparticles were doped with iron powder in a planetary ball-milling system using stainless steel balls. The correlation between milling rotation speeds with structural and morphologic characteristics, optical and magnetic properties, and photocatalytic abilities of bare and Fe-doped TiO₂ powders was studied and discussed.     

TiO2 coating on silica particles by deposition of sol-gel-derived nanoparticles

TiO₂ was coated on nonporous transparent silica particles of 3.2 μm diameter by deposition of sol-gel-derived TiO₂ nanoparticles. Effects of water concentration, feed rate of titanium tetraisopropoxide (TTIP) solution and amount of supplied TTIP solution on the amount of TiO₂ coated on the silica particles were examined. Scanning electron microscopy observation confirmed that TiO₂ was coated on the silica particles in the form of ‘nanoparticles’ by using this method. Because of that, even though the TiO₂ surface area decreased due to sintering after calcination at high temperature to change the crystalline phase of TiO₂ to the anatase phase, the final surface area was still much larger than that of the original silica particles. The results also showed that as the water concentration increased, the amount of coated TiO₂ decreased. On the other hand, when the amount of supplied TTIP solution increased, the amount of coated TiO₂ increased. It was also confirmed that the feed rate of TTIP solution had little effect on the amount of coated TiO₂. The photocatalytic activities of the resulting TiO₂-coated silica particles were also evaluated by the photocatalytic decomposition of 2,4-dinitrophenol as a model substance. The results showed that the photocatalytic activity of the particles is not a function of the total surface area, but of the surface area in which anatase phase TiO₂ is exposed to the reaction space. The sedimentation velocity of the TiO₂-coated silica particles becomes about 5 orders of magnitude faster than that of the primary particles of the TiO₂. This indicates that the handling of the TiO₂ was also improved considerably by coating on the silica particles.     

Solution- and air-recoverable photocatalytic nanofibers by facile and cost-effective electrospinning and co-precipitation processes

While nanostructured materials are of particular academic and practical interest, their recoverability and recyclability have been of paramount industrial and environmental concerns. In the present contribution, co-precipitation was demonstrated as a facile and cost-effective approach to incorporate magnetic sensitivity and enhance the recoverability of nanofibrous materials which were frequently utilized in catalysis, energy and medical applications, etc. In particular, reusable magnetic and photocatalytic hybrid nanofibers were generated by electrospinning and co-precipitation method. First, TiO₂ nanofibers were prepared through sol-gel reaction and electrospinning process. To improve their recoverability, CoFe₂O₄ nanoparticles were decorated onto the nanofibers' surfaces via co-precipitation of cobalt and iron ions in the presence of the nanofibers suspension. Furthermore, the resulting CoFe₂O₄-decorated TiO₂ nanofibers maintained their photocatalytic activity after the modification. When suspended in a solution or spread on a dried surfaces, these nanofibers could be recollected with a magnet. These findings suggested that incorporation of ferromagnetic into the nanofibers maintained their photocatalytic performance and reduced production cost as well as the risk of human and environmental exposure through solution and air.     

Ag surfactant effects of TiO2 films prepared by sputter deposition

The surfactant effect of Ag on the thin film structure of TiO₂ by radio frequency magnetron sputtering has been investigated. Comparisons between the atomic force microscopy images revealed that the surface roughness of TiO₂ film mediated by Ag was smaller than that of the TiO₂ film without Ag. The surface segregation effect of Ag was confirmed using X-ray photoelectron spectroscopy. The results of X-ray diffraction revealed that the initial deposition of a 0.4 nm thick Ag surfactant layer onto a Fe buffer layer prior to the deposition of the TiO₂ film reduced the rutile (110) growth and enhanced the anatase (100) growth. It was concluded that Ag was an effective surfactant for changing the thin film structure of TiO₂ on the Fe buffer layer. The photocatalytic effect of the fabricated TiO₂ film was also investigated using the remote oxidation process. TiO₂ films with the Ag surfactant exhibited higher photocatalytic activity than conventionally deposited TiO₂ films.     

Rapid photokilling of gram-negative Escherichia coli bacteria by platinum dispersed titania nanocomposite films

Superior antimicrobial activity of 2 wt.% Pt-dispersed TiO₂ thin film was observed in photokilling Gram-negative Escherichia coli bacteria within 5 min irradiation (640 μW cm⁻², λ > 340 nm) from UV torch than bare TiO₂ film. Severe disruption of cell membrane has occurred over illuminated Pt-TiO₂ catalysts films coated with 100–300 μg powders per 5 cm² areas over sterilized glass slides. The Pt dispersion onto TiO₂ by impregnation–hydrogen reduction always exhibited better photokilling effect than Pt photodeposition, irrespective of Pt–TiO₂ dose and light exposure time. Similar trend in photoactivity difference between two Pt–TiO₂ catalysts is also observed in aqueous slurry because of the unlike surface structure of TiO₂ due to different annealing temperatures, size and nature of Pt particles dispersion onto TiO₂ photocatalysts.     

Ag surfactant effects of TiO2 films prepared by sputter deposition

The surfactant effect of Ag on the thin film structure of TiO₂ by radio frequency magnetron sputtering has been investigated. Comparisons between the atomic force microscopy images revealed that the surface roughness of TiO₂ film mediated by Ag was smaller than that of the TiO₂ film without Ag. The surface segregation effect of Ag was confirmed using X-ray photoelectron spectroscopy. The results of X-ray diffraction revealed that the initial deposition of a 0.4 nm thick Ag surfactant layer onto a Fe buffer layer prior to the deposition of the TiO₂ film reduced the rutile (110) growth and enhanced the anatase (100) growth. It was concluded that Ag was an effective surfactant for changing the thin film structure of TiO₂ on the Fe buffer layer. The photocatalytic effect of the fabricated TiO₂ film was also investigated using the remote oxidation process. TiO₂ films with the Ag surfactant exhibited higher photocatalytic activity than conventionally deposited TiO₂ films.     

Strong metal-support interactions (SMSIs) between Pt and Ti3+ on Pt/TiOx nanoparticles for enhanced degradation of organic pollutant

In this work, Pt nanoparticles were deposited onto the surface of Magnéli phase titanium suboxide (TiO_x) nanoparticles using a microwave-assisted deposition method. The effect of different concentrations of Pt nanoparticles was investigated to evaluate the strong metal-support interactions (SMSIs) between Pt and TiO_x based on their performance for the degradation of organic pollutant molecules. The adsorption and catalytic performance of the as-synthesized Pt/TiO_x nanoparticles were evaluated with respect to the degradation of rhodamine B (RhB) molecules without any external energy source. The Pt/TiO_x nanoparticles with Pt loading at 10 wt% (10%Pt/TiO_x) exhibited a remarkable performance. The XPS, CV, and FTIR analyses confirmed the presence of RhB degradation reactions under dark condition. This remarkable performance of the Pt/TiO_x nanoparticles was attributed to the SMSIs between Pt and Ti³⁺ atoms, which improves their performance compared with Pt/TiO₂ nanoparticles, and high density of active sites due to their nanometer size, which results in better performance compared with that of Pt/TiO_x submicron particles.     

Photochemical deposition of platinum on titanium dioxide–tungsten trioxide nanocomposites: an efficient photocatalyst under visible light irradiation

Highly ordered titanium dioxide–tungsten trioxide nanotubular composites (TiO₂–WO₃) were fabricated on titanium sheets by electrochemical anodizing. Platinum nanoparticles have been successfully deposited onto TiO₂–WO₃ nanotubes by UV light photoreduction method. In this work, X-ray diffraction, field emission scanning electron microscope, ultraviolet–visible spectroscopy and energy dispersive X-ray spectrometer methods were adopted to characterize the samples. The degradation of methylene blue (MB) was used as a model reaction to evaluate the photocatalytic activity of the obtained samples. After irradiated under visible light for 60 min, the degradation rate of MB solution on unmodified TiO₂–WO₃ and Pt/TiO₂–WO₃ reached 77 and 93 %, respectively. Under the same condition, no obvious photodegradation of MB was found for bare TiO₂ (T). Kinetic research showed that photodegradation process followed the first-order reaction; the apparent reaction rate constant of Pt/TiO₂–WO₃-1 was 4.56 × 10^?2 min^?1 which is approximately 1.75 times higher than that on the unmodified TiO₂–WO₃. This work provides an insight into designing and synthesizing new TiO₂–WO₃ nanotubes based hybrid materials for effective visible light-activated photocatalysis.     

Photocatalytic activity of polypyrrole/TiO<Subscript>2</Subscript> nanocomposites under visible and UV light

A series of polypyrrole (PPy)/titanium dioxide (TiO₂) nanocomposites were prepared in different polymerization conditions by ‘in situ’ chemical oxidative polymerization. The nanocomposites were characterized by transmission electron microscopy (TEM), Fourier transform infrared spectra (FT-IR), X-ray photoelectron spectroscopy spectra (XPS), and UV–Vis diffuse reflectance spectra. The photocatalytic degradation of methyl orange (MO) was chosen as a model reaction to evaluate the photocatalytic activities of TiO₂/PPy catalysts. The results show that a strong interaction exists at the interface between TiO₂ and PPy, the deposition of PPy on TiO₂ nanoparticles can alleviate their agglomeration, PPy/TiO₂ nanocomposites show stronger absorbance than neat TiO₂ under the whole range of visible light. The obtained PPy/TiO₂ nanocomposites exhibit significantly higher photocatalytic activity than the neat TiO₂ on the degradation of MO aqueous solution under visible and UV light illumination. The reasons for improving the photocatalytic activity were also discussed.     

Novel synthesis of quaternary nanocomposites based on chemical vapor grown graphene for photocatalytic hydrogen evolution

Pd-Pt/graphene-TiO₂ nanocomposites were synthesized via a facile ultrasonic and hydrothermal method. For the functionalization of graphene, large area graphene obtained by chemical vapor deposition method was oxidized by 3-chloroperoxybenzoic acid. The functionalized graphene oxide was decorated with TiO₂. And then, Pt and Pd nanoparticles were dispersed on graphene surface, simultaneously. The characterizations of “as-prepared” samples were studied by X-ray diffraction (XRD), transmission electron microscope (TEM), Raman, specific surface area (BET) and with energy dispersive X-ray (EDX). The photocatalytic activity of the Pd-Pt/graphene-TiO₂ nanocomposite catalyst was evaluated by H₂ evolution under UV light. Pd-Pt/graphene-TiO₂ (Pd-Pt/G-TiO₂) exhibited higher photocatalytic activities than control experimental group samples (TiO₂, G-TiO₂, Pd/G-TiO₂ and Pt/G-TiO₂) under UV light irradiation.     

Synthesis of TiO2/Pt/TiO2 multilayer films via radio frequency magnetron sputtering and their enhanced photocatalytic activity

TiO₂/Pt/TiO₂ (TPT) multilayered films with different thicknesses of Pt layers from about 0.75 to 12 nm were prepared by radio frequency magnetron sputtering method. The as-prepared films were characterized by X-ray diffraction, scanning electron microscopy, atomic force microscopy, UV-visible diffuse reflectance spectroscopy, and photoluminescence spectroscopy. The photocatalytic activity of the samples was evaluated by the photocatalytic decolorization of methyl blue aqueous solution under ultraviolet light irradiation. The photocatalytic activities of all TPT multilayer films were higher than that of the pure TiO₂ films. When Pt thickness was increased to 3 nm, the measured photocatalytic activity of the TPT film was highest, and exceeded that of the pure TiO₂ films by a factor of more than three times. Such enhancement was ascribed to the presence of Pt layer, which inhibits the recombination of the photogenerated charge and carriers, as well as modifies the crystallinity of the TiO₂ top layer.     

Enhancement of photocatalytic properties of TiO2 nanobelts through surface-coarsening and surface nanoheterostructure construction

In this work, heterostructures were obtained by uniformly assembling NiO nanoparticles on the surface-coarsened TiO₂ nanobelts through a precipitation process. The uniform assembling of NiO nanoparticles led to a large number of nano-p-n-junction heterostructures on the surface of the TiO₂ nanobelts, where NiO and TiO₂ are p- and n-type semiconductors, respectively. Compared with both pure NiO nanoparticles and TiO₂ nanobelts, NiO nanoparticles/TiO₂ surface-coarsened nanobelt heterostructured composite exhibited a greatly enhanced photocatalytic activity in the decomposition of a model dye compound methyl orange under ultraviolet light irradiation. It was argued that the nano-p-n-junctions effectively reduce the recombination of electrons and holes, thus resulting in enhanced photocatalytic property of the heterostructured composites. The better performance of the surface-coarsened nanobelts is due to the increased photo absorption and production of charge carriers, which renders the composites with further enhanced photocatalytic performance. The established approach allows the control of the nano-p-n junction heterostructure on the nanobelts, and hence, their photocatalytic effect.     

Photochemical synthesis and characterization of Ag/TiO2 nanotube composites

TiO₂ nanotubes were fabricated by a hydrothermal method. Silver nanoparticles with diameters around 3–5 nm were loaded onto the surface of TiO₂ nanotubes via a deposition approach followed by a photochemical reduction process under ultraviolet irradiation. Transmission electron microscopy (TEM), N₂ adsorption measurements, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, UV-vis diffuse reflectance spectroscopy (UV-vis), and fluorescence spectroscopy (FL) were applied to characterize the as-prepared Ag/TiO₂ nanotube composites. The photocatalytic activity of the as-prepared materials was investigated by photodegrading of methyl orange. The results showed that silver particles were in zero oxidation state and highly dispersed on the surface of TiO₂ nanotubes when the concentration of Ag⁺ was low. The presence of metallic silver can help the electron-hole separation by attracting photoelectrons. The Ag/TiO₂ nanotube composites with a suitable amount of silver showed a further improvement on the photocatalytic activity for degradation of methyl orange in water.     

Atomic layer deposition of TiO2 thin films on glass fibers for enhanced photocatalytic activity

Photocatalytic wastewater treatment is expected to become a sustainable way of eliminating toxic chemicals. Due to the surface-driven mechanism of the photocatalysis, surface area of the catalyst material plays a crucial role in the efficiency of the process, which is usually achieved by nanoparticles. However, using powder materials introduces a new problem: removing the catalyst materials out of clean water. As an alternative, atomic layer deposition (ALD) can form conformal thin films on high surface area substrates providing an immobilization route with high photocatalytic activity. Textile materials are inexpensive and accessible therefore good candidates for the substrate materials. Here, we deposit thin films on TiO₂ on fiberglass fabrics and investigate the photocatalytic activity. Since the as-deposited ALD TiO₂ films are amorphous, they have very limited photocatalytic activity. Upon thermal treatment of the films after deposition, photocatalytic activity is achieved. After four hours of exposure to the solar simulator and UV lamp, TiO₂-coated fibers demonstrated much higher photocatalytic activity than films on planar substrates previously described in the literature. The photocatalytic activity and structure of the coated fibers were investigated using XRD, XPS, UV–Vis, and PL analyses.

     

Cu-BTC metal organic framework (MOF) derived Cu-doped TiO2 nanoparticles and their use as visible light active photocatalyst for the decomposition of ofloxacin (OFX) antibiotic and antibacterial activity

Herein, we report the ultrasonic-assisted precipitation technique for the fabrication of Cu-doped TiO₂ nanoparticles. The prepared sample showed high crystallinity, purity and nanoparticles like structure with the diameter in the range of 10–22 nm. The bandgap for Cu-doped TiO₂ nanoparticles was estimated to be 2.91 eV using Tauc plot, which is considerable for improving the light-harvesting capacity. Further, the prepared Cu-doped TiO₂ was used as photocatalyst for the eradication of ofloxacin (OFX), an antibiotic from an aqueous phase under visible illuminations. About 72% degradation of OFX (10 mg/L, pH 7) was achieved with Cu-doped TiO₂ nanoparticles after 180 min of visible illumination. The probable photocatalytic mechanism for the decomposition of OFX has been proposed based on reactive species trapping study. Moreover, the antibiotic efficiency of OFX was investigated against Escherichia coli and it was observed that its antimicrobial activity was significantly diminished after the photocatalytic decomposition of the OFX solution with synthesized nanoparticles.     

Preparation and characterization of Pt–TiO2–SiO2 mesoporous materials and visible-light photocatalytic performance

TiO₂–SiO₂ metal oxide materials with a mesostructure have been prepared by a novel method in which hydrolysis and condensation of titanium tetraisopropoxide (TTIP) and tetraethoxysilane (TEOS) were controlled by the pH change of acidic solution. The Pt-modified TiO₂–SiO₂ catalysts were synthesized by the photo-reduction method. The resulting materials showed a high photocatalytic activity for the photodegradation of methyl orange in the visible-light range. A reaction mechanism was proposed and discussed.