Simple fabrication of rod-like N-doped TiO2/Ag with enhanced visible-light photocatalytic activity

Rod-like N-doped TiO₂/Ag composites were successfully synthesized by a modified sol–gel method, without adding any surfactants. The entire preparation differs from the traditional sol–gel synthesis of TiO₂ that the reaction can get controlled by adjusting the flow speed of water vapor and NH₃. Characterization results show that as-prepared samples were uniform nanorods with an average length of ca. 3 µm and a cross section diameter of ca. 150 nm. The rod-like structure was formed during the annealing process. A possible mechanism was proposed to illustrate the formation of rod-like Ag–N–TiO₂. The degradation of methylene blue performed under visible light with the prepared nanorods as the photocatalyst demonstrated the photocatalytic activities of TiO₂ can be improved by the synergistic effect of N doping and Ag modification. In addition, as-prepared TiO₂-based photocatalyst exhibits a significantly enhanced photo-chemical stability after 5 catalytic cycles mainly due to the rod-like morphology. This indicated that they have some potential value in practical application.     

Visible light photocatalytic degradation of thiophene using Ag–TiO2/multi-walled carbon nanotubes nanocomposite

Ag–TiO₂ nanocatalyst, supported on multi-walled carbon nanotubes, was synthesized successfully via a modified sol–gel method, and the prepared photocatalyst was used to remediate aqueous thiophene environmentally by photocatalytic oxidation under visible light. The prepared Ag–TiO₂/multi-walled carbon nanotubes nanocomposite photocatalyst was characterized through X-ray diffraction, Brunauer–Emmett–Teller (BET), transmission electron microscopy, and UV–vis spectra (UV–vis). The results showed that both Ag and TiO₂ nanoparticles were well-dispersed over the MWCNTs and formed a uniform nanocomposite. Ag doping can eliminate the recombination of electron–hole pairs in the catalyst, and the presence of MWCNTs in the TiO₂ composite can change surface properties to achieve sensitivity to visible light. The optimum mass ratio of MWCNT:TiO₂:Ag was 0.02:1.0:0.05, which resulted in the photocatalyst's experimental performance in oxidizing about 100% of the thiophene in a 600 mg/L solution within 30 min and with 1.4 g L⁻¹ amount of catalyst used.     

Preparation and characterization of SiO2/polydopamine/Ag nanocomposites with long-term antibacterial activity

Silver nanoparticles (Ag NPs) with diameter of approximately 10 nm were prepared by the reduction of silver nitrate using green synthesis, an eco-friendly approach. The synthesized Ag NPs were homogeneously deposited on silicon dioxide (SiO₂) particles modified with dopamine, leading to the formation of SiO₂/polydopamine (PD)/Ag nanocomposites (NCs) with a core–shell–satellite structure investigated by transmission electron microscopy. The Ag content of SiO₂/PD/Ag NCs determined by inductively coupled plasma optical emission spectrometry was approximately 5.92 wt%. The antibacterial properties of both Ag NPs and SiO₂/PD/Ag NCs against Vibrio natriegens (V. natriegens) and Erythrobacter pelagi sp. nov. (E. pelagi) were investigated by bacterial growth curves and inhibition zone. Compared to Ag NPs, the SiO₂/PD/Ag NCs exhibited superior long-term antibacterial activity, attributed to its controlled release of Ag⁺ ions.     

Enhanced photocatalytic activity of Ag doped TiO2 nanoparticles synthesized by a microwave assisted method

Pure anatase TiO₂ photocatalyst with different Ag contents was prepared via a controlled and energy efficient microwave assisted method. The prepared material was further characterized by several analytical techniques like X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), surface area measurement (BET), Fourier transform-infrared spectroscopy (FT-IR), diffused reflectance spectroscopy (DRS), and thermogravimetric–differential thermal analysis (TGA–DTA). A 10 nm average crystallite size with nano-crystals of pseudo-cube like morphology was obtained for optimal (0.25 mol%) Ag doped TiO₂. The present research work is mainly focused on the enhancement of degradation efficiency of methyl orange (MO) by doping of Ag in TiO₂ matrix using UV light (365 nm). A 99.5% photodegradation efficiency of methyl orange was achieved by utilizing 0.25 mol% Ag doped TiO₂ (1 g/dm³) at pH=3 within 70 min. Recyclability of photocatalyst was also studied, with the material being found to be stable up to five runs.     

A novel shape-controlled synthesis of dispersed silver nanoparticles by combined bioaffinity adsorption and TiO2 photocatalysis

Shape-controlled silver nanoparticles (Ag NPs) were prepared in a well-dispersed mode on the active imprinting sites of chitosan-TiO₂ adsorbent (CTA) by means of bioaffinity adsorption and TiO₂ photocatalysis. Nontoxic hydrogen peroxide (H₂O₂) was used as a suitable etching reagent in our production of shape-controlled Ag NPs, since it could regulate the TiO₂ photocatalysis and accelerate the generation of O₂. With the same amount of H₂O₂ addition, silver nanocubes, nanospheres and truncated triangular nanoplates were individually obtained on the surface of CTA under UV irradiation by facilely adjusting the initial Ag⁺ concentration. The FE-SEM, XRD and UV-visible characterizations confirmed single crystal Ag NPs with different shapes loaded on CTA. The mechanism for the formation of shape-controlled Ag NPs was discussed based on a photocatalytic reaction system. As an example of applications of the Ag NPs, we tested the biocidal properties, and silver nanocubes exhibited the highest antibacterial activity. Our research provided a simple synthesis for shape-regulated Ag NPs steadily loaded on CTA. It might moreover be a guide in preparing metal nanocrystals monodispersely immobilized on chemical substrates.     

Novel porous TiO2 glass-ceramics with highly photocatalytic ability

A porous TiO₂ glass-ceramics with high photo-oxidative activity was successfully obtained from the SiO₂–Al₂O₃–B₂O₃–CaO–TiO₂ glass system. Rutile-type TiO₂ was observed in the crystallization temperature range of 973–1173 K. The band gap of the glass-ceramics coincided approximately with that of rutile-type TiO₂. The photocatalytic activity of this glass-ceramics was about four times larger than that of a TiO₂-coated photocatalyst fabricated by the sol–gel process. Furthermore, as this porous TiO₂ glass-ceramics contained TiO₂ in composition form, it could prevent peeling of the TiO₂ from the substrate. As well, this glass-ceramics can be easily shaped into sheets, tubes, rods, etc.     

Effects of tungsten thickness and annealing temperature on the electrical properties of W-TiO2 thin films

TiO₂ thin films were prepared by RF magnetron sputtering onto glass substrates and tungsten was deposited onto these thin films (deposition time 15-60 s) to form W-TiO₂ bi-layer thin films. The crystal structure, morphology, and transmittance of these TiO₂ and W-TiO₂ bi-layer thin films were investigated. Amorphous, rutile, and anatase TiO₂ phases were observed in the TiO₂ and W-TiO₂ bi-layer thin films. Tungsten thickness and annealing temperature had large effects on the transmittance of the W-TiO₂ thin films. The W-TiO₂ bi-layer thin films with a tungsten deposition time of 60 s were annealed at 200 °C-400 °C. The band gap energies of the TiO₂ and the non-annealed and annealed W-TiO₂ bi-layer thin films were evaluated using (αhν)^1/2 versus energy plots, showing that tungsten thickness and annealing temperature had major effects on the transmittance and band gap energy of W-TiO₂ bi-layer thin films.     

Aerosol processing of Ag/TiO2 composite nanoparticles for enhanced photocatalytic water treatment under UV and visible light irradiation

In this study, we investigated the effect of Ag addition on the photocatalytic reactivity of TiO₂ nanoparticles (NPs). Controlled amounts of Ag were incorporated in TiO₂ NPs using aerosol spray pyrolysis and subsequent calcination. Ag/TiO₂ composite NPs containing different amounts of Ag (e.g., 0, 0.5, 1, 2, and 5 wt%) were successfully fabricated. The photodegradation performances of the as-prepared Ag/TiO₂ composite NPs were tested using methylene blue (MB) solution under UV and visible light irradiation. Upon increasing the Ag content to 1 wt%, the resulting Ag/TiO₂ composite NPs exhibited increased photocatalytic reactivity due to lowered bandgap energy, which promoted both charge generation and separation. However, when the Ag content exceeded 1 wt%, the photocatalytic reactivity of the resulting Ag/TiO₂ composite NPs was considerably deteriorated due to the masking effect of the excess Ag on the reactive sites of TiO₂. Hence, the incorporation of an optimized amount of Ag in the TiO₂ matrix promotes the photocatalytic reactivity of Ag/TiO₂ composite NPs by controlling their bandgap energy and charge generation and separation processes. These results could lead to the development of photodegradation active substances for water treatment in organic solutions.     

Antibacterial and photocatalytic properties of Ag/TiO2/ZnO nano-flowers prepared by facile one-pot hydrothermal process

In this paper, a simple and efficient strategy of one-pot synthesis of Ag doped TiO₂/ZnO photocatalyst was developed using hydrothermal process. Simultaneous crystallization of Ag and ZnO crystals from their precursor solution containing P25 (TiO₂) NPs could form effectively bonded Ag/TiO₂/ZnO composite photocatalyst during hydrothermal treatment. Several analytical techniques, including scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), FT-IR spectroscopy, and photoluminescence spectroscopy have been used to characterize the resulting Ag/TiO₂/ZnO photocatalyst. Results showed that ZnO nano-flowers doped with TiO₂ and Ag NPs were formed by this simple facile one-step process. The unique properties of Ag NPs on binary semiconductor composite not only provide the decreased rate of electron–hole separation but also prevent from the loss of photocatalyst during recovery due to the fixed attachment of Ag and TiO₂ NPs on the surface of flower shaped large ZnO particles. Therefore, as-synthesized composite is an economically and environmentally friendly photocatalyst.     

Effect of Ag addition on the properties of Pd–Ag/TiO2 catalysts containing different TiO2 crystalline phases

Anatase and rutile TiO₂ were used for preparation of the TiO₂ supported Pd and Pd–Ag catalysts for selective hydrogenation of acetylene. It was found that Pd/TiO₂-anatase exhibited higher acetylene conversion and ethylene selectivity than rutile TiO₂ supported ones. However, addition of Ag to Pd/TiO₂-anatase catalyst resulted in lower ethylene selectivity while that of Pd/TiO₂-rutile increased. It is suggested that Ag addition suppressed the beneficial effect of the Ti³⁺ sites presented on the anatase TiO₂ during selective acetylene hydrogenation whereas without Ti³⁺, Ag promoted ethylene selectivity by blocking sites for over-hydrogenation of ethylene to ethane.     

Oxidative energy storage behavior of a porous nanostructured TiO2–Ni(OH)2 bilayer photocatalysis system

TiO₂–Ni(OH)₂ bilayer electrodes were prepared by the cathodic electrodeposition of Ni(OH)₂ layer on a TiO₂/ITO substrate. The porous Ni(OH)₂ layers were obtained at relatively high current densities (≥1.0 mA cm⁻²), and the particle size increased with increasing the deposition current density. A porous nanostructured TiO₂–Ni(OH)₂ bilayer was obtained at a current density of 1.0 mA cm⁻². The effects of OH⁻ concentration in the electrolyte and surface structure in the Ni(OH)₂ layer on storage of the oxidative energy of TiO₂ were investigated. In our experimental conditions the oxidative energy storage of an UV-irradiated TiO₂ photocatalyst in Ni(OH)₂ was obviously enhanced in the electrolyte with 1.0 M OH⁻. The porous nanostructured TiO₂–Ni(OH)₂ bilayer electrode showed the notably improved oxidative energy storage performance, resulting from its porous structure and nanostructured Ni(OH)₂ particles. The TiO₂–Ni(OH)₂ bilayer electrode during UV irradiation exhibited much higher potentials and larger photocurrent than the TiO₂/ITO electrode. The transition from Ni(OH)₂ to NiOOH under UV irradiation proceeded in the potential range of −0.5 to −0.2 V, much more negative than the Ni(OH)₂/NiOOH redox potential. A possible mechanism on the oxidative energy storage of an UV-irradiated TiO₂ photocatalyst in Ni(OH)₂ was proposed, and the related experimental results were discussed in terms of the suggested model.     

Fabrication of multifunctional TiO2–fly ash/polyurethane nanocomposite membrane via electrospinning

In this study, we demonstrate the fabrication of multifunctional composite polyurethane (PU) membrane from a sol gel system containing TiO₂ and fly ash (FA) nanoparticles (NPs). The adsorptive property of FA and photocatalytic property of TiO₂ can introduce different functionalities on PU mat for water purification. Different types of PU nanofiber mats were prepared by varying the composition of NPs in blend solution. FE-SEM, TEM, TGA, XRD, UV–visible spectra, and water contact angle measurement confirmed the incorporation of FA and TiO₂ NPs on/into PU nanofibrous mat. The influence of NPs on PU membrane was evaluated from the adsorption of heavy metals (Hg, Pb), removal of dyes (methylene blue), antibacterial activity, and water flux. The improvement of all these activities is attributed to the adsorptive property of FA and photocatalytic/hydrophilic property of TiO₂ NPs. Therefore, as-synthesized composite membrane can be utilized as an economically friendly filter media for water purification.     

An experimental and theoretical understanding of a UV photodetector based on Ag nanoparticles decorated Er-doped TiO2 thin film

Glancing angle deposition (GLAD) was employed to synthesise plasmonic Silver (Ag) nanoparticles (NPs) on the chemically prepared Erbium-doped Titanium dioxide (Er:TiO₂) thin films (TFs). The impact of using Ag NPs on the morphological, optical, and electrical aspects of Er:TiO₂ TFs were sequentially analysed. From the field emission scanning electron microscopy (FESEM) image, the Ag NPs appeared spherical and uniformly distributed on the Er:TiO₂ TFs. The size (diameter) of the maximum number of Ag NPs was ~15 nm (calculated from FESEM image). Energy dispersive X-ray (EDX) spectra assured the presence of Ag NPs on the TFs. X-ray diffraction (XRD) pattern for Ag NPs decorated Er:TiO₂ TFs closely resembled the face centred cubic crystal structure of Ag NPs and body centred tetragonal Ag–O compound. The optical spectroscopy (UV–visible diffuse reflectance and photoluminescence) elucidated that the absorption of light was significantly enhanced in the UV–visible spectral range for the TFs in which Ag NPs were sandwiched between Er:TiO₂ TF layers (Er:TiO₂/Ag NPs/Er:TiO₂). The Schottky contact-based Au/Er:TiO₂/Si photodetector (PD) and Au/Er:TiO₂/Ag NPs/Er:TiO₂/Si (plasmonic) PD were constructed. The plasmonic PD offered a better photo-responsivity of ~4.5 fold higher as compared to Er:TiO₂ TF-based PD upon 380 nm illumination under ?6 V bias. An increase in detectivity and a decrease in noise equivalent power was observed for the plasmonic device compared to Er:TiO₂ device in the UV region. A theoretical approach had been adopted to calculate the wavelength-dependent responsivity for both devices. Further, the important parameters like photoconductive gain, electron transit time and electron mobility were calculated by simulating the experimental responsivity curves of the devices. These parameters exhibited improvement in the UV regime for the plasmonic PD. The fast temporal response with short rise and decay time proves the excellent efficiency of the plasmonic UV PD.     

Two-Functional Direct Current Sputtered Silver-Containing Titanium Dioxide Thin Films

The article reports on structure, mechanical, optical, photocatalytic and biocidal properties of Ti–Ag–O films. The Ti–Ag–O films were reactively sputter-deposited from a composed Ti/Ag target at different partial pressures of oxygen on unheated glass substrate held on floating potential U _fl. It was found that addition of ~2 at.% of Ag into TiO₂ film has no negative influence on UV-induced hydrophilicity of TiO₂ film. Thick (~1,500 nm) TiO₂/Ag films containing (200) anatase phase exhibit the best hydrophilicity with water droplet contact angle (WDCA) lower than 10° after UV irradiation for 20 min. Thick (~1,500 nm) TiO₂/Ag films exhibited a better UV-induced hydrophilicity compared to that of thinner (~700 nm) TiO2/Ag films. Further it was found that hydrophilic TiO₂/Ag films exhibit a strong biocidal effect under both the visible light and the UV irradiation with 100% killing efficiency of Escherichia coli ATCC 10536 after UV irradiation for 20 min. Reported results show that single layer of TiO₂ with Ag distributed in its whole volume exhibits, after UV irradiation, simultaneously two functions: (1) excellent hydrophilicity with WDCA < 10° and (2) strong power to kill E. coli even under visible light due to direct toxicity of Ag.     

Mortality response of folate receptor-activated,PEG–functionalized TiO2 nanoparticles for doxorubicin loading with and without ultraviolet irradiation

TiO₂ nanoparticles (NPs) were synthesized by hydrothermal assisted sol–gel technique. In the next step, as-synthesized NPs were modified by poly ethylene glycol (PEG). Then, folic acid (FA) was conjugated to TiO₂–PEG. Finally, Doxorubicin (Dox) as an anticancer drug was loaded on as-prepared TiO₂–PEG–FA nanocarrier. The optimization of TiO₂ and FA concentration and the influence of ultraviolet (UV) irradiation on photocatalytic activity of nanocarrier and Dox loaded carrier were assessed by utilizing the 3-(4,5-dimethylthiazol-2yl)-2,5-diphenyltetrazolium bromide (MTT)-assay method.     

Production and characterization of nanocomposites based on poly(amide-imide) containing 4,4′-methylenebis(3-chloro-2,6-diethylaniline) using nano-TiO2 surface-coupled by 3-aminopropyltriethoxysilane

In this work, the poly(amide-imide) (PAI) was synthesized from the polymerization reaction of 4,4′-methylenebis(3-chloro-2,6-diethyl trimellitimidobenzene) as a diacid with 4,4′-methylenebis(3-chloro-2,6-diethylaniline) under green condition using molten tetra-n-butylammonium bromide and triphenylphosphite. Ultrasonic technique was used for preparation of PAI/TiO₂ nanocomposites (PAI/TiO₂ NCs). For the improvement of TiO₂ nanoparticles (NPs) dispersion and enhancing interactions between NPs and polymeric matrix the surface of TiO₂ was successfully modified by silane coupling agent (3-aminopropyltriethoxysilane). The resulting NCs were characterized by FT-IR, X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and thermogravimetric analysis (TGA). The TGA of the obtained NCs proves the enhancement in the thermal stability with an increase in the percentage of titania NPs. TEM and FE-SEM images showed that the NPs were uniformly dispersed in the polymer matrix. The shielding effect of nano TiO₂ under UV radiation was examined by UV–vis.     

Photocatalytic activity of TiO2 supported on multi-walled carbon nanotubes under simulated solar irradiation

TiO₂ particles supported on multi-walled carbon nanotubes (MWCNTs) were prepared using a sol–gel method to investigate their photocatalytic activity under simulated solar irradiation for the degradation of methyl orange (MO) in aqueous solution. The prepared composites were analyzed using XRD, SEM, EDS and UV–vis absorption spectroscopy. The results of this study indicated that there was little difference in the shape and structure of MWCNTs/TiO₂ composite and pure TiO₂ particles. The composite exhibited enhanced absorption properties in the visible light range compared to pure TiO₂. The degradation of MO by MWCNTs/TiO₂ composite photocatalysts was investigated under irradiation with simulated solar light. The results of this study indicated that MWCNTs played a significant role in improving photocatalytic performance. Different amounts of MWCNTs had different effects on photodegradation efficiency, and the most efficient MO photodegradation was observed for a 2% MWCNT/TiO₂ mass ratio. Photocatalytic reaction kinetics were described using the Langmuir–Hinshelwood (L–H) model. The photocatalyst was reused for eight cycles, and it retained over 95.2% photocatalytic degradation efficiency. Possible decomposition mechanisms were also discussed. The results of this study indicated that photocatalytic reactions with TiO₂ particles supported on MWCNTs under simulated solar light irradiation are feasible and effective for degrading organic dye pollutants.     

Synthesis and dielectric properties of polyaniline/titanium dioxide nanocomposites

Two series of polyaniline–TiO₂ nanocomposite materials were prepared in base form by in situ polymerization of aniline with inorganic fillers using TiO₂ nanoparticles (P25) and TiO₂ colloids (Hombikat), respectively. The effect of particle sizes and contents of TiO₂ materials on their dielectric properties was evaluated. The as-synthesized polyaniline–TiO₂ nanocomposite materials were characterized by transmission electron microscopy (TEM), Fourier transform infrared (FTIR), thermal analysis (DTA/TGA), and X-ray diffraction (XRD). Dielectric properties of polyaniline–TiO₂ nanocomposites in the form of films were measured at 1 KHz–1 MHz and a temperature range of 35–150 °C. Higher dielectric constants and dielectric losses of polyaniline–TiO₂ nanocomposites than those of neat PANI were found. PANI–TiO₂ nanocomposites derived from P25 exhibited higher dielectric constants and losses than those from Hombikat TiO₂ colloids. Electrical conductivity measurements indicate that the conductivity of nanocomposites is increased with TiO₂ content. The dielectric properties and conductivities are considered to be enhanced due to the addition of TiO₂, which might induce the formation of a more efficient network for charge transport in the base polyaniline matrix.     

Photocatalytic degradation of dairy effluent using AgTiO2 nanostructures/polyurethane nanofiber membrane

Dairy effluent (DE) is environmentally toxic and needs special attention. Photocatalytic degradation of DE was studied using novel polyurethane (PU)-based membranes. Typically, silver–titanium dioxide nanofibers (AgTiO₂ NFs) and silver–titanium dioxide nanoparticles (AgTiO₂ NPs) were individually incorporated in PU electrospun nanofibers to overcome the mandatory sophisticated separation of the nanocatalysts, which can create a secondary pollution, after the treatment process. These nanomembranes were characterized in SEM, TEM, XRD and UV studies. The polymeric electrospun nanofibers were smooth and continuous, with an average diameter of about 550 nm, and held their nanofibrous morphology even after more than 2 h of photocatalytic degradation of DE, due to the good stability of PU in the aqueous solutions, which indicates good imprisoning of the functional photocatalysts. The PU–AgTiO₂ NPs and PU–AgTiO₂ NFs were effective materials for degradation of DE, even after two successive cycles. PU–AgTiO₂ NPs and PU–AgTiO₂ NFs showed a maximum degradation of 75% and 95%, respectively after 2 h. The significant enhancement of degradation in the PU–Ag–TiO₂ NPs and PU–Ag–TiO₂ NFs is attributed to the photoactivity of Ag–TiO₂ material under visible light irradiation.