Fabrication of Gold-Doped Titanium Dioxide (Tio2:Au) Nanofibers Photocatalyst by Vacuum Ion Sputter Coating

Gold-doped titanium dioxide (TiO₂:Au) nanofibers were prepared by a combination of an electrospinning method and sputtering technology and characterized by scanning electron microscopy and X-ray photoelectron spectroscopy. The results show that the morphologies of Au-deposited TiO₂ nanofibers can be well controlled by the sputtering time. The photocatalytic decomposition of acetaldehyde on TiO₂:Au nanofibers was investigated at room temperature. The photocatalytic effect of the TiO₂ nanofiber was improved by using the Au-doped titania nanofibers catalyst and increased as the Au depositing time was increased from 40 s to 3 min. The photocatalytic removal rate of acetaldehyde remained above 94% on the TiO₂:Au nanofibers (2 min) catalyst under ultraviolet (UV) irradiation for 70 min, 1.7 times that of pure TiO₂ fibers.     

Titanium dioxide-coated nanofibers for advanced filters

This article reports on titanium dioxide (TiO₂)-coated nanofibers deposited on a filter surface by the electrospinning process. After depositing a micrometer-thick film of polyamide 11 nanofibers on polypropylene fabric, TiO₂ nanoparticles can be directly electrosprayed onto the nanofibers. X-ray diffraction and Raman spectroscopy showed minimal change in the phase composition (anatase and rutile) and no change in the particle size of nanocrystalline TiO₂ after coating. Scanning electron microscopy demonstrated that nanofibers were uniformly coated by titanium dioxide nanoparticles without agglomeration. TiO₂-coated filters showed excellent photocatalytic-bactericidal activity and photo-induced hydrophilicity.     

Preparation and photoluminescence of single conjugated polymer–TiO2 composite nanofibers

TiO₂ nanoparticles were introduced into the soluble sulfonium precursor of PPV (Poly(p-phenylene vinylene)) during the synthesis procedure of precursor. Later, PPV–TiO₂ nanofibers were prepared by electrospinning of precursor–TiO₂ solution, followed by thermal conversion. The fluorescence microscopy images showed that the resulting nanofibers exhibited outstanding emission properties. No significant differences were observed in photoluminescence spectra of PPV–TiO₂ and PPV fibers. A single oriented PPV–TiO₂ nanofiber can be obtained on the substrate by a modified electrospinning method, which is favorable for some practical applications such as electrical and optical nanodevices.     

The potential use of nanosilver-decorated titanium dioxide nanofibers for toxin decomposition with antimicrobial and self-cleaning properties

While chemical and biological attacks pose risk to human health, clean air is of scientific, environmental and physiological concerns. In the present contribution, the potential use of nanosilver-decorated titanium dioxide (TiO₂) nanofibers for toxin decomposition with antimicrobial activity and self-cleaning properties was investigated. Titanium dioxide nanofibers were prepared through sol-gel reaction followed by an electrospinning process. Following the Japan Industrial Standard (JIS) protocol, decompositions of nitrogen oxide (NOx) and volatile organic compound (VOC) by the TiO₂ nanofibers suggested that these materials were capable of air treatment. To further enhance their anti-microbial activity, silver nanoparticles were decorated onto the TiO₂ nanofibers’ surfaces via photoreduction of silver ion in the presence of the nanofibers suspension. Furthermore, tests of photocatalytic activity of the samples were performed by photodegrading methylene blue in water. The nanofibrous membranes prepared from these nanofibers showed superhydrophilicity under UV. Finally, the possibility of using these hybrid nanofibers in environmental and hygienic nanofiltration was proposed, where the self-cleaning characteristics was expected to be valuable in maintenance processes.     

Thickness effect of the TiO2 nanofiber scattering layer on the performance of the TiO2 nanoparticle/TiO2 nanofiber-structured dye-sensitized solar cells

TiO₂ nanofibers (NFs) were fabricated by an electrospinning process and were used as scattering layers in dye-sensitized solar cells (DSSCs). The NF-coated photoanodes of the DSSCs were prepared with a variety of scattering layer thicknesses. The thickness effect of the scattering layer on the double-layered TiO₂ nanoparticle (NP)/TiO₂ NF structure was investigated through structural, morphological, and optical measurements. In the double-layered photoanode, the TiO₂ NP layer plays a major role in dye adsorption and light transmission, and the TiO₂ NF scattering layer improves the absorption of visible light due to the light scattering effects. The scattering effect of TiO₂ NFs layer was examined by the incident monochromatic photon-to-electron conversion efficiency (IPCE) and UV–Vis spectrometry. The conversion efficiency for the 12 μm-thick photoanode composed of a 2 μm-thick TiO₂ NF layer and 10 μm-thick TiO₂ NP layer was higher than that of DSSCs with only TiO₂ NPs photoanode by approximately 33%.     

Highly Active TiO2/Polyelectrolytes Hybrid Multilayered Hollow Nanofibrous Photocatalyst Prepared from Electrouspun Fibers Using Electrostatic Layer-by-Layer Technique

Compared to conventional film photocatalysts, fiber photocatalyst has a greater surface-to-volume ratio and a 3-D open structure that allows its surface active sites to be accessible for reactants more easily and effectively. However, TiO ₂ powder (Degussa P25), by itself, cannot be prepared in the form of fibers, but with the help of a polymer nanofiber, TiO ₂ particles can be immobilized in a fibrous network of polyelectrolyte. Here, hybrid multilayered hollow nanofibers (HMHNFs) composed of TiO ₂ /polyelectrolyte (PE) have been prepared by a combination of a electrospinning method and layer-by-layer (LBL) technology. The results show that both the average diameter and the wall thickness of the HMHNFs can be well controlled by the template, as well as the number of coating layers. The dried morphology of the obtained HMHNFs is dependent on the inner deposited numbers of the polyelectrolyte layers. When compared with other nanostructured TiO ₂ materials, such as commercial TiO ₂ nanoparticles (P25, Degussa) and TiO ₂ films, the hollow TiO ₂ /PE hybrid nanofibers exhibited higher photocatalytic activities.     

Study of SiRNA-loaded PS-mPEG/CaP nanospheres on lung cancer

The TiO₂/BiOI heterostructured nanofibers were prepared by electrospinning–solvothermal two-step process. The BiOI nanosheets, which owned a thickness of tens of nanometers and an average side length of about 300 nm, were intensive and crossed arranging on the TiO₂ nanofibers whose diameter was about 400–550 nm and length was about 15–45 μm. The absorption edge of TiO₂/BiOI heterostructured nanofibers was extended to more than 600 nm in visible-light region and the TiO₂/BiOI exhibited enhanced visible-light photocatalytic performance and excellent recyclability compared to the individual TiO₂ nanofibers and the BiOI microflowers in the photodecomposition of methylene blue, which was ascribed to nanoscale size heterostructure, narrow energy band, peculiar band gap structures, and porous surface structure.     

Electrochemical properties of TiO2 nanoparticle/nanorod composite photoanode for dye-sensitized solar cells

A unique composite of TiO₂ nanoparticles (NPs) and nanorods (NRs) has been used to fabricate a photoelectrode for developing dye-sensitized solar cells (DSSCs) with higher sensitivity. The TiO₂ nanorods were synthesized using a mechanical process, in which electrospun TiO₂ nanofibers was grinded in a controlled way to obtain uniform size distribution. The characteristics of electron transport, recombination lifetime and charge collection were investigated by intensity-modulated photocurrent spectroscopy (IMPS) and intensity-modulated photovoltage spectroscopy (IMVS). Photoelectrodes prepared with the composites of NRs and NPs showed significant improvements in electron transportation compared to only NP photoelectrodes, which would enhance the photovoltaic performance of DSSCs. IMPS and IMVS measurements show that fast electron transport and slightly decreased recombination lifetime resulted in the improvement of efficiency. The highest energy conversion efficiency obtained from the photoelectrodes fabricated with the as-prepared rutile TiO₂ nanofibers at 5 wt% NR content was up to 6.1% under AM1.5G solar illumination. The results demonstrate that the composite nanostructure can take advantage of both the fast electron transport of the nanorods and the high surface area of the nanoparticles.     

Synthesis and characterization of silver/lithium cobalt oxide (Ag/LiCoO2) nanofibers via sol–gel electrospinning

We report on the preparation and characterization of Ag/LiCoO₂ nanofibers (NFs) via the sol–gel electrospinning (ES) technique. Ag nanoparticles (NPs) were produced in an aqueous polyvinyl pyrrolidone (PVP) solution by using AgNO₃ precursor. A viscous lithium acetate/cobalt acetate/polyvinylalcohol/water (LiAc/(CoAc)₂/PVA/water) solution was prepared separately. A Ag NPs/PVP/water solution was prepared and added to this viscous solution and magnetically stirred to obtain the final homogeneous electrospinning solution. After establishing the proper electrospinning conditions, as-spun precursor Ag/LiAc/Co(Ac)₂/PVA/PVP NFs were formed and calcined in air at a temperature of 600 °C for 3 h to form well-crystallized porous Ag/LiCoO₂ NFs. Various analytical characterization techniques such as UV–vis, SEM, TEM, TGA, XRD, and XPS were performed to analyze Ag NPs, as-spun and calcined NFs. It was established that Ag NPs in the precursor Ag/LiAc/Co(Ac)₂/PVA/PVP NFs are highly self-aligned as a result of the behavior of Ag in the electric field of the electrospinning setup and the interaction of Ag ions with Li and Co ions in the NF. Ag/LiCoO₂ NFs exhibit a nanoporous structure compared with un-doped LiCoO₂ NFs because the atomic radius of Ag is larger than the radius of Co and Li ion; thus, no substitution between Ag and Li or Ag and Co atoms occurs, and Ag NPs are located at the interlayer of LiCoO₂ while some are left in the fiber.     

Enhanced photocatalytic degradation of organic dyes by ultrasonic-assisted electrospray TiO2/graphene oxide on polyacrylonitrile/β-cyclodextrin nanofibrous membranes

Polyacrylonitrile (PAN)/β-cyclodextrin (β-CD) composite nanofibrous membranes immobilized with nano-titanium dioxide (TiO₂) and graphene oxide (GO) were prepared by electrospinning and ultrasonic-assisted electrospinning. Scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM), and X-ray diffraction (XRD) confirmed that TiO₂ and GO were more evenly dispersed on the surface and inside of the nanofibers after 45 min of ultrasonic treatment. Adding TiO₂ and GO reduced the fiber diameter; the minimum fiber diameter was 84.66 ± 40.58 nm when the mass ratio of TiO₂-to-GO was 8:2 (PAN/β-CD nanofibrous membranes was 191.10 ± 45.66 nm). Using the anionic dye methyl orange (MO) and the cationic dye methylene blue (MB) as pollutant models, the photocatalytic activity of the nanofibrous membrane under natural sunlight was evaluated. It was found that PAN/β-CD/TiO₂/GO composite nanofibrous membrane with an 8:2 mass ratio of TiO₂-to-GO exhibited the best degradation efficiency for the dyes. The degradation efficiency for MB and MO were 93.52 ± 1.83% and 90.92 ± 1.52%, respectively. Meanwhile, the PAN/β-CD/TiO₂/GO composite nanofibrous membrane also displayed good antibacterial properties and the degradation efficiency for MB and MO remained above 80% after 3 cycles. In general, the PAN/β-CD/TiO₂/GO nanofibrous membrane is eco-friendly, reusable, and has great potential for the removal of dyes from industrial wastewaters.     

In situ Radical Copolymerization in Presence of Surface‐Modified TiO2 Nanoparticles: Influence of a Double Modification on Properties of Unsaturated Polyester (UP) Nanocomposites

In the preparation of nanocomposites, there is competition between the dispersion of nanoparticles and the formation of agglomerates. In this study, radical copolymerization of ethyl acrylate and methyl methacrylate initiated by 2,2‐azobis (isobutyro) nitrile (AIBN) was performed, in the presence of titanium oxide (TiO₂) nanoparticles modified in a new approach; a good dispersion of the nanoparticles in the unsaturated polyester (UP) matrix was obtained. The TiO₂ nanoparticles were exposed to 3‐(methacryloxy) propyl trimethoxy silane as the coupling agent. The presence of coupling agent‐grafted TiO₂ nanoparticles in the copolymerization process resulted in the formation of a polymeric layer on the surface of the TiO₂ nanoparticles (doubly modified‐TiO₂). The grafting of coupling agent molecules and consequently copolymer macromolecular chains onto the surface of TiO₂ nanoparticles was investigated using Fourier transform infrared (FTIR) analysis. It found that the formation of an acrylate layer on the surface of nanoparticles was successful. Then, unsaturated polyester (UP)/TiO₂ nanocomposites were prepared. The morphology was studied using transmission electron microscopy (TEM). Mechanical properties and ultraviolet visible (UV/VIS) spectroscopy of various samples, including the doubly modified‐TiO₂ nanoparticles, with different nanoparticle inclusions and the unmodified‐TiO₂ nanoparticles, were also investigated. The results showed the doubly modified‐TiO₂ nanoparticles, compared to those of unmodified‐TiO₂, had better nanoparticle dispersion causing improvement in the mechanical properties and UV shielding.     

Electrical characterization of nylon-6 composite nanofibers

The electrical characteristics of nylon-6 nanofibers incorporated with TiO₂ and Fe₃O₄ nanoparticles were investigated. The resultant nanofibers exhibited good incorporation of nanoparticles. The impregnated TiO₂ and Fe₃O₄ nanoparticles into the nylon-6 nanofibers were confirmed by high resolution transmission electron microscopy (HR-TEM) and energy dispersive X-ray (EDX) spectroscopy studies. The electrical conductivity of the nylon-6 incorporated with TiO₂ and Fe₃O₄ composite nanofibers were higher than that of the pristine nylon-6 nanofibers. The impregnation of TiO₂ and Fe₃O₄ nanoparticles significantly enhanced the electrical property of the composite nanofibers. These polymeric/nanoparticles composite nanofibers structure may open a new direction for future organic electronics.     

Nanocomposite fabric formation by electrospinning and electrospraying technologies

Electrospraying and electrospinning processes were employed for the production of nanocomposite material of polymer nanofibers blended with nanoparticles. The diameter of polymer nanofibers made of PVC, PSU or nylon was smaller than 500 nm. Metal oxide nanoparticles of TiO₂, MgO, and Al₂O₃ of the size 20–100 nm suspended in methanol were deposited on the polymer nanofibers. Three configurations of electrospray/electrospun nozzles used for the nanocomposite production were tested: 1. simultaneous electrospraying during the electrospinning process, 2. electrospraying onto the same rotating drum after the electrospinning is completed, and 3. electrospraying onto the electrospun mat removed from the drum and placed onto a heated table.     

Fabrication of hydroxyapatite and TiO2 nanorods on microarc-oxidized titanium surface using hydrothermal treatment

AC-type microarc oxidation (MAO) and hydrothermal treatment techniques were used to enhance the bioactivity of commercially pure titanium (CP-Ti). The porous TiO₂ layer fabricated by the MAO treatment had a dominant anatase structure and contained Ca and P ions. The MAO-treated specimens were treated hydrothermally to form HAp crystallites on the titanium oxide layer in an alkaline aqueous solution (OH-solution) or phosphorous-containing alkaline solution (POH-solution). A small number of micro-sized hydroxyapatite (HAp) crystallites and a thin layer composed of nano-sized HAps were formed on the Ti-MAO-OH group treated hydrothermally in an OH-solution, whereas a large number of micro-sized HAp crystallites and dense anatase TiO₂ nanorods were formed on the Ti-MAO-POH group treated hydrothermally in a POH-solution. The layer of bone-like apatite that formed on the surface of the POH-treated sample after soaking in a modified simulated body fluid was thicker than that on the OH-treated samples.     

Surface modification of PMMA/O-MMT composite microfibers by TiO2 coating

In the present work, poly(methyl methacrylate) (PMMA)/organically modified montmorillonite (O-MMT) composite microfibers were firstly prepared by emulsion polymerization combined with electrospinning, and then coated by nanosize titanium dioxide (TiO₂) using RF magnetron sputter technique. The modified surfaces of PMMA/O-MMT composite microfibers were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), UV-vis spectroscopy and drop shape analyzer. Finally, the photocatalytic properties of TiO₂ coated PMMA/O-MMT composite microfiber membranes were evaluated by degradation of methylene blue(MB) under UV illumination. The experimental results revealed that anatase-TiO₂ and rutile-TiO₂ nanoparticles were well spread and physically deposited on the surface of PMMA/O-MMT microfibers, and the wettability of the PMMA/O-MMT composite microfibers was improved after surface modification by sputter coating. Furthermore, the PMMA/O-MMT microfibers membrane coated with TiO₂ performed well in photocatalytic degradation of MB.     

Comparing the Contribution of Visible‐Light Irradiation,Gold Nanoparticles,and Titania Supports in Photocatalytic Nitroaromatic Coupling and Aromatic Alcohol Oxidation

Under visible‐light irradiation, gold nanoparticles (Au NPs) supported by titania (TiO₂) nanofibers show excellent activity and high selectivity for both reductive coupling of nitroaromatics to corresponding azobenzene or azoxylbenzene and selective oxidation of aromatic alcohols to corresponding aldehydes. The Au NPs act as active centers mainly due to their localized surface plasmon resonance (LSPR) effect. They can effectively couple the photonic energy and thermal energy to enhance reaction efficiency. Visible‐light irradiation has more influence on the reduction than on the oxidation, lowering the activation energy by 24.7 kJ mol^?1 and increasing the conversion rate by 88% for the reductive coupling, compared to merely 8.7 kJ mol^?1 and 46% for the oxidation. Furthermore, it is found that the conversion of nitroaromatics significantly depends on the particle size and specific surface area of supported Au NPs; and the catalyst on TiO₂(B) support outperforms that on anatase phase with preferable ability to activate oxygen. In contrast, for the selective oxidation, the effect of surface area is less prominent and Au NPs on anatase exhibit higher photo‐catalytic activity than other TiO₂ phases. The catalysts can be recovered efficiently because the Au NPs stably attach to TiO₂ supports by forming a well‐matched coherent interface observed via high‐resolution TEM.     

Preparation and Characterization of Nano‐TiO2 Doped Polystyrene Materials by Melt Blending for Inertial Confinement Fusion

Abstract

Nano‐TiO₂ doped polystyrene (PS) materials (TiO₂‐d‐PS) used for inertial confinement fusion (ICF) targets were prepared by means of melt blending. The effect of the pretreatment process, including coupling agents and ultrasonic dispersion on nano‐TiO₂, was studied. Tensile tests were conducted to evaluate the mechanical properties of the TiO₂‐d‐PS materials. Scanning electron microscopy (SEM) combined with energy dispersive spectroscopy (EDS) was used to characterize the degree of dispersion of nano‐TiO₂ in the PS matrix. Transmission electron microscopy (TEM) and dynamic contact angle (DCA) measurements were introduced to demonstrate the surface state of untreated and pretreated nano‐TiO₂. The results showed that coupling agents improved the interfacial adhesion between the PS matrix and dopants; ultrasonic dispersion contributed to the increase in the tensile properties of the TiO₂‐d‐PS materials. The dispersion stability of nano‐TiO₂ powder and the stability of the TiO₂‐d‐PS materials were significantly enhanced through pretreatment, which was supported by the increase in the DCA when the nano‐TiO₂ was pretreated by the coupling agent. The results of SEM and EDS indicated that the nano‐TiO₂ dispersed homogeneously in the PS matrix. The pretreatment process is an effective way to break the aggregation of nano‐TiO₂, which was confirmed by TEM results. Melt blending is a feasible method to prepare PS doped high Z element ICF target materials.     

Effect of Nb doping on morphology,crystal structure,optical band gap energy of TiO2 thin films

Nb–TiO₂ nanofibers and thin films were prepared using a sol–gel derived electrospinning and spin coating, respectively, by varying the Nb/Ti molar ratios from 0 to 0.59 to investigate the effect of Nb doping on morphology, crystal structure, and optical band gap energy of Nb–TiO₂. XRD results indicated that Nb–TiO₂ is composed of anatase and rutile phases as a function of Nb/Ti molar ratio. As the Nb/Ti molar ratio rose, the anatase to rutile phase transformation and the reduction in crystallite size occurred. The band gap energy of Nb–TiO₂ was changed from 3.25 eV to 2.87 eV when the anatase phase was transformed to rutile phase with increasing the Nb doping. Experimental results indicated that the Nb doping was mainly attributed to the morphology, the crystal structure, the optical band gap energy of Nb–TiO₂, and the photocatalytic degradation of methylene blue.     

Synthesis and characterisations of Au-nanoparticle-doped TiO2 and CdO thin films

In the present study, pure and gold nanoparticle (Au NP)-doped titanium dioxide (TiO₂) and cadmium oxide (CdO) thin film were prepared by the sol–gel method, and the effect of Au NP doping on the optical, structural and morphological properties of these thin films was investigated. The prepared thin films were characterised by X-ray diffraction (XRD), scanning electron microscopy (SEM) and ultraviolet–visible–near infrared (UV–Vis–NIR) spectra. While the optical band increases from 3.62 to 3.73 for TiO₂ thin films, it decreases from 2.20 to 1.55 for CdO thin films with increasing Au doping concentration. Analysis of XRD indicates that the intensities of peaks of the crystalline phase have increased with the increasing Au NP concentrations in all thin films. SEM images demonstrate that the surface morphologies of the samples were affected by the incorporation of Au NPs. Consequently, the most significant results of the present study are that the Au NPs can be used to modify the optical, structural and morphological properties of TiO₂ and CdO thin films.     

Targeted sonocatalytic cancer cell injury using avidin-conjugated titanium dioxide nanoparticles

In this study, we applied sonodynamic therapy to cancer cells based on the delivery of titanium dioxide (TiO₂) nanoparticles (NPs) modified with avidin protein, which preferentially discriminated cancerous cells from healthy cells. Subsequently, hydroxyl radicals were generated from the TiO₂ NPs after activation by external ultrasound irradiation (TiO₂/US treatment). Although 30% of the normal breast cells (human mammary epithelial cells) exhibited the uptake of avidin-modified TiO₂ NPs, over 80% of the breast cancer cells (MCF-7) exhibited the uptake of avidin-TiO₂ NPs. Next the effect of the TiO₂/US treatment on MCF-7 cell growth was examined for up to 96 h after 1-MHz ultrasound was applied (0.1 W/cm², 30 s) to cells that incorporated the TiO₂ NPs. No apparent cell injury was observed until 24 h after the treatment, but the viable cell concentration declined to 68% compared with the control at 96 h.