Improved photodegradation activity of TiO2 via decoration with SnS2 nanoparticles

The particles of TiO₂ modified with various amounts of SnS₂ nanoparticles (TiO₂/SnS₂) were synthesized via the hydrothermal method by reacting SnCl₄·5H₂O with thioacetamide in 5% (vol.) acetic acid aqueous solution in the presence of TiO₂. The obtained products were characterized by using X-ray diffraction, X-ray photoelectron spectroscopy, UV–Vis diffuse reflection spectra, scanning and transmission electron microscopy. The photodegradation activities of TiO₂/SnS₂ composites have been investigated by using methyl orange as target in water under the light irradiation of 250–400, 360–600 and 400–600 nm. It was found that the photodegradation activity of TiO₂/SnS₂ composites depended on the mass ratio of SnS₂ and the wavelength of the irradiating light. The composites containing 33% SnS₂ exhibited the maximum activity under the light irradiation of 250–400 and 360–600 nm. However, the more SnS₂ in the composites, the higher activity appeared under the irradiation of 400–600 nm light. All the results reveal that the composites possess much better activity than the pristine TiO_2.     

Composite hydroxyapatite/TiO2 materials for photocatalytic oxidation of NOx

Hydroxyapatite/TiO₂ composite photocatalysts were obtained from sol–gel prepared TiO₂ and commercial hydroxyapatite (HA) powders. Composites with different HA/TiO₂ ratio were studied to assess the influence of HA on the morphology and the photocatalytic behavior of the materials. Morphological SEM analysis revealed that the presence of HA diminishes the aggregation of TiO₂ particles and leads to their higher dispersion in the composites that was confirmed by the N₂ adsorption–desorption isotherms and Barret–Joyner–Halenda analysis. The photocatalytic activity of the prepared catalysts was examined by monitoring photocatalytic oxidation of NO_x model gases over catalysts under UV illumination. The NO_x oxidation over the composite catalysts was improved in comparison with pure TiO₂ powder. Moreover, the decrease of the TiO₂ content, which is the photocatalytically active component in the composites, resulted in enhanced NO_x removal. Maximum activity was recorded for composites with HA/TiO₂ ratios 1 and 2 that was related to improved TiO₂ dispersion and NO₂ trapping by the composite materials.     

One-pot synthesis of intestine-like SnO2/TiO2 hollow nanostructures

In the present study the intestine-like binary SnO₂/TiO₂ hollow nanostructures are one-pot synthesized in aqueous phase at room temperature via a colloid seeded deposition process in which the intestine-like hollow SnO₂ spheres and Ti(SO₄)₂ are used as colloid seeds and Ti-source, respectively. The novel core (SnO₂ hollow sphere)-shell (TiO₂) nanostructures possess a large surface area of 122 m²/g (calcined at 350 °C) and a high exposure of TiO₂ surface. The structural change of TiO₂ shell at different temperatures was investigated by means of X-ray diffraction and Raman spectroscopy. It was observed that the rutile TiO₂ could form even at room temperature due to the presence of SnO₂ core and the unique core-shell interaction.     

Solvothermal synthesis and photoluminescence properties of ZnO nanorods and nanorod assemblies from ZnO2 nanoparticles

Without the use of any extra surfactant or template, hexagonal phase ZnO crystallites consisting of individual nanorods or nanorod assemblies were synthesized simply by solvothermal treatment of several nanometer ZnO₂ nanoparticles in three different solvents (including ethanol, 80 wt.% hydrazine hydrate aqueous solution and ethylenediamine) at 150 °C for 24 h. The structures and optical properties of the resultant products were characterized by means of X-ray powder diffraction (XRD), scanning electron microscope (SEM), and room temperature photoluminescence (RTPL) spectra. The RTPL spectra of the resultant products all showed a much stronger ultraviolet bandgap emission peaking at around 387 nm and a weaker emission associated with the defect level. The as-synthesized ZnO crystallites are promising materials for the optoelectronic devices due to their excellent UV emission properties.     

Green hydrothermal synthesis and optical absorption properties of ZnO2 nanocrystals and ZnO nanorods

A green hydrothermal method was proposed for the controllable synthesis of ZnO₂ nanocrystals and ZnO nanorods, using the common and cost-effective 2ZnCO₃·3Zn(OH)₂ powder and 30 mass% H₂O₂ aqueous solution as the raw materials. The characterization results from X-ray diffraction, high resolution transmission electron microscopy, transmission electron microscopy and energy dispersive X-ray spectroscopy indicated that the products synthesized at 100-120 °C for 6 h or at 170 °C for 0 h were cubic phase ZnO₂ nanocrystals; while those synthesized at 170 °C for 3-6 h were hexagonal phase ZnO nanorods. The UV-vis absorption spectra showed that the as-synthesized ZnO₂ nanocrystals and ZnO nanorods had optical band gaps of about 4.1 and 3.3 eV, respectively.     

Colloidal synthesis of Sb2S3 nanorods/bars with strong preferred orientation

We report the synthesis of antimony trisulfide (Sb₂S₃) nanorods/bars via a simple, low-cost and colloidal synthetic method. The as-synthesized Sb₂S₃ nanorods/bars with different heating times from the moment of appearance of the Sb₂S₃ precipitate at 240 °C are the longest and thinnest in the beginning (diameters of 50-100 nm and lengths of 3-5 μm). UV/Vis absorption spectroscopy reveals that the optical band gap energy of the Sb₂S₃ nanorods/bars slightly decreases with increasing the heating times in the range of 1.54, 1.50 to 1.47 eV at the red part of the solar spectrum. The structure of Sb₂S₃ for all free samples was refined down to the R-factor of 9.57, 5.43 and 6.19%. The refinement showed that Sb₂S₃ powder belongs to the orthorhombic type with space group Pbnm (no. 62). It was found that Sb₂S₃ nanorods/bars predominantly grow along the [010] direction. The preferred orientation parameter (τ) refined against experimental data is quite high and is found to be 1.42, 1.21 and 1.19 for all three samples observed. A decrease in unit cell parameter b followed by increasing the heating times was observed.     

Low temperature synthesis and optical properties of CaTiO3 nanoparticles from Ca(NO3)2·4H2O and TiO2 nanocrystals

Choosing low-melting-point Ca(NO₃)₂·4H₂O and high-reactive-activity TiO₂ nanocrystals as the raw materials, a simple and cost-effective route was developed for the synthesis of CaTiO₃ nanoparticles at 600 °C, which is much lower than that (about 1350 °C) used in the conventional solid state reaction methods. X-ray diffraction, energy dispersive X-ray spectroscopy and field emission scanning electron microscopy revealed the formation of orthorhombic phase CaTiO₃ nanoparticles with oxygen-deficiency at the surface. UV-vis absorption spectrum of the as-obtained CaTiO₃ nanoparticles displayed an absorption peak centered at around 325 nm (3.8 eV), together with a tail at lower energy side. Room temperature photoluminescence spectrum of the as-obtained CaTiO₃ nanoparticles upon laser excitation at 325 nm demonstrated a strong and broad visible light emission ranging from about 527 to 568 nm, which may be originated from the surface states and defect levels.     

Synthesis of tapered TiO2 tubes by replication of ZnO

Micrometer-long tapered TiO₂ tubes have been successfully prepared by a vapor phase method, using tetrapodlike ZnO as template and tetrabutyl titanate (TBT) as titanium source. A very homogeneous TiO₂ coating layer was first prepared on tetrapodlike ZnO and the ZnO core was removed by hydrochloric acid solution. It was found that the obtained tubes were uniform and composed of anatase TiO₂ nanocrystallites. The wall thickness of the TiO₂ tubes varies from 20 to 60 nm by adjusting the amount of TBT. The BET surface area reaches 95 m² g^− 1. The combination of the tubular structure and special morphology may improve the mass transport and benefit to the recovery of the TiO₂ tubes photocatalyst from treated waste water.     

Microwave-assisted hydrothermal synthesis and optical property of Co3O4 nanorods

Single crystalline Co₃O₄ nanorods have been successfully synthesized through thermal decomposition of the precursor, which was obtained by the microwave-assisted hydrothermal route. The obtained sample was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectrometer (FT-IR), and X-ray photoelectron spectroscopy (XPS). The results confirm that the resulting oxide was pure single-crystalline Co₃O₄ nanorods. The optical property test indicates that the absorption peak of the nanorods shifts towards short wavelength. And the blue shift phenomenon might be ascribed to the quantum effect.     

Microwave assisted rapid synthesis of Bi2O3 short nanorods

In this research, a highly efficient and rapid approach of synthesizing Bi₂O₃ short nanorods is reported in aqueous solutions using microwave irradiation of bismuth (III) nitrate in the presence of Polyvinylpyrrolidone (PVP), as a stabilizing polymer. Transmission electron and field-emission scanning electron microscope images clearly indicate the formation of short nanorods in 6 min under microwave irradiation. Conventional heat treatment route yields only Bi₂O₃ powder and it is also comparatively complicated and needs high manufacturing cost. Formation of such short Bi₂O₃ nanorods may be due to the formation of a polymer-metal complex with the stabilizing polymer (PVP).     

Electrospun polymeric nanofibrous composites containing TiO2 short nanofibers

In this study, polymeric nanofibrous composites containing anatase TiO₂ short nanofibers (TiO₂-SNF) were successfully produced via electrospinning. The fabrication of the nanofibrous composite structure includes two steps. First, anatase TiO₂ nanofibers were obtained by calcination of electrospun PVP/TiO₂ nanofibers and then crushed into short nanofibers ranging from few microns in length. Second, these TiO₂-SNF were dispersed into polymer solutions and then electrospun into nanofibrous composites. We obtained nanofibers containing TiO₂-SNF from different polymer types including PMMA, PAN, PET and PC. The SEM and TEM imaging indicated that some of the TiO₂-SNF were fully covered by the polymeric matrix whereas some TiO₂-SNF were partially covered and/or stick on the surface of the fibers. The photocatalytic activity of nanofibrous composites containing TiO₂-SNF was evaluated by monitoring the photocatalytic decomposition of a model dye (rhodamine-6G) under UV irradiation.     

A three-dimensional electrode for photoelectrochemical cell: TiO2 coated ITO mesoporous film

In this letter, TiO₂ coated ITO mesoporous film was prepared by dipping doctor-blade ITO mesoporous film in TiO₂ sol, followed by sintering at 500 °C for 30 min. The CdS quantum dots (QDs) were deposited on TiO₂ coated ITO mesoporous film using sequential chemical bath deposition (S-CBD) method to form a three-dimensional (3D) electrode. The photo-activity of ITO mesoporous film/TiO₂/CdS electrode was investigated by forming a photoelectrochemical cell, which indicated that the ITO mesoporous film/TiO₂/CdS electrode was efficient in photoelectrochemical cell as a working electrode. The 3D electrode showed lower performance than the conventional electrode of TiO₂ mesoporous film/CdS, and more works are needed to improve the performance of 3D electrode.     

Nonaqueous sol-gel synthesis and growth mechanism of single crystalline TiO2 nanorods with high photocatalytic activity

In this paper, we report on a nonaqueous synthesis of single crystalline anatase TiO₂ nanorods by reaction between TiCl₄ and benzyl alcohol at a low temperature of 80 °C. The resulting samples were characterized with X-ray diffraction, scanning electron microscopy, transmission electron microscopy, high resolution transmission electron microscopy, nitrogen adsorption, X-ray photoelectron spectrometry and UV-vis diffuse reflectance spectroscopy. We proposed that the TiO₂ nanorods were formed through an oriented attachment mechanism. More importantly, these single crystalline anatase TiO₂ nanorods exhibited significantly higher photocatalytic activities than commercial photocatalyst P25. This study provides an environmentally friendly and economic approach to produce highly active TiO₂ photocatalyst.     

Facile and large-scale synthesis of hollow TiO2 nanostructures from TiCl3 solution

Hollow TiO₂ nanostructures were successfully synthesized by a hydrothermal process using TiCl₃ solution as Ti sources. The as-obtained product consists of quasi-spherical hollow nanostructures in the diameter of about 500 nm with anatase phase. The control experiments indicated that the synergism of H₂O₂ and KBF₄ plays an important role in the formation of hollow TiO₂ nanostructures. Compared with solid TiO₂ nanostructures, the photocatalytic property of hollow TiO₂ nanostructures has been markedly improved in degradation of methyl orange under UV light. This synthesis procedure is facile and thus promotes large-scale production of hollow TiO₂ nanostructures.     

Synthesis and photoluminescence properties of aligned Zn2GeO4 coated ZnO nanorods and Ge doped ZnO nanocombs

Aligned Zn₂GeO₄ coated ZnO nanorods and Ge doped ZnO nanocombs were synthesized on a silicon substrate by a simple thermal evaporation method. The structure and morphology of the as-synthesized nanostructure were characterized using scanning electron microscopy and transmission electron microscopy. The growth of aligned Zn₂GeO₄ coated ZnO nanorods and Ge doped ZnO nanocombs follows a vapor-solid (VS) process. Photoluminescence properties were also investigated at room temperature. The photoluminescence spectrum reveals the nanostructures have a sharp ultraviolet luminescence peak centered at 382 nm and a broad green luminescence peak centered at about 494 nm.     

Visible photoluminescence from Er-doped TiO2 nanofibres by electrospinning

Er³⁺-doped TiO₂ nanofibres were fabricated with electrospinning method followed by annealing in air at 420, 600, 800 and 1000 °C, respectively. The obtained nanofibres are relatively straight and have an average diameter of ∼ 75 nm. X-ray diffraction measurements showed that the crystal structure transforms from anatase to rutile phase with the increase of annealing temperature. Visible photoluminescence peaking at 528.1, 566.6 and 669.3 nm is detected which is ascribed to ²H_11/2 → ⁴I_15/2, ⁴S_3/2 → ⁴I_15/2 and ⁴F_9/2 → ⁴I_15/2 transitions of Er³⁺ ions and the PL intensities increase with the increase of annealing temperature. Meanwhile at high annealing temperatures, near-infrared photoluminescence peaking at 815 nm due to the defect states associated with Ti³⁺ ions is also found. The strong green photoluminescence of Er³⁺ ions may have potential applications in one-dimensional luminescent nanodevices.     

Hybrid photoelectrode by using vertically aligned rutile TiO2 nanowires inlaid with anatase TiO2 nanoparticles for dye-sensitized solar cells

We report a hybrid photoelectrode fabricated by using single crystalline rutile TiO₂ nanowires (NWs) inlaid with anatase TiO₂ nanoparticles (NPs) for efficient dye-sensitized solar cells. For this purpose, ∼4-μm-thick vertically aligned NWs were synthesized on the FTO glass substrate through a solvothermal treatment. Then, as-prepared NW film was treated with the NP colloidal dispersion to construct the NW–NP film. In particular, the NWs offer a fast pathway for electron transport as well as light scattering effect. On the other hand, the inlaid NPs give an extra amount of space for the dye-uptake. Accordingly, the present NW–NP electrode exhibited 6.2% of the conversion efficiency, which corresponds to ∼48% improvement over the efficiency of the NP-DSC. We attribute this notable result to the synergetic effects of the enhanced light confinement, charge collection, and dye-loading.     

Photoexcitation of TiO2 photoanode in water splitting

TiO₂ is one of the most promising photoanodes for solar-hydrogen conversion by water splitting. However, the solar-hydrogen efficiency of TiO₂ remains limited because of a low photocurrent generation. A clear understanding of photoexcitations within photoanodes can predict the quantity of photocurrent and consequently determine the solar-hydrogen efficiency. In this work, hydrothermally synthesized rutile TiO₂ nanorods were investigated for their photoelectrochemical (PEC) performance. A photogenerated hole concentration of TiO₂ photoanode was derived as 8.40 × 10¹⁴ cm⁻³ under one sun illumination. In addition, Fermi level pinning associated with high density of surface states was also observed under PEC operation. Base on these results, a series of band diagrams of TiO₂ photoanode were established to describe the photogeneration of holes and current at various bias potential. The main limitation of photocurrent generation is the distribution of surface-trapped states, which determines the hole concentration at the surface and consequently determines the open-circuit potential and the photocurrent density.     

Hydrothermal synthesis, characterization and properties of TiO2 nanorods on boron-doped diamond film

The rutile TiO₂ nanorods have been hydrothermally synthesized on boron-doped diamond (BDD) film with a ZnO buffer layer. It is demonstrated that the ZnO buffer layer plays a key role in increasing the density and improving the morphology of synthesized TiO₂ nanorods. The heterojunction of n-TiO₂ nanorods/p-BDD shows an evident rectifying behavior with a ratio of ∼ 180 at 6 V. Experimentally, the TiO₂ nanorod-covered BDD exhibits an improved electron field-emission property over that without using a ZnO buffer layer.     

Electrodeposition PbO2-TiO2 and PbO2-ZrO2 and its physicochemical properties

Composite materials based on PbO₂ containing TiO₂ or ZrO₂ were prepared from electrolytes containing a suspension of TiO₂ or ZrO₂. The contents of foreign oxides in the composite depend on the electrolyte composition and conditions of deposition. When a dispersed phase is incorporated into the composite coating, the dimensions of lead dioxide crystals decrease to submicro- and nano-size. Physico-chemical properties of composite materials are mainly determined by their chemical composition.