Enhanced properties for visible-light-driven photocatalysis of Ag nanoparticle modified Bi2MoO6 nanoplates

The visible light driven Bi₂MoO₆ photocatalyst doped with different contents of Ag nanoparticles was successfully synthesized by a combination of hydrothermal and sonochemical methods. The as-synthesized samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning and transmission electron microscopy (SEM and TEM) and UV–visible spectroscopy to investigate crystalline structure, morphology, composition and photocatalytic properties. XRD patterns and TEM images of the samples revealed pure phase orthorhombic Bi₂MoO₆ nanoplates without any detection of Ag dopant due to its low concentration and very tiny particle size. TEM images showed that Ag nanoparticles with the size of 10–15 nm were dispersed randomly on the surface of Bi₂MoO₆. The XPS analysis of Ag/Bi₂MoO₆ nanocomposites revealed the presence of additional metallic Ag. Photocatalytic activities of the Ag/Bi₂MoO₆ nanocomposites were evaluated by determining the degradation of rhodamine B (RhB) under visible light radiation. In this research, the 10 wt% Ag/Bi₂MoO₆ nanocomposites showed the best photocatalytic activity. The results suggest that the dispersion of Ag nanoparticles on the surface of Bi₂MoO₆ significantly enhances its photocatalytic activity.     

Photocatalytic Property and Electronic Structure of Lanthanide-based Oxysulfides

Lanthanide-based oxysulfides and sulfide, LnTaO_3.5S_0.5, Ln₁₀OS₁₄ (Ln = La, Pr, Nd, Sm) and La₄In₅S₁₃, were successively synthesized by sulfurization in a flowing H₂S. The sulfurization decreased the band-gap energies from >4 eV to <3eV, because of the formation of occupied S3p orbitals on the top of valence band. In accordance with the small band gap, the H₂ evolution from a 0.01 M Na₂S and 0.01 M Na₂SO₃ solution system was observed under irradiation of light up to >500 nm. The rate of H₂ evolution under light irradiation of >500 nm increased in the order of Ni/LaTaO_3.5S_0.5 < Ru/La₁₀OS₁₄ < Pt/La₄In₅S₁₃.     

PHOTOCATALYTIC OXIDATION OF ALDEHYDES/PCE USING POROUS ANATASE TITANIA AND VISIBLE-LIGHT-RESPONSIVE BROOKITE TITANIA

We have synthesized an annealed porous aerogel titania (LUAG2), which demonstrates a very high photocatalytic activity for aldehydes and perchloroethylene (PCE) photocatalytic oxidation (PCO) in gas phase under blacklight and fluorescent light irradiation. LUAG2 has a BET surface area of 237 m²/g and a porosity of 0.31 (volume fraction). X-ray diffraction (XRD) analysis shows LUAG2 is nearly pure anatase. It has improved the destruction of PCE and aldehydes as a group by 10-34% with black light compared to Degussa P-25. The optimum water vapor to butyraldehyde molar ratio is around 1/3. LUAG2 also shows better mineralization to CO₂ than Degussa P-25 TiO₂ does. Under irradiation of a 4 W fluorescent lamp LUAG2 gives a consistently higher conversion than that of Degussa P-25. The highly active photocatalyst indicates potential applications in indoor and outdoor environmental pollution control. A visible-light-responsive TiO₂, NTB 200, is also investigated for comparison purposes.     

Removal of paraquat in aqueous suspension of TiO<Subscript>2</Subscript> in an immersed UV photoreactor

Experiments were performed to investigate the effect of operating parameters on the photodegradation efficiency of paraquat in a TiO₂-suspended photoreactor with immersed UV lamps. TiO₂ particles were prepared by a hydrothermal method. The removal rate of paraquat in the reactor was 0.54 mg/l/h with only air-sparging. The removal rate in 24 h with both the UV radiation and air-sparging was 50% higher than that with only the UV radiation. Variations of the paraquat concentration at the UV intensities of 4 and 8 W/m₂ decreased slowly with time, but that at 12 W/m₂ decreased more rapidly. The removal efficiency at the air-sparging flow rate of 1 //min increased as a UV light intensity increased. pH value in the reactor at the UV intensity of 12 W/m₂ decreased with time until 12 h and then increased with time over 12 h.     

Photocatalytic effect of carbon-modified n-TiO2 nanoparticles under visible light illumination

The present research focused on wet process synthesis of visible light active carbon-modified (CM)-n-TiO₂ nanoparticles and their photocatalytic activity. The CM-n-TiO₂ was synthesized by hydrolysis of TiCl₄ in the presence of tetrabutylammonium hydroxide and also in the presence of glucose and sodium hydroxide. UV–vis spectra, X-ray diffraction (XRD), and FT-IR were used to characterize these photocatalysts. It was found that the CM-n-TiO₂ nanoparticles synthesized by hydrolysis with tetrabutylammonium hydroxide or with sodium hydroxide and glucose when subjected to extended aging and subsequent calcinations absorb well into the visible to near infrared region up to 800 nm and exhibit enhanced visible light photocatalytic activity on degradation of 4-chlorophenol. CM-n-TiO₂ synthesized using glucose as the carbon source generated 13-fold increase in the initial rate of photodegradation of 4-chlorophenol compared to those by regular n-TiO₂, whereas, it increased only eight-fold when tetrabutylammonium hydroxide was used as the carbon source.     

Immobilization of TiO2 nanoparticles on Fe-filled carbon nanocapsules for photocatalytic applications

Using a simple sol-gel method, a novel magnetic photocatalyst was produced by immobilization of TiO₂ nano-crystal on Fe-filled carbon nanocapsules (Fe-CNC). High resolution TEM images indicated that the immobilization of TiO₂ on Fe-CNC was driven primarily by heterogeneous coagulation, whereas surface nucleation and growth was the dominant mechanism for immobilizing TiO₂ on acid-functionalized hollow CNC. The TiO₂ immobilized on Fe-CNC exhibited the anatase phase as revealed by the X-ray diffraction (XRD) patterns. In comparison with free TiO₂ and TiO₂-coated CNC, TiO₂-coated Fe-CNC displayed good performance in the removal of NO gas under UV exposure. Due to the advantages of easy recycling and good photocatalytic efficiency, the novel magnetic photocatalyst developed here has potential use in photocatalytic applications for pollution prevention.     

Photocatalytic TiO2 films deposited by reactive magnetron sputtering with unipolar pulsing and plasma emission control systems

TiO₂ films with thickness of about 500 nm were deposited on unheated non-alkali glass substrates by reactive magnetron sputtering using one Ti metal target with unipolar pulsed powering of 50 kHz and the plasma emission feedback system (PCU). In order to keep the very high deposition rate, the depositions were carried out in the “transition region” between the metallic and the reactive (oxide) sputter mode where the target surface was metallic and oxidized, respectively. Stable deposition was successfully carried out in the whole “transition region” with PCU at total gas pressure of 3.0 Pa. All the as-deposited films deposited in the “transition region” showed amorphous structure, which performed very low photocatalytic activity. After the post-annealing in air at higher than 300 °C, all the films crystallized to anatase polycrystalline structure. They performed both photoinduced decomposition of acetaldehyde and photoinduced hydrophilicity under UV light illumination. The highest deposition rate in this study to deposit the photocatalytic TiO₂ films in the “transition region” was 90 nm/min, which was over twenty times higher than that for conventional sputter deposition processes.     

Photocatalytic property of SiO2/TiO2 nanoparticles prepared by sol-hydrothermal process

Silica-embedded nanocrystalline TiO₂ powders were synthesized by sol-hydrothermal process. The influence of the composition of the solvent and the embedded silica content on the phase transition, grain growth and subsequently, on the photoactivity of TiO₂ were investigated. The volume ratio of ethanol to water for the solvent composition was varied from 0.125 to 8 and the mole fraction of silica content was changed from 0 to 0.4, while the condition for hydrothermal reaction was fixed at 250^∘C for 2 hour. With an increase in ethanol content in solvent composition, the crystallite sizes of pure TiO₂ particles decreased from 15 nm to 6 nm and crystal phase changed from rutile/anatase mixed phase to pure anatase phase. Addition of silica to TiO₂ brought about an increase in the photocatalytic activity by suppressing the phase transition from anatase to rutile. Judging from the result of the decomposition of 1, 4-dichlorobenzene, the most efficient catalyst was found to be 0.2 mole fraction SiO₂ embedded TiO₂ prepared with ethanol-rich solvent (the volume ratio of ethanol to water is 4).     

"光触媒"抗菌镍金属网在中央空调上的应用

本文简要叙述光触媒(TiO2)在分解有害气体、杀菌的作用机理,以及复合"光催化"抗菌泡沫镍金属网在中央空调方面的应用情况.     

High photocatalytic activity over starfish-like La-doped ZnO/SiO_2 photocatalyst for malachite green degradation under visible light

In this work,the unique starlike La-doped ZnO-SiO2 photocatalysts were constructed by an evaporation and calcination method and characterized in detail.UV-vis reflectance and DFT calculation confirm that the doping with La allows to obtain a decrease of band gap of ZnO/SiO_2,which enhances visible light absorbance and oxidizing ability.The photoluminescence intensity reduces greatly,indicating more effective separation of the photo generated carriers of La-doped ZnO-SiO2.Photocatalytic activities of Ladoped ZnO-SiO2 with different doping ratios under simulated visible light irradiation were evaluated with malachite green(MG) as a model pollutant.Under optimized conditions including solution pH of 8,15 mg/L of MG solution and 15 mg of catalyst dosage,0.2% La-ZnO-SiO2 exhibits the best catalytic activity in photodegradations of MG in water.The removal and mineralization efficiency of MG can reach 96.1%and 70.9% in 140 min,respectively.The as-prepared catalysts present superior stability and recyclability after four times reuse.Moreover,selective quenching experiments indicate that hydroxyl radical(·OH),hole(h~+) and superoxide radical(·O_2~-) are the main reactive species responsible for MG degradation.Possible mechanism for photocatalytic elimination of MG over La-doped ZnO/SiO_2 photocatalyst is finally proposed.