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1.
Shuang SongCheng Wang Fangyue HongZhiqiao He Qiaolan CaiJianmeng Chen 《Applied Surface Science》2011,257(8):3427-3432
Visible-light-driven TiO2-based catalysts for the degradation of pollutants have become the focus of attention. In the present work, iodine-doped titania photocatalysts (I-TiO2) were improved by doping with gallium (Ga,I-TiO2) and the resulting physicochemical properties and photocatalytic activity were investigated. The structural properties of the catalysts were determined by X-ray diffraction, UV-vis diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, Brunauer-Emmett-Teller analysis and transmission electron microscopy. We found that Ga probably enters the TiO2 framework for doping levels <0.5 mol%. A further increase in Ga content probably leads to dispersal of excess Ga on the TiO2 surface. The photocatalytic activity of Ga,I-TiO2 catalysts was evaluated using 2-chlorophenol (2-CP) as a model compound under visible and UV-vis light irradiation. The results indicate that 0.5 mol% Ga loading and calcination at 400 °C represent optimal conditions in the calcining temperature range 400-600 °C and with doping levels from 0.1% to 1 mol%. The effective enhancement of 2-CP degradation might be attributed to the formation of oxygen vacancies by Ga doping, which could decrease the recombination of electron-hole pairs. 相似文献
2.
We report the deposition of thin zirconium dioxide films on Si(1 0 0) by a technique of ultraviolet-assisted injection liquid source chemical vapor deposition (UVILS-CVD) by using ultraviolet with 222 nm radiation. The alkoxide zirconium(IV) tert-butoxide (Zr[OC(CH3)3]4) was used as precursor while nitrous oxide was driven into the reaction chamber as an oxidizing agent. The ZrO2 films were deposited under various conditions and characterized by ellipsometry, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction and scanning electron microscopy. The growth rate decreased with the increasing of substrate temperatures from 200 to 400 °C. Deposition rate of 20 nm/min was observed at a substrate temperature of 350 °C. There was a liner relation between the thicknesses of the films and deposition times. As a result the thicknesses can be accurately controlled by changing the number of drops of precursor introduced by the injection liquid source. The growth rate increased with the increasing concentrations of the precursor, nevertheless the trend stopped when the concentration exceeded 8.5%. The growth kinetics were also studied and the results were fit to a three-step kinetic model involving a photo chemical reaction, a reversible precursor absorption process and a following irreversible deposition reaction. 相似文献
3.
The novel visible-light-activated La/I/TiO2 nanocomposition photocatalyst was successfully synthesized using precipitation-dipping method, and characterized by X-ray powder diffraction (XRD), the Brunauer-Emmett-Teller (BET) method, transmission electron microscopy (TEM), thermogravimetry-differential scanning calorimetry (TG-DSC) and UV-vis diffuse reflectance spectroscopy (UV-vis DRS). The photocatalytic activity of La/I/TiO2 was evaluated by studying photodegradation of reactive blue 19 as a probe reaction under simulated sunlight irradiation. Photocatalytic experiment results showed that the maximum specific photocatalytic activity of the La/I/TiO2 photocatalyst appeared when the molar ratio of La/Ti was 2.0 at%, calcined at 350 °C for 2 h, due to the sample with good crystallization, high BET surface area and small crystal size. Under simulated sunlight irradiation, the degradation of reactive blue 19 aqueous solution reached 98.6% in 80 min, which showed La/I/TiO2 photocatalyst to be much higher photocatalytic activity compared to standard Degussa P25 photocatalyst. The higher visible light activity is due to the codoping of lanthanum and iodine. 相似文献
4.
R. RamakrishnanS. Kalaivani J. Amala Infant JoiceT. Sivakumar 《Applied Surface Science》2012,258(7):2515-2521
TiO2 although considered a promising photocatalyst for the degradation of aqueous pollutants, it suffers from poor absorption in the visible region and hence requires ultraviolet (UV) light for activation. To make TiO2 a visible active photocatalyst, multielement (C, N, B, and F) doping has been done. The synthesised CNBF/TiO2 catalysts were calcined at different temperatures and characterized by XRD, BET surface area, UV DRS, XPS, HRSEM-EDAX, and TEM techniques. These catalysts found to show less band gap values when compared to bare TiO2. These catalysts were tested for their catalytic activity towards the degradation of a textile dye - congo red (CR) under different reaction conditions. It was found that the photocatalytic activity was dependent on both doping of multielement and the calcination temperature of CNBF/TiO2. The co-doped catalysts which were calcined at 400 °C and 600 °C (100% intensity in anatase phase) were found to be the best catalysts (100% decolourisation of CR in 21/2 h and 2 h respectively). TOC analysis carried out for the samples at the reaction time of 5 h showed very high percentage (83%) degradation of CR over CNBF/TiO2 catalysts calcined at 600 °C when compared to the other catalysts calcined at different temperatures. CNBF/TiO2 (1000 °C) showed very less photocatalytic activity due to the formation of rutile phase. 相似文献
5.
Well-ordered TiO2 nanotube arrays were prepared by electrochemical anodization of titanium in aqueous electrolyte solution of H3PO4 + NH4F at a constant voltage of 20 V for 3 h, followed by calcined at various temperatures. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS) and Photoluminescence (PL) were used to characterize the samples. The results showed that the as-prepared nanotube arrays before being calcined were amorphous and could transform to anatase phase at a heat treatment temperature higher than 400 °C. As the calcination temperatures increased, crystallization of anatase phase enhanced and rutile phase appeared at 600 °C. However, further increasing the calcination temperature would cause the collapse of nanotube arrays. PL intensity of the nanotube arrays annealed at 500 °C was the lowest, which was probably ascribed to better crystallization together with fewer surface defects of the nanotube arrays. 相似文献
6.
D.G. Huang S.J. Liao S.Q. Quan Z.J. He 《Journal of Physics and Chemistry of Solids》2009,70(5):853-692
Sm- and nitrogen-co-doped TiO2 (Sm-N-TiO2) catalysts were prepared via the modified hydrothermal method using tetrabutyl titanate as the precursor and calcination at 200 °C. The microstructure of the sample was characterized by X-ray diffraction (XRD), ultraviolet-visible diffuse reflection spectroscopy (UV-vis-DRS), Fourier transform infrared (FTIR) spectra and X-ray photoelectron spectroscopy (XPS). The average particle size was ca. 16.0 nm as calculated from XRD patterns. Sm-N-TiO2 nanocrystalline showed strong visible-light response and high photocatalytic activity for 4-chlorophenol degradation under irradiation by visible-light (400-500 nm). The high visible-light photocatalytic activity of the obtained Sm-N-TiO2 might result from the incorporation of nitrogen atoms in TiO2, which extended the spectral response to the visible region, and Sm2O3 facilitated the excited electron transfer and hence suppressed efficiently the recombination of photoproduced electron-hole. 相似文献
7.
Xiaojing Wang Yujuan Chen Guohua Zhao Yafei Liu Zubiao Wen 《Applied Surface Science》2009,255(7):3953-3958
TiO2 photocatalysts deposited on activated carbon (TiO2/AC) were prepared by dip-hydrothermal method at 180 °C using peroxotitanate as a precursor, then calcinated at 300-800 °C. The samples were characterized by X-ray diffraction, scanning electron microscopy, Raman spectroscopy and the nitrogen absorption. Their photocatalytic activity was evaluated by degradation of methyl orange (MO). The results showed that TiO2 particles of anatase type were well deposited on the activated carbon surface. TiO2/AC calcinated at 600 °C exhibited the best photocatalytic performance. For the comparison, the same photocatalysis experiment was carried out for two mixtures of commercial TiO2 (Degussa P25) with AC and synthetic TiO2 with AC. It was found that the composite catalyst TiO2/AC was better than the two mixtures. Besides, different from fine powdered TiO2, the granular TiO2/AC photocatalysts could be easily separated from the bulk solution and reused; indeed, its photocatalytic ability was hardly decreased after a five-cycle for MO degradation. The kinetics of the MO degradation fitted well the Langmuir-Hinshelwood model. 相似文献
8.
We report the characterization of nano-size zinc oxide (ZnO) powder synthesized via microwave-assisted heating of Zn(CH3COO)2·2H2O and NaHCO3 solution with deionized water (DI water) as the solvent. The as-synthesized ZnO powder was calcined at temperatures from 400 to 800 °C for 8 h. The X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR) spectra revealed pure wurtzite structure for the ZnO nanopowder (NP) calcined at 800 °C. Scanning electron microscopy (SEM) images showed increasing size ZnO NP with uniform size distribution with increase in calcination temperature. Significant UV emission at about 373 nm has been observed in the photoluminescence (PL) spectra of the as-synthesized and calcined ZnO NP. Our results showed enhanced PL intensity with a reduced full-width at half-maximum (FWHM) for ZnO NP synthesized at higher calcination temperature. 相似文献
9.
Gaoke Zhang Fan Lü Junling Yang Baibiao Huang 《Journal of Physics and Chemistry of Solids》2010,71(4):579-159
Nanometer Bi2WO6 catalyst with visible-light responsive was prepared by a sol-gel method in the presence of EDTA. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectrum, Fourier transform infrared (FTIR) spectrum, Brunauer-Emmet-Teller (BET). The UV-vis diffuse reflectance spectrum of the as-prepared sample shows a markedly blue-shift as compared to that of the sample obtained by a solid-state reaction. The as-prepared samples exhibited higher activities than that synthesized by the solid-state reaction for 4BS photodegradation under visible-light irradiation (λ>400 nm) and the sample prepared at 450 °C exhibited the highest photocatalytic activity. 相似文献
10.
Yanyan Zhang Haibin Yang Qi Qi Tong Zhang Guangtian Zou 《Applied Surface Science》2008,254(17):5545-5547
The highly ordered TiO2 thin films are prepared by anodic oxidation and calcined at 300, 400, 500 and 600 °C, respectively. X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM) are employed to analyze the structure and the morphology of the TiO2 films. We design a novel sensor to investigate the humidity sensing behaviours of the samples. The samples calcined at 600 °C show high sensitivity with nearly two orders change in the resistance and short response and recovery time (<190 s) during the relative humidity variation from 11 to 95%. 相似文献
11.
Kangle Lv Jiaguo Yu Kejian Deng Mei Li 《Journal of Physics and Chemistry of Solids》2010,71(4):519-6235
To study the relationship between the phase structures of TiO2 and the photoinduced hydroxyl radicals (OH), TiO2 nanocrystallines were synthesized by a hydrolysis-precipitate method using tetrabutylorthotitanate (TBOT) as precursor, and then calcined at 450, 600, 700, 800 and 900 °C for 2 h, respectively. The calcined samples were characterized by X-ray diffraction and N2 sorption. The formation rate of OH on the surface of UV-illuminated TiO2 was detected by the photoluminescence (PL) technique using terephthalic acid as a probe molecule. The results show that with increasing calcined temperatures, the amorphous (Am) TiO2 precursor begins to turn into anatase (A) at 450 °C and rutile (R) phase appears at 600 °C, which is completely turned into the rutile phase at 900 °C. The BET specific surface areas of the catalyst decrease as the calcined temperatures increase. TiO2 sample calcined at 600 °C, with a mixed phase of anatase and rutile, shows the highestOH formation rate, and the order of the OH formation rate is as follows: A+R>A>R>Am. Phase structures of TiO2 play a more important role than specific surface areas in the OH formation rate. Two phase structure of anatase and rutile with a proper ratio is beneficial to the OH formation due to decrease of the combination rate of photo-generated electrons and holes. Our experimental result implies that the mixed phase of anatase and rutile can markedly enhance the photocatalytic activity of TiO2. 相似文献
12.
The physicochemical, surface and catalytic properties of pure and doped 0.25CuO-NiO solids prepared by sol-gel method were investigated. The dopant concentration was 2, 4 and 6 mol% ZrO2. The solids investigated were calcined at 400 and 600 °C. The techniques employed were XRD, EDX, TEM, surface excess oxygen, nitrogen adsorption at −196 °C and catalytic oxidation of CO by O2 using both static and flow methods. The results revealed that the investigated system dissolved 4 mol% ZrO2 by heating at 400 °C. This process was accompanied by a significant increase in the SBET and Vp with subsequent decrease in the (r) values of the doped adsorbent. ZrO2-doping of the system investigated followed by calcination at 400 and 600 °C led to a considerable increase in its catalytic activity in CO oxidation by O2 using static and flow methods. The doping process was not accompanied by any change in the activation energy of the catalyzed reaction. 相似文献
13.
Jing Yang 《Applied Surface Science》2006,253(4):1988-1994
To use solar irradiation or interior lighting efficiently, we sought a photocatalyst with high reactivity under visible light. Nitrogen and carbon doping TiO2−x−yNxCy films were obtained by heating the TiO2 gel in an ionized N2 gas and then were calcined at 500 °C. The TiO2−x−yNxCy films have revealed an improvement over the TiO2 films under visible light (wavelength, 500 nm) in optical absorption and photocatalytic activity such as photodegradation of methyl orange. X-ray photoemission spectroscopy, infrared spectrum and UV-visible (UV-vis) spectroscopy were used to find the difference of two kinds of films. Nitrogen and carbon doped into substitutional sites of TiO2 has been proven to be indispensable for band-gap narrowing and photocatalytic activity. 相似文献
14.
The anatase-TiO2 transparent films, containing 3 mol% of Si and P elements (as dopants), were synthesized using a process combining the sol-gel method and spin-coating technique. Effects of relative ratio of dopants and calcination temperature on phase transformation, grain growth, surface morphology, light transmittance, band-gap energy and photocatalytic activity of the P/Si-TiO2 films were examined and their results were compared with those of the undoped-TiO2 and Si-TiO2 films. The P/Si-TiO2 films calcined at temperature between 600 and 900 °C adhered strongly to the surface of fused-silica substrate and were composed of anatase-TiO2 monophase. The photocatalytic activities of the films were measured and represented using a characteristic time constant (τ) for the methylene blue (MB) photodegradation. The small τ stands for high photocatalytic ability of the film. The P/Si-TiO2 film, containing equalmolar Si and P dopants, calcined at 800 °C gave the best performance in photocatalysis; this film had τ=5.7 h and decomposed about 90 mole% of MB in the water after 12 h of the 365-nm UV light irradiation. 相似文献
15.
The photocatalytic application and regeneration of anatase thin films with embedded commercial TiO2 particles deposited on glass microrods 总被引:1,自引:0,他引:1
Anatase thin films (<200 nm in thickness) embedding Degussa P25 TiO2 were prepared by sol-gel method. TiO2-anatase thin films were deposited on a fiberglass substrate and then ground to obtain glass microrods containing the composite films. The film structure was characterized using Raman spectroscopy, atomic absorption and UV-vis spectrophotometry, and atomic force microscopy. The photocatalytic activity of the composite films, calcined at 450 °C, and the regeneration of the activity under the same experimental conditions, were assessed using gas chromatography to study the photodegradation of phenol, an industrial pollutant, in water under 365 nm irradiation. The film with 15.0 wt.% of P25 TiO2 was found to be more photoactive (54 ppm of degraded phenol at 6 h of illumination) than the other ones. 相似文献
16.
Dong Fang Zhiping LuoKelong Huang Dimitris C. Lagoudas 《Applied Surface Science》2011,257(15):6451-6461
Highly ordered titanium oxide (TiO2) nanotubes were prepared by electrolytic anodization of titanium electrodes. Morphological evolution and phase transformations of TiO2 nanotubes on a Ti substrate and that of freestanding TiO2 membranes during the calcinations process were studied by scanning electron microscopy, transmission electron microscopy, and X-ray diffraction microscopy. The detailed results and mechanisms on the morphology and crystalline structure were presented. Our results show that a compact layer exists between the tubular layer and Ti substrate at 600 °C, and the length of the nanotubes shortens dramatically at 750 °C. The freestanding membranes have many particles on their tubes during calcinations from 450 to 900 °C. The TiO2 nanotubes on the Ti substrate transform to rutile crystals at 600 °C, while the freestanding TiO2 membranes retain an anatase crystal with increasing temperature to 800 °C. The photocatalytic activity of TiO2 nanotubes on a Ti substrate annealed at different temperatures was investigated by the degradation of methyl orange in aqueous solution under UV light irradiation. Due to the anatase crystals in the tubular layer and rutile crystals in the compact layer, TiO2 nanotubes annealed at 450 °C with pure anatase crystals have a better photocatalytic activity than those annealed at 600 °C or 750 °C. 相似文献
17.
Pure zirconium oxide nanocrystallites with diameters 6-140 nm are fabricated from ultrafine metallo-organic complexes by thermal hydrolysis at 120 °C and/or heat treatment at 125-1025 °C. X-ray photoelectron spectroscopy shows that effective ionic valence of Zr decreases with decreasing particle diameter. The size dependence of the ionic valences suggests that the phase transition from cubic to tetragonal occurs at an effective Zr valence of 2.0 near 3 nm in diameter and that the phase transition from tetragonal to monoclinic takes place at a critical size of 25 nm diameter with an effective Zr valence of about 2.6. 相似文献
18.
J.S. ShaikhR.C. Pawar A.V. MoholkarJ.H. Kim P.S. Patil 《Applied Surface Science》2011,257(9):4389-4397
We report the synthesis of CuO-Poly (acrylic) acid (PAA) hybrid thin films by a cost-effective spin coating technique for supercapacitor application. Coated films were annealed at 300, 400 and 500 °C, to study the annealing effect on the supercapacitor behavior. Further films were characterized by X-ray diffractometer (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform-Raman spectroscopy (FT-Raman) and Fourier transform-Infrared spectroscopy (FT-IR) techniques. Energy dispersive spectroscopy (EDS) shows the formation of amorphous blend of CuO and Cu2O phases at 300 °C. Further, films annealed at 400 and 500 °C exhibit polycrystalline phase pure CuO with monoclinic structure. The scanning electron microscopy (SEM) micrographs show the transition of island-like structure to CuO crystals surrounded by PAA grafted composite ring with increase in annealing temperature. The possible growth mechanism of PAA and CuO bonding is discussed. Cyclic voltammetry (CV) is employed to calculate the specific capacitance (Csp) in 1 M H2SO4 electrolyte. It is observed that the Csp increases from 41 to136 F g−1 with increase in annealing temperature. 相似文献
19.
Nanoplates of the MgAl2O4 spinel doped with Eu3+ ions were prepared by a microwave assisted hydrothermal method. Structural properties of the precursor calcined at 700 and 1000 oC powders were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). According to the obtained XRD patterns the formation of single-phase spinels after calcination was confirmed. The average spinel particle size was determined to be 11 nm after calcination at 700 °C and it increased up to 14 nm after calcination at 1000 °C. The photoluminescent properties of prepared powders with different Eu3+ ion concentrations (0-5% mol) were investigated using excitation and emission spectroscopy at room and low temperatures (77 K). 相似文献
20.
Be3N2 thin films have been grown on Si(1 1 1) substrates using the pulsed laser deposition method at different substrate temperatures: room temperature (RT), 200 °C, 400 °C, 600 °C and 700 °C. Additionally, two samples were deposited at RT and were annealed after deposition in situ at 600 °C and 700 °C. In order to obtain the stoichiometry of the samples, they have been characterized in situ by X-ray photoelectron (XPS) and reflection electron energy loss spectroscopy (REELS). The influence of the substrate temperature on the morphological and structural properties of the films was investigated using scanning electron microscopy (SEM), atomic force microscopy (AFM) and X-ray diffraction (XRD). The results show that all prepared films presented the Be3N2 stoichiometry. Formation of whiskers with diameters of 100-200 nm appears at the surface of the films prepared with a substrate temperature of 600 °C or 700 °C. However, the samples grown at RT and annealed at 600 °C or 700 °C do not show whiskers on the surface. The average root mean square (RMS) roughness and the average grain size of the samples grown with respect the substrate temperature is presented. The films grown with a substrate temperature between the room temperature to 400 °C, and the sample annealed in situ at 600 °C were amorphous; while the αBe3N2 phase was presented on the samples with a substrate temperature of 600 °C, 700 °C and that deposited with the substrate at RT and annealed in situ at 700 °C. 相似文献