Fabrication of TiO 2 hollow microspheres（TiO 2-HMSs） has attracted considerable attention owing to their low density,high photoreactivity,and easy to separate and reuse. A fluoride-free method for the fabrication of...Fabrication of TiO 2 hollow microspheres（TiO 2-HMSs） has attracted considerable attention owing to their low density,high photoreactivity,and easy to separate and reuse. A fluoride-free method for the fabrication of TiO 2-HMSs is reported by refluxing a mixed solution of H3PW12O40（0.4 mmol）,KCl（2.5 mmol） and Ti（SO4）2（2–25 mmol） at 125 °C for 8 h,followed by decomposition of the K3PW12O40（KPW） template in basic solution. The prepared TiO 2-HMSs are characterized by X-ray diffraction,transmission electron microscopy,scanning electron microscopy,Fourier transform infrared spectroscopy,ultraviolet-visible diffuse reflectance spectroscopy and X-ray photoelectron spectroscopy. The activities of the photocatalysts are evaluated by photocatalytic degradation of Brilliant Red X-3B,an anionic dye,under UV irradiation. It is observed that the TiO 2-HMSs exhibit diameters of approximately 0.5–1 μm,and the photocatalytic activity of TiO 2-HMSs initially increases and then decreases with an increasing amount of Ti（SO4）2. The TiO 2-HMSs prepared in the presence of 4 mmol Ti（SO4）2 exhibit the highest photocatalytic activity,which is 2.1 times higher than TiO 2 nanoparticles（prepared in the absence of the KPW template）. The enhanced photocatalytic activity of the prepared TiO 2-HMSs is ascribed to the improved crystallization,coupling effect between TiO 2and the residual KPW template,and the unique hollow structures of TiO 2-HMSs.展开更多
Bi2WO6 is a typical visible-light-responsive semiconductor photocatalyst with a layered structure.However,the relatively large bandgap(2.6–2.8 eV)and quick recombination of photo-generated carriers result in its low ...Bi2WO6 is a typical visible-light-responsive semiconductor photocatalyst with a layered structure.However,the relatively large bandgap(2.6–2.8 eV)and quick recombination of photo-generated carriers result in its low quantum efficiency.In this paper,Bi-nanospheres-modified flower-like Bi2WO6 was successfully prepared by solvothermal treatment of Bi2WO6 powders in Bi(NO3)3 solution using ethylene glycol as reductant.The photoreactivity of this photocatalyst was evaluated by the oxidation of NO in a continuous-flow reactor under irradiation by a visible LED lamp(λ>400 nm).It was found that both Bi nanospheres and flower-like Bi2WO6 precursor exhibit very poor photocatalytic activity with NO removal rates of only 7.7%and 8.6%,respectively.The photoreactivity of Bi/Bi2WO6 was found to steadily increase from 12.3%to 53.1%with increase in the amount of Bi nanospheres from 0 to 10 wt%.However,with further increase in the loading amount of Bi nanospheres,the photoreactivity of Bi/Bi2WO6 hybridized photocatalyst begins to decrease,possibly due to the light filtering by the Bi nanospheres.The enhanced visible photoreactivity of Bi/Bi2WO6 towards NO abatement was attributed to surface plasmon resonance driven interfacial charge separation.The excellent stability of Bi/Bi2WO6 hybridized photocatalyst towards NO oxidation demonstrates its potential for applications such as air purification.展开更多
Tailoring the microstructure of pristine TiO2 is essential to narrow its band gap and prolong the charge lifetime. In particular, strategies involving fluorine have been used successfully to tune the surface chemistry...Tailoring the microstructure of pristine TiO2 is essential to narrow its band gap and prolong the charge lifetime. In particular, strategies involving fluorine have been used successfully to tune the surface chemistry, electronic structure, and morphology of TiO2 photocatalysts to improve their photocatalytic activity based on the strong complexation between fluoride ions and TiO2 and the high electronegativity of fluorine. In this review, we summarize the strategies involving fluorine to establish highly efficient TiO2 photocatalytic systems or fabricate highly efficient TiO2 photocatalysts. The main fluorine effects(i.e. the effects of fluorine on photocatalysis) include the following four aspects:(1) Surface effects of fluoride on TiO2 photocatalysis,(2) effects of fluorine doping on TiO2 photocatalysis,(3) fluoride-mediated tailoring of the morphology of TiO2 photocatalysts, and(4) the effects of fluorine on non-TiO2 photocatalysis. Additionally, the unique applications of these fluorine effects in photocatalysis, including selective degradation of pollutants, selective oxidation of chemicals, water-splitting to produce H2, reduction of CO2 to produce solar fuels, and improvement of the thermostability of TiO2 photocatalysts, are reviewed.展开更多
基金supported by Program for New Century Excellent Talents in University(NCET-12-0668)the National Natural Science Foundation of China(21373275120977114)~~
文摘Fabrication of TiO 2 hollow microspheres（TiO 2-HMSs） has attracted considerable attention owing to their low density,high photoreactivity,and easy to separate and reuse. A fluoride-free method for the fabrication of TiO 2-HMSs is reported by refluxing a mixed solution of H3PW12O40（0.4 mmol）,KCl（2.5 mmol） and Ti（SO4）2（2–25 mmol） at 125 °C for 8 h,followed by decomposition of the K3PW12O40（KPW） template in basic solution. The prepared TiO 2-HMSs are characterized by X-ray diffraction,transmission electron microscopy,scanning electron microscopy,Fourier transform infrared spectroscopy,ultraviolet-visible diffuse reflectance spectroscopy and X-ray photoelectron spectroscopy. The activities of the photocatalysts are evaluated by photocatalytic degradation of Brilliant Red X-3B,an anionic dye,under UV irradiation. It is observed that the TiO 2-HMSs exhibit diameters of approximately 0.5–1 μm,and the photocatalytic activity of TiO 2-HMSs initially increases and then decreases with an increasing amount of Ti（SO4）2. The TiO 2-HMSs prepared in the presence of 4 mmol Ti（SO4）2 exhibit the highest photocatalytic activity,which is 2.1 times higher than TiO 2 nanoparticles（prepared in the absence of the KPW template）. The enhanced photocatalytic activity of the prepared TiO 2-HMSs is ascribed to the improved crystallization,coupling effect between TiO 2and the residual KPW template,and the unique hollow structures of TiO 2-HMSs.
基金supported by the National Natural Science Foundation of China(51672312,21373275,51808080,21571192)the Fundamental Research Funds for the Central Univsrsity,South-Central University for Nationalities(CZT19006)+2 种基金the Natural Science Foundation Project of CQ CSTC(cstc2018jcyjA 3794)China "post-doctoral innovative talent support program"(BX20180056)China Postdoctoral Science Foundation(2018M643788XB)~~
文摘Bi2WO6 is a typical visible-light-responsive semiconductor photocatalyst with a layered structure.However,the relatively large bandgap(2.6–2.8 eV)and quick recombination of photo-generated carriers result in its low quantum efficiency.In this paper,Bi-nanospheres-modified flower-like Bi2WO6 was successfully prepared by solvothermal treatment of Bi2WO6 powders in Bi(NO3)3 solution using ethylene glycol as reductant.The photoreactivity of this photocatalyst was evaluated by the oxidation of NO in a continuous-flow reactor under irradiation by a visible LED lamp(λ>400 nm).It was found that both Bi nanospheres and flower-like Bi2WO6 precursor exhibit very poor photocatalytic activity with NO removal rates of only 7.7%and 8.6%,respectively.The photoreactivity of Bi/Bi2WO6 was found to steadily increase from 12.3%to 53.1%with increase in the amount of Bi nanospheres from 0 to 10 wt%.However,with further increase in the loading amount of Bi nanospheres,the photoreactivity of Bi/Bi2WO6 hybridized photocatalyst begins to decrease,possibly due to the light filtering by the Bi nanospheres.The enhanced visible photoreactivity of Bi/Bi2WO6 towards NO abatement was attributed to surface plasmon resonance driven interfacial charge separation.The excellent stability of Bi/Bi2WO6 hybridized photocatalyst towards NO oxidation demonstrates its potential for applications such as air purification.
文摘Tailoring the microstructure of pristine TiO2 is essential to narrow its band gap and prolong the charge lifetime. In particular, strategies involving fluorine have been used successfully to tune the surface chemistry, electronic structure, and morphology of TiO2 photocatalysts to improve their photocatalytic activity based on the strong complexation between fluoride ions and TiO2 and the high electronegativity of fluorine. In this review, we summarize the strategies involving fluorine to establish highly efficient TiO2 photocatalytic systems or fabricate highly efficient TiO2 photocatalysts. The main fluorine effects(i.e. the effects of fluorine on photocatalysis) include the following four aspects:(1) Surface effects of fluoride on TiO2 photocatalysis,(2) effects of fluorine doping on TiO2 photocatalysis,(3) fluoride-mediated tailoring of the morphology of TiO2 photocatalysts, and(4) the effects of fluorine on non-TiO2 photocatalysis. Additionally, the unique applications of these fluorine effects in photocatalysis, including selective degradation of pollutants, selective oxidation of chemicals, water-splitting to produce H2, reduction of CO2 to produce solar fuels, and improvement of the thermostability of TiO2 photocatalysts, are reviewed.
