UiO-66-NH2, as typical visible light responsive Zr-based metal-organic frameworks (MOFs), has attracted great interest in recent years. However, rapid combination of the photoinduced carriers limits its further applic...UiO-66-NH2, as typical visible light responsive Zr-based metal-organic frameworks (MOFs), has attracted great interest in recent years. However, rapid combination of the photoinduced carriers limits its further application. Here, we designed a facile precipitation-photoreduction method to post-synthetically decorate Ag/AgCl on the surface of UiO-66-NH2 and form a heterostructure. Metallic Ag can not only transmit electrons between UiO-66-NH2 and AgCl but also absorb visible light, because of the surface plasmon resonance (SPR) effect. The rhodamine B photodegradation rate of UiO-66-NH2/Ag/AgCl (16.2 wt.% Ag) is about 10 and 4 times those of UiO-66-NH2 and Ag/AgCl, respectively. The SPR effect of Ag NPs and the formation of a heterostructure synergistically increase the absorbability of visible light, accelerate the separation of photoinduced charges, and promote the formation of superoxide radicals. We expect that our work could provide a new viewpoint for constructing efficient MOF-based photocatalytic systems.展开更多
Piezoelectric effect,plasma effect and semiconductor heterostructure are important strategies for enhanced photocatalytic performance.Herein,we developed a novel heterostructure piezoelectric photocatalyst,Ag/Ag_(2)S/...Piezoelectric effect,plasma effect and semiconductor heterostructure are important strategies for enhanced photocatalytic performance.Herein,we developed a novel heterostructure piezoelectric photocatalyst,Ag/Ag_(2)S/BiFeO_(3)(AAS/BFO),for photocatalytic degradation of ciprofloxacin from water.Experimental results verified the enhancement of combining heterostructure piezoelectric polarization effect,which promotes efficient migration and separation of photogenerated carriers due to the localized surface plasmon resonance effect of Ag nanoparticles.Additionally,the introduction of Ag_(2)S constructs a new heterostructure,that enhances the electron transport rate and improves the separation efficiency on electron-hole pairs.Under ultrasonic stimulation and visible light irradiation,the degradation efficiencies of 15%-AAS/BFO towards ciprofloxacin,methyl orange and methylene blue are significantly enhanced compared to pure BFO fibers.The demonstrated AAS/BFO material based on the synergistic piezoelectric effect and plasmon heterostructure shows potential in efficient organic pollutants water treatment and transforming mechanical energy into chemical energy.展开更多
Cerium-doped SiO2/TiO2 nanostructured fibers were fabricated by electrospinning technology. The prepared fibers were characterized by thermogravimetric analysis （TGA）, scanning electron microscopy （SEM）, X-ray dif...Cerium-doped SiO2/TiO2 nanostructured fibers were fabricated by electrospinning technology. The prepared fibers were characterized by thermogravimetric analysis （TGA）, scanning electron microscopy （SEM）, X-ray diffraction （XRD） and Fourier transform infrared spectroscopy （FT-IR）. Using the fibers as catalysts, photoeatalytic degradation of Methylene Blue （MB） aqueous solution was carded out under simulated sunlight. The 0.2% Ce doping proved to be the optimal concentration for the doping of TiO2/SiO2, compared to other Ce-doped molar concentrations. The 0.2% Ce-doped SiOdTiO2 fibers exhibited higher photocatalytic activity than industrial Degussa P25 and the samples doped with only Ce or SIO2. The reasons for improving the photocatalytic activity were also discussed. Several operational parameters were studied, which showed that the photocatalytic efficiency of MB was influenced by parameters such as the initial dye concentration, the initial pH, inorganic anions, and so on. In addition, the influences of an electron acceptor and a radical scavenger suggested that OH was the dominant photooxidant during the photocatalytic process. The reuse evaluation of the fibers indicated that their photocatalytic activity had good stability.展开更多
We report a colloidal process to coat a layer of TiO2onto SiO2composite nanofibers containing embedded CdS and upconversion nanoparticles(UCNPs).The SiO2composite nanofibers were fabricated by electrospinning.To impro...We report a colloidal process to coat a layer of TiO2onto SiO2composite nanofibers containing embedded CdS and upconversion nanoparticles(UCNPs).The SiO2composite nanofibers were fabricated by electrospinning.To improve the energy transfer efficiency,UCNPs and CdS nanoparticles were bound in close proximity to each other within the SiO2matrix.β‐NaYF4:Yb(30%),Tm(0.5%)@NaYF4:Yb(20%),Er(2%)core–shell nanoparticles were used as nanotransducers for near infrared light.These nanoparticles exhibited enhanced upconversion fluorescence compared withβ‐NaYF4:Yb(30%),Tm(0.5%)orβ–NaYF4:Yb(30%),Tm(0.5%)@NaYF4nanoparticles.The morphologies,size and chemical compositions have been extensively investigated using field emission scanning electron microscopy(FESEM),transmission electron microscopy(TEM),X‐ray diffraction(XRD)and X‐ray photoelectron spectra(XPS),respectively.The TEM images showed that the TiO2composite nanotubes were embedded with a large amount of UCNPs and CdS nanoparticles.The composite TiO2nanotubes degraded more than90%of rhodamine B(RhB)dye during20min of irradiation by simulated solar light.In particular,more than50%of RhB was decomposed in70min,under irradiation of near infrared light(NIR).This high degradation was attributed to the full spectrum absorption of solar light,and the enhanced transfer efficiency for near infrared light.The as‐prepared nanostructures can harness solar energy,and provide an alternative to overcome energy shortages and environmental protection.展开更多
Photocatalyst was prepared by immobilizing TiO2 on glass beads using the traditional sol-gel method. Ultraviolet light （UV） produced by pulsed streamer discharge was then used to induce photocatalytic activity of Ti...Photocatalyst was prepared by immobilizing TiO2 on glass beads using the traditional sol-gel method. Ultraviolet light （UV） produced by pulsed streamer discharge was then used to induce photocatalytic activity of TiO2 photocatalyst. Decolouration efficiency of the representative azo dye （acid orange 7, AOT） was investigated using the synergistic system of pulsed streamer discharge plasma and TiO2 photocatalysis. The obtained results showed that the decolouration rate of AO7 could be increased by 16.7% under the condition of adding supported TiO2 in the pulsed streamer discharge system, compared to that in the sole pulsed streamer discharge plasma system, due to the synergistic effect of pulsed streamer discharge and TiO2 photocatalysis induced by pulsed streamer discharge. The synergistic system of pulsed streamer discharge and TiO2 photocatalyst was found to have more reactive radicals for degradation of organic compounds in water.展开更多
As efficient water treatment agents, a novel series of rectorite-based ZnO and TiO2 hybrid composites（REC/ZnO/TiO2） were synthesized and characterized in this study. Effects of experimental parameters including TiO2...As efficient water treatment agents, a novel series of rectorite-based ZnO and TiO2 hybrid composites（REC/ZnO/TiO2） were synthesized and characterized in this study. Effects of experimental parameters including TiO2 mass ratio, solution p H and catalyst dosage on the removal of methyl blue（MB） were also conducted. The presence of a little mass ratio（2%-6%） of TiO2 highly promoted the photoactivity of REC/ZnO/TiO2 in removal of MB dye from aqueous solution, in which ZnO and REC played a role of photocatalyst and adsorbent. The promotion effects of TiO2 may result from the accelerated separation of electron-hole on ZnO. The observed kinetic constant for the degradation of MB over REC/ZnO and REC/ZnO/TiO2 were 0.015 and 0.038 min^（-1）, respectively. The degradation kinetics of MB dye, which followed the Langmuir–Hinshelwood model, had a reaction constant of 0.17 mg/（L min）. The decrease of removal ratio of MB after five repetitive experiments was small, indicating REC/ZnO/TiO2 has great potential as an effective and stable catalyst.展开更多
Highly ordered TiO2 nanotube arrays were fabricated via electrochemical anodization of high purity Ti foil in fluoride-containing electrolyte. The effects of applied anodization potential, anodization time on the form...Highly ordered TiO2 nanotube arrays were fabricated via electrochemical anodization of high purity Ti foil in fluoride-containing electrolyte. The effects of applied anodization potential, anodization time on the formation of TiO2 nanotube arrays and the photocatalytic degradation of methylene blue （MB） were discussed. The TiO2 nanotube arrays calcined at 500 ℃ for 2 h show pure anatase phase. The pore diameters of TiO2 nanotube arrays can be adjusted from 30 to 90 nm using a different anodization voltage. Anodization time mainly influenced TiO2 tube length, and by increasing the anodization time, the nanotube length became longer gradually. When the anodization potential was 40 V, the average growth rate of TiO2 nanotube was about 4.17 μm/h. Both anodization potential and time had important effects on the photocatalytic efficiency. The TiO2 nanotube arrays obtained at anodization potential of 40 V for I h showed the best photocatalytic degradation ratio of MB.展开更多
Bandgap engineering by doping and co‐catalyst loading are two primary approaches to designing efficient photocatalysts by promoting visible‐light absorption and charge separation,respectively.Shifting of the TiO2con...Bandgap engineering by doping and co‐catalyst loading are two primary approaches to designing efficient photocatalysts by promoting visible‐light absorption and charge separation,respectively.Shifting of the TiO2conduction band edge is frequently applied to increase visible‐light absorption but also lowers the reductive properties of photo‐excited electrons.Herein,we report a visible‐light‐driven photocatalyst based on valance band edge control induced by oxygen excess defects and modification with a CuxO electron transfer co‐catalyst.The CuxO grafted oxygen‐rich TiO2microspheres were prepared by ultrasonic spray pyrolysis of the peroxotitanate precursor followed by a wet chemical impregnated treatment.We found that oxygen excess defects in TiO2shifted the valence band maximum upward and improved the visible‐light absorption.The CuxO grafted onto the surface acted as a co‐catalyst that efficiently reduced oxygen molecules to active intermediates(i.e.,O2??radial and H2O2),thus consuming the photo‐generated electrons.Consequently,the CuxO grafted oxygen‐rich TiO2microspheres achieved a photocatalytic activity respectively8.6,13.0and11.0as times high as those of oxygen‐rich TiO2,normal TiO2and CuxO grafted TiO2,for degradation of gaseous acetaldehyde under visible‐light irradiation.Our results suggest that high visible‐light photocatalytic efficiency can be achieved by combining oxygen excess defects to improve visible‐light absorption together with a CuxO electron transfer co‐catalyst.These findings provide a new approach to developing efficient heterojunction photocatalysts.展开更多
The photocatalysis of Ti O2nanotubes（Ti/TNT） and Ni-deposited Ti O2nanotubes（Ti/TNT–Ni） for methyl orange degradation was investigated.Methyl orange was selected as the model pollutant,and its photocatalytic degr...The photocatalysis of Ti O2nanotubes（Ti/TNT） and Ni-deposited Ti O2nanotubes（Ti/TNT–Ni） for methyl orange degradation was investigated.Methyl orange was selected as the model pollutant,and its photocatalytic degradation was determined in 1 mol/L KOH solution.Ti/TNT was produced by anodizing method,and the electrodeposition of nickel on TNT was performed galvanostatically.The characterization of electrodes was performed by scanning electron microscopy,energy-dispersive X-ray spectroscopy and X-ray diffraction analysis.The electrochemical behavior of the electrodes was determined by cyclic voltammetry and electrochemical impedance spectroscopy.The irradiation was applied by visible light source（k = 635 nm） for 48 h.UV/vis spectroscopy was used for determination of the concentration of methyl orange.Furthermore,after 48-h irradiation,the solutions were analyzed by Fourier transform infrared spectroscopy.Results showed that the concentration of methyl orange decreased from 100 ppm（10-6） to 16 ppm,after48-h irradiation with the photocatalysis of Ti/TNT–Ni.展开更多
Heterogeneous photocatalysis is one of the advanced oxidation processes (AOP’s). These are very used nowadays for their implementation in tertiary water treatment with solar activation, with very good results. In thi...Heterogeneous photocatalysis is one of the advanced oxidation processes (AOP’s). These are very used nowadays for their implementation in tertiary water treatment with solar activation, with very good results. In this study, TiO2 porous films were synthesized by sol-gel method. Polyethylene glycol (PEG) 4000 was used as a templating reagent, which is oxidized at a lower temperature than TiO2. This allows the formation of a “skeleton” of porous TiO2 with increased surface area, resulting in higher photocatalytic activity. The film characterization was made with help of FE-SEM microscope, XRD diffractometer and scotch tape test. Finally, the oxidation experiments were performed using methylene blue as a model pollutant and they revealed an increase in the photocatalytic activity of porous films in comparison with the non-porous films.展开更多
Photocatalyst CoPcS/TiO2 was prepared by sol-gel method. Composite CoPcS/TiO2/K2Ti4O9 was prepared by dipping. It was incandesced at various temperatures and modification effect was compared. The results showed that o...Photocatalyst CoPcS/TiO2 was prepared by sol-gel method. Composite CoPcS/TiO2/K2Ti4O9 was prepared by dipping. It was incandesced at various temperatures and modification effect was compared. The results showed that optical absorption of sample incandesce at 423K occurred significant red-shift. Light absorption width extended from ultraviolet region to visible region, especially there was an intensive absorption between 600 nm and 680 nm. X-ray diffraction spectrogram showed that TiO2 in sample still maintained anatase crystal form. Under the illumination of visible light, photocatalysis degradation experiment was taken with Eosin B as simulated pollutants. Decoloration rate of Eosin B was much improved. The rate can reach 80% in 300 minutes.展开更多
TiO2 nanotubes were prepared under normal pressure at a temperature of 120 ℃. Ag, Au, Pt nanoparticles supported on TiO2 nanotubes were prepared by m icrowave assisted heating polyol process. TEM images showed that m...TiO2 nanotubes were prepared under normal pressure at a temperature of 120 ℃. Ag, Au, Pt nanoparticles supported on TiO2 nanotubes were prepared by m icrowave assisted heating polyol process. TEM images showed that microwave prepa red Ag, Au, Pt nanoparticles supported on TiO2 nanotubes were small and well dis persed on the surface of the TiO2 nanotubes. UV-Vis absorption spectra showed th at the absorbance of Ag/TiO2 nanotubes and Au/TiO2 nanotubes in the visible ligh t range increased greatly compared to the single titania nanotubes.展开更多
This study reports the successful synthesis of supported TiO<sub>2</sub>_Palygorskite nanocomposites by a one-pot dry mechanochemical route. Indeed, the elaboration procedure involved an in-situ reaction b...This study reports the successful synthesis of supported TiO<sub>2</sub>_Palygorskite nanocomposites by a one-pot dry mechanochemical route. Indeed, the elaboration procedure involved an in-situ reaction between accessories carbonates present in raw fibrous palygorskite clay and titanyl sulfate (TiOSO<sub>4</sub>) precursor under variable grinding conditions, essentially ball/solid matter mass ratio and rotation velocity. This yielded after air annealing at 600%C for 1 h to the immobilization of anatase TiO<sub>2</sub> nanoparticles (≈8 nm of average size) as evidenced by XRD and TEM analyses. Once the conditions of elaboration were optimized, the photocatalytic properties were evaluated under 3 conditions: artificial UV radiation, artificial solar radiation (UV + visible range) and under dynamic solar illumination taking into account the discontinuities of the solar resource. The results allowed the estimation and comparison of the catalyst’s capabilities and showed its ability to work under natural irradiation. The so developed supported photocatalysts TiO<sub>2</sub>/Palygorskite exhibited a good activity towards the removal of Orange G (OG) dye from aqueous media under artificial UV and natural solar radiations.展开更多
基金supported by the National Natural Science Foundation of China(21676182)the National Basic Research Program of China(973 Program,2014CB932403)the Program for Introducing Talents of Discipline to Universities of China(B06006)
文摘UiO-66-NH2, as typical visible light responsive Zr-based metal-organic frameworks (MOFs), has attracted great interest in recent years. However, rapid combination of the photoinduced carriers limits its further application. Here, we designed a facile precipitation-photoreduction method to post-synthetically decorate Ag/AgCl on the surface of UiO-66-NH2 and form a heterostructure. Metallic Ag can not only transmit electrons between UiO-66-NH2 and AgCl but also absorb visible light, because of the surface plasmon resonance (SPR) effect. The rhodamine B photodegradation rate of UiO-66-NH2/Ag/AgCl (16.2 wt.% Ag) is about 10 and 4 times those of UiO-66-NH2 and Ag/AgCl, respectively. The SPR effect of Ag NPs and the formation of a heterostructure synergistically increase the absorbability of visible light, accelerate the separation of photoinduced charges, and promote the formation of superoxide radicals. We expect that our work could provide a new viewpoint for constructing efficient MOF-based photocatalytic systems.
基金supported by the National Natural Science Foundation of China(Nos.52372090 and 52073177)the National Natural Science Foundation of Guangdong,China(No.2023A1515010947)Shenzhen Basic Research Program(No.JCYJ20220531102207017).
文摘Piezoelectric effect,plasma effect and semiconductor heterostructure are important strategies for enhanced photocatalytic performance.Herein,we developed a novel heterostructure piezoelectric photocatalyst,Ag/Ag_(2)S/BiFeO_(3)(AAS/BFO),for photocatalytic degradation of ciprofloxacin from water.Experimental results verified the enhancement of combining heterostructure piezoelectric polarization effect,which promotes efficient migration and separation of photogenerated carriers due to the localized surface plasmon resonance effect of Ag nanoparticles.Additionally,the introduction of Ag_(2)S constructs a new heterostructure,that enhances the electron transport rate and improves the separation efficiency on electron-hole pairs.Under ultrasonic stimulation and visible light irradiation,the degradation efficiencies of 15%-AAS/BFO towards ciprofloxacin,methyl orange and methylene blue are significantly enhanced compared to pure BFO fibers.The demonstrated AAS/BFO material based on the synergistic piezoelectric effect and plasmon heterostructure shows potential in efficient organic pollutants water treatment and transforming mechanical energy into chemical energy.
基金supported by the National Natural Science Foundation of China (No. 20907022,21003094)the Doctoral Program of Higher Education of China(No. 200800551003,20100032120066)the Special Projects of Environmental Protection (No. 2009ZX07526,2009ZX07208,200909101,2009GJA10021)
文摘Cerium-doped SiO2/TiO2 nanostructured fibers were fabricated by electrospinning technology. The prepared fibers were characterized by thermogravimetric analysis （TGA）, scanning electron microscopy （SEM）, X-ray diffraction （XRD） and Fourier transform infrared spectroscopy （FT-IR）. Using the fibers as catalysts, photoeatalytic degradation of Methylene Blue （MB） aqueous solution was carded out under simulated sunlight. The 0.2% Ce doping proved to be the optimal concentration for the doping of TiO2/SiO2, compared to other Ce-doped molar concentrations. The 0.2% Ce-doped SiOdTiO2 fibers exhibited higher photocatalytic activity than industrial Degussa P25 and the samples doped with only Ce or SIO2. The reasons for improving the photocatalytic activity were also discussed. Several operational parameters were studied, which showed that the photocatalytic efficiency of MB was influenced by parameters such as the initial dye concentration, the initial pH, inorganic anions, and so on. In addition, the influences of an electron acceptor and a radical scavenger suggested that OH was the dominant photooxidant during the photocatalytic process. The reuse evaluation of the fibers indicated that their photocatalytic activity had good stability.
基金supported in part by the National Natural Science Foundation of China(21471043,21304028,51403195,31501576)~~
文摘We report a colloidal process to coat a layer of TiO2onto SiO2composite nanofibers containing embedded CdS and upconversion nanoparticles(UCNPs).The SiO2composite nanofibers were fabricated by electrospinning.To improve the energy transfer efficiency,UCNPs and CdS nanoparticles were bound in close proximity to each other within the SiO2matrix.β‐NaYF4:Yb(30%),Tm(0.5%)@NaYF4:Yb(20%),Er(2%)core–shell nanoparticles were used as nanotransducers for near infrared light.These nanoparticles exhibited enhanced upconversion fluorescence compared withβ‐NaYF4:Yb(30%),Tm(0.5%)orβ–NaYF4:Yb(30%),Tm(0.5%)@NaYF4nanoparticles.The morphologies,size and chemical compositions have been extensively investigated using field emission scanning electron microscopy(FESEM),transmission electron microscopy(TEM),X‐ray diffraction(XRD)and X‐ray photoelectron spectra(XPS),respectively.The TEM images showed that the TiO2composite nanotubes were embedded with a large amount of UCNPs and CdS nanoparticles.The composite TiO2nanotubes degraded more than90%of rhodamine B(RhB)dye during20min of irradiation by simulated solar light.In particular,more than50%of RhB was decomposed in70min,under irradiation of near infrared light(NIR).This high degradation was attributed to the full spectrum absorption of solar light,and the enhanced transfer efficiency for near infrared light.The as‐prepared nanostructures can harness solar energy,and provide an alternative to overcome energy shortages and environmental protection.
基金supported by the National Natural Science Foundation Committee of China(No.20377006)Foundation of Education Ministry of China(No.2005141002)
文摘Photocatalyst was prepared by immobilizing TiO2 on glass beads using the traditional sol-gel method. Ultraviolet light （UV） produced by pulsed streamer discharge was then used to induce photocatalytic activity of TiO2 photocatalyst. Decolouration efficiency of the representative azo dye （acid orange 7, AOT） was investigated using the synergistic system of pulsed streamer discharge plasma and TiO2 photocatalysis. The obtained results showed that the decolouration rate of AO7 could be increased by 16.7% under the condition of adding supported TiO2 in the pulsed streamer discharge system, compared to that in the sole pulsed streamer discharge plasma system, due to the synergistic effect of pulsed streamer discharge and TiO2 photocatalysis induced by pulsed streamer discharge. The synergistic system of pulsed streamer discharge and TiO2 photocatalyst was found to have more reactive radicals for degradation of organic compounds in water.
基金Funded by the National High Technology Research and Development Program of China(No.2007AA06Z418)the National Natural Science Foundation of China(Nos.20577036,20777058,20977070)+2 种基金the National Natural Science Foundation of Hubei Province,China(No.2015CFA137)the Open Fund of Hubei Biomass-Resource Chemistry and Environmental Biotechnology Key Laboratory(Wuhan University)the Fund of Eco-environment Technology R&D and Service Center(Wuhan University)
文摘As efficient water treatment agents, a novel series of rectorite-based ZnO and TiO2 hybrid composites（REC/ZnO/TiO2） were synthesized and characterized in this study. Effects of experimental parameters including TiO2 mass ratio, solution p H and catalyst dosage on the removal of methyl blue（MB） were also conducted. The presence of a little mass ratio（2%-6%） of TiO2 highly promoted the photoactivity of REC/ZnO/TiO2 in removal of MB dye from aqueous solution, in which ZnO and REC played a role of photocatalyst and adsorbent. The promotion effects of TiO2 may result from the accelerated separation of electron-hole on ZnO. The observed kinetic constant for the degradation of MB over REC/ZnO and REC/ZnO/TiO2 were 0.015 and 0.038 min^（-1）, respectively. The degradation kinetics of MB dye, which followed the Langmuir–Hinshelwood model, had a reaction constant of 0.17 mg/（L min）. The decrease of removal ratio of MB after five repetitive experiments was small, indicating REC/ZnO/TiO2 has great potential as an effective and stable catalyst.
基金partly supported by the National Natural Science Foundation of China (Grant No. 61405171)the Shandong Province Natural Science Foundation (No. ZR2012FQ014)the Shandong Province Higher Educational Science and Technology Program (No. G12LA08, No. J13LJ05)
文摘Highly ordered TiO2 nanotube arrays were fabricated via electrochemical anodization of high purity Ti foil in fluoride-containing electrolyte. The effects of applied anodization potential, anodization time on the formation of TiO2 nanotube arrays and the photocatalytic degradation of methylene blue （MB） were discussed. The TiO2 nanotube arrays calcined at 500 ℃ for 2 h show pure anatase phase. The pore diameters of TiO2 nanotube arrays can be adjusted from 30 to 90 nm using a different anodization voltage. Anodization time mainly influenced TiO2 tube length, and by increasing the anodization time, the nanotube length became longer gradually. When the anodization potential was 40 V, the average growth rate of TiO2 nanotube was about 4.17 μm/h. Both anodization potential and time had important effects on the photocatalytic efficiency. The TiO2 nanotube arrays obtained at anodization potential of 40 V for I h showed the best photocatalytic degradation ratio of MB.
基金supported by the National Natural Science Foundation of China(51072032,51372036,51702235)~~
文摘Bandgap engineering by doping and co‐catalyst loading are two primary approaches to designing efficient photocatalysts by promoting visible‐light absorption and charge separation,respectively.Shifting of the TiO2conduction band edge is frequently applied to increase visible‐light absorption but also lowers the reductive properties of photo‐excited electrons.Herein,we report a visible‐light‐driven photocatalyst based on valance band edge control induced by oxygen excess defects and modification with a CuxO electron transfer co‐catalyst.The CuxO grafted oxygen‐rich TiO2microspheres were prepared by ultrasonic spray pyrolysis of the peroxotitanate precursor followed by a wet chemical impregnated treatment.We found that oxygen excess defects in TiO2shifted the valence band maximum upward and improved the visible‐light absorption.The CuxO grafted onto the surface acted as a co‐catalyst that efficiently reduced oxygen molecules to active intermediates(i.e.,O2??radial and H2O2),thus consuming the photo‐generated electrons.Consequently,the CuxO grafted oxygen‐rich TiO2microspheres achieved a photocatalytic activity respectively8.6,13.0and11.0as times high as those of oxygen‐rich TiO2,normal TiO2and CuxO grafted TiO2,for degradation of gaseous acetaldehyde under visible‐light irradiation.Our results suggest that high visible‐light photocatalytic efficiency can be achieved by combining oxygen excess defects to improve visible‐light absorption together with a CuxO electron transfer co‐catalyst.These findings provide a new approach to developing efficient heterojunction photocatalysts.
基金Cukurova University Research Fund (No.FEF2013BAP4)
文摘The photocatalysis of Ti O2nanotubes（Ti/TNT） and Ni-deposited Ti O2nanotubes（Ti/TNT–Ni） for methyl orange degradation was investigated.Methyl orange was selected as the model pollutant,and its photocatalytic degradation was determined in 1 mol/L KOH solution.Ti/TNT was produced by anodizing method,and the electrodeposition of nickel on TNT was performed galvanostatically.The characterization of electrodes was performed by scanning electron microscopy,energy-dispersive X-ray spectroscopy and X-ray diffraction analysis.The electrochemical behavior of the electrodes was determined by cyclic voltammetry and electrochemical impedance spectroscopy.The irradiation was applied by visible light source（k = 635 nm） for 48 h.UV/vis spectroscopy was used for determination of the concentration of methyl orange.Furthermore,after 48-h irradiation,the solutions were analyzed by Fourier transform infrared spectroscopy.Results showed that the concentration of methyl orange decreased from 100 ppm（10-6） to 16 ppm,after48-h irradiation with the photocatalysis of Ti/TNT–Ni.
文摘Heterogeneous photocatalysis is one of the advanced oxidation processes (AOP’s). These are very used nowadays for their implementation in tertiary water treatment with solar activation, with very good results. In this study, TiO2 porous films were synthesized by sol-gel method. Polyethylene glycol (PEG) 4000 was used as a templating reagent, which is oxidized at a lower temperature than TiO2. This allows the formation of a “skeleton” of porous TiO2 with increased surface area, resulting in higher photocatalytic activity. The film characterization was made with help of FE-SEM microscope, XRD diffractometer and scotch tape test. Finally, the oxidation experiments were performed using methylene blue as a model pollutant and they revealed an increase in the photocatalytic activity of porous films in comparison with the non-porous films.
基金Acknowledgements： This project is supported by the fund of the Plan of Postgraduate Scientific Research Innovation of Jiangsu Province （No. CX07B_175z） and the Natural Science Foundation of Henan Province （No. 0624720029）.
文摘Photocatalyst CoPcS/TiO2 was prepared by sol-gel method. Composite CoPcS/TiO2/K2Ti4O9 was prepared by dipping. It was incandesced at various temperatures and modification effect was compared. The results showed that optical absorption of sample incandesce at 423K occurred significant red-shift. Light absorption width extended from ultraviolet region to visible region, especially there was an intensive absorption between 600 nm and 680 nm. X-ray diffraction spectrogram showed that TiO2 in sample still maintained anatase crystal form. Under the illumination of visible light, photocatalysis degradation experiment was taken with Eosin B as simulated pollutants. Decoloration rate of Eosin B was much improved. The rate can reach 80% in 300 minutes.
文摘TiO2 nanotubes were prepared under normal pressure at a temperature of 120 ℃. Ag, Au, Pt nanoparticles supported on TiO2 nanotubes were prepared by m icrowave assisted heating polyol process. TEM images showed that microwave prepa red Ag, Au, Pt nanoparticles supported on TiO2 nanotubes were small and well dis persed on the surface of the TiO2 nanotubes. UV-Vis absorption spectra showed th at the absorbance of Ag/TiO2 nanotubes and Au/TiO2 nanotubes in the visible ligh t range increased greatly compared to the single titania nanotubes.
文摘This study reports the successful synthesis of supported TiO<sub>2</sub>_Palygorskite nanocomposites by a one-pot dry mechanochemical route. Indeed, the elaboration procedure involved an in-situ reaction between accessories carbonates present in raw fibrous palygorskite clay and titanyl sulfate (TiOSO<sub>4</sub>) precursor under variable grinding conditions, essentially ball/solid matter mass ratio and rotation velocity. This yielded after air annealing at 600%C for 1 h to the immobilization of anatase TiO<sub>2</sub> nanoparticles (≈8 nm of average size) as evidenced by XRD and TEM analyses. Once the conditions of elaboration were optimized, the photocatalytic properties were evaluated under 3 conditions: artificial UV radiation, artificial solar radiation (UV + visible range) and under dynamic solar illumination taking into account the discontinuities of the solar resource. The results allowed the estimation and comparison of the catalyst’s capabilities and showed its ability to work under natural irradiation. The so developed supported photocatalysts TiO<sub>2</sub>/Palygorskite exhibited a good activity towards the removal of Orange G (OG) dye from aqueous media under artificial UV and natural solar radiations.
