Cs_(x)WO_(3)/TiO_(2) composites with full-spectrum catalytic activity were prepared by solvothermal reaction.The composites were characterized using X-ray diffraction(XRD)analysis,scanning electron microscopy(SEM),tra...Cs_(x)WO_(3)/TiO_(2) composites with full-spectrum catalytic activity were prepared by solvothermal reaction.The composites were characterized using X-ray diffraction(XRD)analysis,scanning electron microscopy(SEM),transmission electron microscopy(TEM),specific surface area testing,X-ray photoelectron spectroscopy(XPS),and UV-Vis diffuse reflectance spectra(UV-Vis DRS).Cs_(x)WO_(3) and TiO_(2) were uniformly bonded together in the compos-ites.The heterojunction structure was formed.The band gap was reduced from 2.75 to 2.65 eV.The photocatalytic property of Cs_(x)WO_(3)/TiO_(2)was demonstrated by the degradation rates of 20 mg·L^(-1) methylene blue dye,which were 99.7%,91.4%,and 70.7%under irradiation from a 300 W high-pressure mercury lamp,a 500 W xenon lamp,and a 400 W infrared lamp,respectively.After five cycles of photocatalytic degradation,the composite photocatalyst still showed a degradation efficiency of 87.6%.This indicates that Cs_(x)WO_(3)/TiO_(2) has good photocatalytic degradability and cyclic stability.The photocatalytic mechanism of Cs_(x)WO_(3)/TiO_(2)was investigated.The trapping experiments of the active species showed that the main active substances were the empty hole(h+)and hydroxyl radical(·OH).展开更多
Metal nanoparticles with high surface area and high electrochemical activity exhibit excellent catalytic performance in the photocatalytic reduction of carbon dioxide(CO_(2)).However,poor stability,small specific surf...Metal nanoparticles with high surface area and high electrochemical activity exhibit excellent catalytic performance in the photocatalytic reduction of carbon dioxide(CO_(2)).However,poor stability,small specific surface area,and less active sites limits its solar energy utilization.Hydrothermal method was utilized to synthesize the bimetallic material of Cu_(x)Co_(1-x)in this work.Co was loaded onto the Cu surface due to the electrons generated by the surface plasmon resonance(SPR)effect occurring on the Cu surface.Cu_(x)Co_(1-x)exhibits high photocatalytic conversion of CO_(2)efficiency under irradiation,which mainly because the Co nanoparticles on the surface of Cu can be used as cocatalysts to enhance the photocharge transfer.Cu_(0.6)Co_(0.4)exhibits the comparatively best photocatalytic conversion efficiency of CO_(2)in the first 6 h light irradiation.The yields of CO and CH_(4)reached 35.26 and 2.71μmol/(g·h),respectively.Upon illumination,electrons were produced,with the majority of them moving towards the interface.This movement contributes to the increased lifetime of photogenerated electron-hole pairs,which in turn boosts the photocatalytic efficiency.The findings of this research provide significant insights for creating photocatalysts that are both highly effective and stable in CO_(2)reduction processes.展开更多
Traditional polymeric photocatalysts are typically constructed using aromatic building blocks to enhanceπ-conjugation.However,their inherent hydrophobicity and rigid structure lead to poor dispersibility in aqueous s...Traditional polymeric photocatalysts are typically constructed using aromatic building blocks to enhanceπ-conjugation.However,their inherent hydrophobicity and rigid structure lead to poor dispersibility in aqueous solutions,resulting in significant optical losses and exciton recombination.In this study,two series of six novel polymer photocatalysts(FLUSO,FLUSO-PEG10,FLUSO-PEG30;CPDTSO,CPDTSO-PEG10,CPDTSO-PEG30)are designed and synthesized by incorporating the hydrophilic,non-conjugated polyethylene glycol(PEG)chain,into both the main and side chains of polymers.By precisely optimizing the ratio of hydrophilic PEG segments,the water dispersibility is significantly improved while the light absorption capability of the polymer photocatalysts is well maintained.The experimental results confirm that the optimized FLUSO-PEG10 exhibits excellent photocatalytic hydrogen evolution rate,reaching up to 33.9 mmol/(g·h),which is nearly three times higher than that of fullyπ-conjugated counterparts.Water contact angles and particle size analyses reveal that incorporating non-conjugated segments into the main chains enhances the capacitance of the polymer/water interface and reduces particle aggregation,leading to improved photocatalyst dispersion and enhanced charge generation.展开更多
Polymeric perylene diimide(PDI)has been evidenced as a good candidate for photocatalytic water oxidation,yet the origin of the photocatalytic oxygen evolution activity remains unclear and needs further exploration.Her...Polymeric perylene diimide(PDI)has been evidenced as a good candidate for photocatalytic water oxidation,yet the origin of the photocatalytic oxygen evolution activity remains unclear and needs further exploration.Herein,with crystal and atomic structures of the self-assembled PDI revealed from the X-ray diffraction pattern,the electronic structure is theoretically illustrated by the first-principles density functional theory calculations,suggesting the suitable band structure and the direct electronic transition for efficient photocatalytic oxygen evolution over PDI.It is confirmed that the carbonyl O atoms on the conjugation structure serve as the active sites for oxygen evolution reaction by the crystal orbital Hamiltonian group analysis.The calculations of reaction free energy changes indicate that the oxygen evolution reaction should follow the reaction pathway of H_(2)O→^(*)OH→^(*)O→^(*)OOH→^(*)O_(2)with an overpotential of 0.81 V.Through an in-depth theoretical computational analysis in the atomic and electronic structures,the origin of photocatalytic oxygen evolution activity for PDI is well illustrated,which would help the rational design and modification of polymeric photocatalysts for efficient oxygen evolution.展开更多
Elemental doping is an effective strategy for tuning the band structure of graphite carbon nitride(CN)to enhance its photocatalytic performance.In this study,sodium(Na)and oxygen(O)co-doped carbon nitride(Na/O-CN_(x),...Elemental doping is an effective strategy for tuning the band structure of graphite carbon nitride(CN)to enhance its photocatalytic performance.In this study,sodium(Na)and oxygen(O)co-doped carbon nitride(Na/O-CN_(x),x=1.0,2.0,3.0,4.0)was synthesized via solid-phase reaction of sodium citrate(NaCA)and pure CN powder in the Teflon-sealed autoclave under air conditions at 180℃.Surface area of Na/O-CN_(3.0) is measured to be 18.8 m^(2)/g,increasing by 60.7%compared to that of pure CN(11.7 m^(2)/g).Bandgap energy of Na/O-CN_(3.0) is determined to be 2.68 eV,marginally lower than that of pure CN(2.70 eV),thereby enhancing its capacity for sunlight absorption.Meanwhile,the incorporation of Na and O atoms into Na/O-CN_(x) is found to effectively reduce recombination rates of photogenerated electron-hole pairs.As a result,Na/O-CN_(x) samples exhibit markedly enhanced photocatalytic hydrogen evolution activity under visible light irradiation.Notably,the optimal Na/O-CN_(3.0) sample achieves a photocatalytic hydrogen production rate of 103.2μmol·g^(–1)·h^(–1),which is 8.2 times greater than that of pure CN(11.2μmol·g^(–1)·h^(–1)).Furthermore,a series of Na/O-CN_(x)-yO_(2)(y=0,20%,40%,60%,80%,100%)samples were prepared by modulating the oxygen content within reaction atmosphere.The catalytic performance evaluations reveal that the incorporation of both Na and O atoms in Na/O-CN_(3.0) enhances photocatalytic activity.This study also introduces novel methodologies for synthesis of metal atom-doped CN materials at lower temperature,highlighting the synergistic effect of Na and O atoms in photocatalytic hydrogen production of Na/O-CN_(x) samples.展开更多
In the paper,we report a highly robust and porous bimetallic Ti-MOF(designated Mg_(2)Ti-ABTC)by utiliz-ing a trinuclear[Mg_(2)TiO(COO)_(6)]cluster and a tetradentate H_(4)ABTC(3,3′,5,5′-azobenzene tetracarboxylic ac...In the paper,we report a highly robust and porous bimetallic Ti-MOF(designated Mg_(2)Ti-ABTC)by utiliz-ing a trinuclear[Mg_(2)TiO(COO)_(6)]cluster and a tetradentate H_(4)ABTC(3,3′,5,5′-azobenzene tetracarboxylic acid)ligand.Mg_(2)Ti-ABTC exhibited permanent porosity for N_(2),CO_(2),CH_(4),C_(2)H_(2),C_(2)H_(4),and C_(2)H_(6)gas adsorption.Further-more,Mg_(2)Ti-ABTC exhibited outstanding photocatalytic activity in the oxidation of aromatic sulfides to the corre-sponding sulfoxides under ambient air conditions.Mechanism studies reveal that photoinduced holes(h^(+)),the super-oxide radical(·O_(2)^(-)),and singlet oxygen(^(1)O_(2))are pivotal species involved in the photocatalytic oxidation reaction.展开更多
In order to realize the photocatalysis of TiO2 in the sunlight and directly apply it to waste water treatment, the Gd-doped TiO2 nanofibre was synthesized using two-step synthesis method as follows: Firstly, potassium...In order to realize the photocatalysis of TiO2 in the sunlight and directly apply it to waste water treatment, the Gd-doped TiO2 nanofibre was synthesized using two-step synthesis method as follows: Firstly, potassium carbonate, titanium dioxide and proper gadolinium oxide （dopant） were calcined in the muffle at high temperature and the doped gadolinium K2Ti4O9 fibres were obtained; secondly, the fibre was heated using glycerol as solvent until Gd-doped TiO2 nanofibres were obtained. The synthesized samples were characterized using scanning electron microscopy, transmission electron microscopy and X-ray diffraction. The results show that Gd-doped TiO2 nanofibre heat-treated by glycerol solvent can inhibit the agglomeration, so the grain diameter of the fibre is smaller than that without heat-treated with glycerol. Meanwhile, the diameter of the fibre decreases with the increase of the heating temperature and time. 97% 98% of Gd-doped TiO2 nanofibre is anatase. The photocatalysis results showed that the photocatalysis activity of Gd-doped TiO2 nanofibre is just a little lower than that of TiO2 powder.展开更多
We reported the fabrication of highly porous graphene/TiO2 composite nanofibers in the form of a nonwoven mat by electrospinning followed by calcination in air at 450°C.The graphene can uniformly disperse in high...We reported the fabrication of highly porous graphene/TiO2 composite nanofibers in the form of a nonwoven mat by electrospinning followed by calcination in air at 450°C.The graphene can uniformly disperse in highly porous TiO2 nanofibers.The highly porous graphene/TiO2 composite nanofibers exhibited excellent catalytic activities.The new method for producing graphene/TiO2 composite nanofibers is versatile and can be extended to fabricate various types of metal oxide and graphene nanocomposites.展开更多
A series of In_(x)Sb_(2-x)S_(3) nanosheets modified g-C_(3)N_(4)(In_(x)Sb_(2-x)S_(3)-TCN)heterojunctions with different g-C_(3)N_(4) contents were fabricated by an in situ deposition method.All the In_(x)Sb_(2-x)S_(3)...A series of In_(x)Sb_(2-x)S_(3) nanosheets modified g-C_(3)N_(4)(In_(x)Sb_(2-x)S_(3)-TCN)heterojunctions with different g-C_(3)N_(4) contents were fabricated by an in situ deposition method.All the In_(x)Sb_(2-x)S_(3)-TCN composites were applied as photocatalysts in Cr(Ⅵ)polluted water treatment and the results displayed that In_(x)Sb_(2-x)S_(3)-TCN could effectively remove Cr(Ⅵ)under visible light through synergistic effects of adsorption and photocatalytic reduction.Especially,In_(x)Sb_(2-x)S_(3)-TCN-70(70 mg g-C_(3)N_(4)) exhibited the most excellent adsorption and photocatalytic reduction performance among all composites,which possessed a high equilibrium adsorption capacity of 12.45 mg/g in a 30.0 mg/L Cr(Ⅵ)aqueous solution,and reduced Cr(Ⅵ)to Cr(Ⅲ)within 10 min under visible light irradiation.DRS and PL results indicated that the interfacial coupling effect between g-C_(3)N_(4)and In_(x)Sb_(2-x)S_(3) enhanced the utilization efficiency of visible light and suppressed photoinduced carrier recombination,which improved the photocatalytic activity of composites.Moreover,the photocatalyst exhibited satisfactory reduction activity and good stability after 5 cycles of Cr(Ⅵ)adsorptionphotoreduction.展开更多
A catalyst of ferroelectric-BaTiO_(3)@photoelectric-TiO_(2) nanohybrids(BaTiO_(3)@TiO_(2))with enhanced photocatalytic activity was synthesized via a hydrolysis precipitation combined with a hydrothermal approach.Comp...A catalyst of ferroelectric-BaTiO_(3)@photoelectric-TiO_(2) nanohybrids(BaTiO_(3)@TiO_(2))with enhanced photocatalytic activity was synthesized via a hydrolysis precipitation combined with a hydrothermal approach.Compared to pure TiO_(2),pure BaTiO_(3) and BaTiO_(3)/TiO_(2) physical mixture,the heterostructured BaTiO_(3)@TiO_(2) exhibits significantly improved photocatalytic activity and cycling stability in decomposing Rhodamine B(RhB)and the degradation efficiency is 1.7 times higher than pure TiO_(2) and 7.2 times higher than pure BaTiO_(3).These results are mainly attributed to the synergy effect of photoelectric TiO_(2),ferroelectric-BaTiO_(3) and the rationally designed interfacial structure.The mesoporous microstructure of TiO_(2) is of a high specific area and enables excellent photocatalytic activity.The ferroelectric polarization induced built-in electric field in BaTiO_(3) nanoparticles,and the intimate interfacial interactions at the interface of BaTiO_(3) and TiO_(2) are effective in driving the separation and transport of photogenerated charge carriers.This strategy will stimulate the design of heterostructured photocatalysts with outstanding photocatalytic performance via interface engineering.展开更多
Ag/ZnO nanosheet composites were prepared by zinc nitrate, sodium hydroxide and silver nitrate via a simple hydrothermal method. The crystal structure, morphology, optical property and photocatalytic performance were ...Ag/ZnO nanosheet composites were prepared by zinc nitrate, sodium hydroxide and silver nitrate via a simple hydrothermal method. The crystal structure, morphology, optical property and photocatalytic performance were studied by means of XRD, SEM, HRTEM, XPS, and PL methods. It is found that both the pure ZnO and composite Ag/ZnO samples have the same morphology of nanosheet. The interaction of spherical Ag particles with ZnO matrix in the Ag/ZnO sample leads to an increase in photocatalytic efficiency for the possible increase of concentration of surface hydroxyl and the photo-induced electrons and holes. The addition of Ag can reduce the recombination rate of photo-generated carriers and the sample with addition of 3 at% Ag to ZnO exhibits the best photocatalytic activity with the degradation rate up to 95% within 15 min.展开更多
The hierarchical BiOCl_(x)Br_(1–x)was synthesized by a simple solvothermal method.The samples were characterized by X-ray diffraction(XRD),field emission scanning electron microscopy(FESEM),UV-visible diffuse reflect...The hierarchical BiOCl_(x)Br_(1–x)was synthesized by a simple solvothermal method.The samples were characterized by X-ray diffraction(XRD),field emission scanning electron microscopy(FESEM),UV-visible diffuse reflectance spectroscopy(UV-vis DRS)and Brunauer-Emmett-Teller adsorption method.Compared to pure BiOCl or BiOBr,the BiOCl_(x)Br_(1–x)solid solution has enhanced photocatalytic degradation activity for rhodamine B.This phenomenon can be explained to the hierarchical structure,lager specific surface area and appropriate energy gap of the obtained BiOCl_(x)Br_(1–x)solid solution.The renewability and stability of photocatalyst were determinated and a possible mechanism of photocatalytic degradation was also proposed.展开更多
Two new coordination polymers[Co(L)_(0.5)(1,3-bib)](1)and[Ni_(2)(L)(1,4-bib)3(H_(2)O)_(2)]·2H_(2)O(2),where H4L=1,2,4,5-benzenetetracarboxylic acid,1,3-bib=1,3-bis((1H-imidazol-1-yl)methyl)benzene,and 1,4-bib=1,4...Two new coordination polymers[Co(L)_(0.5)(1,3-bib)](1)and[Ni_(2)(L)(1,4-bib)3(H_(2)O)_(2)]·2H_(2)O(2),where H4L=1,2,4,5-benzenetetracarboxylic acid,1,3-bib=1,3-bis((1H-imidazol-1-yl)methyl)benzene,and 1,4-bib=1,4-bis((1H-imidazol-1-yl)methyl)benzene,were synthesized under hydrothermal conditions.The structures of 1 and 2 were con-firmed by elemental analysis,FTIR spectroscopy,single-crystal X-ray diffraction,etc.The results show that 1 and 2 are 3D network structures.The completely deprotonated L4-ligand adopts theμ_(4)-к^(2)∶к^(1)∶к^(2)∶к^(1)mode in 1 and theμ_(2)-к^(1)∶к^(0)∶к^(1)∶к^(0)coordination mode in 2.Further studies showed that in the presence of H_(2)O_(2)and visible light irradiation conditions,1 had good photocatalytic performance for the degradation of MO(methyl orange)/MB(methylene blue)in water,and the degradation rates reached 83.2%and 84.5%at 180 min.Under the same conditions,2 also showed good degradation of the dyes MB and RhB(rhodamine B)in aqueous solution,with 87.0%and 77.4%degradation rates at 180 min,respectively.In addition,the mechanism of photocatalytic degradation of the dye by 1 and 2 was investigated.CCDC:2219951,1;2219953,2.展开更多
CdS quantum dots sensitized platelike WO_3 photoelectrodes were successfully synthesized by a facile hydrothermal method and a modified chemical bath deposition(CBD) technique.To further improve the stability of the p...CdS quantum dots sensitized platelike WO_3 photoelectrodes were successfully synthesized by a facile hydrothermal method and a modified chemical bath deposition(CBD) technique.To further improve the stability of the photoelectrodes in alkaline environment,the platelike WO_3 films were treated with TiCl_4 to form a nano-TiO_2 buffer layer on the WO_3 plate surface before loading CdSQDs.The resulting electrodes were characterized by using XRD,SEM,HR-TEM and UV-vis spectrum.The photocatalytic activity of the resulting electrodes was investigated by degradation of methyl orange(MO) in aqueous solution.The photoelectrochemical(PEC) property of the resulting electrodes was also characterized by the linear sweep voltammetry.The results of both the degradation of MO and photocurrent tests indicated that the as-prepared CdSQDs sensitized WO_3 platelike photoelectrodes exhibit a significant improvement in photocatalytic degradation and PEC activity under visible light irradiation,compared with unsupported CdSQDs electrodes.Significantly,coating the WO_3 plates with nano-TiO_2 obviously facilitate the charge separation and retards the charge-pair recombination,and results in a highest activity for QDsCdS/TiO_2/WO_3 photoelectrodes.展开更多
Zirconia-supported CuO （CuO/ZrO2） composite photocatalysts were successfully synthesized via citric acid-assisted sol-gel technique. For comparison, CuO/ZrO2 materials were also prepared by solid state reaction and ...Zirconia-supported CuO （CuO/ZrO2） composite photocatalysts were successfully synthesized via citric acid-assisted sol-gel technique. For comparison, CuO/ZrO2 materials were also prepared by solid state reaction and co-precipitation method. The as-prepared powders were characterized by X-ray diffractometry （XRD）, transmission electron microscopy （TEM）, and thermogravimetric-differential thermal analysis （TG-DTA）. The photocatalytic activity of CuO/ZrO2 catalyst was investigated based on the H2 evolution from oxalic acid solution under simulated sunlight irradiation. The effects of molar ratio of CuO to ZrO2, preparation method, phase change with the calcination temperature and the durability on the photocatalytic activity of the photocatalyst were investigated in detail. It is found that the optimal activity of photocatalytic H2 evolution （2.41 mmol.h i.g-~） can be obtained when CuO/ZrO2 composite photocatalyst is synthesized by sol-gel technique and the mole ratio of CuO to ZrO2 is 40%. The activity of copper oxide supported on monoclinic ZrO2 calcined at higher temperature is much higher than that on tetragonal ZrO2 calcined at lower temperature, and the best calcination temperature is 900 ℃.展开更多
The role of oxygen and the generation of active radicals in the photocatalitic degradation of phenol were investigated using the eosin sensitized TiO2 as photocatalyst under visible light irradiation. Diffuse reflecta...The role of oxygen and the generation of active radicals in the photocatalitic degradation of phenol were investigated using the eosin sensitized TiO2 as photocatalyst under visible light irradiation. Diffuse reflectance spectra show that the absorbancy range of eosin/TiO2 is expanded from 378 nm (TiO2 ) to about 600 nm. The photocatalitic degradation of phenol is almost stopped when the eosin/TiO2 system is saturated with N2 , which indicates the significance of O2 . The addition of NaN 3 (a quencher of single oxygen) causes about a 62% decrease in the phenol degradation. The phenol degradation ratio is dropped from 92% to 75% when the isopropanol (a quencher of hydroxyl radical) is present in the system. The experimental results show that there are singlet oxygen and hydroxyl radical generated in the eosin/TiO2 system under visible light irradiation. The changes of absorbancy indicate that the hydrogen peroxide might be produced. Through the analysis and comparison, it is found that the singlet oxygen is the predominant active radical for the degradation of phenol.展开更多
Nanocrystalline Fe-doped TiO2 with size of 6070 nm was prepared by a sol-gel technique, followed by freeze-drying treatment for 2 h. Thermogravimetric and differential thermal analyses, X-ray diffraction, scanning （e...Nanocrystalline Fe-doped TiO2 with size of 6070 nm was prepared by a sol-gel technique, followed by freeze-drying treatment for 2 h. Thermogravimetric and differential thermal analyses, X-ray diffraction, scanning （electron） microscope, laser diffraction particle size analyzer and UV-Vis spectrophotometer technologies were used to characterize the product. The photocatalytic activities of the samples were evaluated by the degradation of wastewater of paper-making. The effects of Fe ion implantation on the photocatalytic activity of TiO2 were also discussed. The results show that the iron content plays an essential role in affecting the photocatalytic activity of the Fe-doped TiO2 and the optimum content of Fe-doped is 0.05% （mass fraction）. The photocatalytic activity of samples with lower content of Fe-doped is higher than that of pure TiO2 in the treatment of paper-making wastewater. The photo-degradation effect of paper-making effluent is the best by means of Fe-doped TiO2 with 0.05% Fe.展开更多
Nitric oxide(NO) from flue gas is hard to remove because of low solubility and reactivity. A new technology for photocatalytic oxidation of NO using ultraviolet(UV)/TiO2/H2O2 process is studied in an efficient laborat...Nitric oxide(NO) from flue gas is hard to remove because of low solubility and reactivity. A new technology for photocatalytic oxidation of NO using ultraviolet(UV)/TiO2/H2O2 process is studied in an efficient laboratory-scale reactor. Effects of several key operational parameters on NO removal efficiency are studied, including TiO2 content, H2O2 initial concentration, UV lamp power, NO initial content, oxygen volume fraction and TiO2/H2O2 solution volume. The results illustrate that the NO removal efficiency increases with the increasing of H2O2 initial concentration or UV lamp power. Meanwhile, a lower NO initial content or a higher TiO2/H2O2 solution volume will result in higher NO removal efficiency. In addition, oxygen volume fraction has a little effect.The highest NO removal efficiency is achieved at the TiO2 content of 0.75 g/L, H2O2 initial concentration of 2.5 mol/L, UV lamp power of 36 W, NO initial content of 206×10-6 and TiO2/H2O2 solution volume of 600 m L. It is beneficial for the development and application of NO removal from coal-fired flue gas with UV/TiO2/H2O2 process.展开更多
TiO2/bauxite-tailings （TiO2/BTs） composites were prepared via a chemical liquid deposition method and characterized by X-ray diffractometry （XRD）, scanning electronic microscopy （SEM） and N2 adsorption analysis....TiO2/bauxite-tailings （TiO2/BTs） composites were prepared via a chemical liquid deposition method and characterized by X-ray diffractometry （XRD）, scanning electronic microscopy （SEM） and N2 adsorption analysis. The photocatalytic performance of TiO2/BTs composites was evaluated with UV-Vis spectrophotometer following the changes of phenol concentration under different illumination time. Effects of the calcination temperature, the pH and the cycles on the photocatalytic activity of TiO2/BTs composites were investigated. The composites calcined at 500 and 600 ℃ exhibit the best photocatalytic performance, and the phenol degradation ratios reacting for 40 and 160 rain reach 35% and 78% respectively under the same conditions, higher than those of 29% and 76% of the Degussa P25（TiO2）. The ability of TiO2/BTs500 （BTs500 represents bauxite-tailings calcined at 500 ℃） composites to degrade phenol increases with decreasing pH.展开更多
ZnO/ZnGa_2O_4 composite microspheres with heterojunction were successfully synthesized by one-pot hydrothermal method.These samples were characterized by TG/DTA,XRD,TEM,HRTEM,UV-vis DRS,FL and BET techniques.The resul...ZnO/ZnGa_2O_4 composite microspheres with heterojunction were successfully synthesized by one-pot hydrothermal method.These samples were characterized by TG/DTA,XRD,TEM,HRTEM,UV-vis DRS,FL and BET techniques.The results indicated the as-prepared samples showed better degree of crystalline and large specific surface area.The photocatalytic activity was evaluated by degradation of methyl orange with the concentration of 50 mg/L under the irradiation of simulated sunlight.The effects of molar ratio of Zn to Ga and calcination temperature on the photocatalytic activity were investigated in detail.The results showed that the highest photocatalytic degradation efficiency was observed at the molar ratio of Zn to Ga of 1:0.5 in the starting materials and the calcination temperature of 400 °C.The maximum photocatalytic degradation rate of MO was 97.1% within 60 min under the simulated sunlight irradiation,which is greatly higher than that of ZnO and ZnGa_2O_4.展开更多
文摘Cs_(x)WO_(3)/TiO_(2) composites with full-spectrum catalytic activity were prepared by solvothermal reaction.The composites were characterized using X-ray diffraction(XRD)analysis,scanning electron microscopy(SEM),transmission electron microscopy(TEM),specific surface area testing,X-ray photoelectron spectroscopy(XPS),and UV-Vis diffuse reflectance spectra(UV-Vis DRS).Cs_(x)WO_(3) and TiO_(2) were uniformly bonded together in the compos-ites.The heterojunction structure was formed.The band gap was reduced from 2.75 to 2.65 eV.The photocatalytic property of Cs_(x)WO_(3)/TiO_(2)was demonstrated by the degradation rates of 20 mg·L^(-1) methylene blue dye,which were 99.7%,91.4%,and 70.7%under irradiation from a 300 W high-pressure mercury lamp,a 500 W xenon lamp,and a 400 W infrared lamp,respectively.After five cycles of photocatalytic degradation,the composite photocatalyst still showed a degradation efficiency of 87.6%.This indicates that Cs_(x)WO_(3)/TiO_(2) has good photocatalytic degradability and cyclic stability.The photocatalytic mechanism of Cs_(x)WO_(3)/TiO_(2)was investigated.The trapping experiments of the active species showed that the main active substances were the empty hole(h+)and hydroxyl radical(·OH).
基金supported by the Doctoral Research Start-up Project of Yuncheng University(YQ-2023067)Project of Shanxi Natural Science Foundation(202303021211189)+2 种基金Fund Program for the Scientific Activities of Selected Returned Overseas Professionals in Shanxi Provinces(20220036)Shanxi Province Intelligent Optoelectronic Sensing Application Technology Innovation CenterShanxi Province Optoelectronic Information Science and Technology Laboratory,Yuncheng University。
文摘Metal nanoparticles with high surface area and high electrochemical activity exhibit excellent catalytic performance in the photocatalytic reduction of carbon dioxide(CO_(2)).However,poor stability,small specific surface area,and less active sites limits its solar energy utilization.Hydrothermal method was utilized to synthesize the bimetallic material of Cu_(x)Co_(1-x)in this work.Co was loaded onto the Cu surface due to the electrons generated by the surface plasmon resonance(SPR)effect occurring on the Cu surface.Cu_(x)Co_(1-x)exhibits high photocatalytic conversion of CO_(2)efficiency under irradiation,which mainly because the Co nanoparticles on the surface of Cu can be used as cocatalysts to enhance the photocharge transfer.Cu_(0.6)Co_(0.4)exhibits the comparatively best photocatalytic conversion efficiency of CO_(2)in the first 6 h light irradiation.The yields of CO and CH_(4)reached 35.26 and 2.71μmol/(g·h),respectively.Upon illumination,electrons were produced,with the majority of them moving towards the interface.This movement contributes to the increased lifetime of photogenerated electron-hole pairs,which in turn boosts the photocatalytic efficiency.The findings of this research provide significant insights for creating photocatalysts that are both highly effective and stable in CO_(2)reduction processes.
文摘Traditional polymeric photocatalysts are typically constructed using aromatic building blocks to enhanceπ-conjugation.However,their inherent hydrophobicity and rigid structure lead to poor dispersibility in aqueous solutions,resulting in significant optical losses and exciton recombination.In this study,two series of six novel polymer photocatalysts(FLUSO,FLUSO-PEG10,FLUSO-PEG30;CPDTSO,CPDTSO-PEG10,CPDTSO-PEG30)are designed and synthesized by incorporating the hydrophilic,non-conjugated polyethylene glycol(PEG)chain,into both the main and side chains of polymers.By precisely optimizing the ratio of hydrophilic PEG segments,the water dispersibility is significantly improved while the light absorption capability of the polymer photocatalysts is well maintained.The experimental results confirm that the optimized FLUSO-PEG10 exhibits excellent photocatalytic hydrogen evolution rate,reaching up to 33.9 mmol/(g·h),which is nearly three times higher than that of fullyπ-conjugated counterparts.Water contact angles and particle size analyses reveal that incorporating non-conjugated segments into the main chains enhances the capacitance of the polymer/water interface and reduces particle aggregation,leading to improved photocatalyst dispersion and enhanced charge generation.
基金supported by National Natural Science Foundation of China(No.523B2070,No.52225606).
文摘Polymeric perylene diimide(PDI)has been evidenced as a good candidate for photocatalytic water oxidation,yet the origin of the photocatalytic oxygen evolution activity remains unclear and needs further exploration.Herein,with crystal and atomic structures of the self-assembled PDI revealed from the X-ray diffraction pattern,the electronic structure is theoretically illustrated by the first-principles density functional theory calculations,suggesting the suitable band structure and the direct electronic transition for efficient photocatalytic oxygen evolution over PDI.It is confirmed that the carbonyl O atoms on the conjugation structure serve as the active sites for oxygen evolution reaction by the crystal orbital Hamiltonian group analysis.The calculations of reaction free energy changes indicate that the oxygen evolution reaction should follow the reaction pathway of H_(2)O→^(*)OH→^(*)O→^(*)OOH→^(*)O_(2)with an overpotential of 0.81 V.Through an in-depth theoretical computational analysis in the atomic and electronic structures,the origin of photocatalytic oxygen evolution activity for PDI is well illustrated,which would help the rational design and modification of polymeric photocatalysts for efficient oxygen evolution.
基金National Natural Science Foundation of China(21806023)Natural Science Foundation of Hunan Province(2021JJ40199)+2 种基金Education Department Foundation of Hunan Province(20C0813)Hunan University of Science and Technology Fundamental Research FundsPostgraduate Scientific Research Innovation Project of Hunan Province(CX20240877)。
文摘Elemental doping is an effective strategy for tuning the band structure of graphite carbon nitride(CN)to enhance its photocatalytic performance.In this study,sodium(Na)and oxygen(O)co-doped carbon nitride(Na/O-CN_(x),x=1.0,2.0,3.0,4.0)was synthesized via solid-phase reaction of sodium citrate(NaCA)and pure CN powder in the Teflon-sealed autoclave under air conditions at 180℃.Surface area of Na/O-CN_(3.0) is measured to be 18.8 m^(2)/g,increasing by 60.7%compared to that of pure CN(11.7 m^(2)/g).Bandgap energy of Na/O-CN_(3.0) is determined to be 2.68 eV,marginally lower than that of pure CN(2.70 eV),thereby enhancing its capacity for sunlight absorption.Meanwhile,the incorporation of Na and O atoms into Na/O-CN_(x) is found to effectively reduce recombination rates of photogenerated electron-hole pairs.As a result,Na/O-CN_(x) samples exhibit markedly enhanced photocatalytic hydrogen evolution activity under visible light irradiation.Notably,the optimal Na/O-CN_(3.0) sample achieves a photocatalytic hydrogen production rate of 103.2μmol·g^(–1)·h^(–1),which is 8.2 times greater than that of pure CN(11.2μmol·g^(–1)·h^(–1)).Furthermore,a series of Na/O-CN_(x)-yO_(2)(y=0,20%,40%,60%,80%,100%)samples were prepared by modulating the oxygen content within reaction atmosphere.The catalytic performance evaluations reveal that the incorporation of both Na and O atoms in Na/O-CN_(3.0) enhances photocatalytic activity.This study also introduces novel methodologies for synthesis of metal atom-doped CN materials at lower temperature,highlighting the synergistic effect of Na and O atoms in photocatalytic hydrogen production of Na/O-CN_(x) samples.
文摘In the paper,we report a highly robust and porous bimetallic Ti-MOF(designated Mg_(2)Ti-ABTC)by utiliz-ing a trinuclear[Mg_(2)TiO(COO)_(6)]cluster and a tetradentate H_(4)ABTC(3,3′,5,5′-azobenzene tetracarboxylic acid)ligand.Mg_(2)Ti-ABTC exhibited permanent porosity for N_(2),CO_(2),CH_(4),C_(2)H_(2),C_(2)H_(4),and C_(2)H_(6)gas adsorption.Further-more,Mg_(2)Ti-ABTC exhibited outstanding photocatalytic activity in the oxidation of aromatic sulfides to the corre-sponding sulfoxides under ambient air conditions.Mechanism studies reveal that photoinduced holes(h^(+)),the super-oxide radical(·O_(2)^(-)),and singlet oxygen(^(1)O_(2))are pivotal species involved in the photocatalytic oxidation reaction.
文摘In order to realize the photocatalysis of TiO2 in the sunlight and directly apply it to waste water treatment, the Gd-doped TiO2 nanofibre was synthesized using two-step synthesis method as follows: Firstly, potassium carbonate, titanium dioxide and proper gadolinium oxide （dopant） were calcined in the muffle at high temperature and the doped gadolinium K2Ti4O9 fibres were obtained; secondly, the fibre was heated using glycerol as solvent until Gd-doped TiO2 nanofibres were obtained. The synthesized samples were characterized using scanning electron microscopy, transmission electron microscopy and X-ray diffraction. The results show that Gd-doped TiO2 nanofibre heat-treated by glycerol solvent can inhibit the agglomeration, so the grain diameter of the fibre is smaller than that without heat-treated with glycerol. Meanwhile, the diameter of the fibre decreases with the increase of the heating temperature and time. 97% 98% of Gd-doped TiO2 nanofibre is anatase. The photocatalysis results showed that the photocatalysis activity of Gd-doped TiO2 nanofibre is just a little lower than that of TiO2 powder.
基金Project(41271332)supported by the National Natural Science Foundation of China
文摘We reported the fabrication of highly porous graphene/TiO2 composite nanofibers in the form of a nonwoven mat by electrospinning followed by calcination in air at 450°C.The graphene can uniformly disperse in highly porous TiO2 nanofibers.The highly porous graphene/TiO2 composite nanofibers exhibited excellent catalytic activities.The new method for producing graphene/TiO2 composite nanofibers is versatile and can be extended to fabricate various types of metal oxide and graphene nanocomposites.
基金Projects(41977129,21607176,42007138) supported by the National Natural Science Foundation of ChinaProject(kq1802011) supported by the Changsha Outstanding Innovative Youth Training Program,ChinaProject(2017JJ3516)supported by the Natural Science Foundation of Hunan Province,China。
文摘A series of In_(x)Sb_(2-x)S_(3) nanosheets modified g-C_(3)N_(4)(In_(x)Sb_(2-x)S_(3)-TCN)heterojunctions with different g-C_(3)N_(4) contents were fabricated by an in situ deposition method.All the In_(x)Sb_(2-x)S_(3)-TCN composites were applied as photocatalysts in Cr(Ⅵ)polluted water treatment and the results displayed that In_(x)Sb_(2-x)S_(3)-TCN could effectively remove Cr(Ⅵ)under visible light through synergistic effects of adsorption and photocatalytic reduction.Especially,In_(x)Sb_(2-x)S_(3)-TCN-70(70 mg g-C_(3)N_(4)) exhibited the most excellent adsorption and photocatalytic reduction performance among all composites,which possessed a high equilibrium adsorption capacity of 12.45 mg/g in a 30.0 mg/L Cr(Ⅵ)aqueous solution,and reduced Cr(Ⅵ)to Cr(Ⅲ)within 10 min under visible light irradiation.DRS and PL results indicated that the interfacial coupling effect between g-C_(3)N_(4)and In_(x)Sb_(2-x)S_(3) enhanced the utilization efficiency of visible light and suppressed photoinduced carrier recombination,which improved the photocatalytic activity of composites.Moreover,the photocatalyst exhibited satisfactory reduction activity and good stability after 5 cycles of Cr(Ⅵ)adsorptionphotoreduction.
基金Project(cstc2020jcyj-msxm X0930) supported by the Natural Science Foundation of Chongqing,ChinaProject(KJQN201901522) supported by Technological Research Program of Chongqing Municipal Education Commission,ChinaProject(cx2020068) supported by the Venture&Innovation Support Program for Chongqing Overseas Returnees,China。
文摘A catalyst of ferroelectric-BaTiO_(3)@photoelectric-TiO_(2) nanohybrids(BaTiO_(3)@TiO_(2))with enhanced photocatalytic activity was synthesized via a hydrolysis precipitation combined with a hydrothermal approach.Compared to pure TiO_(2),pure BaTiO_(3) and BaTiO_(3)/TiO_(2) physical mixture,the heterostructured BaTiO_(3)@TiO_(2) exhibits significantly improved photocatalytic activity and cycling stability in decomposing Rhodamine B(RhB)and the degradation efficiency is 1.7 times higher than pure TiO_(2) and 7.2 times higher than pure BaTiO_(3).These results are mainly attributed to the synergy effect of photoelectric TiO_(2),ferroelectric-BaTiO_(3) and the rationally designed interfacial structure.The mesoporous microstructure of TiO_(2) is of a high specific area and enables excellent photocatalytic activity.The ferroelectric polarization induced built-in electric field in BaTiO_(3) nanoparticles,and the intimate interfacial interactions at the interface of BaTiO_(3) and TiO_(2) are effective in driving the separation and transport of photogenerated charge carriers.This strategy will stimulate the design of heterostructured photocatalysts with outstanding photocatalytic performance via interface engineering.
基金Project(21373273)supported by the National Natural Science Foundation of ChinaProject(2019CG033)supported by the Deepening Reform Project of Innovation and Entrepreneurship Education of Central South University,China+1 种基金Project(2019JG067)supported by the Graduate Education and Teaching Reform Research Project of Central South University,ChinaProject(201810533278)supported by the National College Students’ Innovative Experiment Project of Central South University,China
文摘Ag/ZnO nanosheet composites were prepared by zinc nitrate, sodium hydroxide and silver nitrate via a simple hydrothermal method. The crystal structure, morphology, optical property and photocatalytic performance were studied by means of XRD, SEM, HRTEM, XPS, and PL methods. It is found that both the pure ZnO and composite Ag/ZnO samples have the same morphology of nanosheet. The interaction of spherical Ag particles with ZnO matrix in the Ag/ZnO sample leads to an increase in photocatalytic efficiency for the possible increase of concentration of surface hydroxyl and the photo-induced electrons and holes. The addition of Ag can reduce the recombination rate of photo-generated carriers and the sample with addition of 3 at% Ag to ZnO exhibits the best photocatalytic activity with the degradation rate up to 95% within 15 min.
基金Project(2016TP1007)supported by the Hunan Provincial Science and Technology Plan Project,China
文摘The hierarchical BiOCl_(x)Br_(1–x)was synthesized by a simple solvothermal method.The samples were characterized by X-ray diffraction(XRD),field emission scanning electron microscopy(FESEM),UV-visible diffuse reflectance spectroscopy(UV-vis DRS)and Brunauer-Emmett-Teller adsorption method.Compared to pure BiOCl or BiOBr,the BiOCl_(x)Br_(1–x)solid solution has enhanced photocatalytic degradation activity for rhodamine B.This phenomenon can be explained to the hierarchical structure,lager specific surface area and appropriate energy gap of the obtained BiOCl_(x)Br_(1–x)solid solution.The renewability and stability of photocatalyst were determinated and a possible mechanism of photocatalytic degradation was also proposed.
文摘Two new coordination polymers[Co(L)_(0.5)(1,3-bib)](1)and[Ni_(2)(L)(1,4-bib)3(H_(2)O)_(2)]·2H_(2)O(2),where H4L=1,2,4,5-benzenetetracarboxylic acid,1,3-bib=1,3-bis((1H-imidazol-1-yl)methyl)benzene,and 1,4-bib=1,4-bis((1H-imidazol-1-yl)methyl)benzene,were synthesized under hydrothermal conditions.The structures of 1 and 2 were con-firmed by elemental analysis,FTIR spectroscopy,single-crystal X-ray diffraction,etc.The results show that 1 and 2 are 3D network structures.The completely deprotonated L4-ligand adopts theμ_(4)-к^(2)∶к^(1)∶к^(2)∶к^(1)mode in 1 and theμ_(2)-к^(1)∶к^(0)∶к^(1)∶к^(0)coordination mode in 2.Further studies showed that in the presence of H_(2)O_(2)and visible light irradiation conditions,1 had good photocatalytic performance for the degradation of MO(methyl orange)/MB(methylene blue)in water,and the degradation rates reached 83.2%and 84.5%at 180 min.Under the same conditions,2 also showed good degradation of the dyes MB and RhB(rhodamine B)in aqueous solution,with 87.0%and 77.4%degradation rates at 180 min,respectively.In addition,the mechanism of photocatalytic degradation of the dye by 1 and 2 was investigated.CCDC:2219951,1;2219953,2.
基金Project(2014FJ3041)supported by the Research Funds of Science and Technology Agency of Hunan Provincial,ChinaProject(14A076)supported by the Research Funds of Education Agency of Hunan Provincial,ChinaProject supported by the Postdoctoral Science Foundation of Central South University,China
文摘CdS quantum dots sensitized platelike WO_3 photoelectrodes were successfully synthesized by a facile hydrothermal method and a modified chemical bath deposition(CBD) technique.To further improve the stability of the photoelectrodes in alkaline environment,the platelike WO_3 films were treated with TiCl_4 to form a nano-TiO_2 buffer layer on the WO_3 plate surface before loading CdSQDs.The resulting electrodes were characterized by using XRD,SEM,HR-TEM and UV-vis spectrum.The photocatalytic activity of the resulting electrodes was investigated by degradation of methyl orange(MO) in aqueous solution.The photoelectrochemical(PEC) property of the resulting electrodes was also characterized by the linear sweep voltammetry.The results of both the degradation of MO and photocurrent tests indicated that the as-prepared CdSQDs sensitized WO_3 platelike photoelectrodes exhibit a significant improvement in photocatalytic degradation and PEC activity under visible light irradiation,compared with unsupported CdSQDs electrodes.Significantly,coating the WO_3 plates with nano-TiO_2 obviously facilitate the charge separation and retards the charge-pair recombination,and results in a highest activity for QDsCdS/TiO_2/WO_3 photoelectrodes.
基金Project(20876039) supported by the National Natural Science Foundation of ChinaProject(09JJ3023) supported by the Natural Science Foundation of Hunan Province,China
文摘Zirconia-supported CuO （CuO/ZrO2） composite photocatalysts were successfully synthesized via citric acid-assisted sol-gel technique. For comparison, CuO/ZrO2 materials were also prepared by solid state reaction and co-precipitation method. The as-prepared powders were characterized by X-ray diffractometry （XRD）, transmission electron microscopy （TEM）, and thermogravimetric-differential thermal analysis （TG-DTA）. The photocatalytic activity of CuO/ZrO2 catalyst was investigated based on the H2 evolution from oxalic acid solution under simulated sunlight irradiation. The effects of molar ratio of CuO to ZrO2, preparation method, phase change with the calcination temperature and the durability on the photocatalytic activity of the photocatalyst were investigated in detail. It is found that the optimal activity of photocatalytic H2 evolution （2.41 mmol.h i.g-~） can be obtained when CuO/ZrO2 composite photocatalyst is synthesized by sol-gel technique and the mole ratio of CuO to ZrO2 is 40%. The activity of copper oxide supported on monoclinic ZrO2 calcined at higher temperature is much higher than that on tetragonal ZrO2 calcined at lower temperature, and the best calcination temperature is 900 ℃.
基金Project(8451063201001261) supported by the Guangdong Natural Science Fund Committee,ChinaProject(LYM08022) supported by the Foundation for Distinguished Young Talents in Higher Education of Guangdong,China+1 种基金Project (2007A032400001, 2008A030202010) supported by the Scientific and Technological Planning of Guangdong Province,ChinaProject(216113132) supported by the Scientific Research Cultivation and Innovation Fund, Jinan University,China
文摘The role of oxygen and the generation of active radicals in the photocatalitic degradation of phenol were investigated using the eosin sensitized TiO2 as photocatalyst under visible light irradiation. Diffuse reflectance spectra show that the absorbancy range of eosin/TiO2 is expanded from 378 nm (TiO2 ) to about 600 nm. The photocatalitic degradation of phenol is almost stopped when the eosin/TiO2 system is saturated with N2 , which indicates the significance of O2 . The addition of NaN 3 (a quencher of single oxygen) causes about a 62% decrease in the phenol degradation. The phenol degradation ratio is dropped from 92% to 75% when the isopropanol (a quencher of hydroxyl radical) is present in the system. The experimental results show that there are singlet oxygen and hydroxyl radical generated in the eosin/TiO2 system under visible light irradiation. The changes of absorbancy indicate that the hydrogen peroxide might be produced. Through the analysis and comparison, it is found that the singlet oxygen is the predominant active radical for the degradation of phenol.
文摘Nanocrystalline Fe-doped TiO2 with size of 6070 nm was prepared by a sol-gel technique, followed by freeze-drying treatment for 2 h. Thermogravimetric and differential thermal analyses, X-ray diffraction, scanning （electron） microscope, laser diffraction particle size analyzer and UV-Vis spectrophotometer technologies were used to characterize the product. The photocatalytic activities of the samples were evaluated by the degradation of wastewater of paper-making. The effects of Fe ion implantation on the photocatalytic activity of TiO2 were also discussed. The results show that the iron content plays an essential role in affecting the photocatalytic activity of the Fe-doped TiO2 and the optimum content of Fe-doped is 0.05% （mass fraction）. The photocatalytic activity of samples with lower content of Fe-doped is higher than that of pure TiO2 in the treatment of paper-making wastewater. The photo-degradation effect of paper-making effluent is the best by means of Fe-doped TiO2 with 0.05% Fe.
基金Project(2011CB201505)supported by the National Key Basic Research Program of ChinaProject(BA2011031)supported by the Special Fund of Transformation of Scientific and Technological Achievements of Jiangsu Province,China
文摘Nitric oxide(NO) from flue gas is hard to remove because of low solubility and reactivity. A new technology for photocatalytic oxidation of NO using ultraviolet(UV)/TiO2/H2O2 process is studied in an efficient laboratory-scale reactor. Effects of several key operational parameters on NO removal efficiency are studied, including TiO2 content, H2O2 initial concentration, UV lamp power, NO initial content, oxygen volume fraction and TiO2/H2O2 solution volume. The results illustrate that the NO removal efficiency increases with the increasing of H2O2 initial concentration or UV lamp power. Meanwhile, a lower NO initial content or a higher TiO2/H2O2 solution volume will result in higher NO removal efficiency. In addition, oxygen volume fraction has a little effect.The highest NO removal efficiency is achieved at the TiO2 content of 0.75 g/L, H2O2 initial concentration of 2.5 mol/L, UV lamp power of 36 W, NO initial content of 206×10-6 and TiO2/H2O2 solution volume of 600 m L. It is beneficial for the development and application of NO removal from coal-fired flue gas with UV/TiO2/H2O2 process.
基金Project(2005CB623701) supported by the National Key Basic Research Program of China
文摘TiO2/bauxite-tailings （TiO2/BTs） composites were prepared via a chemical liquid deposition method and characterized by X-ray diffractometry （XRD）, scanning electronic microscopy （SEM） and N2 adsorption analysis. The photocatalytic performance of TiO2/BTs composites was evaluated with UV-Vis spectrophotometer following the changes of phenol concentration under different illumination time. Effects of the calcination temperature, the pH and the cycles on the photocatalytic activity of TiO2/BTs composites were investigated. The composites calcined at 500 and 600 ℃ exhibit the best photocatalytic performance, and the phenol degradation ratios reacting for 40 and 160 rain reach 35% and 78% respectively under the same conditions, higher than those of 29% and 76% of the Degussa P25（TiO2）. The ability of TiO2/BTs500 （BTs500 represents bauxite-tailings calcined at 500 ℃） composites to degrade phenol increases with decreasing pH.
基金Projects(21306041,21271071)supported by the National Natural Science Foundation of ChinaProject(15A076)supported by the Scientific Research Foundation of Hunan Provincial Education Department of China
文摘ZnO/ZnGa_2O_4 composite microspheres with heterojunction were successfully synthesized by one-pot hydrothermal method.These samples were characterized by TG/DTA,XRD,TEM,HRTEM,UV-vis DRS,FL and BET techniques.The results indicated the as-prepared samples showed better degree of crystalline and large specific surface area.The photocatalytic activity was evaluated by degradation of methyl orange with the concentration of 50 mg/L under the irradiation of simulated sunlight.The effects of molar ratio of Zn to Ga and calcination temperature on the photocatalytic activity were investigated in detail.The results showed that the highest photocatalytic degradation efficiency was observed at the molar ratio of Zn to Ga of 1:0.5 in the starting materials and the calcination temperature of 400 °C.The maximum photocatalytic degradation rate of MO was 97.1% within 60 min under the simulated sunlight irradiation,which is greatly higher than that of ZnO and ZnGa_2O_4.
