The metal complex 5-(4-aminophenyl)-10,15,20-triphenylporphyrin copper (CuAPTPP) was covalently linked on the surface of TiO2 microspheres by using toluene disocyanate (TDI) as a bridging bond unit. The hydroxyl...The metal complex 5-(4-aminophenyl)-10,15,20-triphenylporphyrin copper (CuAPTPP) was covalently linked on the surface of TiO2 microspheres by using toluene disocyanate (TDI) as a bridging bond unit. The hydroxyl group (-OH) of TiO2 microspheres surface and the amino group (-NH2) of CuAPTPP reacted respectively with the active -NCO groups of TDI to form a surface conjugated microsphere CuAPTPP-TDI-TiO2 that was confirmed by FT-IR spectra. The CuAPTPP-TDI-TiO2 microspheres were characterized with UV-visible, elemental analysis, XRD, SEM, and UV-Vis diffuse reflectance spectra. The effect of amounts of linked TDI on the performance of photocatalytic microspheres was discussed, and the optimal molar ratio of TDI:TiO2 was established. The photocatalytic activity of CuAPTPP- TDI-TiO2 was evaluated using the photocatalytic degradation of methylene blue (MB) under visible-light irradiation. The results showed that, TDI, as a bond unit, was used to form a steady chemical brigdging bond linking CuAPTPP and the surface of TiO2 microspheres, and the prepared catalyst exhibited higher photocatalytic activity under visible-light irradiation for MB degradation. The degradation rate of 20 mg/L MB could reach 98.7% under Xe- lamp (150 W) irradiation in 120 rain. The degradation of MB followed the first-order reaction model under visible light irradiation, and the rate constant of 5.1× 10^-2 min-1 and the half- life of 11.3 min were achieved. And the new photocatalyst can be recycled for 4 times, remaining 90.0% MB degradation rate.展开更多
The photocatalytic reduction of CO2 with H2O to fuels and chemicals using solar energy is one of the most attractive but highly difficult routes.Thus far,only a very limited number of photocatalysts has been reported ...The photocatalytic reduction of CO2 with H2O to fuels and chemicals using solar energy is one of the most attractive but highly difficult routes.Thus far,only a very limited number of photocatalysts has been reported to be capable of catalyzing the photocatalytic reduction of CO2 under visible light.The utilization of the localized surface plasmon resonance(LSPR)phenomenon is an attractive strategy for developing visible-light photocatalysts.Herein,we have succeeded in synthesizing plasmonic MoO3?x-TiO2 nanocomposites with tunable LSPR by a simple solvothermal method.The well-structured nanocomposite containing two-dimensional(2D)molybdenum oxide(MoO3?x)nanosheets and one-dimensional(1D)titanium oxide nanotubes(TiO2-NT)showed LSPR absorption band in the visible-light region,and the incorporation of TiO2-NT significantly enhanced the LSPR absorption band.The MoO3?x-TiO2-NT nanocomposite is promising for application in the photocatalytic reduction of CO2 with H2O under visible light irradiation.展开更多
Biofabrication of noble monometallic platinum nanoparticles(Pt-NPs) and bimetallic gold–silver nanoparticles(Au Ag-NPs) using aqueous extract of Delonix regia is presented here. Antioxidant activity of biomatrix-load...Biofabrication of noble monometallic platinum nanoparticles(Pt-NPs) and bimetallic gold–silver nanoparticles(Au Ag-NPs) using aqueous extract of Delonix regia is presented here. Antioxidant activity of biomatrix-loaded metallic nanoparticles is estimated for scavenging of two model radicals i.e., 2,2′-Azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt and 1,1′-Diphenyl-2-picrylhydrazyl. Broad spectral continuum spanning from visible to ultra-violet region(Pt-NPs: 30 min) and broad high intensity absorption peak around at 500 nm(Au Ag-NPs: 10 min) in two different UV–Visible spectra confirmed the biofabrication. Nanoparticles fabricated with distorted spherical shape and crystalline face-centred-cubic geometry. Strong signal around at 2.10 ke V(pure-phase platinum) and typical X-ray peaks observed at 2.20 and 3 ke V suggested, co-existence and alloying interaction of Au and Ag in Au Ag-NPs. ζ potential(-15.2 mV: Pt-NPs and -13.9 mV: Au Ag-NPs) values suggested surface adsorption of polyphenolic compounds to provide stability. Nanoparticles exhibited pronounced antioxidant activity against free radicals through their electron/hydrogen transfer ability.展开更多
The interaction between silver nanoparticles and Methylene Blue (MB) is studied by UV-Vis spectroscopy and fluorescence spec- trometry. The UV-Vis absorption of the silver nanoparticles changes dramatically with the...The interaction between silver nanoparticles and Methylene Blue (MB) is studied by UV-Vis spectroscopy and fluorescence spec- trometry. The UV-Vis absorption of the silver nanoparticles changes dramatically with the addition of MB. However, no obvious changes of absorption spectra of MB are observed when silver colloids are added into the MB solution. In the presence of surfactant SDS, the catalysis of the silver nanoparticles in the reduction of MB by sodium borohydride is exhibited by UV-Vis and fluorescence spectrosopy of MB displaying faster response compared with the absence of the silver nanoparticles. The results show that the activity of surfactant SDS modified silver nanoparticles is great and a strong physical adsorption to MB exists.展开更多
This paper reports on the synthesis of copper doped sulfated titania nano-crystalline powders with varying (2.0%-10.0%, by mass) by single step sol gel method. The synthesized photo catalyst has been characterized b...This paper reports on the synthesis of copper doped sulfated titania nano-crystalline powders with varying (2.0%-10.0%, by mass) by single step sol gel method. The synthesized photo catalyst has been characterized by employing various techniques like X-ray Diffraction (XRD), Ultraviolet-Visible Diffuse Reflection Spectroscopy (UV-Vis DRS), X-ray Photoelectron Spectroscopy (XPS), Scanning Electron Microscopy (SEM), Energy Dispersive Spectrometry (EDS), Fourier Transform Infrared Spectroscopic Studies (FT-IR), and Transmission Electron Microscopy (TEM). From the XRD and TEM results, all the samples were reported in anatase phase with reduction in particle size in the range of 7 to 12 nm. SEM indicated the change in morphology of the particles. The presence of copper in titania lattice was evidenced by XPS. From UV-Vis DRS and FT-IR studies indicated that prominent absorption shift is observed towards visible region (red shift), the entry ofCu2 + into Ti02 lattice as a substitution- al dopant and S042- ions were covalently bonded with Ti4+ on the surface of the copper doped titania respectively. The photocatalytic activity studies were investigated by considering methyl orange (MO) as dye pollutant in the presence of the visible light. The effect of various parameters like effect of dosage of the catalyst, dopant concentration, pH of the solution, and concentration of the dye was studied in detail.展开更多
The visible light photocatalytic activity of two-dimensional (2D) BiOl microplates was intensively enhanced through simply dipping in Na2CO3 solutions at room temperature. The X-ray powder diffrac- tion (XRD) and ...The visible light photocatalytic activity of two-dimensional (2D) BiOl microplates was intensively enhanced through simply dipping in Na2CO3 solutions at room temperature. The X-ray powder diffrac- tion (XRD) and scanning electron microscopy (SEM) investigations suggest that little amount of (BiO)2CO3 phase was formed on the surface of 2D BiOI via the in situ chemical conversion. The concen- tration of Na2CO3 solutions affected the structure, morphology, light absorption and surface element component of 2D BiOl. The surface loaded (BiO)2CO3 mainly trapped the photoinduced electrons of BiOI, improved the separation efficiency of photocharges and finally raised the photocatalytic activity of BiOl under visible light (λ 〉 420 nm). Furthermore, the product of the as-prepared (BiO)2CO3/BiOI displayed excellent stability in the repeated experiment. This study provides a facile way to improve the photocatalytic activity of BiOX (X = CI, Br, I) by means of surface treatment with Na2CO3 solutions.展开更多
基金ACKNOWLEDGMENTS This work was supported by the National Natural Science Foundation of China (No.21276208), the Doctor Fundation of Education Ministry of China (No.20096118110008), the Special Research Fund of Shaanxi Provincial Department of Education of China (No.12JK0606), and the Research Fund for Excellent Doctoral Thesis of Xi'an University of Technology (No.207-002J1304).
文摘The metal complex 5-(4-aminophenyl)-10,15,20-triphenylporphyrin copper (CuAPTPP) was covalently linked on the surface of TiO2 microspheres by using toluene disocyanate (TDI) as a bridging bond unit. The hydroxyl group (-OH) of TiO2 microspheres surface and the amino group (-NH2) of CuAPTPP reacted respectively with the active -NCO groups of TDI to form a surface conjugated microsphere CuAPTPP-TDI-TiO2 that was confirmed by FT-IR spectra. The CuAPTPP-TDI-TiO2 microspheres were characterized with UV-visible, elemental analysis, XRD, SEM, and UV-Vis diffuse reflectance spectra. The effect of amounts of linked TDI on the performance of photocatalytic microspheres was discussed, and the optimal molar ratio of TDI:TiO2 was established. The photocatalytic activity of CuAPTPP- TDI-TiO2 was evaluated using the photocatalytic degradation of methylene blue (MB) under visible-light irradiation. The results showed that, TDI, as a bond unit, was used to form a steady chemical brigdging bond linking CuAPTPP and the surface of TiO2 microspheres, and the prepared catalyst exhibited higher photocatalytic activity under visible-light irradiation for MB degradation. The degradation rate of 20 mg/L MB could reach 98.7% under Xe- lamp (150 W) irradiation in 120 rain. The degradation of MB followed the first-order reaction model under visible light irradiation, and the rate constant of 5.1× 10^-2 min-1 and the half- life of 11.3 min were achieved. And the new photocatalyst can be recycled for 4 times, remaining 90.0% MB degradation rate.
文摘The photocatalytic reduction of CO2 with H2O to fuels and chemicals using solar energy is one of the most attractive but highly difficult routes.Thus far,only a very limited number of photocatalysts has been reported to be capable of catalyzing the photocatalytic reduction of CO2 under visible light.The utilization of the localized surface plasmon resonance(LSPR)phenomenon is an attractive strategy for developing visible-light photocatalysts.Herein,we have succeeded in synthesizing plasmonic MoO3?x-TiO2 nanocomposites with tunable LSPR by a simple solvothermal method.The well-structured nanocomposite containing two-dimensional(2D)molybdenum oxide(MoO3?x)nanosheets and one-dimensional(1D)titanium oxide nanotubes(TiO2-NT)showed LSPR absorption band in the visible-light region,and the incorporation of TiO2-NT significantly enhanced the LSPR absorption band.The MoO3?x-TiO2-NT nanocomposite is promising for application in the photocatalytic reduction of CO2 with H2O under visible light irradiation.
文摘Biofabrication of noble monometallic platinum nanoparticles(Pt-NPs) and bimetallic gold–silver nanoparticles(Au Ag-NPs) using aqueous extract of Delonix regia is presented here. Antioxidant activity of biomatrix-loaded metallic nanoparticles is estimated for scavenging of two model radicals i.e., 2,2′-Azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt and 1,1′-Diphenyl-2-picrylhydrazyl. Broad spectral continuum spanning from visible to ultra-violet region(Pt-NPs: 30 min) and broad high intensity absorption peak around at 500 nm(Au Ag-NPs: 10 min) in two different UV–Visible spectra confirmed the biofabrication. Nanoparticles fabricated with distorted spherical shape and crystalline face-centred-cubic geometry. Strong signal around at 2.10 ke V(pure-phase platinum) and typical X-ray peaks observed at 2.20 and 3 ke V suggested, co-existence and alloying interaction of Au and Ag in Au Ag-NPs. ζ potential(-15.2 mV: Pt-NPs and -13.9 mV: Au Ag-NPs) values suggested surface adsorption of polyphenolic compounds to provide stability. Nanoparticles exhibited pronounced antioxidant activity against free radicals through their electron/hydrogen transfer ability.
基金supported by the National Natural Science Foundation of China(No.20875059)
文摘The interaction between silver nanoparticles and Methylene Blue (MB) is studied by UV-Vis spectroscopy and fluorescence spec- trometry. The UV-Vis absorption of the silver nanoparticles changes dramatically with the addition of MB. However, no obvious changes of absorption spectra of MB are observed when silver colloids are added into the MB solution. In the presence of surfactant SDS, the catalysis of the silver nanoparticles in the reduction of MB by sodium borohydride is exhibited by UV-Vis and fluorescence spectrosopy of MB displaying faster response compared with the absence of the silver nanoparticles. The results show that the activity of surfactant SDS modified silver nanoparticles is great and a strong physical adsorption to MB exists.
文摘This paper reports on the synthesis of copper doped sulfated titania nano-crystalline powders with varying (2.0%-10.0%, by mass) by single step sol gel method. The synthesized photo catalyst has been characterized by employing various techniques like X-ray Diffraction (XRD), Ultraviolet-Visible Diffuse Reflection Spectroscopy (UV-Vis DRS), X-ray Photoelectron Spectroscopy (XPS), Scanning Electron Microscopy (SEM), Energy Dispersive Spectrometry (EDS), Fourier Transform Infrared Spectroscopic Studies (FT-IR), and Transmission Electron Microscopy (TEM). From the XRD and TEM results, all the samples were reported in anatase phase with reduction in particle size in the range of 7 to 12 nm. SEM indicated the change in morphology of the particles. The presence of copper in titania lattice was evidenced by XPS. From UV-Vis DRS and FT-IR studies indicated that prominent absorption shift is observed towards visible region (red shift), the entry ofCu2 + into Ti02 lattice as a substitution- al dopant and S042- ions were covalently bonded with Ti4+ on the surface of the copper doped titania respectively. The photocatalytic activity studies were investigated by considering methyl orange (MO) as dye pollutant in the presence of the visible light. The effect of various parameters like effect of dosage of the catalyst, dopant concentration, pH of the solution, and concentration of the dye was studied in detail.
基金supported by the National Natural Science Foundation of China (51472005, 51272081)the Natural Science Foundation of Educational Committee of Anhui Province (gxyq ZD2016413, gxyq ZD2016414, and KJ2015A027)+1 种基金the Natural Science Foundation of Anhui Province (1708085MB32)Innovation Team of Design and Application of Advanced Energetic Materials
文摘The visible light photocatalytic activity of two-dimensional (2D) BiOl microplates was intensively enhanced through simply dipping in Na2CO3 solutions at room temperature. The X-ray powder diffrac- tion (XRD) and scanning electron microscopy (SEM) investigations suggest that little amount of (BiO)2CO3 phase was formed on the surface of 2D BiOI via the in situ chemical conversion. The concen- tration of Na2CO3 solutions affected the structure, morphology, light absorption and surface element component of 2D BiOl. The surface loaded (BiO)2CO3 mainly trapped the photoinduced electrons of BiOI, improved the separation efficiency of photocharges and finally raised the photocatalytic activity of BiOl under visible light (λ 〉 420 nm). Furthermore, the product of the as-prepared (BiO)2CO3/BiOI displayed excellent stability in the repeated experiment. This study provides a facile way to improve the photocatalytic activity of BiOX (X = CI, Br, I) by means of surface treatment with Na2CO3 solutions.