TiO 2 nanoparticles, doped with different Pt contents, were prepared by a modified photodeposition method using Degussa P-25 TiO 2 , H 2 PtCl 6 ·6H 2 O and methanol as the solvents. The physicochemical properties...TiO 2 nanoparticles, doped with different Pt contents, were prepared by a modified photodeposition method using Degussa P-25 TiO 2 , H 2 PtCl 6 ·6H 2 O and methanol as the solvents. The physicochemical properties of Pt/TiO 2 were investigated by the nitrogen adsorption and desorption isotherm measurement technique, X-ray diffraction analysis and photoluminescence spectra, respectively. Reaction rates from photocatalytic removal of dichloromethane over Degussa P-25 TiO 2 and Pt/TiO 2 were evaluated. The average diameter and BET surface area of the TiO 2 catalyst particles were 300 nm and 50 m 2 /g, respectively. The degradation efficiency was 99.0%, 82.7%, 55.2%, and 57.9% with TiO 2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. And the degradation efficiency was 99.3%, 79.7%, 76.5%, and 73.4% with a 0.005 wt.% Pt/TiO 2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. In addition, we found that the photoluminescence emission peak intensities decreased with increases in the doping amount of Pt, which indicates that the irradiative recombination was weakened. Furthermore, the results showed that the UV/0.005 wt.% Pt/TiO 2 process was capable of efficiently decomposing gaseous DCM in air.展开更多
Photoelectrocatalytic water splitting is an effective way to utilize the solar energy to solve the energy shortage. The valence band edge of WO3 located at 3V vs. normal hydrogen electrode（NHE）, which can offer enou...Photoelectrocatalytic water splitting is an effective way to utilize the solar energy to solve the energy shortage. The valence band edge of WO3 located at 3V vs. normal hydrogen electrode（NHE）, which can offer enough potential to kinetically oxidize water for oxygen evolution reaction. However, water oxidation reaction kinetics is sluggish when only WO3 is used as the photoanode. It is highly desirable to use cocatalyst to promote the kinetics. Mn Oxloaded on the WO3 photoanode through photodeposition methods improves the photoelectrochemical water oxidation performance. A maximum photocurrent density of composite photoanode is achieved with a deposition time of 3 min, which is higher than that of pristine WO3 photoanode around 40%. Mn O2 is not only a cocatalyst for water splitting but also for improving oxidation selectivity. We tried to use two means to load Mn Oxon WO3 photoanode material. It is observed that loading a moderate amount of Mn Oxon the WO3 by photodeposition can promote the performance of the WO3 photoanode.展开更多
基金financial supports forthe project of"Research and Development on ResourceRecovery Technology of the Opto-Electronic Industry Wastes"(No.99-EC-17-A-10-S1-151)from Taiwan's Ministry of Economic Affairs(MOEA)the projects(No.NSC99-2221-E-197-011-MY3)from Taiwan's"National"Science Council for the work
文摘TiO 2 nanoparticles, doped with different Pt contents, were prepared by a modified photodeposition method using Degussa P-25 TiO 2 , H 2 PtCl 6 ·6H 2 O and methanol as the solvents. The physicochemical properties of Pt/TiO 2 were investigated by the nitrogen adsorption and desorption isotherm measurement technique, X-ray diffraction analysis and photoluminescence spectra, respectively. Reaction rates from photocatalytic removal of dichloromethane over Degussa P-25 TiO 2 and Pt/TiO 2 were evaluated. The average diameter and BET surface area of the TiO 2 catalyst particles were 300 nm and 50 m 2 /g, respectively. The degradation efficiency was 99.0%, 82.7%, 55.2%, and 57.9% with TiO 2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. And the degradation efficiency was 99.3%, 79.7%, 76.5%, and 73.4% with a 0.005 wt.% Pt/TiO 2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. In addition, we found that the photoluminescence emission peak intensities decreased with increases in the doping amount of Pt, which indicates that the irradiative recombination was weakened. Furthermore, the results showed that the UV/0.005 wt.% Pt/TiO 2 process was capable of efficiently decomposing gaseous DCM in air.
基金financially supported by the National Natural Science Foundation of China (Nos. 21173105, 21773096)Fundamental Research Funds for the Central Universities (No. lzujbky2016-k08)+1 种基金Open fund by Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control (No. KHK1701)the Natural Science Foundation of Gansu (No. 17JR5RA186)
文摘Photoelectrocatalytic water splitting is an effective way to utilize the solar energy to solve the energy shortage. The valence band edge of WO3 located at 3V vs. normal hydrogen electrode（NHE）, which can offer enough potential to kinetically oxidize water for oxygen evolution reaction. However, water oxidation reaction kinetics is sluggish when only WO3 is used as the photoanode. It is highly desirable to use cocatalyst to promote the kinetics. Mn Oxloaded on the WO3 photoanode through photodeposition methods improves the photoelectrochemical water oxidation performance. A maximum photocurrent density of composite photoanode is achieved with a deposition time of 3 min, which is higher than that of pristine WO3 photoanode around 40%. Mn O2 is not only a cocatalyst for water splitting but also for improving oxidation selectivity. We tried to use two means to load Mn Oxon WO3 photoanode material. It is observed that loading a moderate amount of Mn Oxon the WO3 by photodeposition can promote the performance of the WO3 photoanode.
