Rod-shaped PbW O4 microcrystals of length 1 μm were fabricated by a hydrothermal route and subsequent calcination. Pt nanoparticles（NPs） of different contents（0.5 wt%,1 wt% and 2 wt%） were subsequently deposited ...Rod-shaped PbW O4 microcrystals of length 1 μm were fabricated by a hydrothermal route and subsequent calcination. Pt nanoparticles（NPs） of different contents（0.5 wt%,1 wt% and 2 wt%） were subsequently deposited on the PbW O4 microcrystals,producing robust Pt/PbW O4 composite microcrystals. The PbW O4 microcrystals and Pt/PbW O4 photocatalysts were characterized by X-ray diffraction,N2 sorption measurements,scanning electron microscopy,transmission electron microscopy,and X-ray photoelectron,photoluminescence,Fourier-transform infrared,and ultraviolet-visible diffuse reflectance spectroscopies. The photocatalytic performances of the catalysts were evaluated by the consecutive photocatalytic degradation of acid orange II dye. The Pt/PbW O4 composite microcrystals exhibited high photocatalytic activity and stability. The deposition of Pt NPs produced surface plasmon resonance（SPR）,which induced a large visible light absorption. A Pt NP content of 1-2 wt% resulted in an ~2 times increase in photocatalytic activity,compared with the activity of Pt/PbW O4. The crystal structure and high crystallinity of PbW O4 resulted in its favorable photocatalytic property,and the SPR effect of the Pt NPs promoted visible light harvesting. The Pt NPs also enhanced the separation of photo-generated electrons and holes,which further promoted the photocatalytic reaction.展开更多
CO self-poisoning and slow surface kinetics pose major challenges to a CO oxidation catalyst that should work at ambient temperature.Furthermore,the presence of moisture would cause passivation of the catalyst A highl...CO self-poisoning and slow surface kinetics pose major challenges to a CO oxidation catalyst that should work at ambient temperature.Furthermore,the presence of moisture would cause passivation of the catalyst A highly active ceria promoted Pt catalyst（4%Pt-12%CeO_2/SiO_2;conversion≥99%at low（ 500 ppm） and high（ 2500 ppm） CO concentrations was developed for CO oxidation at ambient temperature in humid air.Catalyst preparation variables such as Pt and CeO_2 loading,ceria deposition method,drying and calcination conditions for the ceria and Pt precursors were optimized experimentally.The activity was correlated with surface properties using CO/H_2 chemisorption,O_2-H_2 titration,X-ray diffraction and BET surface area analysis.The method of CeO_2 deposition had a significant impact on the catalytic activity.CeO_2 deposition by impregnation resulted in a catalyst that was three times more active than that prepared by deposition precipitation or CeO_2grafting.O_2-H_2 titration results revealed that the close association of ceria and Pt in the case of CeO_2deposition by impregnation resulted in higher activity.The catalyst support used was also crucial as a silica supported catalyst was five times more active than an alumina supported catalyst.The particle size and pore structure of the catalyst support were also crucial as the reaction was diffusion controlled.The drying and calcination conditions of the ceria and Pt precursors also played a crucial role in determining the catalytic activity.The Pt-CeO_2/SiO_2 catalysts with Pt 2.5 wt%and CeO_2 15 wt%were highly active（TOF 0.02 s^（-1）） and stable（conversion 99%after 15 h） at ambient conditions.展开更多
基金supported by the National Natural Science Foundation of China(2106700421567008+5 种基金21263005)Project of Jiangxi Province Natural Science Foundation China(20133BAB21003)Training Programs of Innovation and Entrepreneurship for Undergraduates of Jiangxi Province(201310407046)The Landing Project of Science and Technology of Colleges and Universities in Jiangxi Province(KJLD14046)Young Scientist Training Project of Jiangxi Province(20122BCB23015)Yuanhang Engineering of Jiangxi Province~~
文摘Rod-shaped PbW O4 microcrystals of length 1 μm were fabricated by a hydrothermal route and subsequent calcination. Pt nanoparticles（NPs） of different contents（0.5 wt%,1 wt% and 2 wt%） were subsequently deposited on the PbW O4 microcrystals,producing robust Pt/PbW O4 composite microcrystals. The PbW O4 microcrystals and Pt/PbW O4 photocatalysts were characterized by X-ray diffraction,N2 sorption measurements,scanning electron microscopy,transmission electron microscopy,and X-ray photoelectron,photoluminescence,Fourier-transform infrared,and ultraviolet-visible diffuse reflectance spectroscopies. The photocatalytic performances of the catalysts were evaluated by the consecutive photocatalytic degradation of acid orange II dye. The Pt/PbW O4 composite microcrystals exhibited high photocatalytic activity and stability. The deposition of Pt NPs produced surface plasmon resonance（SPR）,which induced a large visible light absorption. A Pt NP content of 1-2 wt% resulted in an ~2 times increase in photocatalytic activity,compared with the activity of Pt/PbW O4. The crystal structure and high crystallinity of PbW O4 resulted in its favorable photocatalytic property,and the SPR effect of the Pt NPs promoted visible light harvesting. The Pt NPs also enhanced the separation of photo-generated electrons and holes,which further promoted the photocatalytic reaction.
基金supported as part of the Catalysis Center for Energy Innovation, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Basic Energy Sciences under Award Number DE-SC0001004Program for New Century Excellent Talents in University of China (NCET-12-0297)~~
基金supported by US Army contract(W56HZV-05-C0686) at Auburn University administered through TARDEC
文摘CO self-poisoning and slow surface kinetics pose major challenges to a CO oxidation catalyst that should work at ambient temperature.Furthermore,the presence of moisture would cause passivation of the catalyst A highly active ceria promoted Pt catalyst（4%Pt-12%CeO_2/SiO_2;conversion≥99%at low（ 500 ppm） and high（ 2500 ppm） CO concentrations was developed for CO oxidation at ambient temperature in humid air.Catalyst preparation variables such as Pt and CeO_2 loading,ceria deposition method,drying and calcination conditions for the ceria and Pt precursors were optimized experimentally.The activity was correlated with surface properties using CO/H_2 chemisorption,O_2-H_2 titration,X-ray diffraction and BET surface area analysis.The method of CeO_2 deposition had a significant impact on the catalytic activity.CeO_2 deposition by impregnation resulted in a catalyst that was three times more active than that prepared by deposition precipitation or CeO_2grafting.O_2-H_2 titration results revealed that the close association of ceria and Pt in the case of CeO_2deposition by impregnation resulted in higher activity.The catalyst support used was also crucial as a silica supported catalyst was five times more active than an alumina supported catalyst.The particle size and pore structure of the catalyst support were also crucial as the reaction was diffusion controlled.The drying and calcination conditions of the ceria and Pt precursors also played a crucial role in determining the catalytic activity.The Pt-CeO_2/SiO_2 catalysts with Pt 2.5 wt%and CeO_2 15 wt%were highly active（TOF 0.02 s^（-1）） and stable（conversion 99%after 15 h） at ambient conditions.
基金supported by the National Natural Science Foundation of China (21173153)the Science and Technology Department of Science and Technology Support Project of Sichuan Province,China (2011GZ0035)~~
