Electron trapping material CaS:Eu,Sm has been prepared by the technique of direct doping rare earth.It can convert infrared light (0.8～1.6μm) to visible light (～672nm) and its quantum efficiency is more than 76%.Hi...Electron trapping material CaS:Eu,Sm has been prepared by the technique of direct doping rare earth.It can convert infrared light (0.8～1.6μm) to visible light (～672nm) and its quantum efficiency is more than 76%.High efficiency and portable cards for infrared laser detection have been made of electron trapping material by using various expertiese and tested on many conditions,such as waterlogging at high and low temperature.According to the test,this kind of infrared detecting card can convert infrared light (0.8～1.6μm) to visible light at room temperature efficiently and can be used extensively for adjusting and detecting infrared laser emitted by YAG,GaAs,InGaAsP.展开更多
To increase the number of active sites and defects in TiO2 and promote rapid and efficient transfer of photogenerated charges, a g-C3N4@C-TiO2 composite photocatalyst was prepared via in situ deposition of g-C3N4 on a...To increase the number of active sites and defects in TiO2 and promote rapid and efficient transfer of photogenerated charges, a g-C3N4@C-TiO2 composite photocatalyst was prepared via in situ deposition of g-C3N4 on a carbon-doped anatase TiO2 surface. The effects of carbon doping state and surface modification of g-C3N4 on the performance of g-C3N4@C-TiO2 composite photocatalysts were studied by X-ray diffraction, X-ray photoelectron spectroscopy, UV-visible diffuse-reflectance spectroscopy, transmission electron microscopy, electrochemical impedance spectroscopy, photoluminescence, and electron paramagnetic resonance. With increasing carbon doping content, the carbon doping state in TiO2 gradually changed from gap to substitution doping. Although the number of oxygen vacancies gradually increased, the degradation efficiency of g-C3N4@C-TiO2 for RhB (phenol) initially increased and subsequently decreased with increasing carbon content. The g-C3N4@10C-TiO2 sample exhibited the highest apparent reaction rate constant of 0.036 min儃1 (0.039 min儃1) for RhB (phenol) degradation, which was 150 (139), 6.4 (6.8), 2.3 (3), and 1.7 (2.1) times higher than that of pure TiO2, 10C-TiO2, g-C3N4, and g-C3N4@TiO2, respectively. g-C3N4 was grown in situ on the surface of C-TiO2 by surface carbon hybridization and bonding. The resultant novel g-C3N4@C-TiO2 photocatalyst exhibited direct Z-scheme heterojunctions with non-local impurity levels. The high photocatalytic activity can be attributed to the synergistic effects of the improved visible light response ability, higher photogenerated electron transfer efficiency, and redox ability arising from Z-type heterojunctions.展开更多
The mixed oxides La1 -xCexFe1-y-nCOyRunO3 were prepared by sol-gel method and used as catalysts for NO direct decomposition. The catalysts were characterized by DTA - TG, XRD, IR and BET. XRD analysis reveals that th...The mixed oxides La1 -xCexFe1-y-nCOyRunO3 were prepared by sol-gel method and used as catalysts for NO direct decomposition. The catalysts were characterized by DTA - TG, XRD, IR and BET. XRD analysis reveals that the samples are in a pure perovskite phase in 550 - 650 ℃, and catalyst structure keeps long else 20 decrease, and lattice parameters enhance when Ru is introduced. The characteristic peaks of samples are stronger during a temperature increase, and the particle size grows faster. IR analysis shows that the position and shape of adsorption peaks are almost the same among all samples, but with the Ru content increasing, 600 cm^-1 peak stretches to a high frequency and changes to disorder. The wave numbers move to low frequency when n = 0. 05, yet it doesn＇ t vary obviously when n 〉 0. 05. The BET surface area testifies that particle sizes of all catalysts increase with temperature increasing.展开更多
Doped phosphide is promising in earthabundant element based catalysts for hydrogen evolution reaction(HER). Here we employ ammonium hypophosphite(NH4H2PO2) to synthesize a novel parallel doped catalyst,nitrogen doped ...Doped phosphide is promising in earthabundant element based catalysts for hydrogen evolution reaction(HER). Here we employ ammonium hypophosphite(NH4H2PO2) to synthesize a novel parallel doped catalyst,nitrogen doped molybdenum phosphide nanoparticles(NPs)supported on nitrogen doped carbon nanotubes(N-MoP/N-CNTs). The NH4H2PO2 as a bifunctional agent severs as both phosphidation agent and nitrogen source, which makes the synthetic route simple and efficient. The as-obtained parallel doped N-MoP/N-CNTs show an overpotential of 103±5 mV at 10 mA cm-2, which is 140 mV lower than that of MoP NPs. The enhanced HER performance is attributed to the electronic effect by doped MoP and CNTs supports. This work provides a facile route to synthesize doped phosphides for the potential applications in hydrogen energy.展开更多
文摘Electron trapping material CaS:Eu,Sm has been prepared by the technique of direct doping rare earth.It can convert infrared light (0.8～1.6μm) to visible light (～672nm) and its quantum efficiency is more than 76%.High efficiency and portable cards for infrared laser detection have been made of electron trapping material by using various expertiese and tested on many conditions,such as waterlogging at high and low temperature.According to the test,this kind of infrared detecting card can convert infrared light (0.8～1.6μm) to visible light at room temperature efficiently and can be used extensively for adjusting and detecting infrared laser emitted by YAG,GaAs,InGaAsP.
基金supported by the National Natural Science Foundation of China(51772140)the Natural Science Foundation of Jiangxi Province,China(20161BAB206111,20171ACB21033)the Scientific Research Foundation of Jiangxi Provincial Education Department,China(GJJ170578)~~
文摘To increase the number of active sites and defects in TiO2 and promote rapid and efficient transfer of photogenerated charges, a g-C3N4@C-TiO2 composite photocatalyst was prepared via in situ deposition of g-C3N4 on a carbon-doped anatase TiO2 surface. The effects of carbon doping state and surface modification of g-C3N4 on the performance of g-C3N4@C-TiO2 composite photocatalysts were studied by X-ray diffraction, X-ray photoelectron spectroscopy, UV-visible diffuse-reflectance spectroscopy, transmission electron microscopy, electrochemical impedance spectroscopy, photoluminescence, and electron paramagnetic resonance. With increasing carbon doping content, the carbon doping state in TiO2 gradually changed from gap to substitution doping. Although the number of oxygen vacancies gradually increased, the degradation efficiency of g-C3N4@C-TiO2 for RhB (phenol) initially increased and subsequently decreased with increasing carbon content. The g-C3N4@10C-TiO2 sample exhibited the highest apparent reaction rate constant of 0.036 min儃1 (0.039 min儃1) for RhB (phenol) degradation, which was 150 (139), 6.4 (6.8), 2.3 (3), and 1.7 (2.1) times higher than that of pure TiO2, 10C-TiO2, g-C3N4, and g-C3N4@TiO2, respectively. g-C3N4 was grown in situ on the surface of C-TiO2 by surface carbon hybridization and bonding. The resultant novel g-C3N4@C-TiO2 photocatalyst exhibited direct Z-scheme heterojunctions with non-local impurity levels. The high photocatalytic activity can be attributed to the synergistic effects of the improved visible light response ability, higher photogenerated electron transfer efficiency, and redox ability arising from Z-type heterojunctions.
基金Sponsored by the National Natural Science Foundation of China(Grant No.20271019 and 20576027)the Natural Science Foundation of HeilongjiangProvince(Grant No.B200504)+1 种基金the Postdoctoral Foundation of Heilongjiang Province(Grant No.LBH-Z05066)Education Office Foundation ofHeilongjiang Province(Grant No.11511270).
文摘The mixed oxides La1 -xCexFe1-y-nCOyRunO3 were prepared by sol-gel method and used as catalysts for NO direct decomposition. The catalysts were characterized by DTA - TG, XRD, IR and BET. XRD analysis reveals that the samples are in a pure perovskite phase in 550 - 650 ℃, and catalyst structure keeps long else 20 decrease, and lattice parameters enhance when Ru is introduced. The characteristic peaks of samples are stronger during a temperature increase, and the particle size grows faster. IR analysis shows that the position and shape of adsorption peaks are almost the same among all samples, but with the Ru content increasing, 600 cm^-1 peak stretches to a high frequency and changes to disorder. The wave numbers move to low frequency when n = 0. 05, yet it doesn＇ t vary obviously when n 〉 0. 05. The BET surface area testifies that particle sizes of all catalysts increase with temperature increasing.
基金supported by the National Key Research and Development Program of China (2017YFA0206500)the National Natural Science Foundation of China (21671014)the Fundamental Research Funds for the Central Universities (buctrc201522)
文摘Doped phosphide is promising in earthabundant element based catalysts for hydrogen evolution reaction(HER). Here we employ ammonium hypophosphite(NH4H2PO2) to synthesize a novel parallel doped catalyst,nitrogen doped molybdenum phosphide nanoparticles(NPs)supported on nitrogen doped carbon nanotubes(N-MoP/N-CNTs). The NH4H2PO2 as a bifunctional agent severs as both phosphidation agent and nitrogen source, which makes the synthetic route simple and efficient. The as-obtained parallel doped N-MoP/N-CNTs show an overpotential of 103±5 mV at 10 mA cm-2, which is 140 mV lower than that of MoP NPs. The enhanced HER performance is attributed to the electronic effect by doped MoP and CNTs supports. This work provides a facile route to synthesize doped phosphides for the potential applications in hydrogen energy.
