BiOI-sensitized titanium dioxide (TiO2) photocatalysts were prepared by a deposition method at room temperature and characterized by X-ray diffraction, X-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller su...BiOI-sensitized titanium dioxide (TiO2) photocatalysts were prepared by a deposition method at room temperature and characterized by X-ray diffraction, X-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller surface area measurements. The photocatalytic activities of the catalysts were evaluated for the degradation of methyl orange (MO) solution under UV and visible light irradiation. The effects of catalyst amount, initial pH value, initial concentration of MO, as well as KI amount were investigated. The repeatability of photocatalytic activity of the 1.7% BiOI/TiO2 catalyst was also tested. It is shown that BiOI sensitization enhances the photocatalytic activities of TiO2. With BiOI content increasing, the photocatalytic activities of BiOI/TiO2 under UV and visible light irradiation first increase, reaching a maximum around BiOI content of 1.7%, and then decrease with further increasing BiOI content. The 1.7% BiOI/TiO2 catalyst obviously exhibits much higher visible light photocatalytic activity than P25, and its UV light photocatalytic activity is slightly higher than that of P25. Under the conditions of a catalytic dose of 1.5 g.L-1, initial pH of 3.0, initial MO concentration of 20 mg.L-1, UV power of 300 W, and air flow rate of 0.8 L.min-1, complete degradatio is achieved within 60 min. The repeatability of photocatalytic activity of the 1.7% BiOI/TiO2 catalyst is highly reliable.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
The microporous nanocry'sta1line TiO2 electrode with large surface roughness factor hasbeen prepared on a conducting glass support. Modification of the TiO2 electrode by in situ preparingquantum sized RuS2 particl...The microporous nanocry'sta1line TiO2 electrode with large surface roughness factor hasbeen prepared on a conducting glass support. Modification of the TiO2 electrode by in situ preparingquantum sized RuS2 particles on the surface of TiO2 electrode extends the optical absorptionspectrum and photocurrent action specmim into visible region. In addition, compared with RuS2 bulknlaterials- a blue shifi in both absorption spectrum and photocurrent action speCtrum of RuS2rriO2elcctrode is obserived and explained in terms of quantum sized effect.展开更多
For better performance of dye sensitized solar cells （DSSCs）, a bilayer structured electrode was constructed by employing a mesoporous anatase TiO2 overlayer above a commercial P25 TiO2 nanoparticles underlayer. The...For better performance of dye sensitized solar cells （DSSCs）, a bilayer structured electrode was constructed by employing a mesoporous anatase TiO2 overlayer above a commercial P25 TiO2 nanoparticles underlayer. The mesoporous anatase TiO2, prepared through a facile surfactant-assisted sol-gel process, possessed large pore size and well inter-connected network structure, both beneficial for dye adsorption and electron transfer. The dye adsorption capability of the mesoporous TiO2 was nearly twice that of the P25 counterpart. In the electrode, the mesoporous TiO2 film enhanced both dye adsorption and lightharvest, to increase photocurrent （Jsc） from 12.32 to 14.78 mA/cm^2. Compared to the single P25 TiO2 film, the synergy of the mesoporous TiO2 and the P25 TiO2 nanoparticle films in the electrode resulted in a 24% improvement in light-to-electricity conversion efficiency （η）. This bilayered electrode provides an alternative approach for further developing a photovoltaic device with better cell performance.展开更多
基金financially supported by the National Natural Science Foundation of China(No.21171091)the Natural Science Foundation of Higher Education Institutions in Anhui Province(Nos.KJ2012A217,KJ2012B135,and KJ2012B136)
文摘BiOI-sensitized titanium dioxide (TiO2) photocatalysts were prepared by a deposition method at room temperature and characterized by X-ray diffraction, X-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller surface area measurements. The photocatalytic activities of the catalysts were evaluated for the degradation of methyl orange (MO) solution under UV and visible light irradiation. The effects of catalyst amount, initial pH value, initial concentration of MO, as well as KI amount were investigated. The repeatability of photocatalytic activity of the 1.7% BiOI/TiO2 catalyst was also tested. It is shown that BiOI sensitization enhances the photocatalytic activities of TiO2. With BiOI content increasing, the photocatalytic activities of BiOI/TiO2 under UV and visible light irradiation first increase, reaching a maximum around BiOI content of 1.7%, and then decrease with further increasing BiOI content. The 1.7% BiOI/TiO2 catalyst obviously exhibits much higher visible light photocatalytic activity than P25, and its UV light photocatalytic activity is slightly higher than that of P25. Under the conditions of a catalytic dose of 1.5 g.L-1, initial pH of 3.0, initial MO concentration of 20 mg.L-1, UV power of 300 W, and air flow rate of 0.8 L.min-1, complete degradatio is achieved within 60 min. The repeatability of photocatalytic activity of the 1.7% BiOI/TiO2 catalyst is highly reliable.
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The microporous nanocry'sta1line TiO2 electrode with large surface roughness factor hasbeen prepared on a conducting glass support. Modification of the TiO2 electrode by in situ preparingquantum sized RuS2 particles on the surface of TiO2 electrode extends the optical absorptionspectrum and photocurrent action specmim into visible region. In addition, compared with RuS2 bulknlaterials- a blue shifi in both absorption spectrum and photocurrent action speCtrum of RuS2rriO2elcctrode is obserived and explained in terms of quantum sized effect.
基金supported by the National Natural Science Foundation of China (20925621)Shanghai Rising-Star Program (09QH1400700,09QA1401500)+4 种基金Special Projects for Key Laboratories in Shanghai (09DZ2202000,10DZ2211100)Special Projects for Nanotechnology of Shanghai (0952nm02100)Shanghai Pujiang Program (09PJ1403200)Basic Research Program of Shanghai (10JC1403300)Fundamental Research Funds for the Central Universities
文摘For better performance of dye sensitized solar cells （DSSCs）, a bilayer structured electrode was constructed by employing a mesoporous anatase TiO2 overlayer above a commercial P25 TiO2 nanoparticles underlayer. The mesoporous anatase TiO2, prepared through a facile surfactant-assisted sol-gel process, possessed large pore size and well inter-connected network structure, both beneficial for dye adsorption and electron transfer. The dye adsorption capability of the mesoporous TiO2 was nearly twice that of the P25 counterpart. In the electrode, the mesoporous TiO2 film enhanced both dye adsorption and lightharvest, to increase photocurrent （Jsc） from 12.32 to 14.78 mA/cm^2. Compared to the single P25 TiO2 film, the synergy of the mesoporous TiO2 and the P25 TiO2 nanoparticle films in the electrode resulted in a 24% improvement in light-to-electricity conversion efficiency （η）. This bilayered electrode provides an alternative approach for further developing a photovoltaic device with better cell performance.
