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作 者:LI ShunJun1, MA ZiChuan1,2, WANG Lin1 & LIU JingZe2 1 College of Chemistry and Material Sciences, Hebei Normal University, Shijiazhuang 050016, China 2 College of Life Science, Hebei Normal University, Shijiazhuang 050016, China
出 处:《Science China Chemistry》2008年第2期179-185,共7页中国科学(化学英文版)
基 金:the National Natural Science Foundation of China (Grant No. 20477009);the Natural Science Foundation of Hebei Province (Grant No. E2005000183)
摘 要:Influences of α-MnO2, β-MnO2, and δ-MnO2 on the photocatalytic activity of Degussa P-25 TiO2 have been investigated through the photocatalytic degradation of methyl orange. The TiO2 photocatalyst, before and after being contaminated by MnO2, was characterized by UV-visible diffuse reflectance spectroscopy (UV-vis DRS), photoluminescence (PL), and X-ray photoelectron spectroscopy (XPS). The results showed that photocatalytic activity of TiO2 could be inhibited significantly or completely deactivated due to the presence of even a small amount of MnO2 particles. It was found that the poisoning effect varied with the crystal phases of MnO2 and the effect was in the order δ-MnO2 >α-MnO2 >β-MnO2. The poisoning effect was attributed to the formation of heterojunctions between MnO2 and TiO2 particles. The heterojunctions changed the chemical state of Ti4+ and O2 sites in the crystalline phase of TiO2. MnO2 in contact with TiO2 particles also broadens the band-gap of TiO2, which decreases UV absorption of TiO2. It can also create some deep impurity energy levels serving as photoelec-tron-photohole recombination center, which accelerates the electron-hole recombination.Influences of α-MnO2, β-MnO2, and δ-MnO2 on the photocatalytic activity of Degussa P-25 TiO2 have been investigated through the photocatalytic degradation of methyl orange. The TiO2 photocatalyst, before and after being contaminated by MnO2, was characterized by UV-visible diffuse reflectance spectroscopy (UV-vis DRS), photoluminescence (PL), and X-ray photoelectron spectroscopy (XPS). The results showed that photocatalytic activity of TiO2 could be inhibited significantly or completely deactivated due to the presence of even a small amount of MnO2 particles. It was found that the poisoning effect varied with the crystal phases of MnO2 and the effect was in the order δ-MnO2 >α-MnO2 >β-MnO2. The poisoning effect was attributed to the formation of heterojunctions between MnO2 and TiO2 particles. The heterojunctions changed the chemical state of Ti4+ and O2 sites in the crystalline phase of TiO2. MnO2 in contact with TiO2 particles also broadens the band-gap of TiO2, which decreases UV absorption of TiO2. It can also create some deep impurity energy levels serving as photoelec-tron-photohole recombination center, which accelerates the electron-hole recombination.
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