Abstract
Two kinds of Ag2CO3/TiO2 nanocomposite photocatalysts, Ag2CO3/P25 (P25 refers to TiO2 of Degussa Company of Germany produced by gas-phase method) and Ag2CO3/TiO2(Vo•) (Vo• refers to single-electron-trapped oxygen vacancy (abridged as SETOV)), were prepared by precipitation method with commercial P25-TiO2 and TiO2(Vo•) as the precursors. The photocatalytic activity of as-prepared Ag2CO3/P25 and Ag2CO3/TiO2(Vo•) was compared by monitoring the oxidation of propylene under visible light irradiation with pure Ag2CO3 photocatalyst as a reference. The oxidation reaction of propylene was performed in two different reaction systems, i.e., a glass reactor combined with a home-made xenon lamp (denoted as system I) and a quartz reactor combined with a commercial xenon lamp (denoted as system II), respectively. Furthermore, X-ray photoelectron spectroscopic analysis, X-ray diffraction analysis, and diffuse reflection spectrometric analysis of Ag2CO3/P25 and Ag2CO3/TiO2(Vo•) before and after visible light irradiation were conducted to investigate the effect of Ag2CO3 photo-corrosion on the activity of the two kinds of photocatalysts, and their photocatalytic mechanisms were proposed. It was found that in system I (light intensity irradiated on to-be-tested samples at λ=420nm: about 9mW/cm2), Ag2CO3/TiO2(Vo•) shows highly efficient and stable visible light activity and provides a propylene removal rate of up to 90% which remains unchanged within 4h of irradiation, while the degradation rate of propylene over Ag2CO3/P25 is reduced gradually from 35% to nearly zero within 2.5h of irradiation. In system II (light intensity at λ=420nm: about 40mW/cm2), both Ag2CO3/P25 and Ag2CO3/TiO2(Vo•) exhibit similar photocatalytic activity of up to ca. 90%. Besides, photo-corrosion of Ag2CO3 happens during photocatalytic process to afford metallic Ag, and such a photo-corrosion is originally non-conducive to the photocatalysts. Nevertheless, metallic Ag is responsible for strong surface plasmon resonance effect of Ag2CO3/P25 and desired electron capture ability of Ag2CO3/TiO2(Vo•) as well, leading to highly efficient visible light activity of Ag2CO3/P25 in system II. As to Ag2CO3/TiO2(Vo•), a large amount of SETOV induces a new sub-band between the valence band and conduction band of TiO2(Vo•), and this sub-band synergistically functions with nascent surface metallic Ag to result in highly visible light activity. Thus the present approach could provide a versatile strategy for the synthesis of novel and efficient visible light-activated photocatalysts.
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