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Surface chemical structure of titania-silica nanocomposite powder

Surface chemical structure of titania-silica nanocomposite powder
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摘要 Titania-silica (TS) nanocomposite powder with three different composite structures, containing 10―30 mol% SiO2 in each structure, have been prepared by sol-gel processes. The surface characteristics of these titania-silica samples have been investigated by X-ray photo-emission spectroscopy (XPS) and high resolution transmission electron microscopy (HRTEM). The study for all TS oxides annealed at 773 and 1173 K showed: an abnormal surface enrichment in Si increased with increasing annealing temperature; the Ti3+, Ti2+, Si3+ and Si2+ oxides coexisted with Ti4+ and Si4+ oxides, and the contents of these Ti/Si suboxides increased with increasing SiO2 content and annealing temperature; there was a layer rich in O on the topmost surface and the excess O could be attributed to the chemadsorption of H2O; different composite structures could lead to different contents of Ti/Si suboxides. These results indi- cated that the surface of TS oxide powder derived by sol-gel process was a double layer with enriched O first and then SiOx/TiOy (x, y<2). Ti/Si suboxides could result from the thermal diffusion of Ti4+ and Si4+, which might be induced by the strong interaction between Ti4+ and Si4+. Titania-silica (TS) nanocomposite powder with three different composite structures, containing 10-30 mol% SiO2 in each structure, have been prepared by sol-gel processes. The surface characteristics of these titania-silica samples have been investigated by X-ray photo-emission spectroscopy (XPS) and high resolution transmission electron microscopy (HRTEM). The study for all TS oxides annealed at 773 and 1173 K showed: an abnormal surface enrichment in Si increased with increasing annealing temperature; the Ti^3+, Ti^2+, Si^3+ and Si^2+ oxides coexisted with Ti^4+ and Si^4+ oxides, and the contents of these Ti/Si suboxides increased with increasing SiO2 content and annealing temperature; there was a layer rich in O on the topmost surface and the excess O could be attributed to the chem-adsorption of H2O; different composite structures could lead to different contents of Ti/Si suboxides. These results indicated that the surface of TS oxide powder derived by sol-gel process was a double layer with enriched O first and then SiOx/TiOy(x, y〈2). Ti/Si suboxides could result from the thermal diffusion of Ti^4+ and Si^4+, which might be induced by the strong interaction between Ti^4+ and Si^4+.
出处 《Chinese Science Bulletin》 SCIE EI CAS 2008年第19期2964-2972,共9页
基金 Supported by the National Natural Science Foundation of China (Grant Nos. 20776091 and 90306014)
关键词 表面结构 三氧化钛 硅石 低值氧化物 surface structure, titania-silica, sol-gel, suboxide, nanocomposite
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参考文献13

  • 1ZHANG XingWang LEI LeCheng.A kinetic model for describing effect of the external surface concentration of TiO_2 on the reactivity of egg-shell activated carbon supported TiO_2 photocatalys[J].Chinese Science Bulletin,2007,52(24):3339-3345. 被引量:2
  • 2Jiaguo Yu,Jimmy C. Yu,Bei Cheng,Xiujian Zhao.Photocatalytic Activity and Characterization of the Sol-Gel Derived Pb-Doped TiO2 Thin Films[J].Journal of Sol - Gel Science and Technology.2002(1)
  • 3G. M. Ingo,C. Riccucci,G. Bultrini,S. Dirè,G. Chiozzini.Thermal and Microchemical Characterisation of Sol-Gel SiO2, TiO2 and xSiO2–(1–x)TiO2 Ceramic Materials[J].Journal of Thermal Analysis and Calorimetry.2001(1)
  • 4Orlando Martins,Rui M. Almeida.Sintering Anomaly in Silica-Titania Sol-Gel Films[J].Journal of Sol - Gel Science and Technology (-).2000(1-3)
  • 5Fujishima A,Honda K.Electrochemical photolysis of water at a semiconductor electrode[].Nature.1972
  • 6R. Wang,K. Hashimoto,,A. Fujishima,,M. Chikuni,,E. Kojima,,A. Kitamura,,M. Shimohigoshi,and T. Watanabe.Light-induced Amphiphilic Surfaces[].Nature.1997
  • 7Kozlov D V,Paukshtis E A,Savinov E N.The comparative studies of titanium dioxide in Gas-phase ethanol photocatalytic oxidation by the FTIR in situ method[].Applied Catalysis B Environmental.2000
  • 8Zhaoyang Liu Xie Quan Hongbo Fu,Xinyong Li and Kai Yang.Effect of embedded-silica on microstructure and photocatalytic activity of titania prepared by ultrasound-assisted hydrolysis[].Applied Catalysis.2004
  • 9Yingxu,Chen,Kan,Wang,Liping,Lou.Photodegradation of Dye Pollutants on Silica Gel Supported TiO2 Particles under Visible Light Irradiation[].Journal of Photochemistry and Photobiology A Chemistry.2004
  • 10Hong S S,Lee M S,Park S S,Lee G D.Synthesis of nanosized TiO2 /SiO2 particles in the microemulsion and their photocatalytic activity on the decomposition of p-nitrophenol[].Catalysis Today.2003

二级参考文献10

  • 1Konstantinou I,Albanis T.TiO2-assisted photocatalytic degradation of azo dyes in aqueous solution: kinetic and mechanistic investigations: A review[].Appl Catal B Environ.2004
  • 2Sopyan I,Watanabe M,Murasawa S et al.An efficient TiO2 thin-film photocatalyst: Photocatalytic properties in gas-phase acetaldehyde degradation[].J Photochem Photobiol A.1996
  • 3Ara?a J,Do?a-Rodríguez J,Tello Rendón E et al.TiO2 activation by using activated carbon as a support: Part I. Surface characterisation and decantability study[].Appl Catal B Environ.2003
  • 4Chen Y,Dionysiou D.TiO2 photocatalytic films on stainless steel: The role of degussa P 25 in modified sol-gel methods[].Appl Catal B Environ.2006
  • 5Zhang X,Zhou M,Lei L.TiO2 photocatalyst deposition by MOCVD on activated carbon[].Carbon.2006
  • 6Lu M,Chen J,Chang K.Effect of adsorbents coated with titanium dioxide on the photocatalytic degradation of propoxur[].Chemosphere.
  • 7Snell F,Ettre L.Encyclopedia of Industrial Chemical Analysis[]..1974
  • 8Eagles D.Polar modes of lattice vibration and polaron coupling con- stants in rutile (TiO2)[].J Phys Chem Solids.1964
  • 9P.K. Song,Y. Irie,Y. Shigesato.Crystallinity and photocatalytic activity of TiO2 films deposited by reactive sputtering with radio frequency substrate bias[].Thin Solid films.2006
  • 10Gerischer H.particles and the dependence of the quantum yield on particle size and light intensity[].Electrochimica Acta.1995

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