Photocatalytic activity under visible light irradiation was generated by doping a small amount of Co 2+ ions into TiO 2 particles. Nanometer-sized particles with the composition xCoO-(100x) TiO 2 (xCo/TiO 2 ; 0 โค x โค 6.0) were prepared from TiOSO 4 โข 4.5H 2 O and Co(CH 3 COO) 2 โข 4H 2 O in an ethano
Visible-light responsive dye-modified TiO2 photocatalyst
โ Scribed by Dong Jiang; Yao Xu; Dong Wu; Yuhan Sun
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 682 KB
- Volume
- 181
- Category
- Article
- ISSN
- 0022-4596
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โฆ Synopsis
A series of dye-modified TiO 2 photocatalysts were synthesized using dye Chrysoidine G (CG), tolylene-2,4-diisocyanate (TDI), and commercial TiO 2 (Degussa P25) as starting materials. TDI was used as a bridging molecule whose two -NCO groups reacted with Ti-OH of TiO 2 and -NH 2 groups of CG, respectively. As a result, special organic complexes were formed on the TiO 2 surface via stable p-conjugated chemical bonds between TiO 2 and dye molecules, confirmed by FT-IR, XPS, and UV-vis spectra. Due to the existence of p-conjugated surface organic complexes, the as-synthesized photocatalysts showed a great improvement in visible absorption (400-550 nm). Methylene blue, as a photodegradation target, was used to evaluate the photocatalytic performance, and the dye-modified TiO 2 exhibited much better activity under the visible light irradiation than bare TiO 2 .
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