کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1333728 | 979094 | 2008 | 10 صفحه PDF | دانلود رایگان |

A series of dye-modified TiO2 photocatalysts were synthesized using dye Chrysoidine G (CG), tolylene-2,4-diisocyanate (TDI), and commercial TiO2 (Degussa P25) as starting materials. TDI was used as a bridging molecule whose two –NCO groups reacted with Ti–OH of TiO2 and –NH2 groups of CG, respectively. As a result, special organic complexes were formed on the TiO2 surface via stable π-conjugated chemical bonds between TiO2 and dye molecules, confirmed by FT-IR, XPS, and UV–vis spectra. Due to the existence of π-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 TiO2 exhibited much better activity under the visible light irradiation than bare TiO2.
Dye-modified TiO2 photocatalysts were synthesized via the reaction between Chrysoidine G (CG), Degussa P25 (TiO2), and tolylene-2,4-diisocyanate (TDI) as a bridging molecule. As a result, π-conjugated surface organic complexes were formed on TiO2 surface. Due to the existence of organic complexes, dye-modified TiO2 catalysts showed great visible absorption and high activity under the visible light irradiation.Figure optionsDownload as PowerPoint slide
Journal: Journal of Solid State Chemistry - Volume 181, Issue 3, March 2008, Pages 593–602