Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
69133 | Journal of Molecular Catalysis A: Chemical | 2006 | 8 Pages |
Surfaces of SiO2-covered titanium dioxide (TiO2) photocatalysts (SiO2-TiO2) were modified with alkylsilyl groups such as hydrocarbon, fluorocarbon, and phenyl groups. Oxidation of propanal, hexanal, nonanal, pentafuluorobenzaldehyde, and benzaldehyde proceeded much more efficiently on the surface-modified SiO2-TiO2 particles than on SiO2-TiO2 photocatalysts without surface modification. In the case of SiO2-TiO2 photocatalysts modified with hydrocarbon chains, one of the most important factors for improvement of the photocatalytic activities of surface-modified TiO2 photocatalysts is the hydrophobic interaction between substrates and alkylsilyl groups introduced onto SiO2-TiO2 photocatalysts. SiO2-TiO2 modified with phenyl groups is more active in the photocatalytic oxidation of benzaldehyde than SiO2-TiO2-C6. Furthermore, oxidation of pentafluorobenzaldehyde proceeded more favorably on SiO2-TiO2-C8(F) chains than on SiO2-TiO2-C8. These results indicated that the functional groups introduced onto the surface of SiO2-TiO2 play an important role in showing selectivity for photocatalytic oxidation of organic compounds.
Graphical abstractSurfaces of SiO2-covered titanium dioxide (TiO2) photocatalysts (SiO2-TiO2) were modified with organosilyl groups such as hydrocarbon- and fluorocarbon-derived groups. Oxidation of hexanal, nonanal, pentafuluorobenzaldehyde, and benzaldehyde proceeded much more efficiently on the surface-modified SiO2-TiO2 particles than on SiO2-TiO2 photocatalysts without surface modification. Figure optionsDownload full-size imageDownload as PowerPoint slide