Abstract
The photo-induced vapor-phase decomposition of ethanol was investigated on pure, N-doped, and metal-promoted TiO 2. The catalysts were characterized by bandgap determination and by FTIR and XPS spectroscopy. In harmony with previous findings, the bandgap of N-doped TiO 2 continuously decreased from 3.15 to 2.17 eV with elevation of the temperature of its modification. IR studies revealed that illumination of the C 2H 5OH–TiO 2 system initiated the decomposition of adsorbed ethoxy species to yield acetaldehyde. The photodecomposition of ethanol on pure TiO 2 occurs to only a very limited extent; N-doped TiO 2 displays much higher activity and gives acetaldehyde and hydrogen as the primary products. The acetaldehyde formed is photolyzed to afford methane and CO. The efficiency of the N-doped TiO 2 increased with the narrowing of the bandgap, a feature attributed to the prevention of electron–hole recombination. The deposition of Rh on pure and doped TiO 2 dramatically enhanced the extent of photodecomposition of ethanol, even in visible light.
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