TY - JOUR
T1 - N-doped anatase/rutile photocatalysts for the synthesis of aromatic aldehydes under Ultraviolet and solar irradiation
AU - Tek, Bilge Sina
AU - Yurdakal, Sedat
AU - Özcan, Levent
AU - Augugliaro, Vincenzo
AU - Loddo, Vittorio
AU - Palmisano, Giovanni
PY - 2015
Y1 - 2015
N2 - N-doped anatase/rutile photocatalysts were prepared by a sol-gel method, using TiCl4 as TiO2 precursor and urea as N-dopant source. The catalysts required a thermal treatment at temperature higher than 300 °C to achieve actual nitrogen doping; this treatment also allowed obtaining crystalline and hydrophobic samples. Moreover, nitrogen doping modified the surface of samples by increasing the anatase to rutile phase ratio and hydrophilicity. The catalysts were characterized by BET specific surface area, XRD, ESEM, TGA, FT-IR, DRS and XPS measurements, with particular attention to the assessment of the N-doping effect. It was found that XPS analysis should be used together with DRS and FT-IR to discriminate whether N had been incorporated in TiO2 lattice or N species had just adsorbed on the TiO2 surface. Moreover, XPS analysis could be also used for determining the crystallinity of TiO2. The photocatalytic activity of the samples was tested for the partial oxidation of 4-methoxybenzyl alcohol to p-anisaldehyde in water under near-UV, visible, UV-visible and simulated solar light, respectively. Commercial (Degussa P25) and undoped home-prepared TiO2 anatase-rutile catalysts were also used for comparison. The results show that N-doping improves absorption of visible light by the catalysts, but the reaction rate does not increase accordingly. Selectivity was higher in the presence of poorly crystallized catalysts, whereas doping seemed to have a slightly improving effect.
AB - N-doped anatase/rutile photocatalysts were prepared by a sol-gel method, using TiCl4 as TiO2 precursor and urea as N-dopant source. The catalysts required a thermal treatment at temperature higher than 300 °C to achieve actual nitrogen doping; this treatment also allowed obtaining crystalline and hydrophobic samples. Moreover, nitrogen doping modified the surface of samples by increasing the anatase to rutile phase ratio and hydrophilicity. The catalysts were characterized by BET specific surface area, XRD, ESEM, TGA, FT-IR, DRS and XPS measurements, with particular attention to the assessment of the N-doping effect. It was found that XPS analysis should be used together with DRS and FT-IR to discriminate whether N had been incorporated in TiO2 lattice or N species had just adsorbed on the TiO2 surface. Moreover, XPS analysis could be also used for determining the crystallinity of TiO2. The photocatalytic activity of the samples was tested for the partial oxidation of 4-methoxybenzyl alcohol to p-anisaldehyde in water under near-UV, visible, UV-visible and simulated solar light, respectively. Commercial (Degussa P25) and undoped home-prepared TiO2 anatase-rutile catalysts were also used for comparison. The results show that N-doping improves absorption of visible light by the catalysts, but the reaction rate does not increase accordingly. Selectivity was higher in the presence of poorly crystallized catalysts, whereas doping seemed to have a slightly improving effect.
KW - Green synthesis
KW - N-doped TiO
KW - p-anisaldehyde
KW - Photocatalysis
KW - Solar irradiation
KW - X-ray photoelectron spectroscopy
UR - https://www.scopus.com/pages/publications/84947343116
U2 - 10.1166/sam.2015.2280
DO - 10.1166/sam.2015.2280
M3 - Article
AN - SCOPUS:84947343116
SN - 1947-2935
VL - 7
SP - 2306
EP - 2319
JO - Science of Advanced Materials
JF - Science of Advanced Materials
IS - 11
ER -