Artículo de revista
Photocatalytic thin films containing TiO2:N nanopowders obtained by the layer-by-layer self-assembling method
Fecha
2012Registro en:
Applied Surface Science 258 (2012) 2103– 2106
doi:10.1016/j.apsusc.2011.03.150
Autor
Rojas Blanco, L.
Urzúa Acevedo, Marcela
Ramírez Bon, R.
Espinoza Beltrán, F. J.
Institución
Resumen
In this work, TiO2–N powders were synthesized by high-energy ball milling, using commercial titanium
dioxide (TiO2) in the anatase phase and urea to introduce nitrogen into TiO2 in order to enhance their
photocatalytic properties in the visible spectral region. Several samples were prepared by milling a mixture
of TiO2–urea during 2, 4, 8, 12 and 24 h and characterized by spectroscopic and analytical techniques.
X-ray diffraction (XRD) results showed the coexistence of anatase and high-pressure srilankite TiO2 crystalline
phases in the samples. Scanning electron microscopy (SEM) revealed that the grain size of the
powder samples decreases to 200 nm at 24 h milling time. UV–Vis diffuse reflectance spectroscopic data
showed a clear red-shift in the onset of light absorption from 387 to 469 nm as consequence of nitrogen
doping in the samples. The photocatalytic activity of the TiO2–N samples was evaluated by methylene
blue degradation under visible light irradiation. It was found that TiO2–N samples had higher photocatalytic
activity than undoped TiO2 samples, which could be assigned to the effect of introducing N atoms
and XPS results confirm it. Using polyethylenimine (PEI), transparent thin films of TiO2–N nanoparticles
were prepared by layer-by-layer self assembly method. UV–visible spectrophotometry was employed in
a quantitative manner to monitor the adsorbed mass of TiO2 and PEI after each dip cycle. The adsorption
of both TiO2 and PEI showed a saturation dip time of 15 min.