TY - JOUR
T1 - E-beam evaporated TiO2 and Cu-TiO2 on glass
T2 - Performance in the discoloration of methylene blue and 2-propanol oxidation
AU - Garlisi, Corrado
AU - Scandura, Gabriele
AU - Szlachetko, Jakub
AU - Ahmadi, Sareh
AU - Sa, Jacinto
AU - Palmisano, Giovanni
N1 - Funding Information:
Masdar Institute of Science and Technology is gratefully acknowledged for financial support ( FA2014-000010 ). Particular thanks to Cyril Aubry, Thomas Delclos, Leslie George, Adrian Darcie Clark, Rajakumar Devarapalli, Florent Ravaux and Mustapha Jouiad for their technical support and to Steven Griffiths, Mohamed Sassi and Mike Tiner for their initial financial support allowing for a fast establishment of the Photocatalysis Lab in Masdar Institute. The Core Technology Platform at New York University Abu Dhabi is acknowledged for the XRD diffractions performed by James Weston. Jakub Szlachetko acknowledges National Science Centre, Poland (NCN) for support under grant no. 2015/18/E/ST3/00444.
Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2016/9/25
Y1 - 2016/9/25
N2 - TiO2 and Cu-TiO2 thin films were deposited by e-beam evaporation and then annealed at 350 and 500 °C. Their structure, surface morphology and optical properties were studied by X-ray diffraction, scanning electron microscopy, cross-sectional TEM, UV–vis, FT-IR spectroscopy and X-ray absorption spectroscopy. A single-phase source material was used for the first time in the deposition process, thus avoiding preferential evaporation of Cu with respect to TiO2, and resulting in an even concentration of Cu in the doped films. The photocatalytic activity was evaluated by degradation of pre-adsorbed methylene blue (MB) in dry conditions and gaseous 2-propanol in oxygen atmosphere under visible and simulated solar light, respectively. Results suggested that high surface hydroxylation of the as-deposited films is an important factor for MB oxidation occurring through a dye-sensitized mechanism activated by visible light absorption. Conversely, the rate of photodegradation of 2-propanol is enhanced in annealed samples due to the greater crystallinity and less electron-hole recombination, with the TiO2 annealed at 500 °C being the most efficient photocatalyst. However, Cu-doped samples resulted the most active samples during the degradation of MB under visible radiation. Finally, the performance at increasing thickness (250, 500, 1000, up to 2000 nm) was tested for the most reactive films revealing a marked rise in photocatalytic activity up to 1000 nm.
AB - TiO2 and Cu-TiO2 thin films were deposited by e-beam evaporation and then annealed at 350 and 500 °C. Their structure, surface morphology and optical properties were studied by X-ray diffraction, scanning electron microscopy, cross-sectional TEM, UV–vis, FT-IR spectroscopy and X-ray absorption spectroscopy. A single-phase source material was used for the first time in the deposition process, thus avoiding preferential evaporation of Cu with respect to TiO2, and resulting in an even concentration of Cu in the doped films. The photocatalytic activity was evaluated by degradation of pre-adsorbed methylene blue (MB) in dry conditions and gaseous 2-propanol in oxygen atmosphere under visible and simulated solar light, respectively. Results suggested that high surface hydroxylation of the as-deposited films is an important factor for MB oxidation occurring through a dye-sensitized mechanism activated by visible light absorption. Conversely, the rate of photodegradation of 2-propanol is enhanced in annealed samples due to the greater crystallinity and less electron-hole recombination, with the TiO2 annealed at 500 °C being the most efficient photocatalyst. However, Cu-doped samples resulted the most active samples during the degradation of MB under visible radiation. Finally, the performance at increasing thickness (250, 500, 1000, up to 2000 nm) was tested for the most reactive films revealing a marked rise in photocatalytic activity up to 1000 nm.
KW - Cu-TiO on glass
KW - E-beam evaporation
KW - Photocatalysis
UR - http://www.scopus.com/inward/record.url?scp=84988037181&partnerID=8YFLogxK
U2 - 10.1016/j.apcata.2016.08.022
DO - 10.1016/j.apcata.2016.08.022
M3 - Article
AN - SCOPUS:84988037181
SN - 0926-860X
VL - 526
SP - 191
EP - 199
JO - Applied Catalysis A: General
JF - Applied Catalysis A: General
ER -