TY - JOUR
T1 - N and F codoped TiO2 thin films on stainless steel for photoelectrocatalytic removal of cyanide ions in aqueous solutions
AU - Castellanos-Leal, Edgar Leonardo
AU - Acevedo-Peña, Próspero
AU - Güiza-Argüello, Viviana Raquel
AU - Córdoba-Tuta, Elcy María
N1 - Funding Information:
The authors would like to acknowledge financial support from COLCIENCIAS (Project 1102-521-28875) and Universidad Industrial de Santander (DIEF Ingenierías Fisicoquímicas, Project 9416). The authors would also like to thank Dr. Hugo A. Estupiñán from Universidad Nacional de Colombia (Medellín) for technical assistance with AFM measurements.
PY - 2017/3/1
Y1 - 2017/3/1
N2 - N-F codoped TiO2 films were immobilized on stainless steel sheets through a combined approach involving a dip-coating technique and a hydrothermal treatment, followed by calcination at 400°C in the presence of air. Photocatalyst characterization was conducted using XRD, Raman and UV-VIS spectroscopy as well as SEM. The films were tested in a three-electrode cell for the photoelectrocatalytic degradation of CN-containing compounds. The results showed that the increase in the degradation rate of CN-containing compounds is both influenced by a synergistic effect of the doping agents and strongly dependent on the concentration of CN-containing compounds in the solution. Nitrogen contributed to the enhanced photoactivity under visible light due to the generation of localized states within the band gap of TiO2, whereas the presence of fluoride improved the superficial properties of the film, which resulted in higher amounts of CN-containing compounds that were degraded by direct charge transfer through the photogenerated holes.
AB - N-F codoped TiO2 films were immobilized on stainless steel sheets through a combined approach involving a dip-coating technique and a hydrothermal treatment, followed by calcination at 400°C in the presence of air. Photocatalyst characterization was conducted using XRD, Raman and UV-VIS spectroscopy as well as SEM. The films were tested in a three-electrode cell for the photoelectrocatalytic degradation of CN-containing compounds. The results showed that the increase in the degradation rate of CN-containing compounds is both influenced by a synergistic effect of the doping agents and strongly dependent on the concentration of CN-containing compounds in the solution. Nitrogen contributed to the enhanced photoactivity under visible light due to the generation of localized states within the band gap of TiO2, whereas the presence of fluoride improved the superficial properties of the film, which resulted in higher amounts of CN-containing compounds that were degraded by direct charge transfer through the photogenerated holes.
KW - Codoped tio2
KW - Cyanide oxidation
KW - Non-metallic doping
KW - Photoelectrocatalysis
UR - http://www.scopus.com/inward/record.url?scp=85018624632&partnerID=8YFLogxK
U2 - 10.1590/1980-5373-MR-2016-0214
DO - 10.1590/1980-5373-MR-2016-0214
M3 - Artículo en revista científica indexada
AN - SCOPUS:85018624632
SN - 1516-1439
VL - 20
SP - 487
EP - 495
JO - Materials Research
JF - Materials Research
IS - 2
ER -