Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/43221
Título: NO photooxidation with TiO2 photocatalysts modified with gold and platinum
Autores/as: García Santiago, D. 
Navío, J. A. 
Doña Rodríguez, J. M. 
Hernandez Rodriguez, María José 
Pulido Melián, Elisenda 
Gonzalez-Diaz, Oscar M. 
Clasificación UNESCO: 2391 Química ambiental
2210 Química física
221001 Catálisis
221007 Espectroscopia electrónica
Palabras clave: Photocatalysis
Au
Pt
NOx
TiO2
Fecha de publicación: 2017
Editor/a: 0926-3373
Proyectos: Hormigones Fotocatalíticos 
Eliminacion Fotocatalitica de Mezclas de Nox y Covs en Emisiones Gaseosas Con Ti02 y Oxidos Mixtos. 
Publicación seriada: Applied Catalysis B: Environmental 
Resumen: In this study, a comparative analysis is made of TiO2 modified with Pt or Au in NO photoxidation under different radiation and humidity conditions. The metals were deposited on the TiO2 surface using two methods, photodeposition and chemical reduction. All catalysts were supported on borosilicate 3.3 plates using a dip-coating technique. These modified photocatalysts were characterized by X-ray diffraction analysis (XRD), UV–vis diffuse reflectance spectra (DRS), Brunauer-Emmett-Teller measurements (BET), transmission electron microscopy (TEM) and X-ray photoelectron spectrum analysis (XPS). It was found from the XPS results that Pt0 and oxidized Pt species coexist on the samples obtained by photodeposition and chemical reduction. In the case of Au, though other oxidation states were also detected the dominant oxidation state for both catalysts is Au0. TEM results showed most Au-C particles are below 5 nm, whereas for Au-P the nanoparticles are slightly bigger. With UV irradiation, the Pt modified catalysts do not show any significant improvement in NO photocatalytic oxidation in comparison with the unmodified P25. For Au, both modified photocatalysts (Au-P and Au-C) exceed the photocatalytic efficiency of the unmodified P25, with Au-C giving slightly better results. The incorporation of metals on the TiO2 increases its activity in the visible region.
URI: http://hdl.handle.net/10553/43221
ISSN: 0926-3373
DOI: 10.1016/j.apcatb.2016.12.006
Fuente: Applied Catalysis B: Environmental [ISSN 0926-3373], v. 205, p. 148-157
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