Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/43221
Title: NO photooxidation with TiO2 photocatalysts modified with gold and platinum
Authors: García Santiago, D. 
Navío, J. A. 
Doña Rodríguez, J. M. 
Hernandez Rodriguez, María José 
Pulido Melián, Elisenda 
Gonzalez-Diaz, Oscar M. 
UNESCO Clasification: 2391 Química ambiental
2210 Química física
221001 Catálisis
221007 Espectroscopia electrónica
Keywords: Photocatalysis
Au
Pt
NOx
TiO2
Issue Date: 2017
Publisher: 0926-3373
Project: Hormigones Fotocatalíticos 
Eliminacion Fotocatalitica de Mezclas de Nox y Covs en Emisiones Gaseosas Con Ti02 y Oxidos Mixtos. 
Journal: Applied Catalysis B: Environmental 
Abstract: 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
Source: Applied Catalysis B: Environmental [ISSN 0926-3373], v. 205, p. 148-157
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