Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/43230
Título: Production of hydrogen by water photo-splitting over commercial and synthesised Au/TiO2 catalysts
Autores/as: Ortega Méndez, José Alejandro 
López, Cristina R.
Pulido Melián, Elisenda 
González Díaz, Óscar Manuel 
Doña Rodríguez, José Miguel 
Fernández Hevia, Daniel
Macías, Manuel
Clasificación UNESCO: 221001 Catálisis
Palabras clave: Methanol
H2 production
Photocatalysis
Photo-splitting
Au plasmon
Fecha de publicación: 2014
Editor/a: 0926-3373
Proyectos: Sistema Completo de Caracterización de la Relación Entre Composición, Estructura y Fotoactividad de Sólidos Sintéticos Con Aplicaciones Fotocatalíticas. 
Publicación seriada: Applied Catalysis B: Environmental 
Resumen: H2 production from methanol/water photo-splitting was compared using various commercial photocatalysts (Evonik P25 (P25), Hombikat UV-100 (HB) and Kronos vlp7000 (KR)) and others synthesised with a sol–gel-hydrothermal (HT) process and a sol–gel method followed by calcination (SG400 and SG750). All photocatalysts had been surface modified with Au at different concentrations, from 0.2 to 6.0 wt.%, using the photodeposition method. A complete characterisation study of the different photocatalysts was performed (BET, XRD, TEM, SEM-EDX, FTIR, UV–vis Reflectance Diffuse Spectra and aggregate size). The experiments were conducted for 3.5 h using 1 g L−1 of photocatalyst with methanol (25 vol.%) as sacrificial agent. In addition to H2 generation, production of the main intermediates, formaldehyde and formic acid, and of CO2 was also evaluated. The commercial photocatalyst KR at 0.8 wt.% Au had the highest H2 production of all the photocatalysts studied with 1542.9 μmol h−1. Of the photocatalysts synthesised by our group, SG750 at Au loading of 2.0 wt.% gave the highest H2 production of 723.1 μmol h−1. The SG750 photocatalyst at Au loading of 2.0 wt.% also had the highest H2 production yield per unit of surface area at 45.5 μmol g h−1 m−2.
URI: http://hdl.handle.net/10553/43230
ISSN: 0926-3373
DOI: 10.1016/j.apcatb.2013.09.029
Fuente: Applied Catalysis B: Environmental [ISSN 0926-3373], v. 147, p. 439-452
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