Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/53588
Título: Influence of nickel in the hydrogen production activity of TiO2
Autores/as: Pulido Melián, Elisenda 
Jardiel, Teresa 
Doña Rodríguez, José Miguel 
Caballero Cuesta, Amador 
González Calatayud, David
González Díaz, Óscar Manuel 
Suárez Rodríguez, María Nereida 
Araña Mesa, Francisco Javier 
Clasificación UNESCO: 221001 Catálisis
Palabras clave: Hydrogen
Photocatalysis
Nickel
TiO2
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: Sol–gel synthesised TiO2 developed by our group was modified through the addition of nickel nitrate and ammonium carbonate in the synthesis process. Photocatalysts were synthesised with different Ni/Ti molar ratios (0.015, 0.030, 0.045) and constant Ni/N ratio equal to 1.5 and subjected to post-calcination at temperatures of between 400 °C and 700 °C. Characterisation was carried out with: X-ray diffraction (XRD), UV–vis diffusive reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy-energy dispersive X-ray analysis (TEM-EDX), thermal analysis (TGA, DTA), aggregate size distribution, Fourier transform infrared spectroscopy (FTIR) and nitrogen adsorption-desorption isotherm (BET). Photoactivity in terms of photocatalytic hydrogen production was tested using a suspension of photocatalyst at 25 vol.% methanol. With a continuous flow of N2 in headspace the hydrogen produced was conducted to a gas chromatograph for quantification. No evidence of the presence of N was found in the photocatalyst. However, the presence of Ni enhanced TiO2 photoactivity, with a calcination temperature of 550 °C resulting in the highest photoactivity value of 260.76 μmol h−1.
URI: http://hdl.handle.net/10553/53588
ISSN: 0926-3373
DOI: 10.1016/j.apcatb.2014.01.039
Fuente: Applied Catalysis B: Environmental [ISSN 0926-3373], v. 152-153, p. 192-201
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