Abstract: In this study relationships between preparation conditions, structure and activity of Pt-containing TiO2 photocatalysts in photoinduced reforming of glycerol for H2 production were explored. Commercial Aerolyst (P25 based TiO2) and homemade TiO2 prepared by precipitation-aging method were used as semiconductors. Pt co-catalysts were prepared by incipient wetness impregnation from aqueous solution of Pt(NH3)4(NO3)2 and activated by calcination, high temperature hydrogen or nitrogen treatments. The chemico-physical and structural properties were evaluated by XRD, 1H MAS NMR, ESR XPS, TG-MS and TEM.The highest H2 evolution rate was observed over Aerolyst based samples and the H2 treatment resulted in more active samples than the other co-catalyst formation methods. In all calcined samples, reduction of Pt occurred during the photocatalytic reaction. Platinum was more easily reducible in all of the Aerolyst-supported samples compared to those obtained from the more water-retentive homemade TiO2. This result was related to the negative effect of the adsorbed water content of the homemade TiO2 on Pt reduction and on particle growth during co-catalyst formation.

Study of PtOx/TiO2 Photocatalysts in the Photocatalytic Reforming of Glycerol: The Role of Co-Catalyst Formation

Giuseppe Bonura;Catia Cannilla;Francesco Frusteri;
2018

Abstract

Abstract: In this study relationships between preparation conditions, structure and activity of Pt-containing TiO2 photocatalysts in photoinduced reforming of glycerol for H2 production were explored. Commercial Aerolyst (P25 based TiO2) and homemade TiO2 prepared by precipitation-aging method were used as semiconductors. Pt co-catalysts were prepared by incipient wetness impregnation from aqueous solution of Pt(NH3)4(NO3)2 and activated by calcination, high temperature hydrogen or nitrogen treatments. The chemico-physical and structural properties were evaluated by XRD, 1H MAS NMR, ESR XPS, TG-MS and TEM.The highest H2 evolution rate was observed over Aerolyst based samples and the H2 treatment resulted in more active samples than the other co-catalyst formation methods. In all calcined samples, reduction of Pt occurred during the photocatalytic reaction. Platinum was more easily reducible in all of the Aerolyst-supported samples compared to those obtained from the more water-retentive homemade TiO2. This result was related to the negative effect of the adsorbed water content of the homemade TiO2 on Pt reduction and on particle growth during co-catalyst formation.
2018
Istituto di Tecnologie Avanzate per l'Energia - ITAE
TiO2; co-catalyst; Pt(NH3)4(NO3)2; high temperature H2 treatment; high temperature N2 treatment; calcination; glycerol; H2 evolution
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/348723
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