Hydrogen Evolution over New Heteronanostructured Photocatalysts Pt‒Nb3O7(OH) and Cu‒Nb3O7(OH)
a American University of Beirut, Chemistry, Beirut, 11, Lebanon
b University of Toronto, Materials Chemistry Research Group, Department of Chemistry, Saint George Street, 80, Toronto, Canada
c Physics Department, University of Texas at San Antonio, One UTSA Circle,, San Antonio, United States
Proceedings of International Conference on New Advances in Materials Research for Solar Fuels Production (SolarFuel14)
Montréal, Canada, 2014 June 25th - 26th
Organizer: Thomas Hamann
Poster, Mohamad Hmadeh, 033
Publication date: 16th April 2014
Publication date: 16th April 2014
Photocatalytic solar fuel production has attracted much attention since Fujishima and Honda’s work using the TiO2 photocatalyst as a photoanode. Following this initial discovery, numerous families of semiconductors (e.g. ZnO, ZrO2, CdS, ZnS, SiC) have been developed for solar fuel production. At present, the main obstacle in the development of photocatalytic materials is to increase their efficiency. Several strategies have been employed in the design of novel materials to enhance the photocatalytic activity. The utilization of multi-component nanostructures rather than single semiconductors is one of the most efficient and practical approaches in achieving these highly sought after characteristics. Although titania is the most commonly studied photocatalyst, a series of niobium based semiconductors (e.g. HNb3O8, HNbO3, H4Nb2O7, H4Nb6O17) have attracted much attention recently, due to their favorable properties such as high stability under light irradiation, chemical inertness, and non-toxicity. Furthermore, it is believed that the protonic acidity in these semiconductors can promote adsorption of water, and CO2. Herein, the synthesis and characterization of Nb3O7(OH) nanorods as well as their Pt- and CuO-decorated heteronanostructures is reported. The resulting Pt- and CuO-decorated Nb3O7(OH) nanorods demonstrated uniform particle dispersion and were fully characterized by X-ray diffraction, electron microscopy, and spectroscopic analysis. Furthermore, the solar powered photocatalytic hydrogen production properties of these heteronanostructures were studied. The solar driven H2 formation rate over Pt‒Nb3O7(OH) was determined to be 710.4 ± 1.7 μmol g‒1 h‒1 with a quantum efficiency of f = 5.40 % at λ = 380 nm. Interestingly, the as-prepared CuO–Nb3O7(OH) heteronanostructure was found to be inactive under solar irradiation during an induction phase whereupon it undergoes an in situ photoreduction process to form the photocatalytically active Cu–Nb3O7(OH). This restructuring process was monitored by an in situ measurement of the time evolution of the optical absorption spectra. The solar powered H2 production for the restructured compound was determined to be 290.3 ± 5.1 μmol g‒1 h‒1.
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