Identification of valence shifts in Au during the water-gas shift reaction |
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Authors: | Nina Hammer Ingvar Kvande Wouter van Beek De Chen Magnus Rønning |
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Affiliation: | (1) Department of Chemical Engineering, NTNU, N-7491 Trondheim, Norway;(2) The Swiss-Norwegian Beam Lines (SNBL) at ESRF, BP 220, F-38043 Grenoble, France |
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Abstract: | In situ X-ray absorption spectroscopy (XAS) has been performed to investigate the active site on Au-based catalysts in the water-gas
shift (WGS) reaction. The surface area and hence the WGS activity is higher for AuTiO2 catalysts supported on carbon nanofibres (CNF) than TiO2. The WGS reaction rate depends on the Au coordination number with an apparent maximum close to eight which corresponds to
a particle size of approximately 2.5–3.0 nm. A likely cause for the changes in the electronic structure of Au is the adsorption
of CO on the surface, which also creates a small positive charge in the Au atoms. The catalytic activity significantly improves
when titania is present compared to Au deposited directly on CNF. |
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Keywords: | Au catalyst XAS water-gas shift valence state titania carbon nanofibres |
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