Abstract
The oxidation of CO is a fundamental model reaction in heterogeneous catalysis. This contribution presents an uncommon approach to investigate a catalytic gas-phase reaction by using colloidal gold and provides a unified picture of the CO oxidation of supported gold nanoparticles at room temperature. Our experiments on ligand-free colloidal gold nanoparticles prove that gold activates molecular oxygen independently from the presence of any support. Isotope experiments along with studies on colloidal stability reveal that the active oxygen species is a stable surface oxide that can be protonated. The role of the support is to provide water for protonation steps. Therefore, the hydrophilicity is the main property of the support which determines the catalytic activity and not, as is often assumed, its acidity or reducibility. The deduced model provides explanations for experimental results described in the literature for various gold catalysts and reaction conditions.
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