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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Casati, R. |
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Kočí, Jan | Prague |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Dononelli, Wilke
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article
Understanding Oxygen Activation on Nanoporous Gold
Abstract
<p>Nanoporous gold (np-Au) is a catalytically highly active material, prepared by selectively dealloying silver from a gold-silver alloy. It can promote aerobic CO oxidation and a range of other oxidation reactions. It has been debated whether the remarkable catalytic properties of np-Au are mainly due to its structural features or whether the residual Ag remaining in the material after dealloying is decisive for the activity, especially for the activation of O<sub>2</sub>. Recent theoretical studies provided evidence that Ag impurities can facilitate the adsorption and dissociation of O<sub>2</sub> on np-Au. However, these studies predicted quite a high activation barrier for O<sub>2</sub> dissociation on Au-Ag alloy catalysts, whereas experimentally reported activation energies are much lower. In this work we use the stepped Au(321) surface with Ag impurities, which is arguably a realistic model for np-Au material as well as for Au-Ag catalysts in general. We present alternative routes for O<sub>2</sub> activation via its direct reaction with adsorbed CO or H<sub>2</sub>O. In all of the reactions considered, surface atomic O is generated via a sequence of elementary steps with calculated low activation energies of <0.4 eV with respect to coadsorbed reactants. Ag impurities are shown to increase the adsorption energy of O<sub>2</sub> and hence the probability of a surface-mediated reaction versus desorption. We considered four possible mechanisms of CO oxidation in dry and humid environments in a microkinetic modeling study. We show that via the proposed mechanisms water indeed promotes O<sub>2</sub> dissociation; nevertheless, the "dry" mechanism, in which CO directly reacts with O<sub>2</sub>, is by far the fastest route of CO<sub>2</sub> formation on pure Au and on Au with Ag impurities. Ag impurities lead to significantly higher turnover rates; thus, calculations point to the key role of Ag in promoting the catalytic activity of Au-Ag alloy systems.</p>