Adsorption of O 2 on the Preferred -O-Au Sites of Small Gold Oxide Clusters: Charge-dependent Interaction and Activation.

Decades of research have illuminated the significant roles of gold/gold oxide clusters in small molecule catalytic oxidation. However, many fundamental questions, such as the actual sites to adsorb and activate O 2 and the impact of charge, remain unanswered. Here, we have utilized an improved genetic algorithm program coupled with the DFT method to systematically search for the structures of Au 1-5 O x -/+/0 ( x = 1-4) and calculated binding interactions between Au 1-5 O x -/+/0 ( x = 1-2) and O 2 , aiming to determine the active sites and to elucidate the impact of different charge states in gold oxide systems. The results revealed that the reactivity of all three kinds of small gold oxide clusters toward O 2 is strongly site-dependent, with clusters featuring an -O-Au site exhibiting a preference for adsorption. The charges on small gold oxide clusters significantly impact the interaction strength and the activation degree of adsorbed O 2 : in the case of anionic cluster, the interaction between O 2 and the -O-Au sites leads to a chemical reaction involving electron transfer, thereby significantly activating O 2 ; in neutral and cationic clusters, the adsorption of O 2 on their -O-Au sites can be viewed as an electrostatic interaction. Pointedly, for cationic clusters, the highly concentrated positive charge on the Au atom of the -O-Au sites can strongly adsorb but hardly activate the adsorbed O 2 . These results have certain reference points for understanding the gold oxide interfaces and the improved catalytic oxidation performance of gold-based systems in the presence of atomic oxygen species.