Runhai Ouyang

Atomistic Theory of Ostwald Ripening and Disintegration of Supported Metal Particles under Reaction Conditions

Understanding Ostwald ripening and disintegration of supported metal particles under operating conditions has been of central importance in the study of sintering and dispersion of heterogeneous catalysts for long-term industrial implementation. To achieve a quantitative description of these complicated processes, an atomistic and generic theory taking into account the reaction environment, particle size and morphology, and metal-support interaction is developed. It includes (1) energetics of supported metal particles, (2) formation of monomers (both the metal adatoms and metal-reactant complexes) on supports, and (3) corresponding sintering rate equations and total activation energies, in the presence of reactants at arbitrary temperature and pressure. The thermodynamic criteria for the reactant assisted Ostwald ripening and induced disintegration are formulated, and the influence of reactants on sintering kinetics and redispersion are mapped out. Most energetics and kinetics barriers in the theory can be obtained conveniently by first-principles theory calculations. This allows for the rapid exploration of sintering and disintegration of supported metal particles in huge phase space of structures and compositions under various reaction environments. General strategies of suppressing the sintering of the supported metal particles and facilitating the redispersions of the low surface area catalysts are proposed. The theory is applied to TiO(2)(110) supported Rh particles in the presence of carbon monoxide, and reproduces well the broad temperature, pressure, and particle size range over which the sintering and redispersion occurred in such experiments. The result also highlights the importance of the metal-carbonyl complexes as monomers for Ostwald ripening and disintegration of supported metal catalysts in the presence of CO.

CO oxidation at the perimeters of an FeO/Pt(111) interface and how water promotes the activity: a first-principles study.

The catalytic role of the Pt--Fe cation ensemble presented at the perimeters of the FeO film supported on Pt(111) for low-temperature CO oxidation and the promotion of water on activity were studied by using DFT calculations. We found that the perimeter sites along the edge of the FeO islands on Pt provided a favorable ensemble that consisted of coordinatively unsaturated ferrous species and nearby Pt atoms for O(2) and H(2) O activation free from CO poison. A dissociative oxygen atom at the Pt--Fe cation ensemble reacts easily with CO adsorbed on nearby Pt. The OH group from water dissociation not only facilitates activation of the oxygen molecule, more importantly it opens a facile reaction channel for CO oxidation through the formation of the carboxyl intermediate. The presence of the OH group on the FeO film strengthens interfacial interactions between FeO and Pt(111), which would make the FeO film more resistant to further oxidation. The importance of the Pt--Fe cation ensemble and the role of water as a cocatalyst for low-temperature CO oxidation is highlighted.