Structures and Stabilities of (MgO)n Nanoclusters

Global minima for (MgO)(n) structures were optimized using a tree growth-hybrid genetic algorithm in conjunction with MNDO/MNDO/d semiempirical molecular orbital calculations followed by density functional theory geometry optimizations with the B3LYP functional. New lowest energy isomers were found for a number of (MgO)(n) clusters. The most stable isomers for (MgO)(n) (n > 3) are 3-dimensional. For n < 20, hexagonal tubular (MgO)(n) structures are more favored in energy than the cubic structures. The cubic structures and their variations dominate after n = 20. For the cubic isomers, increasing the size of the cluster in any dimension improves the stability. The effectiveness of increasing the size of the cluster in a specific dimension to improve stability diminishes as the size in that dimension increases. For cubic structures of the same size, the most compact cubic structure is expected to be the more stable cubic structure. The average Mg-O bond distance and coordination number both increase as n increases. The calculated average Mg-O bond distance is 2.055 angstrom at n = 40, slightly smaller than the bulk value of 2.104 angstrom. The average coordination number is predicted to be 4.6 for the lowest energy (MgO)(40) as compared to the bulk value of 6. As n increases, the normalized clustering energy Delta E(n) for the (MgO)(n) increases and the slope of the Delta E(n) vs n curve decreases. The value of Delta E(40) is predicted to be 150 kcal/mol, as compared to the bulk value Delta E(infinity) = 176 kcal/mol. The electronic properties of the clusters are presented and the reactive sites are predicted to be at the corners.