Primary nucleation processes in binary oxide growth: The case of MgO

The smallest forms of stoichiometric and non-stoichiometric MgO clusters appearing on the MgO(0 0 1) surface during the growth under atomic and/or molecular deposition are investigated from first-principles and empiric potentials. The basic entities (MgO molecule and (MgO)₂ cluster) result from a very exoenergetic and spontaneous redox reaction that involves directly the deposited species (Mg and O atoms, O₂ molecule). The stoichiometric clusters, resulting from the agglomeration of MgO molecules, are very stable under non-polar forms. Their formation energy is modelized, down to very small sizes, within an independent defect model. We point out the specificity of such clusters in the framework of the classical nucleation theory. The high-energy polar isomers are associated to destabilizing macroscopic electric fields and dipoles. These forms may nevertheless be strongly stabilized by incorporating extra Mg adatoms that give part of their valence shell to the cluster and decrease the total dipole in this way, illustrating the delicate coupling between chemistry and electrostatics in growth processes of oxides. Based on these considerations, we propose a scenario describing MgO growth both in the step-flow and in the nucleation regime.