Origin of the size dependence of Au nanoparticles toward molecular oxygen dissociation

Density functional theory calculations using a plane-wave basis set and a generalized gradient approach exchange-correlation potential have been carried out to study the dissociation of molecular oxygen by Au nanoparticles and its dependence with particle size. The analysis of the energy related data shows that the reactivity is dominated by the energy barrier height from adsorbed O-2 to the dissociated state and by the stability of molecular oxygen on the nanoparticle. The energy barrier is found to be only slightly dependent on the particles size where large variations are found for the adsorption energy of the O-2 molecule on the different nanoparticles. A careful analysis of the electronic structure shows that the driving force for O-2 adsorption by these nanoparticles is the existence of a clear gap between occupied and unoccupied states for the naked particle. This allows accommodating bonding states with O-2 below the Fermi level resulting in a strong interaction. On the contrary, the Au nanoparticles with a more metallic electronic structure have necessarily to accommodate bonding and antibonding states below the Fermi level with a concomitant weaker interaction with O-2.