0000000000017509
AUTHOR
Mauro Causà
On the mechanism of the interaction between oxygen and close-packed single-crystal aluminum surfaces
Abstract Using periodic first principles simulations we investigate the interaction of oxygen molecules with both regular Al(111) and Al(001) surfaces as well as a stepped Al(111) substrate. The limitation of this approach is the use of thin metallic slabs with a limited range for their coverage by adsorbed oxygen. The advantage is the detailed modeling that is possible at an atomic level. On the regular Al(111) surface, we have been able to follow the oxidation process from the approach of O 2 molecules to the surface, through the chemisorption and absorption of O atoms, up to the formation of first Al 2 O 3 formula units. An energetically feasible mechanism for the formation of these Al 2…
The adhesion nature of the Ag/MgO(100) interface: an ab initio study
The atomic and electronic structure of the Ag/MgO(100) interface are calculated by means of the ab initio Hartree-Fock approach combined with a supercell model. The electronic density distribution and the interface binding energy/distance are analyzed for different Ag adsorption positions, slabs of different thicknesses and varying Ag surface coverage. It is demonstrated that the adhesion energy arises mainly due to the electrostatic interaction of substrate atoms with a complicated charge redistribution in the metal layer(s), characterized by large quadrupole moments as well as electron density redistribution towards bridge and hollow positions between the nearest and next-nearest Ag atoms…