First-principles calculations that clarify energetics and reactions of oxygen adsorption and carbon desorption on 4H-SiC ($11\bar{2}0$) surface

Abstract

We report static and dynamic first-principles calculations that provide atomistic pictures of the initial stage of the oxidation processes occurring at the ($11\bar{2}0$) surface of 4H-SiC. Our results unveil reaction pathways and their associated free-energy barriers for the adsorption of oxygen and the desorption of carbon atoms. We find that oxygen adsorption shows structural multi-stability and that the surface-bridge sites are the most stable and crucial sites for subsequent oxidation. We find that an approaching O${}_2$ molecule is adsorbed, then dissociated and finally migrates toward these surface-bridge sites with a free-energy barrier of 0.7 eV at the ($11\bar{2}0$) surface. We also find that a CO molecule is desorbed from the metastable oxidized structure upon the overcoming of a free-energy barrier of 2.4$\sim$2.6 eV, thus constituting one of the annihilation process of C during the oxidation. The results of the CO molecule desorption on the ($11\bar{2}0$) surface are compared with the ($000\bar{1}$) surface. A catalytic effect of dangling bonds at the surface, causing a drastic reduction of the CO desorption energy, is found on the ($000\bar{1}$) surface and the microscopic picture of the effect is ascribed to an electron transfer from the Si to C dangling bonds. The intrinsic ($11\bar{2}0$) surface does not show this catalytic effect, and this is because the surface consists of an equal amount of Si and C dangling bonds and the electron transfer occurs before the desorption.

11 pages, 9 figures