Abstract

An initial oxidation dynamics of 4H-SiC(0001)-(√3×√3)R30° surface has been studied using high resolution X-ray photoelectron spectroscopy and supersonic molecular beams. Clean 4H-SiC(0001)-(√3×√3)R30° surface was exposed to oxygen molecules with translational energy of 0.5eV at 300K. In the first step of initial oxidation, oxygen molecules are immediately dissociated and atomic oxygens are inserted into Si–Si back bonds to form stable oxide species. At this stage, drastic increase in growth rate of stable oxide species by heating molecular beam source to 1400K was found. We concluded that this increase in growth rate of stable oxide is mainly caused by molecular vibrational excitation. It suggests that the dissociation barrier is located in the exit channel on potential energy hypersurface. A metastable molecular oxygen species was found to be adsorbed on a Si-adatom that has two oxygen atoms inserted into the back bonds. The adsorption of the metastable species is neither enhanced nor suppressed by molecular vibrational excitation.

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