Abstract
The angular dependence of the dissociative adsorption of molecular hydrogen at terrace and step sites of vicinal single-domain Si(001) surfaces was investigated by means of molecular beam techniques and optical second-harmonic generation. A strongly anisotropic behavior was observed for terrace adsorption with polar distributions of and parallel and perpendicular to the dimer, respectively. The -steps show enhanced reactivity under glancing incidence in the upwards direction. The results are traced back to the directionality of the covalent surface bonds.
- Received 30 August 2001
DOI:https://doi.org/10.1103/PhysRevLett.88.076107
©2002 American Physical Society