ENERGY DEPENDENCE OF ABSTRACTIVE VERSUS DISSOCIATIVE CHEMISORPTION OF FLUORINE MOLECULES ON THE SILICON (111)-(7X7) SURFACE

摘要

Scanning tunneling microscopy and monoenergetic molecular beams have been used to obtain real-space atomic images of the competition between abstractive and dissociative chemisorption. The size distribution of Si-F adsorbates on the Si(111)-(7x7) surface was examined as a function of the incident translational energy of the F-2 molecules. For F-2 molecules with 0.03 electron volt of incident energy, the dominant adsorbate sites were isolated Si-F species. As an F-2 molecule with low translational energy collides with the surface, abstraction occurs and only one of the F atoms chemisorbs; the other is ejected into the gas phase. For F-2 molecules with 0.27 electron volt of incident energy, many adjacent Si-F adsorbates (dimer sites) were observed because F-2 molecules with high translational energy collide with the surface and chemisorb dissociatively so that both F atoms react to form adjacent Si-F adsorbates. For halogens with very high incident energy (0.5-electron volt Br-2), dissociative chemisorption is the dominant adsorption mechanism and dimer sites account for nearly all adsorbates.