PRECURSOR AND DIRECT ACTIVATED CHEMISORPTION OF CHLORINE MOLECULES ONTO SI(111) (7X7) AND SI(100) (2X1) SURFACES

Citation
Djd. Sullivan et al., PRECURSOR AND DIRECT ACTIVATED CHEMISORPTION OF CHLORINE MOLECULES ONTO SI(111) (7X7) AND SI(100) (2X1) SURFACES, Journal of physical chemistry, 97(46), 1993, pp. 12051-12060
Citations number
64
Categorie Soggetti
Chemistry Physical
ISSN journal
00223654
Volume
97
Issue
46
Year of publication
1993
Pages
12051 - 12060
Database
ISI
SICI code
0022-3654(1993)97:46<12051:PADACO>2.0.ZU;2-K
Abstract
The zero-coverage sticking/chemisorption probabilities (S-0) of a mono energetic Cl-2 beam are measured on two faces of silicon: Si(111) (7x7 ) and Si(100) (2x1). The initial sticking probabilities (S-0) are meas ured as a function of the incident translational energy (E(i)), the su rface temperature (T-s), and the angle between the incident beam and t he surface normal (theta(i)). For Cl-2 chemisorption on Si(111) (7X7) at 300 K, there is a moderate increase in S-0 from 54% at 0.038 eV to 75% at 0.66 eV. S-0 is nearly insensitive to the surface temperature f or E(i) > 0.11 eV. At E(i) less than or equal to 0.11 eV there is a dr op in S-0 when the T-s is elevated. These data indicate that the prima ry mechanism for adsorption of Cl-2 onto Si(111) (7x7) is direct activ ated chemisorption with an average barrier approximate to 0.04 eV and that there is a precursor mediated chemisorption channel at low E(i). Conversely, the initial sticking probability is a strong function of t he incident molecular beam energy for Cl-2 onto Si(100) (2x1). For the Si(100) (2x1) surface at 300 K, there is a decrease in S-0 from 58% a t 0.038 eV to 42% at 0.045 eV and then a sharp increase to 72% at 0.16 eV. At the very lowest incident translational energy (0.038 eV), S-0 is a strong function of the surface temperature while for higher incid ent translational energy (greater than or equal to 0.38 eV) S-0 is ind ependent of the surface temperature. These data indicate that Cl-2 ads orbs on Si(100) (2X1) via precursor-mediated chemisorption at low tran slational energies and via direct activated chemisorption with an aver age barrier of approximate to 0.055 +/- 0.010 eV at high translational energies. The S-0 is independent of the incident angle of the molecul ar beam for all incident energies on both surfaces.