We have studied the etching of Si(100)-2 x 1 by Cl and Br, using scanning t
unneling microscopy to obtain morphological information that can be related
to reaction and desorption pathways. Clean surfaces were exposed to molecu
lar halogens at room temperature to produce well-defined chemisorption stru
ctures for coverages of 0.2-1.0 ML. Heating to 750-850 K induced etching by
thermal desorption, as well as the diffusion of vacancies and adatoms. Ana
lysis of the halogen concentration before and after heating indicated that
the rates of desorption for SiX2 were greatest for intermediate coverages a
nd that etching was suppressed as saturation was approached. This unexpecte
d result is discussed in terms of an isomerization reaction involving adsor
bed species 2SiX(a)<->SiX2(a) + Si(a), followed by the transfer of Si(a) to
a terrace site. The creation of a monomer vacancy adjacent to the SiX2(a)
unit frustrated the reverse reaction and increased the likelihood that it w
ould desorb. However, vacancy-assisted desorption is impeded when terrace s
ites are blocked by halogens, and the etch rate drops. The decrease is less
profound for Br than Cl because there is a high-concentration phase, Br-Si
(100)-3 x 1, in which Si dimerization can occur after isomerization. The ef
fect is again to increase the lifetime of the SiBr2(a)state. In this case,
desorption results in lines of single atom vacancies between dimer rows.