P. Moriarty et al., PHOTOELECTRON CORE-LEVEL SPECTROSCOPY AND SCANNING-TUNNELING-MICROSCOPY STUDY OF THE SULFUR-TREATED GAAS(100) SURFACE, Physical review. B, Condensed matter, 50(19), 1994, pp. 14237-14245
A study of the adsorption of sulfur on the GaAs(100)surface after in s
itu thermal desorption of a protective As capping layer is presented.
The sulfur flux was generated by the decomposition of silver sulfide i
n an UHV compatible electrochemical cell. Use of As-capped samples pro
vided a means to study the interaction of sulfur with both the c(2X8)
and (4X1) surface reconstructions. Scanning-tunneling-microscopy image
s of the sulfur-covered surface indicated the formation of disordered
surface layers which display a diffuse (1X1) low-energy-electron-diffr
action pattern. This (1X1) phase is attributed to the symmetry of the
bulk structure visible through the disordered surface overlayer, cause
d by the adsorbed sulfur breaking the surface dimer bonds. Synchrotron
radiation core-level photoemission spectra indicate evidence of sulfu
r bonding td both gallium and arsenic at room temperature, but that th
e relative magnitude of these bonding interactions depends on the Ga/A
s ratio of the clean surface. Sulfur 2p photoemission spectra from the
annealed surfaces show that sulfur diffuses into the topmost atomic l
ayers as well as bonding to the surface. Annealing the sulfur covered
surface above 400 degrees C results in the formation of a (2X1) low-en
ergy-electron-diffraction pattern with a dimer-row structure clearly v
isible in scanning-tunneling-microscopy images; Our results would sugg
est that the adsorption of sulfur on the c (2X8) clean surface results
in dimer rows consisting of both arsenic and sulfur dimers, while onl
y sulfur dimers are observed after adsorption on the (4X1) surface. Th
e degree to which the clean surface band bending is altered on these r
espective,surfaces appears to be related to the precise chemical compo
sition of the dimer rows.