Modification of the surface termination of GaAs(001) using photon-activated electron-transfer reactions

Citation
Ka. Khan et al., Modification of the surface termination of GaAs(001) using photon-activated electron-transfer reactions, SURF SCI, 458(1-3), 2000, pp. 53-62
Citations number
30
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
SURFACE SCIENCE
ISSN journal
00396028 → ACNP
Volume
458
Issue
1-3
Year of publication
2000
Pages
53 - 62
Database
ISI
SICI code
0039-6028(20000620)458:1-3<53:MOTSTO>2.0.ZU;2-6
Abstract
We report the use of a photon-activated electron-transfer chemical reaction to modify the surface termination of the (001) face of single-crystal GaAs . The technique involves the extraction of surface Ga atoms as a result of reaction with bromine. The bromine is produced at the surface by photoiniti ated dissociative electron attachment to methyl bromide molecules in a sing le monolayer physisorbed at similar to 80 K. Subsequent to the photoinduced surface reaction, the gallium is removed by annealing to desorb a gallium halide product. We have demonstrated that variation in photon exposure and thermal treatment allows the surface reconstruction to be controllably adju sted from the Ga-rich c(8 x 2) to the (4 x 6), (3 x 1) and As-rich c(2 x 8) terminations. A comparison of the results obtained with several surface di agnostics, including low energy electron diffraction, temperature programme d desorption and energy-resolved photofragment angular distribution measure ments, indicates that the most As-rich surface obtained by our technique is identical in structure to that of a control surface prepared using the sta ndard thermal reaction technique. In principle, the use of this photon-acti vated reaction, and others like it, allows precise adjustment and patternin g of the surface structure based on control of photon or electron exposure, molecular coverage, thermal treatment and lateral patterning of the incide nt photon or electron beam. (C) 2000 Elsevier Science B.V. All rights reser ved.