z-logo
Premium
Ultrathin films of Ge on the Si(100)2 × 1 surface
Author(s) -
Kamaratos M.,
Sotiropoulos A.K.,
Vlachos D.
Publication year - 2018
Publication title -
surface and interface analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.52
H-Index - 90
eISSN - 1096-9918
pISSN - 0142-2421
DOI - 10.1002/sia.6358
Subject(s) - dangling bond , overlayer , silicon , auger electron spectroscopy , annealing (glass) , germanium , materials science , electron diffraction , crystallography , low energy electron diffraction , amorphous solid , substrate (aquarium) , analytical chemistry (journal) , chemistry , diffraction , optoelectronics , optics , metallurgy , physics , oceanography , chromatography , geology , nuclear physics
The Ge/Si(100)2 × 1 interface was investigated by means of Auger electron spectroscopy, low‐energy electron diffraction, thermal desorption spectroscopy, and work function measurements, in the regime of a few monolayers. The results show that growth of Ge at room temperature forms a thermally stable amorphous interface without significant intermixing and interdiffusion into the substrate, for annealing up to ~1100 K. Therefore, the Ge‐Si interaction most likely takes place at the outmost silicon atomic plane. The charge transfer between Ge and Si seems to be negligible, indicating a rather covalent bonding. Regarding the Ge overlayer morphology, the growth mode depends on the substrate temperature during deposition, in accordance with the literature. Stronger annealing of the germanium covered substrate (>1100 K) causes desorption of not only Ge adatoms, but also SiGe and Ge 2 species. This is probably due to a thermal Ge‐Si interdiffusion. In that case, deeper silicon planes participate in the Ge‐Si interaction. Above 1200 K, a new Ge superstructure (4 × 4) R 45 o was observed. Based on that symmetry, an atomic model is proposed, where Ge adatom pairs interact with free silicon dangling bonds.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here