Aspects of the formation of self-organized clusters of germanium (Ge) and solid solution of SiGe, first formed in the mode of deposition of subthin polycrystalline silicon films doped with Ge on the nanoscale film of dielectrics were studied by techniques of atomic force microscopy and Raman scattering by optical phonons in germanium clusters. We found that in subthin polycrystalline silicon films (PSF) doped with Ge on the nanoscale films of dielectrics in conditions of PSF film deposition, there appeared correlated spatial distribution of germanium clusters, as well as silicon rich clusters in certain conditions, i.e., clusters of SiGe solid solution, with the modes of their formation. The relationship of the form, size, and density of Ge nanoclusters (NC), with the conditions of their self-organization is considered. The influence of interdiffusion processes on self-organizing of clusters is established, which is significant at high temperatures of the deposition and doping of PSF. It was found that clusters (islands) could occur on the cleavage surface in the form of four types of topographic features in a classical pyramid form, flat-topped pyramids, and domes and sharp spines, depending on the conditions of the deposition of PSF doped with Ge. The systems of highly organized Ge NC, measuring 3.5–40 nm and with a density of 2.7 × 107–3.5 × 10 cm−2 were obtained. The possibility, in principle, of managing the geometric parameters of self-organizing NC (nanoislands) by selecting the conditions of their self-organization in the mode of deposition of PSF doped with Ge, was shown.
Russian Microelectronics – Springer Journals
Published: May 20, 2010
It’s your single place to instantly
discover and read the research
that matters to you.
Enjoy affordable access to
over 18 million articles from more than
15,000 peer-reviewed journals.
All for just $49/month
Query the DeepDyve database, plus search all of PubMed and Google Scholar seamlessly
Save any article or search result from DeepDyve, PubMed, and Google Scholar... all in one place.
All the latest content is available, no embargo periods.
“Whoa! It’s like Spotify but for academic articles.”@Phil_Robichaud