Systematic growth studies of narrow constrictions formed by molecular beamepitaxy on prepatterned substrates

Citation
M. Lipinski et al., Systematic growth studies of narrow constrictions formed by molecular beamepitaxy on prepatterned substrates, MAT SCI E B, 74(1-3), 2000, pp. 25-31
Citations number
11
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
MATERIALS SCIENCE AND ENGINEERING B-SOLID STATE MATERIALS FOR ADVANCED TECHNOLOGY
ISSN journal
09215107 → ACNP
Volume
74
Issue
1-3
Year of publication
2000
Pages
25 - 31
Database
ISI
SICI code
0921-5107(20000501)74:1-3<25:SGSONC>2.0.ZU;2-Q
Abstract
The overgrowth of prepatterned GaAs substrates by molecular beam epitaxy (M BE) of GaAs/AlGaAs heterostructures is investigated by scanning electron mi croscopy (SEM) and atomic force microscopy (AFM). First, mesas with vertica l side walls which have a constriction of 1-5 mu m, are patterned into a Ga As substrate. During the MBE deposition of GaAs/AlGaAs layers onto this sub strate, specific facets form at the boundaries of the patterned area. These facets depend on the shape and orientation of the prepatterning. A detaile d study of an overgrown constriction which consists mainly of {110} and int ermediate {N11}A (N = 3 or 4) facets shows that the constriction narrows an d that a rectangular shape of the prepatterning is maintained in the MBE pr ocess. Inter facet diffusion of adatoms modifies the thickness of the MBE l ayers in the patterned area. The enhanced thickness of layers in the center of the constriction may be utilized to fabricate dot and wire like structu res at well-defined positions. AFM measurements in combination with simulat ions of the surface diffusion clearly demonstrate that the {110} facets yie ld the main contribution to the enhanced thickness. {N11}A facets can only be employed to obtain the above enhancements, if the prepatterned constrict ion is round-shaped. This sets a limit for down-scaling to the submicron ra nge. (C) 2000 Elsevier Science S.A. All rights reserved.