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Title: Formation of strained iron silicide nanodots by Fe deposition on Si nanodots on oxidized Si (111) surfaces

Journal Article · · Physical Review. B, Condensed Matter and Materials Physics
;  [1];  [1]; ;  [2]
  1. Quantum-Phase Electronics Center, Department of Applied Physics, Graduate School of Engineering, University of Tokyo, Bunkyo-ku, Tokyo 113-8656 (Japan)
  2. CREST Japan Science and Technology Agency (Japan)

We studied the epitaxial growth of iron silicide ({epsilon}-FeSi,{beta}-FeSi{sub 2}, and {alpha}-FeSi{sub 2}) nanodots on Si (111) substrates by Fe deposition on Si nanodots on Si (111) substrates with ultrathin Si oxide films using reflection high-energy electron diffraction, scanning tunneling microscopy, and transmission electron microscope (TEM). We formed almost single phase iron silicide nanodots by controlling the Fe deposition conditions; growth temperature, deposition rate, and amount. The {epsilon}-FeSi or {alpha}-FeSi{sub 2} nanodots were epitaxially grown in a dome shape with an average size of {approx}5 nm and an ultrahigh density (>10{sup 12} cm{sup -2}) on the surface. We formed {approx}2-nm high and {approx}8-nm wide {beta}-FeSi{sub 2} nanodots in a dome shape with a density of {approx}5x10{sup 11} cm{sup -2} on the surface. Cross-sectional TEM images revealed that the {beta}-FeSi{sub 2} growth continued beneath the Si surface. The part of the {beta}-FeSi{sub 2} nanodot beneath the surface was a disk shape, which was {approx}5 nm thick and {approx}20 nm wide, with an abrupt interface parallel to the Si (111) plane. The nanodots were epitaxially grown and had almost no misfit dislocations near the {beta}-FeSi{sub 2}/Si interface, which were strained by the lattice mismatch. The size distribution of the iron silicide dots was determined by Ostwald ripening with the activation energy of dot edge mobility of {approx}1.3 eV.

OSTI ID:
20719338
Journal Information:
Physical Review. B, Condensed Matter and Materials Physics, Vol. 72, Issue 7; Other Information: DOI: 10.1103/PhysRevB.72.075404; (c) 2005 The American Physical Society; Country of input: International Atomic Energy Agency (IAEA); ISSN 1098-0121
Country of Publication:
United States
Language:
English