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Kinetic processes in the transition from Ag(111) crystallites to ({radical}(3){times}{radical}(3))R30{degree} domains for Ag/Si(111)-(7{times}7)

Journal Article · · Physical Review, B: Condensed Matter
 [1];  [2]
  1. Department of Physics and Astronomy, Southwest Missouri State University, Springfield, Missouri 65804 (United States)
  2. Solid State Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 (United States)

Kinetic processes in the transition from metastable Ag(111) crystallites to ({radical}(3){times}{radical}(3))R30{degree} domains in the initial growth of Ag on the Si(111)-(7{times}7) surface have been investigated using spot profile analysis low-energy electron diffraction. Upon annealing above 468 K, the number density M(t) of metastable Ag(111) crystallites (deposited at T{sub d}{approximately}333K) is found to decrease exponentially with time t. Simultaneously, the average size of {radical}(3) domains increases as R(t){approximately}t{sup x}, with the exponent x increasing with initially deposited coverage and limited to a range of 1/3{le}x{le}2/5. A theoretical model for this structural transition is established to explain these observations, which is based on a kinetic process driven by the step-edge line tension of terraces in the Ag(111) crystallites. Also, a dissociation energy of an atom from the step edge of a Ag(111) crystallite is determined to be E{sub dis}{approximately}1.38eV. {copyright} {ital 1997} {ital The American Physical Society}

Research Organization:
Oak Ridge National Laboratory
DOE Contract Number:
AC05-96OR22464
OSTI ID:
565527
Journal Information:
Physical Review, B: Condensed Matter, Journal Name: Physical Review, B: Condensed Matter Journal Issue: 7 Vol. 56; ISSN 0163-1829; ISSN PRBMDO
Country of Publication:
United States
Language:
English

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