Nucleation on Defects in Heteroepitaxy

1996 ◽  
Vol 440 ◽  
Author(s):  
J. A. Venables

AbstractThe rate equation treatment of nucleation and growth on perfect substrates has been extended to cover nucleation on random defect sites, and problems involving 1-dimensional (1D) diffusion to sinks. This paper recaps the results of rate equation treatments on perfect terraces, and sumnarises some new models, including: 1) nucleation on point defects, with application to nm-sized Fe and Co particles grown on various CaF2substrates; 2) nucleation and diffusion in finite 1D deposits, with application to diffusion over, and the break-up of, multilayer deposits of Ag/Ge(111) and Ag/Fe(110); 3) 1D models developed for nucleation in competition with step capture. Comparison of rate-diffusion equations with experiment can result in values for, or bounds on, the controlling energies, in a way which illuminates the main features of interatomic forces at surfaces. The use of defects to grow thin film arrays for practical application presents some interesting challenges at both the nucleation and growth stages, which are discussed briefly.

1995 ◽  
Vol 5 (1-2) ◽  
pp. 39-52 ◽  
Author(s):  
Jeffrey R. Hufton ◽  
Douglas M. Ruthven ◽  
Ronald P. Danner

2006 ◽  
Vol 249 ◽  
pp. 1-6 ◽  
Author(s):  
Jean Philibert

After some biographical notes, Fick’s 1855 seminal paper is analysed and the contributions of Stefan and Roberts-Austen are briefly mentioned.


2002 ◽  
Vol 389-393 ◽  
pp. 471-476 ◽  
Author(s):  
M. Bockstedte ◽  
Matthias Heid ◽  
Alexander Mattausch ◽  
Oleg Pankratov

1999 ◽  
Vol 570 ◽  
Author(s):  
J. A. Venables ◽  
G. Haas ◽  
H. Brune ◽  
J.H. Harding

ABSTRACTNucleation and growth of metal clusters at defect sites is discussed in terms of rate equation models, which are applied to the cases of Pd and Ag on MgO(001) and NaCl(001) surfaces. Pd/MgO has been studied experimentally by variable temperature atomic force microscopy (AFM). The island density of Pd on Ar-cleaved surfaces was determined in-situ by AFM for a wide range of deposition temperature and flux, and stays constant over a remarkably wide range of parameters; for a particular flux, this plateau extends from 200 K ≤ T ≤ 600 K, but at higher temperatures the density decreases. The range of energies for defect trapping, adsorption, surface diffusion and pair binding are deduced, and compared with earlier data for Ag on NaCl, and with recent calculations for these metals on both NaCl and MgO


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