In situ high-temperature scanning tunneling microscopy studies of two-dimensional TiN island coarsening kinetics on TiN(001)

被引:33
|
作者
Kodambaka, S [1 ]
Petrova, V [1 ]
Vailionis, A [1 ]
Petrov, I [1 ]
Greene, JE [1 ]
机构
[1] Univ Illinois, Frederick Seitz Mat Res Lab, Dept Mat Sci, Urbana, IL 61801 USA
关键词
surface diffusion; surface thermodynamics (including phase transitions); scanning tunneling microscopy; adatoms; clusters; single crystal surfaces;
D O I
10.1016/S0039-6028(02)02570-0
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In situ high-temperature (1023-1223 K) scanning tunneling microscopy was used to study the coarsening/decay kinetics of two-dimensional (2D) TiN adatom islands on TiN(0 0 1) terraces and in single-atom-deep vacancy pits. Island coarsening/decay behavior was found to be non-linear with time and to depend on the local environment (i.e., on adatom concentration gradients on the terrace), the signature of surface-diffusion-limited kinetics. Two simple island geometries-a single 2D adatom island on an atomically smooth terrace and a single 2D adatom island within a vacancy island-were used to extract adatom surface transport parameters. We model diffusion-limited island decay kinetics for these configurations based upon steady-state diffusion equations solved by adaptive finite-element methods with a form of the Gibbs-Thomson equation describing anisotropic islands serving as the boundary condition. Calculated decay rates were compared with the experimental results to obtain an activation energy E-a for adatom formation and diffusion on TiN(0 0 1). E-a was found to be 2.6 +/- 0.6 and 3.1 +/- 0.5 eV for adatom islands in vacancy pits and on terraces, respectively. The difference in the two E-a values corresponds to the step edge Ehrlich barrier, which for TiN(0 0 1) is less than the experimental uncertainties in the measurements. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:85 / 96
页数:12
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