Communication: Diverse nanoscale cluster dynamics: Diffusion of 2D epitaxial clusters

被引:9
|
作者
Lai, King C. [1 ,2 ]
Evans, James W. [1 ,2 ]
Liu, Da-Jiang [2 ]
机构
[1] Iowa State Univ, Dept Phys & Astron, Ames, IA 50011 USA
[2] Iowa State Univ, US DOE, Div Chem & Biol Sci, Ames Lab, Ames, IA 50011 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2017年 / 147卷 / 20期
关键词
METAL; 100; SURFACES; ISLAND DIFFUSION; SHAPE CHANGES; STEP; NANOSTRUCTURES; NANOPARTICLES; NANOCLUSTERS; SIMULATIONS; EVOLUTION; MOBILITY;
D O I
10.1063/1.5008424
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
The dynamics of nanoscale clusters can be distinct from macroscale behavior described by continuum formalisms. For diffusion of 2D clusters of N atoms in homoepitaxial systems mediated by edge atom hopping, macroscale theory predicts simple monotonic size scaling of the diffusion coefficient, D-N similar to N-beta, with beta = 3/2. However, modeling for nanoclusters on metal(100) surfaces reveals that slow nucleation-mediated diffusion displaying weak size scaling beta < 1 occurs for "perfect" sizes N-p = L-2 and L(L+1) for integer L = 3,4,... (with unique square or near-square ground state shapes), and also for N-p+3, N-p+4,.... In contrast, fast facile nucleation-free diffusion displaying strong size scaling beta approximate to 2.5 occurs for sizes N-p+1 and N-p+2. D-N versus N oscillates strongly between the slowest branch (for N-p+3) and the fastest branch (for N-p+1). All branches merge for N = O(10(2)), but macroscale behavior is only achieved for much larger N = O(10(3)). This analysis reveals the unprecedented diversity of behavior on the nanoscale. Published by AIP Publishing.
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页数:4
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