Paredis K, Smeets D, Vantomme A
Instituut voor Kern- en Stralingsfysica and INPAC, K. U. Leuven, Celestijnenlaan 200D, 3001 Leuven, Belgium.
Nanoscale Res Lett. 2009 Dec;4(12):1447-1451. doi: 10.1007/s11671-009-9418-3. Epub 2009 Aug 26.
Using scanning tunneling microscopy, the influence of a thin Au layer on the diffusion of Fe adatoms and the subsequent island nucleation on a Si(111) surface is investigated. The adsorbate induces the Si(111)-√3×√3-Au structure that increases the surface mobility of subsequently deposited Fe atoms, resulting in the formation well-defined nanoclusters. Surprisingly, the domain walls-inherent to the √3×√3-Au reconstruction-do not influence the surface diffusion, which demonstrates that the passivation is of much more importance for the self-assembly than the surface corrugation. Using the decoupling of the diffusion and nucleation on the surface and the reaction with the surface and conventional nucleation theory, the activation energy for surface diffusion E(d) = 0.61 eV and the critical cluster size i = 3 are determined, which reveal the microscopic details of the diffusion and nucleation processes.
利用扫描隧道显微镜,研究了薄金层对硅(111)表面铁吸附原子扩散以及随后岛状核形成的影响。吸附质诱导形成了Si(111)-√3×√3-Au结构,该结构增加了后续沉积铁原子的表面迁移率,从而形成了定义明确的纳米团簇。令人惊讶的是,√3×√3-Au重构固有的畴壁并不影响表面扩散,这表明钝化对于自组装比表面起伏更为重要。利用表面扩散与成核的解耦、与表面的反应以及传统成核理论,确定了表面扩散的活化能E(d)=0.61 eV以及临界团簇尺寸i=3,揭示了扩散和成核过程的微观细节。