Diverse growth of Mn, In and Sn islands on thallium-passivated Si(111) surface

被引:8
作者
Matvija, P. [1 ]
Sobotik, P. [1 ]
Ost'adal, I. [1 ]
Kocan, P. [1 ]
机构
[1] Charles Univ Prague, Fac Math & Phys, Prague, Czech Republic
关键词
Thallium; Si(111); Passivation; Thin film growth; Growth modes; Scanning tunneling microscopy; SCANNING-TUNNELING-MICROSCOPY; INITIAL-STAGES; OVERLAYERS; NUCLEATION; DIFFUSION; STM; STABILITY; SI(100); EPITAXY; ATOMS;
D O I
10.1016/j.apsusc.2015.01.067
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
Controlled growth of thin films on highly reactive silicon surfaces has been a challenge for decades. High density of surface dangling bonds, however, hinders the adsorbate diffusion and its self-organization. In our work, we propose a novel use of the T1-(1 x 1) layer as a passivating agent, which highly enhances diffusion of adsorbates by saturating all dangling bonds of the Si substrate. We use room-temperature scanning tunneling microscopy to study structures formed on the Si(1 1 I)/T1 - (1 x 1) surface after deposition of submonolayer amounts of three elemental adsorbates: Mn, In and Sn. As a result, three significantly different surface structures are observed. Manganese atoms aggregate to stable dendritic islands nucleated on Si steps. Indium islands are compact and unstable during observation. Unlike Mn and In, Sn atoms intermix with Tl atoms and arrange into an array of triangular objects. The growth kinetics of the three deposited metals on the Tl - (1 x 1) layer is discussed and compared with the kinetics observed in previously studied systems. The comparison shows that the growth of the layers adsorbed on the Tl-passivated surface is similar to the growth of the adsorbate layers on less reactive metal surfaces. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:339 / 345
页数:7
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