Stochastic switching of subphthalocyanine arrays triggered by scanning tunneling microscopy

被引:10
作者
Yanagi, H [1 ]
Ikuta, K [1 ]
机构
[1] Kobe Univ, Fac Engn, Nada Ku, Kobe, Hyogo 6578501, Japan
关键词
density functional calculations; equilibrium thermodynamics and statistical mechanics; molecular beam epitaxy; scanning tunneling microscopy; physical adsorption;
D O I
10.1016/j.susc.2005.02.024
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
Single-molecular switching phenomena in monolayer arrays of subphthalocyanine adsorbed on Cu(100) surface were investigated by scanning tunneling microscopy (STM) under ultrahigh vacuum. The molecules evaporated on the surface arranged in a square lattice taking the Cu(100)SubPc(5 x 5) epitaxy. During continuous STM imaging at fixed tunneling conditions the topography of the individual molecules spontaneously changed between the high and low states. This topographic change was attributed to orientational switching between the upward and downward adsorption of the axial Cl atom of the molecule on the Cu surface. Molecular energy calculations and statistical thermodynamic evaluation concluded that the tip-triggered disturbance in the close-packed molecular array induced the molecular rearrangement accompanied with the stochastic orientational switching. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:9 / 16
页数:8
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