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利用电场控制金属上分子的扩散。

Diffusivity control in molecule-on-metal systems using electric fields.

机构信息

Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing, China.

出版信息

Nano Lett. 2010 Apr 14;10(4):1184-8. doi: 10.1021/nl903473p.

Abstract

The development of methods for controlling the motion and arrangement of molecules adsorbed on a metal surface would provide a powerful tool for the design of molecular electronic devices. Recently, metal phthalocyanines (MPc) have been extensively considered for use in such devices. Here we show that applied electric fields can be used to turn off the diffusivity of iron phthalocyanine (FePc) on Au(111) at fixed temperature, demonstrating a practical and direct method for controlling and potentially patterning FePc layers. Using scanning tunneling microscopy, we show that the diffusivity of FePc on Au(111) is a strong function of temperature and that applied electric fields can be used to retard or enhance molecular diffusion at fixed temperature. Using spin-dependent density-functional calculations, we then explore the origin of this effect, showing that applied fields modify both the molecule-surface binding energies and the molecular diffusion barriers through an interaction with the dipolar Fe-Au adsorption bond. On the basis of these results FePc on Au(111) is a promising candidate system for the development of adaptive molecular device structures.

摘要

发展控制吸附在金属表面的分子的运动和排列的方法将为设计分子电子器件提供有力的工具。最近,金属酞菁(MPc)已被广泛应用于此类器件。在这里,我们展示了可以在固定温度下使用外加电场来关闭铁酞菁(FePc)在 Au(111)上的扩散性,这证明了一种实用且直接的控制和潜在图案化 FePc 层的方法。使用扫描隧道显微镜,我们表明 FePc 在 Au(111)上的扩散性是温度的强烈函数,并且外加电场可用于在固定温度下延迟或增强分子扩散。然后,我们使用自旋相关的密度泛函计算,探索了这种效应的起源,表明外加场通过与偶极 Fe-Au 吸附键相互作用,同时改变了分子-表面结合能和分子扩散势垒。基于这些结果,FePc 在 Au(111)上是开发自适应分子器件结构的有前途的候选体系。

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