Directed long-range molecular migration energized by surface reaction

被引:0
|
作者
Harikumar K.R. [1 ]
Polanyi J.C. [1 ]
Zabet-Khosousi A. [1 ]
Czekala P. [2 ]
Lin H. [2 ]
Hofer W.A. [2 ]
机构
[1] Department of Chemistry, Institute for Optical Sciences, University of Toronto, Toronto, ON M5S 3H6
[2] Surface Science Research Centre, University of Liverpool
基金
加拿大自然科学与工程研究理事会;
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D O I
10.1038/nchem.1029
中图分类号
学科分类号
摘要
The recoil of adsorbates away (desorption) and towards (reaction) surfaces is well known. Here, we describe the long-range recoil of adsorbates in the plane of a surface, and accordingly the novel phenomenon of reactions occurring at a substantial distance from the originating event. Three thermal and three electron-induced surface reactions are shown by scanning tunnelling microscopy to propel their physisorbed ethylenic products across the rough surface of Si(100) over a distance of up to 200Å before an attachment reaction. The recoil energy in the ethylenic products comes from thermal exoergicity or from electronic excitation of chemisorbed alkenes. We propose that the mechanism of migration is a rolling motion, because the recoiling molecule overcomes raised surface obstacles. Electronic excitation of propene causes directional recoil and often end-to-end inversion, suggesting cartwheeling. Ab initio calculations of the halogenation and electron-induced reactions support a model in which asymmetric forces between the molecule and the surface induce rotation and therefore migration. © 2011 Macmillan Publishers Limited. All rights reserved.
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页码:400 / 408
页数:8
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