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https://doi.org/10.1021/nn404254y
Title: | Contacting a conjugated molecule with a surface dangling bond dimer on a hydrogenated Ge(001) surface allows imaging of the hidden ground electronic state | Authors: | Godlewski, S. Kolmer, M. Kawai, H. Such, B. Zuzak, R. Saeys, M. De Mendoza, P. Echavarren, A.M. Joachim, C. Szymonski, M. |
Keywords: | atomic-scale contacts hydrogenated semiconductor molecule manipulation organic molecule scanning tunneling microscope single-molecule devices surface dangling bonds |
Issue Date: | 26-Nov-2013 | Citation: | Godlewski, S., Kolmer, M., Kawai, H., Such, B., Zuzak, R., Saeys, M., De Mendoza, P., Echavarren, A.M., Joachim, C., Szymonski, M. (2013-11-26). Contacting a conjugated molecule with a surface dangling bond dimer on a hydrogenated Ge(001) surface allows imaging of the hidden ground electronic state. ACS Nano 7 (11) : 10105-10111. ScholarBank@NUS Repository. https://doi.org/10.1021/nn404254y | Abstract: | Fabrication of single-molecule logic devices requires controlled manipulation of molecular states with atomic-scale precision. Tuning molecule-substrate coupling is achieved here by the reversible attachment of a prototypical planar conjugated organic molecule to dangling bonds on the surface of a hydrogenated semiconductor. We show that the ground electronic state resonance of a Y-shaped polyaromatic molecule physisorbed on a defect-free area of a fully hydrogenated surface cannot be observed by scanning tunneling microscopy (STM) measurements because it is decoupled from the Ge bulk states by the hydrogen-passivated surface. The state can be accessed by STM only if the molecule is contacted with the substrate by a dangling bond dimer. The reversibility of the attachment processes will be advantageous in the construction of surface atomic-scale circuits composed of single-molecule devices interconnected by the surface dangling bond wires. © 2013 American Chemical Society. | Source Title: | ACS Nano | URI: | http://scholarbank.nus.edu.sg/handle/10635/63651 | ISSN: | 19360851 | DOI: | 10.1021/nn404254y |
Appears in Collections: | Staff Publications |
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