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Adsorption and switching properties of a N-benzylideneaniline based molecular switch on a Au(111) surface

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Wolf,  Martin
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Citation

Óvári, L., Luo, Y., Leyssner, F., Haag, R., Wolf, M., & Tegeder, P. (2010). Adsorption and switching properties of a N-benzylideneaniline based molecular switch on a Au(111) surface. Journal of Chemical Physics, 133(4), 044707–1-044707–8. doi:10.1063/1.3460647.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-F534-A
Abstract
High resolution electron energy loss spectroscopy is employed to analyze the adsorption geometry and the photoisomerization ability of the molecular switch carboxy-benzylideneaniline (CBA) adsorbed on Au(111). CBA adopts on the Au(111) surface a planar (trans) configuration in the first monolayer (ML) as well as for higher coverages (up to 6 ML), contrary to the geometry in solution, which is strongly non-planar. Illumination with UV light of CBA in direct contact with the Au(111) surface (≤ 1 ML) caused no changes in the vibrational structure, whereas at higher coverages ( > 1 ML) pronounced modifications of vibrational features are observed, which we assign to a trans → cis isomerization. Thermal activation induced the back reaction to trans-CBA. We propose that the photoisomerization is driven by a direct (intramolecular) electronic excitation of the adsorbed CBA molecules in the second ML (and above) analogous to CBA in the liquid phase.