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Reversible and Efficient Light-Induced Molecular Switching on an Insulator Surface

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Department of Physical Chemistry, University of Graz, Heinrichstrasse 28, Graz 8010, Austria
Department of Physical Chemistry, University of Mainz, Duesbergweg 10-14, Mainz 55122, Germany
§ Department of Chemistry, Humboldt-Universität zu Berlin, Brook-Taylor-Straße 2, Berlin 10099, Germany
Cite this: ACS Nano 2018, 12, 2, 1821–1828
Publication Date (Web):January 9, 2018
https://doi.org/10.1021/acsnano.7b08624
Copyright © 2018 American Chemical Society

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    Abstract

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    Prototypical molecular switches such as azobenzenes exhibit two states, i.e., trans and cis, with different characteristic physical properties. In recent years various derivatives were investigated on metallic surfaces. However, bulk insulators as supporting substrate reveal important advantages since they allow electronic decoupling from the environment, which is key to control the switching properties. Here, we report on the light-induced isomerization of an azobenzene derivative on a bulk insulator surface, in this case calcite (101̅4), studied by atomic force microscopy with submolecular resolution. Surprisingly, cis isomers appear on the surface already directly after preparation, indicating kinetic trapping. The photoisomerization process is reversible, as the use of different light sources results in specific molecular assemblies of each isomer. The process turns out to be very efficient and even comparable to molecules in solution, which we assign to the rather weak molecular interaction with the insulator surface, in contrast to metals.

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    The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acsnano.7b08624.

    • Details on AFM experiments and the illumination setup; deposition of M-TBA on the cold Au(111) surface; molecular geometry from X-ray crystal diffraction; isomerization cross sections (PDF)

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