Clemens Simbrunner, Dmitrii Nabok, Gerardo Hernandez-Sosa, Martin Oehzelt, Tatjana Djuric, Roland Resel, Lorenz Romaner, Peter Puschnig, Claudia Ambrosch-Draxl, Ingo Salzmann, Günther Schwabegger, Irene Watzinger, Helmut Sitter
Index: J. Am. Chem. Soc. 133 , 3056-62, (2011)
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During the last years, self-assembled organic nanostructures have been recognized as a proper fundament for several electrical and optical applications. In particular, phenylenes deposited on muscovite mica have turned out to be an outstanding material combination. They tend to align parallel to each other forming needlelike structures. In that way, they provide the key for macroscopic highly polarized emission, waveguiding, and lasing. The resulting anisotropy has been interpreted so far by an induced dipole originating from the muscovite mica substrate. Based on a combined experimental and theoretical approach, we present an alternative growth model being able to explain molecular adsorption on sheet silicates in terms of molecule-surface interactions only. By a comprehensive comparison between experiments and simulations, we demonstrate that geometrical changes in the substrate surface or molecule lead to different molecular adsorption geometries and needle directions which can be predicted by our growth model.
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