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Issue 32, 2011
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Photoinduced work function changes by isomerization of a densely packed azobenzene-based SAM on Au: a joint experimental and theoretical study

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Abstract

Responsive monolayers are key building blocks for future applications in organic and molecular electronics in particular because they hold potential for tuning the physico-chemical properties of interfaces, including their energetics. Here we study a photochromic SAM based on a conjugated azobenzene derivative and its influence on the gold work function (ΦAu) when chemisorbed on its surface. In particular we show that the ΦAu can be modulated with external stimuli by controlling the azobenzenetrans/cisisomerization process. This phenomenon is characterized experimentally by four different techniques, kelvin probe, kelvin probe force microscopy, electroabsorption spectroscopy and ultraviolet photoelectron spectroscopy. The use of different techniques implies exposing the SAM to different measurement conditions and different preparation methods, which, remarkably, do not alter the observed work function change (Φtrans–Φcis). Theoretical calculations provided a complementary insight crucial to attain a deeper knowledge on the origin of the work function photo-modulation.

Graphical abstract: Photoinduced work function changes by isomerization of a densely packed azobenzene-based SAM on Au: a joint experimental and theoretical study

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Publication details

The article was received on 21 Mar 2011, accepted on 13 May 2011 and first published on 22 Jun 2011


Article type: Paper
DOI: 10.1039/C1CP20851A
Citation: Phys. Chem. Chem. Phys., 2011,13, 14302-14310
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    Photoinduced work function changes by isomerization of a densely packed azobenzene-based SAM on Au: a joint experimental and theoretical study

    N. Crivillers, A. Liscio, F. Di Stasio, C. Van Dyck, S. Osella, D. Cornil, S. Mian, G. M. Lazzerini, O. Fenwick, E. Orgiu, F. Reinders, S. Braun, M. Fahlman, M. Mayor, J. Cornil, V. Palermo, F. Cacialli and P. Samorì, Phys. Chem. Chem. Phys., 2011, 13, 14302
    DOI: 10.1039/C1CP20851A

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