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Issue 45, 2016
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Two-dimensional core–shell donor–acceptor assemblies at metal–organic interfaces promoted by surface-mediated charge transfer

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Abstract

Organic charge transfer (CT) complexes obtained by combining molecular electron donors and acceptors have attracted much interest due to their potential applications in organic opto-electronic devices. In order to work, these systems must have an electronic matching – the highest occupied molecular orbital (HOMO) of the donor must couple with the lowest unoccupied molecular orbital (LUMO) of the acceptor – and a structural matching, so as to allow direct intermolecular CT. Here it is shown that, when molecules are adsorbed on a metal surface, novel molecular organizations driven by surface-mediated CT can appear that have no counterpart in condensed phase non-covalent assemblies of donor and acceptor molecules. By means of scanning tunneling microscopy and spectroscopy it is demonstrated that the electronic and self-assembly properties of an electron acceptor molecule can change dramatically in the presence of an additional molecular species with marked electron donor character, leading to the formation of unprecedented core–shell assemblies. DFT and classical force-field simulations reveal that this is a consequence of charge transfer from the donor to the acceptor molecules mediated by the metallic substrate.

Graphical abstract: Two-dimensional core–shell donor–acceptor assemblies at metal–organic interfaces promoted by surface-mediated charge transfer

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Publication details

The article was received on 17 Aug 2016, accepted on 18 Oct 2016 and first published on 02 Nov 2016


Article type: Paper
DOI: 10.1039/C6NR06527A
Citation: Nanoscale, 2016,8, 19004-19013
  • Open access: Creative Commons BY license
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    Two-dimensional core–shell donor–acceptor assemblies at metal–organic interfaces promoted by surface-mediated charge transfer

    A. Della Pia, M. Riello, D. Stassen, T. S. Jones, D. Bonifazi, A. De Vita and G. Costantini, Nanoscale, 2016, 8, 19004
    DOI: 10.1039/C6NR06527A

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