Della Pia, A, Riello, M, Stassen, D, Jones, T.S., Bonifazi, Davide ![]() |
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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.
Item Type: | Article |
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Date Type: | Published Online |
Status: | Published |
Schools: | Schools > Chemistry |
Subjects: | Q Science > QD Chemistry |
Publisher: | Royal Society of Chemistry |
ISSN: | 2040-3372 |
Date of First Compliant Deposit: | 10 January 2017 |
Date of Acceptance: | 18 October 2016 |
Last Modified: | 07 Nov 2024 01:00 |
URI: | https://orca.cardiff.ac.uk/id/eprint/97307 |
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