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Adsorption and Organization of the Organic Radical 3-Carboxyproxyl on a Cu(110) Surface: A Combined STM, RAIRS, and DFT Study
University of Liverpool, UK.
University of Liverpool, UK.
University of Liverpool, UK.
University of Liverpool, UK.
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2009 (English)In: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 113, no 30, 13223-13230 p.Article in journal (Refereed) Published
Abstract [en]

We report on a combined experimental and theoretical study of the adsorption of the paramagnetic organic radical 2,2,5,5-tetramethyl-3-carboxypyrrolidine nitroxide (3-carboxyproxyl, 3CP) on a Cu(110) surface. Information from scanning tunneling microscopy (STM), reflection absorption infrared spectroscopy, and periodic density functional theory (DFT) calculations reveals important insights into the nature of the molecule-metal interface. We find that the molecule is robustly anchored to the surface via the formation of two Cu-O bonds between the carboxylate functionality and specific short-bridge adsorption sites on the Cu(110) surface. The adsorbed organic radicals appear in STM as discrete entities on the surface and can be imaged with submolecular resolution. We observe a tendency for local 2D ordering. Importantly, 3CP molecules adopt a preferred site, dictated by the strong interaction of the carboxylate groups and the steric repulsion of the methyl groups with the surface which orient the molecular ring almost perpendicular with respect to the surface. This conformation forces the NO radical away from the surface, and DFT calculations provide strong indications for the survival of the unpaired spin localized on the NO radical.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2009. Vol. 113, no 30, 13223-13230 p.
National Category
Physical Chemistry Condensed Matter Physics
Identifiers
URN: urn:nbn:se:liu:diva-85267DOI: 10.1021/jp9017579OAI: oai:DiVA.org:liu-85267DiVA: diva2:567759
Available from: 2012-11-14 Created: 2012-11-14 Last updated: 2017-12-07

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Björk, Jonas

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