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Issue 32, 2016
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Ultrafast electron injection into photo-excited organic molecules

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Abstract

Charge transfer rates at metal/organic interfaces affect the efficiencies of devices for organic based electronics and photovoltaics. A quantitative study of electron transfer rates, which take place on the femtosecond timescale, is often difficult, especially since in most systems the molecular adsorption geometry is unknown. Here, we use X-ray resonant photoemission spectroscopy to measure ultrafast charge transfer rates across pyridine/Au(111) interfaces while also controlling the molecular orientation on the metal. We demonstrate that a bi-directional charge transfer across the molecule/metal interface is enabled upon creation of a core-exciton on the molecule with a rate that has a strong dependence on the molecular adsorption angle. Through density functional theory calculations, we show that the alignment of molecular levels relative to the metal Fermi level is dramatically altered when a core-hole is created on the molecule, allowing the lowest unoccupied molecular orbital to fall partially below the metal Fermi level. We also calculate charge transfer rates as a function of molecular adsorption geometry and find a trend that agrees with the experiment. These findings thus give insight into the charge transfer dynamics of a photo-excited molecule on a metal surface.

Graphical abstract: Ultrafast electron injection into photo-excited organic molecules

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Publication details

The article was received on 13 Jun 2016, accepted on 14 Jul 2016 and first published on 14 Jul 2016


Article type: Paper
DOI: 10.1039/C6CP04099C
Citation: Phys. Chem. Chem. Phys., 2016,18, 22140-22145
  • Open access: Creative Commons BY-NC license
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    Ultrafast electron injection into photo-excited organic molecules

    D. Cvetko, G. Fratesi, G. Kladnik, A. Cossaro, G. P. Brivio, L. Venkataraman and A. Morgante, Phys. Chem. Chem. Phys., 2016, 18, 22140
    DOI: 10.1039/C6CP04099C

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