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Struktur und Dynamik Poster: Mi., 14:00–16:30 M-P144<br />

Time-Resolved Structural Investigation of Excimer Evolution in Organic<br />

Molecules<br />

Henrik Till Lemke 1 , Tine Ejdrup 1 , Nerijus Rusteika 1 , Peter Hammershøj 1 ,<br />

Theis Ivan Sølling 1 , Niels Harrit 1 , Klaus Bechgaard 1 , Robert<br />

Feidenhans’l 1 , Martin Meedom Nielsen 1<br />

1 Centre for Molecular Movies, Niels Bohr Institute, University of Copenhagen, Universitetsparken<br />

5, DK-2100 Copenhagen Ø, Denmark<br />

Excited aromatic molecules like pyrene, perylene and pentacene can relax to a short<br />

lived (≈100 ps) excited dimer state (excimer) that decays radiatively. Although this<br />

state is well characterised by time resolved optical spectroscopy the structural change<br />

upon dimerization remains unknown. We employ pump laser probe X-ray experiments<br />

in order to investigate structural changes during excimer evolution. X-ray pulses are<br />

either obtained from Kα secondary radiation from a plasma source or as synchrotron radiation<br />

from individual electron bunches at the ESRF. Using grazing incidence diffraction<br />

on polycrystalline thin films we can achieve a high excitation density within the<br />

probed volume and thus enhance the scattering signal. We have demonstrated a preferential<br />

uniaxial alignment of crystallites along the substrate surface, resembling a<br />

2D-powder, as well as bi-axial alignment on substrates with friction deposited PTFE<br />

alignment layers. This enables us to take advantage of the grazing incidence scattering<br />

geometry to enhance the scattering signal. Results for this first time-resolved structural<br />

observations of transient excimers are reported.

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