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Struktur und Dynamik Poster: Mi., 14:00–16:30 M-P140<br />

Energy-dispersive X-ray reflectivity for real-time growth studies of organic<br />

thin films<br />

Stefan Kowarik 1,2 , Alexander Gerlach 1,2 , Frank Schreiber 1 , Wolfram<br />

Leitenberger 3 , Ullrich Pietsch 4<br />

1 Tübingen University, Institute for Applied Physics, 72076 Tübingen, Germany –<br />

2 Oxford University, Physical and Theoretical Chemistry, Oxford OX1 3QZ, UK –<br />

3 Potsdam, Institute for Physics, 14469 Potsdam, Germany – 4 Siegen University, Department<br />

of Physics, 57068 Siegen, Germany<br />

We employ energy-dispersive as well as angle-dispersive X-ray reflectivity to study<br />

the growth and structure of the organic semiconductors rubrene and pentacene in in<br />

situ and real time. Following the surface morphology of rubrene films during organic<br />

molecular beam deposition, we find relatively smooth films (surface roughness below<br />

∼15 ˚A for thicknesses up to at least 600 ˚A) and a significant delay before the onset<br />

of roughening. This anomalous roughening in the beginning and crossover to normal<br />

roughening later during growth may be related to conformational changes of rubrene<br />

in the early stages of growth. Studying pentacene in real-time during growth with<br />

energy-dispersive reflectometry we can follow the growth oscillations for a wide range<br />

in q-space including the anti-Bragg point. These growth oscillations give a detailed<br />

picture of the crossover from layer-by-layer growth for the first pentacene monolayers<br />

to roughening for thicker films. Finally, we discuss the chances and li<strong>mit</strong>ations of energy<br />

dispersive as compared to conventional angle-dispersive measurements [1].<br />

[1] S. Kowarik et al., PCCP 8 (2006) 1834<br />

Fig. 1: Following the evolution<br />

of the X-ray reflectivity<br />

during pentacene thin film<br />

growth with energy dispersive<br />

measurements allows to determine<br />

the growth mode.

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