Excitonic intraband relaxation and polarization anisotropies in PTCDA on femtosecond and picosecond timescales

被引:6
作者
Engel, E [1 ]
Koschorreck, M [1 ]
Leo, K [1 ]
Hoffmann, M [1 ]
机构
[1] Tech Univ Dresden, Inst Angew Photophys, D-01062 Dresden, Germany
关键词
organic molecular crystals; ultrafast spectroscopy; time-resolved luminescence;
D O I
10.1016/j.jlumin.2004.09.098
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We report on investigations of optical excitations in polycrystalline organic molecular crystals with quasi-1D-stacked crystal structure and negative exciton dispersion. As model system, we choose thin films of the perylene derivative 3,4,9, 10-perylenetetracarboxylic dianhydride (PTCDA). Using pump-probe spectroscopy, we show how the relaxation from the absorbing state towards the border of the Brillouin zone occurs on a 120 fs timescale. Time-resolved luminescence anisotropy gives evidence that as a result of the coherent coupling between adjacent stacks, populations of the Davydovsplit states that are prepared during photo-excitation relax into the emitting states in less than 5 ps. The behavior of the luminescence anisotropy can be explained by the orientation of the two PTCDA molecules in the unit cell. However, a full understanding of the ultrafast pump-probe anisotropy requires novel explanations beyond current models. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:299 / 302
页数:4
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