Ultrafast relaxation and exciton-exciton annihilation in PTCDA thin films at high excitation densities

被引:128
作者
Engel, E [1 ]
Leo, K [1 ]
Hoffmann, M [1 ]
机构
[1] Tech Univ Dresden, Inst Angew Phys, D-01062 Dresden, Germany
关键词
PTCDA; organic molecular crystals; ultrafast spectroscopy; exciton-exciton annihilation; exciton diffusion;
D O I
10.1016/j.chemphys.2005.09.004
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Femtosecond pump-probe spectroscopy is applied to thin films of the quasi-one-dimensional organic semiconductor 3,4,9,10-perylene tetracarboxylic dianhydride (PTCDA). We present transient absorption spectra over a broad spectral range. Ultrafast intraband relaxation in the S, manifold towards the border of the Brillouin zone is shown to depend on temperature and excitation density. The intraband relaxation time is of the order of 100 fs. At high excitation densities (> 10(19) cm(-3)), the major de-excitation mechanism for the relaxed excitons is exciton-exciton annihilation. The experimental decay dynamics can be explained very well by two alternative annihilation models: one-dimensional diffusion limited bimolecular recombination or single-step long range Forster-type annihilation. In contrast, a three-dimensional diffusion limited annihilation model is significantly inferior. For all three models, we extract annihilation rates, diffusion constants, diffusion lengths, and Forster radii for room and liquid Helium temperature. (c) 2005 Elsevier B.V. All rights reserved.
引用
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页码:170 / 177
页数:8
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