Photoexcited carrier relaxation dynamics in pentacene probed by ultrafast optical spectroscopy: Influence of morphology on relaxation processes

被引:24
作者
Thorsmolle, V. K. [1 ,2 ]
Averitt, R. D. [2 ,3 ]
Demsar, J. [2 ,4 ,5 ,6 ]
Smith, D. L. [2 ]
Tretiak, S. [2 ]
Martin, R. L. [2 ]
Chi, X. [2 ,7 ]
Crone, B. K. [2 ]
Ramirez, A. P. [2 ,8 ]
Taylor, A. J. [2 ]
机构
[1] Ecole Polytech Fed Lausanne, CH-1015 Lausanne, Switzerland
[2] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
[3] Boston Univ, Boston, MA 02215 USA
[4] Univ Konstanz, Dept Phys, D-78457 Constance, Germany
[5] Univ Konstanz, Ctr Appl Photon, D-78457 Constance, Germany
[6] Jozef Stefan Inst, Dept Complex Matter, Ljubljana, Slovenia
[7] Texas A&M Univ Kingsville, Kingsville, TX 78363 USA
[8] Bell Labs, Alcatel Lucent, Murray Hill, NJ 07974 USA
关键词
Ultrafast spectroscopy; Organic semiconductors; Sample morphology; EXCITON DYNAMICS; CHARGE-TRANSFER; LOW-COST; POLYMERS; FILMS; CELLS;
D O I
10.1016/j.physb.2009.07.063
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
We present a comparative study of ultrafast photoexcited state relaxation in pentacene single crystals and in pure and C(60)-doped pentacene films using optical pump-probe spectroscopy. The photoinduced absorption spectra in pentacene crystals is consistent with a dominant singlet-triplet fission decay channel for above-gap excitation. This decay channel is suppressed in thin films and even further suppressed by electron trapping in C60-doped films. Thus we show that suppression of triplet state production, which is necessary for free carrier formation and thus photovoltaic and photodiode performance, is controllable via sample morphology. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:3127 / 3130
页数:4
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