Femtosecond study of exciton transport dynamics in (phthalocyaninato)polysiloxane

被引:22
|
作者
Ern, J
Bock, A
Oddos-Marcel, L
Rengel, H
Wegner, G
Trommsdorff, HP
Kryschi, C
机构
[1] Univ Dusseldorf, Lehrstuhl Festkorperspektroskopie, IPKM, D-40225 Dusseldorf, Germany
[2] Univ Grenoble 1, Spectrometrie Phys Lab, F-38402 St Martin Dheres, France
[3] Max Planck Inst Polymerforsch, D-55128 Mainz, Germany
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 1999年 / 103卷 / 14期
关键词
D O I
10.1021/jp984064w
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
The transport and relaxation dynamics of singlet excitons of rodlike [tetramethoxytetrakis(octyloxy)-phthalocyaninato]polysiloxane (PcPSi) in tetrahydrofuran solution were investigated on the femtosecond scale by transient absorption spectroscopy. Singlet excitons are generated upon excitation into the ground-state absorption at 555 nm using laser pulses of 120 fs duration with different intensities. Transient absorption spectra were recorded at variable delays using a white-light continuum probe pulse. Both photoinduced bleaching and transient absorption show nonexponential decay dynamics with a pronounced dependence on the excitation energy density. The analysis of the decay dynamics of the photo-induced bleaching and transient absorption at lower excitation densities is made by including, in addition to the monomolecular, exponential decay with lifetime tau, a time-dependent bimolecular exciton-exciton annihilation rate constant gamma t(-1/2) characteristic of one-dimensional diffusive exciton transport. At high excitation densities, the observed decay strongly deviates from this behavior, as a new relaxation channel is opened, which is attributed to short-lived, charge-separated states.
引用
收藏
页码:2446 / 2450
页数:5
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