Electronic photon echo spectroscopy and vibrations

被引:10
作者
Christensson, N. [1 ]
Dietzek, B. [2 ,3 ]
Yartsev, A. [1 ]
Pullerits, T. [1 ]
机构
[1] Lund Univ, Dept Chem Phys, S-22100 Lund, Sweden
[2] Univ Jena, Inst Phys Chem, D-07743 Jena, Germany
[3] Inst Photon Technol Jena, D-07745 Jena, Germany
关键词
Photon echo; Fluorescence line narrowing; System-bath interaction; Huang-Rhys factor; Spectral density; Vibrational relaxation; ENERGY-GAP LAW; SOLVATION DYNAMICS; PEAK SHIFT; RELAXATION; SPECTRA; PROPAGATION; ABSORPTION; SYSTEMS;
D O I
10.1016/j.vibspec.2010.01.009
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Coupling between electronic and nuclear degrees of freedom in Rhodamine 800 has been studied using fluorescence line narrowing (FLN) and three-pulse photon echo peak shift (3PEPS). From the FLN measurement we extract the Huang-Rhys S-factors and frequencies of 16 Franck-Condon active vibrations clustered in two groups centred around 350 cm(-1) and 1400 cm(-1). The five modes below 500 cm(-1) covered by the excitation pulse spectral band create a complex beating pattern in the 3PEPS measurements. After determining the reorganisation energy of the modes involved in the peak shift measurement we are able to obtain the S-factors of the modes. The S-factors from two different experiments are in good agreement. The dephasing rates of these vibrations deviate significantly from the band-gap law. We propose that the main channel for the dephasing of the modes above 225 cm(-1) is a second order process involving one phonon and a molecular vibration. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:2 / 5
页数:4
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