Excited and ground state vibrational dynamics revealed by two-dimensional electronic spectroscopy

被引:39
|
作者
Caram, Justin R. [1 ]
Fidler, Andrew F.
Engel, Gregory S.
机构
[1] Univ Chicago, Dept Chem, Chicago, IL 60637 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2012年 / 137卷 / 02期
基金
美国国家科学基金会;
关键词
FEMTOSECOND PUMP-PROBE; QUANTUM COHERENCE; PHYSIOLOGICAL TEMPERATURE; ROOM-TEMPERATURE; ENERGY-TRANSFER; CYANINE DYE; PHOTOSYNTHESIS; SPECTRA; COMPLEX; SOLVENT;
D O I
10.1063/1.4733710
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
Broadband two-dimensional electronic spectroscopy (2DES) can assist in understanding complex electronic and vibrational signatures. In this paper, we use 2DES to examine the electronic structure and dynamics of a long chain cyanine dye (1,1-diethyl-4,4-dicarbocyanine iodide, or DDCI-4), a system with a vibrational progression. Using broadband pulses that span the resonant electronic transition, we measure two-dimensional spectra that show a characteristic six peak pattern from coherently excited ground and excited state vibrational modes. We model these features using a spectral density formalism and the vibronic features are assigned to Feynman pathways. We also examine the dynamics of a particular set of peaks demonstrating anticorrelated peak motion, a signature of oscillatory wavepacket dynamics on the ground and excited states. These dynamics, in concert with the general structure of vibronic two-dimensional spectra, can be used to distinguish between pure electronic and vibrational quantum coherences. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.4733710]
引用
收藏
页数:10
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