Determining the static electronic and vibrational energy correlations via two-dimensional electronic-vibrational spectroscopy

被引:37
|
作者
Dong, Hui [1 ]
Lewis, Nicholas H. C.
Oliver, Thomas A. A.
Fleming, Graham R.
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2015年 / 142卷 / 17期
关键词
MOLECULAR-STRUCTURE DISTORTIONS; REAL-TIME; DYNAMICS; PHOTOSYNTHESIS; LIGHT; BACTERIORHODOPSIN; ISOMERIZATION; MODES;
D O I
10.1063/1.4919684
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
Changes in the electronic structure of pigments in protein environments and of polar molecules in solution inevitably induce a re-adaption of molecular nuclear structure. Both changes of electronic and vibrational energies can be probed with visible or infrared lasers, such as two-dimensional electronic spectroscopy or vibrational spectroscopy. The extent to which the two changes are correlated remains elusive. The recent demonstration of two-dimensional electronic-vibrational (2DEV) spectroscopy potentially enables a direct measurement of this correlation experimentally. However, it has hitherto been unclear how to characterize the correlation from the spectra. In this paper, we present a theoretical formalism to demonstrate the slope of the nodal line between the excited state absorption and ground state bleach peaks in the spectra as a characterization of the correlation between electronic and vibrational transition energies. We also show the dynamics of the nodal line slope is correlated to the vibrational spectral dynamics. Additionally, we demonstrate the fundamental 2DEV spectral line-shape of a monomer with newly developed response functions. (C) 2015 AIP Publishing LLC.
引用
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页数:8
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