The separation of overlapping transitions in β-carotene with broadband 2D electronic spectroscopy

被引:21
|
作者
Calhoun, Tessa R. [1 ,2 ]
Davis, Jeffrey A. [3 ]
Graham, Matthew W. [1 ,2 ]
Fleming, Graham R. [1 ,2 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Phys Biosci Div, Berkeley, CA 94720 USA
[3] Swinburne Univ Technol, Ctr Atom Opt & Ultrafast Spect, Hawthorn, Vic 3122, Australia
基金
美国国家科学基金会;
关键词
STIMULATED RAMAN-SPECTROSCOPY; EXCITED-STATE DYNAMICS; ULTRAFAST DYNAMICS; CONVERSION;
D O I
10.1016/j.cplett.2011.10.051
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 2D electronic spectroscopy is applied to beta-carotene, revealing new insight into the excited state dynamics of carotenoids by exploring the full energetic range encompassing the S-0 -> S-2 and S-1 -> S-1n transitions at 77 K. Multiple signals are observed in the regime associated with the proposed S* state and isolated through separate analysis of rephasing and nonrephasing contributions. Peaks in rephasing pathways display dynamic lineshapes characteristic of coupling to high energy vibrational modes, and simulation with a simple model supports their assignment to impulsive stimulated Raman scattering. A signal persisting beyond 10 ps in the nonrephasing spectra is still under investigation. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 5
页数:5
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