Potential pitfalls of the early-time dynamics in two-dimensional electronic spectroscopy

被引:26
作者
Palecek, David [1 ,2 ,4 ]
Edlund, Petra [3 ]
Gustavsson, Emil [3 ]
Westenhoff, Sebastian [3 ]
Zigmantas, Donatas [1 ]
机构
[1] Lund Univ, Dept Chem Phys, POB 124, SE-22100 Lund, Sweden
[2] Charles Univ Prague, Dept Chem Phys, Ke Karlovu 3, Prague 12116 2, Czech Republic
[3] Univ Gothenburg, Dept Chem & Mol Biol, Box 462, SE-40530 Gothenburg, Sweden
[4] Univ Cambridge, Cavendish Lab, JJ Thomson Ave, Cambridge CB3 0HE, England
基金
瑞典研究理事会;
关键词
ENERGY-TRANSFER; REACTION CENTERS; COHERENCE; PHOTOSYNTHESIS; COMPLEX; STATES;
D O I
10.1063/1.5079817
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
Two-dimensional electronic spectroscopy, and especially the polarization-controlled version of it, is the cutting edge technique for disentangling various types of coherences in molecules and molecular aggregates. In order to evaluate the electronic coherences, which often decay on a 100 fs time scale, the early population times have to be included in the analysis. However, signals in this region are typically plagued by several artifacts, especially in the unavoidable pulse overlap region. In this paper, we show that, in the case of polarization-controlled two-dimensional spectroscopy experiment, the early-time dynamics can be dominated by the "incorrect" pulse ordering signals. These signals can affect kinetics at positive times well beyond the pulse overlap region, especially when the "correct" pulse ordering signals are much weaker. Moreover, the "incorrect" pulse ordering contributions are oscillatory and overlap with the spectral signatures of energy transfer, which may lead to misinterpretation of "incorrect" pulse ordering signals for fast-decaying coherences.
引用
收藏
页数:8
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