Ultrafast solvation dynamics explored by femtosecond photon echo spectroscopies

被引:264
作者
de Boeij, WP [1 ]
Pshenichnikov, MS [1 ]
Wiersma, DA [1 ]
机构
[1] Univ Groningen, Ctr Mat Sci, Ultrafast Laser & Spect Lab, NL-9747 AG Groningen, Netherlands
关键词
ultrafast spectroscopy; correlation function;
D O I
10.1146/annurev.physchem.49.1.99
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
Chemical reaction and optical dynamics in the liquid phase are strongly affected by specific solute-solvent interactions. The dynamical part of this coupling leads to energy fluctuations. The associated energy gap dynamics can be probed by using various nonlinear optical spectroscopies. We discuss various forms of photon echo-time-integrated, time-gated, and heterodyne-detected photon echo-as well as Fourier transform spectral interferometry. It is shown that for solutions of the dye molecule DTTCI, a system-bath correlation function can be acquired that provides a quantitative description of all (non)linear spectroscopic experiments. The deduced correlation function is projected onto the multimode Brownian oscillator model, which allows for a physical interpretation of the multiple-time correlation function and a determination of the spectral density relevant to the solvation process. The following applications of photon echo to condensed phase dynamics are discussed: enhanced vibrational mode suppression, Liouville pathways interference, and dynamical Stokes shift. Recent results of echo-peak shift experiments on the hydrated electron are also presented The review concludes that photon echo should be useful as a novel tool to explore transition state dynamics.
引用
收藏
页码:99 / 123
页数:25
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