Wave-packet interferometry and molecular state reconstruction: Spectroscopic adventures on the left-hand side of the Schrodinger equation

被引:50
作者
Cina, Jeffrey A. [1 ,2 ]
机构
[1] Univ Oregon, Dept Chem, Eugene, OR 97403 USA
[2] Univ Oregon, Oregon Ctr Opt, Eugene, OR 97403 USA
关键词
femtosecond chemical dynamics; multi dimensional electronic spectroscopy; coherent control;
D O I
10.1146/annurev.physchem.59.032607.093753
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
This article summarizes theoretical studies of molecular state determination by wave-packet interferometry (WPI) and recounts some recent experimental applications of molecular WPI. Calculations predict that two-color nonlinear WPI data can be used to reconstruct a rovibronic target wave packet evolving under an incompletely characterized nuclear Hamiltonian. This can be accomplished by the isolation via phase cycling or wave-vector matching of an exhaustive collection of overlaps between the unknown target and the members of a family of reference wave packets whose form is known by construction. This review highlights recent experiments employing WPI to gain amplitude-level information about the photoexcited-state dynamics of small molecules in the gas phase and in rare-gas crystals. I briefly describe a new semiclassical theory for condensed-phase WPI and other coherence-spectroscopy measurements, such as time-resolved coherent anti-Stokes Raman scattering, and mention our initial studies of nonlinear WPI from electronic energy-transfer complexes.
引用
收藏
页码:319 / 342
页数:24
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