Nonperturbative response function: A tool for the interpretation of four-wave-mixing signals beyond third order

被引:13
作者
Chen, Lipeng [1 ]
Palacino-Gonzalez, Elise [1 ]
Gelin, Maxim F. [1 ]
Domcke, Wolfgang [1 ]
机构
[1] Tech Univ Munich, Dept Chem, D-85747 Garching, Germany
关键词
ENERGY-TRANSFER; QUANTUM COHERENCE; NONLINEAR SPECTROSCOPY; TRANSIENT ABSORPTION; PROBE SPECTROSCOPY; ULTRAFAST DYNAMICS; MOLECULAR-SYSTEMS; PHOTON-ECHO; SPECTRA; EXCITATION;
D O I
10.1063/1.5004763
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
Considering an electronic two-level system coupled to vibrational degrees of freedom and driven by short and intense non-overlapping laser pulses, we introduce the concept of nonperturbative response functions. These response functions are expressed in terms of effective electronic transition dipole moments which depend on the strength of the field-matter coupling and on the pulse durations. It is shown that the nonlinear polarization representing four-wave-mixing signals can elegantly be expressed in terms of these nonperturbative response functions to all orders in the field-matter coupling. The nonperturbative response functions generalize the interpretative power of the familiar third-order response functions to four-wave-mixing experiments with intense laser pulses. Published by AIP Publishing.
引用
收藏
页数:12
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