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

被引:16
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
相关论文
共 71 条
[1]   Dephasing in semiconducting single-walled carbon nanotubes induced by exciton-exciton annihilation [J].
Abramavicius, Darius ;
Ma, Ying-Zhong ;
Graham, Matthew W. ;
Valkunas, Leonas ;
Fleming, Graham R. .
PHYSICAL REVIEW B, 2009, 79 (19)
[2]  
[Anonymous], 1987, OPTICAL RESONANCE 2
[3]   IMPULSIVE EXCITATION OF COHERENT VIBRATIONAL MOTION GROUND SURFACE DYNAMICS INDUCED BY INTENSE SHORT PULSES [J].
BANIN, U ;
BARTANA, A ;
RUHMAN, S ;
KOSLOFF, R .
JOURNAL OF CHEMICAL PHYSICS, 1994, 101 (10) :8461-8481
[4]   Feedback quantum control of molecular electronic population transfer [J].
Bardeen, CJ ;
Yakovlev, VV ;
Wilson, KR ;
Carpenter, SD ;
Weber, PM ;
Warren, WS .
CHEMICAL PHYSICS LETTERS, 1997, 280 (1-2) :151-158
[5]   Ultrafast dynamics of single molecules [J].
Brinks, Daan ;
Hildner, Richard ;
van Dijk, Erik M. H. P. ;
Stefani, Fernando D. ;
Nieder, Jana B. ;
Hernando, Jordi ;
van Hulst, Niek F. .
CHEMICAL SOCIETY REVIEWS, 2014, 43 (08) :2476-2491
[6]   Non-perturbative calculation of 2D spectra in heterogeneous systems:: Exciton relaxation in the FMO complex [J].
Bruggemann, Ben ;
Kjellberg, Par ;
Pullerits, Tonu .
CHEMICAL PHYSICS LETTERS, 2007, 444 (1-3) :192-196
[7]   Control of excited-state population and vibrational coherence with shaped-resonant and near-resonant excitation [J].
Buckup, T. ;
Hauer, J. ;
Serrat, C. ;
Motzkus, M. .
JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS, 2008, 41 (07)
[8]   Vibrational vs. electronic coherences in 2D spectrum of molecular systems [J].
Butkus, Vytautas ;
Zigmantas, Donatas ;
Valkunas, Leonas ;
Abramavicius, Darius .
CHEMICAL PHYSICS LETTERS, 2012, 545 :40-43
[9]   Molecular vibrations-induced quantum beats in two-dimensional electronic spectroscopy [J].
Butkus, Vytautas ;
Valkunas, Leonas ;
Abramavicius, Darius .
JOURNAL OF CHEMICAL PHYSICS, 2012, 137 (04) :8231
[10]   Optimal Energy Transfer in Light-Harvesting Systems [J].
Chen, Lipeng ;
Shenai, Prathamesh ;
Zheng, Fulu ;
Somoza, Alejandro ;
Zhao, Yang .
MOLECULES, 2015, 20 (08) :15224-15272