Coherent nonlinear spectroscopy: From femtosecond dynamics to control

被引:93
作者
Dantus, M [1 ]
机构
[1] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA
[2] Michigan State Univ, Ctr Fundamental Mat Res, E Lansing, MI 48824 USA
关键词
ultrafast; four-wave mixing; photon echo; transient-grating; wavepacket;
D O I
10.1146/annurev.physchem.52.1.639
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 review focuses on the study of the dynamics of isolated molecules and their control using coherent nonlinear spectroscopic methods. Emphasis is placed on topics such as bound-to-free excitation and the study of concerted elimination reactions, free-to-bound excitation and the study of bimolecular reactions, and bound-to-bound excitation and the study of intramolecular rovibrational dynamics and coherence relaxation. For each case the detailed time-resolved information reveals possible strategies to control the outcome. Experimental results are shown for each of the reactions discussed. The methods discussed include pump-probe and four-wave mixing processes such as transient grating and photon echo spectroscopy. Off-resonance transient-grating experiments are shown to be ideal for the study of ground state dynamics, molecular structure, and the molecular response to strong field excitation.
引用
收藏
页码:639 / +
页数:48
相关论文
共 284 条
[11]   Control of photoassociation yield: a quantum-dynamical study of the mercury system to explore the role of pulse duration from nanoseconds to femtoseconds [J].
Backhaus, P ;
Schmidt, B ;
Dantus, M .
CHEMICAL PHYSICS LETTERS, 1999, 306 (1-2) :18-24
[12]  
Bahns JT, 1996, J CHEM PHYS, V104, P9689, DOI 10.1063/1.471731
[13]   MULTIPHOTON ABSORPTION VIA CHIRPED-PULSE ADIABATIC PASSAGE - DYNAMICS WITHIN THE EXCITED-STATE MANIFOLDS [J].
BAND, YB .
PHYSICAL REVIEW A, 1994, 50 (06) :5046-5050
[14]   ULTRACOLD-MOLECULE PRODUCTION BY LASER-COOLED ATOM PHOTOASSOCIATION [J].
BAND, YB ;
JULIENNE, PS .
PHYSICAL REVIEW A, 1995, 51 (06) :R4317-R4320
[15]   COMPLETE ALIGNMENT AND ORIENTATION OF ATOMS AND MOLECULES BY STIMULATED RAMAN-SCATTERING WITH TEMPORALLY SHIFTED LASERS [J].
BAND, YB ;
JULIENNE, PS .
JOURNAL OF CHEMICAL PHYSICS, 1992, 96 (04) :3339-3341
[16]   High-order harmonic generation by one- and two-electron molecular ions with intense laser pulses [J].
Bandrauk, AD ;
Yu, HT .
PHYSICAL REVIEW A, 1999, 59 (01) :539-548
[17]   DIRECT OBSERVATION OF PREFERENTIAL BOND FISSION BY EXCITATION OF A VIBRATIONAL FUNDAMENTAL - PHOTODISSOCIATION OF HOD (0,0,1) [J].
BAR, I ;
COHEN, Y ;
DAVID, D ;
ROSENWAKS, S ;
VALENTINI, JJ .
JOURNAL OF CHEMICAL PHYSICS, 1990, 93 (03) :2146-2148
[18]   Femtosecond chirped pulse excitation of vibrational wave packets in LD690 and bacteriorhodopsin [J].
Bardeen, CJ ;
Wang, Q ;
Shank, CV .
JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (17) :2759-2766
[19]   SELECTIVE EXCITATION OF VIBRATIONAL WAVE-PACKET MOTION USING CHIRPED PULSES [J].
BARDEEN, CJ ;
WANG, Q ;
SHANK, CV .
PHYSICAL REVIEW LETTERS, 1995, 75 (19) :3410-3413
[20]   Quantum control of NaI photodissociation reaction product states by ultrafast tailored light pulses [J].
Bardeen, CJ ;
Che, JW ;
Wilson, KR ;
Yakovlev, VV ;
Cong, PJ ;
Kohler, B ;
Krause, JL ;
Messina, M .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (20) :3815-3822