DETECTION AND CONTROL OF MOLECULAR QUANTUM DYNAMICS

被引:30
作者
CHE, JW
KRAUSE, JL
MESSINA, M
WILSON, KR
YAN, YJ
机构
[1] HONG KONG UNIV SCI & TECHNOL, DEPT CHEM, KOWLOON, HONG KONG
[2] UNIV CALIF SAN DIEGO, DEPT CHEM & BIOCHEM, LA JOLLA, CA 92093 USA
[3] UNIV FLORIDA, QUANTUM THEORY PROJECT, GAINESVILLE, FL 32611 USA
关键词
D O I
10.1021/j100041a008
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
We combine a theory of quantum control in the weak-response regime with the conventional theory of pump-probe spectroscopy, in order to provide a clear theoretical basis for control experiments of the type recently carried out in our group. In the control scenario considered here, we compute the pump field that best drives a quantum system to a desired target or goal. To monitor the temporal evolution of the quantum system, we employ an optical scheme in which the wave packet created by the pump, or control, field is probed with a second ultrafast pulse to a higher-lying electronic state. The absorption of the probe pulse is proportional to the laser-induced fluorescence (LIF) signal observed in an experiment and thus gives a measure of the quantum distribution of the wave packet in the target region. By using a series of such probe pulses at different times and/or different photon energies, the quantum temporal evolution of the control system can be mapped out. Numerical examples are presented for the control and subsequent detection of the vibrational dynamics of the I-2 molecule on an electronically excited potential energy surface. By comparing the LIF signal for the globally optimal field for a specific target with the signal obtained from a deliberately nonoptimal field, the time reversal of the optimal field, which has the same frequency spectrum, we demonstrate that a clear signature of control can be obtained by monitoring a spectroscopic observable. Finally, we compare the detected signal as computed by exact quantum mechanics and as approximated by the computationally simpler classical Condon approximation.
引用
收藏
页码:14949 / 14958
页数:10
相关论文
共 78 条
[51]   DYNAMICS OF VIBRATIONAL WAVE-PACKETS IN THE C1-PI-U STATE OF CS-2 [J].
RODRIGUEZ, G ;
EDEN, JG .
CHEMICAL PHYSICS LETTERS, 1993, 205 (4-5) :371-379
[52]   PHASE-DEPENDENT EFFECTS IN MULTIPHOTON IONIZATION INDUCED BY A LASER FIELD AND ITS 2ND HARMONIC [J].
SCHAFER, KJ ;
KULANDER, KC .
PHYSICAL REVIEW A, 1992, 45 (11) :8026-8033
[53]   TIME RESOLVED DYNAMICS OF ISOLATED MOLECULAR-SYSTEMS STUDIED WITH PHASE-LOCKED FEMTOSECOND PULSE PAIRS [J].
SCHERER, NF ;
RUGGIERO, AJ ;
DU, M ;
FLEMING, GR .
JOURNAL OF CHEMICAL PHYSICS, 1990, 93 (01) :856-857
[54]   CONTROLLED PHOTON INDUCED SYMMETRY-BREAKING - CHIRAL MOLECULAR PRODUCTS FROM ACHIRAL PRECURSORS [J].
SHAPIRO, M ;
BRUMER, P .
JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (11) :8658-8661
[55]   LASER CONTROL OF PRODUCT QUANTUM STATE POPULATIONS IN UNIMOLECULAR REACTIONS [J].
SHAPIRO, M ;
BRUMER, P .
JOURNAL OF CHEMICAL PHYSICS, 1986, 84 (07) :4103-4104
[56]   COHERENT AND INCOHERENT LASER CONTROL OF PHOTOCHEMICAL-REACTIONS [J].
SHAPIRO, M ;
BRUMER, P .
INTERNATIONAL REVIEWS IN PHYSICAL CHEMISTRY, 1994, 13 (02) :187-229
[57]   SIMPLIFIED LASER CONTROL OF UNIMOLECULAR REACTIONS - SIMULTANEOUS (OMEGA-1,OMEGA-3) EXCITATION [J].
SHAPIRO, M ;
HEPBURN, JW ;
BRUMER, P .
CHEMICAL PHYSICS LETTERS, 1988, 149 (5-6) :451-454
[58]   WEAK-FIELD OPTIMAL-CONTROL OVER PRODUCT YIELDS - THE PUMP DUMP SCENARIO [J].
SHAPIRO, M ;
BRUMER, P .
CHEMICAL PHYSICS LETTERS, 1993, 208 (3-4) :193-196
[59]   OPTIMAL PULSE SHAPING FOR COHERENT CONTROL BY THE PENALTY ALGORITHM [J].
SHEN, H ;
DUSSAULT, JP ;
BANDRAUK, AD .
CHEMICAL PHYSICS LETTERS, 1994, 221 (5-6) :498-506
[60]   OPTIMAL-CONTROL OF SELECTIVE VIBRATIONAL-EXCITATION OF HARMONIC MOLECULES - ANALYTIC SOLUTION AND RESTRICTED FORMS FOR THE OPTIMAL FIELDS [J].
SHI, SH ;
RABITZ, H .
JOURNAL OF CHEMICAL PHYSICS, 1990, 92 (05) :2927-2937