OPTIMAL-CONTROL OF THE ELECTRIC SUSCEPTIBILITY OF A MOLECULAR GAS BY DESIGNED NONRESONANT LASER-PULSES OF LIMITED AMPLITUDE

被引:17
作者
SHEN, LY
SHI, S
RABITZ, H
LIN, C
LITTMAN, M
HERITAGE, JP
WEINER, AM
机构
[1] PRINCETON UNIV, DEPT MECH & AEROSP ENGN, PRINCETON, NJ 08544 USA
[2] UNIV CALIF DAVIS, DEPT ELECT ENGN, DAVIS, CA 95616 USA
[3] BELLCORE, RED BANK, NJ 07701 USA
关键词
D O I
10.1063/1.464587
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 present a theoretical study on optimal control of the electric susceptibility change of a homogeneous molecular gas resulting from orientational anisotropy induced by nonresonant lasers with limited intensity. It is assumed that the molecular gas is initially in thermal equilibrium. Two types of optimal control objectives have been considered: terminal control and temporal profile control (i.e., trajectory control). A step function is introduced into the cost functionals which successfully helps to realize the restriction on the magnitude of the field amplitude in numerical optimization, as demonstrated by the examples. Calculations are carried out for CS2 which has a small rotational constant (B=0.1091 cm-1) and a quite large polarizability anisotropy (DELTAalpha=9.6 angstrom3). For terminal control of a maximal susceptibility change at a target time T, it is found that the optimal control field is composed of a series of rectangular pulses with identical amplitudes equal to a preassigned bound value. All of the optimal fields for terminal control are functions of (T-t) over the time interval [0,T] with characteristic time 1/8B and period 1/2B. For temporal profile control, the degree of control is strongly dependent on the length of time interval over which a target profile is defined. Usually, if a time interval is shorter than 1/8B and a target profile is a smooth and non-negative function with a reasonable maximal value, the control can be achieved perfectly. In other cases the detailed assignment of the weight function in the cost functional plays an important role in determining how to make an optimally controlled susceptibility change profile approach the target profile. Furthermore, we have also examined the temperature effects on optimal control in this paper. It can be shown that the general optimal control properties observed by CS2 will also be valid for other linear molecular gases with small rotational constants.
引用
收藏
页码:7792 / 7803
页数:12
相关论文
共 71 条
[1]   THE USE OF PULSE SHAPING TO CONTROL THE PHOTODISSOCIATION OF A DIATOMIC MOLECULE - PREVENTING THE BEST FROM BEING THE ENEMY OF THE GOOD [J].
AMSTRUP, B ;
CARLSON, RJ ;
MATRO, A ;
RICE, SA .
JOURNAL OF PHYSICAL CHEMISTRY, 1991, 95 (21) :8019-8027
[2]   POLARIZATION CONTROL OF BRANCHING RATIOS IN PHOTODISSOCIATION [J].
ASARO, C ;
BRUMER, P ;
SHAPIRO, M .
PHYSICAL REVIEW LETTERS, 1988, 60 (16) :1634-1637
[3]  
BENSTEIN RB, 1982, CHEM DYNAMICS VIA MO
[4]   APPLICATION OF OPTIMAL-CONTROL THEORY FOR SELECTIVE VIBRATIONAL-EXCITATION IN MOLECULES MODELED AS HARMONIC PHYSICAL SYSTEMS [J].
BEUMEE, JGB ;
RABITZ, H .
JOURNAL OF MATHEMATICAL PHYSICS, 1990, 31 (05) :1253-1260
[5]  
BRUMER P, 1990, CHEM PHYS, V144, P146
[6]   COHERENCE CHEMISTRY - CONTROLLING CHEMICAL-REACTIONS WITH LASERS [J].
BRUMER, P ;
SHAPIRO, M .
ACCOUNTS OF CHEMICAL RESEARCH, 1989, 22 (12) :407-413
[7]   ONE PHOTON MODE SELECTIVE CONTROL OF REACTIONS BY RAPID OR SHAPED LASER-PULSES - AN EMPEROR WITHOUT CLOTHES [J].
BRUMER, P ;
SHAPIRO, M .
CHEMICAL PHYSICS, 1989, 139 (01) :221-228
[8]   CONTROL OF UNIMOLECULAR REACTIONS USING COHERENT-LIGHT [J].
BRUMER, P ;
SHAPIRO, M .
CHEMICAL PHYSICS LETTERS, 1986, 126 (06) :541-546
[9]  
BRUMER P, 1986, FARADAY DISCUSS, V82, P177
[10]   CONTROL OF VIBRATIONAL-EXCITATION AND DISSOCIATION OF SMALL MOLECULES BY CHIRPED INTENSE INFRARED-LASER PULSES [J].
CHELKOWSKI, S ;
BANDRAUK, AD .
CHEMICAL PHYSICS LETTERS, 1991, 186 (2-3) :264-269