FINITE-RANGE SCATTERING WAVE-FUNCTION METHOD FOR SCATTERING AND RESONANCE LIFETIMES

被引:29
作者
JANG, HW [1 ]
LIGHT, JC [1 ]
机构
[1] UNIV CHICAGO,JAMES FRANCK INST,CHICAGO,IL 60637
关键词
D O I
10.1063/1.465405
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
A generic expression for the scattering wave function in terms of the full discrete spectral Green's function on a finite range is used to obtain the ''finite range scattering wave function (FRSW)'' which is accurate over a finite range of the scattering coordinate. We show that the representation of the FRSW in a finite basis set can be used to compute the scattering matrix and related quantities when the interaction potential is also restricted to this range. Comparisons of numerical results for several model problems with those of other methods and with analytical results indicate that the FRSW method is very accurate when converged and requires comparable or less computation than other methods. The main difference between the present method and other variational scattering methods is that the real Green's function is used and that the scattering wave function itself is calculated nonvariationally. Thus the FRSW can be used to solve quantum mechanical problems involving scattering wave functions over a finite range such as scattering theory, resonance studies, and photodissociation. Results of two implementations are presented. Both require only one representation of the real Green's function in a finite basis. One requires energy dependent matrix elements, while the other does not.
引用
收藏
页码:1057 / 1069
页数:13
相关论文
共 39 条
[1]  
Abramowitz M.., 1972, HDB MATH FUNCTIONS
[2]  
Calogero F., 1967, VARIABLE PHASE APPRO
[3]   DETERMINATION OF THE BOUND AND QUASI-BOUND STATES OF AR-HCL VANDERWAALS COMPLEX - DISCRETE VARIABLE REPRESENTATION METHOD [J].
CHOI, SE ;
LIGHT, JC .
JOURNAL OF CHEMICAL PHYSICS, 1990, 92 (04) :2129-2145
[4]   COMPLEX COORDINATE CALCULATIONS OF FESHBACH RESONANCE ENERGIES AND WIDTHS FOR A COLLINEAR TRIATOMIC SYSTEM [J].
CHRISTOFFEL, KM ;
BOWMAN, JM .
JOURNAL OF CHEMICAL PHYSICS, 1983, 78 (06) :3952-3958
[5]   DIRECT CALCULATION OF COLLISIONAL PROPERTIES THAT REQUIRE ENERGY DERIVATIVES OF THE S-MATRIX - RESULTS FOR THE REACTION HE+H2+-REVERSIBLEHEH++H [J].
DARAKJIAN, Z ;
HAYES, EF ;
PARKER, GA ;
BUTCHER, EA ;
KRESS, JD .
JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (04) :2516-2522
[6]   CONVERGED VARIATIONAL QUANTUM SCATTERING RESULTS FOR THE 3-DIMENSIONAL F+D2 REACTION [J].
DMELLO, M ;
MANOLOPOULOS, DE ;
WYATT, RE .
CHEMICAL PHYSICS LETTERS, 1990, 168 (02) :113-118
[7]   ACCURATE QUANTUM-MECHANICAL REACTION PROBABILITIES FOR THE REACTION O+H2-]OH+H [J].
HAUG, K ;
SCHWENKE, DW ;
TRUHLAR, DG ;
ZHANG, YC ;
ZHANG, JZH ;
KOURI, DJ .
JOURNAL OF CHEMICAL PHYSICS, 1987, 87 (03) :1892-1894
[8]   OBSERVATION OF PADE SUMMABILITY IN DIVERGENT L2 COMPLEX COORDINATE CALCULATIONS OF TERT-MATRIX AMPLITUDES IN THE PRESENCE OF LONG-RANGE FORCES [J].
JOHNSON, BR ;
REINHARDT, WP .
PHYSICAL REVIEW A, 1984, 29 (05) :2933-2935
[9]   RESONANCE STATES USING THE OPTICAL-POTENTIAL MODEL - STUDY OF FESHBACH RESONANCES AND BROAD SHAPE RESONANCES [J].
JOLICARD, G ;
LEFORESTIER, C ;
AUSTIN, EJ .
JOURNAL OF CHEMICAL PHYSICS, 1988, 88 (02) :1026-1031
[10]   RECENT COMPUTATIONAL DEVELOPMENTS IN THE USE OF COMPLEX SCALING IN RESONANCE PHENOMENA [J].
JUNKER, BR .
ADVANCES IN ATOMIC AND MOLECULAR PHYSICS, 1982, 18 :207-263