Do semiclassical trajectory theories provide an accurate picture of radiationless decay for systems with accessible surface crossings?

被引:55
作者
Hack, MD
Jasper, AW
Volobuev, YL
Schwenke, DW
Truhlar, DG [1 ]
机构
[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Inst Supercomp, Minneapolis, MN 55455 USA
[3] NASA, Ames Res Ctr, Moffett Field, CA 94035 USA
关键词
D O I
10.1021/jp993353x
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 quantum mechanical and semiclassical calculations of Feshbach funnel resonances that correspond to long-lived exciplexes in the (A) over tilde B-2(2) State of NaH2. These exciplexes decay to the ground state, (X) over tilde (2)A(1), by a surface crossing in C-2v geometry. The quantum mechanical lifetimes and the branching probabilities for competing decay mechanisms are computed for two different NaH2 potential energy matrices, and we explain the results in terms of features of the potential energy matrices. We compare the quantum mechanical calculations of the lifetimes and the average vibrational and rotational quantum numbers of the decay product, H-2, to two kinds of semiclassical trajectory calculations: the trajectory surface hopping method and the Ehrenfest self-consistent potential method (also called the time-dependent self-consistent field method). The trajectory surface hopping calculations use Tully's fewest switches algorithm and two different prescriptions for adjusting the momentum during a hop. Both the adiabatic and the diabatic representations are used for the trajectory surface hopping calculations. We show that the diabatic surface hopping calculations agree better with the quantum mechanical calculations than the adiabatic surface hopping calculations or the Ehrenfest calculations do for one potential energy matrix, and the adiabatic surface hopping calculations agree best with the quantum mechanical calculations for the other potential energy matrix. We test three criteria for predicting which representation is most accurate for surface hopping calculations. We compare the ability of the semiclassical methods to accurately reproduce the quantum mechanical trends between the two potential matrices, and we review other recent comparisons of semiclassical and quantum mechanical calculations for a variety of potential matrices. On the basis of the evidence so far accumulated, we conclude that for general three-dimensional two-state systems, Tully's fewest switches method is the most accurate semiclassical method currently available if (i) one uses the nonadiabatic coupling vector as the hopping vector and (ii) one propagates the trajectories in the representation that minimizes the number of surface hops.
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页码:217 / 232
页数:16
相关论文
共 42 条
[1]  
BISCHOF C, 1998, ADIFOR VERSION 2 0
[2]   THE EFFECT OF A CONICAL INTERSECTION ON CROSS-SECTIONS FOR COLLISION-INDUCED DISSOCIATION [J].
BLAIS, NC ;
TRUHLAR, DG ;
MEAD, CA .
JOURNAL OF CHEMICAL PHYSICS, 1988, 89 (10) :6204-6208
[3]   MONTE-CARLO TRAJECTORY STUDY OF AR+H2 COLLISIONS .1. POTENTIAL-ENERGY SURFACE AND CROSS-SECTIONS FOR DISSOCIATION, RECOMBINATION, AND INELASTIC-SCATTERING [J].
BLAIS, NC ;
TRUHLAR, DG .
JOURNAL OF CHEMICAL PHYSICS, 1976, 65 (12) :5335-5356
[4]   TRAJECTORY-SURFACE-HOPPING STUDY OF NA(3P2P) +H2-]NA(3S2S)+H2(V',J',THETA) [J].
BLAIS, NC ;
TRUHLAR, DG .
JOURNAL OF CHEMICAL PHYSICS, 1983, 79 (03) :1334-1342
[5]  
COHENTANNOUDJI C, 1977, QUANTUM MECH, V2, pCHR13
[6]   THEORY OF WIDTH AND SHIFT OF MOLECULAR SPECTRAL LINES IN GASES [J].
GORDON, RG .
JOURNAL OF CHEMICAL PHYSICS, 1966, 44 (08) :3083-+
[7]   Quantum mechanical and quasiclassical trajectory surface hopping studies of the electronically nonadiabatic predissociation of the (A)over-tilde state of NaH2 [J].
Hack, MD ;
Jasper, AW ;
Volobuev, YL ;
Schwenke, DW ;
Truhlar, DG .
JOURNAL OF PHYSICAL CHEMISTRY A, 1999, 103 (32) :6309-6326
[8]   Analytic potential energy surfaces and their couplings for the electronically nonadiabatic chemical processes Na(3p)+H2→Na(3s)+H2 and Na(3p)+H2→NaH+H [J].
Hack, MD ;
Truhlar, DG .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (09) :4315-4337
[9]   A NEW DIABATIC REPRESENTATION OF THE COUPLED POTENTIAL-ENERGY SURFACES FOR NA(3P P-2)+H2-]NA(3S S-2)+H2 OR NAH+H [J].
HALVICK, P ;
TRUHLAR, DG .
JOURNAL OF CHEMICAL PHYSICS, 1992, 96 (04) :2895-2909
[10]  
HERZBERG G, 1966, MOLECULAR SPECTRA MO, V3, pCH4