Quantum and Classical Fall of a Charged Particle onto a Stationary Dipolar Target

被引:8
作者
Dashevskaya, E. I. [1 ,2 ]
Litvin, I. [1 ,2 ]
Nikitin, E. E. [1 ,2 ]
Troe, J. [1 ,3 ]
机构
[1] Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
[2] Technion Israel Inst Technol, Schulich Fac Chem, IL-32000 Haifa, Israel
[3] Univ Gottingen, Inst Phys Chem, D-37077 Gottingen, Germany
关键词
MOLECULE CAPTURE PROCESSES; ADIABATIC CHANNEL MODEL; STARK ENERGY-LEVELS; SYMMETRICAL-TOP; INSERTION REACTIONS; RIGIDITY FACTORS; RATE-CONSTANT; TRANSITION; COLLISION; FIELD;
D O I
10.1021/jp901515e
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
The quantum dynamics of the fall of a charged particle (i.e., the capture of a charged particle) onto a stationary dipolar target is considered. Extending previous approaches for the calculation of rate coefficients in the lowest channels, we now determine rate coefficients for all channels until the quantum rate coefficients converge to their classical counterpart. The results bridge the gap between the capture of light particles (electrons) and heavy particles (ions) in the limit of sudden dynamics, when the collision time is short in comparison to the rotational period of the molecular target. The quantum-classical correspondence is discussed in terms of semiclassical numbers or channels which are open for capture in effective potentials formed by charge-dipole attraction and centrifugal repulsion. The quantum capture rate coefficients are presented through classical rate coefficients and correction factors that converge to unity for high temperatures and whose behavior at ultralow temperatures, for not too small values of the dipole moment, is determined by semiclassical numbers of capture channels.
引用
收藏
页码:14212 / 14219
页数:8
相关论文
共 25 条
[1]   Product multiplet branching in the O(1D)+H2→OH(2Π)+H reaction [J].
Alexander, MH ;
Rackham, EJ ;
Manolopoulos, DE .
JOURNAL OF CHEMICAL PHYSICS, 2004, 121 (11) :5221-5235
[2]   Cross sections and thermal rate constants for the isotope exchange reaction:: D(2S)+OH(2Π)→OD(2Π)+H(2S) -: art. no. 204306 [J].
Atahan, S ;
Alexander, MH ;
Rackham, EJ .
JOURNAL OF CHEMICAL PHYSICS, 2005, 123 (20)
[3]   Nuclear physics B. Nuclear dynamics, theoretical [J].
Bethet, HA .
REVIEWS OF MODERN PHYSICS, 1937, 9 (02) :0069-0244
[4]   Modelling low-energy electron-molecule capture processes [J].
Dashevskaya, E. I. ;
Litvin, I. ;
Nikitin, E. E. ;
Troe, J. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2008, 10 (09) :1270-1276
[5]   Low-temperature behavior of capture rate constants for inverse power potentials [J].
Dashevskaya, EI ;
Maergoiz, AI ;
Troe, J ;
Litvin, I ;
Nikitin, EE .
JOURNAL OF CHEMICAL PHYSICS, 2003, 118 (16) :7313-7320
[6]   On the sudden limit in the capture of particles for long-range anisotropic interactions [J].
Dashevskaya, EI ;
Maergoiz, AI ;
Ushakov, VG .
ZEITSCHRIFT FUR PHYSIKALISCHE CHEMIE-INTERNATIONAL JOURNAL OF RESEARCH IN PHYSICAL CHEMISTRY & CHEMICAL PHYSICS, 2002, 216 :605-613
[7]  
Fabrikant II, 2001, PHYS REV A, V63, DOI 10.1103/PhysRevA.63.022706
[8]   Dissociative electron attachment to dipolar molecules at low energies with meV resolution:: CFCl3, 1,1,1-C2Cl3F3, and HI [J].
Klar, D ;
Ruf, MW ;
Fabrikant, II ;
Hotop, H .
JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS, 2001, 34 (19) :3855-3878
[9]  
Landau L. D., 1965, COURSE THEORETICAL P, V3
[10]  
Landau L. D., 1976, CLASSICAL MECH