Abstract
Nonadiabatic effects in quantum dynamics are described using a mixed polar/coordinate space representation of the wave function. The polar part evolves on dynamically determined potential surfaces that have diabatic and adiabatic potentials as limiting cases of weak localized and strong extended diabatic couplings. The coordinate space part, generalized to a matrix form, describes transitions between the surfaces. Choice of the effective potentials for the polar part and partitioning of the wave function enables one to represent the total wave function in terms of smooth components that can be accurately propagated semiclassically using the approximate quantum potential and small basis sets. Examples are given for two-state one-dimensional problems that model chemical reactions that demonstrate the capabilities of the method for various regimes of nonadiabatic dynamics.
| Original language | English (US) |
|---|---|
| Article number | 174108 |
| Journal | Journal of Chemical Physics |
| Volume | 123 |
| Issue number | 17 |
| DOIs | |
| State | Published - Nov 1 2005 |
Funding
Acknowledgment is made to the Donors of the American Chemical Society Petroleum Research Fund and to the Chemistry Division of NSF for support of this research.
ASJC Scopus subject areas
- General Physics and Astronomy
- Physical and Theoretical Chemistry