Time-resolved photoelectron angular distributions in linear molecules were calculated using a nonperturbative theory. The approach was extended to study electronic and rotational symmetries for nonlinear systems. The formally exact expressions were reduced to cruder forms applicable to complex systems by using approximations.
|Original language||English (US)|
|Number of pages||3825378|
|Journal||Physical Review A. Atomic, Molecular, and Optical Physics|
|State||Published - Oct 2001|
ASJC Scopus subject areas
- Atomic and Molecular Physics, and Optics