Journal
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 6, Issue 11, Pages 2140-2146Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.5b00929
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Funding
- National Science Foundation [CHE1212281, CHE1464450]
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1464450] Funding Source: National Science Foundation
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The angle-dependence of strong field ionization of O-2, N-2, CO2, and CH2O has been studied theoretically using a time-dependent configuration interaction approach with a complex absorbing potential (TDCIS-CAP). Calculation of the ionization yields as a function of the direction of polarization of the laser pulse produces three-dimensional surfaces of the angle-dependent ionization probability. These three-dimensional shapes and their variation with laser intensity can be interpreted in terms of ionization from the highest occupied molecular orbital (HOMO) and lower lying orbitals, and the Dyson orbitals for the ground and excited states of the cations.
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