Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5404241 | Journal of Luminescence | 2007 | 7 Pages |
Abstract
Contrary to a standard definition of diabatic states (i.e., those without momentum-dependent coupling), based on the construction from adiabatic ones, we defined diabatic states as bright and dark states of a given experiment. Namely, they are defined as states providing maximum, respectively, zero value of electronic transition dipole moments projected to a given polarization vector. Second, the state from (or to) which the optical transition is performed is not from the space of investigated electronic excited state manifold, but it is chosen by the observer. It is shown, for this case, that the inter-state coupling is a general function of vibrational coordinates. The explicit dependence of the inter-state coupling on vibrational coordinates is particularly important for system with strong Stokes shift. The role of exact definitions of bright and dark states as well as the inter-state coupling is discussed with respect to the coherent structure of electronic population observed in optical spectroscopy.
Keywords
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Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Miroslav MenÅ¡Ãk, Stanislav NeÅ¡půrek,