Resonance fluorescence as a probe to elucidate mechanisms of intramolecular relaxation processes
Density matrix formalism is used to study resonance fluorescence processes of isolated gaseous molecules. The Wangsness--Bloch--Fano theory is applied to the irreversible intramolecular relaxation process. In the present treatment, it is assumed that the rotational angular momentum J is a constant of motion in the zeroth order approximation. Thus intramolecular interactions can be classified as tensor operators with respect to J. The fluorescence decay patterns depend on excitation bandwidths and monitoring conditions. Under narrow band excitation, the population (monopole), orientation (dipole), and alignment (quadrupole) of the excited state density matrix rho/sub e/ can be prepared. For a sharply prepared angular momentum state under pulsed excitation, the population does not undergo radiationless decay and the resonance fluorescence intensity is a sum of three exponentials in general. For cw experiments, where lifetime limited linewidth or polarized fluorescence intensities are measured, the population can decay via an intramolecular relaxation channel providing the orientation component is initially prepared. Explicit J dependences of lifetimes are given for pulsed experiments. Under broad band excitation, quantum beats due to the coherence of rho/sub e/ are derived from the Liouville equation. Most important of all, the population can decay under pulsed, broad-band excitation conditions. The scalar part of the nonadiabatic coupling becomes an additional contributor to the intramolecular relaxation process in this last case.
- Research Organization:
- Ames Laboratory, U.S. Department of Energy and Department of Chemistry, Iowa State University, Ames, Iowa 50011
- OSTI ID:
- 5865569
- Journal Information:
- J. Chem. Phys.; (United States), Vol. 71:12
- Country of Publication:
- United States
- Language:
- English
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