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Photoionization dynamics of excited molecular states. Photoelectron angular distributions and rotational and vibrational branching ratios for H2 C ¹Πu, v=0–4

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.450959· OSTI ID:5086257
Photoelectron angular distributions following three photonresonant, four photon (3+1) ionization of H2 via the C ¹Πu, v'=0-4←X ¹Σg⁺, v''= 0 Q(1) transitions are reported. The observed angular distributions are generally more isotropic for v⁺≠v' than for v⁺=v'. Photoelectron spectra obtained along the polarization axis of the laser following (3+1)= ionization via the C ¹Πu, v'= 4←X ¹Σg⁺, v"= 0 R(0) and R(1) transitions are also reported. These spectra are rotationally resolved and exhibit strongly v⁺-dependent rotational branching ratios. The comparison of the angular distribution data with available theoretical calculations indicates good agreement for some transitions and poor agreement for others, suggesting the need for substantial progress in understanding the photoionizationdynamics of even the simplest excited molecular states.
Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE; Office of Health and Environmental Research (OHER); Office of Naval Research (ONR)
DOE Contract Number:
W-31109-ENG-38
OSTI ID:
5086257
Journal Information:
Journal of Chemical Physics, Journal Name: Journal of Chemical Physics Journal Issue: 6 Vol. 85; ISSN JCPSA6; ISSN 0021-9606
Publisher:
American Institute of Physics (AIP)
Country of Publication:
United States
Language:
English