Photoelectron angular distributions from autoionizing 4s14p 66p1 states in atomic krypton probed with femtosecond time resolution
Photoelectron angular distributions (PADs) are obtained for a pair of 4s14p66p1 (a singlet and a triplet) autoionizing states in atomic krypton. A high-order harmonic pulse is used to excite the pair of states and a time-delayed 801 nm ionization pulse probes the PADs to the final 4s14p6 continuum with femtosecond time resolution. The ejected electrons are detected with velocity map imaging to retrieve the time-resolved photoelectron spectrum and PADs. The PAD for the triplet state is inherently separable by virtue of its longer autoionization lifetime. Measuring the total signal over time allows for the PADs to be extracted for both the singlet state and the triplet state. Anisotropy parameters for the triplet state are measured to be β2 = 0.55 ± 0.17 and β4 = -0.01 ± 0.10, while the singlet state yields β2 = 2.19 ± 0.18 and β4 = 1.84 ± 0.14. For the singlet state, the ratio of radial transition dipole matrix elements, X, of outgoing S to D partial waves and total phase shift difference between these waves, Δ , are determined to be X = 0.56± 0.08 andΔ = 2.19 ± 0.11 rad. The continuum quantum defect difference between the S and D electron partial waves is determined to be -0.15± 0.03 for the singlet state. Based on previous analyses, the triplet state is expected to have anisotropy parameters independent of electron kinetic energy and equal to β2 5/7 and β4 -12/7. Deviations from the predicted values are thought to be a result of state mixing by spin-orbit and configuration interactions in the intermediate and final states; theoretical calculations are required to quantify these effects. © 2011 American Institute of Physics.
Publication Source (Journal or Book title)
Journal of Chemical Physics
Doughty, B., Haber, L., Hackett, C., & Leone, S. (2011). Photoelectron angular distributions from autoionizing 4s14p 66p1 states in atomic krypton probed with femtosecond time resolution. Journal of Chemical Physics, 134 (9) https://doi.org/10.1063/1.3547459