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Rotationally resolved photoionization with coherent VUV radiation

Conference ·
OSTI ID:10172085
Pulsed field ionization (PFI) has been used in conjunction with coherent VUV radiation to investigate the rotational state distributions of molecular cations following single photon ionization. The rotational state distributions for several linear cations (O{sub 2}, NO, OH(OD), HCl and N{sub 2}0) can be interpreted predominately on the basis of the near-threshold, one-electron photoionization dynamics; however, field-induced autoionization is often the dominate ionization pathway for rotational branches involving negative changes in core angular momentum. For photoionization of the H{sub 2}X (X = 0, S) non-linear triatomic molecules, transitions between asymmetric top levels involving the rotational angular momentum projections, K{sub a} and K{sub c} permit resolution of the photoelectron continua according to symmetry. The observed spectra clearly demonstrate the importance of the non-spherical nature of the molecular ion potential which leads to photoelectron final states which are unexpected from atomic-like analogies.
Research Organization:
Brookhaven National Lab., Upton, NY (United States)
Sponsoring Organization:
USDOE, Washington, DC (United States)
DOE Contract Number:
AC02-76CH00016
OSTI ID:
10172085
Report Number(s):
BNL--47814; CONF-920735--3; ON: DE92019257
Country of Publication:
United States
Language:
English