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(2+1 prime ) rotationally resolved resonance enhanced multiphoton ionization via the E sup 2. Sigma. sup + (4 s ,3 d ) and H sup 2. Sigma. sup + (3 d ,4 s ) Rydberg states of NO

Journal Article · · Journal of Chemical Physics; (USA)
DOI:https://doi.org/10.1063/1.459428· OSTI ID:6162539
;  [1]
  1. Arthur Amos Noyes Laboratory of Chemical Physics, California Institute of Technology, Pasadena, CA (USA)
The results of studies of ionic rotational branching ratios and photoelectron angular distributions resulting from (2+1{prime}) resonance enhanced multiphoton ionization of NO via various high {ital J} ({approx}21.5) rotational branches of the {ital E}{sup 2}{Sigma}{sup +}(4{ital s},3{ital d}) and {ital H}{sup 2}{Sigma}{sup +}(3{ital d},4{ital s}) Rydberg states are presented. The rotational branching ratios show the expected {Delta}N=even rotational propensity rule with very small {Delta}N=odd signals. The branching ratios for the {ital E}{sup 2}{Sigma}{sup +} state are seen to be independent of photoelectron energy with the {Delta}N=+2 signals strongest and no appreciable higher rotational transfer peaks ({vert bar}{Delta}N{vert bar}{ge}3). The higher rotational transfer signal for ionization of the {ital H}{sup 2}{Sigma}{sup +} state are also negligible but the rotational branching ratios are strongly energy dependent due to a Cooper minimum in the {ital l}=3 partial wave of the {ital k}{sigma}- and {ital k}{pi}-continua at a photoelectron kinetic energy of 2.6 eV and 2.9 eV, respectively. This leads to a strong rotational selectivity that can be exploited to produce ions in a specific rotational level. These consequences of Cooper minima close to threshold are quite general and their influence on rotational distributions should be readily observable in other molecular systems. The photoelectron angular distributions via both states show a strong energy dependence with a rapid change in the angular distributions around the Cooper minimum associated with the {ital H}{sup 2}{Sigma}{sup +} state.
DOE Contract Number:
FG03-87ER60513
OSTI ID:
6162539
Journal Information:
Journal of Chemical Physics; (USA), Journal Name: Journal of Chemical Physics; (USA) Vol. 93:10; ISSN JCPSA; ISSN 0021-9606
Country of Publication:
United States
Language:
English