Abstract
The results of combined experimental and theoretical studies of the rotationally resolved photoelectron spectra of OH and OD following single-photon ionization are presented. The measured zero-kinetic-energy (ZEKE) spectra were obtained using pulsed field ionization in conjunction with a vacuum ultraviolet laser source. The OH+ and OD+ (X3Σ-, v+ = 0) rotational distributions were studied over the range 95.0-95.4 nm. Agreement between the observed and calculated spectra is very encouraging. Improved values for the ionization potentials of OH and OD (104 989 and 105 085 ± 2 cm-1, respectively) are reported and the unusual dynamics favoring ΔN < 0 transitions are discussed.
| Original language | English |
|---|---|
| Pages (from-to) | 768-772 |
| Number of pages | 5 |
| Journal | Journal of Chemical Physics |
| Volume | 97 |
| Issue number | 2 |
| DOIs | |
| State | Published - 1992 |
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