VACUUM ULTRAVIOLET SPECTROSCOPY AND CHEMISTRY BY PHOTOIONIZATION AND PHOTOELECTRON METHODS
- 1 October 2002
- journal article
- Published by Annual Reviews in Annual Review of Physical Chemistry
- Vol. 53 (1) , 101-140
- https://doi.org/10.1146/annurev.physchem.53.082001.144416
Abstract
The recent developments of vacuum ultraviolet (VUV) laser and third generation synchrotron radiation sources, together with the introduction of pulsed field ionization (PFI) schemes for photoion-photoelectron detection, have had a profound impact on the field of VUV spectroscopy and chemistry. Owing to the mediation of near-resonant autoionizing states, rovibronic states of ions with negligible Franck-Condon factors for direct photoionization can be examined by VUV-PFI measurements with rotational resolutions. The VUV-PFI spectra thus obtained have provided definitive ionization energies (IEs) for many small molecules. The recent synchrotron-based PFI-photoelectron-photoion coincidence experiments have demonstrated that dissociative photoionization thresholds for a range of molecules can be determined to the same precision as in PFI-photoelectron measurements. Combining appropriate dissociation thresholds and IEs measured in PFI studies, thermochemical data for many neutrals and cations can be determined with unprecedented precision. The further development of two-color excitation-ionization schemes promises to expand the scope of spectroscopic and chemical applications using the photoionization-photoelectron method.Keywords
This publication has 129 references indexed in Scilit:
- Ab initio MO study of the A, D and third 2Π states of CO+Journal of Electron Spectroscopy and Related Phenomena, 2000
- Time- and frequency-resolved photoionisation of the allyl radicalFaraday Discussions, 2000
- Rotationally resolved pulsed field ionization photoelectron bands of O2+(X 2Π1/2,3/2g, v+=0–38) in the energy range of 12.05–18.15 eVThe Journal of Chemical Physics, 1999
- Rotational-resolved pulsed field ionization photoelectron study of NO+(a 3Σ+,v+=0–16) in the energy range of 15.6–18.2 eVThe Journal of Chemical Physics, 1999
- High-resolution pulsed field ionization photoelectron study of O2: Predissociation lifetimes and high-n Rydberg lifetimes converging to O2+(c 4Σu−, v+=0,1)The Journal of Chemical Physics, 1998
- Autoionizing Rydberg and zero electron kinetic energy states in ArThe Journal of Chemical Physics, 1995
- Collisional and electric field effects in the delayed pulsed field ionization zero-kinetic-energy photoelectron spectrum of argonThe Journal of Chemical Physics, 1994
- Dissociation energy of neutral and ionic benzene-noble gas dimers by pulsed field threshold ionization spectroscopyThe Journal of Chemical Physics, 1993
- Electric field effects in the near-threshold photoionization spectrum of nitric oxideThe Journal of Chemical Physics, 1993
- Mass analyzed threshold ionization spectroscopyThe Journal of Chemical Physics, 1991