The vibrational quenching of NO (u= I-11) by N20 in gas phase was studied by means of the time-resolved Fourier transform infrared emission spectroscopy. NO(v) was formed from the reaction of NsO and O( 'D) which was generated by laser photolysis of NsO at 193 nm. Twenty IR spectra of nx 30 ps delay
The vibrational quenching of O+2(v) by Kr as a function of relative kinetic energy
โ Scribed by M. Kriegl; R. Richter; P. Tosi; W. Federer; W. Lindinger; E.E. Ferguson
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 278 KB
- Volume
- 124
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
The collisional relaxation of vibrationally excited 02 ions by Kr has been measured from thermal energy to 2 eV relative center-of-mass kinetic energy. The rate constant decreases from 1.5 x lo-*' cm3 s-' at 300 K to a broad minimum of 9 X lo-l2 cm3 s-' between 0.1 and 0.3 eV and then increases to 6 X lo-" cm3 s-' at 2 eV. The quenching at low kinetic energies ( < 0.1 eV) is attributed to the long-range chemical attraction arising from the specific chemical bonding of 02 and Kr, while the quenching at higher kinetic energies ( > 0.3 ev) is presumably due to the short-range repulsive forces. This is the first observation of this transition for vibrational quenching of a molecular ion.
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