Hydrogen atoms produced by photodissociation of H202 using 193 nm laser light have been observed for the first time. The H atoms are detected by VUV spectroscopy. The yield is 12 rt 1%. The H atoms are produced by a one-photon process.
Photofragmentation dynamics of H2O2 at 193 nm
β Scribed by Axel Ulrich Grunewald; Karl-Heinz Gericke; Franz Josef Comes
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 627 KB
- Volume
- 132
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The photofragmentation dynamics of Hz02 at 193 nm have been analyzed by probing the OH products by Doppler spectroscopy Using laser-induced fluorescence. The excess energy (Eav = 4 17 kJ/mol) appears mostly as translational motion of the fragments with ft = 0.84. No vibrational excitation was observed cfv < 0.003). The rotational state distribution is strongly inverted, peaking for N" = 12 which results in fr = 0.16. Our results indicate that previously published rotational state distributions are not nascent in character, but are perturbed by rotational relaxation. Individual fragment recoil velocities obtained from Doppler lineshapes are u = 4950 m s-l [OH(N" = 4)] and v = 4550 m s-l [OH(N" = lo)]. The effective anisotropy parameter Peff is slightly negative at high N" (Jeff = 0.35 at N" = 10).
π SIMILAR VOLUMES
Photodissociation of H$ has been studied at 193.3 nm using H atom photofragment-translational speclroscopy with massspectrometric detection. H t HS( v) product branching ratios are reported which are not in quantitative agreement with other recent experimental results. Secondary photodissociation of
A molecular beam of SO\* has been photodissociated at I93 nm to measure both the translational energy and angular distributions, from which it is concluded that the photodissociation is predissociative and that the vibrational population is peaked at un =2.
The 193 nm photodissociation of the isotopomers SOz, SO: and SOO' (with O\*= '\*O) was studied by high-resolution photofragment translational spectroscopy. The translational energy distributions P(&) of the fragment pairs SOtO, SO'tff, SOt(T and SO\*+0 were determined from systematic analysis of the