Abstract

O 2( 1Δ g) was generated in the gas phase at atmospheric pressure by direct laser excitation. A Holobeam model 255 Nd—YAG laser with an output at 1065 nm was used to achieve the transition O 2( 3Σ g −, v = 0) → O 2( 1Δ g, v = 1) The mean lifetime τ of the resulting excited oxygen species in the gas phase at atmospheric pressure was measured to be 0.124 ± 0.012 s. This corresponds to a bimolecular rate constant k 2 for the overall reaction O 2( 1Δ g, v = 1) + O 2( 3Σ g −) → 2O 2( 3Σ g −) of (3.3 ± 0.4) × 10 −19 molecule −1 cm 3 s −1, a factor of 10 below the currently accepted value for ground state oxygen deactivation of singlet oxygen. Possible reasons for this difference are discussed.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.