Quantum yields for product formation in the 120-133 nm photodissociation of O2
- 1. Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853-1301 (United States)
Description
The photodissociation of O2 in the region from 120-133 nm has been investigated using product imaging. The spectrum in this region is dominated by transitions from the ground state to the first three vibrational levels of the E 3Σu- state. The O(1D)+O(3P) channel is the only product channel observed by product imaging for dissociation at either 124.4 nm or 120.4 nm. The O(1D2) product is aligned in the molecular frame in such a way that its J vector is perpendicular to the relative velocity vector between the O(1D) and the O(3P). The variation in the anisotropy of dissociation is approximately predicted by considering transitions on individual lines and then taking into account the coherent excitation of overlapping resonances. At 132.7 nm, both the O(1D)+O(3P) and the O(3P)+O(3P) channels are observed with branching ratios of 0.40±0.08 and 0.60±0.09, respectively. At 130.2 nm, the quantum yield for production of O(1D) is 0.76±0.28
Additional details
Identifiers
- DOI
- 10.1063/1.1809114;
Publishing Information
- Journal Title
- Journal of Chemical Physics
- Journal Volume
- 121
- Journal Issue
- 21
- Journal Page Range
- p. 10437-10446
- ISSN
- 0021-9606
- CODEN
- JCPSA6
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 36096842
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S74: ATOMIC AND MOLECULAR PHYSICS;
- Descriptors DEI
- ANISOTROPY; BRANCHING RATIO; BY-PRODUCTS; DISSOCIATION; EXCITATION; GROUND STATES; OXYGEN; PHOTOCHEMISTRY; RESONANCE; ULTRAVIOLET SPECTRA; VIBRATIONAL STATES
- Descriptors DEC
- CHEMISTRY; ELEMENTS; ENERGY LEVELS; ENERGY-LEVEL TRANSITIONS; EXCITED STATES; NONMETALS; SPECTRA
Optional Information
- Notes
- (c) 2004 American Institute of Physics.