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Excitation of the <i>b</i> 1Σ+<i>g</i> state of O2 by low energy electrons
292
Citations
43
References
1978
Year
Charge ExcitationsEngineeringLocalized Excited StateAtomic Emission SpectroscopyLow Energy ElectronsExcitation Energy TransferChemistryElectronic Excited StateElectron SpectroscopyQuantum MaterialsO2 MoleculesIon EmissionO2 MoleculeQuantum SciencePhotoluminescencePhysicsAtomic PhysicsPhysical ChemistryQuantum ChemistryO2 DensitiesAb-initio MethodExcited State PropertyNatural SciencesSpectroscopyCondensed Matter PhysicsApplied PhysicsChemical Kinetics
Rate coefficients for excitation of the b 1Σ+g state of O2 by low energy electrons have been measured using a drift tube technique. The time dependence of the absolute intensity of the 762 nm band emission was measured for O2 densities between 1016 and 2×1018 molecules/cm3. When corrected for electron attachment, ionization, and metastable diffusion, the number of b 1Σ+g molecules produced per centimeter of electron drift and per O2 molecule calculated from the 762 nm emission varied from 1.3×10−18 cm2 at E/N=5×10−17V cm2 to 2.1×10−16 cm2 at E/N=2×10−15V cm2. These values of electric field to oxygen density ratio E/N correspond to mean electron energies of 0.75 and 6 eV, respectively. Measured decay constants for the 762 nm radiation yield a value for the product of the diffusion coefficient and the O2 density of (5.0±0.3) ×108 cm−1 sec−1 and a quenching coefficient for the b 1Σ+g state of (3.9±0.2) ×10−17 cm3 sec−1. Comparison of measured excitation coefficients with values calculated using a recommended set of electron collision cross sections for O2 show that the cross sections for direct excitation of the b 1Σ+g state are accurate near threshold and suggest that essentially all of the O2 molecules excited to levels at and above 1.63 eV result in the formation of molecules in the b 1Σ+g state.
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