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A flasch photolysis–resonance fluorescence study of the formation of O(1<i>D</i>) in the photolysis of water and the reaction of O(1<i>D</i>) with H2, Ar, and He −
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1975
Year
Excited State PropertyChemical EngineeringPhosphorescence ImagingResonance FluorescenceEngineeringPhotochemistryNatural SciencesSpectroscopyRelative ImportanceMechanistic PhotochemistryPhotocatalysisPhysical ChemistryPhotophysical PropertyChemistryQuantum ChemistryElectronic Excited StateChemical KineticsRate Constants
The relative importance of two primary processes in the photolysis of water, H2O+hν → H+OH d in Processes I and II, respectively. The initially formed O(1D) was deactivated to ground state O(3P) prior to detection via resonance fluorescence. The relative quantum yields for Porcesses I and II are 0.89 and 0.11 for the wavelength interval 105–145 nm and ?0.99 and ?0.01 for the wavelength interval 145–185 nm. Rate constants at 300 °K have been determined relative to that for Reaction (1), O(1D)+O2 → O(3P)+O2 decrease in O signal as a function of H2, Ar, or He pressure for the following reactions: O(1D)+H2 → H+OH % (2), O(1D)+Ar → O(3P)+Ar e−1⋅s−1, we obtain the following results: %k2 = (2.5±1.5) ×10−10, k3 = (8±4) ×10−13, and k4 &lt; 5×10−14 cm3 molecule−1⋅s−1.
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