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Argon, krypton, and xenon excimer luminescence: From the dilute gas to the condensed phase
85
Citations
59
References
1989
Year
Localized Excited StateEngineeringLow Density LimitAbsorption SpectroscopyChemistryElectronic Excited StateLuminescence PropertySpectroscopic PropertyPhotophysical PropertyPhotoluminescencePhysicsDilute GasAtomic PhysicsPhysical ChemistryQuantum ChemistrySynchrotron RadiationExcited State PropertyCondensed PhaseNatural SciencesSpectroscopyApplied PhysicsCondensed Matter PhysicsNumber DensityExciton Appearance
For the first time, the evolution of luminescence from rare gases was studied as a function of number density. Synchrotron radiation served as a light source for selective and pulsed excitation of the samples. The excitation spectra confirm previous results on perturbed Rydberg states and exciton appearance in dense media. In time-resolved emission spectra the peak energies and widths of the luminescence bands were followed. The energy separation between the fast and slow components is found to be density independent. A model proposed by Cheshnovsky et al. [Chem. Phys. Lett. 15, 475 (1972)] accounts for the change in peak width with temperature. Both lifetimes decrease with increasing density. The data extrapolate to 3.3±0.1 ns (Ar); 3.4±0.1 ns, 270±5 ns (Kr); 4.5±0.1 ns, 100±5 ns (Xe) for the low density limit. For the solid at the triple point, we obtain 1.3±0.1 ns, 82±5 ns (Kr) and 1.1±0.1 ns, 18.5±0.5 ns (Xe). Theories on density dependence of lifetimes give only a qualitative description of the experimental results.
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