Time-resolved optical emission spectroscopy of laser-produced air plasma

Time-resolved optical emission spectroscopy (OES) is used to analyze a mesh-initiated air breakdown plasma induced by a transverse excitation atmospheric CO 2 pulsed laser ( λ = 10.591   μ m , 64 ns (full width at half maximum), 70 - 160   J / cm 2 ). Emission from excited N, O, C, H, and Ar; ionic...

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Veröffentlicht in:Journal of applied physics 2010-04, Vol.107 (8), p.083306-083306-9
Hauptverfasser: Camacho, J. J., Díaz, L., Santos, M., Juan, L. J., Poyato, J. M. L.
Format: Artikel
Sprache:eng
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Zusammenfassung:Time-resolved optical emission spectroscopy (OES) is used to analyze a mesh-initiated air breakdown plasma induced by a transverse excitation atmospheric CO 2 pulsed laser ( λ = 10.591   μ m , 64 ns (full width at half maximum), 70 - 160   J / cm 2 ). Emission from excited N, O, C, H, and Ar; ionic fragment N + , O + , N 2 + , O 2 + , C + , and molecular band systems of N 2 + ( B Σ 2 u + − X Σ 2 g + ;   D Π 2 g − A Π 2 u ) , N 2 ( C Π 3 u − B Π 3 g ) , and OH ( A Σ 2 + − X Π 2 ) is observed. Plasma characteristics are examined in detail on the emission lines of N + , O + , and C by time-resolved OES technique. The results show a faster decay of continuum and ionic spectral species than of neutral atomic and molecular ones. The velocity and kinetic energy distributions for the different species were obtained from time-of-flight measurements. Excitation temperature and electron density in the laser-induced plasma were estimated from the analysis of spectral data at various times from the laser pulse incidence. Temporal evolution of electron density has been used for the estimation of the three-body recombination rate constant.
ISSN:0021-8979
1089-7550
DOI:10.1063/1.3382914