The deactivation of PH2(A2A1;v’2=1,0) and PH2(X2B1;v”2=1) due to collisions with CO2, N2O, and SO2 have been measured. Comparison with data due to rare gas and diatomic quenchers have shown that the electronically excited PH2 species are probably quenched by multiple channel mechanisms of both physical and chemical nature for SO2 and of prevalently physical nature for CO2 and N2O. A V-V energy transfer is clearly responsible for the vibrational relaxation of PH2(X2B1;v”2=1) by these triatomic quenchers.

COLLISIONAL DEACTIVATION OF PH2(A2A1;v'2=1,0) AND PH2(X2B1;v"2=1) BY SOME TRIATOMIC MOLECULES

Nguyen Xuan C;
2002

Abstract

The deactivation of PH2(A2A1;v’2=1,0) and PH2(X2B1;v”2=1) due to collisions with CO2, N2O, and SO2 have been measured. Comparison with data due to rare gas and diatomic quenchers have shown that the electronically excited PH2 species are probably quenched by multiple channel mechanisms of both physical and chemical nature for SO2 and of prevalently physical nature for CO2 and N2O. A V-V energy transfer is clearly responsible for the vibrational relaxation of PH2(X2B1;v”2=1) by these triatomic quenchers.
2002
Istituto di Nanotecnologia - NANOTEC
Photochemistry
Chemical Kinetics
Molecular Dynamics
Energy Transfer
Laser photolysis-LIF
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/152326
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