Temperature dependence of vibrational relaxation in the HF, DF, HF–CO2, and DF–CO2 systems

Abstract

The laser excited fluorescence method has been employed to determine rate constants for V → V, R and V → R, T relaxation HF(ν = 1) and DF(ν = 1) by CO2 over the temperature range from 295 to 670°K. The self-deactivation rates for HF(ν = 1) and DF(ν = 1) by ground state molecules and the rate of V → V, R transfer from HF(ν = 1) and DF(ν = 1) to the CO2 (00°1) state exhibit a marked decrease with increasing temperature. The results provide additional evidence for the conversion of the large vibrational energy defects of the present systems into rotational motion of the hydrogen halide under the influence of a sizable attractive intermolecular potential well.