“…A set of experimental data for the mixtures He-Ar = 50:1, 75:1, 100:1 and 200:1 at gas pressures from p = 1.75 to 4.0 atm was numerically calculated with a step of 0.25 atm. In the coordinates of figure 5a the function (12) corresponds to the function ln(1/T) = p ex exp(-k ex (t-t 0 )) + p d exp(-(γg (t-t 0 )) 2 ) exp(-γk d (t-t 0 )), (13) where the first, slowly-decaying term of the right-hand side of (13) p ex exp(-k ex (t-t 0 )) (14) describes a broadband absorption (γ = 1) of the probe pulse by the excimer molecules, whereas the second term p d exp(-(γg (t-t 0 )) 2 ) exp(-γk d (t-t 0 )) (15) describes the studied exponential process of collisional quenching of o 2 4s[3/2] metastable state exp(-γk d (t-t 0 )) (16) with "Gaussian pre-exponent" exp(-(γg (t-t 0 )) 2 ), (17) which provides a correction for the recombination and relaxation processes of populating this state [11,12]. Obtaining a true form of the Gaussian pre-exponent in analytical form is hardly possible because of the variety and complexity of the relevant reactions depending, in particular, on the time-varying temperature and density of the secondary electrons.…”