Abstract

Absorbing UV radiation, ozone protects life on Earth and plays a fundamental role in Earth's temperature balance. The formation of ozone occurs through the ternary recombination reaction: O2_2+O+M →\rightarrow O3_3+M, where M can be N2_2, O2_2 or Ar. Here, we developed a theoretical approach capable of modeling the formation of ozone molecules in ternary collisions, and applied it to the reaction with M=Ar because of extensive experimental data available. The rate coefficients for the direct formation of O3_3 in ternary collisions O+O2_2+Ar were computed for the first time as a function of collision energy, and thermally-averaged coefficients were derived for temperatures 5-900~K leading to a good agreement with available experimental data for temperatures 100-900~K. The present study shows that the formation of ozone in ternary collisions O+O2_2+Ar at temperatures below 200~K proceeds through a formation of a temporary complex ArO2_2, while at temperatures above 1000~K, the reaction proceeds mainly through a formation of long-lived vibrational resonances of O3∗_3^*. At intermediate temperatures 200~K-1000~K, the process cannot be viewed as a two-step mechanism. In addition, it is found that the majority of O3_3 molecules formed initially are weakly bound.

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