Product State-Resolved Reactive Scattering Studies of the H + Cl2 (v0 = 1-3, j0 = 0) → HCl + Cl Reaction by the Time-Dependent Wave Packet Method.

The typical hydrogen atom plus halogen molecule reaction H + Cl2 → HCl + Cl has implications across many fields. In this paper, product state-resolved quantum dynamics calculations for the vibrationally excited reaction H + Cl2 (v0 = 1-3, j0 = 0) → HCl + Cl were conducted using the time-dependent wave packet method on a newly developed accurate potential energy surface. Numerical results indicate that the initial vibrational excitation of Cl2 does enhance the reactivity for this early barrier reaction, although less than the enhancement of the translational energy. The calculated product vibrational state-resolved integral cross sections and rate constants reveal that the product vibrational state distribution and the initial vibrational state of Cl2 are highly correlated. The thermal rate constant in the temperature range from 100 to 1000 K was given and is found to be in reasonable agreement with the experimental measurements.