Accurate Time-dependent Wave Packet Study of the H++LiH Reaction at Early Universe Conditions

The dynamics and kinetics of the H+ + LiH reaction have been studied using a quantum reactive time-dependent wave packet (TDWP) coupled-channel quantum mechanical method on an ab initio potential energy surface at conditions of the early universe. The total reaction probabilities for the H+ + LiH(nu = 0, j = 0) -> H-2(+) + Li process have been calculated from 5 x 10(-3) eV up to 1 eV for total angular momenta J from 0 to 110. Using a Langevin model, integral cross sections have been calculated in that range of collision energies and extrapolated for energies below 5 x 10(-3) eV. The calculated rate constants are found to be nearly independent of temperature in the 10-1000 K interval with a value of approximate to 10(-9) cm(3) s(-1), which is in good agreement with estimates used in evolutionary models of the early universe lithium chemistry.