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International Journal of Quantum Chemistry

Comparative study of the photoassociation reaction of He + X+→ HeX+ (X = H, D): Including multiphoton transitions and dissociations

Su‐Hua Jing, Binbin Wang, Xiao‐Yun Zhou, Tixian Zeng

Published Feb 24, 2020• 1 citation
Publisher

Abstract

Abstract Using the time‐dependent quantum wave packet method, the photoassociation (PA) processes of He + H +→ HeH+ and He + D +→ HeD+, driven by the sin2‐shaped femtosecond laser pulse in the electronic ground state, including multiphoton transitions and dissociations, are investigated for a wide range of initial collision momenta spanning from 1 to 4 a.u. (or for the collision energy roughly in the ranges of 0.009∼0.148 eV and 0.006∼0.089 eV for HeH+ and HeD+ systems, respectively). It is found that, at some collision momenta, multiphoton transitions to deeply bound states are inevitable to occur and can greatly decrease the PA probability of the target state that selected is the vibrational state v = 6. For the dissociation process, the higher‐order (two‐ and three‐photon) dissociations, measured from the target state, tend to be significant at relative high collision energies, which implies that above‐threshold dissociations may also be an important loss mechanism in the PA process. In addition, it is also shown that the higher‐order dissociation is much stronger for HeH+ systems than that for HeD+ systems at a given collision momentum, and could be enhanced by the strong transitions among deeply bound states.

DOI
10.1002/qua.26196

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The laser-induced vibrational state-selectivity of product HF in photoassociation reaction H+F→HF is theoretically investigated by using the time-dependent quantum wave packet method. The population transfer process from the continuum state down to the bound vibrational states can be controlled by the driving laser. The effects of laser pulse parameters and the initial momentum of the two collision atoms on the vibrational population of the product HF are discussed in detail. Photodissociation accompanied with the photoassociation process is also described.
In this work, we simulate the laser‐induced photoassociation of the collision reaction O+H to generate the OH molecule. The photoassociation process involves the continuum‐discrete transition, and the initial wavepacket corresponding to the collision pair is generally given by a superposition of continuum state. By numerically solving the Schrödinger equation with split‐operator method, we can take into account implicitly but completely for the continuum state in the photoassociation process. In our simulation, we find interestingly the above threshold dissociation spectrum due to the continuum‐continuum transition as well as the target bound states by the photoassociation. In order to analyze the continuum state involved, we show the effective method by means of the quasicontinuum state on the Morse potential obtained by numerically diagonalizing the total system.
Photoassociation via reverse ladder transition controlled by two and four laser pulses is investigated using the time-dependent quantum wave packet method. The calculated results show that the amplitudes of the pulses have an enormous effect on the target population and total yield of association. For the target state with a high energy level, the population of background states can reduce the state-selectivity. Although, the total yield of association is decreased, the four pulses can induce the population transferring to low vibrational levels, and the state-selectivity of the target state is high.