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Theoretical study of dissociation dynamics of HD<sup>+</sup> and its quantum control with an intense laser field
Author(s) -
Hongbin Yao,
XinDong Jiang,
Chengang Cao,
Wenliang Li
Publication year - 2019
Publication title -
wuli xuebao
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.199
H-Index - 47
ISSN - 1000-3290
DOI - 10.7498/aps.68.20190400
Subject(s) - dissociation (chemistry) , atomic physics , physics , laser , absorption spectroscopy , chemistry , optics
The dissociation dynamics of HD + molecule in an intense field is investigated by using an accurate three-dimensional time-dependent wave packet approach. When the 790-nm laser pulse interacts with HD + molecule, the lowest electronic 1sσ and 2pσ states are coupled. Due to the existence of the permanent electric dipole moment, the transitions in HD + molecule involve the direct absorption of an odd and even number of photons, thereby opening different pathways for dissociation. The model of the photon-dressed states is presented to analyze the possible dissociation pathways of HD + molecule. The laser-induced dissociation of HD + molecule is mainly composed of the four pathways: the direct one-photon absorption, the net two-photon absorption, the direct two-photon absorption, and the direct two-photon absorption. To reveal the dissociation mechanism of HD + molecule, the kinetic energy resolved spectra are calculated at the given laser intensities. It is found that the dissociation pathways are strongly dependent on laser intensity, especially for the net one-photon absorption dissociation and direct two-photon absorption dissociation. With further research, the dissociation pathways of HD + are controlled by regulating the intensity of laser pulse. At a laser intensity of 4.0 × 10 13 W/cm 2 , the kinetic energy resolved spectrum for the vibrational state ν = 3 includes the contributions from the net two-photon absorption dissociation and the direct two-photon absorption dissociation. For the vibrational state ν = 6, HD + molecule is preferentially dissociated via the net one-photon absorption. However, the dissociation mechanism of HD + molecule at the vibrational states ν = 3 and ν = 6 have significant changes as the laser intensity increases to 2.0 × 10 14 W/cm 2 . For the vibrational state ν = 3, the branching ratio between the dissociation pathway of the net two-photon absorption and that of the direct two-photon absorption has a dramatic change with the increase of laser intensity. Compared with the kinetic energy resolved spectra at laser energy of 4.0 × 10 13 W/cm 2 , the height of the dissociation peak from the net two-photon absorption decreases, and that of the direct two-photon absorption increases at laser intensity of 2.0 × 10 14 W/cm 2 . For the vibrational state ν = 6, the dissociation process of the net one-photon absorption almost disappears at laser intensity of 2.0 × 10 14 W/cm 2 , and it is replaced by the dissociation pathway of the direct two-photon absorption.

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