z-logo
open-access-imgOpen Access
Two-photon dissociation of vibrationally excited HD+: The inhomogeneous differential equation approach
Author(s) -
C. Laughlin,
K K Datta,
ShihI Chu
Publication year - 1986
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.451229
Subject(s) - diatomic molecule , dissociation (chemistry) , excited state , photon , atomic physics , photon energy , spectroscopy , molecule , physics , chemistry , optics , quantum mechanics
We extend the inhomogenous‐differential‐equation (IDE) approach of Dalgarno and Lewis for a detailed study of two‐photon dissociation (TPD) of HD+ from high vibrational levels of the 1sσg electronic state. Contrary to the H+2 case, where the TPD cross sections σ(2)L are largest near TPD thresholds and decrease monotonically with increasing photon energy, the HD+ cross sections are characterized by rich resonant and interference structures. We present σ(2)L results for TPD from the initial vi =6, 8, 10, 12, 14, 16, and ji=0 levels as well as from vi=14, ji=0, 2, 4 levels for a wide range of wavelengths of linearly polarized radiation accessible by CO2 and CO lasers. It is found that while there are four TPD pathways, the channel 1sσg(vi ji)→ω 1sσg(v, j=ji±1) →ω2pσu(k, j f=j±1) dominates the two‐photon process in most of the cases we have studied. Further, the results show that σ(2)L increases rather rapidly as the initial vibrational quantum number vi increases, indicating that the hereronuclear diatomic m...

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom