Time evolution and anti-bunching effect of diatomic molecules coherent states
The vibrations inside diatomic molecules are well modeled by the Morse potential and, therefore, the Morse nonlinear coherent states can be considered as approximations of diatomic molecules coherent states. Currently, the experimental realization of nonlinear coherent states for molecular systems i...
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Published in | Annals of physics Vol. 423; p. 168331 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
01.12.2020
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Subjects | |
Online Access | Get full text |
ISSN | 0003-4916 1096-035X |
DOI | 10.1016/j.aop.2020.168331 |
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Summary: | The vibrations inside diatomic molecules are well modeled by the Morse potential and, therefore, the Morse nonlinear coherent states can be considered as approximations of diatomic molecules coherent states. Currently, the experimental realization of nonlinear coherent states for molecular systems is an interesting subject of investigation. In this paper, we analyze the nonclassical properties of different coherent states for a particle in the Morse potential. We find that the su(2) algebra can be generalized by using an appropriate monotonically increasing function and that the bound states of particular diatomic molecules can be well described by the introduced algebra. We construct two types of generalized su(2) coherent states satisfying all necessary requirements, mainly the resolution of identity, for the molecule 27Al1H. We notice an anti-bunching effect for both types of coherent states by analyzing the second order correlation function.
•We introduce a new generalized su(2) algebra.•The algebra can be applied to particular Morse oscillators.•We apply the approach to the molecule 27Al1H.•We construct the associated Klauder’s coherent states.•We analyze the physical properties of the coherent states for 27Al1H. |
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ISSN: | 0003-4916 1096-035X |
DOI: | 10.1016/j.aop.2020.168331 |