Long range forces between polar alkali diatoms aligned by external electric fields
arXiv:1207.3546 · doi:10.1103/PhysRevA.86.032711
Abstract
Long range electrostatic, induction and dispersion coefficients including terms of order have been calculated by the sum over states method using time dependent density functional theory. We also computed electrostatic moments and static polarizabilities of the individual diatoms up to the octopole order using coupled cluster and density functional theory. The laboratory-frame transformed electrostatic moments and van der Waals coefficients corresponding to the alignment of the diatomic molecules were found. We use this transformation to obtain the coupling induced by an external DC electric field, and present values for all XY combinations of like polar alkali diatomic molecules with atoms from Li to Cs. Analytic solutions to the dressed-state laboratory-frame electrostatic moments and long range intermolecular potentials are also given for the DC low-field limit.
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- Optical trapping of ultracold dysprosium atoms: transition probabilities, dynamic dipole polarizabilities and van der Waals coefficients
- Diatomic molecules of alkali-metal and alkaline-earth-metal atoms: interaction potentials, dipole moments, and polarizabilities
- Photoassociation of ultracold long-range polyatomic molecules
- On cold gases with anisotropic interactions