Electronic structure of ultralong-range Rydberg pentaatomic molecules with two polar diatomic molecules
arXiv:1710.01393 · doi:10.1103/PhysRevA.96.052509
Abstract
We explore the electronic structure of ultralong-range pentaatomic Rydberg molecules from a merger of a Rydberg atom and two ground state heteronuclear diatomic molecules. Our focus is on the interaction of Rb() and Rb(, ) Rydberg states with ground and rotationally excited KRb diatomic polar molecules. For symmetric and asymmetric configurations of the pentaatomic Rydberg molecule, we investigate the metamorphosis of the Born-Oppenheimer potential curves, essential for the binding of the molecule, with varying distance from the Rydberg core and analyze the alignment and orientation of the polar diatomic molecules.
12 pages, 12 figures
References in corpus (8)
- A High Phase-Space-Density Gas of Polar Molecules
- Quantum technologies with hybrid systems
- Production of trilobite Rydberg molecule dimers with thousand-Debye permanent electric dipole moments
- Experimental characterization of singlet scattering channels in long-range Rydberg molecules
- Hybrid quantum systems with trapped charged particles
- Loss of molecules in magneto-electrostatic traps due to nonadiabatic transitions
- Rotational hybridization, and control of alignment and orientation in triatomic ultralong-range Rydberg molecules
- Lifetimes of ultralong-range strontium Rydberg molecules in a dense BEC