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Register a new userTheory of long range interactions for Rydberg states attached to hyperfine split cores
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The theory is developed for one and two atom interactions when the atom has a Rydberg electron attached to a hyperfine split core state. This situation is relevant for some of the rare earth and alkaline earth atoms that have been proposed for experiments on Rydberg-Rydberg interactions. For the rare earth atoms, the core electrons can have a very substantial total angular momentum, $J$, and a non-zero nuclear spin, $I$. In the alkaline earth atoms there is a single, $s$, core electron whose spin can couple to a non-zero nuclear spin for odd isotopes. The resulting hyperfine splitting of the core state can lead to substantial mixing between the Rydberg series attached to different thresholds. Compared to the unperturbed Rydberg series of the alkali atoms, the series perturbations and near degeneracies from the different parity states could lead to qualitatively different behavior for single atom Rydberg properties (polarizability, Zeeman mixing and splitting, etc) as well as Rydberg-Rydberg interactions ($C_5$ and $C_6$ matrices).
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Long-range dipole-dipole and quadrupole-quadrupole interactions between pairs of Rydberg atoms are calculated perturbatively for calcium, strontium and ytterbium within the Coulomb approximation. Quantum defects, obtained by fitting existing laser spectroscopic data, are provided for all $S$, $P$, $D$ and $F$ series of strontium and for the $^3P_2$ series of calcium. The results show qualitative differences with the alkali metal atoms, including isotropically attractive interactions of the strontium $^1S_0$ states and a greater rarity of Forster resonances. Only two such resonances are identified, both in triplet series of strontium. The angular dependence of the long range interaction is briefly discussed.
The interaction of two excited hydrogen atoms in metastable states constitutes a theoretically interesting problem because of the quasi-degenerate 2P_{1/2} levels which are removed from the 2S states only by the Lamb shift. The total Hamiltonian of the system is composed of the van der Waals Hamiltonian, the Lamb shift and the hyperfine effects. The van der Waals shift becomes commensurate with the 2S-2P_{3/2} fine-structure splitting only for close approach (R < 100 a_0, where a_0 is the Bohr radius) and one may thus restrict the discussion to the levels with n=2 and J=1/2 to good approximation. Because each S or P state splits into an F=1 triplet and an F=0 hyperfine singlet (eight states for each atom), the Hamiltonian matrix {em a priori} is of dimension 64. A careful analysis of symmetries the problem allows one to reduce the dimensionality of the most involved irreducible submatrix to 12. We determine the Hamiltonian matrices and the leading-order van der Waals shifts for states which are degenerate under the action of the unperturbed Hamiltonian (Lamb shift plus hyperfine structure). The leading first- and second-order van der Waals shifts lead to interaction energies proportional to 1/R^3 and 1/R^6 and are evaluated within the hyperfine manifolds. When both atoms are metastable 2S states, we find an interaction energy of order E_h chi (a_0/R)^6, where E_h and L are the Hartree and Lamb shift energies, respectively, and chi = E_h/L ~ 6.22 times 10^6 is their ratio.
In high orbital angular momentum ($ell geq 3$) Rydberg states, the centrifugal barrier hinders close approach of the Rydberg electron to the ion-core. As a result, these core-nonpenetrating Rydberg states can be well described by a simplified model in which the Rydberg electron is only weakly perturbed by the long-range electric properties (i.e., multipole moments and polarizabilities) of the ion-core. We have used a long-range model to describe the vibrational autoionization dynamics of high-$ell$ Rydberg states of nitric oxide (NO). In particular, our model explains the extensive angular momentum exchange between the ion-core and Rydberg electron that had been previously observed in vibrational autoionization of $f$ ($ell=3$) Rydberg states. These results shed light on a long-standing mechanistic question around these previous observations, and support a direct, vibrational mechanism of autoionization over an indirect, predissociation-mediated mechanism. In addition, our model correctly predicts newly measured total decay rates of $g$ ($ell=4$) Rydberg states because, for $ellgeq4$, the non-radiative decay is dominated by autoionization rather than predissociation. We examine the predicted NO$^+$ ion rotational state distributions generated by vibrational autoionization of $g$ states and discuss applications of our model to achieve quantum state selection in the production of molecular ions.
The lifetimes of the lower-lying vibrational states of ultralong-range strontium Rydberg molecules comprising one ground-state 5s2 1S0 atom and one Rydberg atom in the 5s38s 3S1 state are reported. The molecules are created in an ultracold gas held in an optical dipole trap and their numbers determined using field ionization, the product electrons being detected by a microchannel plate. The measurements show that, in marked contrast to earlier measurements involving rubidium Rydberg molecules, the lifetimes of the low-lying molecular vibrational states are very similar to those of the parent Rydberg atoms. This results because the strong p-wave resonance in low-energy electronrubidium scattering, which plays an important role in determining the molecular lifetimes, is not present for strontium. The absence of this resonance offers advantages for experiments involving strontium Rydberg atoms as impurities in quantum gases and for testing theories of molecular formation and decay.
We theoretically investigate trapped ions interacting with atoms that are coupled to Rydberg states. The strong polarizabilities of the Rydberg levels increases the interaction strength between atoms and ions by many orders of magnitude, as compared to the case of ground state atoms, and may be mediated over micrometers. We calculate that such interactions can be used to generate entanglement between an atom and the motion or internal state of an ion. Furthermore, the ion could be used as a bus for mediating spin-spin interactions between atomic spins in analogy to much employed techniques in ion trap quantum simulation. The proposed scheme comes with attractive features as it maps the benefits of the trapped ion quantum system onto the atomic one without obviously impeding its intrinsic scalability. No ground state cooling of the ion or atom is required and the setup allows for full dynamical control. Moreover, the scheme is to a large extent immune to the micromotion of the ion. Our findings are of interest for developing hybrid quantum information platforms and for implementing quantum simulations of solid state physics.
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