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arXiv:2504.21241

Microwave-Dressing of Rydberg States in a Trapped Calcium Ion

Han Bao, Alexander Schulze-Makuch, Ferdinand Schmidt‐Kaler

Published Apr 30, 2025• 0 citations
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Abstract

We are using optical- and microwave-fields to excite Rydberg states in trapped cold 40Ca+ ions. We employ a single ion and observe spectroscopically in the manifold of a principal quantum number n=49 the dressing of Rydberg states of angular momentum states S and P. We compare our experimental spectra with a multi-level calculation of dressed states and find good agreement. The results are important for controlling the interaction of single ions in Rydberg states with electric fields of the ion trap, and for tailoring the interactions in an ion crystal in Rydberg states.

DOI
10.48550/arxiv.2504.21241

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We are using optical- and microwave-fields to excite Rydberg states in trapped cold 40Ca+ ions. We employ a single ion and observe spectroscopically in the manifold of a principal quantum number n=49 the dressing of Rydberg states of angular momentum states S and P. We compare our experimental spectra with a multi-level calculation of dressed states and find good agreement. The results are important for controlling the interaction of single ions in Rydberg states with electric fields of the ion trap, and for tailoring the interactions in an ion crystal in Rydberg states.
Abstract We are using optical and microwave fields to excite Rydberg states in trapped cold ions. We employ a single ion and observe spectroscopically in the manifold of a principal quantum number n = 49 the dressing of Rydberg states of angular momentum states S and P. We compare our experimental spectra with a multi-level calculation of dressed states and find good agreement. The results are important for controlling the interaction of single ions in Rydberg states with electric fields of the ion trap and for tailoring the interactions in an ion crystal in Rydberg states.
Microwave dressing of Rydberg ions creates tunable eigenstates with controllable polarizability and interaction strength, but coherent navigation between these states has remained elusive. Here, we report on the first demonstration of coherent population transfer between different Rydberg states of a trapped ion. We investigate both microwave-mediated Rabi oscillations between Rydberg S and P states and adiabatic transfer between microwave-dressed Rydberg states. Between Rydberg S and P states we achieve a population transfer efficiency of 91.5(5)% in a single microwave πππ-pulse. Microwave dressing hybridizes the S and P Rydberg states into new eigenstates with tunable polarizability, enabling both noise-resilient zero-polarizability states and maximally interacting states. We demonstrate adiabatic transfer between these zero-polarizability and maximally dressed states, enabling experiments that combine noise-resilient excitation with strong dipole-dipole interactions and Förster resonance control within a single measurement sequence.
Trapped Rydberg ions are a promising new platform for quantum computation and simulation. They combine the exquisite control of trapped ion systems with the strong dipole-dipole interactions available in Rydberg atom systems. In order to realize strong interactions between Rydberg ions, microwave dressing is required to induce strong oscillating dipoles. Additionally, microwave dressing of Rydberg states with polarizabilities of opposite sign allows for the realization of Rydberg states with vanishing polarizability. Such states are insensitive to external electric fields and can be trapped independently of their state. Vanishing-polarizability Rydberg states allow for implementing Rydberg entangling gates in large ion crystals.
We study the dynamics of Rydberg ions trapped in a linear Paul trap, and discuss the properties of ionic Rydberg states in the presence of the static and time-dependent electric fields constituting the trap. The interactions in a system of many ions are investigated and coupled equations of the internal electronic states and the external oscillator modes of a linear ion chain are derived. We show that strong dipole–dipole interactions among the ions can be achieved by microwave dressing fields. Using low-angular momentum states with large quantum defect, the internal dynamics can be mapped onto an effective spin model of a pair of dressed Rydberg states that describes the dynamics of Rydberg excitations in the ion crystal. We demonstrate that excitation transfer through the ion chain can be achieved on a nanosecond timescale and discuss the implementation of a fast two-qubit gate in the ion chain.
We report on the observation of interactions between ultracold Rydberg atoms and ions in a Paul trap. The rate of observed inelastic collisions, which manifest themselves as charge transfer between the Rydberg atoms and ions, exceeds that of Langevin collisions for ground state atoms by about 3 orders of magnitude. This indicates a huge increase in interaction strength. We study the effect of the vacant Paul trap's electric fields on the Rydberg excitation spectra. To quantitatively describe the exhibited shape of the ion loss spectra, we need to include the ion-induced Stark shift on the Rydberg atoms. Furthermore, we demonstrate Rydberg excitation on a dipole-forbidden transition with the aid of the electric field of a single trapped ion. Our results confirm that interactions between ultracold atoms and trapped ions can be controlled by laser coupling to Rydberg states. Adding dynamic Rydberg dressing may allow for the creation of spin-spin interactions between atoms and ions, and the elimination of collisional heating due to ionic micromotion in atom-ion mixtures.
Abstract We present a method for measuring the polarizability of Rydberg ions confined in the harmonic potential of a Paul trap. For a highly excited electronic state, the coupling between the electronic wave function and the trapping field modifies the excitation spectra depending on the motional state of the ion. This interaction strongly depends on the polarizability of the excited state and manifests itself in the state-dependent secular frequencies of the ion. We initialize a single trapped 40 Ca + ion from the motional ground state into coherent states with | α | up to 12 using electric voltages on the trap segments. The internal state, firstly initialised in the long-lived 3D 5 / 2 state, is excited to a Rydberg S 1 / 2 -state via the 5P 3 / 2 state in a two-photon process. We probe the depletion of the 3D 5 / 2 state owing to the Rydberg excitation followed by a decay into the internal ground 4S 1 / 2 state. By analysing the obtained spectra we extract the polarizability of Rydberg states which agree with numerical calculations. The method is applicable to different Rydberg states regardless of their principal or angular quantum numbers. An accurate value of the state polarizability is needed for quantum gate operations with Rydberg ion crystals.