Jonas Vogel

Fast entangling gate operations are a fundamental prerequisite for quantum simulation and computation. We propose an entangling scheme for arbitrary pairs of ions in a linear crystal, harnessing the high electric polarizability of highly excited Rydberg states. An all-to-all quantum gate connectivity is based on an initialization of a pair of ions to a superposition of ground- and Rydberg-states by laser excitation, followed by the entangling gate operation which relies on a state-dependent frequency shift of collective vibrational modes of the crystal. This gate operation requires applying an electric waveform to trap electrodes. Employing transverse collective modes of oscillation, we reveal order of $μs$ operation times within any of the qubit pairs in a small crystal. In our calculation, we are taking into account realistic experimental conditions and feasible electric field ramps. The proposed gate operation is ready to be combined with a scalable processor architecture to reconfigure the qubit register, either by shuttling ions or by dynamically controlling optical tweezer potentials.

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 probability 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 easy-to-implement and 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.

A complete set of spectroscopic data is indispensable when using Rydberg states of trapped ions for quantum information processing. We carried out Rydberg series spectroscopy for $nS_{1/2}$ states with $38 \leq n \leq 65$ and for $nD_{5/2}$ states with $37\leq n \leq 50$ on a single trapped $^{40}$Ca$^+$ ion. From a nonlinear regression to resonance frequencies, we determined the ionization energy of 2 870 575.582(15) GHz, measured 60 times more accurately as compared to the accepted value and contradicting it by 7.5 standard deviations. We confirm quantum defect values of $δ_{S_{1/2}}=1.802995(5)$ and $δ_{D_{5/2}}=0.626888(9)$ for $nS_{1/2}$ and $nD_{5/2}$ states respectively, which allow for unambiguous addressing of Rydberg levels of Ca$^+$ ions.

We present an experimental investigation of the Rydberg 23 P$_{1/2}$ state of laser-cooled $^{40}$Ca$^+$ ions in a radiofrequency ion trap. Using micromotion sideband spectroscopy on a narrow quadrupole transition, the oscillating electric field at the ion position was precisely characterised, and the modulation of the Rydberg transition due to this field was minimised. From a correlated fit to this P line and previously measured P and F level energies of Ca II, we have determined the ionization energy of 95 751.916(32) $\rm {cm}^{-1}$, in agreement with the accepted value, and the quantum defect for the $n$ P$_{1/2}$ states.