Trapped ions are among the most advanced platforms for quantum simulation and computation. Their capabilities can be further augmented by making use of electronically highly excited Rydberg states, which enable the realization of long-range electric dipolar interactions. Most experimental and theoretical studies so far have focused on the excitation of ionic Rydberg states in linear Paul traps, which generate confinement by a combination of static and oscillating electric fields. These two fields need to be carefully aligned to minimize so-called micromotion, caused by the time-dependent electric field. The purpose of this work is to systematically understand the qualitative impact of micromotion on the Rydberg excitation spectrum, when the symmetry axes of the two electric fields do not coincide. Considering this scenario not only is important in the case of possible field misalignment but becomes inevitable for Rydberg excitations in two- and three-dimensional ion crystals, we develop a minimal model describing a single trapped Rydberg ion, which we solve numerically via Floquet theory and analytically using a perturbative approach. We calculate the excitation spectra and analyze in which parameter regimes addressable and energetically isolated Rydberg lines persist, which are important requirements for conducting coherent manipulations.

In this work, we present a method for measuring the motional state of a two-level system coupled to a harmonic oscillator. Our technique uses ultranarrowband composite pulses on the blue sideband transition to scan through the populations of the different motional states. Our approach does not assume any previous knowledge of the motional state distribution and is easily implemented. It is applicable both inside and outside of the Lamb-Dicke regime. For higher phonon numbers especially, the composite pulse sequence can be used as a filter for measuring phonon number ranges. We demonstrate this measurement technique using a single trapped ion and show good detection results with the numerically evaluated pulse sequence.

Trapped Rydberg ions are a novel approach to quantum information processing [1, 2]. Qubit rotations in the ion's lower lying electronic states are combined with entanglement operations that take advantage of strong Rydberg interactions [3]. In our experimental setup we excite trapped strontium ions from the metastable 4D state to the Rydberg manifold using a two photon excitation process. Certain properties of the ion become more prominent for highly excited states. One example is the polarizabilty which reacts to the surrounding electric field of the trapping electrodes. While effects due to the polarizability are negligible for lower lying states, they become more prominent for highly-excited states. This change leads to an altered trapping potential for the high lying Rydberg states, as shown in Fig. 1 [4]. For previous experiments those shifts have always been compensated for to perform, for example, sub-microsecond entangling gates between trapped ions [5]. However, this trapping field displacement can also be used to coherently control the ions' motion.

We present a single-shot method to measure motional states in the number basis. The technique can be applied to systems with at least three nondegenerate energy levels which can be coupled to a linear quantum harmonic oscillator. The method relies on probing an Autler-Townes splitting that arises when a phonon-number changing transition is strongly coupled. We demonstrate the method using a single trapped ion and show that it may be used in a nondemolition fashion to prepare phonon number states. We also show how the Autler-Townes splitting can be used to measure phonon number distributions.

We propose a scheme to dissipatively produce steady-state entanglement in a two-qubit system, via an interaction with a bosonic mode. The system is driven into a stationary entangled state, while we compensate the mode dissipation by injecting energy via a coherent pump field. We also present a scheme which allows us to adiabatically transfer all the population to the desired entangled state. The dynamics leading to the entangled state in these schemes can be understood in analogy with electromagnetically induced transparency and stimulated Raman adiabatic passage, respectively.