Fabian Thielemann

Neutral atoms trapped in optical tweezers and excited to Rydberg states, together with trapped ions, are among the most advanced platforms for quantum simulation and quantum computing. Current experiments often rely on additional atoms in neighboring traps to encode ancilla qubits for local manipulation and readout. Here, we demonstrate a dual ion-Rydberg system comprising two qubits encoded in two individually controlled electrons of the same alkaline-earth atom. The first, a microwave qubit, is encoded in a pair of circular Rydberg states, while the second, an optical qubit, is encoded on a narrow quadrupole transition of the Rydberg atom's ionic core. We demonstrate coherent control of the optical qubit and achieve coherence times of several hundred microseconds under dynamical decoupling. Furthermore, we realize coherent coupling between the two electrons via electrostatic quadrupole interactions over the large separation between the Rydberg electron and the ionic core, and map out its angular tunability. Finally, we demonstrate a two-qubit operation, reminiscent of a Mølmer-Sørensen gate, that evolves through an entangled state of the two qubits driven by the quadrupole coupling. Our work opens a pathway to exploit a pair of individually controlled electronic qubits with tunable coupling for quantum simulation and quantum metrology.

We report the optical trapping of multiple ions localized at individual lattice sites of a one-dimensional optical lattice. We observe a fivefold increase in robustness against axial DC-electric fields and an increase of the axial eigenfrequency by two orders of magnitude compared to an optical dipole trap without interference but similar intensity. Our findings motivate an alternative pathway to extend arrays of trapped ions in size and dimension, enabling quantum simulations with particles interacting at long range.

Controlling physical systems and their dynamics on the level of individual quanta propels both fundamental science and quantum technologies. Trapped atomic and molecular systems, neutral and charged, are at the forefront of quantum science. Their extraordinary level of control is evidenced by numerous applications in quantum information processing and quantum metrology. Studying the long-range interactions between these systems when combined in a hybrid atom-ion trap has lead to landmark results. Reaching the ultracold regime, however, where quantum mechanics dominates the interaction, e.g., giving access to controllable scattering resonances, has been elusive so far. Here we demonstrate Feshbach resonances between ions and atoms, using magnetically tunable interactions between $^{138}$Ba$^{+}$ ions and $^{6}$Li atoms. We tune the experimental parameters to probe different interaction processes - first, enhancing three-body reactions and the related losses to identify the resonances, then making two-body interactions dominant to investigate the ion's sympathetic cooling in the ultracold atomic bath. Our results provide deeper insights into atom-ion interactions, giving access to complex many-body systems and applications in experimental quantum simulation.

For conventional ion traps, the trapping potential is close to independent of the electronic state, providing confinement for ions dependent primarily on their charge-to-mass ratio $Q/m$. In contrast, storing ions within an optical dipole trap results in state-dependent confinement. Here we experimentally study optical dipole potentials for $^{138}\mathrm{Ba}^+$ ions stored within two distinctive traps operating at 532 nm and 1064 nm. We prepare the ions in either the $6\mathrm{S}_{\mathrm{1/2}}$ electronic ground or the $5\mathrm{D}_{\mathrm{3/2}}$/ $5\mathrm{D}_{\mathrm{5/2}}$ metastable excited state and probe the relative strength and polarity of the potential. On the one hand, we apply our findings to selectively remove ions from a Coulomb crystal, despite all ions sharing the same $Q/m$. On the other hand, we deterministically purify the trapping volume from parasitic ions in higher-energy orbits, resulting in reliable isolation of Coulomb crystals down to a single ion within a radio-frequency trap.

We study a method for mass-selective removal of ions from a Paul trap by parametric excitation. This can be achieved by applying an oscillating electric quadrupole field at twice the secular frequency $ω_{\text{sec}}$ using pairs of opposing electrodes. While excitation near the resonance with the frequency $ω_{\text{sec}}$ only leads to a linear increase of the amplitude with excitation duration, parametric excitation near $2\, ω_{\text{sec}}$ results in an exponential increase of the amplitude. This enables efficient removal of ions from the trap with modest excitation voltages and narrow bandwidth, therefore substantially reducing the disturbance of ions with other charge-to-mass ratios. We numerically study and compare the mass selectivity of the two methods. In addition, we experimentally show that the barium isotopes with 136 and 137 nucleons can be removed from small ion crystals and ejected out of the trap while keeping $^{138}\text{Ba}^{+}$ ions Doppler cooled, corresponding to a mass selectivity of better than $Δm / m = 1/138$. This method can be widely applied to ion trapping experiments without major modifications, since it only requires modulating the potential of the ion trap.