Weibin Li

Trapped ions excited to high-lying electronic states, so-called Rydberg states, open new opportunities for quantum simulation and quantum computing. Generally, the fidelity of quantum coherent operations critically depends on the longevity of Rydberg states. However, scaling laws predict that the lifetimes of Rydberg states in singly charged alkaline-earth metal ions are 16 times shorter, compared to their neutral atom counterparts. Here, we show that this is not generally the case. We report an anomalous lifetime enhancement of certain low angular momentum ionic Rydberg series by factors larger than eight. The anomaly is present at both zero and finite temperature, although it is caused by different mechanisms. At zero temperature, the anomalously enhanced lifetimes are caused by accidental cancellations of the relevant dipole transition matrix elements, while at room temperature the anomaly originates from the enlarged energetic separation of ionic Rydberg levels with respect to neutral-atom levels.

The quantum Mpemba effect (ME) in Markovian systems is conventionally explained by a smaller overlap between the initial state and the slowest decay mode (SDM). Such state, initially farther away from equilibrium or steady state, relaxes faster than closer ones, resulting to a crossing of their trajectories. This picture, by neglecting the transient dynamics, holds in the long-time limit. Here we experimentally observe multiple trajectory crossings (multi-ME) in the relaxation dynamics of a trapped ion. Such novel dynamics takes place in a unusual scenario where the initial state instead has a larger overlap with the SDM. We develop a theoretical framework based on relaxation speed to understand the multi-ME. We show that the initial relaxation speed is governed by the fastest decay mode, which together with the SDM overlap gives a phase diagram that reveals both the occurrence and the types of quantum ME observed in our experiment. Our study goes beyond the simple picture based on the long-time limit, tracks continuously the quantum ME dynamics, and establishes a comprehensive framework to describe the transient quantum relaxation.

Trapped ions as one of the most promising quantum-information-processing platforms, yet conventional entangling gates mediated by collective motion remain slow and difficult to scale. Exciting trapped ions to high-lying electronic Rydberg states provides a promising route to overcome these limitations by enabling strong, long-range dipole-dipole interactions that support much faster multi-qubit operations. Here, we introduce the first scheme for implementing a native controlled-controlled-Z gate with microwave-dressed Rydberg ions by optimizing a single-pulse protocol that accounts for the finite Rydberg-state lifetime. The resulting gate outperforms standard decompositions into one- and two-qubit gates by achieving fidelities above 97% under realistic conditions, with execution times of about 2 microseconds at cryogenic temperatures. To explore the potential of trapped Rydberg ions for fault-tolerant quantum error correction, and to illustrate the utility of three-qubit Rydberg-ion gates in this context, we develop and analyze a proposal for fault-tolerant, measurement-free quantum error correction using the nine-qubit Bacon-Shor code. Our simulations confirm that quantum error correction can be performed in a fully fault-tolerant manner on a linear Rydberg-ion chain despite its limited qubit connectivity. These results establish native multiqubit Rydberg-ion gates as a valuable resource for fast, high-fidelity quantum computing and highlight their potential for fault-tolerant quantum error correction.

We study spin-phonon coupled dynamics in the vicinity of a sloped conical intersection created by laser coupling the electronic (spin) and vibrational degrees of freedom of a pair of trapped Rydberg ions. We show that the shape of the potential energy surfaces can be engineered and controlled by exploiting the sideband transitions of the crystal vibration and dipole-dipole interactions between Rydberg ions in the Lamb-Dicke regime. Using the sideband transition, we realize a sloped conical intersection whose cone axis is only tilted along one spatial axis. When the phonon wavepacket is located in the potential minimum of the lower potential surface, the spin and phonon dynamics are largely frozen owing to the geometric phase effect. When starting from the upper potential surface, the electronic and phonon states tunnel to the lower potential surface, leading to a partial revival of the initial state. In contrast, the dynamics drastically change when the initial wavepackets are away from the conical intersection. The initial state is revived, and is almost entirely irrelevant to whether it is from the lower or upper potential surface. Complete Rabi oscillations of the adiabatic states are found when the wavepacket is initialized on the upper potential surface. The dynamics occur on the microsecond and nanometer scales, implying that Rydberg ions provide a platform for simulating nonadiabatic processes in the vicinity of a sloped conical intersection.

State-dependent conformational changes play a central role in molecular dynamics, yet they are often difficult to observe or simulate due to their complexity and ultrafast nature. One alternative approach is to emulate such phenomena using quantum simulations with cold, trapped ions. In their electronic ground state, these ions form long-lived Wigner crystals. When excited to high-lying electronic Rydberg states, the ions experience a modified trapping potential, resulting in a strong coupling between their electronic and vibrational degrees of freedom. In an ion crystal, this vibronic coupling creates electronic state-dependent potential energy surfaces that can support distinct crystal structures -- closely resembling the conformational changes of molecules driven by electronic excitations. Here, we present the first experimental observation of this effect, by laser-coupling a single ion at the centre of a three-ion crystal to a Rydberg state. By tuning the system close to a structural phase transition, the excitation induces a state-dependent conformational change, transforming the Wigner crystal from a linear to a zigzag configuration. This structural change leads to a strong hybridisation between vibrational and electronic states, producing a clear spectroscopic signature in the Rydberg excitation. Our findings mark the first experimental step towards using Rydberg ions to create and study artificial molecular systems. change leads to a strong hybridisation between vibrational and electronic states, producing a clear spectroscopic signature in the Rydberg excitation. Our findings mark the first experimental step towards using Rydberg ions to create and study artificial molecular systems.

Non-adiabatic processes near conical intersections are rooted in the stronger coupling between electronic and nuclear degrees of freedom. Using a system of two trapped Rydberg ions, their high polarizability and strong dipolar interactions allow to form a conical intersection, where dynamics takes place on a microsecond time scale. Rydberg lifetimes are typically from a few to tens of microseconds, which could affect the conical dynamics. We study the effect of the finite lifetime of the Rydberg state on the vibronic dynamics around the conical intersection via analyzing the master equation. Through mean field and numerical calculations, damping dynamics are found in both the phonon populations and electronic states depending on the initial states. It is found that oscillatory vibronic dynamics can be seen clearly within the Rydberg lifetime, permitting to observe the conical effect in the trapped Rydberg ion system.

An ancient and counterintuitive phenomenon know as the Mpemba effect (water can cool faster when initially heated up) showcases the critical role of initial conditions in relaxation processes. How to realize and utilize this effect for speeding up relaxation is an important but challenging task in purely quantum system till now. Here, we report the first experiment, as far as we know,about the strong Mpemba effect in a single trapped ion system in which an exponentially expedited relaxation in time is observed by preparing an optimal initial state with no excitation of the slowest decaying mode. Also, we find that the condition of realizing such effect coincides with the Liouvillian exceptional point, featuring the coalescence of both the eigenvalues and the eigenmodes of the system. Our work provides an efficient strategy to exponentially accelerate relaxations of quantum system to their stationary state, and suggests a link unexplored yet between the Mpemba effect and the non-Hermitian physics. It could open up the door to engineer a wide range of dissipative quantum systems by utilizing the anomalous Mpemba effect, for applications in quantum simulation and quantum information processing.

We investigate a tripartite quantum Rabi model (TQRM) wherein a bosonic mode concurrently couples to two spin-$1/2$ particles through a spin-spin interaction, resulting in a spin-spin-boson coupling -- a departure from conventional quantum Rabi models featuring bipartite spin-boson couplings. The symmetries of the TQRM depend on the detuning parameter, representing the energy difference between the spin states. At zero detuning a parity symmetry renders the TQRM reducible to a quantum Rabi model. A subradiant to superradiant transition in the groundstate is predicted as the tripartite coupling strength increases. For non-zero detuning the total spin emerges as the sole conserved quantity in the TQRM. It is found that superradiance prevails in the groundstate as long as the tripartite coupling remains non-zero. We derive the Braak $\mathcal{G}$-function of the TQRM analytically, with which the eigenspectra are obtained. The TQRM can be realized in a viable trapped Rydberg ion quantum simulator, where the required tripartite couplings and single body interactions in the TQRM are naturally present. Our study opens opportunities to explore and create novel correlations and entanglement in the spin and motional degrees of freedoms with the TQRM.

Atoms and ions confined with electric and optical fields form the basis of many current quantum simulation and computing platforms. When excited to high-lying Rydberg states, long-ranged dipole interactions emerge which strongly couple the electronic and vibrational degrees of freedom through state-dependent forces. This vibronic coupling and the ensuing hybridization of internal and external degrees of freedom manifest through clear signatures in the many-body spectrum. We illustrate this by considering the case of two trapped Rydberg ions, for which the interaction between the relative vibrations and Rydberg states realizes a quantum Rabi model. We proceed to demonstrate that the aforementioned hybridization can be probed by radio frequency spectroscopy and discuss observable spectral signatures at finite temperatures and for larger ion crystals.

We investigate speeding up of relaxation of Markovian open quantum systems with the Liouvillian exceptional point (LEP), where the slowest decay mode degenerate with a faster decay mode. The degeneracy significantly increases the gap of the Liouvillian operator, which determines the timescale of such systems in converging to stationarity, and hence accelerates the relaxation process. We explore an experimentally relevant three level atomic system, whose eigenmatrices and eigenspectra are obtained completely analytically. This allows us to gain insights in the LEP and examine respective dynamics with details. We illustrate that the gap can be further widened through Floquet engineering, which further accelerates the relaxation process. Finally, we extend this approach to analyze laser cooling of trapped ions, where vibrations (phonons) couple to the electronic states. An optimal cooling condition is obtained analytically, which agrees with both existing experiments and numerical simulations. Our study provides analytical insights in understanding LEP, as well as in controlling and optimizing dissipative dynamics of atoms and trapped ions.

Trapped ions provide a platform for quantum technologies that offers long coherence times and high degrees of scalability and controllability. Here, we use this platform to develop a realistic model of a thermal device consisting of two laser-driven, strongly coupled Rydberg ions in a harmonic trap. We show that the translational degrees of freedom of this system can be utilized as a flywheel storing the work output that is generated by a cyclic thermodynamic process applied to its electronic degrees of freedom. Mimicking such a process through periodic variations of external control parameters, we use a mean-field approach underpinned by numerical and analytical calculations to identify relevant physical processes and to determine the charging rate of the flywheel. Our work paves the way for the design of microscopic thermal machines based on Rydberg ions that can be equipped with both many-body working media and universal work storages.

We propose an adiabatic method for optimal phonon temperature estimation using trapped ions which can be operated beyond the Lamb-Dicke regime. The quantum sensing technique relies on a time-dependent red-sideband transition of phonon modes, described by the non-linear Jaynes-Cummings model in general. A unique feature of our sensing technique is that the relevant information of the phonon thermal distributions can be transferred to the collective spin-degree of freedom. We show that each of the thermal state probabilities is adiabatically mapped onto the respective collective spin-excitation configuration and thus the temperature estimation is carried out simply by performing a spin-dependent laser fluorescence measurement at the end of the adiabatic transition. We characterize the temperature uncertainty in terms of the Fisher information and show that the state projection measurement saturates the fundamental quantum Cramér-Rao bound for quantum oscillator at thermal equilibrium.

Conical intersections between electronic potential energy surfaces are paradigmatic for the study of non-adiabatic processes in the excited states of large molecules. However, since the corresponding dynamics occurs on a femtosecond timescale, their investigation remains challenging and requires ultrafast spectroscopy techniques. We demonstrate that trapped Rydberg ions are a platform to engineer conical intersections and to simulate their ensuing dynamics on larger length and time scales of the order of nanometers and microseconds, respectively; all this in a highly controllable system. Here, the shape of the potential energy surfaces and the position of the conical intersection can be tuned thanks to the interplay between the high polarizability and the strong dipolar exchange interactions of Rydberg ions. We study how the presence of a conical intersection affects both the nuclear and electronic dynamics demonstrating, in particular, how it results in the inhibition of the nuclear motion. These effects can be monitored in real-time via a direct spectroscopic measurement of the electronic populations in a state-of-the-art experimental setup.

Trapped Rydberg ions represent a flexible platform for quantum simulation and information processing which combines a high degree of control over electronic and vibrational degrees of freedom. The possibility to individually excite ions to high-lying Rydberg levels provides a system where strong and long-range interactions between pairs of excited ions can be engineered and tuned via external laser fields. We show that the coupling between Rydberg pair interactions and collective motional modes gives rise to effective long-range multi-body interactions, consisting of two, three, and four-body terms. Their shape, strength, and range can be controlled via the ion trap parameters and strongly depends on both the equilibrium configuration and vibrational modes of the ion crystal. By focusing on an experimentally feasible quasi one-dimensional setup of $ {}^{88}\mathrm{Sr}^+ $ Rydberg ions, we demonstrate that multi-body interactions are enhanced by the emergence of a soft mode associated, e.g., with a structural phase transition. This has a striking impact on many-body electronic states and results, for example, in a three-body anti-blockade effect. Our study shows that trapped Rydberg ions offer new opportunities to study exotic many-body quantum dynamics driven by enhanced multi-body interactions.

Generating quantum entanglement in large systems on time scales much shorter than the coherence time is key to powerful quantum simulation and computation. Trapped ions are among the most accurately controlled and best isolated quantum systems with low-error entanglement gates operated via the vibrational motion of a few-ion crystal within tens of microseconds. To exceed the level of complexity tractable by classical computers the main challenge is to realise fast entanglement operations in large ion crystals. The strong dipole-dipole interactions in polar molecule and Rydberg atom systems allow much faster entangling gates, yet stable state-independent confinement comparable with trapped ions needs to be demonstrated in these systems. Here, we combine the benefits of these approaches: we report a $700\,\mathrm{ns}$ two-ion entangling gate which utilises the strong dipolar interaction between trapped Rydberg ions and produce a Bell state with $78\%$ fidelity. The sources of gate error are identified and a total error below $0.2\%$ is predicted for experimentally-achievable parameters. Furthermore, we predict that residual coupling to motional modes contributes $\sim 10^{-4}$ gate error in a large ion crystal of 100 ions. This provides a new avenue to significantly speed up and scale up trapped ion quantum computers and simulators.

Trapped Rydberg ions are a promising new system for quantum information processing. They have the potential to join the precise quantum operations of trapped ions and the strong, long-range interactions between Rydberg atoms. Technically, the ion trap will need to stay active while exciting the ions into the Rydberg state, else the strong Coulomb repulsion will quickly push the ions apart. Thus, a thorough understanding of the trap effects on Rydberg ions is essential for future applications. Here we report the observation of two fundamental trap effects. First, we investigate the interaction of the Rydberg electron with the quadrupolar electric trapping field. This effect leads to Floquet sidebands in the spectroscopy of Rydberg D-states whereas Rydberg S-states are unaffected due to their symmetry. Second, we report on the modified trapping potential in the Rydberg state compared to the ground state which results from the strong polarizability of the Rydberg ion. We observe the resultant energy shifts as a line broadening which can be suppressed by cooling the ion to the motional ground state in the directions orthogonal to the excitation laser.

We investigate quantum synchronization theoretically in a system consisting of two cold ions in microtraps. The ions' motion is damped by a standing-wave laser whilst also being driven by a blue-detuned laser which results in self-oscillation. Working in a non-classical regime, where these oscillations contain only a few phonons and have a sub-Poissonian number variance, we explore how synchronization occurs when the two ions are weakly coupled using a probability distribution for the relative phase. We show that strong correlations arise between the spin and vibrational degrees of freedom within each ion and find that when two ions synchronize their spin degrees of freedom in turn become correlated. This allows one to indirectly infer the presence of synchronization by measuring the ions' internal state.

We explore trapped ions as a setting to investigate non-equilibrium phases in a generalised Dicke model of dissipative spins coupled to phonon modes. We find a rich dynamical phase diagram including superradiant-like regimes, dynamical phase-coexistence and phonon-lasing behaviour. A particular advantage of trapped ions is that these phases and transitions among them can be probed in situ through fluorescence. We demonstrate that the main physical insights are captured by a minimal model and consider an experimental realisation with Ca+ ions trapped in a linear Paul trap.

We present a theoretical analysis of the implementation of an entangling quantum gate between two trapped Ca$^+$ ions which is based on the dipolar interaction among ionic Rydberg states. In trapped ions the Rydberg excitation dynamics is usually strongly affected by mechanical forces due to the strong couplings between electronic and vibrational degrees of freedom in inhomogeneous electric fields. We demonstrate that this harmful effect can be overcome by using dressed states that emerge from the microwave coupling of nearby Rydberg states. At the same time these dressed states exhibit long range dipolar interactions which we use to implement a controlled adiabatic phase gate. Our study highlights a route towards a trapped ion quantum processor in which quantum gates are realized independently of the vibrational modes.