Two rubidium atoms, one in its ground state and the other with a highly excited electron, form a metastable polar molecule.

In a combined experimental and theoretical effort we report on two novel types of ultracold long-range Rydberg molecules. First, we demonstrate the creation of triatomic molecules of one Rydberg atom and two ground-state atoms in a single-step photoassociation. Second, we assign a series of excited dimer states that are bound by a so far unexplored mechanism based on internal quantum reflection at a steep potential drop. The properties of the Rydberg molecules identified in this work qualify them as prototypes for a new type of chemistry at ultracold temperatures.

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 while also being driven by a blue-detuned laser which results in self-oscillation. Working in a nonclassical 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.

An ancient and counterintuitive phenomenon known 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 experimentally study the strong Mpemba effect in a single trapped ion system in which an exponentially accelerated relaxation in time is observed by preparing an optimal quantum initial state with no excitation of the slowest decaying mode. Also, we demonstrate 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 systems. Our work provides an efficient strategy to engineer the dynamics of open quantum system, and suggests a link unexplored yet between the Mpemba effect and the non-Hermitian physics.

Progress in the creation of large-scale, artificial quantum coherent structures demands the investigation of their nonequilibrium dynamics when strong interactions, even between remote parts, are non-perturbative. Analysis of multiparticle quantum correlations in a large system in the presence of decoherence and external driving is especially topical. Still, the scaling behavior of dynamics and related emergent phenomena are not yet well understood. We investigate how the dynamics of a driven system of several quantum elements (e.g., qubits or Rydberg atoms) changes with increasing number of elements. Surprisingly, a two-element system exhibits chaotic behaviors. For larger system sizes, a highly stochastic, far from equilibrium, hyperchaotic regime emerges. Its complexity systematically scales with the size of the system, proportionally to the number of elements. Finally, we demonstrate that these chaotic dynamics can be efficiently controlled by a periodic driving field. The insights provided by our results indicate the possibility of a reduced description for the behavior of a large quantum system in terms of the transitions between its qualitatively different dynamical regimes. These transitions are controlled by a relatively small number of parameters, which may prove useful in the design, characterization, and control of large artificial quantum structures.