Stability achieved by large angular momentum is ubiquitous in nature, with examples ranging from classical mechanics, over optics and chemistry, to nuclear physics. In atoms, angular momentum can protect excited electronic orbitals from decay due to selection rules. This manifests spectacularly in highly excited Rydberg states. Low angular momentum Rydberg states are at the heart of recent breakthroughs in quantum computing, simulation and sensing with neutral atoms. For these applications the lifetime of the Rydberg levels sets fundamental limits for gate fidelities, coherence times, or spectroscopic precision. The quest for longer Rydberg state lifetimes has motivated the generation, coherent control and trapping of circular Rydberg atoms, which are characterized by the maximally allowed electron orbital momentum and were key to seminal experiments with single atoms and photons. Here, we report the observation of individually trapped circular Rydberg atoms with lifetimes of more than 10 milliseconds, two orders of magnitude longer-lived than the established low angular momentum orbitals. This is achieved via Purcell suppression of blackbody modes at room temperature. We coherently control individual circular Rydberg levels at so far elusive principal quantum numbers of up to n = 103, and observe tweezer trapping of the Rydberg atoms on the hundred millisecond scale. Our results pave the way for quantum information processing and sensing utilizing the combination of extreme lifetimes and giant Rydberg blockade.
Stability achieved by large angular momentum is ubiquitous in nature, with examples ranging from classical mechanics, over optics and chemistry, to nuclear physics. In atoms, angular momentum can protect excited electronic orbitals from decay due to selection rules. This manifests spectacularly in highly excited Rydberg states. Low angular momentum Rydberg states are at the heart of recent breakthroughs in quantum computing, simulation and sensing with neutral atoms. For these applications the lifetime of the Rydberg levels sets fundamental limits for gate fidelities, coherence times, or spectroscopic precision. The quest for longer Rydberg state lifetimes has motivated the generation, coherent control and trapping of circular Rydberg atoms, which are characterized by the maximally allowed electron orbital momentum and were key to seminal experiments with single atoms and photons. Here, we report the observation of individually trapped circular Rydberg atoms with lifetimes of more than 10 milliseconds, two orders of magnitude longer-lived than the established low angular momentum orbitals. This is achieved via Purcell suppression of blackbody modes at room temperature. We coherently control individual circular Rydberg levels at so far elusive principal quantum numbers of up to n = 103, and observe tweezer trapping of the Rydberg atoms on the hundred millisecond scale. Our results pave the way for quantum information processing and sensing utilizing the combination of extreme lifetimes and giant Rydberg blockade.
Stability achieved by large angular momentum is ubiquitous in nature, with examples ranging from classical mechanics, over optics and chemistry, to nuclear physics. In atoms, angular momentum can protect excited electronic orbitals from decay due to selection rules. This manifests spectacularly in highly excited Rydberg states. Low angular momentum Rydberg states are at the heart of recent breakthroughs in quantum computing, simulation and sensing with neutral atoms. For these applications the lifetime of the Rydberg levels sets fundamental limits for gate fidelities, coherence times, or spectroscopic precision. The quest for longer Rydberg state lifetimes has motivated the generation, coherent control and trapping of circular Rydberg atoms, which are characterized by the maximally allowed electron orbital momentum and were key to seminal experiments with single atoms and photons. Here, we report the observation of individually trapped circular Rydberg atoms with lifetimes of more than 10 milliseconds, two orders of magnitude longer-lived than the established low angular momentum orbitals. This is achieved via Purcell suppression of blackbody modes at room temperature. We coherently control individual circular Rydberg levels at so far elusive principal quantum numbers of up to n = 103, and observe tweezer trapping of the Rydberg atoms on the hundred millisecond scale. Our results pave the way for quantum information processing and sensing utilizing the combination of extreme lifetimes and giant Rydberg blockade.
Coherence time and gate fidelities in Rydberg atom quantum simulators and computers are fundamentally limited by the Rydberg state lifetime. Circular Rydberg states are highly promising candidates to overcome this limitation by orders of magnitude, as they can be effectively protected from decay due to their maximum angular momentum. We report the first realization of alkaline-earth circular Rydberg atoms trapped in optical tweezers, which provide unique and novel control possibilities due to the optically active ionic core. Specifically, we demonstrate creation of very high- n ( n = 79 ) circular states of Sr 88 . We measure lifetimes as long as 2.55 ms at room temperature, which are achieved via cavity-assisted suppression of black-body radiation. We show coherent control of a microwave qubit encoded in circular states of nearby manifolds, and characterize the qubit coherence time via Ramsey and spin-echo spectroscopy. Finally, circular-state tweezer trapping exploiting the Sr + core polarizability is quantified via measurements of the trap-induced light shift on the qubit. Our work opens routes for quantum simulations with circular Rydberg states of divalent atoms, exploiting the emergent toolbox associated with the optically active core ion. Published by the American Physical Society 2024
Circular Rydberg atoms (CRAs), i.e., Rydberg atoms with maximal orbital momentum, are highly promising for quantum computation, simulation, and sensing. They combine long natural lifetimes with strong interatomic interactions and coupling to electromagnetic fields. Trapping individual CRAs is essential to harness these unique features. We report the first demonstration of CRAs laser trapping in a programmable array of optical bottle beams. We observe the decay of a trapped rubidium circular level over 5 ms using a novel optical detection method. This first optical detection of alkali CRAs is both spatially and level selective. We finally observe the mechanical oscillations of the CRAs in the traps. This work opens the route to the use of circular levels in quantum devices. It is also promising for quantum simulation and information processing using the full extent of Rydberg manifolds.
In recent years, advances in optical tweezers arrays have enabled the trapping and control of individual atoms. This makes it possible to simulate condensed matter systems by arranging atoms in an array that mimics the crystalline structure of real materials. This approach, known as quantum simulation, was first envisioned by R. Feynman and is now being implemented by several research groups worldwide. In order to induce interactions between atoms, they are prepared in highly excited atomic states, known as Rydberg states. In particular, circular Rydberg states, which possess maximal angular momentum, exhibit lifetimes of several milliseconds, much longer than those of other Rydberg states. This property makes them particularly interesting for the development of new quantum technologies. In this work, we present the first building blocks of a quantum simulator based on circular Rydberg states of strontium atoms. This includes the development of a new cryogenic apparatus in which individual strontium atoms are trapped in optical tweezers. Using an alkaline-earth element allows us to exploit its two valence electrons for different tasks. One electron is excited to the circular state with principal quantum number n = 52, while the ionic core behaves as a Sr+ ion, which can be directly trapped by the tweezers. Moreover, we observe coherent oscillations between singlet and triplet spin states, due to the spin-orbit coupling of the electron in the circular state. These oscillations allow us to measure, with high precision, QED corrections to the Landé g5S1/2 factor of the ground state of Sr+.
Summary form only given. Condensed-matter systems are interesting and important to understand, for fundamental science as well as towards more applied objectives in the development of new materials for instance. Unfortunately, these many-body quantum systems are difficult to study: both the theoretical approach and the numerical simulation are proving impossible to carry out to relevant system sizes. Quantum simulation proposes to mimic those out-of-reach systems with more controllable and accessible quantum systems. Rydberg atoms gained renewed interest in the last decades thanks to their very high polarizability, allowing for strong and tunable short-range interactions. They constitute an interesting candidate for a quantum simulation platform. However, low angular momentum Rydberg states have limited, despite relatively long, lifetimes which limit the scope of such a quantum simulator. Moreover, low-l Rydberg states cannot be efficiently laser-trapped. In order to overcome these limitations, we propose to use circular Rydberg states, i.e., of maximum angular momentum. Circular Rydberg states exhibit much longer lifetimes, and can be trapped using laser light. By placing the circular Rydberg atoms inside a spontaneous emission-inhibiting capacitor, we hope to achieve the deterministic preparation of a 1D-chain of 40 atoms, with a collective lifetime of over 2 seconds. With expected exchange energies in the 10-100 kHz range, this would provide a platform capable of simulating quantum many-body physics up to 105exchange times. The first step towards the experimental realization of such a quantum simulator is the demonstration of the laser-trapping of circular Rydberg atoms. To this end, we use a Laguerre-Gauss hollow beam at 1064 nm, imposing a ponderomotive potential on the nearly-free electron of the Rydberg atoms. I will present our latest experimental results of light-trapping of circular Rydberg atoms.
Summary form only given. Quantum simulation offers a highly promising way to understand large correlated quantum systems, and many experimental platforms are now being developed. Rydberg atoms are specially appealing thanks to their strong and short-range dipole-dipole interaction and to their long lifetime. Low-angular momentum Rydberg atoms have been successfully used recently to realize early quantum simulators. These experiments suffer, however, from the limited (despite long) lifetime of these levels and the fact that they cannot be efficiently trapped [1, 2].Here, we propose to use circular Rydberg atoms, i.e., Rydberg atoms with maximum angular momentum, to realize a quantum simulator: A chain of circular atoms is laser trapped inside a spontaneous emission inhibiting structure. A defect-free chain of 40 atoms could be prepared. It is expected to live several seconds inside the inhibition structure. Given the strong interaction frequencies between nearby Rydberg atoms, such a system would, thus, allow us to observe the dynamics of the spin chain over several 10 4 interaction cycles. In addition, the solid state Hamiltonian that would be simulated is fully tuneable experimentally. The proposed circular atoms quantum simulator should therefore open the way towards the simulations of systems and of their dynamics beyond the grasp of classical computation.