Circular states of strontium are promising platforms for quantum technologies. They exhibit much longer lifetimes than laser-accessible Rydberg states and possess an optically active ionic core that can be manipulated with laser light. Here we trap circular states in optical tweezers by exploiting the dynamical polarizability of the ionic core. We measure the decay of the orbital component of a n=51 circular state and observe singlet-triplet spin oscillations arising from the interplay of vector light shifts induced by the optical tweezers, spin-orbit coupling associated with the Rydberg electron, and the difference in Landé $g$-factor between the ionic core and the Rydberg electrons. By observing the two electron spin dynamics, we measure the spin-orbit interaction and the correction $δg \sim$ 10^(-5) of the Landé $g$-factor of the Sr$^+$ 5s$_{1/2}$ ionic core electron with respect to that of a free electron. This provides a first high-precision measurement of $g_{\textrm{Sr}^+, 5s_{1/2}}$ = 2.002290(1).
Measuring the Sr+ 5s1/2 Landé g-factor Using Singlet-Triplet Oscillations in a Circular Rydberg State of Strontium
Circular states of strontium are promising platforms for quantum technologies. They exhibit much longer lifetimes than laser-accessible Rydberg states and possess an optically active ionic core that can be manipulated with laser light. Here we trap circular states in optical tweezers by exploiting the dynamical polarizability of the ionic core. We measure the decay of the orbital component of a n=51 circular state and observe singlet-triplet spin oscillations arising from the interplay of vector light shifts induced by the optical tweezers, spin-orbit coupling associated with the Rydberg electron, and the difference in Landé g-factor between the ionic core and the Rydberg electrons. By observing the two electron spin dynamics, we measure the spin-orbit interaction and the correction δg∼ 10^(-5) of the Landé g-factor of the Sr+ 5s1/2 ionic core electron with respect to that of a free electron. This provides a first high-precision measurement of gSr+,5s1/2 = 2.002290(1).
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+.
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
Alkaline earth Rydberg atoms are very promising tools for quantum technologies. Their highly excited outer electron provides them with the remarkable properties of Rydberg atoms and, notably, with a huge coupling to external fields or to other Rydberg atoms while the ionic core retains an optically active electron. However, low angular-momentum Rydberg states suffer almost immediate autoionization when the core is excited. Here, we demonstrate that strontium circular Rydberg atoms with a core excited in a 4D metastable level are impervious to autoionization over more than a few millisecond time scale. This makes it possible to trap and laser-cool Rydberg atoms. Moreover, we observe singlet to triplet transitions due to the core optical manipulations, opening the way to a microwave to optical quantum interface.
Divalent atoms provide excellent means for advancing control in Rydberg atom-based quantum simulation and computing due to the second optically active valence electron available. Particularly promising in this context are circular Rydberg atoms, for which long-lived ionic core excitations can be exploited without suffering from detrimental autoionization. Here, we report the implementation of electric quadrupole coupling between the metastable 4D_{3/2} level and a very high-n (n=79) circular Rydberg qubit, realized in doubly excited ^{88}Sr atoms prepared from an optical tweezer array. We measure the kHz-scale differential level shift on the circular Rydberg qubit via beat-node Ramsey interferometry comprising spin echo. Observing this coupling requires coherent interrogation of the Rydberg states for more than 100 μs, which is assisted by tweezer trapping and circular state lifetime enhancement in a black-body radiation suppressing capacitor. Further, we find no noticeable loss of qubit coherence under continuous photon scattering on the ion core, paving the way for laser cooling and imaging of Rydberg atoms. Our results demonstrate access to weak electron-electron interactions in Rydberg atoms and expand the quantum simulation toolbox for optical control of highly excited circular state qubits via ionic core manipulation.
Circular Rydberg atoms (CRAs), i.e., Rydberg atoms with maximal orbital momentum, ideally combine long coherence times and strong interactions, a key property of quantum systems, in particular for the development of quantum technologies. However, the dipole-dipole interaction between CRAs has not been observed so far. We report the measurement and characterization of the resonant dipole-dipole interaction between two CRAs, individually trapped in optical tweezers, and find excellent agreement with theoretical predictions. We demonstrate a dynamic control over the strength of the interaction by tuning the orientation of an electric field. We use the interaction between the CRAs as a meter for the interatomic distance, and record the relative motion between two atoms in their traps. This motion, that we induce through the interaction between Rydberg levels with permanent electric dipoles, transiently populated during the preparation of the circular states, is a signature of spin-motion coupling.
Alkaline-earth Rydberg atoms are very promising tools for quantum technologies. They benefit from the remarkable properties of Rydberg atoms and, notably, a huge coupling to external fields and to other Rydberg atoms while the ionic core retains an optically active electron. However, low angular-momentum Rydberg states suffer almost immediate autoionization when the core is excited. Classically, the two electrons “collide” and one is expelled. However, this is not the case for circular states. Here, we demonstrate that Strontium circular Rydberg atoms with a core excited in a 4d metastable level are stable for more than a few milliseconds. We verify this property while the ionic core is either in a 4d, j = 3/2 state or a 4d, j = 5/2 state. Furthermore, we measure the energy difference between the Zeeman sublevels of metastable 4d states of the ionic-core electron, resulting from the electric-quadrupole coupling between the two valence electrons, with one prepared in a Rydberg state. We show that the energy difference is a function of the principal and magnetic quantum numbers of the Rydberg electron. We show that this coupling between the two valence electrons leads to control the state of one depending on the state of the other. This opens the way to detect non-destructively the state of the Rydberg atom. Using the fluorescence emitted by the core electron allows us to envision a selective, optical detection of the circular states with remarkable sensitivity. The results presented in this work are important in the context of the realization of a Rydberg quantum simulator, exploiting the circular states of Strontium to build the qubits.