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arXiv:1912.08754

Trapped arrays of alkaline earth Rydberg atoms in optical tweezers

Wilson, Jack, Samuel Saskin, Yijian Meng, Shuo Ma, Rohit Dilip, A. P. Burgers, Jeff Thompson

Published Dec 18, 2019• 21 citations
arXivHTMLPDF

Abstract

Neutral atom qubits with Rydberg-mediated interactions are a leading platform for developing large-scale coherent quantum systems. In the majority of experiments to date, the Rydberg states are not trapped by the same potential that confines ground state atoms, resulting in atom loss and constraints on the achievable interaction time. In this work, we demonstrate that the Rydberg states of an alkaline earth atom, ytterbium, can be stably trapped by the same red-detuned optical tweezer that also confines the ground state, by leveraging the polarizability of the Yb$^+$ ion core. Using the previously unobserved \tripletS series, we demonstrate trapped Rydberg atom lifetimes exceeding $100\,μ$s, and observe no evidence of auto- or photo-ionization from the trap light for these states. We measure a coherence time of $T_2 = 59$ $μ$s between two Rydberg levels, exceeding the 28 $μ$s lifetime of untrapped Rydberg atoms under the same conditions. These results are promising for extending the interaction time of Rydberg atom arrays for quantum simulation and computing, and are vital to capitalize on the extended Rydberg lifetimes in circular states or cryogenic environments.

DOI
10.48550/arxiv.1912.08754

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Neutral atom qubits with Rydberg-mediated interactions are a leading platform for developing large-scale coherent quantum systems. In the majority of experiments to date, the Rydberg states are not trapped by the same potential that confines ground state atoms, resulting in atom loss and constraints on the achievable interaction time. In this work, we demonstrate that the Rydberg states of an alkaline earth atom, ytterbium, can be stably trapped by the same red-detuned optical tweezer that also confines the ground state, by leveraging the polarizability of the Yb+^++ ion core. Using the previously unobserved \tripletS series, we demonstrate trapped Rydberg atom lifetimes exceeding 100 μ100\,μ100μs, and observe no evidence of auto- or photo-ionization from the trap light for these states. We measure a coherence time of T2=59T_2 = 59T2​=59 μμμs between two Rydberg levels, exceeding the 28 μμμs lifetime of untrapped Rydberg atoms under the same conditions. These results are promising for extending the interaction time of Rydberg atom arrays for quantum simulation and computing, and are vital to capitalize on the extended Rydberg lifetimes in circular states or cryogenic environments.
Neutral atom qubits with Rydberg-mediated interactions are a leading platform for developing large-scale coherent quantum systems. In the majority of experiments to date, the Rydberg states are not trapped by the same potential that confines ground state atoms, resulting in atom loss and constraints on the achievable interaction time. In this Letter, we demonstrate that the Rydberg states of an alkaline earth atom, ytterbium, can be stably trapped by the same red-detuned optical tweezer that also confines the ground state, by leveraging the polarizability of the Yb^{+} ion core. Using the previously unobserved ^{3}S_{1} series, we demonstrate trapped Rydberg atom lifetimes exceeding 100 μs, and observe no evidence of auto- or photoionization from the trap light for these states. We measure a coherence time of T_{2}=59 μs between two Rydberg levels, exceeding the 28 μs lifetime of untrapped Rydberg atoms under the same conditions. These results are promising for extending the interaction time of Rydberg atom arrays for quantum simulation and computing, and are vital to capitalize on the extended Rydberg lifetimes in circular states or cryogenic environments.
Neutral atom arrays have emerged as a powerful platform for quantum computation, simulation, and metrology.Among them, alkaline-earth-like atoms exhibit distinct advantages, including long coherence time, high-fidelity Rydberg gates, and erasure correction for efficient quantum error correction. However, their scalability has lagged behind that of the alkali atoms. Here, we report 2400 ytterbium-174 atoms trapped in an optical tweezer array with enhanced loading efficiency of 83.5(1)\% via blue-detuned light-assisted collisions. We develop a quantitative model of the collision dynamics and find good agreement between the calculated inelastic collision rates and the experimentally measured loading efficiencies.Notably, the loading efficiency is largely maintained for array sizes ranging from dozens to thousands, exhibiting excellent scalability. We further demonstrate that the enhancement exists robustly across a range of interatomic potentials, suggesting its utility for other atomic species. To establish the capability of the 174^{174}174Yb arrays toward universal quantum computation, we propose to encode the qubit in the ground-clock state manifold and estimate a 99.9\% two-qubit gate fidelity with experimentally feasible parameters. Our work advances the prospects for realizing large-scale quantum computers using alkaline-earth-like atoms.
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
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+.
New experimental quantum simulation platforms have recently been implemented with divalent atoms trapped in optical tweezer arrays, with promising performance.The second valence electron also brings about new prospects through the so-called isolated core excitation (ICE).However, autoionization presents a strong limitation to this use.In this study, we propose and demonstrate a new approach to applying a sizable light shift to a Rydberg state with close-to-resonant ICE while avoiding autoionization.In particular, we investigate the ICE of ytterbium atoms in 1 S 0 Rydberg states.Spectroscopic studies of the induced autoionization and the light shift imparted to the Rydberg states are well accounted for with multichannel quantum defect theory.Such control over the inner electron without disturbing the Rydberg electron brings about a new tool for the targeted coherent manipulation of Rydberg states in quantum simulation or quantum computing experiments performed with alkaline-earth atoms.
We report on the realization of a 133^{133}133Cs optical tweezer array in a cryogenic blackbody radiation (BBR) environment. By enclosing the array within a 4K radiation shield, we measure long Rydberg lifetimes, up to 406(36) μ406 (36)\,μ406(36)μs for the 55P3/255 P_{3/2}55P3/2​ Rydberg state, a factor of 3.3(3) longer than the room-temperature value. We employ single-photon coupling for coherent manipulation of the ground-Rydberg qubit. We measure a small differential dynamic polarizability of the transition, beneficial for reducing dephasing due to light intensity fluctuations. Our results pave the path for advancing neutral-atom two-qubit gate fidelities as their error budgets become increasingly dominated by T1T_1T1​ relaxation of the ground-Rydberg qubit.