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arXiv:2205.15484 · Nature Communications

Prospects of a thousand-ion Sn2+ Coulomb-crystal clock with sub-10−19 inaccuracy

David R. Leibrandt, S. G. Porsev, Charles Cheung, Marianna S. Safronova

Published Jul 5, 2024• 24 citations
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Abstract

Abstract Optical atomic clocks are the most accurate and precise measurement devices of any kind, enabling advances in international timekeeping, Earth science, fundamental physics, and more. However, there is a fundamental tradeoff between accuracy and precision, where higher precision is achieved by using more atoms, but this comes at the cost of larger interactions between the atoms that limit the accuracy. Here, we propose a many-ion optical atomic clock based on three-dimensional Coulomb crystals of order one thousand Sn2+ ions confined in a linear RF Paul trap with the potential to overcome this limitation. Sn2+ has a unique combination of features that is not available in previously considered ions: a 1S0 ↔ 3P0 clock transition between two states with zero electronic and nuclear angular momentum (I = J = F = 0) making it immune to nonscalar perturbations, a negative differential polarizability making it possible to operate the trap in a manner such that the two dominant shifts for three-dimensional ion crystals cancel each other, and a laser-accessible transition suitable for direct laser cooling and state readout. We present calculations of the differential polarizability, other relevant atomic properties, and the motion of ions in large Coulomb crystals, in order to estimate the achievable accuracy and precision of Sn2+ Coulomb-crystal clocks.

DOI
10.1038/s41467-024-49241-w

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Abstract Optical atomic clocks are the most accurate and precise measurement devices of any kind, enabling advances in international timekeeping, Earth science, fundamental physics, and more. However, there is a fundamental tradeoff between accuracy and precision, where higher precision is achieved by using more atoms, but this comes at the cost of larger interactions between the atoms that limit the accuracy. Here, we propose a many-ion optical atomic clock based on three-dimensional Coulomb crystals of order one thousand Sn2+ ions confined in a linear RF Paul trap with the potential to overcome this limitation. Sn2+ has a unique combination of features that is not available in previously considered ions: a 1S0 ↔ 3P0 clock transition between two states with zero electronic and nuclear angular momentum (I = J = F = 0) making it immune to nonscalar perturbations, a negative differential polarizability making it possible to operate the trap in a manner such that the two dominant shifts for three-dimensional ion crystals cancel each other, and a laser-accessible transition suitable for direct laser cooling and state readout. We present calculations of the differential polarizability, other relevant atomic properties, and the motion of ions in large Coulomb crystals, in order to estimate the achievable accuracy and precision of Sn2+ Coulomb-crystal clocks.
Clocks have been among the most accurate man-made devices for centuries. Atomic clocks, which have been defining time by means of a microwave transition in the 133Cs atom since 1967, represent a major step in this development. A redefinition of the SI unit of time based on optical atomic clocks is currently under discussion. This forthcoming redefinition requires, among other criteria, the repeated demonstration of the consistency of different optical frequency standards in the low 10−18 range. In this work, the first evaluation of the systematic shifts and their uncertainties in a 115In+–172Yb+ Coulomb crystal clock is presented. This clock utilizes the 1S0 ↔ 3P0 transition in 115In+. 172Yb+ ions are co-trapped with the 115In+ ions in a segmented Paul trap and used for sympathetic cooling. With a systematic uncertainty of 2.5×10−18 when operating with a 1In+–3Yb+ crystal and 2.6×10−18 when operating with a 2In+–4Yb+ crystal, this clock is one of the most accurate clocks in the world. In addition, the operation of the clock with multiple clock ions is the first of its kind at this level of uncertainty. Measurements with up to four clock ions show a reduction in instability from 1.6×10−15/√ τ for a single indium ion to 9.2(4)×10−16/√τ when operating with four indium ions. By using an additional quench laser, the instability in another series of measurements was reduced from a single-ion instability of 1.5×10−15/√ τ to a four-ion instability of 7.1(15)×10−16/√τ , which is consistent with the expected scaling of 1/√N with the number of clock ions N. In this work, the hyperfine structure of the 3P0 ↔ 1P1 transition used for quenching was also resolved for the first time and the hyperfine constants were determined to be AHFS = 265.42(75)MHz and BHFS = 291.4(135) MHz. In frequency comparisons with other clocks, the optical frequency ratios 115In+/171Yb+(E3) and 115In+/87Sr were determined. With a relative total uncertainty of 4.2 × 10−18, the former ratio is the most accurate frequency ratio of different species published to date. It is also the first to meet one of the requirements defined on the roadmap for redefining the SI unit of the second: Measurements of frequency ratios with relative total measurement uncertainties below 5 × 10−18. The determination of the absolute frequency results in an uncertainty of 1.3 × 10−16 for the 1S0 ↔ 3P0 transition in 115In+, which is limited by that of the cesium fountains. The results obtained summarized: ν115In+ ν171Yb+(E3) =1.973 773 591 557 215 788(8) ν115In+ ν87Sr =2.952 748 749 874 860 781(27) ν115In+ =1 267 402 452 901 038.87(16) Hz
Trapped-ion optical clocks are capable of achieving systematic fractional frequency uncertainties of 10−1810^{-18}10−18 and possibly below. However, the stability of current ion clocks is fundamentally limited by the weak signal of single-ion interrogation. We present an operational, versatile platform for extending clock spectroscopy to arrays of Coulomb crystals consisting of several tens of ions, while allowing systematic shifts as low as 10−1910^{-19}10−19. The concept is applicable to all clock transitions with low differential electric quadrupole moments. We observe 3D excess micromotion amplitudes of all individual ions inside a Coulomb crystal with nm resolution and prove that the related frequency shifts can be controlled simultaneously at the 10−1910^{-19}10−19 level. Using this method, we demonstrate regions of 400400400 μ\muμm and 222 mm length in our trap array with time dilation shifts due to micromotion close to 1×10−191\times10^{-19}1×10−19 and below 10−1810^{-18}10−18, respectively. Further measurements of the trapping environment and cooling dynamics calculations for mixed In+{}^++ / Yb+{}^++ crystals show that achievable clock uncertainties due to multi-ion operation in our setup are below 1×10−191\times10^{-19}1×10−19. This work will enable clock operation with multiple ions and open up the possibility of new interrogation schemes which allow optical clock stabilities beyond classical limits.
We investigate the feasibility of precision frequency metrology with large ion crystals. For clock candidates with a negative differential static polarizability, we show that micromotion effects should not impede the performance of the clock. Using Lu+{\mathrm{Lu}}^{+}Lu+ as a specific example, we show that quadrupole shifts due to the electric fields from neighboring ions do not significantly affect clock performance. We also show that effects from the tensor polarizability can be effectively managed with a compensation laser at least for a small number of ions ($\ensuremath{\lesssim}{10}^{3}$). These results provide new possibilities for ion-based atomic clocks, allowing them to achieve stability levels comparable to neutral atoms in optical lattices and a viable path to greater levels of accuracy.
The electronic and motional degrees of freedom of trapped ions can be controlled and coherently coupled on the level of individual quanta.Assembling complex quantum systems ion by ion while keeping this unique level of control remains a challenging task.For many applications, linear chains of ions in conventional traps are ideally suited to address this problem.However, driven motion due to the magnetic or radio-frequency electric trapping fields sometimes limits the performance in one dimension and severely affects the extension to higher-dimensional systems.Here, we report on the trapping of multiple barium ions in a single-beam optical dipole trap without radio-frequency or additional magnetic fields.We study the persistence of order in ensembles of up to six ions within the optical trap, measure their temperature, and conclude that the ions form a linear chain, commonly called a one-dimensional Coulomb crystal.As a proof-of-concept demonstration, we access the collective motion and perform spectrometry of the normal modes in the optical trap.Our system provides a platform that is free of driven motion and combines advantages of optical trapping, such as state-dependent confinement and nanoscale potentials, with the desirable properties of crystals of trapped ions, such as long-range interactions featuring collective motion.Starting with small numbers of ions, it has been proposed that these properties would allow the experimental study of many-body physics and the onset of structural quantum phase transitions between one-and two-dimensional crystals.
Optical clocks have garnered widespread attention due to their unparalleled precision in the fields of time-frequency standards, geodetic measurements, and fundamental physics research. Among recent advances, highly charged ion (HCI)-based optical clocks have attracted significant scientific interest owing to their remarkable insensitivity to electromagnetic perturbations and enhanced sensitivity to potential variations of the fine-structure constant $(\ensuremath{\alpha})$. Although the recent successful demonstration of an Ar13+{\mathrm{Ar}}^{13+}Ar13+ optical clock has validated the feasibility of HCI-based systems, Ni12+{\mathrm{Ni}}^{12+}Ni12+ (featuring an ultranarrow clock transition linewidth) stands out as a superior candidate for achieving HCI optical clocks with ${10}^{\ensuremath{-}19}$ level uncertainty and stability. In this work, we report the Coulomb crystallization of highly charged nickel ions (Ni-HCIs). Through a precise deceleration and sympathetic cooling protocol in a room-temperature linear Paul trap, high-energy Ni-HCI bunches were sympathetically cooled from megakelvin energies down to the hundred-millikelvin range using laser-cooled Be+{\mathrm{Be}}^{+}Be+ ions. This work represents a pivotal step toward the realization of an optical clock based on Ni12+{\mathrm{Ni}}^{12+}Ni12+ ion.
We report on the design of a segmented linear Paul trap for optical clock applications using trapped ion Coulomb crystals. For an optical clock with an improved short-term stability and a fractional frequency uncertainty of 10−18, we propose 115In+ ions sympathetically cooled by 172Yb+. We discuss the systematic frequency shifts of such a frequency standard. In particular, we elaborate on high-precision calculations of the electric radiofrequency field of the ion trap using the finite element method. These calculations are used to find a scalable design with minimized excess micromotion of the ions at a level at which the corresponding second-order Doppler shift contributes less than 10−18 to the relative uncertainty of the frequency standard.