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arXiv:2505.06440 · Physical Review A

Direct measurement of the P 0 3 clock state natural lifetime in Sr 87

Jonathan Dolde, D. Ganapathy, Xin Zheng, Shuo Ma, K. Beloy, Shimon Kolkowitz

Published Jul 29, 2025• 4 citations
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Abstract

Optical lattice clocks based on the narrow ( 5 s 2 ) S 0 1 − ( 5 s 5 p ) P 0 3 transition in neutral strontium (Sr) are among the most precise and accurate measurement devices in existence. Although this transition is completely forbidden by selection rules, state mixing from the hyperfine interaction in Sr 87 provides a weakly allowed transition that can be coherently driven with practical clock laser intensities. While the coherent interrogation times of optical clocks are typically set by the linewidth of the probe laser, this limitation can be overcome in synchronous differential comparisons between ensembles. In such measurements the natural lifetime of the S 0 1 – P 0 3 clock transition becomes the fundamental limiting factor to the duration of a single run of the experiment. However, a direct measurement of the decay rate of the clock excited state is quite challenging due to the competing effects of other loss channels such as Raman scattering, inelastic collisions, and atom loss due to background gas. In this work, we monitor the decay of Sr atoms trapped in an optical lattice and initialized in the P 0 3 state. By making measurements of high and low density ensembles of both Sr 87 and Sr 88 across varying lattice trap depths, we isolate radiative decay, which accounts for a significant fraction of the observed decays at low depths. We obtain a natural radiative decay lifetime of 167 − 40 + 79 s for the P 0 3 clock state in Sr 87 , a value that is consistent with previously reported measurements and theoretical predictions. We also introduce an additional measurement scheme that involves repeated measurements of the ground-state population within a single experimental sequence, validating our model and the consistency of the measured rates. We expect that the techniques introduced in this work are applicable to lifetime measurements of long-lived metastable states in other atoms and ions used for clocks and quantum computing. The results presented in this work inform performance estimates of proposed gravitational wave detectors and long-baseline atom interferometers making use of Sr 87 .

DOI
10.1103/f6pt-flnt

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Optical lattice clocks based on the narrow ( 5 s 2 ) S 0 1 − ( 5 s 5 p ) P 0 3 transition in neutral strontium (Sr) are among the most precise and accurate measurement devices in existence. Although this transition is completely forbidden by selection rules, state mixing from the hyperfine interaction in Sr 87 provides a weakly allowed transition that can be coherently driven with practical clock laser intensities. While the coherent interrogation times of optical clocks are typically set by the linewidth of the probe laser, this limitation can be overcome in synchronous differential comparisons between ensembles. In such measurements the natural lifetime of the S 0 1 – P 0 3 clock transition becomes the fundamental limiting factor to the duration of a single run of the experiment. However, a direct measurement of the decay rate of the clock excited state is quite challenging due to the competing effects of other loss channels such as Raman scattering, inelastic collisions, and atom loss due to background gas. In this work, we monitor the decay of Sr atoms trapped in an optical lattice and initialized in the P 0 3 state. By making measurements of high and low density ensembles of both Sr 87 and Sr 88 across varying lattice trap depths, we isolate radiative decay, which accounts for a significant fraction of the observed decays at low depths. We obtain a natural radiative decay lifetime of 167 − 40 + 79 s for the P 0 3 clock state in Sr 87 , a value that is consistent with previously reported measurements and theoretical predictions. We also introduce an additional measurement scheme that involves repeated measurements of the ground-state population within a single experimental sequence, validating our model and the consistency of the measured rates. We expect that the techniques introduced in this work are applicable to lifetime measurements of long-lived metastable states in other atoms and ions used for clocks and quantum computing. The results presented in this work inform performance estimates of proposed gravitational wave detectors and long-baseline atom interferometers making use of Sr 87 .
Optical atomic clocks have spurred a range of precision frequency comparison experiments and proposals including tests of general relativity, gravitational wave detection, and relativistic geodesy. Current measurements using optical atomic clocks are often limited by the coherence of the clock laser rather than the atomic samples used as a frequency reference. In order to overcome the performance limits imposed by clock laser coherence, we realize a multiplexed optical clock system where multiple spatially resolved ensembles each consisting of thousands of strontium atoms trapped in a 1D optical lattice function as separate atomic frequency references that can be simultaneously interrogated with a shared clock laser. This scheme allows us to make differential frequency comparisons with a quantum projection noise limited fractional instability of 9.7(4)×10−18/ √τ and a differential fractional uncertainty of 8.9×10−20 after 3.3 hours of averaging. We then use this system to perform a lab-based test of the gravitational redshift at the centimeter scale, where we measure a fractional frequency gradient of [−12.4±0.7stat ±2.5sys]×10−19/cm, consistent with the predicted value of 10.9×10−19/cm. Having demonstrated that our differential comparisons are no longer limited by the local oscillator, we turn to fundamental limits on atom–atom coherence. We perform a direct decay measurement of the natural lifetime of the excited clock state 3P0 in 87Sr, in which we use measurements of simultaneously loaded high and low density atomic ensembles and compare decay rates of 87Sr and 88Sr to help isolate natural lifetime decay from other population dynamics. We measure a lifetime of 167+79 −40, which is consistent with previously reported experimental and theoretical values. Lastly, we demonstrate a hyperfine-resolved readout scheme in 87Sr that converts depolarization errors during interrogation into erasure errors, extending coherence times between ensembles in our optical lattice clock up to 150s using spin-echo measurements. These results taken together demonstrate the advantages of differential clock measurements that aren’t limited by clock laser coherence and how to characterize and improve on the performance limits that arise in that regime.
Cavity-QED determination of the natural linewidth of the 87^{87}87Sr millihertz clock transition with 30μ\muμHz resolution
We present a new method for determining the intrinsic natural linewidth or lifetime of exceptionally long-lived optical excited states. Such transitions are key to the performance of state-of-the-art atomic clocks, have potential applications in searches for fundamental physics and gravitational wave detectors, as well as novel quantum many-body phenomena. With longer lifetime optical transitions, sensitivity is increased, but so far it has proved challenging to determine the natural lifetime of many of these long lived optical excited states because standard population decay detection techniques become experimentally difficult. Here, we determine the ratio of a poorly known ultranarrow linewidth transition (3^33P0_00​ to 1^11S0_00​ in 87^{87}87Sr) to that of another narrow well known transition (3^33P1_11​ to 1^11S0_00​) by coupling the two transitions to a single optical cavity and performing interleaved nondestructive measurements of the interaction strengths of the atoms with cavity modes near each transition frequency. We use this approach to determine the natural linewidth of the clock transition 3^33P0_00​ to 1^11S0_00​ in 87^{87}87Sr to be γ0/(2π)=1.35(3) \gamma_0/(2\pi) = 1.35(3)~γ0​/(2π)=1.35(3) mHz or τ=118(3) \tau= 118(3)~τ=118(3) s. The 30 μ~\mu μHz resolution implies that we could detect states with lifetimes just below 2 hours, and with straightforward future improvements, we could detect states with lifetimes up to 15 hours, using measurement trials that last only a few hundred milliseconds, eliminating the need for long storage times in optical potentials.
We explore the limits of atomic coherence and measurement precision in a ^{87}Sr optical lattice clock. We perform a detailed characterization of key effects, including lattice Raman scattering and atomic collisions in a shallow lattice configuration, determining a 174(28) s ^{3}P_{0} clock state lifetime. Investigation of atomic coherence across a range of lattice depths and atomic densities reveals decoherence mechanisms related to photon scattering and atomic interaction. At a reduced density, we observe a coherence time of 118(9) s, approaching the fundamental limit set by spontaneous emission. Guided by this coherence understanding, we demonstrate a clock instability for an atomic ensemble of 1.5×10^{-18} at 1 s in fractional frequency units. Our results are important for further advancing the state of the art of an optical lattice clock for fundamental physics applications.
Increasing coherent interrogation times is central to advancing the precision of optical clocks. Synchronous differential optical clock comparisons have now demonstrated atomic coherence times that far exceed the coherence time of the clock laser. While atom coherence times are then primarily limited by errors induced by lattice Raman scattering, excited clock state radiative decay, and broadening from two-body collisions, many of these errors take the atoms out of the clock transition subspace, and can therefore be converted into “erasure” errors if the appropriate readout scheme is employed. Here we experimentally demonstrate a hyperfine-resolved readout technique for 87 Sr optical lattice clocks that mitigates decoherence from Raman scattering induced by the lattice as well as radiative decay. By employing hyperfine-resolved readout in synchronous differential comparisons between 87 Sr ensembles with both Ramsey and spin-echo spectroscopy sequences, we achieve enhanced atomic coherence times exceeding 100 and 150 s, respectively, enabling longer coherent measurements without a reduction in performance. We anticipate that this hyperfine-resolved readout technique will benefit applications of state-of-the-art optical lattice clock comparisons in which the coherence times are constrained by Raman scattering or radiative decay.
We report an optical lattice clock with a total systematic uncertainty of 8.1×10^{-19} in fractional frequency units, representing the lowest uncertainty of any clock to date. The clock relies on interrogating the ultranarrow ^{1}S_{0}→^{3}P_{0} transition in a dilute ensemble of fermionic strontium atoms trapped in a vertically-oriented, shallow, one-dimensional optical lattice. Using imaging spectroscopy, we previously demonstrated record high atomic coherence time and measurement precision enabled by precise control of collisional shifts and the lattice light shift. In this work, we revise the black body radiation shift correction by evaluating the 5s4d ^{3}D_{1} lifetime, necessitating precise characterization and control of many body effects in the 5s4d ^{3}D_{1} decay. Last, we measure the second order Zeeman coefficient on the least magnetically sensitive clock transition. All other systematic effects have uncertainties below 1×10^{-19}.
We explore the limits of atomic coherence and measurement precision in a 87Sr optical lattice clock. We perform a detailed characterization of key effects, including lattice Raman scattering and atomic collisions in a shallow lattice configuration, determining a 174(28) s 3P0 clock state lifetime. Investigation of atomic coherence across a range of lattice depths and atomic densities reveals decoherence mechanisms related to photon scattering and atomic interaction. At a reduced density, we observe a coherence time of 118(9) s, approaching the fundamental limit set by spontaneous emission. Guided by this coherence understanding, we demonstrate a clock instability of 1.5E-18 at 1 s in fractional frequency units. Our results are important for further advancing the state-of-the-art of an optical lattice clock for fundamental physics applications.