Half-minute-scale atomic coherence and high relative stability in a tweezer clock

The preparation of large, low-entropy, highly coherent ensembles of identical quantum systems is fundamental for many studies in quantum metrology1, simulation2 and information3. However, the simultaneous realization of these properties remains a central challenge in quantum science across atomic and condensed-matter systems2,4–7. Here we leverage the favourable properties of tweezer-trapped alkaline-earth (strontium-88) atoms8–10, and introduce a hybrid approach to tailoring optical potentials that balances scalability, high-fidelity state preparation, site-resolved readout and preservation of atomic coherence. With this approach, we achieve trapping and optical-clock excited-state lifetimes exceeding 40 seconds in ensembles of approximately 150 atoms. This leads to half-minute-scale atomic coherence on an optical-clock transition, corresponding to quality factors well in excess of 1016. These coherence times and atom numbers reduce the effect of quantum projection noise to a level that is comparable with that of leading atomic systems, which use optical lattices to interrogate many thousands of atoms in parallel11,12. The result is a relative fractional frequency stability of 5.2(3) × 10−17τ−1/2 (where τ is the averaging time in seconds) for synchronous clock comparisons between sub-ensembles within the tweezer array. When further combined with the microscopic control and readout that are available in this system, these results pave the way towards long-lived engineered entanglement on an optical-clock transition13 in tailored atom arrays. A tweezer clock containing about 150 88Sr atoms achieves trapping and optical excited-state lifetimes exceeding 40 seconds, and shows relative fractional frequency stability similar to that of leading atomic clocks.