Abstract
Trapped-ion optical clocks are capable of achieving systematic fractional frequency uncertainties of 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, scalable platform for extending clock spectroscopy to arrays of Coulomb crystals consisting of several tens of ions while allowing systematic shifts as low as . We observe three-dimensional excess micromotion amplitudes inside a Coulomb crystal with atomic spatial resolution and subnanometer amplitude uncertainties, and show that in ion Coulomb crystals of length and 2 mm, time-dilation shifts of ions due to micromotion can be close to and below , respectively. In previous ion traps, excess micromotion would have dominated the uncertainty budget for spectroscopy of even a few ions. By minimizing its contribution and providing a means to quantify it, we open up a path to precision spectroscopy in many-body ion systems, enabling entanglement-enhanced ion clocks and providing a well-controlled, strongly coupled quantum system.
- Received 24 March 2018
- Revised 21 October 2018
DOI:https://doi.org/10.1103/PhysRevApplied.11.011002
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