We report precise measurements of inter-level interactions in a bosonic optical lattice clock based on
88Sr atoms. We observe a nonlinear density dependence of the clock shift, even without reaching quantum degeneracy. In a 2D lattice, the Rabi line shape exhibits an interaction sideband consistent with a collective spin model, while in a 1D lattice the shift is modified by density-induced dephasing. These findings, combined with a careful choice of interrogation detuning and atomic density, can enable operation at a net-zero systematic density shift in
88Sr lattice clocks. We discuss the implications of these findings in many-body physics, quantum simulation, and precision isotope shift measurements, which provide a powerful probe for new physics beyond the Standard Model.
Atoms deeply trapped in magic wavelength optical lattices provide a Doppler- and collision-free dense ensemble of quantum emitters ideal for high-precision spectroscopy and they are the basis of some of the best optical atomic clocks to date. However, despite their minute optical dipole moments the inherent long-range dipole-dipole interactions in such lattices still generate line shifts, dephasing and modified decay. We show that in a perfectly filled lattice line shifts and decay are resonantly enhanced depending on the lattice constant and geometry. Potentially, this yields clock shifts of many atomic linewidths and reduces the measurement by optimizing the lattice geometry. Such collective effects can be tailored to yield zero effective shifts and prolong dipole lifetimes beyond the single-atom decay. In particular, we identify dense 2D hexagonal or square lattices as the most promising configurations for an accuracy and precision well below the independent ensemble limit. This geometry should also be an ideal basis for related applications such as superradiant lasers, precision magnetometry or long-lived quantum memories.
We experimentally and theoretically determine the magic wavelength of the (5s^{2})^{1}S_{0}-(5s5p)^{3}P_{0} clock transition of ^{111}Cd to be 419.88(14) and 420.1(7) nm. To perform Lamb-Dicke spectroscopy of the clock transition, we use narrow-line laser cooling on the ^{1}S_{0}-^{3}P_{1} transition to cool the atoms to 6 μK and load them into an optical lattice. Cadmium is an attractive candidate for optical lattice clocks because it has a small sensitivity to blackbody radiation and its efficient narrow-line cooling mitigates higher order light shifts. We calculate the blackbody shift, including the dynamic correction, to be fractionally 2.83(8)×10^{-16} at 300 K, an order of magnitude smaller than that of Sr and Yb. We also report calculations of the Cd ^{1}P_{1} lifetime and the ground state C_{6} coefficient.