We explore the potential of direct spectroscopy of ultra-narrow optical transitions of atoms localized in an optical cavity. In contrast to stabilization against a reference cavity, which is the approach currently used for the most highly stabilized
lasers, stabilization against an atomic transition does not suffer from Brownian thermal noise. Spectroscopy of ultra-narrow optical transitions in a cavity operates in a very highly saturated regime in which non-linear effects such as bistability play an important role. From the universal behavior of the Jaynes-Cummings model with dissipation, we derive the fundamental limits for laser stabilization using direct spectroscopy of ultra-narrow atomic lines. We find that with current lattice clock experiments, laser linewidths of about 1 mHz can be achieved in principle, and the ultimate limitations of this technique are at the 1 $mu$ Hz level.
We investigate the influence of atomic motion on precision Rabi spectroscopy of ultracold fermionic atoms confined in a deep, one dimensional (1D) optical lattice. We analyze the spectral components of longitudinal sideband spectra and present a mode
l to extract information about the transverse motion and sample temperature from their structure. Rabi spectroscopy of the clock transition itself is also influenced by atomic motion in the weakly confined transverse directions of the optical lattice. By deriving Rabi flopping and Rabi lineshapes of the carrier transition, we obtain a model to quantify trap state dependent excitation inhomogeneities. The inhomogeneously excited ultracold fermions become distinguishable, which allows s-wave collisions. We derive a detailed model of this process and explain observed density shift data in terms of a dynamic mean field shift of the clock transition.
At ultracold temperatures, the Pauli exclusion principle suppresses collisions between identical fermions. This has motivated the development of atomic clocks using fermionic isotopes. However, by probing an optical clock transition with thousands of
lattice-confined, ultracold fermionic Sr atoms, we have observed density-dependent collisional frequency shifts. These collision effects have been measured systematically and are supported by a theoretical description attributing them to inhomogeneities in the probe excitation process that render the atoms distinguishable. This work has also yielded insights for zeroing the clock density shift.
