Analysis of collision shift assessments in ion-based clocks
M. D. Barrett, K. J. Arnold
TL;DR
The paper addresses collision-induced frequency shifts in ion-based clocks by unifying classical Langevin and quantum treatments within a simple interaction model, showing that the shift is bounded by the Langevin collision rate diminished by a recoil-induced suppression factor. It introduces the Ramsey Suppression Factor (RSF) to quantify laser–ion decoupling due to recoil and derives bounds that apply to any single-ion clock, with consistent results across hard-sphere and Lennard-Jones potentials. The study demonstrates that glancing collisions contribute negligibly to the clock shift, while the dominant effect arises from the loss of laser coupling during recoil, enabling a practical, analytic bound without heavy molecular-potential calculations. The bound is robust against reasonable short-range potential details and provides a clear path to experimentally measure collision rates via RSF, with important implications for achieving accuracies near the $10^{-19}$ level and for evaluating pressures in vacuum systems. Overall, the work offers a tractable framework for estimating and bounding collision shifts in ion clocks, bridging classical intuition and quantum scattering theory, and guiding future refinements through molecular-potential physics.
Abstract
We consider back-ground gas collision shifts in ion-based clocks. We give both a classical and quantum description of a collision between an ion and a polarizable particle with a simple hard-sphere repulsion. Both descriptions give consistent results, which shows that a collision shift bound is determined by the classical Langevin collision rate reduced by a readily calculated factor describing the decoupling of the clock laser from the ion due to the recoil motion. We also show that the result holds when using a more general Lennard-Jones potential to describe the interaction between the ion and its collision partner. This leads to a simple bound for the collision shift applicable to any single ion clock without resorting to large-scale Monte-Carlo simulations or determination of molecular potential energy curves describing the collision. It also provides a relatively straightforward means to measure the relevant collision rate.
