Rotational spectroscopy of cold, trapped molecular ions in the Lamb-Dicke regime

TL;DR

This paper introduces a novel Doppler-free rotational spectroscopy method for cold, trapped molecular ions, achieving unprecedented resolution and precision, enabling advanced tests of molecular theory and fundamental constants.

Contribution

The authors develop a general approach using ion trapping and crystallization to reach the Lamb-Dicke regime for molecular rotations, significantly improving spectroscopic resolution.

Findings

Achieved a fractional line width of 1×10^{-9}

Demonstrated the most precise test of ab initio molecular theory

Performed the most precise proton mass measurement

Abstract

Sympathetic cooling of trapped ions has been established as a powerful technique for manipulation of non-laser-coolable ions (Raizen1992,Waki1992,Bowe1999,Barrett2003). For molecular ions, it promises vastly enhanced spectroscopic resolution and accuracy. However, this potential remains untapped so far, with the best resolution achieved being not better than $5\times10^{-8}$ fractionally, due to residual Doppler broadening being present in ion clusters even at the lowest achievable translational temperatures (Bressel2012). Here we introduce a general and accessible approach that enables Doppler-free rotational spectroscopy. It makes use of the strong radial spatial confinement of molecular ions when trapped and crystallized in a linear quadrupole trap, providing the Lamb-Dicke regime for rotational transitions. We achieve a line width of $1\times10^{-9}$ fractionally and $1.3~\textrm{kHz}$ absolute, an improvement by $50$ and nearly $3\times10^{3}$, respectively, over other methods. The systematic uncertainty is $2.5\times10^{-10}$. As an application, we demonstrate the most precise test of $\textit{ab initio}$ molecular theory and the most precise ($1.3~\textrm{PPB}$) spectroscopic determination of the proton mass. The results represent the long overdue extension of Doppler-free microwave spectroscopy of laser-cooled atomic ion clusters (Berkeland1998) to higher spectroscopy frequencies and to molecules. This approach enables a vast range of high-precision measurements on molecules, both on rotational and, as we project, vibrational transitions.