Monika Leibscher

We suggest a protocol for the sympathetic cooling of a molecular asymmetric top rotor co-trapped with laser-cooled atomic ions, based on resonant coupling between the molecular ion's electric dipole moment and a common normal mode of the trapped particles. By combining sympathetic sideband laser cooling with coherent microwave excitation, we demonstrate the efficient depopulation of arbitrary rotational subspaces and the ability to cool an incoherent distribution of rotational states into a single, well-defined quantum state. This capability opens the door to exploiting the rotational Hilbert space for applications in quantum information processing and high-precision spectroscopy.

Planar rotors can be realized by confining molecular ions or charged nanoparticles together with atomic ions in a Paul trap. We study the case of molecular ions or charged nanoparticles that have an electric dipole moment which couples to modes of the common vibrational motion in the trap. We calculate the strength of the coupling with specific vibrational modes for rotor masses ranging from $10^2$ atomic units, as typical for diatomic molecules, to $10^{6}\,$ atomic units, corresponding to nanoclusters. Either, the coupling manifests as a resonant energy exchange between rotational states and one of ion crystal vibrational modes. Or, in the off-resonant case, the dipole-phonon coupling results in energy shifts. In both cases we discuss how the effect may be experimentally detected using sideband-resolved laser spectroscopy and measurements of decoherence.