We discuss laser-dressed dipolar and van der Waals interactions between atoms and polar molecules, so that a cold atomic gas with laser admixed Rydberg levels acts as a designed reservoir for both elastic and inelastic collisional processes. The elastic scattering channel is characterized by large elastic scattering cross sections and repulsive shields to protect from close encounter collisions. In addition, we discuss a dissipative (inelastic) collision where a spontaneously emitted photon carries away (kinetic) energy of the collision partners, thus providing a significant energy loss in a single collision. This leads to the scenario of rapid thermalization and cooling of a molecule in the mK down to the μK regime by cold atoms.
Atom-ion interactions occur through the electric dipole which is induced by the ion on the neutral atom. In a Langevin collision, in which the atom and ion overcome the centrifugal barrier and reach a short internuclear distance, their internal electronic states deform due to their interaction and can eventually alter. Here we explore the outcome products and the energy released from a single Langevin collision between a single cold
88Sr
+ ion initialized in the metastable
4d2D5/2,3/2 states, and a cold
87Rb atom in the
5s2S1/2 ground state. We found that the long-lived
D5/2 and
D3/2 states quench after roughly three Langevin collisions, transforming the excitation energy into kinetic energy. We identify two types of collisional quenching. One is an Electronic Excitation-Exchange process, during which the ion relaxes to the
S state and the atom is excited to the
P state, followed by energy release of
∼ 3000 K
⋅k
B. The second is Spin-Orbit Change where the ion relaxes from the higher fine-structure
D5/2 level to the lower
D3/2 level releasing
∼ 400 K
⋅k
B into kinetic motion. These processes are theoretically understood to occur through Landau-Zener avoided crossings between the different molecular potential curves. We also found that these relaxation rates are insensitive to the mutual spin orientation of the ion and atoms. This is explained by the strong inertial Coriolis coupling present in ultracold atom-ion collisions due to the high partial wave involved, which strongly mixes different angular momentum states. This inertial coupling explains the loss of the total electronic angular-momentum which is transferred to the external rotation of nuclei. Our results provide deeper understanding of ultracold atom-ion inelastic collisions and offer additional quantum control tools for the cold chemistry field.
We present an experimental and theoretical study of atom-molecule collisions in a mixture of cold, trapped N atoms and NH molecules at a temperature of $\ensuremath{\sim}600\text{ }\text{ }\mathrm{mK}$. We measure a small
N+NH trap loss rate coefficient of ${k}_{\mathrm{loss}}^{(\mathrm{N}+\mathrm{NH})}=9(5)(3)\ifmmode\times\else\texttimes\fi{}{10}^{\ensuremath{-}13}\text{ }\text{ }{\mathrm{cm}}^{3}\text{ }{\mathrm{s}}^{\ensuremath{-}1}$. Accurate quantum scattering calculations based on ab initio interaction potentials are in agreement with experiment and indicate the magnetic dipole interaction to be the dominant loss mechanism. Our theory further indicates the ratio of
N+NH elastic-to-inelastic collisions remains large (
>100) into the mK regime.