No Arabic abstract
Collisions between cold molecules are essential for studying fundamental aspects of quantum chemistry, and may enable formation of quantum degenerate molecular matter by evaporative cooling. However, collisions between trapped, naturally occurring molecules have so far eluded direct observation due to the low collision rates of dilute samples. We report the first directly observed collisions between cold, trapped molecules, achieved without the need of laser cooling. We magnetically capture molecular oxygen in a 0.8K x kB deep superconducting trap, and set bounds on the ratio between the elastic and inelastic scattering rates, the key parameter determining the feasibility of evaporative cooling. We further co-trap and identify collisions between atoms and molecules, paving the way to studies of cold interspecies collisions in a magnetic trap.
Measurements of interactions between cold molecules and ultracold atoms can allow for a detailed understanding of fundamental collision processes. These measurements can be done using various experimental geometries including where both species are in a beam, where one species is trapped, or when both species are trapped. Simultaneous trapping offers significantly longer interaction times and an associated increased sensitivity to rare collision events. However, there are significant practical challenges associated with combining atom and molecule systems, which often have competing experimental requirements. Here, we describe in detail an experimental system that allows for studies of cold collisions between ultracold atoms and cold molecules in a dual trap, where the atoms and molecules are trapped using static magnetic and electric fields, respectively. As a demonstration of the systems capabilities, we study cold collisions between ammonia ($^{14}$ND$_{3}$ and $^{15}$ND$_{3}$) molecules and rubidium ($^{87}$Rb and $^{85}$Rb) atoms.
We prepare mixtures of ultracold CaF molecules and Rb atoms in a magnetic trap and study their inelastic collisions. When the atoms are prepared in the spin-stretched state and the molecules in the spin-stretched component of the first rotationally excited state, they collide inelastically with a rate coefficient of $k_2 = (6.6 pm 1.5) times 10^{-11}$ cm$^{3}$/s at temperatures near 100~$mu$K. We attribute this to rotation-changing collisions. When the molecules are in the ground rotational state we see no inelastic loss and set an upper bound on the spin relaxation rate coefficient of $k_2 < 5.8 times 10^{-12}$ cm$^{3}$/s with 95% confidence. We compare these measurements to the results of a single-channel loss model based on quantum defect theory. The comparison suggests a short-range loss parameter close to unity for rotationally excited molecules, but below 0.04 for molecules in the rotational ground state.
We present an experimental and theoretical study of atom-molecule collisions in a mixture of cold, trapped atomic nitrogen and NH molecules at a temperature of $sim 600$~mK. We measure a small N+NH trap loss rate coefficient of $k^{(mathrm{N+NH})}_mathrm{loss} = 8(4) times 10^{-13}$~cm$^{3}$s$^{-1}$. Accurate quantum scattering calculations based on {it 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.
Trapping of atoms and molecules in electrostatic, magnetic and optical traps has enabled studying atomic and molecular interactions on a timescale of many seconds, allowing observations of ultra-cold collisions and reactions. Here we report the first magnetic deceleration and trapping of neutral carbon atoms in a static magnetic trap. When co-trapping the carbon atoms with oxygen molecules in a superconducting trap, the carbon signal decays in a non-exponential manner, consistent with losses resulting from atom-molecule collisions. Our findings pave the way to studying both elastic and inelastic collisions of species that cannot be laser cooled, and specifically may facilitate the observation of reactions at low temperatures, such as C + O2 --> CO + O, which is important in interstellar chemistry.
We present an experimental realization of a moving magnetic trap decelerator, where paramagnetic particles entrained in a cold supersonic beam are decelerated in a co-moving magnetic trap. Our method allows for an efficient slowing of both paramagnetic atoms and molecules to near stopping velocities. We show that under realistic conditions we will be able to trap and decelerate a large fraction of the initial supersonic beam. We present our first results on deceleration in a moving magnetic trap by bringing metastable neon atoms to near rest. Our estimated phase space volume occupied by decelerated particles at final velocity of 50 m/s shows an improvement of two orders of magnitude as compared to currently available deceleration techniques.