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arXiv:2006.08388 · New Journal of Physics

Low-energy collisions between carbon atoms and oxygen molecules in a magnetic trap

Michael Karpov, Martin Pitzer, Yair Segev, Julia Narevicius, Edvardas Narevicius

Published Oct 1, 2020• 12 citations
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Abstract

Abstract 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 the decay model describing 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.

DOI
10.1088/1367-2630/abc391

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Abstract 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 the decay model describing 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.
Synopsis We decelerate and trap molecular oxygen using time-dependent magnetic fields and superconducting magnets. The density-dependent, non-exponential decay in particle number provides a clear proof of molecule-molecule collisions within the trapped ensemble. The spatial distribution of molecules in the trap is found to change over time, allowing to set limits on the ratio between the elastic and inelastic collision cross sections. Our experimental scheme opens up new possibilities for studying quantum effects in chemistry as well as for evaporative cooling of molecules.
Abstract Collisions between cold molecules are essential for studying fundamental aspects of quantum chemistry, and may enable the formation of quantum degenerate molecular matter by evaporative cooling. However, collisions between trapped, naturally occurring molecules have not been directly observed so far owing to the low collision rates of dilute samples. Here we report the direct observation of collisions between cold trapped molecules, without the need for laser cooling. We magnetically capture molecular oxygen in an 800-millikelvin-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 atoms and molecules and identify collisions between them, paving the way for studies of cold interspecies collisions in a magnetic trap.
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 down 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 a final velocity of 50 m s -1 shows an improvement of two orders of magnitude as compared to currently available deceleration techniques.Cold chemistry (at temperature of ∼1 K) is a fast developing field with many interesting theoretical predictions yet only a few experiments [1][2][3][4].It has been predicted that in the cold chemistry regime, reactions might proceed through resonance states [5] and both reaction rate and path could be controlled [6] via external magnetic or electrostatic fields.Low-temperature chemistry is not limited to artificially created conditions alone but occurs naturally at the low temperature of interstellar space [7] and the atmospheres of remote planets and moons [8].It is anticipated that cold chemistry will follow the enormous progress in molecular chemistry that was spurred by the advent of supersonic beams more than half a century ago [9].However, the progress in experimental cold chemistry is rather slow partly due to the absence of a general method of atomic and molecular cooling.Although the low-temperature environment created within a supersonic expansion has been used to observe many reactions [10], a direct 1 Author to whom any correspondence should be addressed.
We demonstrate simultaneous deceleration and trapping of a cold atomic and molecular mixture. This is the first step towards studies of cold atom-molecule collisions at low temperatures as well as application of sympathetic cooling. Both atoms and molecules are cooled in a supersonic expansion and are loaded into a moving magnetic trap that brings them to rest via the Zeeman interaction from an initial velocity of 375 m/s. We use a beam seeded with molecular oxygen, and entrain it with lithium atoms by laser ablation prior to deceleration. The deceleration ends with loading of the mixture into a static quadrupole trap, which is generated by two permanent magnets. We estimate 10^{9} trapped O_{2} molecules and 10^{5} Li atoms with background pressure limited lifetime on the order of 1 sec. With further improvements to lithium entrainment we expect that sympathetic cooling of molecules is within reach.
Collision cross sections and rate constants between two ground-state oxygen molecules are investigated theoretically at translational energies below $\ensuremath{\sim}1$ K and in zero magnetic field. We present calculations for elastic and spin-changing inelastic collision rates for different isotopic combinations of oxygen atoms as a prelude to understanding their collisional stability in ultracold magnetic traps. A numerical analysis has been made in the framework of a rigid-rotor model that accounts fully for the singlet, triplet, and quintet potential-energy surfaces in this system. The results offer insights into the effectiveness of evaporative cooling and the properties of molecular Bose-Einstein condensates, as well as estimates of collisional lifetimes in magnetic traps. Specifically, 17O2{}^{17}{\mathrm{O}}_{2}17O2​ looks like a good candidate for ultracold studies, while 16O2{}^{16}{\mathrm{O}}_{2}16O2​ is unlikely to survive evaporative cooling. Since 17O2{}^{17}{\mathrm{O}}_{2}17O2​ is representative of a wide class of molecules that are paramagnetic in their ground state we conclude that many molecules can be successfully magnetically trapped at ultralow temperatures.
A unique property of Zeeman effect based manipulation of paramagnetic particle's motion is the ability to control velocities of both atoms and molecules. In particular the moving magnetic trap decelerator is capable of slowing and eventually trapping mixtures of both cold atoms and cold molecules generated in a supersonic expansion. Here we report the deceleration of molecular oxygen together with metastable argon atoms. The cold mixture with temperature below 1 K is slowed from an initial velocity of 430 m s −1 down to 100 m s −1 . Our decelerator spans 2.4 m and consists of 480 quadrupole traps. Our results pave the way for the study of sympathetic cooling of molecules by laser cooled atoms.