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Physical Review A

One-dimensional confinement of magnetically decelerated supersonic beams of O2 molecules

Yang Liu, Sida Zhou, Wei Zhong, Pavle Djuricanin, Takamasa Momose

Published Feb 27, 2015• 23 citations
Publisher

Abstract

We have demonstrated that supersonic beams of oxygen molecules $({\text{O}}_{2})$ in the ground rotational state were slowed to a near standstill by a linear Zeeman decelerator and successfully confined spatially in an anti-Helmholtz magnetic trap. The translational temperature of the decelerated ${\text{O}}_{2}$ molecules was about 800 mK. The demonstrated trapping capability of paramagnetic species opens up various possibilities for the investigation of cold collisions and reactions of various radicals in the sub-kelvin regime by spatially confining them in a magnetic trap.

DOI
10.1103/physreva.91.021403

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We have demonstrated that supersonic beams of oxygen molecules (O2)({\text{O}}_{2})(O2​) in the ground rotational state were slowed to a near standstill by a linear Zeeman decelerator and successfully confined spatially in an anti-Helmholtz magnetic trap. The translational temperature of the decelerated O2{\text{O}}_{2}O2​ molecules was about 800 mK. The demonstrated trapping capability of paramagnetic species opens up various possibilities for the investigation of cold collisions and reactions of various radicals in the sub-kelvin regime by spatially confining them in a magnetic trap.
We have demonstrated that a supersonic beam of methyl radicals (CH_{3}) in the ground rotational state of both para and ortho species has been slowed down to standstill with a magnetic molecular decelerator, and successfully captured spatially in an anti-Helmholtz magnetic trap for >1 s. The trapped CH_{3} radicals have a mean translational temperature of about 200 mK with an estimated density of >5.0×10^{7} cm^{-3}. The methyl radical is an ideal system for the study of cold molecules not only because of its high reactivities at low temperatures, but also because further cooling below 1 mK is plausible via sympathetic cooling with ultracold atoms. The demonstrated trapping capability of methyl radicals opens up various possibilities for realizing ultracold ensembles of molecules towards Bose-Einstein condensation of polyatomic molecules and investigations of reactions governed by quantum statistics.
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.
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.
The long standing goal of chemical physics is finding a convenient method to create slow and cold beams intense enough to observe chemical reactions in the temperature range of a few Kelvin. We present an extensive numerical analysis of our moving magnetic trap decelerator showing that a 3D confinement throughout the deceleration process enables deceleration of almost all paramagnetic particles within the original supersonic expansion to stopping velocities. We show that the phase space region containing the decelerating species is larger by two orders of magnitude as compared to other available deceleration methods.
Control of the translational motion of methyl radicals is demonstrated by using pulsed magnetic fields created by a series of solenoid coils. By synchronously switching the magnetic fields corresponding to the motion of the radicals, we have observed the deceleration and focusing of a supersonic radical beam. The present result shows that Zeeman deceleration of polyatomic free radicals in the doublet state can be realized. This opens possibilities for trapping cold polyatomic free radicals in a spatially confined area leading to further studies of cold collisions and reactions.
Cold samples of oxygen molecules in supersonic beams have been decelerated from initial velocities of 390 and 450 m s−1 to final velocities in the range between 150 and 280 m s−1 using a 90-stage Zeeman decelerator. (2 + 1) resonance-enhanced-multiphoton-ionization (REMPI) spectra of the 3sσ g 3Π g (C) two-photon transition of O2 have been recorded to characterize the state selectivity of the deceleration process. The decelerated molecular sample was found to consist exclusively of molecules in the J ′′ = 2 spin–rotational component of the X ground state of O2. Measurements of the REMPI spectra using linearly polarized laser radiation with polarization vector parallel to the decelerator axis, and thus to the magnetic-field vector of the deceleration solenoids, further showed that only the magnetic sublevel of the N′′ = 1, J ′′ = 2 spin–rotational level is populated in the decelerated sample, which therefore is characterized by a fully oriented total-angular-momentum vector. By maintaining a weak quantization magnetic field beyond the decelerator, the polarization of the sample could be maintained over the 5 cm distance separating the last deceleration solenoid and the detection region.