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Bulletin of the American Physical Society

Toward trapping cold molecules produced via ``kinematic'' cooling

Jeffrey J Kay, Sebastiaan Y. T. van de Meerakker, Kevin E. Strecker, David W. Chandler

Published May 28, 2008• 0 citations
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We have produced translationally cold ammonia (ND3) molecules in various quantum states by kinematic cooling. In these experiments, ND3 molecules are brought nearly to rest in the (J, K) = (2,0), (2,1), (2,2), (3,1), (3,2), and (3,3) rotational levels of the ground vibronic state by rotationally-inelastic collisions with Ne atoms. The cold molecules are produced in quantum-state-dependent velocity distributions whose laboratory frame velocities are measured to be between 21 m s(-1) (E(trans)/k = 530 mk) and 32 m s(-1) (E(trans)/k = 1.2 K), and are calculated to be between 7.5 m s(-1) (E(trans)/k = 70 mK) and 27 m s(-1) (E(trans)/k = 880 mK). Due to systematic experimental effects, the measured velocities are upper limits to the actual velocities. These temperatures are low enough that it should be possible to use electrostatic traps to confine cold molecules in many of these quantum states.

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Recently we developed a technique for producing cold molecules from a supersonic molecular beam via single collisions with a supersonic atomic beam [M. S. Elioff, J. J. Valentini, and D. W. Chandler, Science 302, 1940 (2003)]. This cooling technique necessarily produces the cold molecules at the relatively high density crossing of the atomic and molecular beams. In previous reports, secondary glancing collisions with the remnant atomic and molecular beams lead to rapid depletion of the cold molecules limiting the observation time to less than $10\phantom{\rule{0.3em}{0ex}}\ensuremath{\mu}\mathrm{s}$ with an estimated temperature of $440\phantom{\rule{0.3em}{0ex}}\mathrm{mK}$. Here we present experimental conditions for the kinematic cooling technique which overcome the limitations of the previous experiments. We demonstrate the success of this experiment for the production of cold nitric oxide (NO) in the ground vibrational, $j=7.5$ rotational, state in order to compare with our previously reported data. With the present setup, we are able to extract the cold molecules from the pulsed molecular and atomic beams and we observe these cold $\mathrm{NO}{(X)}_{j=7.5}$ persisting for over $150\phantom{\rule{0.3em}{0ex}}\ensuremath{\mu}\mathrm{s}$. This long observation time demonstrates our ability to temporally and spatially separate the cold molecules from the parent atomic and molecular beams, simultaneously allowing for a better measurement of the final average velocity for the kinematically cooled molecules. From the data we find a final average velocity of the $\mathrm{NO}{(X)}_{j=7.5}$ of approximately $4.5\phantom{\rule{0.3em}{0ex}}\mathrm{m}∕\mathrm{s}$, consistent with simulations. The final observed average velocity is equated to a temperature of approximately $35\phantom{\rule{0.3em}{0ex}}\mathrm{mK}$, over an order of magnitude colder than our previous measurements.

Physical Review A•Dec 3, 2008•21 citations
We have produced translationally cold ammonia (ND3) molecules in various quantum states by kinematic cooling. In these experiments, ND3 molecules are brought nearly to rest in the (J, K) = (2,0), (2,1), (2,2), (3,1), (3,2), and (3,3) rotational levels of the ground vibronic state by rotationally-inelastic collisions with Ne atoms. The cold molecules are produced in quantum-state-dependent velocity distributions whose laboratory frame velocities are measured to be between 21 m s(-1) (E(trans)/k = 530 mk) and 32 m s(-1) (E(trans)/k = 1.2 K), and are calculated to be between 7.5 m s(-1) (E(trans)/k = 70 mK) and 27 m s(-1) (E(trans)/k = 880 mK). Due to systematic experimental effects, the measured velocities are upper limits to the actual velocities. These temperatures are low enough that it should be possible to use electrostatic traps to confine cold molecules in many of these quantum states.
Recently we developed a technique for producing cold molecules from a supersonic molecular beam via single collisions with a supersonic atomic beam [M. S. Elioff, J. J. Valentini, and D. W. Chandler, Science 302, 1940 (2003)]. This cooling technique necessarily produces the cold molecules at the relatively high density crossing of the atomic and molecular beams. In previous reports, secondary glancing collisions with the remnant atomic and molecular beams lead to rapid depletion of the cold molecules limiting the observation time to less than $10\phantom{\rule{0.3em}{0ex}}\ensuremath{\mu}\mathrm{s}$ with an estimated temperature of 440mK440\phantom{\rule{0.3em}{0ex}}\mathrm{mK}440mK. Here we present experimental conditions for the kinematic cooling technique which overcome the limitations of the previous experiments. We demonstrate the success of this experiment for the production of cold nitric oxide (NO) in the ground vibrational, j=7.5j=7.5j=7.5 rotational, state in order to compare with our previously reported data. With the present setup, we are able to extract the cold molecules from the pulsed molecular and atomic beams and we observe these cold NO(X)j=7.5\mathrm{NO}{(X)}_{j=7.5}NO(X)j=7.5​ persisting for over $150\phantom{\rule{0.3em}{0ex}}\ensuremath{\mu}\mathrm{s}$. This long observation time demonstrates our ability to temporally and spatially separate the cold molecules from the parent atomic and molecular beams, simultaneously allowing for a better measurement of the final average velocity for the kinematically cooled molecules. From the data we find a final average velocity of the NO(X)j=7.5\mathrm{NO}{(X)}_{j=7.5}NO(X)j=7.5​ of approximately 4.5m∕s4.5\phantom{\rule{0.3em}{0ex}}\mathrm{m}∕\mathrm{s}4.5m∕s, consistent with simulations. The final observed average velocity is equated to a temperature of approximately 35mK35\phantom{\rule{0.3em}{0ex}}\mathrm{mK}35mK, over an order of magnitude colder than our previous measurements.