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Journal of Physics Conference Series

Ion-ion collision-induced evaporative cooling of atomic and molecular ions by autoresonance in an electrostatic ion beam trap

O. Heber, Reetesh Kumar Gangwar, K Saha, Michael L. Rappaport, D. Zajfman

Published Jan 1, 2020• 0 citations
Publisher

Abstract

Synopsis A new method for cooling beams of any ion is introduced. The method is autoresonance acceleration of ions inside an Electrostatic Ion Beam Trap. Intrabunch collisions of trapped (molecular) ions transfer energy from the “cold” part of the population of the ion distribution to the “hot” part, which, in turn, evaporates from the bunch. As a result, bunches of ions were cooled from about 45 K to well below 1 K.

DOI
10.1088/1742-6596/1412/12/122003

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Synopsis A new method for cooling beams of any ion is introduced. The method is autoresonance acceleration of ions inside an Electrostatic Ion Beam Trap. Intrabunch collisions of trapped (molecular) ions transfer energy from the “cold” part of the population of the ion distribution to the “hot” part, which, in turn, evaporates from the bunch. As a result, bunches of ions were cooled from about 45 K to well below 1 K.
Autoresonance (AR) cooling of a bunch of ions oscillating inside an electrostatic ion beam trap is demonstrated for the first time. The relatively wide initial longitudinal velocity distribution is reduced by at least an order of magnitude using AR acceleration and ramping forces. The hot ions escaping the bunch are not lost from the system but continue to oscillate in the trap outside of the bunch and may be further cooled by successive AR processes. Ion-ion collisions inside the bunch close to the turning points in the trap's mirrors contribute to the thermalization of the ions. This cooling method can be applied to any mass and any charge.
Cooling all degrees of freedom of a molecule, a cluster, or even a nanoparticle which is suspended in a vacuum, is an experimental challenge. Without suitable schemes, cold or ultracold chemical reactions are not feasible. Methods such as laser based preparation of very slow atoms, decelerating molecules to low velocities with electric fields or freezing molecular ions into Coulomb crystals, are generally not suitable to cool the vibrational or rotational motion of molecules. This contribution describes a new method in which a beam of slow atoms or molecules (H, He, H2, or D2) is used for cooling charged particles confined in a multi-electrode rf trap. For reaching sub-K temperatures, the fast part of a cold effusive beam is removed with a shutter before the slow remaining neutrals interact with the ion cloud. The development of a pulsed cold beam source is discussed as well as suitable methods for determining the ion temperature. A challenging application is to prepare internally cold CH5+ for spectroscopy or chemistry. New experimental results for hydrogen abstraction in collisions with slow H atoms are reported at energies of a few meV. For evaluating these measurements and for predicting effective rate coefficients at lower energies, the kinematic conditions of the slow neutral beam-ion trap arrangement have been analyzed in detail. The potential of cooling ions such as protonated methane or H3+ with slow energy selected H atoms is briefly mentioned. An interesting process is the formation of weakly bound ions such as H4+ or CH6+ via radiative or ternary association. Such ions are ideal candidates for preparing the corresponding collision complexes very close (microeV) to the dissociation continuum using infrared transitions.
Externally, in an electron beam ion trap, generated Ar16+ ions were retrapped in a Penning trap and evaporatively cooled in their axial motion. The cooling was observed by a novel extraction technique based on the excitation of a coherent axial oscillation which yields short ion bunches of well-defined energies. The initial temperature of the ion cloud was decreased by a factor of more than 140 within 1 s, while the phase-space density of the coldest extracted ion pulses was increased by a factor of up to about 9.
The study of cold and controlled molecular ions is pivotal for fundamental research in modern physics and chemistry. Investigations into cooling molecular anions, in particular, have proven to be of key consequence for the production of cold antihydrogen, the creation, and study of anionic Coulomb crystals as well as in atmospheric research and astrochemistry. The commonly used anion cooling technique via collisions with a buffer gas is limited by the temperature of the used cryogenic cooling medium. Here, we demonstrate forced evaporative cooling of anions via a laser beam with photon energies far above the photodetachment threshold of the anion. We reach runaway evaporative cooling of an anionic OH−^{-}− ensemble from an initial temperature of 370(12) K down to 2.2(8) K. This corresponds to three orders of magnitude increase in the ions' phase space density approaching the near-strong Coulomb coupling regime. A quantitative analysis of the experimental results, via a full thermodynamic model including the role of intrinsic collisional heating, represents the anion cooling dynamics without any fitting parameters. This technique can be used to cool, in principle, any anionic species below liquid helium temperature, providing a novel tool to push the frontiers of anion cooling to much lower than the state-of-the-art temperature regimes.