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CHIMIA International Journal for Chemistry

Low-temperature Collisions between Neutral Molecules in Merged Molecular Beams

Benjamin Bertsche, Justin Jankunas, Andreas Osterwalder

Published Apr 30, 2014• 30 citations
Publisher

Abstract

We have developed an experiment for the investigation of neutral molecular collisions in the gas phase at temperatures as low as 100 mK. These low temperatures are obtained by merging two supersonic expansions, using an electric and a magnetic guide, and by matching the velocities of the beams. Since the energy available for the collisions, or the temperature, is determined only by the relative velocity of the reaction partners this enables the study of chemical processes at very low temperatures without the need to prepare slow molecules in the laboratory frame of reference. This paper describes the method and presents results on the Ne((3)P2)+NH3 Penning ionization.

DOI
10.2533/chimia.2014.256

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We have developed an experiment for the investigation of neutral molecular collisions in the gas phase at temperatures as low as 100 mK. These low temperatures are obtained by merging two supersonic expansions, using an electric and a magnetic guide, and by matching the velocities of the beams. Since the energy available for the collisions, or the temperature, is determined only by the relative velocity of the reaction partners this enables the study of chemical processes at very low temperatures without the need to prepare slow molecules in the laboratory frame of reference. This paper describes the method and presents results on the Ne((3)P2)+NH3 Penning ionization.
Molecular collisions can be studied at very low relative kinetic energies, in the milliKelvin range, by merging codirectional beams with much higher translational energies, extending even to the kiloKelvin range, provided that the beam speeds can be closely matched. This technique provides far more intensity and wider chemical scope than methods that require slowing both collision partners. Previously, at far higher energies, merged beams have been widely used with ions and/or neutrals formed by charge transfer. Here, we assess for neutral, thermal molecular beams the range and resolution of collision energy that now appears attainable, determined chiefly by velocity spreads within the merged beams. Our treatment deals both with velocity distributions familiar for molecular beams formed by effusion or supersonic expansion, and an unorthodox variant produced by a rotating supersonic source capable of scanning the lab beam velocity over a wide range.
Within this thesis two experiments will be described. In the first experiment a velocity filter was used to obtain a beam of polar molecules (ND3) with a translational temperature of less than 5K. For the first time the dynamics of individual rotational states inside a velocity filter could be investigated directly. Usually a velocity filter defines only a maximumvelocity that can pass the filter. We successfully implemented two different approaches where molecules below a certain minimal velocity are removed from the beam, turning the velocity filter into a bandpass filter. The second and more interesting experiment is the merged beamexperiment. We developed and constructed the first apparatus which successfullymerged two guided beams, one consisting of polar molecules, the other of paramagnetic particles, into an overlapping parallel movement. With this approach we could lower the temperature at which the reaction of metastable Ne* with ND3, NH3 and CH3F has been investigated by 3 orders of magnitude down to the sub-kelvin regime. Especially the stereochemistry of those reactions revealed an unexpected energy-insensitivity at temperatures below 200K. As our setup is very general the investigation of manymore neutral-neutral reactions will be possible, opening a new route into an temperature regime where only a few reactions have been studied before.
Experiments have lagged theory in exploring chemical interactions at temperatures so low that translational degrees of freedom can no longer be treated classically. The difficulty has been to realize in the laboratory low-enough collisional velocities between neutral reactants to access this regime. We report here the realization of merged neutral supersonic beams and the manifestation of clear nonclassical effects in the resulting reactions. We observed orbiting resonances in the Penning ionization reaction of argon and molecular hydrogen with metastable helium, leading to a sharp absolute ionization rate increase in the energy range corresponding to a few degrees kelvin down to 10 millikelvin. Our method should be widely applicable to many canonical chemical reactions.
Recent merged neutral beam experiments have introduced the possibility of measuring reactive collisions in the cold regime down to 10 mK. The lowest temperature attained in these experiments cannot be explained using the standard formalism developed for crossed molecular beam scattering. These low temperatures become accessible because pulsed supersonic beams develop a correlation in velocity-position space during free propagation such that the local velocity standard deviation decreases. This effect is responsible for a reduction in the attainable collision energy by more than 2 orders of magnitude along with an order of magnitude improvement in the resolution. We show that supersonic nozzles with short pulsed opening durations compared to the time-of-flight, such as the Even-Lavie valve, have a clear advantage in achieving low collision energies with improved resolution. We discuss possible improvements in the energy resolution by varying the detection time duration.
A detailed description of a merged beam apparatus for the study of low energy molecular scattering is given. This review is intended to guide any scientist who plans to construct a similar experiment, and to provide some inspiration in describing the approach we chose to our goal. In our experiment a supersonic expansion of paramagnetic particles is merged with one of polar molecules. A magnetic and an electric multipole guide are used to bend the two beams onto the same axis. We here describe in detail how the apparatus is designed, characterised, and operated.
Studying chemical reactions at very low temperatures is of importance for the understanding of fundamental physical and chemical processes. At very low energies, collisions are dominated by only a few partial waves. Thus, studies in this regime allow the characterisation of quantum effects which depend on the collisional angular momentum, e.g., reactive scattering resonances and tunneling through centrifugal barriers. Additionally, the dynamics of ultralow-energy collisions is dominated by long-range interactions, i.e., "universal" chemical forces. Thus, experiments in this domain probe the details of intermolecular interactions which is of general relevance for the understanding of chemical processes. Moreover, the increasingly more precise experiments provide valuable data for benchmarking theoretical models and quantum-chemical calculations. Studies of cold ion-neutral reactions in the laboratory rely on techniques for the generation of cold ions and cold neutrals. Many of these techniques do not only allow the translational cooling of the molecules, but also a precise reparation of their internal quantum state. Thus, by an accurate preparation of both the energy and state of the reaction partners as well as by the application of external electric, magnetic or optical fields, prospects open up to study and control chemical processes at an unprecedented level of accuracy. In this chapter, we will review salient theoretical concepts and recent experimental developments for studies of ion-molecule reactions at low temperatures. We first discuss the theoretical background for the description of low-energy ion-molecule reactions. Next we present key experimental methods for laboratory studies of cold ion-molecule reactions. The chapter concludes with a review of illustrative results and an outlook on future directions.