Alignment of ND3 molecules in dc-electric fields.

The control of movement and orientation of gas-phase molecules has become the focus of many research areas in molecular physics. Here, ND3 molecules are polarized in a segmented, curved electrostatic guide and adiabatically aligned inside a rotatable mass spectrometer (MS). Alignment is probed by photoionization using a linearly polarized laser. Rotation of the polarization at fixed MS orientation has the same effect as the rotation of the MS at fixed polarization, proving that the molecular alignment adiabatically follows the MS axis. Polarization-dependent ion signals reveal state-specific populations and allow for a quantification of the aligned sample in the space-fixed reference frame.

Cold Ion-Molecule Chemistry: The Very Different Reactions of He⁺ with CO and NO.

The ion-molecule reactions He+ + CO → He + C+ + O and He+ + NO → He + N+ + O have been measured at collision energies between 0 and kB · 10 K. Strong variations of the rate coefficients are observed below kB · 5 K. The rate of the He+ + CO reaction decreases by ~30% whereas that of the He+ + NO reaction increases by a factor of ~1.5. These observations are interpreted in the realm of an adiabatic-channel capture model as arising from interactions between the ion charge and the dipole and quadrupole moments of CO and NO. We show that the different low-energy behavior of these reactions originates from the closed- vs. open-shell electronic structures of CO and NO.

Imaging of Chemical Kinetics at the Water-Water Interface in a Free-Flowing Liquid Flat-Jet.

We present chemical kinetics measurements of the luminol oxidation chemiluminescence (CL) reaction at the interface between two aqueous solutions, using liquid jet technology. Free-flowing liquid microjets are a relatively recent development that have found their way into a growing number of applications in spectroscopy and dynamics. A variant thereof, called flat-jet, is obtained when two cylindrical jets of a liquid are crossed, leading to a chain of planar leaf-shaped structures of the flowing liquid. We here show that in the first leaf of this chain, the fluids do not exhibit turbulent mixing, providing a clean interface between the liquids from the impinging jets. We also show, using the example of the luminol CL reaction, how this setup can be used to obtain kinetics information from friction-less flow and by circumventing the requirement for rapid mixing by intentionally suppressing all turbulent mixing and instead relying on diffusion.

Study of He*/Ne*+Ar, Kr, N2, H2, D2 Chemi-Ionization Reactions by Electron Velocity-Map Imaging.

The chemi-ionization of Ar, Kr, N2, H2, and D2 by Ne(3P2) and of Ar, Kr, and N2 by He(3S1) was studied by electron velocity map imaging (e-VMI) in a crossed molecular beam experiment. A curved magnetic hexapole was used to state-select the metastable species. Collision energies of 60 meV were obtained by individually controlling the beam velocities of both reactants. The chemi-ionization of atoms and molecules can proceed along different channels, among them Penning ionization and associative ionization. The evolution of the reaction is influenced by the internal redistribution of energy, which happens at the first reaction step that involves the emission of an electron. We designed and built an e-VMI spectrometer in order to investigate the electron kinetic energy distribution, which is related to the internal state distribution of the ionic reaction products. The analysis of the electron kinetic energy distributions allows an estimation of the ratio between the two-reaction channel Penning and associative ionization. In the molecular cases the vibrational or electronic excitation enhanced the conversion of internal energy into the translational energy of the forming ions, thus influencing the reaction outcome.

Investigation of the low-energy stereodynamics in the Ne(3P2) + N2, CO reactions.

We report on an experimental investigation of the low-energy stereodynamics of the energy transfer reactions Ne(3P2) + X, producing Ne(1S) + X+ and [Ne-X]+ (X = N2 or CO). Collision energies in the range 0.2 K-700 K are obtained by using the merged beam technique. Two kinds of product ions are generated by Penning and associative ionization, respectively. The intermediate product [Ne-X]+ in vibrationally excited states can predissociate into bare ions (X+). The experimental ratio of the NeX+ and X+ product ion yields is similar for both molecules at high collision energies but diverge at collision energies below 100 K. This difference is explained by the first excited electronic state of the product ions, which is accessible in the case of CO but lies too high in energy in the case of N2.

Sub-Kelvin Stereodynamics of the Ne(

We present an experimental study of the low-energy stereodynamics of the Ne(^{3}P_{2})+N_{2} reaction. Supersonic expansions of the two reactants are superposed in a merged beam experiment, where individual velocity control of the two beams allows us to reach average relative velocities of zero, yielding minimum collision energies around 60 mK. We combine the merged beam technique with the orientation of the metastable neon atoms and measure the branching between two reaction channels, Penning ionization and associative ionization, as a function of neon orientation and collision energy, covering the range 0.06-700 K. We find that we lose the ability to orient Ne below ≈100 K due to dynamic reorientation. Associative ionization products Ne-N_{2}^{+} predissociate with a probability of 30%-60% and that associative ionization is entirely due to reactions of the Ω=2 state, where the singly occupied p orbital of the Ne^{*} is oriented along the interatomic axis.

Energy and orientation independence of the channel branching in Ne* + ND3 chemi-ionisation.

Collisions of excited neon atoms with ammonia molecules can lead to two reaction processes, dissociative ionisation and Penning ionisation. Both processes result in the ionisation of the ammonia molecule and redistribution of the electronic energy into the internal ammonia ion rovibrational modes. We performed energy dependent, crossed-beam stereodynamics studies of the branching ratio between the two ionisation processes. It was found that the branching ratio is totally and completely insensitive to both the neon orientation and the collision energy across the range we sampled, 370-520 cm-1. The total lack of stereodynamics can be explained by the structure of the ammonia and that its orientation, which we do not attempt to control, is the critical factor in the reaction outcome.

Quantum-state-controlled channel branching in cold Ne(3P2)+Ar chemi-ionization.

A prerequisite to gain a complete understanding of the most basic aspects of chemical reactions is the ability to perform experiments with complete control over the reactant degrees of freedom. By controlling these, details of a reaction mechanism can be investigated and ultimately manipulated. Here, we present a study of chemi-ionization-a fundamental energy-transfer reaction-under completely controlled conditions. The collision energy of the reagents was tuned from 0.02 K to 1,000 K, with the orientation of the excited Ne atom relative to Ar fully specified by an external magnetic field. Chemi-ionization of Ne(3P2) and Ar in these conditions enables a detailed investigation of how the reaction proceeds, and provides us with a means to control the branching ratio between the two possible reaction outcomes. The merged-beam experimental technique used here allows access to a low-energy regime in which the atoms dynamically reorient into a favourable configuration for reaction, irrespective of their initial orientations.

Stereodynamics of Ne(3P2) reacting with Ar, Kr, Xe, and N2.

Stereodynamics experiments of Ne(3P2) reacting with Ar, Kr, Xe, and N2 leading to Penning and associative ionization have been performed in a crossed molecular beam apparatus. A curved magnetic hexapole was used to state-select and polarize Ne(3P2) atoms which were then oriented in a rotatable magnetic field and crossed with a beam of Ar, Kr, Xe, or N2. The ratio of associative to Penning ionization was recorded as a function of the magnetic field direction for collision energies between 320 cm-1 and 500 cm-1. Reactivities are obtained for individual states that differ only in Ω, the projection of the neon total angular momentum vector on the inter-particle axis. The results are rationalized on the basis of a model involving a long-range and a short-range reaction mechanism. Substantially lower probability for associative ionization was observed for N2, suggesting that predissociation plays a critical role in the overall reaction pathway.

Energy Dependent Stereodynamics of the Ne(

The stereodynamics of the Ne(^{3}P_{2})+Ar Penning and associative ionization reactions have been studied using a crossed molecular beam apparatus. The experiment uses a curved magnetic hexapole to polarize the Ne(^{3}P_{2}), which is then oriented with a shaped magnetic field in the region where it intersects with a beam of Ar(^{1}S). The ratios of Penning to associative ionization were recorded over a range of collision energies from 320 to 500 cm^{-1} and the data were used to obtain Ω state dependent reactivities for the two reaction channels. These reactivities were found to compare favorably to those predicted in the theoretical work of Brumer et al.

Experimental and Theoretical Studies of Low-Energy Penning Ionization of NH3 , CH3 F, and CHF3.

We present results from a joint theoretical and experimental study of the low-energy Penning ionization of NH3 , CH3 F, and CHF3 by metastable Ne(3 P2 ) and He(3 S1 ) atoms. We combine the merged neutral beams experiment, covering a range of collision energies between 0.1-150 K, with multichannel quantum defect theory calculations based on interaction potentials from symmetry-adapted perturbation theory. The three symmetric tops provide several distinct properties that make them interesting targets for cold chemistry studies. Of these three, only NH3 has a lone electron pair that leads to a strong binding with rare gas atoms. The CHF3 molecule has much smaller rotational constants than both NH3 and CH3 F, and thus has a considerably higher density of rotational states already at low energies. Their presence opens inelastic collision channels that reduce the observed reactive cross section. We show that this effect dominates the total rate coefficient in heavy molecules already at relatively low collision energies but is much less prominent for lighter molecules.

Communication: Importance of rotationally inelastic processes in low-energy Penning ionization of CHF3.

Low energy reaction dynamics can strongly depend on the internal structure of the reactants. The role of rotationally inelastic processes in cold collisions involving polyatomic molecules has not been explored so far. Here we address this problem by performing a merged-beam study of the He((3)S1)+CHF3 Penning ionization reaction in a range of collision energies E/kB = 0.5-120 K. The experimental cross sections are compared with total reaction cross sections calculated within the framework of quantum defect theory. We find that the broad range of collision energies combined with the relatively small rotational constants of CHF3 makes rotationally inelastic collisions a crucial player in the total reaction dynamics. Quantitative agreement between theory and experiment is only obtained if the energy-dependent probability for rotational excitation is included in the calculations, in stark contrast to previous experiments where classical scaling laws were able to describe the results.

Observation of orbiting resonances in He((3)S(1)) + NH3 Penning ionization.

Resonances are among the clearest quantum mechanical signatures of scattering processes. Previously, shape resonances and Feshbach resonances have been observed in inelastic and reactive collisions involving atoms or diatomic molecules. Structure in the integral cross section has been observed in a handful of elastic collisions involving polyatomic molecules. The present paper presents the observation of shape resonances in the reactive scattering of a polyatomic molecule, NH3. A merged-beam study of the gas phase He((3)S1) + NH3 Penning ionization reaction dynamics is described in the collision energy range 3.3 µeV < Ecoll < 10 meV. In this energy range, the reaction rate is governed by long-range attraction. Peaks in the integral cross section are observed at collision energies of 1.8 meV and 7.3 meV and are assigned to ℓ = 15,16 and ℓ = 20,21 partial wave resonances, respectively. The experimental results are well reproduced by theoretical calculations with the short-range reaction probability Psr = 0.035. No clear signature of the orbiting resonances is visible in the branching ratio between NH3 (+) and NH2 (+) formation.

Preparation of state purified beams of He, Ne, C, N, and O atoms.

The production and guiding of ground state and metastable C, N, and O atoms in a two-meter-long, bent magnetic guide are described. Pure beams of metastable He((3)S1) and Ne((3)P2), and of ground state N((4)S3/2) and O((3)P2) are obtained using an Even-Lavie valve paired with a dielectric barrier discharge or electron bombardment source. Under these conditions no electronically excited C, N, or O atoms are observed at the exit of the guide. A general valve with electron impact excitation creates, in addition to ground state atoms, electronically excited C((3)P2; (1)D2) and N((2)D5/2; (2)P3/2) species. The two experimental conditions are complimentary, demonstrating the usefulness of a magnetic guide in crossed or merged beam experiments such as those described in Henson et al. [Science 338, 234 (2012)] and Jankunas et al. [J. Chem. Phys. 140, 244302 (2014)].

Cold and controlled molecular beams: production and applications.

The field of cold molecules has become an important source of new insight in fundamental chemistry and molecular physics. High-resolution spectroscopy benefits from translationally and internally cold molecules by increased interaction times and reduced spectral congestion. Completely new effects in scattering dynamics become accessible with cold and controlled molecules. Many of these experiments use molecular beams as a starting point for the generation of molecular samples. This review gives an overview of methods to produce beams of cold molecules, starting from supersonic expansions or effusive sources, and provides examples of applications in spectroscopy and molecular dynamics studies.

Dynamics of gas phase Ne(*) + NH3 and Ne(*) + ND3 Penning ionisation at low temperatures.

Two isotopic chemical reactions, Ne(*) + NH3, and Ne(*) + ND3, have been studied at low collision energies by means of a merged beams technique. Partial cross sections have been recorded for the two reactive channels, namely, Ne(*) + NH3 → Ne + NH3(+) + e(-), and Ne(*) + NH3 → Ne + NH2(+) + H + e(-), by detecting the NH3(+) and NH2(+) product ions, respectively. The cross sections for both reactions were found to increase with decreasing collision energy, Ecoll, in the range 8 µeV < Ecoll < 20 meV. The measured rate constant exhibits a curvature in a log(k)-log(Ecoll) plot from which it is concluded that the Langevin capture model does not properly describe the Ne(*) + NH3 reaction in the entire range of collision energies covered here. Calculations based on multichannel quantum defect theory were performed to reproduce and interpret the experimental results. Good agreement was obtained by including long range van der Waals interactions combined with a 6-12 Lennard-Jones potential. The branching ratio between the two reactive channels, Γ = [NH2(+)]/[NH2(+)] + [NH3(+)], is relatively constant, Γ ≈ 0.3, in the entire collision energy range studied here. Possible reasons for this observation are discussed and rationalized in terms of relative time scales of the reactant approach and the molecular rotation. Isotopic differences between the Ne(*) + NH3 and Ne(*) + ND3 reactions are small, as suggested by nearly equal branching ratios and cross sections for the two reactions.

Low-temperature collisions between neutral molecules in merged molecular beams.

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.

Study of the Ne((3)P2) + CH3F electron-transfer reaction below 1 K.

Relatively little is known about the dynamics of electron-transfer reactions at low collision energy. We present a study of Penning ionization of ground-state methyl fluoride molecules by electronically excited neon atoms in the 13 µeV­4.8 meV (150 mK­56 K) collision energy range, using a neutral­neutral merged beam setup. Relative cross sections have been measured for three Ne((3)P2) + CH3F reaction channels by counting the number of CH3F(+), CH2F(+), and CH3(+) product ions as a function of relative velocity between the neon and methyl fluoride molecular beams. Experimental cross sections markedly deviate from the Langevin capture model at collision energies above 20 K. The branching ratios are constant. In other words, the chemical shape of the CH3F molecule, as seen by the Ne((3)P2) atom, appears not to change as the collision energy is varied, in contrast to related Ne((3)PJ) + CH3X (X = Cl and Br) reactions at higher collision energies.

A traveling wave decelerator for neutral polar molecules.

Recently, a decelerator for neutral polar molecules has been presented that operates on the basis of macroscopic, three-dimensional, traveling electrostatic traps [A. Osterwalder, S. A. Meek, G. Hammer, H. Haak, and G. Meijer, Phys. Rev. A 81, 051401 (2010)]. In the present paper, a complete description of this decelerator is given, with emphasis on the electronics and the mechanical design. Experimental results showing the transverse velocity distributions of guided molecules are shown and compared to trajectory simulations. An assessment of non-adiabatic losses is made by comparing the deceleration signals from (13)CO with those from (12)CO and with simulated signals.