Generation of Sub-nanosecond H Atom Pulses for Scattering from Single-Crystal Epitaxial Graphene.

Pulsed molecular beams allow high-density gas samples to be cooled to low internal temperatures and to produce narrow speed distributions. They are particularly useful in combination with pulsed-laser-based detection schemes and have also been used as pump pulses in pump-probe experiments with neutral matter. The mechanical response of pulsed valves and chopper wheels limits the duration of these pulses typically to about 10-100 µs. Bunch compression photolysis has been proposed as a means to produce atomic pulses shorter than 1 ns─an experimental capability that would allow new measurements to be made on chemical systems. This technique employs a spatially chirped femtosecond duration photolysis pulse that produced an ensemble of H atom photoproducts that rebunches into a short pulse downstream. To date, this technique could not produce strong enough beams to allow new experiments to be carried out. In this paper, we report production of pulsed H atom beams consistent with a 700 ps pulse duration and with sufficient intensity to carry out differentially resolved inelastic H scattering experiments from a graphene surface. We observe surprisingly narrow angular distributions for H atoms incident normal to the surface. At low incidence energies quasi-elastic scattering dominates, and at high incidence energy we observe a strongly inelastic scattering channel. These results provide the basis for future experiments where the H atoms synchronously collide with a pulsed-laser-excited surface.

Controlling the Spin-Orbit Branching Fraction in Molecular Collisions.

The collision geometry, that is, the relative orientation of reactants before interaction, can have a large effect on how a collision or reaction proceeds. Certain geometries may prevent access to a given product channel, while others might enhance it. In this Letter, we demonstrate how the initial orientation of NO molecules relative to approaching Ar atoms determines the branching between the spin-orbit changing and the spin-orbit conserving rotational product channels. We use a recently developed quantum treatment to calculate differential and integral branching fractions, at any arbitrary orientation, from theoretical and experimental data points. Our results show that a substantial degree of control over the final spin-orbit state of the scattering products can be achieved by tuning the initial collision geometry.

Probing the location of the unpaired electron in spin-orbit changing collisions of NO with Ar.

Understanding the molecular forces that drive a reaction or scattering process lies at the heart of molecular dynamics. Here, we present a combined experimental and theoretical study of the spin-orbit changing scattering dynamics of oriented NO molecules with Ar atoms. Using our crossed molecular beam apparatus, we have recorded velocity-map ion images and extracted differential and integral cross sections of the scattering process in the side-on geometry. We observe an overall preference for collisions close to the N atom in the spin-orbit changing manifold, which is a direct consequence of the location of the unpaired electron on the potential energy surface. In addition, a prominent forward scattered feature is observed for intermediate, even rotational transitions when the atom approaches the molecule from the O-end. The appearance of this peak originates from an attractive well on the A' potential energy surface, which efficiently directs high impact parameter trajectories towards the region of high unpaired electron density near the N-end of the molecule. The ability to orient molecules prior to collision, both experimentally and theoretically, allows us to sample different regions of the potential energy surface(s) and unveil the associated collision pathways.

Steric Effects in the Inelastic Scattering of NO(X) + Ar: Side-on Orientation.

The rotationally inelastic collisions of NO(X) with Ar, in which the NO bond-axis is oriented side-on (i.e., perpendicular) to the incoming collision partner, are investigated experimentally and theoretically. The NO(X) molecules are selected in the |j = 0.5, Ω = 0.5, ε = -1, f⟩ state prior to bond-axis orientation in a static electric field. The scattered NO products are then state selectively detected using velocity-map ion imaging. The experimental bond-axis orientation resolved differential cross sections and integral steric asymmetries are compared with quantum mechanical calculations, and are shown to be in good agreement. The strength of the orientation field is shown to affect the structure observed in the differential cross sections, and to some extent also the steric preference, depending on the ratio of the initial e and f Λ-doublets in the superposition determined by the orientation field. Classical and quantum calculations are compared and used to rationalize the structures observed in the differential cross sections. It is found that these structures are due to quantum mechanical interference effects, which differ for the two possible orientations of the NO molecule due to the anisotropy of the potential energy surface probed in the side-on orientation. Side-on collisions are shown to maximize and afford a high degree of control over the scattering intensity at small scattering angles (θ < 90°), while end-on collisions are predicted to dominate in the backward scattered region (θ > 90°).

Side-impact collisions of Ar with NO.

In the realm of molecular collision dynamics, stereochemistry refers to the dependence of the collision outcome on the mutual orientation of the colliding partners. This may involve directed end-on collisions along a molecular bond axis or encounters in which the partner approaches the bond of an oriented molecule from the side. Using both experiment and theory, we show here that in the simplest case of an inelastic collision between an atom and a nearly homonuclear diatom, in which the two atoms have almost the same mass, the scattering dynamics are very distinct for impacts on either side of the molecule. By recording the direction of the scattered particles after the collision, we demonstrate that the intensity of products scattered in the forward direction, near parallel to the initial motion, can be substantially controlled and even maximized by altering the side-on orientation of the quantum state selected NO molecules that collide with Ar atoms. In addition, our findings provide valuable information about the preferred collision mechanism and reveal interesting quantum interference effects.