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.

Anisotropy is a fundamental property of particle interactions. It occupies a central role in cold and ultra-cold molecular processes, where long-range forces have been found to significantly depend on orientation in ultra-cold polar molecule collisions 1,2 . Recent experiments have demonstrated the emergence of quantum phenomena such as scattering resonances in the cold collisions regime due to quantization of the intermolecular degrees of freedom 3-8 . Although these states have been shown to be sensitive to interaction details, the effect of anisotropy on quantum resonances has eluded experimental observation so far. Here, we directly measure the anisotropy in atom-molecule interactions via quantum resonances by changing the quantum state of the internal molecular rotor. We observe that a quantum scattering resonance at a collision energy of appears in the Penning ionization of molecular hydrogen with metastable helium only if the molecule is rotationally excited. We use state of the art ab initio and multichannel quantum molecular dynamics calculations to show that the anisotropy contributes to the effective interaction only for molecules in the first excited rotational state, whereas rotationally ground state interacts purely isotropically with metastable helium. Control over the quantum state of the internal molecular rotation allows us to switch the anisotropy on or off and thus disentangle the isotropic and anisotropic parts of the interaction. These quantum phenomena provide a challenging benchmark for even the most advanced theoretical descriptions, highlighting the advantage of using cold collisions to advance the microscopic understanding of particle interactions.

Quantum phenomena in the translational motion of reactants, which are usually negligible at room temperature, can dominate reaction dynamics at low temperatures. In such cold conditions, even the weak centrifugal force is enough to create a potential barrier that keeps reactants separated. However, reactions may still proceed through tunnelling because, at low temperatures, wave-like properties become important. At certain de Broglie wavelengths, the colliding particles can become trapped in long-lived metastable scattering states, leading to sharp increases in the total reaction rate. Here, we show that these metastable states are responsible for a dramatic, order-of-magnitude-strong, quantum kinetic isotope effect by measuring the absolute Penning ionization reaction rates between hydrogen isotopologues and metastable helium down to 0.01 K. We demonstrate that measurements of a single isotope are insufficient to constrain ab initio calculations, making the kinetic isotope effect in the cold regime necessary to remove ambiguity among possible potential energy surfaces.

The role of internal molecular degrees of freedom, such as rotation, has scarcely been explored experimentally in low-energy collisions despite their significance to cold and ultracold chemistry. Particularly important to astrochemistry is the case of the most abundant molecule in interstellar space, hydrogen, for which two spin isomers have been detected, one of which exists in its rotational ground state whereas the other is rotationally excited. Here we demonstrate that quantization of molecular rotation plays a key role in cold reaction dynamics, where rotationally excited ortho-hydrogen reacts faster due to a stronger long-range attraction. We observe rotational state-dependent non-Arrhenius universal scaling laws in chemi-ionization reactions of para-H2 and ortho-H2 by He(2(3)P2), spanning three orders of magnitude in temperature. Different scaling laws serve as a sensitive gauge that enables us to directly determine the exact nature of the long-range intermolecular interactions. Our results show that the quantum state of the molecular rotor determines whether or not anisotropic long-range interactions dominate cold collisions.

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.