Stereodynamic control of cold rotationally inelastic CO + HD collisions
arXiv:2107.00259 · doi:10.1039/D1CP02755G
Abstract
Quantum control of molecular collision dynamics is an exciting emerging area of cold collisions. Co-expansion of collision partners in a supersonic molecular beam combined with precise control of their quantum states and alignment/orientation using Stark-induced Adiabatic Raman Passage allows exquisite stereodynamic control of the collision outcome. This approach has recently been demonstrated for rotational quenching of HD in collisions with H2, D2, and He and D2 by He. Here we illustrate this approach for HD(v=0,j=2)+CO(v=0,j=0) -> HD(v'=0,j')+CO(v'=0,j') collisions through full-dimensional quantum scattering calculations at collision energies near 1 K. It is shown that the collision dynamics at energies between 0.01--1K are controlled by an interplay of L=1 and L=2 partial wave resonances depending on the final rotational levels of the two molecules. Polarized cross-sections resolved into magnetic sub-levels of the initial and final rotational quantum numbers of the two molecules also reveal a significant stereodynamic effect in the cold energy regime. Overall, the stereodynamic effect is controlled by both geometric and dynamical factors, with parity conservation playing an important role in modulating these contributions depending on the particular final state.
References in corpus (10)
- Cold molecules: Progress in Quantum Engineering of Chemistry and Quantum Matter
- Observation of Quantum Effects in sub Kelvin Cold Reactions
- Assembly of a rovibrational ground state molecule in an optical tweezer
- Quantum dynamics of CO-H in full dimensionality
- Quantum calculations of H2-H2 collisions: from ultracold to thermal energies
- Vibrational energy transfer in ultracold molecule - molecule collisions
- Complete quantum coherent control of ultracold molecular collisions
- Stereodynamic control of overlapping resonances in cold molecular collisions
- Coherent control of reactive scattering at low temperatures: Signatures of quantum interference in the differential cross sections for F + H2 and F + HD
- Beyond universality: parametrizing ultracold complex-mediated reactions using statistical assumptions