Imaging rotational energy transfer: comparative stereodynamics in CO + N2 and CO + CO inelastic scattering

Zhong-Fa Sun; Roy J A Scheidsbach; Marc C van Hemert; Ad van der Avoird; Arthur G Suits; David H Parker

doi:10.1039/d3cp02229c

Imaging rotational energy transfer: comparative stereodynamics in CO + N₂ and CO + CO inelastic scattering

Phys Chem Chem Phys. 2023 Jul 12;25(27):17828-17839. doi: 10.1039/d3cp02229c.

Authors

Zhong-Fa Sun¹, Roy J A Scheidsbach², Marc C van Hemert³, Ad van der Avoird⁴, Arthur G Suits⁵, David H Parker^{1

2}

Affiliations

¹ Anhui Province Key Laboratory of Optoelectric Materials Science and Technology, Department of Physics, Anhui Normal University, Wuhu, Anhui 241000, China. zfsun@ahnu.edu.cn.
² Department of Molecular and Laser Physics, Institute for Molecules and Materials, Radboud University, Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands. parker@science.ru.nl.
³ Leiden Institute of Chemistry, Gorlaeus Laboratories, Leiden University, Einsteinweg 55, 2333 CC Leiden, The Netherlands.
⁴ Theoretical Chemistry, Institute for Molecules and Materials, Radboud University, Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands.
⁵ Department of Chemistry, University of Missouri, Columbia, MO 65211, USA.

PMID: 37377093
DOI: 10.1039/d3cp02229c

Abstract

State-to-state rotational energy transfer in collisions of ground ro-vibrational state ¹³CO molecules with N₂ molecules has been studied using the crossed molecular beam method under kinematically equivalent conditions used for ¹³CO + CO rotationally inelastic scattering described in a previously published report (Sun et al., Science, 2020, 369, 307-309). The collisionally excited ¹³CO molecule products are detected by the same (1 + 1' + 1'') VUV (Vacuum Ultra-Violet) resonance enhanced multiphoton ionization scheme coupled with velocity map ion imaging. We present differential cross sections and scattering angle resolved rotational angular momentum alignment moments extracted from experimentally measured ¹³CO + N₂ scattering images and compare them with theoretical predictions from quasi-classical trajectories (QCT) on a newly calculated ¹³CO-N₂ potential energy surface (PES). Good agreement between experiment and theory is found, which confirms the accuracy of the ¹³CO-N₂ potential energy surface for the 1460 cm^-1 collision energy studied by experiment. Experimental results for ¹³CO + N₂ are compared with those for ¹³CO + CO collisions. The angle-resolved product rotational angular momentum alignment moments for the two scattering systems are very similar, which indicates that the collision induced alignment dynamics observed for both systems are dominated by a hard-shell nature. However, compared to the ¹³CO + CO measurements, the primary rainbow maximum in the DCSs for ¹³CO + N₂ is peaked consistently at more backward scattering angles and the secondary maximum becomes much less obvious, implying that the ¹³CO-N₂ PES is less anisotropic. In addition, a forward scattering component with high rotational excitation seen for ¹³CO + CO does not appear for ¹³CO-N₂ in the experiment and is not predicted by QCT theory. Some of these differences in collision dynamics behaviour can be predicted by a comparison between the properties of the PESs for the two systems. More specific behaviour is also predicted from analysis of the dependence on the relative collision geometry of ¹³CO + N₂ trajectories compared to ¹³CO + CO trajectories, which shows the special 'do-si-do' pathway invoked for ¹³CO + CO is not effective for ¹³CO + N₂ collisions.