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Resonant scattering of highly vibrationally excited and aligned D2 in cold collisions with Ne has recently been probed experimentally using the Stark-induced adiabatic Raman passage technique [Perreault et al., J. Chem. Phys. 157, 144301 (2022)]. A partial-wave analysis and numerical fitting of the experimental data attributed the measured angular distribution to an l = 2 shape resonance near Ec/kB = 1 K (≈0.7 cm−1). Here, we report the computation of a new potential energy surface for the Ne–H2 interaction suitable for the study of collisions between highly vibrationally excited H2/D2 with Ne as well as quantum scattering calculations of stereodynamics of D2 (v = 4, j = 2) + Ne collisions probing Δj = −2 rotational transition in D2. Our results show that collisions are dominated by a strong l = 5 resonance near 3 K (≈2.09 cm−1) and a weaker l = 6 resonance near 8 K (≈5.56 cm−1) and not an l = 2 resonance, as suggested in the analysis of the experimental data. A reasonable agreement between our calculations and the experiments is obtained only when an artificial energy cutoff is applied to the integral over the collision energy to exclude contributions from the l = 5 resonance while retaining contributions from l = 0, 1, and 2. However, our calculations do not support the claim that the measured angular distributions are dominated by a single l = 2 partial-wave resonance characteristic of orbiting collisions.
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Probing the Dependence of Long-Range, Four-Atom Interactions on Intermolecular Orientation. 4. The Dissociation Dynamics of H2/D2···ICl(B,v′=3) and the Observation of Efficient Vibrational–Rotational Energy Transfer
The vibrational predissociation dynamics of H2/D2···I35Cl(B,v′=3) complexes containing both para- and ortho-hydrogen prepared in different intermolecular vibrational levels were investigated. The Δv = −1 I35Cl(B,v = 2,j) rotational product-state distributions measured for excitation to the lowest-energy T-shaped levels of these complexes are mostly bimodal. The rotational distributions measured for excitation of the H2···I35Cl(B,v′=3) complexes are colder than those of the D2···I35Cl(B,v′=3) complexes, and there are only slight differences between those measured for the para- and ortho-hydrogen containing complexes. Excitation of the delocalized bending levels results in slightly colder rotational product-state distributions. The distributions suggest the dynamics result from more than impulsive dissociation off of the inner repulsive wall of the lower-energy H2/D2 + I35Cl(B,v = 2) potential surfaces of the products. The depths of these potentials and the energies available to these products also contribute to the dynamics. The formation of the Δv = −2, I35Cl(B,v = 1) product channel was only identified for excitation of levels within the ortho(j = 0)-D2 + I35Cl(B,v′=3) potential. The formation of this channel occurs via I35Cl(B,v′=3) vibrational to D2 rotational energy transfer forming the ortho(j = 2)-D2 + I35Cl(B,v = 1,j) products.
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- Award ID(s):
- 2102241
- PAR ID:
- 10484200
- Publisher / Repository:
- American Chemical Society
- Date Published:
- Journal Name:
- The Journal of Physical Chemistry A
- Volume:
- 126
- Issue:
- 43
- ISSN:
- 1089-5639
- Page Range / eLocation ID:
- 7916 to 7923
- Subject(s) / Keyword(s):
- Binding energy, Dissociation,Energy, Energy transfer, Molecular structure
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1021/acs.jpca.2c05817
