H2O-CO and D2O-CO complexes: Intra- and intermolecular rovibrational states from full-dimensional and fully coupled quantum calculations

Peter M Felker; Zlatko Bačić

doi:10.1063/5.0020566

H₂O-CO and D₂O-CO complexes: Intra- and intermolecular rovibrational states from full-dimensional and fully coupled quantum calculations

J Chem Phys. 2020 Aug 21;153(7):074107. doi: 10.1063/5.0020566.

Authors

Peter M Felker¹, Zlatko Bačić²

Affiliations

¹ Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1569, USA.
² Department of Chemistry, New York University, New York, New York 10003, USA.

PMID: 32828109
DOI: 10.1063/5.0020566

Abstract

We present efficient yet rigorous, full-dimensional quantum bound-state calculations of the fully coupled J = 0 and one intra- and intermolecular rovibrational levels of H₂O-CO and D₂O-CO complexes. The new ab initio nine-dimensional (9D) potential energy surface (PES) [Y. Liu and J. Li, Phys. Chem. Chem. Phys. 21, 24101 (2019)] is employed. In the spirit of the recently introduced general procedure [P. M. Felker and Z. Bačić, J. Chem. Phys. 151, 024305 (2019)], the 9D rovibrational Hamiltonian is partitioned into a 5D (rigid-monomer) intermolecular Hamiltonian, two intramolecular vibrational Hamiltonians-one for the water monomer (3D) and another for the CO monomer (1D), and a 9D remainder term. The low-energy eigenstates of the three reduced-dimension Hamiltonians are used to build up the 9D product contracted basis, in which the matrix of the full rovibrational Hamiltonian is diagonalized. In line with the findings of our earlier study referenced above, the 5D intermolecular eigenstates included in the 9D bases extend up to at most 230 cm^-1 above the lowest-energy state of the given parity, much less than the intramolecular fundamentals of the two complexes that span the range of energies from about 1200 cm^-1 to 3800 cm^-1. The resulting Hamiltonian matrices are small for the 9D quantum problem considered, ≈ 10 000 for J = 0 and 13 500 for J = 1 calculations, allowing for direct diagonalization. The 9D calculations permit exploring a number of features of the rovibrational level structure of H₂O-CO and D₂O-CO that are beyond the quantum 5D rigid-monomer treatments reported to date. These include the differences in the magnitudes of the hydrogen-exchange tunneling splittings computed in 9D and 5D, the sensitivity of the tunneling splittings to the intramolecular vibrational excitation, the frequency shifts of the intramolecular vibrational modes, which, depending on the mode, can be either blue- or redshifts, and the effects of the excitation of the intramolecular fundamentals on the low-lying intermolecular eigenstates. Also examined is the extent of the eigenstate delocalization over the two minima on the PES. Whenever possible, a comparison is made with the experimental data in the literature.