Issue 21, 2024

A two-step quadrature-based variational calculation of ro-vibrational levels and wavefunctions of CO2 using a bisector-x molecule-fixed frame

Abstract

In this paper, we propose a new two-step strategy for computing ro-vibrational energy levels and wavefunctions of a triatomic molecule and apply it to CO2. A two-step method [J. Tennyson and B. T. Sutcliffe, Mol. Phys., 1986, 58, 1067] uses a basis whose functions are products of K-dependent “vibrational” functions and symmetric top functions. K is the quantum number for the molecule-fixed z component of the angular momentum. For a linear molecule, a two-step method is efficient because the Hamiltonian used to compute the basis functions includes the largest coupling term. The most important distinguishing feature of the two-step method we propose is that it uses an associated Legendre basis and quadrature rather than a K-dependent discrete variable representation. This reduces the cost of the calculation and simplifies the method. We have computed ro-vibrational energy levels with J up to 100 for CO2, on an accurate available potential energy surface which is known as the AMES-2 PES and present a subset of those levels. We have converged most levels up to 20 000 cm−1 to 0.0001 cm−1.

Graphical abstract: A two-step quadrature-based variational calculation of ro-vibrational levels and wavefunctions of CO2 using a bisector-x molecule-fixed frame

Supplementary files

Article information

Article type
Paper
Submitted
14 फरवरी 2024
Accepted
02 अप्रैल 2024
First published
25 अप्रैल 2024

Phys. Chem. Chem. Phys., 2024,26, 15181-15191

A two-step quadrature-based variational calculation of ro-vibrational levels and wavefunctions of CO2 using a bisector-x molecule-fixed frame

X. Wang and T. Carrington, Phys. Chem. Chem. Phys., 2024, 26, 15181 DOI: 10.1039/D4CP00655K

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