Computational study of the rovibrational spectrum of CO2–N2
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Authors
Quintas-Sánchez, Ernesto
Dawes, Richard
Wang, Xiao-Gang
Carrington, Tucker Jr
Date
2020-09-17
Type
journal article
Language
en
Keyword
Alternative Title
Abstract
The CO2–N2 complex is formed from two key components of Earth's atmosphere, and as such, has received some attention from both experimental and theoretical studies. On the theory side, a potential energy surface (PES) based on high level ab initio data was reported [Nasri et al., J. Chem. Phys., 2015, 142, 174301] and then used in more recently reported rovibrational calculations [Lara-Moreno et al., Phys. Chem. Chem. Phys., 2019, 21, 3550]. Accuracy of about 1 percent was achieved for calculated rotational transitions of the ground vibrational state of the complex, compared with previously reported microwave spectra. However, a very recent measurement of the geared bending mode frequency [Barclay et al., J. Chem. Phys., 2020, 153, 014303] recorded a value of 21.4 cm−1, which is wildly different from the corresponding calculated value of 45.9 cm−1. To provide some insight into this discrepancy, we have constructed a new more accurate PES, and used it to perform highly converged variational rovibrational calculations. Our new results yield a value of 21.1 cm−1 for that bending frequency, in close agreement with the experiment. We also obtain significantly improved predicted rotational transitions. Finally, we note that a very shallow well, previously reported as a distinct second isomer, is not found on our new PES, but rather a transition structure is seen in that location.
Description
Citation
Quintas-Sánchez, E., Dawes, R., Wang, X.-G., & Carrington, T. (2020). Computational study of the rovibrational spectrum of CO2–N2. Physical Chemistry Chemical Physics, 22(39), 22674–22683. https://doi.org/10.1039/D0CP04186F
Publisher
Royal Society of Chemistry