Electronically excited states of formic acid investigated by theoretical and experimental methods

Randi, P. A. S.; Pastega, D. F.; Bettega, M. H. F.; Jones, N. C.; Hoffmann, S. V.; Eden, S.; Souza Barbosa, A. and Limão-Vieira, P. (2023). Electronically excited states of formic acid investigated by theoretical and experimental methods. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 289, article no. 122237.

DOI: https://doi.org/10.1016/j.saa.2022.122237


Absolute cross-section values are reported from high-resolution vacuum ultraviolet (VUV) photoabsorption measurements of formic acid in the photon energy range 4.7–10.8 eV (265–115 nm), together with quantum chemical calculations to provide vertical energies and oscillator strengths. The combination of experimental and theoretical methods has allowed a comprehensive assignment of the electronic transitions. The VUV spectrum reveals various vibronic features not previously reported in the literature, notably associated with (3pa'←10a'), (3p'a'←10a'), (3sa'←2a'') and (3pa' ←2a'') Rydberg transitions. The assignment of vibrational features in the absorption bands reveal that the C=O stretching, v'3(a'), the H′–O–′C deformation, v'5(a'), the C–O stretching, v'6(a'), and the O=C–O′ deformation, v'7(a') modes are mainly active. The measured absolute photoabsorption cross sections have also been used to estimate the photolysis lifetime of HCOOH in the upper stratosphere (30–50 km), showing that solar photolysis is an important sink at altitudes above 30 km but not in the troposphere. Potential energy curves for the lowest-lying electronic excited states, as a function of the C=O coordinate, are obtained employing time dependent density functional theory (TD-DFT). These calculations have shown the relevance of internal conversion from Rydberg to valence character governing the nuclear dynamics, yielding clear evidence of the rather complex multidimensional nature of the potential energy surfaces involved.

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