| Literature DB >> 33100382 |
Hélène Fleurbaey1, Hongming Yi1, Erin M Adkins1, Adam J Fleisher1, Joseph T Hodges1.
Abstract
The λ = 2.06 μm absorption band of CO2 is widely used for the remote sensing of atmospheric carbon dioxide, making it relevant to many important top-down measurements of carbon flux. The forward models used in the retrieval algorithms employed in these measurements require increasingly accurate line intensity and line shape data from which absorption cross-sections can be computed. To overcome accuracy limitations of existing line lists, we used frequency-stabilized cavity ring-down spectroscopy to measure 39 transitions in the 12C16O2 absorption band. The line intensities were measured with an estimated relative combined standard uncertainty of u r = 0.08 %. We predicted the J-dependence of the measured intensities using two theoretical models: a one-dimensional spectroscopic model with Herman-Wallis rotation-vibration corrections, and a line-by-line ab initio dipole moment surface model [Zak et al. JQSRT 2016;177:31-42]. For the second approach, we fit only a single factor to rescale the theoretical integrated band intensity to be consistent with the measured intensities. We find that the latter approach yields an equally adequate representation of the fitted J-dependent intensity data and provides the most physically general representation of the results. Our recommended value for the integrated band intensity equal to 7.183 × 10-21 cm molecule-1 ± 6 × 10-24 cm molecule-1 is based on the rescaled ab initio model and corresponds to a fitted scale factor of 1.0069 ± 0.0002. Comparisons of literature intensity values to our results reveal systematic deviations ranging from -1.16 % to +0.33 %.Entities:
Keywords: Carbon dioxide; Cavity ring-down spectroscopy; Dipole moment surfaces; Herman-Wallis expansion; Line lists; Precision molecular spectroscopy
Year: 2020 PMID: 33100382 PMCID: PMC7579847
Source DB: PubMed Journal: J Quant Spectrosc Radiat Transf ISSN: 0022-4073 Impact factor: 2.468