jp6b09489_si_006.pdf (15.33 MB)

# Modeling Carbon Dioxide Vibrational Frequencies in
Ionic Liquids: I. *Ab Initio* Calculations

journal contribution

posted on 2016-12-30, 20:06 authored by Eric J. Berquist, Clyde A. Daly, Thomas Brinzer, Krista K. Bullard, Zachary M. Campbell, Steven A. Corcelli, Sean Garrett-Roe, Daniel S. LambrechtThis
work elucidates the molecular binding mechanism of CO

_{2}in [C_{4}C_{1}IM][PF_{6}] ionic liquid (IL) and its interplay with the CO_{2}asymmetric stretch frequency ν_{3}, and establishes computational protocols for the reliable construction of spectroscopic maps for simulating ultrafast 2D-IR data of CO_{2}solvated in ILs. While charge transfer drives the static frequency shift between*different*ionic liquids (J. Chem. Phys. 2015, 142, 212425), we find here that electrostatic and Pauli repulsion effects dominate the dynamical frequency shift between different geometries sampled from the finite-temperature dynamics*within*a single ionic liquid. This finding is also surprising because dispersion interactions dominate the CO_{2}–IL interaction energies, but are comparably constant across different geometries. An important practical consequence of this finding is that density functional theory is expected to be sufficiently accurate for constructing potential energy surfaces for CO_{2}in [C_{4}C_{1}IM][PF_{6}], as needed for accurate anharmonic calculations to construct a reliable spectroscopic map. Similarly, we established appropriate computational and chemical models for treating the extended solvent environment. We found that a QM/MM treatment including at least 2 cation-ion pairs at the QM level and at least 32 pairs at the MM level is necessary to converge vibrational frequencies to within 1 cm^{–1}. Using these insights, this work identifies a computational protocol as well as a chemical model necessary to construct accurate spectroscopic maps from first principles.