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Quantum calculations on a new CCSD(T) machine-learned PES reveal the leaky nature of gas-phase $trans$ and $gauche$ ethanol conformers

Ethanol is a molecule of fundamental interest in combustion, astrochemistry, and condensed phase as a solvent. It is characterized by two methyl rotors and $trans$ ($anti$) and $gauche$ conformers, which are known to be very close in energy. Here we show that based on rigorous quantum calculations of the vibrational zero-point state, using a new ab initio potential energy surface (PES), the ground state resembles the $trans$ conformer but substantial delocalization to the $gauche$ conformer is present. This explains experimental issues about the identification and isolation of the two conformers. This "leak" effect is partially quenched when deuterating the OH group, which further demonstrates the need for a quantum mechanical approach. Diffusion Monte Carlo (DMC) and full-dimensional semiclassical dynamics calculations are employed. The new PES is obtained by means of a $Δ$-Machine learning approach starting from a pre-existing low level (LL) density functional theory (DFT) surface. This surface is brought to the CCSD(T) level of theory using a relatively small number of $ab$ $initio$ CCSD(T) energies. Agreement between the corrected PES and direct $ab$ $initio$ results for standard fidelity tests is excellent. One- and two-dimensional discrete variable representation calculations focusing on the $trans$-$gauche$ torsional motion are also reported, in reasonable agreement with the experiment.