Benchmarking the computed proton solvation energy and absolute potential in non-aqueous solvents. (1st March 2023)

• Record Type: Journal Article
• Authors: Sotoudeh, Mohsen; Laasonen, Kari; Busch, Michael
• Is Part Of: Electrochimica acta. Volume 443(2023)
• Publication Date: 2023-03-01
• Subjects: Absolute potential -- Proton solvation energy -- Non-aqueous solvents -- Water -- Dft -- Quantum chemistry; Electrochemistry -- Periodicals; Electrochemistry, Industrial -- Periodicals; 541.37
• DOI: 10.1016/j.electacta.2022.141785
• Languages: English
• ISSNs: 0013-4686

Abstract

Highlights: The most accurate guess of the absolute potential in water is 4.31(±0.07) eV. The most accurate guess of the proton solvation energy in water is −11.38(±0.07) eV. Predictions in non-aqueous solvents are unreliable owing to shortcomings of the implicit solvation models. Abstract: Proton solvation energies and absolute potentials are of critical importance in all areas of chemistry. But despite their relevance they are only known in water with a sufficient degree of accuracy while we still lack fundamental understanding in non-aqueous solvents. Here, we report an extensive benchmark for different DFT or ab-initio methods, the solvation models, and the choice of reference compounds for computing proton solvation energies and absolute potentials. Our computations indicate, that cationic acids (ammonium and iminium ions) allow for the most accurate prediction of these parameters in water while neutral acids (e.g. alcohols, carboxylic acids) display an unphysical correlation between their pKa and the proton solvation energy. The CCSD(T)/SMD computations are the most accurate method for predicting the proton solvation energy. For non-aqueous solvents, excellent error cancelation has been observed for all considered parameters. Furthermore, we report a fundamental flaw in solvation models for non-aqueous solvents, causing an unphysical correlation between the pKa and the proton solvation energy in DMSO. This work thoroughly evaluates the most critical parameters affecting the computed proton solvation energies using DMSO as a test case. Graphical abstract: Image, graphical abstract