Assessing the correctness of pressure correction to solvation theories in the study of electron transfer reactions

Abstract

Liquid states theories have emerged as a numerically efficient alternative to costly molecular dynamics simulations of electron transfer reactions in solution. In a recent paper [Chem. Sci., 2019, 10, 2130], we introduced the framework to compute energy gap, free energy profile and reorganization free energy using molecular density functional theory. However, this technique, as other molecular liquid state theories, overestimates the bulk pressure of the fluids. Because of the too high pressure, the predicted free energy is dramatically exaggerated. Several attempts were made to fix this issue, either based on simple a posteriori correction or by improving the description of the liquid introducing bridge terms. By studying two model half reactions in water, Cl -> Cl+ and Cl -> Cl-, we assess the correctness of these two types of corrections to study electron transfer reactions. We found that a posteriori corrections, because they violate the functional principle, lead to an inconsistency in the definition of the reorganization free energy and should not be used to study electron transfer reactions. The bridge approach, because it is theoretically well grounded, is perfectly suitable for this type of systems.

15 pages, 4 figures

References in corpus (5)

• Fast Computation of Solvation Free Energies with Molecular Density Functional Theory: Thermodynamic-Ensemble Partial Molar Volume Corrections
• Scalar fundamental measure theory for hard spheres in three dimensions. Application to hydrophobic solvation
• Efficient molecular density functional theory using generalized spherical harmonics expansions
• Molecular Density Functional Theory for water with liquid-gas coexistence and correct pressure
• Integral equations for simple fluids in a general reference functional approach