The phenomena of solvent exchange control the process of solvating ions, protons, and charged molecules. Building upon our extension of Marcus’ philosophy of electron transfer, we provide a new perspective of ultrafast solvent exchange mechanism around ions measurable by two-dimensional infrared (2DIR) spectroscopy. In this theory, solvent rearrangement drives an ion-bound water to an activated state of higher coordination number, triggering ion-water separation that leads to the solvent-bound state of the water molecule. This ion-bound to solvent-bound transition rate for a BF4- water system is computed using ab initio molecular dynamics and Marcus theory, and is found to be in excellent agreement with the 2DIR measurement.
Revised: May 23, 2018 |
Published: January 16, 2018
Citation
Roy S., M. Galib, G.K. Schenter, and C.J. Mundy. 2018.On the Relation between Marcus Theory and Ultrafast Spectroscopy of Solvation Kinetics.Chemical Physics Letters 692.PNNL-SA-130814.doi:10.1016/j.cplett.2017.12.041