January 16, 2018
Journal Article

On the Relation between Marcus Theory and Ultrafast Spectroscopy of Solvation Kinetics

Abstract

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