Electron-transfer diabatic free energy surfaces from first-principles molecular dynamics

ORAL

Abstract

Electron transfer in aqueous solution is a fundamental process in physical chemistry, and since the introduction of Marcus theory it has been extensively studied using classical force-fields molecular dynamics. However, classical potentials contain fitted parameters, and have obvious limitations in describing structural effects related to hybridization and electronic polarization. In this work, we investigate electron transfer fully from first-principles, using the case of ferrous-ferric ions solvated in water as a paradigmatic example. The structure and dynamics of the aqua ions at ambient conditions are studied via Car-Parrinello molecular dynamics. The diabatic free energy surfaces in the limit of two ions infinitely apart are calculated with umbrella sampling, obtaining parabolic free energy curves, in agreement with Marcus theory. The extension of our approach to ions at finite distances is also discussed, and our solution to the specific challenges that this problem entails, ranging from self-interaction effects to localization constraints.

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Authors

  • P. H.-L. Sit

    Department of Physics, MIT, Cambridge, MA 02139

  • Matteo Cococcioni

    DMSE, MIT, Cambridge, MA 02139, DMSE and ISN Massachusetts Institute of Technology, DMSE and ISN, Massachusetts Institute of Technology

  • Nicola Marzari

    Department of Materials Science and Engineering, MIT, DMSE, MIT, Cambridge, MA 02139, Department of Materials Science and Engineering, Massachusetts Institute of Technology, DMSE-MIT, Department of Materials Science and Engineering and Institute for Soldier Nanotechnologies, Massachusetts Institute of Technology, DMSE and ISN Massachusetts Institute of Technology, Materials Science and Engineering, MIT, Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139