Inner-Sphere Reorganization in Optical Electron Transfer.

Abstract

Free energies for photoelectron emission by aqueous solutions of hexaquocations (V2+, Cr2+, Fe2+) - metal complexes (Fe(CN)6 4-, Co (NH3)6 2+) and inorganic anions (OH, C1-, Br-, I-) are calculated from theory and compared with experimental threshold energies. Good agreement is obtained within the estimated error (+ or - 0.2 eV) on emission free energies. The free energy for outer-sphere reorganization is calculated from a continuous medium model. The inner-sphere reorganization energy is obtained from a bond-stretching model for hexaquo cations and metal complexes. A new method is developed for the calculation of the inner-sphere reorganization energies of univalent anions from their free energies of hydration, Reorganization free energies for electron transfer reactions (V(2+)/(3+), Cr(2+)/(3+), Mn(2+)/(3+), Fe(2+)/(3+), Fe(CN)6 (4-)/(3-) calculated from experimental threshold energies and computed outersphere reorganization free energies yield activation free energies in agreement with the values obtained from kinetic measurements. Improvements are discussed for the determination of threshold energies by extrapolation. (Author)

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Document Details

Document Type
Technical Report
Publication Date
Mar 01, 1984
Accession Number
ADA139722

Entities

People

  • A. Dziedzic
  • Paul Delahay

Organizations

  • New York University

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Aqueous Solutions
  • Chemical Engineering
  • Chemistry
  • Computer Science
  • Coordination Complexes
  • Electron Transfer
  • Engineering
  • Equations
  • Free Energy
  • Jet Propulsion
  • Materials
  • Materials Science
  • Military Research
  • Molecular Dynamics
  • New Jersey
  • New York
  • Standards

Fields of Study

  • Physics

Readers

  • Electrochemical Surface Science
  • Solar Physics

Technology Areas

  • Microelectronics