Abstract
The electron transfer mechanism in a titanium containing system was investigated by electrochemical and quantum-chemical methods. The kinetics of charge transfer for the Ti(IV)/Ti(III) redox couple in the (NaCl–KCl)equimol–NaF (10 wt%)-K2TiF6 melt with addition of Ca2+ cations was studied by cyclic voltammetry. The standard rate constants of charge transfer (k
s
) were calculated by Nicholson’s method. The increase values of the k
s
reaching the maximum at mole ratio Ca2+/Ti(IV) equals 1:1 was found. Values of activation energy for system with Ca2+ cations are considerably less than activation energies of the system without Ca2+ cations. The quantum-chemical calculations were performed using the Firefly quantum-chemical package by methods of the density functional theory. Structures with a high probability of the electron transfer from the cathode to the titanium complex were found. Using the Frontier molecular orbital method made it possible with a small amount of computer time to determine the structure of the transition state of the TiF6
2− complex. The calculated activation energy of the electron transfer was in a good agreement with experimentally determined value.
Publisher
The Electrochemical Society
Subject
Materials Chemistry,Electrochemistry,Surfaces, Coatings and Films,Condensed Matter Physics,Renewable Energy, Sustainability and the Environment,Electronic, Optical and Magnetic Materials
Cited by
1 articles.
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