Study of the Mechanism of the Vanadium 4+/5+ Redox Reaction in Acidic Solutions
Author(s) -
M. Gattrell,
Jung O. Park,
B. MacDougall,
J. Apte,
Sarah McCarthy,
Chang-Shuo Wu
Publication year - 2003
Publication title -
journal of the electrochemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.258
H-Index - 271
eISSN - 1945-7111
pISSN - 0013-4651
DOI - 10.1149/1.1630594
Subject(s) - vanadium , redox , mechanism (biology) , chemistry , reaction mechanism , inorganic chemistry , catalysis , organic chemistry , physics , quantum mechanics
The mechanism of the vanadium VO21/VO2 1 redox couple has been examined in acidic aqueous solutions. A detailed understanding of this chemistry is of interest for improving and optimizing the performance of vanadium redox-flow batteries, a promising electrochemical electricity storage technology. The vanadium 41/51 redox reactions were studied at a rotating disk graphite electrode and polarization curves were obtained in sulfuric acid and perchloric acid, with varying pH and vanadium concentrations. The results were compared to model predictions for different mechanisms. The data were consistent with a model with a multistep chemical-electrochemical-chemical mechanism at low overpotentials, which changes to a multistep electrochemicalchemical- chemical mechanism at higher anodic or cathodic overpotentials. Unusually high Tafel slopes ~350-450 mV/decade! were observed for the reduction of VO2 1 at higher overpotentials. While this could not be directly explained by the model, insights gained through the use of the model can provide the basis for some suggestions.Peer reviewed: YesNRC publication: Ye
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