(Invited) Some Aspects of Electrode Kinetics and Electrolyte Stability in Vanadium Flow Batteries

The electrochemical kinetics of the V II /V III redox reaction on carbon electrodes is enhanced by anodic treatment of the electrode and inhibited by cathodic treatment. Contrastingly, the kinetics of the V IV /V V redox reaction is inhibited by anodic treatment of the electrode and enhanced by cath...

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Veröffentlicht in:ECS transactions 2022-09, Vol.109 (10), p.3-22
Hauptverfasser: Buckley, D. Noel, Bourke, Andrea, Oboroceanu, Daniela, Lenihan, Catherine, Al Hajji Safi, Maria, Quill, Nathan, Miller, Mallory A., Savinell, Robert F., Wainright, Jesse S., Sasikumar S P, Varsha, Rybalchenko, Maria, Amini, Pupak, Lynch, Robert P.
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Sprache:eng
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Zusammenfassung:The electrochemical kinetics of the V II /V III redox reaction on carbon electrodes is enhanced by anodic treatment of the electrode and inhibited by cathodic treatment. Contrastingly, the kinetics of the V IV /V V redox reaction is inhibited by anodic treatment of the electrode and enhanced by cathodic treatment. The observed effects are attributed to oxygen-containing species on the surface of carbon electrodes and it is likely that enhancement of both V II /V III and V IV /V V occurs on the same (meso) state of the electrode. Oxidation of this active meso state leads to inhibition of V IV /V V while reduction of the active meso state leads to inhibition of V II /V III .We have investigated the thermal stability of VFB catholytes using a standard methodology. The induction time for precipitation of V 2 O 5 decreases exponentially with increasing temperature or V V concentration but increases exponentially with increasing sulphate concentration. Arrhenius plots show two linear regimes, at 45–70 °C and 30–45 °C, respectively. We model this behavior to estimate acceleration factors for testing of electrolyte stability over a range of test and use temperatures. Group V additives (phosphate and arsenate) are effective for improving the thermal stability of VFB catholytes.
ISSN:1938-5862
1938-6737
DOI:10.1149/10910.0003ecst