An Amperometric, Temperature-Independent, and Calibration-Free Method for the Real-Time State-of-Charge Monitoring of Redox Flow Battery Electrolytes
A simple mathematical framework for a calibration-free real-time state-of-charge (SOC) monitoring of redox flow battery (RFB) electrolytes, which is based on mass-transfer limited amperometry, is theoretically derived. The equations are initially validated with literature data for a vanadium-based R...
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Veröffentlicht in: | Chemistry of materials 2019-08, Vol.31 (15), p.5363-5369 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A simple mathematical framework for a calibration-free real-time state-of-charge (SOC) monitoring of redox flow battery (RFB) electrolytes, which is based on mass-transfer limited amperometry, is theoretically derived. The equations are initially validated with literature data for a vanadium-based RFB electrolyte, revealing absolute root-mean-square deviations (RMSD) of 4–6% for the obtained SOC estimates. Subsequently, our own experimental results based on a microelectrode as an amperometric sensor are presented. Absolute RMSDs of 2–7% are obtained for ferri-/ferrocyanide-based RFB electrolytes at two different concentrations in an offline measurement. Furthermore, the real-time SOC monitoring capability is demonstrated for the capacity limiting half-cell of a symmetric aqueous RFB utilizing N,N,N-2,2,6,6-heptamethylpiperidinyloxy-4-ammonium chloride (TEMPTMA) as an active organic molecule, yielding an absolute RMSD of below 3%. The theoretical considerations and the experimental results imply a complete independence of the presented approach from, e.g., the type of mass-transfer limiting process, the temperature, the RFB type (organic/inorganic, aqueous/nonaqueous), and the electrolyte composition. |
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ISSN: | 0897-4756 1520-5002 |
DOI: | 10.1021/acs.chemmater.9b02376 |