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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creator | Stolze, Christian Meurer, Jan P Hager, Martin D Schubert, Ulrich S |
description | 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. |
doi_str_mv | 10.1021/acs.chemmater.9b02376 |
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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%. 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Mater</addtitle><description>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.</description><issn>0897-4756</issn><issn>1520-5002</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkNFKwzAUhoMoOKePIOQBlpm0TZtczrHpYCLovC5pcrp2tMlIM3QP4vuaMfHWm3M4_P9_-PkQumd0ymjCHpQeprqBvlcB_FRWNEmL_AKNGE8o4ZQml2hEhSxIVvD8Gt0Mw45SFqNihL5nFs_6PXjXQ_CtnuANnE4VDh7IyhrYQxw2TLCyBs9V11ZRbJ0lSw-AXyA0zuDaeRwawG-gOrJpe8DvIbYhribzRvltNDrbBudbu8Wujj7jvvCyc5_4UYVY-4gXHejgXXcMMNyiq1p1A9z97jH6WC4282eyfn1azWdrohLJAwFTMJlBBYXMtay0UKkQuaIFo5RLTY0wFQeeZ8pkIq8lZFJoJZQoqjTJKpaOET__1d4Ng4e63Pu2V_5YMlqe2JaRbfnHtvxlG3PsnDvJO3fwNrb8J_MD5puEpg</recordid><startdate>20190813</startdate><enddate>20190813</enddate><creator>Stolze, Christian</creator><creator>Meurer, Jan P</creator><creator>Hager, Martin D</creator><creator>Schubert, Ulrich S</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0003-4978-4670</orcidid><orcidid>https://orcid.org/0000-0002-6373-6600</orcidid></search><sort><creationdate>20190813</creationdate><title>An Amperometric, Temperature-Independent, and Calibration-Free Method for the Real-Time State-of-Charge Monitoring of Redox Flow Battery Electrolytes</title><author>Stolze, Christian ; Meurer, Jan P ; Hager, Martin D ; Schubert, Ulrich S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a295t-ed7194ebe796c9bc8a3886a0710059c0d8db5e564ad486f9e498ca8a87b324b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stolze, Christian</creatorcontrib><creatorcontrib>Meurer, Jan P</creatorcontrib><creatorcontrib>Hager, Martin D</creatorcontrib><creatorcontrib>Schubert, Ulrich S</creatorcontrib><collection>CrossRef</collection><jtitle>Chemistry of materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stolze, Christian</au><au>Meurer, Jan P</au><au>Hager, Martin D</au><au>Schubert, Ulrich S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An Amperometric, Temperature-Independent, and Calibration-Free Method for the Real-Time State-of-Charge Monitoring of Redox Flow Battery Electrolytes</atitle><jtitle>Chemistry of materials</jtitle><addtitle>Chem. Mater</addtitle><date>2019-08-13</date><risdate>2019</risdate><volume>31</volume><issue>15</issue><spage>5363</spage><epage>5369</epage><pages>5363-5369</pages><issn>0897-4756</issn><eissn>1520-5002</eissn><abstract>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.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.chemmater.9b02376</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-4978-4670</orcidid><orcidid>https://orcid.org/0000-0002-6373-6600</orcidid></addata></record> |
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title | An Amperometric, Temperature-Independent, and Calibration-Free Method for the Real-Time State-of-Charge Monitoring of Redox Flow Battery Electrolytes |
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