AbstractThe stepwise oxidation of vanadium ions in electrolytes, as used in all vanadium redox flow batteries (VRFB), is studied offline by a combination of potentiometric titration and simultaneous UV/Vis/NIR spectroscopy. Eight different total vanadium concentrations between 0.2 mol L−1 and 1.6 mol L−1 have been investigated. The analyte (titrand, V2+ solution) is the anolyte (V2+/V3+ side) of a fully charged laboratory vanadium redox flow battery (VRFB). Absorption maxima are observed at λ = 850 nm for V2+ and at λ = 400 nm for V3+, the corresponding absorption coefficients are determined. In the former case an extrapolation procedure is necessary because during transfer from the VRFB to the titration cell, oxidation to V3+ by ambient oxygen cannot completely be avoided. Based on the knowledge of the absorption coefficients, via simultaneous photometry of V2+ and V3+, the state-of-charge of the anolyte of a VRFB can be determined. In the catholyte (V4+/V5+ side) of a VRFB the formation of an intermediate mixed valence VIV–VV complex at large vanadium concentration prevents a simple photometric SOC determination.
Monitoring the State‐of‐Charge of a Vanadium Redox Flow Battery with the Acoustic Attenuation Coefficient: An In Operando Noninvasive Method
