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Spectroscopic Measurement of State of Charge in Vanadium Flow Batteries with an Analytical Model of V-IV-V-V Absorbance

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posted on 2022-08-22, 14:57 authored by Cattleya Petchsing, NATHAN QUILL, Jennifer Joyce, DEIRDRE NI EIDHINDEIRDRE NI EIDHIN, Daniela Oboroceanu, Catherine Lenihan, Xin Gao, ROBERT LYNCHROBERT LYNCH, NOEL BUCKLEYNOEL BUCKLEY
The ultraviolet-visible spectra of catholytes for vanadium flow batteries (VFBs) were measured and analyzed for a range of V-IV:V-V ratios and vanadium concentrations. Using a model of V2O33+ in equilibrium with VO2+ and VO2+, the spectra were characterized in terms of an excess absorbance parameter p and the molar extinction coefficients epsilon(4) and epsilon(5) of VO2+ and VO2+, respectively. The results showed that p varies weakly with the vanadium concentration C and this variation was quantified relative to a reference concentration C-r by means of a concentration coefficient phi(r). Experimental data showed that plots of fr versus C phi(r) and plots of 1/phi(r) versus C are linear and, based on this linearity, phi(r) was expressed as a simple function of C in terms of its reference concentration C-r and a single parameter M that is independent of the choice of C-r. Standard spectra of p at a concentration C-0 = 1 mol dm(-3) and of epsilon(4) and epsilon(5) were generated from which the spectrum of any catholyte may be simulated using the measured value of M in a governing equation. This enables determination of the state of charge for any VFB catholyte using absorbance measurements at a small number of wavelengths. (C) The Author(s) 2015. Published by ECS. All rights reserved.

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Publication

Journal of the Electrochemical Society;163 (1), pp. A5068-A5083

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Electrochemical Society

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peer-reviewed

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© The Author(s) 2015. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives 4.0 License (CC BY-NC-ND, http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is not changed in any way and is properly cited. For permission for commercial reuse, please email: oa@electrochem.org. [DOI: 10.1149/2.0091601jes] All rights reserved

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English

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