Influence of crossover on capacity fade of symmetric redox flow cells

Journal Article · 02 October 2024 · Energy Advances

DOI: https://doi.org/10.1039/d4ya00407h · OSTI ID:2466273

George, Thomas Y.  ^[1]; Fell, Eric M.  ^[1]; Lee, Kyumin  ^[1]; Emanuel, Michael S.  ^[1]; Aziz, Michael J.  ^[1]

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1. Harvard University, Cambridge, MA (United States)

Volumetrically unbalanced compositionally symmetric cell cycling with potentiostatic (CV) or galvanostatic-with-potential-hold (CCCV) protocols is a rigorous technique for evaluating the calendar lifetime of reactants for redox flow batteries. Here, we evaluate the influence of reactant crossover through the membrane on symmetric cell cycling behavior. We tested symmetric cells of anthraquinone disulfonic acid (AQDS) with Nafion membranes of varied thickness and manufacture (NR211, NR212, N115, and N117, ranging 25–183 μm). Membranes were tested both as-received and pretreated with a common procedure of soaking in water at elevated temperature and then in dilute hydrogen peroxide. We found no significant difference in capacity fade rates of symmetric cells with any of the membranes as-received, indicating a negligible influence of crossover. However, we observed increased capacity fade with increased permeability through pretreated membranes. Supported by zero-dimensional modeling and operando UV-vis spectrophotometry, we propose a mechanism for net crossover in AQDS symmetric cells based on a higher time-averaged concentration of quinhydrone dimers in the non-capacity limiting side (NCLS) compared to the capacity limiting side (CLS), driving net crossover of AQDS reactants out of the CLS. Further, we illustrate other hypothetical scenarios of net crossover using the zero-dimensional model. Overall, many membrane–electrolyte systems used in symmetric cell studies have sufficiently low crossover flux as to avoid the influence of crossover on capacity fade, but under conditions of higher crossover flux, complex interactions of crossover and chemical reactions may result in diverse capacity fade trajectories, the mechanisms of which may be untangled with operando characterization and modeling.

• Research Organization: Harvard University, Cambridge, MA (United States)
• Sponsoring Organization: USDOE
• Grant/Contract Number: AC05-76RL01830
• OSTI ID: 2466273
• Journal Information: Energy Advances, Journal Name: Energy Advances Journal Issue: 12 Vol. 3; ISSN 2753-1457
• Publisher: Royal Society of ChemistryCopyright Statement
• Country of Publication: United States
• Language: English