Aqueous organic redox flow batteries (AORFBs) hold great
promise
in the storage of fluctuating renewable energy output for later use
when there is a demand for electricity. Anthrarufin (AN), reported
earlier as an anolyte material for the AORFB application, offered
limited energy density due to its poor solubility. Here, we present
a derivative of AN, 1,5-dihydroxy-9,10-dioxo-9,10-dihydroanthracene-2,6-disulfonic
acid (DSAN) as an anolyte to improve the energy density of the AORFB.
Sulfonic acid functional groups were introduced to hike the solubility
of DSAN in an alkaline medium. DSAN is soluble up to 110 mM in 0.4
M KOH and offers a theoretical capacity of 5.9 A h L–1, which is more than twice that of AN. Cyclic voltammetry studies
reveal the quasi-reversible nature of DSAN with the redox potential
centered at around −0.64 V versus Ag/AgCl. However, upon cycling,
the cell enters into capacity imbalance mainly due to DSAN reacting
with water in the presence of carbon felt producing H2.
This parasitic reaction makes catholyte the capacity-limiting side.
Hence, an in situ electrolysis route is introduced to restore the
capacity of the battery in the event of capacity decay. In addition,
the use of d-fructose as an additive in the anolyte compartment
increases the overpotential for H2 evolution and minimizes
capacity fading. Hence, we believe that the work is relevant as it
addresses a much bigger problem of parasitic reactions in an alkaline
medium and benefits a broader spectrum of work.