The hydrogen-bromate flow battery represents one of the promising variants for hybrid power sources. Its membrane-electrode assembly (MEA) combines a hydrogen gas diffusion anode and a porous flow-through cathode where bromate reduction takes place from its acidized aqueous solution: BrO3− + 6 H+ + 6 e− = Br− + 3 H2O (*). The process of electric current generation occurs on the basis of the overall reaction: 3 H2 + BrO3− = Br− + 3 H2O (**), which has been studied in previous publications. Until this work, it has been unknown whether this device is able to function as a rechargeable power source. This means that the bromide anion, Br−, should be electrooxidized into the bromate anion, BrO3−, in the course of the charging stage inside the same cell under strongly acidic conditions, while until now this process has only been carried out in neutral or alkaline solutions with specially designed anode materials. In this study, we have demonstrated that processes (*) and (**) can be performed in a cyclic manner, i.e., as a series of charge and discharge stages with the use of MEA: H2, Freidenberg H23C8 Pt-C/GP-IEM 103/Sigracet 39AA, HBr + H2SO4; square cross-section of 4 cm2 surface area, under an alternating galvanostatic mode at a current density of 75 mA/cm2. The coulombic, voltaic and energy efficiencies of the flow battery under a cyclic regime, as well as the absorption spectra of the catholyte, were measured during its operation. The total amount of Br-containing compounds penetrating through the membrane into the anode space was also determined.
Keywords: bromate anions reduction; bromide anions oxidation; crossover; flow battery; fuel cell; redox mediator cycle.