Abstract
The MnIII /MnII redox couple with a standard potential of +1.51 V versus the standard hydrogen electrode (SHE) has attracted interest for the design of V/Mn redox flow batteries (RFBs). However, MnIII disproportionation leads to a loss of capacity, an increase in pressure drop, and electrode passivation caused by the formation of MnO2 particles during battery cycling. In this work, the influence of TiIV or/and VV on MnIII stability in acidic conditions is studied by formulating four different electrolytes in equimolar ratios (Mn, Mn/Ti, Mn/V, Mn/V/Ti). Voltammetry studies have revealed an ECi process for MnII oxidation responsible for the electrode passivation. SEM and XPS analysis demonstrate that the nature and morphology of the passivating oxides layer depend strongly on the electrolyte composition. Spectroelectrochemistry highlights the stabilization effect of TiIV and VV on MnIII . At a comparable pH, the amount of MnIII loss through disproportionation is decreased by a factor of 2.5 in the presence of TiIV or/and VV . Therefore, VV is an efficient substitute for TiIV to stabilize the MnIII electrolyte for RFB applications.
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