Poor cycling stability and mechanistic controversies have hindered the wider application of rechargeable aqueous Zn-MnO2 batteries. Herein, direct evidence was provided of the importance of Mn2+ in this type of battery by using a bespoke cell. Without pre-addition of Mn2+ , the cell exhibited an abnormal discharge-charge profile, meaning it functioned as a primary battery. By adjusting the Mn2+ content in the electrolyte, the cell recovered its charging ability through electrodeposition of MnO2 . Additionally, a dynamic pH variation was observed during the discharge-charge process, with a precipitation of Zn4 (OH)6 (SO4 )⋅5H2 O buffering the pH of the electrolyte. Contrary to the conventional Zn2+ intercalation mechanism, MnO2 was first converted into MnOOH, which reverted to MnO2 through disproportionation, resulting in the dissolution of Mn2+ . The charging process occurred by the electrodeposition of MnO2 , thus improving the reversibility through the availability of Mn2+ ions in the solution.
Keywords: Mn2+ dissolution; aqueous Zn-MnO2 batteries; conversion; degradation; electrodeposition.
© 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.