Abstract

Development of aqueous zinc-ion batteries (ZIBs) promises low-cost and safe energy storage systems. From the existing natural resources manganese-based compounds are desirable cathodes materials for aqueous ZIBs. We present a layered birnessite-type δ–K0.32MnO2·0·15H2O (MnO2) as a candidate cathode material. By adding reduced graphene oxide (rGO) to enhance electron transport, we present the electrode performance in Al pouch cells (3.2 × 3.4 cm2) achieving a high-capacity of 373 mAh g1− at 0.1C which retained over 99 % for 120 cycles. Additionally, performance is highlighted at 5C and 10C, retaining 89 % for 500 cycles and 35 % for 2,000 cycles, respectively. The main redox process involves the Mn4+/Mn3+ redox couple, accompanied by a conversion reaction through the de/protonation process. Operando XRD, operando pH measurement, and time-of-flight secondary-ion mass spectroscopy prove that the de/protonation process of solvated zinc ions [Zn(H2O)6]2+, followed by protonation of the active material leads to the formation of KxMnOOH(1- x) during discharge and vice versa during charging. The conversion reaction resulting from the de/protonation processes leads to the amorphization of the active material after the prolonged cycles. Operando pH analysis shows the influence of the pH on de/protonation of [Zn(H2O)6]2+ complex, thus implicating it as a determinant of the capacity.

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