Abstract

Layered birnessite-type manganese oxide is exfoliated into single-layer manganese oxide nanosheets. Then, the exfoliated manganese oxide nanosheets are spontaneously restacked by a self-assembly process, which is driven mainly by electrostatic interactions between the negatively charged manganese oxide nanosheets and the positively charged tetramethylammonium (TMA+) ions, yielding a new ordered layered structure of MnO2 (self-assembled MnO2) with a large interlayer spacing of 0.67nm, suggesting the formation of a layered hybrid form, intercalated with TMA+ ions in residence between the manganese oxide nanosheets. The large interlayer spacing facilitates rapid ion exchange and the intercalation and deintercalation of electrolyte cations. The supercapacitive behavior of the as-prepared self-assembled MnO2 is evaluated by cyclic voltammetry (CV), galvanostatic charge–discharge (CD) experiments and electrochemical impedance spectroscopy (EIS). The specific capacitance value is 180Fg−1 at a current density of 0.5Ag−1. After 10,000 cycles, the specific capacitance is still approximately 90% of the maximum specific capacitance. In addition, the intercalation of TMA+ ions between the manganese oxide nanosheets leads to a low charge-transfer resistance. These experimental results demonstrate that this self-assembled MnO2 is a promising candidate for use as electrode material in supercapacitor applications.

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