Enhanced Pseudocapacitive Performance of α-MnO₂ by Cation Preinsertion

Although the theoretical capacitance of MnO₂ is 1370 F g⁻¹ based on the Mn³⁺/Mn⁴⁺ redox couple, most of the reported capacitances in literature are far below the theoretical value even when the material goes to nanoscale. To understand this discrepancy, in this work, the electrochemical behavior and charge storage mechanism of K⁺-inserted α-MnO₂ (or KxMnO₂) nanorod arrays in broad potential windows are investigated. It is found that electrochemical behavior of KxMnO₂ is highly dependent on the potential window. During cyclic voltammetry cycling in a broad potential window, K⁺ ions can be replaced by Na⁺ ions, which determines the pseudocapacitance of the electrode. The K⁺ or Na⁺ ions cannot be fully extracted when the upper cutoff potential is less than 1 V vs Ag/AgCl, which retards the release of full capacitance. As the cyclic voltammetry potential window is extended to 0-1.2 V, enhanced specific capacitance can be obtained with the emerging of new redox peaks. In contrast, the K⁺-free α-MnO₂ nanorod arrays show no redox peaks in the same potential window together with much lower specific capacitance. This work provides new insights on understanding the charge storage mechanism of MnO₂ and new strategy to further improve the specific capacitance of MnO₂-based electrodes.