摘要
Micro-supercapacitors (MSCs) have emerged as indispensable power solutions for modern microelectronics, offering rapid charge/discharge capabilities, high power delivery, and exceptional cycling stability. However, their energy density remains limited due to the lower electrode capacitance and narrower voltage window of conventional symmetrical micro-supercapacitors (SMSCs). In this study, a novel strategy is presented to maximize the energy density of MnO 2 -based SMSCs by modulating their electrode polarity and redox activity. Specifically, the non-lattice oxygen concentration in MnO 2 is focused on tuning to introduce additional redox-active sites, thus improving charge storage capacity and energy density. Using operando electrochemical quartz crystal microbalance (EQCM) analysis reveals a multi-step redox mechanism involving lattice water-assisted transformations and non-lattice oxygen pathways, providing unprecedented insights into MnO 2 ’s electrochemical behavior in alkaline electrolytes. The engineered symmetric MnO 2 MSCs achieve an outstanding energy density of 33.63 µW h cm −2 at a power density of 1.12 mW cm −2 , retaining full performance under mechanical deformation. The alkaline electrolyte further inhibits disproportionation reaction, preserving active material integrity and cycling durability. This work not only unveils the pivotal role of non-lattice oxygen in MnO 2 electrochemical polarity but also provides a promising pathway for designing high-energy-density, flexible MSCs to power next-generation microdevices.
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