超级电容器
材料科学
氧化还原
极性(国际关系)
储能
电极
纳米技术
电化学储能
假电容器
计算机数据存储
化学工程
电化学
计算机科学
冶金
计算机硬件
化学
生物化学
功率(物理)
物理
物理化学
量子力学
工程类
细胞
作者
Situo Cheng,Zhihui Zhang,Jianfeng Yan,Tianyu Yang,Junli Zhang,Jiecai Fu
标识
DOI:10.1002/adfm.202502526
摘要
Abstract 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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