Cao Zhiqian, Zhu Yin-Bo, Chen Kai, Wang Quan, Li Yujin, Xing Xianjun, Ru Jie, Meng Ling-Guo, Shu Jie, Shpigel Netanel, Chen Li-Feng
Key Laboratory of Green and Precise Synthetic Chemistry and Applications, Ministry of Education, School of Chemistry and Materials Science, Huaibei Normal University, Huaibei, Anhui, 235000, China.
CAS Key Laboratory of Mechanical Behavior and Design of Materials (LMBD), School of Engineering Science, School of Chemistry and Materials Science, Division of Nanomaterials &Chemistry, Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, Anhui, 230026, China.
Adv Mater. 2024 Jun;36(26):e2401271. doi: 10.1002/adma.202401271. Epub 2024 Apr 5.
The advancement of aqueous micro-supercapacitors offers an enticing prospect for a broad spectrum of applications, spanning from wearable electronics to micro-robotics and sensors. Unfortunately, conventional micro-supercapacitors are characterized by low capacity and slopy voltage profiles, limiting their energy density capabilities. To enhance the performance of these devices, the use of 2D MXene-based compounds has recently been proposed. Apart from their capacitive contributions, these structures can be loaded with redox-active nanowires which increase their energy density and stabilize their operation voltage. However, introducing rigid nanowires into MXene films typically leads to a significant decline in their mechanical properties, particularly in terms of flexibility. To overcome this issue, super stretchable micro-pseudocapacitor electrodes composed of MXene nanosheets and in situ reconstructed Ag nanoparticles (Ag-NP-MXene) are herein demonstrated, delivering high energy density, stable operation voltage of ≈1 V, and fast charging capabilities. Careful experimental analysis and theoretical simulations of the charging mechanism of the Ag-NP-MXene electrodes reveal a dual nature charge storage mechanism involving ad(de)sorption of ions and conversion reaction of Ag nanoparticles. The superior mechanical properties of synthesized films obtained through in situ construction of Ag-NP-MXene structure show an ultra stretchability, allowing the devices to provide stable voltage and energy output even at 100% elongation.
水性微型超级电容器的发展为从可穿戴电子设备到微型机器人和传感器等广泛的应用领域提供了诱人的前景。不幸的是,传统的微型超级电容器具有容量低和电压分布斜率大的特点,限制了它们的能量密度性能。为了提高这些器件的性能,最近有人提出使用基于二维MXene的化合物。除了它们的电容贡献外,这些结构还可以负载氧化还原活性纳米线,从而提高它们的能量密度并稳定其工作电压。然而,将刚性纳米线引入MXene薄膜通常会导致其机械性能显著下降,特别是在柔韧性方面。为了克服这个问题,本文展示了由MXene纳米片和原位重构的银纳米颗粒(Ag-NP-MXene)组成的超可拉伸微型赝电容器电极,其具有高能量密度、约1V的稳定工作电压和快速充电能力。对Ag-NP-MXene电极充电机制的仔细实验分析和理论模拟揭示了一种双重性质的电荷存储机制,涉及离子的吸附/解吸和银纳米颗粒的转化反应。通过原位构建Ag-NP-MXene结构获得的合成薄膜具有优异的机械性能,表现出超拉伸性,使器件即使在100%伸长率下也能提供稳定的电压和能量输出。