超级电容器
电解质
乙烯醇
材料科学
电容
化学工程
自愈水凝胶
电化学
储能
纳米技术
制作
离子电导率
聚合物
复合材料
电极
高分子化学
化学
工程类
物理
病理
物理化学
功率(物理)
医学
量子力学
替代医学
作者
Jingyang Tian,Zhe Sun,Cai Shi,Zhanhua Huang
标识
DOI:10.1016/j.ijbiomac.2023.125937
摘要
With the rapid development of flexible portable devices, polymer-based hydrogel electrolytes have drawn tremendous attention and widespread interest to replace conventional liquid electrolytes. Herein, an eco-friendly, low cost and fast method was adopted to synthesize novel cross-linked dual-network hydrogel electrolytes (PVA/SA/MXene-NaCl) within 5 min due to the formation of borate bonds. The unique dual-network structure of hydrogel enabled hydrogel electrolytes to efficiently dissipate energy under deformation and the formation of borate bonds endowed hydrogel with self-healing ability. Benefited from the introduction of NaCl and MXene, the hydrogels displayed a high ionic conductivity (40.8 mS/cm) and enhanced mechanical strength (650 kPa). Notedly, the flexible supercapacitor with low concentration of NaCl (0.3 mol L−1) delivered a superior areal capacitance of 130.8 mF cm−2 at 1 mA cm−2 and 106.2 mF cm−2 at 3 mA cm−2, and simultaneously offered remarkable capacitance retention under the state of bending, self-healing (five cycles), compression and stretching. Moreover, as-assembled supercapacitor maintained about 88.9 % of its original capacitance and 90.5 % of Coulombic efficiency after 5000 charge-discharge cycles. Our research presented a simple and universally pathway to prepare flexible energy storage devices with excellent mechanical and electrochemical properties.
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