假电容
超级电容器
材料科学
电容
氧化物
电极
电解质
电化学
堆积
石墨烯
化学工程
多孔性
水平扫描速率
纳米技术
储能
重量分析
复合材料
循环伏安法
化学
冶金
物理化学
物理
工程类
功率(物理)
有机化学
量子力学
作者
Yongzheng Fang,Bowen Yang,Dongtong He,Huipeng Li,Kai Zhu,Lin Wu,Ke Ye,Kui Cheng,Jun Yan,Guiling Wang,Dianxue Cao
标识
DOI:10.1016/j.cclet.2019.08.043
摘要
MXene-based electrode materials exhibit favorable supercapacitor performance in sulfuric acid due to praised pseudocapacitance charge storage mechanism. However, self-stacking of conventional MXene electrodes severely restricts their electrochemical performance, especially at high loading. Herein, a flexible cross-linked porous Ti3C2Tx-MXene-reduced graphene oxide (Ti3C2Tx-RGO) film is skillfully designed and synthesized by microscopic explosion of graphene oxide (GO) at sudden high temperature. The generated chamber structure between layers could hold a few of electrolyte, leading to a close-fitting reaction at interlayer and avoiding complex ions transmission paths. The Ti3C2Tx-RGO film displayed a preferable rate performance than that of pure Ti3C2Tx film and a high capacitance of 505 F/g at 2 mV/s. Furthermore, the uniform intralayer structure and unique energy storage process lead to thickness-independenct electrochemical performances. This work provides a simple and feasible improvement approach for the design of MXene-based electrodes, which can be spread other electrochemical systems limited by ions transport, such as metal ions batteries and catalysis.
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