插层(化学)
嫁接
碳化钛
材料科学
表面改性
MXenes公司
热重分析
最大相位
电化学
离子
化学工程
混合材料
芳基
碳化物
超级电容器
电极
化学
纳米技术
无机化学
复合材料
有机化学
烷基
物理化学
聚合物
工程类
作者
Hongbing Wang,Jianfeng Zhang,Yuping Wu,Huajie Huang,Quanguo Jiang
标识
DOI:10.1016/j.jpcs.2017.12.039
摘要
Two-dimensional Ti3C2 MXene nanosheets were functionalized with phenylsulfonic groups derived from in situ generated diazonium ions by the corresponding amine. During the functionalization process, the aryl groups were attached onto the MXene surfaces in the form of strong MXene-aryl (TiOC) linkages. Simultaneously, the intercalation of diazonium ions enabled Ti3C2 multi-layers to be delaminated into separate few-layer nanosheets via weak sonication with low energy. As a result of chemical functionalization for MXene Ti3C2, the dispersibility was greatly improved and the specific surface area increased significantly. The grafted functional groups are still stable up to at least 200 °C upon thermogravimetric analysis measurements. With diazonium ions intercalating and electroactive groups grafting between-in MXene layers, the chemically functionalized Ti3C2 electrodes exhibited an enhanced supercapacitive performance, which acquired a specific capacitance more than double that of pristine Ti3C2 samples and excellent cycling stability (91% capacity retention after 10,000 cycles at 3 A g−1). This feasible modification scheme can be also extended to functionalize other types of MXenes materials with this or other aryl diazonium ions as surface modifiers and intercalants, thus offering scope for full potential applications of the new 2D materials.
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