1.西南交通大学材料科学与工程学院,四川 成都610031
2.西南交通大学智慧城市与交通学院,四川 成都611756
薛曜东(2005—),男,本科生,专业为材料科学与工程,E-mail:3219891134@qq.com;
张海涛,教授,从事高功率储能科学与功率调度技术研究,E-mail:haitaozhang@swjtu.edu.cn。
收稿:2026-03-26,
修回:2026-04-24,
纸质出版:2026-05-28
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薛曜东, 史睿洋, 唐靓, 等. 褶皱状少层Ti3C2 MXene的制备及超级电容性能研究[J]. 储能科学与技术, 2026, 15(5): 1618-1625.
XUE Yaodong, SHI Ruiyang, TANG Liang, et al. Preparation of few-layer corrugated Ti3C2 MXene and its supercapacitor performance[J]. Energy Storage Science and Technology, 2026, 15(5): 1618-1625.
薛曜东, 史睿洋, 唐靓, 等. 褶皱状少层Ti3C2 MXene的制备及超级电容性能研究[J]. 储能科学与技术, 2026, 15(5): 1618-1625. DOI: 10.19799/j.cnki.2095-4239.2026.0244.
XUE Yaodong, SHI Ruiyang, TANG Liang, et al. Preparation of few-layer corrugated Ti3C2 MXene and its supercapacitor performance[J]. Energy Storage Science and Technology, 2026, 15(5): 1618-1625. DOI: 10.19799/j.cnki.2095-4239.2026.0244.
为解决Ti
3
C
2
MXene电极材料因层间自堆叠导致离子传输受阻、超级电容性能衰减的关键问题,本研究以高比例少层Ti
3
C
2
MXene水溶液(1~3层占比96%)为前驱体,选取不同种类的有机溶剂如乙醇(ET)、乙腈(AN)、二甲基亚砜(DMSO),协同旋蒸工艺对材料进行结构与形貌调控,系统探究有机溶剂种类对材料层间距、微观形貌及电化学行为的影响规律。通过X射线衍射、扫描电子显微镜、傅里叶变换红外光谱对材料结构与形貌进行表征,结合循环伏安、恒流充放电、电化学阻抗谱及弛豫时间分布分析,评估褶皱状Ti
3
C
2
MXene在对称超级电容器与柔性微型超级电容器中的储能性能。X射线衍射结果表明,有机溶剂处理可显著增大MXene层间距并呈现DMSO
>
ET
>
AN的规律;扫描电子显微镜显示改性后材料均形成褶皱状形貌,有效抑制层间堆叠。电化学测试表明,乙醇改性样品在低电流密度下输出最高比容量,适合高容量储能应用;乙腈改性样品电荷转移电阻与离子扩散电阻最小,高倍率充放电性能最优。在微型超级电容器中,乙醇改性电极的面积比电容与容量保持率显著优于未改性样品。本研究通过无外源插层剂的有机溶剂改性策略,实现Ti
3
C
2
MXene结构精准调控,为高性能MXene基储能器件的设计与制备提供实验依据与新的思路。
To address the critical issue o
f hindered ion transport and degraded supercapacitor performance caused by interlayer self-stacking of Ti
3
C
2
MXene electrode materials
this study employed an aqueous solution of high-proportion few-layer Ti
3
C
2
MXene (96% consisting of 1-3 layers) as the precursor. Different organic solvents
ethanol (ET)
acetonitrile (AN)
and dimethyl sulfoxide (DMSO)
were combined with a rotary evaporation process to regulate the structure and morphology of the material. The influences of the organic solvent type on the interlayer spacing
micromorphology
and electrochemical behavior of the material were systematically investigated. The structure and morphology of the material were characterized using X-ray diffraction
scanning electron microscopy
and Fourier transform infrared spectroscopy. The energy storage performance of the corrugated Ti
3
C
2
MXene in symmetric supercapacitors and flexible micro-supercapacitors was evaluated using cyclic voltammetry
galvanostatic charge-discharge
electrochemical impedance spectroscopy
and relaxation time distribution analysis. X-ray diffraction results demonstrate that organic solvent treatment significantly enlarges the interlayer spacing of MXene
with the extent of expansion following the order DMSO
>
ET
>
AN. Scanning electron microscopy images reveal that all modified materials exhibit a corrugated morphology
which effectively suppresses interlayer stacking. Electrochemical tests indicate that the ET-modified sample delivers the highest specific capacitance at low current densities
making it suitable for high-capacity energy storage applications. The AN-modified sample exhibits the lowest charge transfer resistance and ion diffusion resistance
resulting in optimal high-rate charge-discharge performance. In micro-supercapacitors
the ET-modified electrode presents significantly higher areal specific capacitance and better capacity retention rate than the unmodified sample. This study achieves precise structur
al regulation of Ti
3
C
2
MXene via an organic solvent modification strategy without the use of exogenous intercalators
providing experimental evidence and a viable route for the design and fabrication of high-performance MXene-based energy storage devices.
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