Wu Wenling, Wang Chengwei, Zhao Chunhui, Wei Dan, Zhu Jianfeng, Xu Youlong
School of Material Science and Engineering, Shaanxi Key Laboratory of Green Preparation and Functionalization for Inorganic Materials, Shaanxi University of Science and Technology, Xi'an 710021, PR China; Electronic Materials Research Laboratory, Key Laboratory of the Ministry of Education & International Center for Dielectric Research, School of Electronic Science and Engineering, Xi'an Jiaotong University, Xi'an 710049, PR China.
School of Material Science and Engineering, Shaanxi Key Laboratory of Green Preparation and Functionalization for Inorganic Materials, Shaanxi University of Science and Technology, Xi'an 710021, PR China.
J Colloid Interface Sci. 2020 Nov 15;580:601-613. doi: 10.1016/j.jcis.2020.07.052. Epub 2020 Jul 15.
Titanium carbide MXene (TiC) has attracted significant research interest because of its extraordinary advantages as advanced electrode material for energy storage. In this work, we explored a facile strategy to construct TiC-based hierarchical composite materials by surface modification using pseudocapacitive materials. The method involved the synthesis of the exfoliation of ultrathin TiC nanosheets, followed by one-pot in situ polymerization and surface decoration using polyaniline nanotubes (PANI-NTs). Herein, the self-aggregation of TiC layers had been effectively suppressed, resulting in an enhanced interlamellar spacing and enlarged ion contact area. Furthermore, the novel hierarchical structure of TiC/PANI-NTs can facilitate the electrolyte ions diffusion, which also boosted more electrochemical active sites to become more accessible. In addition, the electrochemical test in the three-electrode system demonstrated that the specific capacitance of the TiC/PANI-NTs-1 composite can be as high as 596.6F g at 0.1 A g, remaining 94.7% retention of initial capacitance after 5000 cycles of charge/discharge. Moreover, the symmetric supercapacitor device based on TiC/PANI-NTs-1 composite exhibited a maximum energy density of 25.6 Wh kg (at 153.2 W kg) and an impressive power density of 1610.8 W kg (at 13.2 Wh kg), as well as outstanding cycling stability (81.1% retention of the capacitance after 4000 cycles). These electrochemical measurements indicated that the performance of TiC-based supercapacitors could be immensely improved by designing and constructing the hierarchical structure with abundant pseudocapacitive materials. Furthermore, this strategy could be extended to other MXenes composite materials as advanced electrodes by taking full advantage of their potentials for new symmetric supercapacitors.
碳化钛MXene(TiC)因其作为储能先进电极材料的非凡优势而引起了广泛的研究兴趣。在这项工作中,我们探索了一种简便的策略,通过使用赝电容材料进行表面改性来构建基于TiC的分级复合材料。该方法包括合成超薄TiC纳米片的剥离,然后通过聚苯胺纳米管(PANI-NTs)进行一锅原位聚合和表面修饰。在此,TiC层的自聚集得到了有效抑制,导致层间距增大和离子接触面积扩大。此外,TiC/PANI-NTs的新型分级结构可以促进电解质离子扩散,这也增加了更多的电化学活性位点,使其更容易接近。此外,三电极系统中的电化学测试表明,TiC/PANI-NTs-1复合材料在0.1 A g时的比电容高达596.6F g,在5000次充放电循环后初始电容保持率为94.7%。此外,基于TiC/PANI-NTs-1复合材料的对称超级电容器装置表现出最大能量密度为25.6 Wh kg(在153.2 W kg时)和令人印象深刻的功率密度为1610.8 W kg(在13.2 Wh kg时),以及出色的循环稳定性(在4000次循环后电容保持率为81.1%)。这些电化学测量表明,通过设计和构建具有丰富赝电容材料的分级结构,可以极大地提高基于TiC的超级电容器的性能。此外,通过充分利用其在新型对称超级电容器方面的潜力,该策略可以扩展到其他MXenes复合材料作为先进电极。