Su Weiming, Liang Yue, Zuo Yinze, Tang Yuefeng
National Laboratory of Solid State Microstructures, Department of Energy Science and Engineering, College of Engineering and Applied Sciences, Nanjing University, Nanjing, 210093, China.
Dalton Trans. 2019 Sep 14;48(34):12964-12973. doi: 10.1039/c9dt02902h. Epub 2019 Aug 9.
SiC&Si@CNT composite 3D frameworks were successfully synthesized via an in situ reduction method of a C@SiO@CNT precursor. Owing to the extremely large amount of heat derived from magnesiothermic reduction, SiC particles of the SiC&Si@CNT composite were obtained by a reaction between Si and C. The amount of SiC could be adjusted by changing the poly-dopamine coating time. The SiC&Si@CNT composite is composed of reduced nano Si, fine SiC and CNTs. The as-prepared materials, particularly the SiC&Si@CNT-1 sample, show superior cycling performance and electrochemical characteristics as anode materials for lithium-ion batteries. In particular, the specific capacity of the SiC&Si@CNT-1 electrode reaches 1051.44 mA h g at 1 A g even after 880 cycles. Furthermore, the SiC&Si@CNT-1 electrode delivered ideal reversible capacities of 671.58 mA h g and 476.71 mA h g at high current densities of 4 A g and 8 A g, respectively. The porous nanostructure of the SiC&Si@CNT composite 3D framework is beneficial for shortening the path of lithium-ion diffusion inside the electrode, alleviating the volume expansion and contraction during the cycling process. These results suggest that the SiC&Si@CNT composite 3D frameworks can be used as appropriate anode materials for lithium-ion batteries.
通过C@SiO@CNT前驱体的原位还原法成功合成了SiC&Si@CNT复合三维框架。由于镁热还原产生的大量热量,SiC&Si@CNT复合材料中的SiC颗粒是通过Si与C之间的反应获得的。SiC的量可以通过改变聚多巴胺包覆时间来调节。SiC&Si@CNT复合材料由还原的纳米Si、细SiC和CNT组成。所制备的材料,特别是SiC&Si@CNT-1样品,作为锂离子电池的负极材料表现出优异的循环性能和电化学特性。特别是,即使在880次循环后,SiC&Si@CNT-1电极在1 A g下的比容量仍达到1051.44 mA h g。此外,SiC&Si@CNT-1电极在4 A g和8 A g的高电流密度下分别提供了671.58 mA h g和476.71 mA h g的理想可逆容量。SiC&Si@CNT复合三维框架的多孔纳米结构有利于缩短电极内部锂离子扩散的路径,减轻循环过程中的体积膨胀和收缩。这些结果表明,SiC&Si@CNT复合三维框架可作为锂离子电池合适的负极材料。