Wang Taohong, Shen Dongyang, Liu Huan, Chen Hongyi, Liu Quanhui, Lu Bingan
School of Physics and Electronics, Hunan University, Changsha 410082, P. R. China.
College of Materials Science and Engineering, Hunan Provincial Key Lab of Advanced Materials for New Energy Storage And Conversion, Hunan University of Science and Technology, Xiangtan, Hunan, 411201, P. R. China.
ACS Appl Mater Interfaces. 2020 Dec 30;12(52):57907-57915. doi: 10.1021/acsami.0c18285. Epub 2020 Dec 17.
Potassium-ion batteries (PIBs) are prospective for energy storage systems owing to their low price and high operating voltage. Antimony-based electrode materials have the advantage of high capacity for PIBs, while suffering from huge volume expansion and inferior stability because of the large radius of K. Therefore, developing suitable antimony-based electrode materials with high performance is highly challenging. Herein, self-assembled SbS nanoflowers on the surfaces of MXene (TiC) flakes are synthesized through a solvothermal reaction along with a calcination method. The highly conductive two-dimensional TiC soft substrate could not only boost the charge transfer kinetics but also buffer the volumetric expansion of SbS effectively. In addition, the structural stability is enhanced because the SbS nanoflowers are in situ grown on TiC flakes through the strong interfacial coupling. Consequently, the TiC-SbS anode exhibits a high reversible capacity of 461 mAh g at 100 mA g, long cycling life (capacity retention of 79% for 500 cycles), and superior rate performance (102 at 2000 mA g). This work may provide a pathway for designing advanced materials for PIBs.
钾离子电池(PIBs)因其价格低廉和工作电压高而在储能系统方面具有前景。锑基电极材料对钾离子电池而言具有高容量的优势,但由于钾离子半径较大,会出现巨大的体积膨胀且稳定性较差。因此,开发合适的高性能锑基电极材料极具挑战性。在此,通过溶剂热反应结合煅烧法,在MXene(TiC)薄片表面合成了自组装的SbS纳米花。高导电性的二维TiC软基底不仅可以促进电荷转移动力学,还能有效缓冲SbS的体积膨胀。此外,由于SbS纳米花通过强界面耦合原位生长在TiC薄片上,结构稳定性得到增强。因此,TiC-SbS负极在100 mA g下表现出461 mAh g的高可逆容量、长循环寿命(500次循环后容量保持率为79%)以及优异的倍率性能(在2000 mA g下为102)。这项工作可能为设计用于钾离子电池的先进材料提供一条途径。