Yao Kai, Xu Zhanwei, Huang Jianfeng, Ma Meng, Fu Licai, Shen Xuetao, Li Jia, Fu Maosen
School of Materials Science and Engineering, Shaanxi Key Laboratory of Green Preparation and Functionalization for Inorganic Materials, Shaanxi University of Science and Technology, Xi'an, 710021, China.
College of Material Science and Engineering, Hunan University, Changsha, 410082, China.
Small. 2019 Mar;15(12):e1805405. doi: 10.1002/smll.201805405. Epub 2019 Feb 20.
Molybdenum disulfide (MoS ), a 2D-layered compound, is regarded as a promising anode for sodium-ion batteries (SIBs) due to its attractive theoretical capacity and low cost. The main challenges associated with MoS are the low rate capability suffering from the sluggish kinetics of Na intercalation and the poor cycling stability owning to the stack of MoS sheets. In this work, a unique architecture of bundled defect-rich MoS (BD-MoS ) that consists of MoS with large vacancies bundled by ultrathin MoO is achieved via a facile quenching process. When employed as anode for a SIB, the BD-MoS electrode exhibits an ultrafast charge/discharge due to the pseudocapacitive-controlled Na storage mechanism in it. Further experimental and theoretical calculations show that Na is able to cross the MoS layer by vacancies, not only limited to diffusion along the layer, thus realizing a 3D Na diffusion with faster kinetics. Meanwhile, the bundling architecture reduces the stack of sheets with a superior cycle life illustrating the highly reversible capacities of 350 and 272 mAh g at 2 and 5 A g after 1000 cycles.
二硫化钼(MoS₂)是一种二维层状化合物,因其具有诱人的理论容量和低成本,被视为钠离子电池(SIBs)颇具前景的负极材料。与MoS₂相关的主要挑战在于,由于钠离子嵌入动力学缓慢,其倍率性能较低,且由于MoS₂片层的堆叠,循环稳定性较差。在这项工作中,通过一种简便的淬火工艺,实现了一种独特的富含缺陷的束状MoS₂(BD-MoS₂)结构,该结构由具有大量空位的MoS₂被超薄的MoO₂束状包裹而成。当用作SIBs的负极时,BD-MoS₂电极由于其赝电容控制的钠存储机制而表现出超快的充放电性能。进一步的实验和理论计算表明,钠离子能够通过空位穿过MoS₂层,而不仅限于沿层扩散,从而实现了具有更快动力学的三维钠扩散。同时,束状结构减少了片层的堆叠,具有优异的循环寿命,在1000次循环后,在2 A g和5 A g下分别表现出350和272 mAh g的高可逆容量。