材料科学
阳极
二硫化钼
动力学
扩散
钠离子电池
插层(化学)
堆栈(抽象数据类型)
钠
硫系化合物
离子
化学工程
电极
化学物理
电池(电)
纳米技术
光电子学
无机化学
复合材料
热力学
化学
物理化学
冶金
计算机科学
功率(物理)
有机化学
程序设计语言
法拉第效率
工程类
物理
量子力学
作者
Kai Yao,Zhanwei Xu,Jianfeng Huang,Meng Ma,Licai Fu,Xuetao Shen,Jia Li,Maosen Fu
出处
期刊:Small
[Wiley]
日期:2019-02-20
卷期号:15 (12)
被引量:170
标识
DOI:10.1002/smll.201805405
摘要
Molybdenum disulfide (MoS2 ), 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 MoS2 are the low rate capability suffering from the sluggish kinetics of Na+ intercalation and the poor cycling stability owning to the stack of MoS2 sheets. In this work, a unique architecture of bundled defect-rich MoS2 (BD-MoS2 ) that consists of MoS2 with large vacancies bundled by ultrathin MoO3 is achieved via a facile quenching process. When employed as anode for a SIB, the BD-MoS2 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 MoS2 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-1 at 2 and 5 A g-1 after 1000 cycles.
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