插层(化学)
材料科学
单层
阳极
电化学
电极
离子
化学工程
碳纤维
纳米技术
退火(玻璃)
锂(药物)
二硫化钼
无机化学
储能
复合材料
复合数
有机化学
化学
功率(物理)
量子力学
物理
物理化学
医学
内分泌学
工程类
作者
Laiying Jing,Gang Lian,Feier Niu,Jian Yang,Qilong Wang,Deliang Cui,Ching‐Ping Wong,Xizheng Liu
出处
期刊:Nano Energy
[Elsevier]
日期:2018-06-30
卷期号:51: 546-555
被引量:106
标识
DOI:10.1016/j.nanoen.2018.06.084
摘要
Abstract Despite high theoretical specific capacity and uniform interlayer channel for accommodation of ions, poor cycling stability and rate capacity have been identified as critical roadblocks to further development of MoS 2 -based lithium ion batteries (LIBs) or sodium ion batteries (SIBs). In this study, few-atomic-layered MoS 2 hollow nanospheres with expanded interlayer spacing, due to alternate intercalation of N-doped monolayer carbon (m-C) between the adjacent MoS 2 monolayers, have been designed and synthesized via an annealing-followed soft-template approach. As an anode of SIBs, the ultrathin-layered m-C/MoS 2 superstructures electrode can deliver a reversible discharge capacity of 401 mA h g −1 at 200 mA g −1 after 150 cycles. It can maintain 262 mA h g −1 at 2000 mA g −1 after 600 cycles with a capacity retention of 105% in comparison with that of the 2nd cycle. For LIBs, the hollow nanospheres can also deliver a reversible discharge capacity of 1025 mA h g −1 at 1000 mA g −1 after 80 cycles. The excellent electrochemical performance can be attributed to the synergy effect of expanded interlayer spacing (improving ion diffusion mobility), ultrathin feature (shortening ion diffusion paths) and alternate intercalation of monolayer carbon (improving the electrical conductivity and maintaining the structural integrity), which ensures new opportunities for designing advanced two-dimensional hosts for energy storage devices.
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