阳极
法拉第效率
电解质
材料科学
二硫化钼
傅里叶变换红外光谱
钠离子电池
极化(电化学)
化学工程
电化学
电极
化学
工程类
物理化学
冶金
作者
Jingjing Wang,Chao Luo,Tao Gao,Alex Langrock,A. C. Mignerey,Chunsheng Wang
出处
期刊:Small
[Wiley]
日期:2014-09-25
卷期号:11 (4): 473-481
被引量:414
标识
DOI:10.1002/smll.201401521
摘要
Molybdenum disulfide (MoS2) is a promising anode for high performance sodium-ion batteries due to high specific capacity, abundance, and low cost. However, poor cycling stability, low rate capability and unclear electrochemical reaction mechanism are the main challenges for MoS2 anode in Na-ion batteries. In this study, molybdenum disulfide/carbon (MoS2/C) nanospheres are fabricated and used for Na-ion battery anodes. MoS2/C nanospheres deliver a reversible capacity of 520 mAh g−1 at 0.1 C and maintain at 400 mAh g−1 for 300 cycles at a high current density of 1 C, demonstrating the best cycling performance of MoS2 for Na-ion batteries to date. The high capacity is attributed to the short ion and electron diffusion pathway, which enables fast charge transfer and low concentration polarization. The stable cycling performance and high coulombic efficiency (∼100%) of MoS2/C nanospheres are ascribed to (1) highly reversible conversion reaction of MoS2 during sodiation/desodiation as evidenced by ex-situ X-ray diffraction (XRD) and (2) the formation of a stable solid electrolyte interface (SEI) layer in fluoroethylene carbonate (FEC) based electrolyte as demonstrated by fourier transform infrared spectroscopy (FTIR) measurements.
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