插层(化学)
阳极
碳纤维
材料科学
溶剂
储能
化学工程
电池(电)
X射线光电子能谱
钠
电极
纳米技术
无机化学
化学
有机化学
复合数
物理化学
复合材料
冶金
工程类
物理
功率(物理)
量子力学
作者
Nan Jiang,Long Chen,Hao Jiang,Yanjie Hu,Chunzhong Li
出处
期刊:Small
[Wiley]
日期:2022-03-01
卷期号:18 (15)
被引量:19
标识
DOI:10.1002/smll.202108092
摘要
As the most successful anode material for sodium-ion batteries, hard carbon has attracted extensive attention from researchers. However, its storage mechanism is still controversial. In this paper, a solvent co-intercalation mechanism into hard carbon is proposed and is proved by in situ XRD and ex situ TEM XPS results successfully. Thanks to the co-intercalation of solvent, the platform capacity of hard carbon maintains well at very high current densities. It can even exhibit 245 mAh g-1 at 5 A g-1 , which is the best rate performance obtained for hard carbon anode as far as it is known. The full battery assembled with Na3 V2 (PO4 )3 has a high energy density of 157 Wh kg-1 at 3800 W kg-1 (relative to the electrode). This finding brings new insights with regard to the design of hard carbon materials and sodium storage mechanisms.
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