插层(化学)
钠
阴极
离子
磷酸盐
磷酸铁
材料科学
同步加速器
化学工程
体积热力学
储能
化学
无机化学
冶金
有机化学
热力学
物理化学
工程类
物理
功率(物理)
核物理学
作者
Xiaobo Zhu,T. Mochiku,Hiroki Fujii,Kaibin Tang,Yuxiang Hu,Zhenguo Huang,Bin Luo,Kiyoshi Ozawa,Lianzhou Wang
出处
期刊:Nano Research
[Springer Nature]
日期:2018-07-12
卷期号:11 (12): 6197-6205
被引量:31
标识
DOI:10.1007/s12274-018-2139-0
摘要
Low-cost room-temperature sodium-ion batteries (SIBs) are expected to promote the development of stationary energy storage applications. However, due to the large size of Na+, most Na+ host structures resembling their Li+ counterparts show sluggish ion mobility and destructive volume changes during Na ion (de)intercalation, resulting in unsatisfactory rate and cycling performances. Herein, we report a new type of sodium iron phosphate (Na0.71Fe1.07PO4), which exhibits an extremely small volume change (~ 1%) during desodiation. When applied as a cathode material for SIBs, this new phosphate delivers a capacity of 78 mA·h·g−1 even at a high rate of 50 C and maintains its capacity over 5,000 cycles at 20 C. In situ synchrotron characterization disclosed a highly reversible solid-solution mechanism during charging/discharging. The findings are believed to contribute to the development of high-performance batteries based on Earth-abundant elements.
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