锂(药物)
离子
氧化还原
材料科学
相(物质)
数码产品
化学工程
纳米技术
能量密度
化学
工程物理
冶金
物理化学
有机化学
物理
医学
工程类
内分泌学
作者
Prabeer Barpanda,Mohamed Ati,Brent C. Melot,Gwenaëlle Rousse,Jean‐Noël Chotard,Marie‐Liesse Doublet,Moulay Tahar Sougrati,Serena A. Corr,J.C. Jumas,J-M. Tarascon
出处
期刊:Nature Materials
[Springer Nature]
日期:2011-08-21
卷期号:10 (10): 772-779
被引量:320
摘要
Li-ion batteries have empowered consumer electronics and are now seen as the best choice to propel forward the development of eco-friendly (hybrid) electric vehicles. To enhance the energy density, an intensive search has been made for new polyanionic compounds that have a higher potential for the Fe²⁺/Fe³⁺ redox couple. Herein we push this potential to 3.90 V in a new polyanionic material that crystallizes in the triplite structure by substituting as little as 5 atomic per cent of Mn for Fe in Li(Fe(1-δ)Mn(δ))SO₄F. Not only is this the highest voltage reported so far for the Fe²⁺/Fe³⁺ redox couple, exceeding that of LiFePO₄ by 450 mV, but this new triplite phase is capable of reversibly releasing and reinserting 0.7-0.8 Li ions with a volume change of 0.6% (compared with 7 and 10% for LiFePO₄ and LiFeSO₄F respectively), to give a capacity of ~125 mA h g⁻¹.
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