材料科学
锂(药物)
电解质
阳极
电化学
重量分析
阴极
储能
离子
纳米技术
电极
化学工程
磁滞
物理化学
化学
热力学
医学
功率(物理)
物理
有机化学
量子力学
工程类
内分泌学
作者
Qiao Huang,Travis P. Pollard,Xiaolei Ren,Do Youb Kim,Alexandre Magasinski,Oleg A. Borodin,Gleb N. Yushin
出处
期刊:Small
[Wiley]
日期:2019-01-15
卷期号:15 (6): e1804670-e1804670
被引量:89
标识
DOI:10.1002/smll.201804670
摘要
Abstract The rapid development of ultrahigh‐capacity alloying or conversion‐type anodes in rechargeable lithium (Li)‐ion batteries calls for matching cathodes for next‐generation energy storage devices. The high volumetric and gravimetric capacities, low cost, and abundance of iron (Fe) make conversion‐type iron fluoride (FeF2 and FeF3)‐based cathodes extremely promising candidates for high specific energy cells. Here, the substantial boost in the capacity of FeF2 achieved with the addition of NiF2 is reported. A systematic study of a series of FeF2–NiF2 solid solution cathodes with precisely controlled morphology and composition reveals that the presence of Ni may undesirably accelerate capacity fading. Using a powerful combination of state‐of‐the‐art analytical techniques in combination with the density functional theory calculations, fundamental mechanisms responsible for such a behavior are uncovered. The unique insights reported in this study highlight the importance of careful selection of metals and electrolytes for optimizing electrochemical properties of metal fluoride cathodes.
科研通智能强力驱动
Strongly Powered by AbleSci AI