成核
相(物质)
材料科学
亚稳态
阴极
相图
化学工程
纳米颗粒
化学物理
纳米技术
衍射
电极
锂(药物)
化学
物理
物理化学
热力学
内分泌学
工程类
有机化学
光学
医学
作者
Hao Liu,Fiona C. Strobridge,Olaf J. Borkiewicz,Kamila M. Wiaderek,Karena W. Chapman,Peter J. Chupas,Clare P. Grey
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2014-06-26
卷期号:344 (6191)
被引量:527
标识
DOI:10.1126/science.1252817
摘要
The absence of a phase transformation involving substantial structural rearrangements and large volume changes is generally considered to be a key characteristic underpinning the high-rate capability of any battery electrode material. In apparent contradiction, nanoparticulate LiFePO4, a commercially important cathode material, displays exceptionally high rates, whereas its lithium-composition phase diagram indicates that it should react via a kinetically limited, two-phase nucleation and growth process. Knowledge concerning the equilibrium phases is therefore insufficient, and direct investigation of the dynamic process is required. Using time-resolved in situ x-ray powder diffraction, we reveal the existence of a continuous metastable solid solution phase during rapid lithium extraction and insertion. This nonequilibrium facile phase transformation route provides a mechanism for realizing high-rate capability of electrode materials that operate via two-phase reactions.
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