Rate-Dependent, Li-Ion Insertion/Deinsertion Behavior of LiFePO4 Cathodes in Commercial 18650 LiFePO4 Cells

被引:59
|
作者
Liu, Qi [1 ]
He, Hao [1 ]
Li, Zhe-Fei [1 ]
Liu, Yadong [1 ]
Ren, Yang [2 ]
Lu, Wenquan [3 ]
Lu, Jun [3 ]
Stach, Eric A. [4 ]
Xie, Jian [1 ]
机构
[1] Indiana Univ Purdue Univ, Purdue Sch Engn & Technol, Dept Mech Engn, Indianapolis, IN 46202 USA
[2] Argonne Natl Lab, Xray Sci Div, Adv Photon Source, Lemont, IL 60439 USA
[3] Argonne Natl Lab, Chem Sci & Engn Div, Lemont, IL 60439 USA
[4] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
关键词
lithium insertion/deinsertion mechanism; lithiation/delithiation LiFePO4; synchrotron high-energy X-ray diffraction; commercial cells; PHASE-TRANSFORMATION; PHOSPHO-OLIVINES; MISCIBILITY GAP; SOLID-SOLUTION; LITHIUM; NANOPARTICLES; MECHANISMS; INSERTION; FEPO4; INSERTION/EXTRACTION;
D O I
10.1021/am405150c
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We have performed operando synchrotron high-energy X-ray diffraction (XRD) to obtain nonintrusive, real-time monitoring of the dynamic chemical and structural changes in commercial 18650 LiFePO4/C cells under realistic cycling conditions. The results indicate a nonequilibrium lithium insertion and extraction in the LiFePO4 cathode, with neither the LiFePO4 phase nor the FePO4 phase maintaining a static composition during lithium insertion/extraction. On the basis of our observations, we propose that the LiFePO4 cathode simultaneously experiences both a two-phase reaction mechanism and a dual-phase solid-solution reaction mechanism over the entire range of the flat voltage plateau, with this dual-phase solid-solution behavior being strongly dependent on charge/ discharge rates. The proposed dual-phase solid-solution mechanism may explain the remarkable rate capability of LiFePO4 in commercial cells.
引用
收藏
页码:3282 / 3289
页数:8
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