Evaluation of real performance of LiFePO4 by using single particle technique

被引:77
作者
Munakata, Hirokazu [1 ]
Takemura, Bunpei [1 ]
Saito, Takamitsu [1 ]
Kanamura, Kiyoshi [1 ]
机构
[1] Tokyo Metropolitan Univ, Dept Appl Chem, Grad Sch Urban Environm Sci, Hachioji, Tokyo 1920397, Japan
关键词
Lithium-ion battery; Lithium iron phosphate; Single particle measurement; Rate capability; Diffusion coefficient; Exchange current density; LITHIUM-ION BATTERIES; LAYERED CATHODE MATERIAL; ELECTRODE; CAPACITY; SIMULATION; BEHAVIOR; DESIGN;
D O I
10.1016/j.jpowsour.2012.06.037
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Single particle technique was employed to investigate the intrinsic electrochemical properties of LiFePO4. A micro-size LiFePO4 single particle composed of a plurality of primary particles was contacted with a micro Pt electrode in an electrolyte solution using a micromanipulator under optical microscope observation, and then galvanostatic charge/discharge tests were performed. The specific capacity of the particle with a diameter of 24 pm was estimated to be 1.5 nA h in the potential rage of 2.0-4.2 V vs. Li/Lit The particle had a good reversibility for charge/discharge processes, and also showed excellent rate performance, for example, that more than 50% of the full capacity was maintained even when the discharge current was as high as 750 nA corresponding to 4 s discharge (900 C rate). From the dependency of over-potential in the single particle electrode on discharge current density, it was expected that the discharge reaction was controlled at the discharge current densities higher than 2.56 mA cm(-2) by Li+ diffusion step in the particle accompanied with the phase conversion from FePO4 to LiFePO4. According to this assumption, Li+ diffusion coefficient in the particle was estimated as 2.7 x 10(-9) cm(2) s(-1). (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:444 / 448
页数:5
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