The Delithiation Behavior of LiFePO4 Particles with Broad Particle Size Distribution during Chemically Delithiation

材料科学 粒子(生态学) 粒径 电化学 电极 阴极 相(物质) 离心机 粒度分布 纳米颗粒 化学工程 化学物理 纳米技术 化学 物理化学 物理 有机化学 核物理学 工程类 地质学 海洋学
作者
Sunyoung Yoo,Byoungwoo Kang
出处
期刊:Meeting abstracts [Institute of Physics]
卷期号:MA2014-02 (5): 305-305
标识
DOI:10.1149/ma2014-02/5/305
摘要

LiFePO 4 is the most promising cathode material, especially for electric vehicle (EV) because of its inexpensive cost, superior thermal and structural safety, and non-toxicity. Although LiFePO 4 has been believed to be poor conductor due to its low electronic conductivity and 1D lithium diffusion, nano-sized LiFePO 4 shows the fastest electrochemical reaction during charge and discharge. To understand these intriguing behaviors, we have to consider delithiation behavior of particles in the electrode which consists of 10 10 ~ 10 17 particles in addition to the transport properties in the material because a particle has a non-monotonic chemical potential [1] . The non-monotonic chemical potential of single particle in multi-particle electrode leads to characteristic electrochemical behaviors such as a flat potential in voltage curve of the electrode and a sequential phase transformation between particles. Thus, delithiation behaviors in a particle in the electrode should be understood. In this study, we will explore delithiation behaviors of LiFePO 4 with broad particle size distribution. For this purpose, chemical delithiation and followed centrifuge method were applied to understand the delithiation behavior of LiFePO 4 depending on particle size. This simple method shows phase transformation behaviors more directly. We synthesized LiFePO 4 with broad particle size distribution by solid state reaction. And then, we can easily separate chemically delithiated small and large particles by centrifuge method. In this talk, we will introduce simple centrifuge method and will discuss about delithiation behavior of LiFePO 4 with broad particle size distribution during chemical delithiation. [1] W. Dreyer et al 2010 The thermodynamic origin of hysteresis in insertion batteries Nature Mat. 9 , 448.

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