Impact of LiFePO[sub 4]∕C Composites Porosity on Their Electrochemical Performance

多孔性 扫描电子显微镜 材料科学 电化学 粒子(生态学) 热分解 粒径 复合材料 吸附 化学工程 化学 电极 有机化学 物理化学 工程类 地质学 海洋学
作者
Robert Dominko,Jean‐Michel Goupil,Marjan Bele,Miran Gaberšček,Maja Remškar,D. Hanžel,J. Jamnik
出处
期刊:Journal of The Electrochemical Society [The Electrochemical Society]
卷期号:152 (5): A858-A858 被引量:129
标识
DOI:10.1149/1.1872674
摘要

citrate was used as a source for synthesis of microsized porous particles. All samples, prepared either by solid-state or by sol-gel techniques, are phase-pure triphylite phases, which, however, have different morphology highly influenced by the type of synthesis and synthesis parameters. Their common feature is porosity due to thermal decomposition of citrate anion. The impact of particle porosity on the electrochemical behavior is discussed in terms of qualitative results obtained from scanning electron microscopy (SEM) micrographs and in terms of quantitative results obtained from adsorption isotherms. The best electrochemical behavior (above at rate during continuous cycling) was obtained with composites prepared at a relatively high heating rate (above ). This suggests that interlaced pores were formed inside particles. A strong correlation between the electrochemical results and the heating rate was observed, which could easily be explained based on SEM micrographs and on some trends found in porosity measurements. The latter reveal the main difference between samples prepared by solid-state and by sol-gel techniques.

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