In Situ Hydrothermal Synthesis of LiFePO4 Studied by Synchrotron X-ray Diffraction

成核 同步加速器 溶解 材料科学 结晶 原位 水热合成 衍射 化学工程 电极 热液循环 纳米技术 化学 物理化学 光学 物理 工程类 有机化学
作者
Jiajun Chen,Jianming Bai,Haiyan Chen,Jason Graetz
出处
期刊:Journal of Physical Chemistry Letters [American Chemical Society]
卷期号:2 (15): 1874-1878 被引量:63
标识
DOI:10.1021/jz2008209
摘要

The development of high capacity, safe lithium battery materials requires new tools to better understand how reaction conditions affect nucleation and crystallization, particle size, morphology, and defects. We present a general approach for studying the synthesis of Li battery electrode materials in real time. The formation of LiFePO4 was investigated by time-resolved in situ synchrotron X-ray diffraction under hydrothermal conditions, and the reaction kinetics were determined by changes of the Bragg reflections. We provide the first evidence in support of a dissolution–reprecipitation process for the formation of LiFePO4, which occurs at temperatures as low as 105 °C and appears to be a three-dimensional diffusion-controlled process. Lattice parameters and their evolution were monitored in situ, as well as the formation of antisite defects and their subsequent elimination under various synthesis conditions. The ability to characterize and tailor synthesis reactions in situ is essential for rapid optimization of the synthesis procedures and, ultimately, the development of new battery electrodes.
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