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通过原位中子衍射可视化锂离子电池中的化学和结构动力学。

Visualizing the chemistry and structure dynamics in lithium-ion batteries by in-situ neutron diffraction.

机构信息

Chemical and Engineering Materials Division, Oak Ridge National Laboratory Oak Ridge, TN 37831-6465, USA.

出版信息

Sci Rep. 2012;2:747. doi: 10.1038/srep00747. Epub 2012 Oct 19.

Abstract

We report an in-situ neutron diffraction study of a large format pouch battery cell. The succession of Li-Graphite intercalation phases was fully captured under an 1C charge-discharge condition (i.e., charge to full capacity in 1 hour). However, the lithiation and dilithiation pathways are distinctively different and, unlike in slowing charging experiments with which the Li-Graphite phase diagram was established, no LiC₂₄ phase was found during charge at 1C rate. Approximately 75 mol. % of the graphite converts to LiC₆ at full charge, and a lattice dilation as large as 4% was observed during a charge-discharge cycle. Our work demonstrates the potential of in-situ, time and spatially resolved neutron diffraction study of the dynamic chemical and structural changes in "real-world" batteries under realistic cycling conditions, which should provide microscopic insights on degradation and the important role of diffusion kinetics in energy storage materials.

摘要

我们报告了一项原位中子衍射研究,研究对象是一种大型袋式电池。在 1C 的充放电条件下(即在 1 小时内充满电),成功地捕获了完整的 Li-石墨嵌入相序列。然而,锂化和双锂化途径明显不同,而且与建立 Li-石墨相图的缓慢充电实验不同,在 1C 速率下充电时没有发现 LiC₂₄ 相。在完全充电时,大约有 75%的石墨转化为 LiC₆,在充放电循环过程中观察到高达 4%的晶格膨胀。我们的工作证明了在实际循环条件下,对“真实世界”电池中的动态化学和结构变化进行原位、时间和空间分辨中子衍射研究的潜力,这应该为降解和扩散动力学在储能材料中的重要作用提供微观见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b6/3475991/05f7e86bdd06/srep00747-f1.jpg

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