拉曼光谱
相(物质)
材料科学
转化(遗传学)
衍射
原位
分析化学(期刊)
粒子(生态学)
锂(药物)
光谱学
原子单位
化学工程
化学
光学
基因
海洋学
医学
物理
地质学
工程类
内分泌学
有机化学
量子力学
生物化学
色谱法
作者
N.A. Siddique,Amir Salehi,Zi Wei,Dong Liu,Syed D. Sajjad,Fuqiang Liu
出处
期刊:ChemPhysChem
[Wiley]
日期:2015-06-12
卷期号:16 (11): 2383-2388
被引量:17
标识
DOI:10.1002/cphc.201500299
摘要
The charge and discharge of lithium ion batteries are often accompanied by electrochemically driven phase-transformation processes. In this work, two in situ and operando methods, that is, micro-Raman spectroscopy and X-ray diffraction (XRD), have been combined to study the phase-transformation process in LiFePO4 at two distinct length scales, namely, particle-level scale (∼1 μm) and macroscopic scale (∼several cm). In situ Raman studies revealed a discrete mode of phase transformation at the particle level. Besides, the preferred electrochemical transport network, particularly the carbon content, was found to govern the sequence of phase transformation among particles. In contrast, at the macroscopic level, studies conducted at four different discharge rates showed a continuous but delayed phase transformation. These findings uncovered the intricate phase transformation in LiFePO4 and potentially offer valuable insights into optimizing the length-scale-dependent properties of battery materials.
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