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In situ X-ray diffraction and electrochemical impedance spectroscopy of a nanoporous Li2FeSiO4/C cathode during the initial charge/discharge cycle of a Li-ion battery

机译:锂离子电池初始充电/放电循环期间纳米多孔Li2FesiO4 / C阴极的原位X射线衍射和电化学阻抗谱

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摘要

Understanding of the structural evolution of the cathode during the charge/discharge processes is crucial to describe the Li insertion/de-insertion mechanisms in a Li-ion battery. An in situ XRD cell has been specially fabricated to study a nanostructured electrode using a standard laboratory diffractometer. This cell was used to investigate phase transformations of a nanoporous Li2FeSiO4/C cathode in the initial charge/discharge cycle by in situ XRD as well as analyzing the full Li-ion battery by electrochemical impedance spectroscopy (EIS). The battery was operated in chronocoulometric mode for the in situ XRD and galvanostatic intermittent titration technique (GITT) mode for the EIS. Coexistence of two different polymorphs, P21/n and Pmn21 of Li2FeSiO4, was observed in the in situ XRD patterns. The amount of P21/n phase, which was the only phase present before cycling, decreased while the amount of Pmn21 phase increased during the first cycle. In the fully discharged state the Pmn21 phase appeared as the main phase. An inductive loop was observed in the impedance spectra which is believed to arise from the formation of a concentration cell (Li|P21/n||Pmn21|Li) from which current flows in opposition to the Li being intercalated/de-intercalated into and out of the Li2−xFeSiO4 electrode.
机译:了解充电/放电过程中阴极的结构演变对于描述锂离子电池中的锂插入/去插入机理至关重要。使用标准实验室衍射仪专门制造了原位XRD电池,以研究纳米结构电极。该电池用于通过原位XRD研究纳米多孔Li2FeSiO4 / C阴极在初始充电/放电循环中的相变,以及通过电化学阻抗谱(EIS)分析完整的锂离子电池。对于原位XRD,电池以计时容积模式运行,而对于EIS,则采用恒电流间歇滴定技术(GITT)模式运行。在原位XRD图谱中观察到Li2FeSiO4的两种不同的多晶型物P21 / n和Pmn21共存。在第一个循环中,P21 / n相的量减少,而Pmn21相的量增加,这是循环前存在的唯一相。在完全放电状态下,Pmn21相为主要相。在阻抗谱中观察到一个感应环路,该阻抗谱被认为是由于形成了一个浓度单元(Li | P21 / n || Pmn21 | Li)而引起的,该电流从中流过,而与Li相反/相反地流过Li在Li2-xFeSiO4电极中。

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