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Combined operando X-ray diffraction–electrochemical impedance spectroscopy detecting solid solution reactions of LiFePO4 in batteries

机译:组合操作X射线衍射-电化学阻抗谱检测电池中LiFePO4的固溶反应

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摘要

Lithium-ion batteries are widely used for portable applications today; however, often suffer from limited recharge rates. One reason for such limitation can be a reduced active surface area during phase separation. Here we report a technique combining high-resolution operando synchrotron X-ray diffraction coupled with electrochemical impedance spectroscopy to directly track non-equilibrium intermediate phases in lithium-ion battery materials. LiFePO4, for example, is known to undergo phase separation when cycled under low-current-density conditions. However, operando X-ray diffraction under ultra-high-rate alternating current and direct current excitation reveal a continuous but current-dependent, solid solution reaction between LiFePO4 and FePO4 which is consistent with previous experiments and calculations. In addition, the formation of a preferred phase with a composition similar to the eutectoid composition, Li0.625FePO4, is evident. Even at a low rate of 0.1C, ∼20% of the X-ray diffractogram can be attributed to non-equilibrium phases, which changes our understanding of the intercalation dynamics in LiFePO4.
机译:锂离子电池今天广泛用于便携式应用。但是,经常会受到充电率有限的困扰。这种限制的一个原因可能是相分离过程中有效表面积的减小。在这里,我们报告结合高分辨率操作同步辐射X射线衍射与电化学阻抗谱的技术来直接跟踪锂离子电池材料中的非平衡中间相。例如,已知在低电流密度条件下循环使用时,LiFePO4会发生相分离。然而,超高速交流电和直流电激励下的操作X射线衍射显示LiFePO4和FePO4之间发生了连续但依赖电流的固溶反应,这与以前的实验和计算是一致的。另外,明显形成了具有与共析组分Li0.625FePO4相似的组分的优选相。即使在0.1C的低速率下,约20%的X射线衍射图也可归因于非平衡相,这改变了我们对LiFePO4插层动力学的理解。

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