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Important Variation in Vibrational Properties of LiFePO4 and FePO4 Induced by Magnetism

机译:磁性引起的LiFePO4和FePO4振动特性的重要变化

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摘要

A new thermodynamically self-consistent (TSC) method, based on the quasi-harmonic approximation (QHA), is used to obtain the Debye temperatures of LiFePO4 (LFP) and FePO4 (FP) from available experimental specific heat capacities for a wide temperature range. The calculated Debye temperatures show an interesting critical and peculiar behavior so that a steep increase in the Debye temperatures is observed by increasing the temperature. This critical behavior is fitted by the critical function and the adjusted critical temperatures are very close to the magnetic phase transition temperatures in LFP and FP. Hence, the critical behavior of the Debye temperatures is correlated with the magnetic phase transitions in these compounds. Our first-principle calculations support our conjecture that the change in electronic structures, i.e. electron density of state and electron localization function, and consequently the change in thermophysical properties due to the magnetic transition may be the reason for the observation of this peculiar behavior of the Debye temperatures.
机译:基于准谐波近似(QHA)的一种新的热力学自洽(TSC)方法用于在宽温度范围内从可用的实验比热容中获得LiFePO4(LFP)和FePO4(FP)的德拜温度。 。计算得出的德拜温度显示出有趣的临界和特殊行为,因此通过升高温度可以观察到德拜温度急剧上升。该临界行为由临界函数拟合,并且调整后的临界温度非常接近LFP和FP中的磁相变温度。因此,德拜温度的临界行为与这些化合物中的磁性相变有关。我们的第一性原理计算支持我们的推测,即电子结构的变化,即状态的电子密度和电子局部化函数,因此由于磁跃迁而引起的热物理性质的变化可能是观察到这种奇异行为的原因。德拜温度。

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