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Molecular dynamics investigation of dynamical heterogeneity and local structure in the supercooled liquid and glass states of Al

机译:Al过冷液相和玻璃态动力学非均质性和局部结构的分子动力学研究

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Molecular dynamics simulations are performed to study the structure and dynamical heterogeneity in the liquid and glass states of Al using a frequently employed embedded atom potential. While the pair correlation function of the glass and liquid states displays only minor differences, the icosahedral short-range order (ISRO) and the dynamics of the two states are very different. The ISRO is much stronger in the glass than in the liquid. It is also found that both the most mobile and the most immobile atoms in the glass state tend to form clusters, and the clusters formed by the immobile atoms are more compact. In order to investigate the local environment of each atom in the liquid and glass states, a local density is defined to characterize the local atomic packing. There is a strong correlation between the local packing density and the mobility of the atoms. These results indicate that dynamical heterogeneity in glasses is directly correlated to the local structure. We also analyze the diffusion mechanisms of atoms in the liquid and glass states. It is found that for the mobile atoms in the glass state, initially they are confined in the cages formed by their nearest neighbors and vibrating. On the time scale of β relaxation, the mobile atoms try to break up the cage confinement and hop into new cages. In the supercooled liquid states, however, atoms continuously diffuse. Furthermore, it is found that on the time scale of β relaxation, some of the mobile atoms in the glass state cooperatively hop, which is facilitated by the stringlike cluster structures. On the longer time scale, it is found that a certain fraction of atoms can simultaneously hop, although they are not nearest neighbors. Further analysis shows that these hopping atoms form big and more compact clusters than the characterized most mobile atoms. The cooperative rearrangement of these big compact clusters might facilitate the simultaneous hopping of atoms in the glass states on the long time scale.
机译:使用常用的嵌入原子势进行分子动力学模拟以研究Al的液态和玻璃态的结构和动力学异质性。虽然玻璃态和液态的成对相关函数仅显示微小差异,但二十面体短程有序(ISRO)和两种态的动力学却有很大差异。玻璃中的ISRO比液体中的ISRO强得多。还发现在玻璃态中最易移动和最不易移动的原子都倾向于形成簇,并且由不易移动的原子形成的簇更致密。为了研究处于液态和玻璃态的每个原子的局部环境,定义了局部密度来表征局部原子堆积。局部堆积密度与原子迁移率之间存在很强的相关性。这些结果表明,玻璃中的动态异质性与局部结构直接相关。我们还分析了液态和玻璃态原子的扩散机理。已经发现,对于处于玻璃态的移动原子,最初它们被限制在由它们最近的邻居形成并振动的笼中。在β弛豫的时间尺度上,可移动原子试图打破笼的限制并跳入新的笼。然而,在过冷液态下,原子连续扩散。此外,发现在β弛豫的时间尺度上,玻璃态中的一些可移动原子协同跳跃,这由线状簇结构促进。在更长的时间尺度上,发现尽管不是最邻近的原子,但一定比例的原子可以同时跳跃。进一步的分析表明,这些跳跃原子比大多数可移动原子形成更大且更紧凑的簇。这些大的紧密团簇的协同重排可能会促进长时间尺度上玻璃态原子的同时跳跃。

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