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Breakdown of the Stokes-Einstein relation above the melting temperature in a liquid phase-change material

机译:液相变化材料中高于熔化温度的斯托克斯-爱因斯坦关系的分解

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The dynamic properties of liquid phase-change materials (PCMs), such as viscosity η and the atomic self-diffusion coefficient D, play an essential role in the ultrafast phase switching behavior of novel nonvolatile phase-change memory applications. To connect η to D, the Stokes-Einstein relation (SER) is commonly assumed to be valid at high temperatures near or above the melting temperature Tm and is often used for assessing liquid fragility (or crystal growth velocity) of technologically important PCMs. However, using quasi-elastic neutron scattering, we provide experimental evidence for a breakdown of the SER even at temperatures above Tm in the high–atomic mobility state of a PCM, Ge1Sb2Te4. This implies that although viscosity may have strongly increased during cooling, diffusivity can remain high owing to early decoupling, being a favorable feature for the fast phase switching behavior of the high-fluidity PCM. We discuss the origin of the observation and propose the possible connection to a metal-semiconductor and fragile-strong transition hidden below Tm.
机译:液相相变材料(PCM)的动态特性,例如粘度η和原子自扩散系数D,在新型非易失性相变存储应用的超快速相转换行为中起着至关重要的作用。为了将η连接到D,通常假定斯托克斯-爱因斯坦关系(SER)在接近或高于熔化温度Tm的高温下有效,并且通常用于评估技术上重要的PCM的液体脆性(或晶体生长速度)。但是,使用准弹性中子散射,即使在PCM,Ge1Sb2Te4的高原子迁移率状态下,即使在Tm以上的温度下,SER的分解也提供了实验证据。这意味着,尽管在冷却过程中粘度可能已大大增加,但由于过早的去耦,扩散率仍可保持较高,这对于高流动性PCM的快速相转换行为是有利的。我们讨论了观测的起源,并提出了与隐藏在Tm下的金属半导体和易碎的强过渡的可能联系。

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