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Effects of microstructure formation on the stability of vapor-deposited glasses

机译:微观结构的形成对气相沉积玻璃稳定性的影响

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摘要

Glasses formed by physical vapor deposition (PVD) are an interesting new class of materials, exhibiting properties thought to be equivalent to those of glasses aged for thousands of years. Exerting control over the structure and properties of PVD glasses formed with different types of glass-forming molecules is now an emerging challenge. In this work, we study coarse-grained models of organic glass formers containing fluorocarbon tails of increasing length, corresponding to an increased tendency to form microstructures. We use simulated PVD to examine how the presence of the microphase-separated domains in the supercooled liquid influences the ability to form stable glasses. This model suggests that increasing molecule tail length results in decreased thermodynamic stability of the molecules in PVD films. The reduced stability is further linked to the reduced ability of these molecules to equilibrate at the free surface during PVD. We find that, as the tail length is increased, the relaxation times near the surface of the supercooled equilibrium liquid films of these molecules are slowed and become essentially bulk-like, due to the segregation of the fluorocarbon tails to the free surface. Surface diffusion is also markedly reduced due to clustering of the molecules at the surface. Based on these results, we propose a trapping mechanism where tails are unable to move between local phase-separated domains on the relevant deposition time scales.
机译:通过物理气相沉积(PVD)形成的玻璃是一类有趣的新型材料,其性能被认为等同于数千年老化的玻璃。现在,对由不同类型的玻璃形成分子形成的PVD玻璃的结构和性能进行控制是一个新的挑战。在这项工作中,我们研究了有机玻璃形成剂的粗粒度模型,其中包含长度不断增加的碳氟化合物尾部,这对应于形成微观结构的趋势增加。我们使用模拟的PVD来检查过冷液体中微相分离域的存在如何影响形成稳定玻璃的能力。该模型表明,增加分子尾长会导致PVD膜中分子的热力学稳定性降低。降低的稳定性还与这些分子在PVD期间在自由表面平衡的能力降低有关。我们发现,随着尾部长度的增加,由于碳氟化合物尾部向自由表面的偏析,这些分子的过冷平衡液膜表面附近的弛豫时间变慢,并且基本上变为块状。由于分子在表面的聚集,表面扩散也明显减少。基于这些结果,我们提出了一种捕集机制,其中尾部无法在相关的沉积时间尺度上在局部相分离域之间移动。

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