Monnier Xavier, Cangialosi Daniele, Ruta Beatrice, Busch Ralf, Gallino Isabella
Donostia International Physics Center, Paseo Manuel de Lardizabal, 20018 San Sebastián, Spain.
Centro de Física de Materiales (CSIC-UPV/EHU), Paseo Manuel de Lardizabal, 50018 Sebastián, Spain.
Sci Adv. 2020 Apr 24;6(17):eaay1454. doi: 10.1126/sciadv.aay1454. eCollection 2020 Apr.
Understanding how glasses form, the so-called vitrification, remains a major challenge in materials science. Here, we study vitrification kinetics, in terms of the limiting fictive temperature, and atomic mobility related to the α-relaxation of an Au-based bulk metallic glass former by fast scanning calorimetry. We show that the time scale of the α-relaxation exhibits super-Arrhenius temperature dependence typical of fragile liquids. In contrast, vitrification kinetics displays milder temperature dependence at moderate undercooling, and thereby, vitrification takes place at temperatures lower than those associated to the α-relaxation. This finding challenges the paradigmatic view based on a one-to-one correlation between vitrification, leading to the glass transition, and the α-relaxation. We provide arguments that at moderate to deep undercooling, other atomic motions, which are not involved in the α-relaxation and that originate from the heterogeneous dynamics in metallic glasses, contribute to vitrification. Implications from the viewpoint of glasses fundamental properties are discussed.
理解玻璃是如何形成的,即所谓的玻璃化转变,仍然是材料科学中的一个重大挑战。在此,我们通过快速扫描量热法研究了基于金的块状金属玻璃形成体的玻璃化转变动力学,具体是从极限虚构温度以及与α弛豫相关的原子迁移率方面进行研究。我们表明,α弛豫的时间尺度呈现出典型的易碎液体的超阿伦尼乌斯温度依赖性。相比之下,在适度过冷条件下,玻璃化转变动力学表现出较弱的温度依赖性,因此,玻璃化转变发生在低于与α弛豫相关的温度下。这一发现挑战了基于玻璃化转变(导致玻璃化转变)与α弛豫之间一一对应关系的范式观点。我们提出论据表明,在适度到深度过冷条件下,其他不参与α弛豫且源于金属玻璃中非均匀动力学的原子运动对玻璃化转变有贡献。从玻璃基本性质的角度讨论了其影响。