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Structural instability of metallic glasses under radio-frequency-ultrasonic perturbation and its correlation with glass-to-crystal transition of less-stable metallic glasses

机译:射频-超声波扰动下金属玻璃的结构不稳定性及其与较不稳定金属玻璃的玻璃-晶体转变的相关性

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It has been reported that the structural stability is significantly deteriorated under radio-frequency-ultrasonic perturbation at relatively low temperatures, e.g., near/below the glass transition temperature T-g, even for thermally stable metallic glasses. Here, we consider an underlying mechanism of the ultrasound-induced instability, i.e., crystallization, of a glass structure to grasp the nature of the glass-to-liquid transition of metallic glasses. Mechanical spectroscopy analysis indicates that the instability is caused by atomic motions resonant with the dynamic ultrasonic-strain field, i.e., atomic jumps associated with the beta relaxation that is usually observed for low frequencies of the order of 1 Hz at temperatures far below T-g. Such atomic motions at temperatures lower than the so-called kinetic freezing temperature T-g originate from relatively weakly bonded (and/or low-density) regions in a nanoscale inhomogeneous microstructure of glass, which can be straightforwardly inferred from a partially crystallized microstructure obtained by annealing of a Pd-based metallic glass just below T-g under ultrasonic perturbation. According to this nanoscale inhomogeneity concept, we can reasonably understand an intriguing characteristic feature of less-stable metallic glasses (fabricated only by rapid melt quenching) that the crystallization precedes the glass transition upon standard heating but the glass transition is observable at extremely high rates. Namely, in such less-stable metallic glasses, atomic motions are considerably active at some local regions even below the kinetic freezing temperature. Thus, the glass-to-crystal transition of less-stable metallic glasses is, in part, explained with the present nanoscale inhomogeneity concept. (c) 2006 American Institute of Physics.
机译:据报道,即使对于热稳定的金属玻璃,在相对较低的温度下,例如在玻璃化转变温度T-g附近/之下,在射频-超声波扰动下,结构稳定性也会显着降低。在这里,我们考虑了由超声引起的玻璃结构的不稳定性,即结晶的潜在机理,以掌握金属玻璃从玻璃到液体的转变的本质。机械光谱分析表明,不稳定性是由与动态超声应变场共振的原子运动引起的,即,与β弛豫相关的原子跃迁,通常在远低于T-g的温度下以1Hz量级的低频观察到。在低于所谓的动态冻结温度Tg的温度下,这种原子运动源自玻璃的纳米级非均质微结构中相对较弱的键合(和/或低密度)区域,这可以直接通过退火获得的部分结晶的微结构来推断。在超声波扰动下刚好低于Tg的Pd基金属玻璃根据这种纳米级的不均匀性概念,我们可以合理地理解不太稳定的金属玻璃(仅通过快速熔体淬火制造)的一个有趣的特征,即在标准加热条件下结晶先于玻璃化转变,但可以观察到极高的转化率。即,在这种不那么稳定的金属玻璃中,甚至在低于运动冻结温度的情况下,原子运动在某些局部区域也相当活跃。因此,用当前的纳米级不均匀性概念部分地解释了较不稳定的金属玻璃的玻璃到晶体的转变。 (c)2006年美国物理研究所。

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