Thaiyanurak Tittaya, Gordon Olivia, Ye Muyang, Wang Zhengming, Xu Donghua
Materials Science Program, Oregon State University, Corvallis, OR 97331, USA.
School of Mechanical, Industrial and Manufacturing Engineering, Oregon State University, Corvallis, OR 97331, USA.
Molecules. 2025 Jun 16;30(12):2602. doi: 10.3390/molecules30122602.
The mechanical properties of materials are fundamentally determined by the behavior of atomic bonds under stress. Probing bond behavior during deformation, however, is highly challenging, particularly for materials with complex chemical compositions and/or atomic structures, such as metallic glasses (MGs). As a result, a significant gap exists in the current understanding of the mechanical properties of MGs in relation to the atomic bond behavior and how this relationship is influenced by metallurgical factors (e.g., alloy composition, processing conditions). Here, we present our study of the compositional effects on the tensile behavior of atomic bonds in CuZrAl (x = 40, 50, 60 at.%) MGs using large-scale molecular dynamics (MD) simulations and statistical analysis. Specifically, we examine the populations (fractions), mean bond lengths, mean bond z-lengths, and mean bond z-strains of the different bond types before and during tensile loading (in the z-direction), and we compare these quantities across the different alloy compositions. Among our key findings, we show that increasing the Zr content in the alloy composition leads to shortened Zr-Zr, Al-Cu, Al-Zr, and Cu-Zr bonds and elongated Cu-Cu bonds, as evidenced by their mean bond lengths. During deformation, the shorter Zr-Zr bonds and longer Cu-Cu bonds in the higher-Zr-content alloys, compared with those in the x = 40 alloy, appear stronger (more elastic stretching in the z-direction) and weaker (less z-stretching), respectively, consistent with general expectations. In contrast, the Al-Cu, Al-Zr, and Cu-Zr bonds in the higher-Zr-content alloys appear weaker in the elastic regime, despite their shortened mean bond lengths. This apparent paradox can be reconciled by considering the fractions of these bonds associated with icosahedral clusters, which are known to be more resistant to deformation than the rest of the glassy structure. We also discuss how the compositional effects on the bond behavior relate to variations in the overall stress-strain behavior of the different alloys.
材料的力学性能从根本上由应力作用下原子键的行为决定。然而,探测变形过程中的键行为极具挑战性,尤其是对于具有复杂化学成分和/或原子结构的材料,如金属玻璃(MGs)。因此,目前对于金属玻璃的力学性能与原子键行为之间的关系以及这种关系如何受到冶金因素(如合金成分、加工条件)的影响,存在显著的认知差距。在此,我们利用大规模分子动力学(MD)模拟和统计分析,展示了我们对CuZrAl(x = 40、50、60原子百分比)金属玻璃中原子键拉伸行为的成分效应研究。具体而言,我们研究了拉伸加载前和加载过程中(沿z方向)不同键型的数量(分数)、平均键长、平均键z长度和平均键z应变,并比较了不同合金成分下的这些量。在我们的主要发现中,我们表明合金成分中Zr含量的增加导致Zr-Zr、Al-Cu、Al-Zr和Cu-Zr键缩短,而Cu-Cu键伸长,这通过它们的平均键长得到证明。在变形过程中,与x = 40合金相比,高Zr含量合金中较短的Zr-Zr键和较长的Cu-Cu键分别表现出更强(在z方向上弹性拉伸更多)和更弱(z方向拉伸更少),这与一般预期一致。相比之下,高Zr含量合金中的Al-Cu、Al-Zr和Cu-Zr键在弹性范围内似乎更弱,尽管它们的平均键长缩短了。通过考虑与二十面体团簇相关的这些键的分数,可以解释这个明显的矛盾,已知二十面体团簇比玻璃态结构的其余部分更能抵抗变形。我们还讨论了键行为的成分效应如何与不同合金的整体应力-应变行为变化相关。