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均质和非均质非晶态金属相对于晶相的相形成和相稳定性。

Phase formation and phase stability for the homogenous and heterogeneous amorphous metals versus the crystalline phase.

作者信息

Shen Yidi, Samwer Konrad, Johnson William L, Goddard William A, An Qi

机构信息

Department of Materials Science and Engineering, Iowa State University, Ames, IA 50011.

Materials Process and Simulation Center, California Institute of Technology, Pasadena, CA 91125.

出版信息

Proc Natl Acad Sci U S A. 2025 Jan 28;122(4):e2404489122. doi: 10.1073/pnas.2404489122. Epub 2025 Jan 21.

DOI:10.1073/pnas.2404489122
PMID:39835902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11789084/
Abstract

From molecular dynamics (MD) simulations of melt-quenching and thermal aging procedures in pure Ag, Cu, Ag-Cu binary alloys, and Cu-Zr binary alloys, we have identified two distinct amorphous phases for a metastable undercooled liquid: the homogeneous L-phase with low shear rigidity and the heterogenous G-phase with much higher shear rigidity and a heterogeneity length scale Λ. Here, we examine two-phase equilibration studies showing that the G-phase melts to form the L-phase above 1,000 K, which then transforms to form the crystal (X) phase; however, below the melting point of the G-Phase (990 K), the X- and G-phases do not transform into each other. We suggest the presence of a G-phase is likely responsible for embrittlement often observed in metallic glasses. We also consider how mechanical milling or irradiation-induced defect accumulation in the crystalline metallic alloy triggers a crystal-to-glass transition. We use the CuZr system as a model to investigate random interchange of Zr and Cu atoms at room temperature leading to a transition from a crystalline Laves-phase to an L-glass through formation and growth of amorphous regions and destabilization of the crystal. During relaxation of the nonequilibrium structures by annealing, the configurations either reverted to the crystalline phase or evolve to a heterogeneous G-phase equivalent to the G-phase formed during thermal quenching and aging of the melt. Athermal defect accumulation in the G-phase at low temperature led to a transition back to the L-phase. Our findings show how athermal disordering drives transitions among the X-, L-, and G-phases.

摘要

通过对纯银、铜、银 - 铜二元合金以及铜 - 锆二元合金的熔体淬火和热老化过程进行分子动力学(MD)模拟,我们确定了亚稳态过冷液体的两种不同非晶相:具有低剪切刚度的均匀L相和具有更高剪切刚度及非均匀长度尺度Λ的非均匀G相。在此,我们研究了两相平衡研究,结果表明G相在约1000 K以上熔化形成L相,然后L相转变形成晶体(X)相;然而,在G相熔点(约990 K)以下,X相和G相不会相互转变。我们认为G相的存在可能是金属玻璃中经常观察到的脆化现象的原因。我们还考虑了机械研磨或辐照诱导的晶体金属合金中的缺陷积累如何引发从晶体到玻璃的转变。我们以CuZr体系为模型,研究室温下Zr和Cu原子的随机交换,通过非晶区域的形成和生长以及晶体的失稳,导致从晶体Laves相转变为L玻璃。在通过退火使非平衡结构弛豫的过程中,构型要么恢复到晶相,要么演变成与熔体热淬火和老化过程中形成的G相等效的非均匀G相。低温下G相中的无热缺陷积累导致转变回L相。我们的研究结果展示了无热无序如何驱动X相、L相和G相之间的转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1524/11789084/06374a40354d/pnas.2404489122fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1524/11789084/c87d9ea0c299/pnas.2404489122fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1524/11789084/bf750a197734/pnas.2404489122fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1524/11789084/86995c09c537/pnas.2404489122fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1524/11789084/fa3827668a43/pnas.2404489122fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1524/11789084/06374a40354d/pnas.2404489122fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1524/11789084/c87d9ea0c299/pnas.2404489122fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1524/11789084/bf750a197734/pnas.2404489122fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1524/11789084/86995c09c537/pnas.2404489122fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1524/11789084/fa3827668a43/pnas.2404489122fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1524/11789084/06374a40354d/pnas.2404489122fig05.jpg

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本文引用的文献

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