Atomistic simulation of chemical short-range order on the irradiation resistance of HfNbTaTiZr high entropy alloy

IF 9.4 1区 材料科学 Q1 ENGINEERING, MECHANICAL International Journal of Plasticity Pub Date : 2024-10-24 DOI:10.1016/j.ijplas.2024.104155
Yang Mo , Yanxiang Liang , Wei Guo , Yiming Tian , Qiang Wan
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Abstract

High entropy alloys (HEAs) have been considered as one of the potential structural material candidates for fourth-generation nuclear reactors and fusion reactors due to their excellent irradiation resistance. Current studies have shown that the chemical short-range order (CSRO) usually exists in HEAs, which has a significant effect on the mechanical properties and irradiation resistance of HEAs. Refractory high entropy alloys (RHEAs), as a new class of HEAs have better mechanical properties at high temperatures than face-centered cubic (FCC) HEAs, and therefore have better prospects of application in the nuclear field. In this study, CSRO and its effect on the irradiation resistance of HfNbTaTiZr are analyzed via molecular dynamics (MD) and Monte Carlo (MC). The primary cascade simulations, multi-cascade simulations and surface bombardment simulations are carried out to simulate the generation and accumulation of irradiation damage. The results of the primary cascade simulations and surface bombardment simulations of CSRO models show that the presence of CSRO induces cascade splitting into subcascades. The presence of subcascades reduces the thermal peak enhancement effect and thus lowers the recombination rate of Frenkel pairs (FPs) in the damage zone when FPs concentrations are low. However, the creation of subcascades increases the size of the damage zone caused by the cascade. Thus, when the concentrations of FPs are high, the larger area of damage zone allows more of the already existing FPs to be included, thus promoting their recombination, i.e., impedes their accumulation when concentrations are high. These subcascades lower the recombination of FPs at low FPs concentrations but inhibit their accumulation at high FPs concentrations. The presence of CSRO is also beneficial in inhibiting the growth of point defect clusters, which further improves the resistance of HfNbTaTiZr to dislocation generation. Furthermore, the presence of CSRO facilitates the irradiation-induced phase transition. But it is found that HfNbTaTiZr shows suppression of hexagonal close-packed (HCP) cluster growth. And the tendency to break down large HCP clusters into smaller ones is demonstrated in the CSRO model. From our calculations we also find that the irradiation-induced HCP atoms have a higher potential energy relative to the matrix. The potential energy difference between those energetic HCP atoms and the matrix can lead to generating a great number of insurmountable barriers pervading the matrix and largely suppressing the long-term mobility of FPs, thus limiting their aggregation and growth into clusters.

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原子模拟化学短程有序性对 HfNbTaTiZr 高熵合金耐辐照性的影响
高熵合金(HEAs)因其优异的抗辐照性能,已被视为第四代核反应堆和聚变反应堆的潜在结构材料之一。目前的研究表明,高熵合金中通常存在化学短程有序(CSRO),这对高熵合金的机械性能和抗辐照性能有显著影响。难熔高熵合金(RHEAs)作为一类新型 HEAs,与面心立方(FCC)HEAs 相比,在高温下具有更好的机械性能,因此在核领域具有更好的应用前景。本研究通过分子动力学(MD)和蒙特卡罗(MC)分析了 CSRO 及其对 HfNbTaTiZr 抗辐照性的影响。通过一级级联模拟、多级级联模拟和表面轰击模拟来模拟辐照损伤的产生和累积。CSRO 模型的一级级联模拟和表面轰击模拟结果表明,CSRO 的存在会导致级联分裂成子级联。当 FPs 浓度较低时,子级联的存在会降低热峰值增强效应,从而降低损伤区中 Frenkel 对(FPs)的重组率。然而,子级联的产生会增加级联造成的损伤区的面积。因此,当 FPs 浓度较高时,较大的损伤区面积允许更多已经存在的 FPs 被包括在内,从而促进了它们的重组,即在浓度较高时阻碍了它们的积累。这些子级联降低了低浓度 FPs 时 FPs 的重组,但抑制了高浓度 FPs 时 FPs 的积累。CSRO 的存在还有利于抑制点缺陷簇的生长,从而进一步提高 HfNbTaTiZr 对位错产生的抵抗力。此外,CSRO 的存在还有利于辐照诱导的相变。但研究发现,HfNbTaTiZr 会抑制 HCP 簇的生长。在 CSRO 模型中,大的 HCP 簇有分解成小簇的趋势。通过计算我们还发现,辐照诱导的 HCP 原子相对于基体具有更高的势能。这些高能 HCP 原子与基体之间的势能差会导致在基体中产生大量不可逾越的壁垒,在很大程度上抑制了 FPs 的长期流动性,从而限制了它们聚集和生长成簇。
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来源期刊
International Journal of Plasticity
International Journal of Plasticity 工程技术-材料科学:综合
CiteScore
15.30
自引率
26.50%
发文量
256
审稿时长
46 days
期刊介绍: International Journal of Plasticity aims to present original research encompassing all facets of plastic deformation, damage, and fracture behavior in both isotropic and anisotropic solids. This includes exploring the thermodynamics of plasticity and fracture, continuum theory, and macroscopic as well as microscopic phenomena. Topics of interest span the plastic behavior of single crystals and polycrystalline metals, ceramics, rocks, soils, composites, nanocrystalline and microelectronics materials, shape memory alloys, ferroelectric ceramics, thin films, and polymers. Additionally, the journal covers plasticity aspects of failure and fracture mechanics. Contributions involving significant experimental, numerical, or theoretical advancements that enhance the understanding of the plastic behavior of solids are particularly valued. Papers addressing the modeling of finite nonlinear elastic deformation, bearing similarities to the modeling of plastic deformation, are also welcomed.
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