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通过镁中的形变孪晶实现塑性的恢复。

Rejuvenation of plasticity via deformation graining in magnesium.

作者信息

Liu Bo-Yu, Zhang Zhen, Liu Fei, Yang Nan, Li Bin, Chen Peng, Wang Yu, Peng Jin-Hua, Li Ju, Ma En, Shan Zhi-Wei

机构信息

Center for Advancing Materials Performance from the Nanoscale (CAMP-Nano) and Hysitron Applied Research Center in China (HARCC), State Key Laboratory for Mechanical Behavior of Materials, Xi'an Jiaotong University, Xi'an, 710049, People's Republic of China.

School of Materials Science and Engineering, Hefei University of Technology, Hefei, 230009, China.

出版信息

Nat Commun. 2022 Feb 25;13(1):1060. doi: 10.1038/s41467-022-28688-9.

Abstract

Magnesium, the lightest structural metal, usually exhibits limited ambient plasticity when compressed along its crystallographic c-axis (the "hard" orientation of magnesium). Here we report large plasticity in c-axis compression of submicron magnesium single crystal achieved by a dual-stage deformation. We show that when the plastic flow gradually strain-hardens the magnesium crystal to gigapascal level, at which point dislocation mediated plasticity is nearly exhausted, the sample instantly pancakes without fracture, accompanying a conversion of the initial single crystal into multiple grains that roughly share a common rotation axis. Atomic-scale characterization, crystallographic analyses and molecular dynamics simulations indicate that the new grains can form via transformation of pyramidal to basal planes. We categorize this grain formation as "deformation graining". The formation of new grains rejuvenates massive dislocation slip and deformation twinning to enable large plastic strains.

摘要

镁是最轻的结构金属,当沿其晶体学c轴(镁的“硬”取向)压缩时,通常在环境条件下表现出有限的塑性。在此,我们报道了通过双阶段变形在亚微米级镁单晶的c轴压缩中实现的大塑性。我们表明,当塑性流动使镁晶体逐渐应变硬化至吉帕斯卡水平时,此时位错介导的塑性几乎耗尽,样品会立即被压扁而不发生断裂,同时初始单晶会转变为多个大致共享共同旋转轴的晶粒。原子尺度表征、晶体学分析和分子动力学模拟表明,新晶粒可通过从锥面到基面的转变形成。我们将这种晶粒形成归类为“变形晶粒化”。新晶粒的形成使大量位错滑移和变形孪晶恢复活力,从而实现大的塑性应变。

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