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硅中异常的塑性应变诱导相变现象。

Unusual plastic strain-induced phase transformation phenomena in silicon.

作者信息

Yesudhas Sorb, Levitas Valery I, Lin Feng, Pandey K K, Smith Jesse S

机构信息

Department of Aerospace Engineering, Iowa State University, Ames, Iowa, USA.

Department of Mechanical Engineering, Iowa State University, Ames, Iowa, USA.

出版信息

Nat Commun. 2024 Aug 15;15(1):7054. doi: 10.1038/s41467-024-51469-5.

DOI:10.1038/s41467-024-51469-5
PMID:39147793
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11327322/
Abstract

Pressure-induced phase transformations (PTs) in Si, the most important electronic material, have been broadly studied, whereas strain-induced PTs have never been studied in situ. Here, we reveal in situ various important plastic strain-induced PT phenomena. A correlation between the direct and inverse Hall-Petch effect of particle size on yield strength and pressure for strain-induced PT is predicted theoretically and confirmed experimentally for Si-I→Si-II PT. For 100 nm particles, the strain-induced PT Si-I→Si-II initiates at 0.3 GPa under both compression and shear while it starts at 16.2 GPa under hydrostatic conditions. The Si-I→Si-III PT starts at 0.6 GPa but does not occur under hydrostatic pressure. Pressure in small Si-II and Si-III regions of micron and 100 nm particles is ∼5-7 GPa higher than in Si-I. For 100 nm Si, a sequence of Si-I → I + II → I + II + III PT is observed, and the coexistence of four phases, Si-I, II, III, and XI, is found under torsion. Retaining Si-II and single-phase Si-III at ambient pressure and obtaining reverse Si-II→Si-I PT demonstrates the possibilities of manipulating different synthetic paths. The obtained results corroborate the elaborated dislocation pileup-based mechanism and have numerous applications for developing economic defect-induced synthesis of nanostructured materials, surface treatment (polishing, turning, etc.), and friction.

摘要

硅作为最重要的电子材料,其压力诱导相变(PTs)已得到广泛研究,而应变诱导相变从未进行过原位研究。在此,我们揭示了各种重要的塑性应变诱导PT现象。理论上预测了颗粒尺寸对应变诱导PT的屈服强度和压力的正、反Hall-Petch效应之间的相关性,并通过实验证实了硅-I→硅-II相变的情况。对于100纳米的颗粒,应变诱导的硅-I→硅-II相变在压缩和剪切条件下均在0.3吉帕开始,而在静水压力条件下则在16.2吉帕开始。硅-I→硅-III相变在0.6吉帕开始,但在静水压力下不发生。微米级和100纳米颗粒的小硅-II和硅-III区域中的压力比硅-I中的压力高约5 - 7吉帕。对于100纳米的硅,观察到一系列硅-I→I + II→I + II + III相变,并且在扭转条件下发现了硅-I、II、III和XI四个相的共存。在环境压力下保留硅-II和单相硅-III并实现反向硅-II→硅-I相变,证明了操控不同合成路径的可能性。所获得的结果证实了基于位错堆积的详细机制,并且在开发经济的缺陷诱导纳米结构材料合成、表面处理(抛光、车削等)和摩擦方面有众多应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fdd/11327322/5daf24d41a45/41467_2024_51469_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fdd/11327322/fbc2f24fb15a/41467_2024_51469_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fdd/11327322/5daf24d41a45/41467_2024_51469_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fdd/11327322/fbc2f24fb15a/41467_2024_51469_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fdd/11327322/5daf24d41a45/41467_2024_51469_Fig3_HTML.jpg

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