Phase Transformations, Microstructural Refinement and Defect Evolution Mechanisms in Al-Si Alloys Under Non-Hydrostatic Diamond Anvil Cell Compression

Tingkun Liu, M. Olszta, B. Gwalani, Changyong Park, S. Mathaudhu, A. Devaraj
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引用次数: 6

Abstract

Abstract Non-hydrostatic compression of materials using a diamond anvil cell (DAC) can transform the equilibrium microstructure of an alloy to novel, potentially metastable states. In this study, in situ synchrotron X-ray diffraction (XRD) during compression up to 24 GPa and subsequent ex-situ, high resolution analytical electron microscopy (AEM) after decompression of an Al-Si alloy provided insight into the crystallographic changes during the compression as well as microstructural refinement, and defect structures caused by such a high pressure compression-decompression process. Pressure resolved in-situ synchrotron XRD was used to detail the phase transformation pathway of the eutectic Si phase in Al-Si alloy, from Si-I → Si-XI → Si-V during compression, and a final transformation predominantly to Si-III after decompression. Using scanning and transmission electron microscopy (S/TEM), site specific analysis of the alloy immediately underneath the anvil contact surface demonstrated a highly complex microstructure. A narrow region of thick amorphous Al oxide interspersed with nanocrystalline grains was found at the top surface. Underneath this Al oxide, while the majority of the eutectic Si was transformed into highly-deformed, polycrystalline (PC) Si-III, a complex intermediate layer was discovered at the interface between Al and Si, comprised of a small fraction of Al nanocrystals and a majority of nanocrystalline Si-I. This combination of pressure resolved in-situ synchrotron XRD coupled with subsequent high resolution, electron microscopy resolved the phase transformation as well as non-equilibrium microstructures in a metallic alloy induced by a non-hydrostatic high pressure compression followed by decompression.
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非静压金刚石砧孔压缩下Al-Si合金的相变、显微组织细化及缺陷演化机制
摘要利用金刚石砧细胞(DAC)对材料进行非静压压缩可以将合金的平衡微观结构转变为新的、潜在的亚稳态。在本研究中,对Al-Si合金压缩至24gpa时的原位同步x射线衍射(XRD)和随后的非原位高分辨率分析电子显微镜(AEM)进行了分析,揭示了压缩过程中的晶体学变化、显微组织细化以及这种高压压缩-减压过程引起的缺陷结构。采用压力分辨原位同步加速器XRD分析了Al-Si合金共晶Si相在压缩过程中由Si- i→Si- xi→Si- v,减压后最终以Si- iii为主转变的相变过程。利用扫描和透射电子显微镜(S/TEM),对铁砧接触面下方的合金进行了现场特定分析,显示出高度复杂的微观结构。在顶部表面发现了一窄区分布着纳米晶粒的厚非晶氧化铝。在氧化铝下面,当大部分共晶Si转变为高度变形的多晶Si- iii时,在Al和Si的界面处发现了一个复杂的中间层,由一小部分Al纳米晶和大部分Si- i纳米晶组成。该方法结合了压力分解原位同步加速器XRD和随后的高分辨率电子显微镜,分析了由非流体静力高压压缩和减压引起的金属合金的相变和非平衡组织。
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