Determining the temporal evolution of twinning and/or dislocation slip, in real-time (nanoseconds), in single crystals subjected to plane shock wave loading is a long-standing scientific need. Noncubic crystals pose special challenges because they have many competing slip and twinning systems. Here, we report on time-resolved, in situ, synchrotron Laue x-ray diffraction measurements during shock compression and release of magnesium single crystals that are subjected to compression along the c axis. Significant twinning was observed directly during stress release following shock compression; during compression, only dislocation slip was observed. Our measurements unambiguously distinguish between twinning and dislocation slip on nanosecond timescales in a shocked hexagonal-close-packed metal.
To understand inelastic deformation mechanisms for shocked hexagonal-close-packed (hcp) metals, shock compression and release wave profiles, previously unavailable for hcp single crystals, were measured for c-axis magnesium crystals. The results show that the elastic-inelastic loading response is strongly time-dependent. Measured release wave profiles showed distinct peaked features, which are unusual for inelastic deformation during unloading of shocked metals. Numerical simulations show that pyramidal slip provides a reasonably good description of the inelastic loading response. However, {101¯2} twinning is needed to explain the unloading response. The results and analysis presented here provide insight into the relative roles of dislocation slip and deformation twinning in the response of shocked hcp metals.
To gain insights into the relative contributions of different plastic deformation mechanisms, particularly basal slip, for shocked hexagonal close-packed (hcp) metals, magnesium (Mg) single crystals were subjected to shock compression and release along a low-symmetry (LS) orientation to 1.9 and 4.8 GPa elastic impact stresses. LS-axis is a “nonspecific” direction resulting in propagation of quasilongitudinal and quasishear waves. Wave profiles, measured using laser interferometry, show a small elastic wave followed by two plastic waves in compression; release wave profiles exhibited a structured response for the higher stress and a smooth response for the lower stress. The LS-axis wave profiles are significantly different than profiles published previously for c- and a-axes, demonstrating that Mg single crystals exhibit strong anisotropy under shock compression/release. Numerical simulations, using a time-dependent anisotropic modeling framework, show that shock wave loading along the LS-axis involves the simultaneous operation of multiple deformation mechanisms. Shock compression along LS-axis is dominated by basal slip while prismatic slip and pyramidal I {101¯1}⟨112¯3⟩ slip play a smaller role; coupling between longitudinal and shear deformations was observed. The unloading response is dominated by basal slip with some contribution from prismatic slip; pyramidal I slip is not activated. The present results, unlike results obtained for c- and a-axes, show that the deformation mechanism observed under quasistatic loading conditions along LS-axis is not sufficient to determine the shock response along this orientation. Although requiring numerical simulations for wave analysis, shock propagation along a LS-orientation provides new insights into the plastic deformation response of hcp metal single crystals.
To gain insight into inelastic deformation mechanisms for shocked hexagonal close-packed (hcp) metals, particularly the role of crystal anisotropy, magnesium (Mg) single crystals were subjected to shock compression and release along the a-axis to 3.0 and 4.8 GPa elastic impact stresses. Wave profiles measured at several thicknesses, using laser interferometry, show a sharply peaked elastic wave followed by the plastic wave. Additionally, a smooth and featureless release wave is observed following peak compression. When compared with wave profiles measured previously for c-axis Mg [Winey et al., J. Appl. Phys. 117, 105903 (2015)], the elastic wave amplitudes for a-axis Mg are lower for the same propagation distance, and less attenuation of elastic wave amplitude is observed for a given peak stress. The featureless release wave for a-axis Mg is in marked contrast to the structured features observed for c-axis unloading. Numerical simulations, using a time-dependent anisotropic modeling framework, showed that the wave profiles calculated using prismatic slip or (101¯2) twinning, individually, do not match the measured compression profiles for a-axis Mg. However, a combination of slip and twinning provides a good overall match to the measured compression profiles. In contrast to compression, prismatic slip alone provides a reasonable match to the measured release wave profiles; (101¯2) twinning due to its uni-directionality is not activated during release. The experimental results and wave profile simulations for a-axis Mg presented here are quite different from the previously published c-axis results, demonstrating the important role of crystal anisotropy in the time-dependent inelastic deformation of Mg single crystals under shock compression and release.
Solid-solid and solid-liquid transformations were examined in Ge(100), using in situ xray diffraction measurements during uniaxial strain compression and release. For final stresses above 15.7 GPa, the Ge transformed to a highly textured tetragonal β-Sn phase. At 31.5 GPa and above, Ge transformed to the molten phase. Full stress release (uniaxial strain) from the β-Sn phase, from the melt boundary, and from the completely molten phase, resulted in reversion to an untextured cubic diamond (cd) phase. These findings demonstrate that the cd to β-Sn phase change is reversible, and that recrystallization from the liquid phase occurs on nanosecond timescales during release.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.