Svetlizky Ilya, Kim Seongsoo, Weitz David A, Spaepen Frans
School of Engineering and Applied Sciences (SEAS), Harvard University, Cambridge, MA, USA.
Department of Physics, Harvard University, Cambridge, MA, USA.
Nat Commun. 2023 Sep 16;14(1):5760. doi: 10.1038/s41467-023-41430-3.
The severe difficulty to resolve simultaneously both the macroscopic deformation process and the dislocation dynamics on the atomic scale limits our understanding of crystal plasticity. Here we use colloidal crystals, imaged on the single particle level by high-speed three-dimensional (3D) confocal microscopy, and resolve in real-time both the relaxation of the epitaxial misfit strain and the accompanying evolution of dislocations. We show how dislocation interactions give rise to the formation of complex dislocation networks in 3D and to unexpectedly sharp plastic relaxation. The sharp relaxation is facilitated by attractive interactions that promote the formation of new dislocations that are more efficient in mediating strain. Dislocation networks form fragmented structures, as dislocation growth is blocked by either attractive interactions, which result in the formation of sessile dislocation junctions, or by repulsion from perpendicular segments. The strength of these blocking mechanisms decreases with the thickness of the crystal film. These results reveal the critical role of dislocation interactions in plastic deformation of thin films and can be readily generalized from the colloidal to the atomic scale.
同时解决宏观变形过程和原子尺度上的位错动力学这一严峻困难,限制了我们对晶体可塑性的理解。在此,我们使用通过高速三维(3D)共聚焦显微镜在单粒子水平成像的胶体晶体,并实时解析外延失配应变的弛豫以及伴随的位错演化。我们展示了位错相互作用如何导致三维中复杂位错网络的形成以及意外急剧的塑性弛豫。有吸引力的相互作用促进了新位错的形成,这些新位错在介导应变方面更有效,从而推动了急剧的弛豫。位错网络形成碎片化结构,因为位错生长要么被导致固定位错结形成的吸引力相互作用所阻碍,要么被来自垂直段的排斥力所阻碍。这些阻碍机制的强度随着晶体薄膜的厚度而降低。这些结果揭示了位错相互作用在薄膜塑性变形中的关键作用,并且可以很容易地从胶体尺度推广到原子尺度。