High-entropy alloys (HEAs) are an exciting new class of multi-component alloys some of which haveunusual and remarkable properties. As of yet, little is understood about dislocation core structure and stacking fault energies in these alloys. For this study, a five-component, equiatomicalloy (CrMnFeCoNi) was deformed to 5% plastic strain at room temperature. Posttest observations using diffraction contrast scanning transmission electron microscopy (DC-STEM) analysis provide evidence for numerous planar slip bands composed of ½<110> dislocations. More detailed analyses of dislocation separation distances were performed using high-order diffraction vector DC-STEM and atomic resolution high angle annular dark field (HAADF) STEM on ½<110> dislocations in 60° orientation. Large variations in dissociation distances are found, leading to the concept of a local stacking fault energy (SFE). This finding issupported through embedded-atom-method (EAM) calculations of a model, concentrated, three-element solid solution. For the first time, the Nye tensor and center of symmetry analysis were used collectively to accurately determine dissociation distance. Lastly, using highresolution energy dispersive X-ray spectroscopy, no ordering or segregation was observed,

One of the most potent examples of interstitial solute strengthening in metal alloys is the extreme sensitivity of titanium to small amounts of oxygen. Unfortunately, these small amounts of oxygen also lead to a markedly decreased ductility, which in turn drives the increased cost to purify titanium to avoid this oxygen poisoning effect. Here, we report a systematic study on the oxygen sensitivity of titanium that provides a clear mechanistic view of how oxygen impurities affect the mechanical properties of titanium. The increased slip planarity of Ti-O alloys is caused by an interstitial shuffling mechanism, which is sensitive to temperature, strain rate, and oxygen content and leads to the subsequent alteration of deformation twinning behavior. The insights from our experimental and computational work provide a rationale for the design of titanium alloys with increased tolerance to variations in interstitial content, with notable implications for more widespread use of titanium alloys.

No abstract

No abstract

Two-dimensional monolayers derived from 3D bulk structures remain a relatively unexplored class of materials because of the challenge of stabilizing nonepitaxial interfaces. Here, we report an unusual reconstruction during the deposition of precursors when targeting the synthesis of heterostructures with an odd number of PbSe monolayers. Multilayer elemental precursors of Pb|Se + V|Se were deposited to have the correct number of atoms to form [(PbSe) 1+δ ] q (VSe 2 ) 1 where q is the number of PbSe monolayers in the heterostructure. Structural analysis of the self-assembled precursor via X-ray reflectivity, X-ray diffraction, and HAADF-STEM suggests three different behaviors upon deposition. Precursors with q ≥ 7 and even values of q have the targeted nanoarchitectures after deposition, which are maintained as the products are self-assembled through a near diffusionless process. Significant lateral surface diffusion occurred during the deposition of precursors with q = 1, 3, and 5, resulting in the precursor to have a different nanoarchitecture than targeted. Additional perpendicular long-range diffusion occurs during self-assembly of these precursors, resulting in different final products than targeted. Density functional theory (DFT) calculations of PbSe blocks show that the odd-numbered layers are less stable than the even-numbered layers, which suggests an energetic driving force for the observed rearrangement. This work highlights the importance of understanding the reaction mechanism when attempting to prepare 2D layers of constituents with bulk 3D structures.