Wenjun Lu

Characterizing solute hydrogen and hydrides in pure and alloyed titanium at the atomic scale

Abstract Ti and its alloys have a high affinity for hydrogen and are typical hydride formers. Ti-hydride are brittle phases which probably cause premature failure of Ti-alloys. Here, we used atom probe tomography and electron microscopy to investigate the hydrogen distribution in a set of specimens of commercially pure Ti, model and commercial Ti-alloys. Although likely partly introduced during specimen preparation with the focused-ion beam, we show formation of Ti-hydrides along α grain boundaries and α/β phase boundaries in commercial pure Ti and α+β binary model alloys. No hydrides are observed in the α phase in alloys with Al addition or quenched-in Mo supersaturation.

Large strain synergetic material deformation enabled by hybrid nanolayer architectures.

Nanolayered metallic composites are much stronger than pure nanocrystalline metals due to their high density of hetero-interfaces. However, they are usually mechanically instable due to the deformation incompatibility among the soft and hard constituent layers promoting shear instability. Here we designed a hybrid material with a heterogeneous multi-nanolayer architecture. It consists of alternating 10u2009nm and 100 nm-thick Cu/Zr bilayers which deform compatibly in both stress and strain by utilizing the layers’ intrinsic strength, strain hardening and thickness, an effect referred to as synergetic deformation. Micropillar tests show that the 6.4 GPa-hard 10u2009nm Cu/Zr bilayers and the 3.3u2009GPa 100u2009nm Cu layers deform in a compatible fashion up to 50% strain. Shear instabilities are entirely suppressed. Synergetic strengthening of 768u2009MPa (83% increase) compared to the rule of mixture is observed, reaching a total strength of 1.69u2009GPa. We present a model that serves as a design guideline for such synergetically deforming nano-hybrid materials.

Eliminating deformation incompatibility in composites by gradient nanolayer architectures

Composite materials usually possess a severe deformation incompatibility between the soft and hard phases. Here, we show how this incompatibility problem is overcome by a novel composite design. A gradient nanolayer-structured Cu-Zr material has been synthesized by magnetron sputtering and tested by micropillar compression. The interface spacing between the alternating Cu and Zr nanolayers increases gradually by one order of magnitude from 10u2009nm at the surface to 100u2009nm in the centre. The interface spacing gradient creates a mechanical gradient in the depth direction, which generates a deformation gradient during loading that accumulates a substantial amount of geometrically necessary dislocations. These dislocations render the component layers of originally high mechanical contrast compatible. As a result, we revealed a synergetic mechanical response in the material, which is characterized by fully compatible deformation between the constituent Cu and Zr nanolayers with different thicknesses, resulting in a maximum uniform layer strain of up to 60% in the composite. The deformed pillars have a smooth surface, validating the absence of deformation incompatibility between the layers. The joint deformation response is discussed in terms of a micromechanical finite element simulation.

Bidirectional Transformation Enables Hierarchical Nanolaminate Dual‐Phase High‐Entropy Alloys

Microstructural length-scale refinement is among the most efficient approaches to strengthen metallic materials. Conventional methods for refining microstructures generally involve grain size reduction via heavy cold working, compromising the materials ductility. Here, a fundamentally new approach that allows load-driven formation and permanent refinement of a hierarchical nanolaminate structure in a novel high-entropy alloy containing multiple principal elements is reported. This is achieved by triggering both, dynamic forward transformation from a faced-centered-cubic γ matrix into a hexagonal-close-packed ε nanolaminate structure and the dynamic reverse transformation from ε into γ. This new mechanism is referred to as the bidirectional transformation induced plasticity (B-TRIP) effect, which is enabled through a near-zero yet positive stacking fault energy of γ. Modulation of directionality in the transformation is triggered by local dissipative heating and local micromechanical fields. The simple thermodynamic and kinetic foundations for the B-TRIP effect render this approach generally suited for designing metastable strong and ductile bulk materials with hierarchical nanolaminate substructures.