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M. Odén

Publications and source records attributed to M. Odén.

4 recordsLinked to original sources

Controlled polymorphic competition -- a path to tough and hard ceramics

From nanoscale devices including sensors, electronics, or biocompatible coatings to macroscale structural, automotive or aerospace components, fundamental understanding of plasticity and fracture can guide the realization of materials that ensure safe and durable performance. Identifying the role of atomic-scale plasticity is crucial, especially for applications relying on brittle ceramics. Here, stress-intensity-controlled atomistic simulations of fracture in cubic Ti$_{1-x}$Al$_{x}$N model systems demonstrate how $\overset{\lower.5em\circ}{\mathrm{A}}$-scale plasticity - manifested as lattice distortions, phase transformation, nucleation and emission of dislocations - substantially affects the macroscale fracture toughness (K$_{Ic}$) and fracture strength ($σ$$_{f}$) of brittle ceramics. The extent of plastic deformation in Ti$_{1-x}$Al$_{x}$N increases monotonically with the Al content (x), due to a corresponding decrease in cubic $\rightarrow$ hexagonal polymorph transition energies and unstable stacking fault energies. Overall, plasticity positively affects the mechanical properties, resulting in optimal combinations of strength and toughness for x~0.6. However, for x exceeding ~0.7, the benefits of plasticity diminish. The initial rise followed by a decline in K$_{Ic}$(x) and $σ$$_{f}$(x) is explained based on the interplay between phase transformation, shear-induced faulting, and tensile cleavage on the easiest fracture plane. The results highlight the impact of atomic-scale plasticity on observable properties and point to strategies for toughening ceramics through control of polymorph competition.

cond-mat.mtrl-sci↗

High temperature decomposition and age hardening of single-phase wurtzite Ti$_{1-x}$Al$_{x}$N thin films grown by cathodic arc deposition

We investigated the high temperature decomposition behavior of wurtzite phase Ti$_{1-x}$Al$_{x}$N films using experimental methods and first-principles calculations. Single phase metastable wurtzite Ti$_{1-x}$Al$_{x}$N (x = 0.65, 0.75, 085 and 0.95) solid solution films were grown by cathodic arc deposition using low duty cycle pulsed substrate-bias voltage. First-principles calculated elastic constants of the wurtzite Ti$_{1-x}$Al$_{x}$N phase show a strong dependence on alloy composition. The predicted phase diagram shows a miscibility gap with an unstable region. High resolution scanning transmission electron microscopy and chemical mapping demonstrate decomposition of the films after high temperature annealing (950$^{\circ}$C), which resulted in nanoscale chemical compositional modulations containing Ti-rich and Al-rich regions with coherent or semi coherent interfaces. This spinodal decomposition of the wurtzite film causes age hardening of 1-2 GPa.

cond-mat.mtrl-sci↗

Structural changes in Ti1-xAlxN coatings during turning: A XANES and EXAFS study of worn tools

Structural changes in Ti1-xAlxN coated tool inserts used for turning in 316L stainless steel were investigated by XANES, EXAFS, EDS, and STEM. For coarse-grained fcc-structured Ti1-xAlxN coatings, with 0 \leq x \leq 0.62, the XANES spectrum changes with Al-content. XANES Ti 1s line-scans across the rake face of the worn samples reveals that TiN-enriched domains have formed during turning in Ti0.47Al0.53N and Ti0.38Al0.62N samples as a result of spinodal decomposition. The XANES spectra reveal the locations on the tool in which the most TiN-rich domains have formed, indicating which part of the tool-chip contact area that experienced the highest temperature during turning. Changes in the pre-edge features in the XANES spectra reveal that structural changes occur also in the w-TiAlN phase in fine-grained Ti0.38Al0.62N during turning. EDS shows that Cr and Fe from the steel adhere to the tool rake face during machining. Cr 1s and Fe 1s XANES show that Cr is oxidized in the end of the contact length while the adhered Fe retains in the same fcc-structure as that of the 316L stainless steel.

cond-mat.mtrl-sci↗

Elucidating dislocation core structures in titanium nitride through high-resolution imaging and atomistic simulations

Although titanium nitride (TiN) is among the most extensively studied and thoroughly characterized thin-film ceramic materials, detailed knowledge of relevant dislocation core structures is lacking. By high-resolution scanning transmission electron microscopy (STEM) of epitaxial single crystal (001)-oriented TiN films, we identify different dislocation types and their core structures. These include, besides the expected primary full a/2{110}<1$\bar{1}$0> dislocation, Shockley partial dislocations a/6{111}<11$\bar{2}$> and sessile Lomer edge dislocations a/2{100}<011>. Density-functional theory and classical interatomic potential simulations complement STEM observations by recovering the atomic structure of the different dislocation types, estimating Peierls stresses, and providing insights on the chemical bonding nature at the core. The generated models of the dislocation cores suggest locally enhanced metal-metal bonding, weakened Ti-N bonds, and N vacancy-pinning that effectively reduces the mobilities of {110}<1$\bar{1}$0> and {111}<11$\bar{2}$> dislocations. Our findings underscore that the presence of different dislocation types and their effects on chemical bonding should be considered in the design and interpretations of nanoscale and macroscopic properties of TiN.

cond-mat.mtrl-sci↗