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If all humans vanished tomorrow, almost every metal structure would collapse within a century or less, the metal converting to an oxide. In applications ranging from the mature technology of nuts and bolts to high technology batteries, nuclear fuels and turbine engines, protective oxide films are critical to limiting oxidation. To date models of these oxide films have assumed that they form thermodynamic equilibrium stable or metastable phases doped within thermodynamic solubility limits. Here we demonstrate experimentally and theoretically the formation of unusual non-equilibrium oxide phases, that can be predicted using a scientific framework for solute capture at a moving oxide/substrate interface. The theory shows that solute capture is likely a generic process for many electrochemical processes, and suggests that similar phenomena yielding non-equilibrium phases can occur and be predicted for a wide range of other processes involving solid-fluid and solid-solid chemical reactions.
Epitaxial strain is a proven route to enhancing the properties of complex oxides, however, the details of how the atomic structure accommodates strain are poorly understood due to the difficulty of measuring the oxygen positions in thin films. We pre
We present an extensive first-principles database of solute-vacancy, homoatomic, heteroatomic solute-solute, and solute-solute-vacancy binding energies of relevant alloying elements in aluminum. We particularly focus on the systems with major alloyin
Strong electronic correlations can produce remarkable phenomena such as metal-insulator transitions and greatly enhance superconductivity, thermoelectricity, or optical non-linearity. In correlated systems, spatially varying charge textures also ampl
Recent advances in high-throughput experimentation for combinatorial studies have accelerated the discovery and analysis of materials across a wide range of compositions and synthesis conditions. However, many of the more powerful characterization me
Using resonant X-ray spectroscopies combined with density functional calculations, we find an asymmetric bi-axial strain-induced $d$-orbital response in ultra-thin films of the correlated metal LaNiO$_3$ which are not accessible in the bulk. The sign