Effect of Oxygen in Mo-TM (TM = Ti, Zr, Hf) Solid Solutions as Studied with Density Functional Theory Calculations

Abstract

Mo-Ti-Si, Mo-Zr-B, and Mo-Hf-B are promising alloy systems for high-temperature applications as they show higher toughness and higher creep resistance than other Mo-based alloys. Regarding ductility and toughness, the chemical composition of the Mo solid-solution phase is the main parameter with which to tweak these properties of multiphase Mo-based alloys. Besides the common solid-solution hardening, one goal is to minimize embrittlement by decreasing the detrimental effects of interstitials like oxygen atoms in Mo alloys, which might be present in the bulk material due to trapping. For a better understanding of the trapping mechanisms and behavior of Mo solid solutions, the bonding situation and interaction of Mo atoms with the atoms of the alloying partners, as well as oxygen atoms, is worthwhile to investigate. For this, an in-depth analysis of the chemical bonding situation with calculations based on density functional theory in selected Mo-TM(-O) (TM = Ti, Zr, Hf) solid solutions is conducted in this work. It is shown that Ti atoms in a Mo solid solution are strong traps for oxygen atoms, while Hf and, even more clearly, Zr atoms are not. It is pointed out that the ionic and covalent interactions are the primary influence on the trapping behavior, as the change in ionic and covalent interactions between trapping and nontrapping models follows the trend Mo-1Ti > Mo-1Hf > Mo-1Zr, which resembles the trend of the trapping energy.