Untangling individual cation roles in rock salt high-entropy oxides

• Published in: Acta materialia 2024-10, Vol.279, p.120289, Article 120289
• Main Authors: Almishal, Saeed S.I., Sivak, Jacob T., Kotsonis, George N., Tan, Yueze, Furst, Matthew, Srikanth, Dhiya, Crespi, Vincent H., Gopalan, Venkatraman, Heron, John T., Chen, Long-Qing, Rost, Christina M., Sinnott, Susan B., Maria, Jon-Paul
• Format: Article
• Language: English
• Subjects: Binary phase diagrams; Bulk synthesis; Density functional theory; High-entropy oxides; Linear optical properties; Thin film growth
• ISSN: 1359-6454
• DOI: 10.1016/j.actamat.2024.120289

We unravel the distinct role each cation plays in phase evolution, stability, and properties within the Mg1/5Co1/5Ni1/5Cu1/5Zn1/5O high-entropy oxide (HEO) by integrating experimental findings, thermodynamic analyses, and first-principles predictions. Our approach is through sequentially removing one cation at a time from the five-component high-entropy oxide to create five four-component derivatives. Bulk synthesis experiments indicate that Mg, Ni, and Co act as rock salt phase stabilizers whereas only Mg and Ni enthalpically enhance single-phase rock salt stability in thin film growth; synthesis conditions dictate whether Co is a rock salt phase stabilizer or destabilizer. By examining the competing phases and oxidation state preferences using pseudo-binary phase diagrams and first-principles calculations, we resolve the stability differences between bulk and thin film for all compositions. We systematically explore HEO macroscopic property sensitivity to cation selection employing both predicted and measured optical spectra. This study establishes a framework for understanding high-entropy oxide synthesizability and properties on a per-cation basis that is broadly applicable to tailoring functional property design in other high-entropy materials. [Display omitted]