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High‐entropy oxides (HEOs) are being extensively studied for various functional applications, but there is limited research into the mechanical behavior of these materials, especially at elevated temperatures. Bulk (Co, Cu, Mg, Ni, Zn)O (transition metal (TM)‐HEO) samples are formed into dome shapes at 800 °C and 70 kPa. Deformation experiments and finite element analysis (FEA) reveal that TM‐HEO has a creep stress exponent ofn = 0.6, indicating that TM‐HEO deforms through superplastic deformation and exhibits shear‐thickening behavior. Comparisons of experimental strain rates to those calculated using existing superplasticity mechanism models signify that TM‐HEO deforms through grain boundary sliding accommodated by a solution‐precipitation mechanism from a secondary phase. A Cu‐rich tenorite phase, commonly observed in the grain boundaries of TM‐HEO, is proposed as the secondary phase facilitating deformation. It is important to highlight here that the superplastic deformation behavior in TM‐HEO is active under modest temperature and pressure conditions, as noted above. Low‐temperature superplastic deformation will provide a powerful method of manufacturing HEO ceramics into net shape parts, greatly expanding their potential applications.
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From fabrication to mechanical properties: exploring high-entropy oxide thin films and coatings for high-temperature applications
High-entropy oxides (HEOs) containing five or more cations have garnered significant attention recently due to their vastly tunable compositional space, along with their remarkable physical and mechanical properties, exceptional thermal stability, and phase reversibility at elevated temperatures. These characteristics position HEOs as promising candidates for structural components and coatings in high-temperature applications. While much of the ongoing research on HEOs centers around understanding processing-structure relationships, there remains a dearth of knowledge concerning their mechanical properties, crucial for their prospective high-temperature applications. Whether in bulk form or as coatings, the efficacy of HEOs hinges on robust mechanical properties across a spectrum of temperatures, to ensure structural integrity, fracture resistance, and resilience to thermal stress. This review offers a succinct synthesis of recent advancements in HEO research, spanning from processing techniques to mechanical behaviors under extreme conditions. Emphasis is placed on three key aspects: (1) Investigating the influence of processing parameters on HEO crystal structures. (2) Analyzing the interplay between crystal structure and mechanical properties, elucidating deformation mechanisms. (3) Examining the mechanical behavior of HEOs under extreme temperatures and pressures. Through this review, we aim to illuminate the effective control of HEOs’ unique structures and mechanical properties, paving the way for their future applications in extreme environments.
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- Award ID(s):
- 2104655
- PAR ID:
- 10528154
- Publisher / Repository:
- Frontiers
- Date Published:
- Journal Name:
- Frontiers in Coatings, Dyes and Interface Engineering
- Volume:
- 2
- ISSN:
- 2813-6861
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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We present the successful synthesis and characterization of a one-dimensional high-entropy oxide (1D-HEO) exhibiting nanoribbon morphology. These 1D-HEO nanoribbons exhibit high structural stability at elevated temperatures (to 1000°C), elevated pressures (to 12 gigapascals), and long exposure to harsh acid or base chemical environments. Moreover, they exhibit notable mechanical properties, with an excellent modulus of resilience reaching 40 megajoules per cubic meter. High-pressure experiments reveal an intriguing transformation of the 1D-HEO nanoribbons from orthorhombic to cubic structures at 15 gigapascals followed by the formation of fully amorphous HEOs above 30 gigapascals, which are recoverable to ambient conditions. These transformations introduce additional entropy (structural disorder) besides configurational entropy. This finding offers a way to create low-dimensional, resilient, and high-entropy materials.more » « less
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The prototype high-entropy oxide (HEO) Y0.2La0.2Ce0.2Pr0.2Sm0.2O2−δ represents a particularly complex class of HEOs with significant anion sublattice entropy. The system takes either a fluorite or bixbyite-type crystal structure, depending on synthesis kinetics and thermal history. Here, we synthesize bulk ceramics and epitaxial thin films of Y0.2La0.2Ce0.2Pr0.2Sm0.2O2−δ and use diffraction to explore crystal symmetry and phase. Thin films exhibit the high symmetry fluorite phase, while bulk ceramics adopt the lower symmetry bixbyite phase. The difference in chemical ordering and observed symmetry between vapor-deposited and reactively sintered specimens suggests that synthesis kinetics can influence accessible local atomic configurations, i.e., the high kinetic energy adatoms quench in a higher-effective temperature, and thus higher symmetry structure with more configurational entropy. More generally, this demonstration shows that recovered HEO specimens can exhibit appreciably different local configurations depending on synthesis kinetics, with potential ramifications on macroscopic physical properties.more » « less
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Despite significant interest in their functional properties, the mechanical behavior of high-entropy oxides (HEOs) is not well studied, particularly at elevated temperatures. Bulk (Co,Cu,Mg,Ni,Zn)O (transition metal (TM)-HEO) samples were deformed under compression at applied stresses and temperatures ranging from 5 to 31 MPa and 600 to 850 °C, respectively. All of the deformation conditions result in creep stress exponents of n < 3, indicating that TM-HEO exhibits superplastic deformation. A transition from structural to solution-precipitation-based superplasticity is observed during deformation above 650 °C. Additionally, TM-HEO exhibits shear-thickening behavior when deformed at stresses above 9 MPa. The formation and behavior of a Cu-rich tenorite secondary phase during deformation is identified as a key factor underpinning the deformation mechanisms. The microstructure and phase state of TM-HEO before deformation also influenced the behavior, with finer grain sizes and increasing concentrations of Cu-rich tenorite, resulting in the increased prevalence of solution-precipitation deformation. While complex, the results of this study indicate that TM-HEO deforms through known superplastic deformation mechanisms. Superplasticity is a highly efficient manufacturing method and could prove to be a valuable strategy for forming HEO ceramics into complex geometries.more » « less
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The ability to accommodate multiple principal cations within a single crystallographic structure makes high entropy oxides (HEOs) ideal systems for exploring new composition–property relationships. In this work, the high-entropy design strategy is extended to strained single-crystal HEO-manganite (HEO-Mn) thin films. Phase-pure orthorhombic films of (Gd0.2La0.2Nd0.2Sm0.2Sr0.2)MnO3 were deposited on three different single-crystal substrates: SrTiO3 (STO) (100), NdGaO3 (110), and LaAlO3 (LAO) (100), each inducing different degrees of epitaxial strain. Fully coherent growth of the thin films is observed in all cases, despite the high degree of lattice mismatch between HEO-Mn and LAO. Magnetometry measurements reveal distinct differences in the magnetic properties between epitaxially strained HEO-Mn thin films and their bulk crystalline HEO counterparts. In particular, the bulk polycrystalline HEO-Mn shows two magnetic transitions as opposed to a single one observed in epitaxial thin films. Moreover, the HEO-Mn film deposited on LAO exhibits a significant reduction in the Curie temperature, which is attributed to the strong variation of the in-plane lattice parameter along the thickness of the film and the resulting changes in the Mn–O–Mn bond geometry. Thus, this preliminary study demonstrates the potential of combining high entropy design with strain engineering to tailor the structure and functionality of perovskite manganites.more » « less
- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.3389/frcdi.2024.1417527
