Abstract
High-entropy ceramics are an emerging class of materials with fascinating characteristics. However, elemental immiscibility and crystal complexity limit the development of a general synthesis strategy, and common methods yield bulk materials. Here, we introduce a transformative non-equilibrium flame aerosol technique for synthesizing high-entropy nanoceramics. This scalable, one-step process enables the production of high-entropy oxide nanoceramics with an unprecedented diversity of crystal structures, including fluorite-phase materials that integrate up to 22 distinct cation elements. The method's capacity for entropic stabilization and grain refinement significantly improves the thermal stability of these nanostructures. In a representative application, a Pt-(MgCoNiCuZn)O high-entropy single-atom catalyst showed superior activity and long-term stability for CO2 hydrogenation, maintaining constant CO2 conversion over 670 h and dramatically outperforming conventional catalysts. The general approach opens a vast composition and structure space for the creation of high-entropy oxide nanomaterials for application across diverse fields, including catalysis, energy storage, sensing, and thermal management.
| Original language | English |
|---|---|
| Pages (from-to) | 3994-4013 |
| Number of pages | 20 |
| Journal | Matter |
| Volume | 7 |
| Issue number | 11 |
| DOIs | |
| State | Published - Nov 6 2024 |
Keywords
- CO hydrogenation
- MAP 1: Discovery
- catalysis
- flame aerosol process
- high-entropy nanoceramics
- multi-element mixing
- non-equilibrium synthesis
- single-atom dispersion
- structure diversity
- thermal stability
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