Abstract
Entropy-modulated oxide–metal catalyst exsolving Ni–Fe–Cu alloy nanoparticles from a high-entropy perovskite matrix enables efficient and durable ammonia decomposition. Density functional theory calculations reveal that the high-entropy oxide framework facilitates cation exsolution and lowers the kinetic barriers for NH3 decomposition; additionally, the exsolved Ni–Fe–Cu alloy nanoparticles exhibit markedly higher catalytic activity than single-metal surfaces. Direct ammonia protonic ceramic fuel cells (DA-PCFCs) incorporating the Sr2Fe1Mo0.2Mn0.2Cr0.2Cu0.2Ni0.2O6-δ (SFMMCCN) catalyst layer achieve a record-high power density of 2.04 W cm−2 at 700 °C with stable operation for over 255 h under NH3 fuel, demonstrating the effectiveness of the entropy-modulated catalyst in designing durable and high-performance DA-PCFCs for carbon-free ammonia-to-power technologies.
| Original language | English |
|---|---|
| Article number | 335 |
| Journal | Nano-Micro Letters |
| Volume | 18 |
| Issue number | 1 |
| DOIs | |
| State | Published - 2026.12 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Ammonia
- Anode catalyst layer
- Density functional theory
- High-entropy perovskite
- Protonic ceramic fuel cells (PCFCs)
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