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Entropy-Modulated Oxide–Metal Catalyst Architectures for Direct Ammonia Protonic Ceramic Fuel Cells

  • Dongyeon Kim
  • , Dong Jae Park
  • , Incheol Jeong
  • , Seeun Oh
  • , Hyeonggeun Kim
  • , Mincheol Lee
  • , Sang Won Lee
  • , Kangyong Lee
  • , Daehan Chung
  • , Ki Min Roh*
  • , Joongmyeon Bae*
  • , Tae Ho Shin*
  • , Kang Taek Lee*
  • *Corresponding author for this work
  • Korea Advanced Institute of Science and Technology
  • Korea Institute of Ceramic Engineering And Technology
  • Korea Institute of Geoscience and Mineral Resources

Research output: Contribution to journalJournal articlepeer-review

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 languageEnglish
Article number335
JournalNano-Micro Letters
Volume18
Issue number1
DOIs
StatePublished - 2026.12

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    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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