Abstract
A carbon-free energy system might use ammonia as a hydrogen carrier owing to its high hydrogen concentration, good liquefaction, and worldwide production and transportation infrastructure. Catalytic ammonia breakdown provides a CO2-free hydrogen-generating method, but high temperatures, catalyst deactivation, and expense restrict its practicality. This study covers important aspects of ammonia decomposition catalysts, including Ru-, Ni-, and Co-based systems supported by carbon, Al2O3, and perovskite oxides. To develop structure–activity connections and identify rate-limiting stages under various operating regimes, thermodynamic, kinetic, and fundamental reaction processes are examined. Ru-based catalysts, especially those supported on conductive carbons and tailored perovskites, are standards for low-temperature activity, but their high cost and stability prevent large-scale application. Combining Ni-based catalysts with Al2O3 or basic perovskite supports offers a good balance between activity, cost, and commercial practicality, making them the dominant non-noble alternatives. Due to strong metal–support interactions and alternate reaction routes, Co-based catalysts in perovskite formulations seem promising despite being inherently less active. Support chemistry, promoters, metal dispersion, and oxygen vacancies are discussed, along with low-temperature operation and scale-up problems and research prospects.
| Original language | English |
|---|---|
| Article number | e70200 |
| Journal | Chemical Record |
| Volume | 26 |
| Issue number | 9 |
| DOIs | |
| State | Published - Sep 2026 |
Bibliographical note
Publisher Copyright:© 2026 The Chemical Society of Japan and Wiley-VCH GmbH.
Keywords
- ammonia decomposition
- catalysis
- hydrogen production
- nickel
- perovskite
- Ru catalysts
ASJC Scopus subject areas
- Biochemistry
- General Chemistry
- General Chemical Engineering
- Materials Chemistry
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