Mechanistic Insights Into Nickel-Based Catalysts for Ammonia Decomposition Toward Efficient Hydrogen Generation
M A Shadab Siddiqui1, Md Mamunur Rahman2, Md Shaib Hossain2
1Department of Materials Science and Engineering, King Fahd University of Petroleum and Minerals (KFUPM), Dhahran, Saudi Arabia.
Nickel catalysts efficiently release hydrogen from ammonia, a carbon-free fuel. Advances in catalyst design and support materials enable low-temperature ammonia decomposition for cleaner energy.
Area of Science:
- Materials Science
- Catalysis
- Chemical Engineering
Background:
- Ammonia is a promising carbon-free hydrogen carrier due to its high hydrogen density and existing infrastructure.
- Efficient hydrogen release via ammonia decomposition at low temperatures is kinetically challenging.
Purpose of the Study:
- To review recent advancements in nickel-based catalysis for ammonia decomposition.
- To highlight strategies for optimizing catalyst performance and understanding reaction mechanisms.
Main Methods:
- Review of literature on nickel-based catalysts, oxide supports, promoters, and bimetallic systems.
- Analysis of catalyst design, mechanistic understanding, and performance optimization guided by the Sabatier principle.
- Exploration of atomic-scale catalysts and surface science insights.
Main Results:
- Basic and defect-rich oxide supports (e.g., CeO2, La2O3) enhance Ni dispersion and activity.
- Rare-earth and alkaline-earth promoters improve catalyst stability across temperature ranges.
- Bimetallic Ni-Co and Ni-Fe alloys expand operational windows and activity.
- Single Ni sites on reducible oxides show potential for lower activation barriers near 300°C.
Conclusions:
- Nickel-based catalysts, particularly when supported on basic, defect-rich oxides and enhanced with promoters or bimetallic formulations, offer efficient pathways for hydrogen generation from ammonia.
- Integrating surface science, materials chemistry, and reactor design is crucial for developing cost-effective, durable, low-temperature catalysts.
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