4.6 Article

First-Principles Insights into the Thermocatalytic Cracking of Ammonia-Hydrogen Blends on Fe(110): 1. Thermodynamics

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 126, Issue 46, Pages 19733-19744

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.2c06003

Keywords

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Funding

  1. Air Force Office of Scientific Research (AFOSR) via the Department of Defense Multidisciplinary University Research Initiative (MURI) under AFOSR Award [FA9550-15-1-0022]
  2. University of California, Los Angeles

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Ammonia is considered a practical means for hydrogen transportation due to its higher volumetric energy density. By using density functional theory, the researchers studied the decomposition of NH3 on a catalyst and predicted surface phase diagrams that provide insights for designing efficient catalysts for NH3 decomposition. It was found that a catalyst with weakened N binding is needed to enable high-turnover NH3 decomposition.
Ammonia (NH3) is being considered as a practical means to transport hydrogen (H-2) because of its higher volumetric energy density for the same temperature and pressure. Thermodynamics suggest high temperature is needed to decompose NH3 to nitrogen (N-2) and H-2. Furthermore, overcoming decomposition kinetic barriers requires a catalyst. Via density functional theory, we study this reaction on a model catalyst: the close-packed (110) facet of alpha-Fe. Specifically, we predict detailed in-operando temperature- and pressure-dependent surface phase diagrams on this benchmark catalyst that offer insights for the design of optimal NH3 decomposition catalysts. Here, we explore the equilibrium composition(s) of the Fe(110) surface when exposed to NH3-H-2 mixtures. We predict that both N and NH partially cover the Fe(110) surface at 300-400 degrees C (far above the NH3 decomposition-formation coexistence temperature at standard partial pressures of 1 bar: similar to 180 degrees C) and 2-4 bar of total reactor pressure. At the equilibrium N/NH coverage, these species inhibit coadsorption of H, indicating that direct H-2 production may occur. However, from thermodynamics alone, removal of N/NH as N-2(g) is extremely unfavorable even at these elevated temperatures-effectively deactivating the surface toward further NH3 decomposition. Thus, catalysts that remain active toward N-H bond breaking but with weakened N binding relative to Fe are needed to enable high-turnover catalytic NH3 decomposition to release H-2.

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