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Ammonia Decomposition over Ni Catalysts Supported on Perovskite-type Oxides for the On-site Generation of Hydrogen

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Journal RSC Adv
Specialty Chemistry
Date 2022 May 13
PMID 35547483
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Abstract

Ammonia decomposition has attracted increasing attention as a promising process for the on-site generation of hydrogen. In this study, Ni catalysts supported on perovskite-type oxides (ABO) were prepared and the activity for ammonia decomposition was examined. The Ni/ANbO (A = Na and K) and Ni/AEMnO (AE = Ca, Sr, and Ba) catalysts were less effective for this reaction. Meanwhile, the Ni/REAlO (RE = La, Sm, and Gd) catalysts exhibited relatively high activity. For Ni/AETiO and Ni/AEZrO, the performance strongly depended on the A-site element of the perovskite-type oxides, and the Sr and Ba elements were more effective than the Ca one in the respective series. The catalytic activity for Ni/AEZrO was higher than Ni/AETiO in the case of the same alkaline earth element, and Ni/BaZrO was the most active among the samples investigated in this work. For these series, the order in the performance corresponded well with that in the basic property. The nitrogen desorption profiles revealed that the evolution of nitrogen atoms, which is one of the kinetically slow steps, effectively proceeded for Ni/SrZrO and Ni/BaZrO compared with the conventional Ni catalysts. This promotion effect would be ascribed to the strong basic properties of the SrZrO and BaZrO supports, resulting in the high activity of Ni/SrZrO and Ni/BaZrO for ammonia decomposition.

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References
1.
Karim A, Prasad V, Mpourmpakis G, Lonergan W, Frenkel A, Chen J . Correlating particle size and shape of supported Ru/gamma-Al2O3 catalysts with NH3 decomposition activity. J Am Chem Soc. 2009; 131(34):12230-9. DOI: 10.1021/ja902587k. View

2.
Zheng W, Cotter T, Kaghazchi P, Jacob T, Frank B, Schlichte K . Experimental and theoretical investigation of molybdenum carbide and nitride as catalysts for ammonia decomposition. J Am Chem Soc. 2013; 135(9):3458-64. DOI: 10.1021/ja309734u. View

3.
Hansgen D, Vlachos D, Chen J . Using first principles to predict bimetallic catalysts for the ammonia decomposition reaction. Nat Chem. 2010; 2(6):484-9. DOI: 10.1038/nchem.626. View

4.
Bell T, Zhan G, Wu K, Zeng H, Torrente-Murciano L . Modification of Ammonia Decomposition Activity of Ruthenium Nanoparticles by N-Doping of CNT Supports. Top Catal. 2020; 60(15):1251-1259. PMC: 6961473. DOI: 10.1007/s11244-017-0806-0. View

5.
Stolbov S, Rahman T . First-principles study of some factors controlling the rate of ammonia decomposition on Ni and Pd surfaces. J Chem Phys. 2005; 123(20):204716. DOI: 10.1063/1.2121467. View