High spin polarized Fe2 cluster combined with vicinal nonmetallic sites for catalytic ammonia synthesis from a theoretical perspective

An Fe2 catalyst combined with the vicinal nonmetallic sites may break the Brønsted–Evans–Polanyi limitation and lead to a more efficient ammonia synthesis than previously reported. Our theoretical calculations show that the Fe2 catalyst supported on graphitic carbon nitride (Fe2/mpg-C3N4) strongly f...

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Bibliographic Details
Published in:Inorganic chemistry frontiers 2021-12, Vol.8 (24), p.5299-5311
Main Authors: Zhu, Hongdan, Aarons, Jolyon, Peng, Qian
Format: Article
Language:English
Subjects:
Ammonia
Carbon nitride
Catalysts
Chemical synthesis
Hydrogen bonds
Inorganic chemistry
Polarization (spin alignment)
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Summary:An Fe2 catalyst combined with the vicinal nonmetallic sites may break the Brønsted–Evans–Polanyi limitation and lead to a more efficient ammonia synthesis than previously reported. Our theoretical calculations show that the Fe2 catalyst supported on graphitic carbon nitride (Fe2/mpg-C3N4) strongly favors hydrogenation of *N2 to form *NHNH2 species, which leads to low energy barriers for N–H formation (0.47 eV) and N–N dissociation (0.50 eV). In addition, B–N Lewis pairs constructed on the mpg-C3N4 serve as nonmetallic sites that enable heterolysis of the H–H bond to overcome the relatively high energy barrier of hydrogen transfer. Through a comprehensive study of Fen/mpg-C3N4 (n = 2, 3, 4) and Fe (211) catalysts, we conclude that synergistic Fe2 catalyst shows a significant advantage due to its high spin polarization and thus can avoid harsh reaction conditions for the thermal conversion of N2 to NH3.
ISSN:2052-1545
2052-1553
DOI:10.1039/d1qi01083b