Plasma-Induced Catalytic Conversion of Nitrogen and Hydrogen to Ammonia over Zeolitic Imidazolate Frameworks ZIF‑8 and ZIF-67

Microporous crystals have emerged as highly appealing catalytic materials for the plasma catalytic synthesis of ammonia. Herein, we demonstrate that zeolitic imidazolate frameworks (ZIFs) can be employed as efficient catalysts for the cold plasma ammonia synthesis using an atmospheric dielectric bar...

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Published inACS applied materials & interfaces Vol. 13; no. 18; pp. 21338 - 21348
Main Authors Gorky, Fnu, Lucero, Jolie M, Crawford, James M, Blake, Beth, Carreon, Moises A, Carreon, Maria L
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 12.05.2021
American Chemical Society (ACS)
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Summary:Microporous crystals have emerged as highly appealing catalytic materials for the plasma catalytic synthesis of ammonia. Herein, we demonstrate that zeolitic imidazolate frameworks (ZIFs) can be employed as efficient catalysts for the cold plasma ammonia synthesis using an atmospheric dielectric barrier discharge reactor. We studied two prototypical ZIFs denoted as ZIF-8 and ZIF-67, with a uniform window pore aperture of 3.4 Å. The resultant ZIFs displayed ammonia synthesis rates as high as 42.16 μmol NH3/min gcat. ZIF-8 displayed remarkable stability upon recycling. The dipole–dipole interactions between the polar ammonia molecules and the polar walls of the studied ZIFs led to relatively low ammonia uptakes, low storage capacity, and high observed ammonia synthesis rates. Both ZIFs outperform other microporous crystals including zeolites and conventional oxides in terms of ammonia production. Furthermore, we demonstrate that the addition of argon to the reactor chamber can be an effective strategy to improve the plasma environment. Specifically, the presence of argon helped to improve the plasma uniformity, making the reaction system more energy efficient by operating at a low specific energy input range allowing abundant formation of nitrogen vibrational species.
Bibliography:ObjectType-Article-1
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SC0021357
USDOE Office of Science (SC)
ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.1c03115