1. Direct cleavage of C=O double bond in CO2 by the subnano MoOx surface on Mo2N.
- Author
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Liu, Hao-Xin, Wang, Wei-Wei, Fu, Xin-Pu, Liu, Jin-Cheng, and Jia, Chun-Jiang
- Subjects
DOUBLE bonds ,SCISSORS & shears ,CATALYST synthesis ,HYDROGENATION ,HETEROSTRUCTURES - Abstract
Compared to H
2 -assisted activation mode, the direct dissociation of CO2 into carbonyl (*CO) with a simplified reaction route is advantageous for CO2 -related synthetic processes and catalyst upgrading, while the stable C = O double bond makes it very challenging. Herein, we construct a subnano MoO3 layer on the surface of Mo2 N, which provides a dynamically changing surface of MoO3 ↔MoOx (x < 3) for catalyzing CO2 hydrogenation. Rich oxygen vacancies on the subnano MoOx surface with a high electron donating capacity served as a scissor to directly shear the C = O double bond of CO2 to form CO at a high rate. The O atoms leached in CO2 dissociation are removed timely by H2 to regenerate active oxygen vacancies. Owing to the greatly enhanced dissociative activation of CO2 , this MoOx /Mo2 N catalyst without any supported active metals shows excellent performance for catalyzing CO2 hydrogenation to CO. The construction of highly disordered defective surface on heterostructures paves a new pathway for molecule activation. The direct dissociation of CO2 into carbonyl (*CO) via a simplified reaction pathway benefits CO2 -related synthesis and catalyst improvement, though the stability of the C = O double bond poses a significant challenge. Here, the authors design a subnano MoO3 layer on the surface of Mo2 N, offering a dynamically adaptive surface for catalyzing CO2 hydrogenation. [ABSTRACT FROM AUTHOR]- Published
- 2024
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