An update on the mechanism of the graphene–NO reaction. (May 2015)

• Record Type: Journal Article
• Authors: Oyarzún, Andrea M.; Radovic, Ljubisa R.; Kyotani, Takashi
• Is Part Of: Carbon. Volume 86(2015)
• Page Start: 58
• Page End: 68
• Publication Date: 2015-05
• Subjects: Carbon -- Periodicals; Carbone -- Périodiques; Koolstof; Toepassingen; Electronic journals; 546.681
• DOI: 10.1016/j.carbon.2015.01.020
• Languages: English
• ISSNs: 0008-6223

Abstract

Abstract: Cognizant of the key experimental facts from studies of carbonaceous solids ranging from soot to graphite, we performed a quantum chemistry study of the interaction of NO monomer or dimer with one or more zigzag sites. Thermodynamic and kinetic results were used to examine two alternative mechanisms proposed in the literature, and to compare them with the graphene–O2 reaction mechanism. The chemisorption stoichiometry similarities are striking; but the differences, especially regarding the intermediate role of N2 O, have important practical implications. Monomer chemisorption on an isolated site is a dead-end and temporarily inhibiting process, similar to that of formation of a stable C–O surface complex in the graphene–O2 reaction. When two sites are available, successive monomer adsorption eventually leads to N2 O formation subsequent to parallel reorientation of the first NO molecule. If three contiguous sites are available, N2 and CO are the principal products. Chemisorption of the dimer provides a straightforward path to N2 and CO2 when one site is available and to N2 and CO when two sites are available. The formation of N2 O is also feasible in this case, both during adsorption and desorption; in the adsorption phase it is very sensitive to the details of the electron pairing processes.