Date | 17th, Dec 2018 |
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Home > Press > IMDEA Nanociencia and Universidad Aut'noma de Madrid researchers have demonstrated that graphene deposited on a metal surface promotes an unusual chemical reaction that would hardly take place under noncatalyzed conditions.
Abstract: Graphene monolayers can be epitaxially grown on many single-crystal metal surfaces under ultra-high vacuum. On one side, these monolayers protect highly reactive metallic surfaces from contaminants, but on the other side, the piling of the layers as graphitic carbon poisons the activity of transition metal catalysts. The inertness of the graphite and the physical blockage of the active sites prevents chemical reactions occurring on the metal surface.
Madrid, Spain | Posted on December 14th, 2018
Researchers led by Fernando Mart'n, Emilio P'rez and Amadeo V'zquez de Parga (IMDEA Nanociencia and Universidad Aut'noma de Madrid) have demonstrated that nanostructured graphene monolayers on a metal surface do promote a chemical reaction that would hardly take place under noncatalyzed conditions. A crystal of ruthenium, Ru(0001), has been covered with an epitaxially grown continuous graphene layer. Because of the difference in lattice parameters, a new superperiodicity appears on the graphene layer and modulates its electronic properties. Taking advantage of the modulation, the surface has been functionalized with cyanomethylene groups (-CH2CN), covalently bonded to the center of the hexagonal close-packed areas in the Moir' unit cell, and doped with TCNQ (7,7,8,8-tetracyano-p-quinodimethane). TCNQ is an electron acceptor molecule used to p-dope graphene films. When deposited on the graphene surface, this molecule is absorbed on a bridge position between two ripples. Here, it is worth to notice the important role of the surface and of the graphene layer in catalyzing the reaction of TCNQ and -CH2CN. The reaction of TCNQ with CH3CN (the pristine reactants are in gas phase) plus the loss of a hydrogen atom is very unlikely because of the high energy barrier (about 5 eV). The presence of the graphene layer reduces this energy barrier by a factor of 5, thus favoring the formation of the products.
The nanostructured graphene promotes the reaction in a threefold way: first, holds the -CH2CN in place; second, allows for an efficient charge transfer from the ruthenium; and third, prevents the absorption of TCNQ by ruthenium allowing the molecule to diffuse on the surface. 'A similar clean reaction on pristine ruthenium is not possible, because the reactive character of ruthenium leads to the absorption of CH3CN and hinders the mobility of TCNQ molecules once absorbed on the surface' Amadeo says. The results confirm the catalytic character of graphene in this reaction. 'Such a selectivity would be difficult to obtain by using other forms of carbon' Emilio confirms.
Further, the TCNQ molecules have been injected with electrons using the scanning tunneling microscope (STM). This individual manipulation of the molecules induces a C-C bond breaking, thus leading to the recovery of the initial reactants: CH2CN-graphene and TCNQ. The process is reversible and reproducible at a single-molecule level. As the researchers have observed a Kondo resonance, the reversibility of the process can be thought as a reversible magnetic switch controlled by a chemical reaction.
Fernando Mart'n, Emilio P'rez and Amadeo V'zquez de Parga are researchers at the Madrid's Institute of Advanced Studies IMDEA Nanociencia. The work is a collaboration between IMDEA Nanociencia and Universidad Aut'noma de Madrid, and the Condensed Matter Physics Center IFIMAC. The research has been co-funded by the Spanish Ministry of Economy and Competitiveness, the Government of the Region of Madrid and the European Research Council.
Article:
J. Navarro, M. Pisarra, B. Nieto-Ortega, J. Villalva, C. G. Ayani, C. D'az, F. Calleja, R. Miranda, F. Mart'n, E. M. P'rez, A. L. V'zquez de Parga. Graphene catalyzes the reversible formation of a C'C bond between two molecules. Sci. Adv. 4, eaau9366 (2018).
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