Graphene is usually considered a chemically inert material. Theoretical studies of CO adsorption on free-standing graphene predict quite low adsorption energies (<0.1eV). However, we show here by vibrational spectroscopy and scanning tunneling microscopy that the nondissociative chemisorption of CO occurs at cold, pristine graphene grown on Ni(111). The CO adlayer remains stable up to 125K, although some coverage survives flashes to 225K. This unexpected result is explained qualitatively by the modification of the density of states close to the Fermi energy induced by the relatively strong graphene-substrate interaction. The value of the adsorption energy allows us to estimate an equilibrium coverage of the order of 0.1monolayers at 10mbar pressure, which thus paves the way for the use of graphene as a catalytically active support under realistic conditions.

Enhanced Chemical Reactivity of Pristine Graphene Interacting Strongly with a Substrate: Chemisorbed Carbon Monoxide on Graphene/Nickel(111)

Smerieri M;Carraro G;Bracco G;Savio L;Vattuone L
2015

Abstract

Graphene is usually considered a chemically inert material. Theoretical studies of CO adsorption on free-standing graphene predict quite low adsorption energies (<0.1eV). However, we show here by vibrational spectroscopy and scanning tunneling microscopy that the nondissociative chemisorption of CO occurs at cold, pristine graphene grown on Ni(111). The CO adlayer remains stable up to 125K, although some coverage survives flashes to 225K. This unexpected result is explained qualitatively by the modification of the density of states close to the Fermi energy induced by the relatively strong graphene-substrate interaction. The value of the adsorption energy allows us to estimate an equilibrium coverage of the order of 0.1monolayers at 10mbar pressure, which thus paves the way for the use of graphene as a catalytically active support under realistic conditions.
2015
Istituto dei Materiali per l'Elettronica ed il Magnetismo - IMEM
Chemisorption
Graphene
Nickel
Surface chemistry
Vibrational spectroscopy
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/294265
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