The growth of graphene by molecular beam epitaxy from an elemental carbon precursor is a very promis- ing technique to overcome some of the main limitations of the chemical vapour deposition approach, such as the possibility to synthesize graphene directly on a wide variety of surfaces including semi- conductors and insulators. However, while the individual steps of the chemical vapour deposition growth process have been extensively studied for several surfaces, such knowledge is still missing for the case of molecular beam epitaxy, even though it is a key ingredient to optimise its performance and effectiveness. In this work, we have performed a combined experimental and theoretical study comparing the growth rate of the molecular beam epitaxy and chemical vapour deposition processes on the prototypical Ir (111) surface. In particular, by employing high-resolution fast X-ray photoelectron spectroscopy, we were able to follow the growth of both single- and multi-layer graphene in real time, and to identify the spectro- scopic fingerprints of the different C layers. Our experiments, supported by density functional theory cal- culations, highlight the role of the interaction between different C precursor species and the growing gra- phene flakes on the growth rate of graphene. These results provide an overview of the main differences between chemical vapour deposition and molecular beam epitaxy growth and thus on the main para- meters which can be tuned to optimise growth conditions.

Graphene growth by molecular beam epitaxy: An interplay between desorption, diffusion and intercalation of elemental C species on islands

Presel, Francesco;Bignardi, Luca;Tache, Cristian A.;Baraldi, Alessandro
2018

Abstract

The growth of graphene by molecular beam epitaxy from an elemental carbon precursor is a very promis- ing technique to overcome some of the main limitations of the chemical vapour deposition approach, such as the possibility to synthesize graphene directly on a wide variety of surfaces including semi- conductors and insulators. However, while the individual steps of the chemical vapour deposition growth process have been extensively studied for several surfaces, such knowledge is still missing for the case of molecular beam epitaxy, even though it is a key ingredient to optimise its performance and effectiveness. In this work, we have performed a combined experimental and theoretical study comparing the growth rate of the molecular beam epitaxy and chemical vapour deposition processes on the prototypical Ir (111) surface. In particular, by employing high-resolution fast X-ray photoelectron spectroscopy, we were able to follow the growth of both single- and multi-layer graphene in real time, and to identify the spectro- scopic fingerprints of the different C layers. Our experiments, supported by density functional theory cal- culations, highlight the role of the interaction between different C precursor species and the growing gra- phene flakes on the growth rate of graphene. These results provide an overview of the main differences between chemical vapour deposition and molecular beam epitaxy growth and thus on the main para- meters which can be tuned to optimise growth conditions.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11368/2928943
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