Universidad Autónoma de Madrid


Surface chemical reactions at epitaxial graphene and material beyond graphene

Fecha de celebración:
Desde el 12-09-2017 hasta el 12-09-2017

Hora de celebración:
12 h

Lugar de celebración:
Dpto. Física de la Materia Condensada, Facultad Ciencias, Modulo 3, Sala de Seminarios (5ª Planta)



In this talk, an overview of surface-science investigations on the chemical reactivity of epitaxial graphene (Gr) and materials “beyond graphene” (van der Waals semiconductors, topological insulators, Dirac semimetals, Weyl semimetals) will be provided.


By means of time-resolved X-ray photoemission spectroscopy and high-resolution electron energy loss spectroscopy, different surface chemical reactions in epitaxial Gr have been followed in real time (Gr growth by cracking of hydrocarbons, oxidation, intercalation of chemical species).

In particular, we have observed that, due to the similar work functions, Gr grows as an undoped sheet on the Pt-skin of Pt3Ni(111) but in an oxygen environment Ni segregation toward the surface occurs with selective oxidation of Ni. Subsequently, the Pt skin underneath Gr is replaced by a nickel-oxide skin. In the oxidation process, Gr acquires a p-type doping of 0.3 eV [1].

We have also used surface-science tools for investigating Gr employment in the fields of energy and catalysis. By means of a combination of surface-science spectroscopies and density functional theory [2], we have unveiled the mechanisms ruling the catalytic role of epitaxial Gr grown on transition-metal substrates for the production of hydrogen from water. Water decomposition at the Gr/metal interface at room temperature provides a hydrogenated Gr sheet, which is buckled and decoupled from the metal substrate. Molecular hydrogen is released upon heating above T=400 K.


Moreover, the analysis of the chemical reactivity of surface defects of two-dimensional materials provides important information for the nanofabrication process of electronic devices with active channels of ultrathin flakes of black phosphorus (few-layer phosphorene) [3] or InSe [4], which require the use of capping layers in order to avoid surface degradation in ambient conditions. In particular, we find high reactivity of phosphorene toward water, oxygen and CO [5], while water decomposition at room temperature occurs at Se vacancies of InSe [4].


Furthermore, the chemical inertness of high-quality single crystals of topological insulators toward ambient gases [6] will be discussed. The subsequent ambient stability of uncapped topological insulator-based nanodevices [7] paves the way for the technological exploitation of topological insulators in the fields of plasmonics [8] and Terahertz photodetection [7].

Finally, surface-science investigations on the chemical reactivity of Weyl semimetals and Dirac semimetals, also highlighting their potential applications in catalysis, will be presented.



[1]         A. Politano and G. Chiarello, 2D Mater. 4 (2017) 035003.

[2]          A. Politano et al., ACS Nano 10 (2016) 4543.

[3]          L. Viti et al., Adv. Mater. 27 (2015) 5567; L. Viti et al., Adv. Mater. 28 (2016) 7390.

[4]          A. Politano et al. Nanoscale 8 (2016) 8474.

[5           A. Politano et al., Nano Res. 9 (2016) 2598.

[6]          A. Politano et al., J. Phys. Chem. C 118 (2014) 21517.

[7]           L. Viti et al., Nano Lett. 16 (2016) 80; A. Politano et al. APL Mater. 5 (2017) 035504.

[8]          A. Politano et al., Phys. Rev. Lett. 115 (2015) 216802.

Más información: http://www.ifimac.uam.es/category/seminars/