Articolo in rivista, 2017, ENG, 10.3762/bjnano.8.44
A. Piazza 1,2,3; F. Giannazzo 1; G. Buscarino 2; G. Fisichella 1; A. La Magna 1; F. Roccaforte 1; M. Cannas 2; F.M. Gelardi 2; S. Agnello 2
1.CNR-IMM, Catania (Italy); 2. University of Palermo (Italy); 3. University of Catania (Italy)
The effects of temperature and atmosphere (air and O-2) on the doping of monolayers of graphene (Gr) on SiO2 and Si substrates, and on the doping of MoS2 multilayer flakes transferred on the same substrates have been investigated. The investigations were carried out by in situ micro-Raman spectroscopy during thermal treatments up to 430 degrees C, and by atomic force microscopy (AFM). The spectral positions of the G and 2D Raman bands of Gr undergo only minor changes during treatment, while their amplitude and full width at half maximum (FWHM) vary as a function of the temperature and the used atmosphere. The thermal treatments in oxygen atmosphere show, in addition to a thermal effect, an effect attributable to a p-type doping through oxygen. The thermal broadening of the line shape, found during thermal treatments by in situ Raman measurements, can be related to thermal phonon effects. The absence of a band shift results from the balance between a red shift due to thermal effects and a blue shift induced by doping. This shows the potential of in situ measurements to follow the doping kinetics. The treatment of MoS2 in O-2 has evidenced a progressive erosion of the flakes without relevant spectral changes in their central zone during in situ measurements. The formation of MoO3 on the edges of the flakes is observed indicative of the oxygen-activated transformation.
Beilstein journal of nanotechnology 8 , pp. 418–424
two-dimensional (2D) materials, graphene, MoS2, Raman spectroscopy, thermal doping
Roccaforte Fabrizio, Giannazzo Filippo
ID: 397205
Year: 2017
Type: Articolo in rivista
Creation: 2019-01-02 17:32:34.000
Last update: 2021-03-11 17:01:32.000
CNR authors
CNR institutes
External IDs
CNR OAI-PMH: oai:it.cnr:prodotti:397205
DOI: 10.3762/bjnano.8.44
ISI Web of Science (WOS): 000394460500001