Large area molybdenum disulphide- epitaxial graphene vertical Van der Waals heterostructures

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作者
Debora Pierucci
Hugo Henck
Carl H. Naylor
Haikel Sediri
Emmanuel Lhuillier
Adrian Balan
Julien E. Rault
Yannick J. Dappe
François Bertran
Patrick Le Fèvre
A. T. Charlie Johnson
Abdelkarim Ouerghi
机构
[1] Laboratoire de Photonique et de Nanostructures (CNRS- LPN),Department of Physics and Astronomy
[2] Route de Nozay,undefined
[3] University of Pennsylvania,undefined
[4] Institut des Nanosciences de Paris,undefined
[5] UPMC,undefined
[6] 4 place Jussieu,undefined
[7] Laboratoire d’Innovation en Chimie des Surfaces et Nanosciences,undefined
[8] DSM/NIMBE/LICSEN (CNRS UMR 3685),undefined
[9] CEA Saclay,undefined
[10] Synchrotron-SOLEIL,undefined
[11] Saint-Aubin,undefined
[12] SPEC,undefined
[13] CEA,undefined
[14] CNRS,undefined
[15] Universite Paris-Saclay,undefined
[16] CEA Saclay,undefined
[17] 91191 Gif-sur-Yvette Cedex,undefined
[18] France ,undefined
来源
Scientific Reports | / 6卷
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摘要
Two-dimensional layered transition metal dichalcogenides (TMDCs) show great potential for optoelectronic devices due to their electronic and optical properties. A metal-semiconductor interface, as epitaxial graphene - molybdenum disulfide (MoS2), is of great interest from the standpoint of fundamental science, as it constitutes an outstanding platform to investigate the interlayer interaction in van der Waals heterostructures. Here, we study large area MoS2-graphene-heterostructures formed by direct transfer of chemical-vapor deposited MoS2 layer onto epitaxial graphene/SiC. We show that via a direct transfer, which minimizes interface contamination, we can obtain high quality and homogeneous van der Waals heterostructures. Angle-resolved photoemission spectroscopy (ARPES) measurements combined with Density Functional Theory (DFT) calculations show that the transition from indirect to direct bandgap in monolayer MoS2 is maintained in these heterostructures due to the weak van der Waals interaction with epitaxial graphene. A downshift of the Raman 2D band of the graphene, an up shift of the A1g peak of MoS2 and a significant photoluminescence quenching are observed for both monolayer and bilayer MoS2 as a result of charge transfer from MoS2 to epitaxial graphene under illumination. Our work provides a possible route to modify the thin film TDMCs photoluminescence properties via substrate engineering for future device design.
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