TY - JOUR
T1 - Tunable quasiparticle band gap in few-layer GaSe/graphene van der Waals heterostructures
AU - Ben Aziza, Zeineb
AU - Pierucci, Debora
AU - Henck, Hugo
AU - Silly, Mathieu G.
AU - David, Christophe
AU - Yoon, Mina
AU - Sirotti, Fausto
AU - Xiao, Kai
AU - Eddrief, Mahmoud
AU - Girard, Jean Christophe
AU - Ouerghi, Abdelkarim
N1 - Publisher Copyright:
© 2017 American Physical Society.
PY - 2017/7/7
Y1 - 2017/7/7
N2 - Two-dimensional (2D) materials have recently been the focus of extensive research. By following a similar trend as graphene, other 2D materials, including transition metal dichalcogenides (MX2) and metal mono-chalcogenides (MX), show great potential for ultrathin nanoelectronic and optoelectronic devices. Despite the weak nature of interlayer forces in semiconducting MX materials, their electronic properties are highly dependent on the number of layers. Using scanning tunneling microscopy and spectroscopy, we demonstrate the tunability of the quasiparticle energy gap of few-layered gallium selenide (GaSe) directly grown on a bilayer graphene substrate by molecular beam epitaxy. Our results show that the band gap is about 3.50 ± 0.05 eV for single-tetralayer, 3.00±0.05eV for bi-tetralayer, and 2.30±0.05eV for tri-tetralayer GaSe. This band-gap evolution of GaSe, particularly the shift of the valence band with respect to the Fermi level, was confirmed by angle-resolved photoemission spectroscopy (ARPES) measurements and our theoretical calculations. Moreover, we observed a charge transfer in the GaSe/graphene van der Waals (vdW) heterostructure using ARPES. These findings demonstrate the high impact on the GaSe electronic band structure and electronic properties that can be obtained by the control of 2D materials layer thickness and the graphene induced doping.
AB - Two-dimensional (2D) materials have recently been the focus of extensive research. By following a similar trend as graphene, other 2D materials, including transition metal dichalcogenides (MX2) and metal mono-chalcogenides (MX), show great potential for ultrathin nanoelectronic and optoelectronic devices. Despite the weak nature of interlayer forces in semiconducting MX materials, their electronic properties are highly dependent on the number of layers. Using scanning tunneling microscopy and spectroscopy, we demonstrate the tunability of the quasiparticle energy gap of few-layered gallium selenide (GaSe) directly grown on a bilayer graphene substrate by molecular beam epitaxy. Our results show that the band gap is about 3.50 ± 0.05 eV for single-tetralayer, 3.00±0.05eV for bi-tetralayer, and 2.30±0.05eV for tri-tetralayer GaSe. This band-gap evolution of GaSe, particularly the shift of the valence band with respect to the Fermi level, was confirmed by angle-resolved photoemission spectroscopy (ARPES) measurements and our theoretical calculations. Moreover, we observed a charge transfer in the GaSe/graphene van der Waals (vdW) heterostructure using ARPES. These findings demonstrate the high impact on the GaSe electronic band structure and electronic properties that can be obtained by the control of 2D materials layer thickness and the graphene induced doping.
U2 - 10.1103/PhysRevB.96.035407
DO - 10.1103/PhysRevB.96.035407
M3 - Article
AN - SCOPUS:85026371193
SN - 2469-9950
VL - 96
JO - Physical Review B
JF - Physical Review B
IS - 3
M1 - 035407
ER -