The effects of surface polarity and dangling bonds on the electronic properties of monolayer and bilayer MoS2 on α-quartz

Abstract

We investigate the electronic properties of monolayer and bilayer MoS _2 on α -quartz substrate through first-principles density functional calculations. Due to the coupling of the MoS _2 with the substrate, the valence band edge state at the Brillouin zone center tends to shift upward, reducing the indirect band gap of the MoS _2 , whereas the direct gap at the K valleys is less sensitive to substrate conditions. By taking into account the van der Waals interactions between the MoS _2 and the substrate, we find that monolayer MoS _2 exhibits a transition from direct-gap to indirect-gap semiconductor in the presence of surface O-dangling bonds. Moreover, a charge transfer occurs from MoS _2 to SiO _2 , inducing p -type doping and lifting the Kramers degeneracy by breaking the time reversal symmetry. In bilayer MoS _2 , O-dangling bonds break the inversion symmetry by inducing dipole fields across the interface and thereby lower the energy band associated with the one layer relative to the other. Although the time reversal symmetry is also broken, its effect on the spin splitting is extremely small in the K valleys so that a strong coupling between the spin and valley degrees of freedom takes place, similar to that found in free-standing monolayer MoS _2 .

Keywords

• electronic structure
• molybdenum disulphide
• spin-orbit coupling
• local density functional
• MoS2
• 71.15.Mb