📝 SummarXiv

Abstract

This study presents a comprehensive investigation of hybrid interfaces formed by monolayer MoS$_2$ coupled with the organic molecules perylene (P), perylene diimide (PDI), and perylene orange (PO). Using density functional theory, we demonstrate the extent to which the mechanical and electronic properties of a hybrid system can be altered by the chemical modification of a given chromophore. The three systems exhibit distinct differences due to their chemical composition and van der Waals contact enabled by their geometry. All systems are structurally stable. The binding energies follow the order PD$>$P$>$PO due to the large $\pi$-system (PD) and strong structural distortion (PO). Young's modulus and Poisson's ratio exhibit pronounced anisotropy in all cases. PO exhibits the greatest anisotropy due to steric effects and a permanent dipole, which introduce directionality to the molecule-surface interaction. Physisorption is accompanied by net charge transfer in the same order as the binding energies. The associated interfacial polarization results in a change in the work function compared to pristine MoS$_2$ in the order P$>$PO$>$PD. Finally, the presence of organic molecules introduces states into the MoS$_2$ energy gap, with the band alignment being either type II (P, PO) or type I (PD).