Diverse Excitonic Phenomena in Asymmetric Trilayer Transition Metal Dichalcogenide Heterostructures.

Interlayer excitons formed in two-dimensional transition metal dichalcogenide (TMD) heterostructures can be easily tuned due to the large spatial separation. In this work, we discuss the electronic and excitonic optical properties of trilayer heterostructures MoS/MoSSe/WSe and MoS/MoSSe/MoSe using state-of-the-art +BSE calculations. In both trilayer geometries, we discover a variety of exciton states, including interlayer excitons, every-other-layer excitons, and their hybridized states, -IX. Importantly, the -IXs are optically bright through hybridizing with the intralayer excitons, and the radiative lifetimes of -IXs range from subnanoseconds to tens of microseconds at 77 K, depending on their compositions. We also reveal that the diversity of the low-lying IXs in MoS/MoSSe/MoSe is higher than that of MoS/MoSSe/WSe, because more energy levels participate in transitions in MoS/MoSSe/MoSe. Our findings demonstrate that the appropriate energy alignment via manipulating the Janus layer is crucial for realizing rich excitonic states in trilayer TMD heterostructures.