2022/09/12 by S. Kundu, Tomer Amit, Kundu, Sudipta +7 · 1 citation
Materials Science · #2D Materials and Applications #FOS: Physical sciences #Materials Science (cond-mat.mtrl-sci)
paper · pdf · doi:10.48550/arxiv.2209.05030
openalex publication_date 2022/09/12 · openalex created_date 2022/09/14 · openalex updated_date 2026/07/28
Moiré superlattices of transition metal dichalcogenide (TMD) heterostructures give rise to rich excitonic phenomena associated with the interlayer twist angle and induced changes in the involved quantum states. Theoretical calculations of excitons in such systems are typically based on model moiré potentials to mitigate the computational cost. However, an ab initio understanding of the electron-hole coupling dominating the excitations is crucial to realize the twist-induced modifications of the optical selection rules. In this work we use many-body perturbation theory to compute and analyze the relation between twist angle and exciton properties in twisted TMD heterostructures. We present a general approach for unfolding excitonic states from the moiré Brillouin zone onto the Brillouin zones of the separate layers. Applying this method to a twisted MoS2/MoSe2 bilayer, we find that the optical excitation spectrum is dominated by mixed transitions between electrons and holes with different momenta in the separate monolayers, leading to unexpected and angle-dependent hybridization between interlayer and intralayer excitons. Our findings offer a design pathway for tuning exciton layer-localization in TMD heterostructures as a function of twist angle.