Abstract

Interlayer excitons (IXs) in hetero-bilayers of transition metal dichalcogenides (TMDs) represent an exciting emergent class of long-lived dipolar composite bosons in an atomically thin, near-ideal two-dimensional (2D) system. The long-range interactions that arise from the spatial separation of electrons and holes can give rise to novel quantum, as well as classical multi-particle correlation effects. In order to acquire a detailed understanding of the possible many-body effects, the fundamental interactions between individual IXs have to be studied. Here, we trap a tunable number of dipolar within a nanoscale confinement potential induced by placing a MoSe2_2-WSe2_2 hetero-bilayer (HBL) onto an array of SiO2_2 nanopillars. We control the mean occupation of the IX trap via the optical excitation level and observe discrete sharp-line emission from different configurations of interacting IXs. We identify these features as different multiparticle states with NIX∼1−5N_{IX}\sim1-5 via their power dependencies and directly measure the hierarchy of dipolar and exchange interactions as NIXN_{IX} increases. The interlayer biexciton (NIX=2N_{IX}=2) is found to be an emission doublet that is blue-shifted from the single exciton by ΔE=(8.4±0.6)ΔE=(8.4\pm0.6) meV and split by 2J=(1.2±0.5)2J=(1.2\pm0.5) meV. The blueshift is even more pronounced for triexcitons ((12.4±0.4)(12.4\pm0.4) meV), quadexcitons ((15.5±0.6)(15.5\pm0.6) meV) and quintexcitons ((18.2±0.8)(18.2\pm0.8) meV). These values are shown to be mutually consistent with numerical modelling of dipolar excitons confined to a harmonic trapping potential having a confinement lengthscale in the range ℓ≈3\ell\approx 3 nm. Our results contribute to the understanding of interactions between IXs in TMD HBLs at the discrete limit of only a few excitations and represent a key step towards exploring quantum correlations between them.

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