Probing Interface-Driven Mechanisms of Non-Classical Light in van der Waals Heterostructures

Abstract

Single-photon emitters in two-dimensional semiconductors offer a versatile platform for integrated quantum photonics, yet their performance is strongly influenced by local dielectric environments and substrate-induced disorder. Here, we examine SPEs in monolayer WSe$_2$ incorporated into hBN/WSe$_2$/Clinochlore van der Waals heterostructures and assess how interface-mediated dielectric modulation governs their optical and quantum characteristics. Low-temperature micro-photoluminescence reveals narrow emission lines (100 - 300 $\mu$eV) and robust non-classical behavior, with $g^{(2)}(0) = 0.13 \pm 0.02$ on SiO$_2$ and $0.54 \pm 0.02$ for emitters directly coupled to Clinochlore. Magneto-optical measurements yield effective g-factors near -8, consistent with defect states hybridized with dark excitons. WSe$_2$ on Clinochlore exhibits up to a fivefold enhancement in emission intensity, attributed to coupling with Fe-related substrate states that introduce resonant absorption near 1.75 eV. Kelvin probe force microscopy confirms strong dielectric contrast across thin and thick Clinochlore regions. Time-resolved photoluminescence shows that emitters on SiO$_2$ display a single $\approx 4$ ns lifetime, whereas those on Clinochlore exhibit biexponential dynamics with sub-nanosecond and tens-of-nanoseconds decay components. A phenomenological model incorporating coupling to bright and dark Fe-related states in Clinochlore accounts for modified excitation pathways. These results establish interface dielectric engineering in vdW heterostructures as an effective strategy for tailoring the radiative dynamics and brightness of quantum emitters in atomically thin materials.