arXiv subjects

Arya D. Keni

Publications and source records attributed to Arya D. Keni.

3 recordsLinked to original sources

arXiv2026

Few-Body Decay Dynamics in Colloidal CsPbI3 Quantum-Dot Clusters

Colloidal perovskite quantum dots combine bright emission with the ability to self- assemble into closely spaced structures, enabling radiative dynamics to be studied from isolated emitters to few-dot clusters. Here, we characterize CsPbI3 perovskite quan- tum dots from isolated emitters to self-assembled clusters containing up to ten dots. We estimate the number of emitters in each cluster using a combination of photon autocorrelation, blinking statistics, and emission brightness. Compared with isolated dots, clusters containing two or more emitters exhibit biexponential decay, with a short lifetime that decreases with emitter number and an additional long-lived component. Photon-correlation Fourier spectroscopy shows that the single-dot emission remains far from the lifetime-limited regime. Nevertheless, we observe emitter-number-dependent decay dynamics even in this low-coherence regime. Together, these measurements es- tablish self-assembled perovskite quantum-dot clusters as a platform for studying how collective optical behavior emerges between the single-emitter and ensemble limits

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arXiv2026

Vapor Phase Assembly of Molecular Emitter Crystals for Photonic Integrated Circuits

Organic molecules embedded in an organic matrix exhibit lifetime-limited optical coherence and bright emission at cryogenic temperatures below 3 K. Here we present a simple vapor-phase growth method for synthesizing optically thin DBT-doped anthracene crystals that are compatible with integrated nanophotonics. The crystals are ~200 nm thick with sub-nm surface roughness and a tunable lateral dimension of up to 200 $μ$m. The molecular transitions remain narrow and spectrally stable, with inhomogeneous broadening below 100 GHz, comparable to DBT in bulk anthracene. The dopant density is tunable up to several hundred molecules per $μ$m$^2$, ensuring emitters within the near-field of nanophotonic structures. We demonstrate that the crystals can be micropositioned onto integrated photonic devices with the molecular dipole aligned to the optical mode. This approach opens a path toward on-chip single-photon sources and collective many-emitter effects.

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arXiv2025

Cavity QED with molecular defects coupled to a photonic crystal cavity

We implement permanent spectral tuning to bring lifetime-limited emitters into collective resonance within an integrated photonic cavity. This addresses a fundamental challenge in solid-state cavity QED: combining multiple coherent quantum emitters with scalable nanophotonics. Our hybrid approach decouples emitter synthesis from nanophotonic fabrication using straightforward techniques that make cavity QED broadly accessible. High doping densities allow us to couple several coherent emitters to a single cavity mode, while optically-induced frequency shifting provides long-lived spectral control. By tuning two molecules into resonance, we demonstrate controlled formation of collective quantum states, establishing a scalable platform for many-body cavity QED. This opens pathways toward chemically-designed quantum systems where optical properties are engineered through synthetic chemistry.

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