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Hanna Wahl

Publications and source records attributed to Hanna Wahl.

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Purcell-enhanced single-photon emission from InAs/GaAs quantum dots coupled to broadband cylindrical nanocavities

On-chip emitters that can generate single and entangled photons are essential building blocks for developing photonic quantum information processing technologies in a scalable fashion. Semiconductor quantum dots (QDs) are attractive candidates that emit high-quality quantum states of light on demand, however at a rate limited by their spontaneous radiative lifetime. In this study, we utilize the Purcell effect to demonstrate up to a 38-fold enhancement in the emission rate of InAs QDs by coupling them to metal-clad GaAs nanopillars. These cavities, featuring a sub-wavelength mode volume of 4.5x10-4 (λ/n)3 and low quality factor of 62, enable Purcell-enhanced single-photon emission across a large bandwidth of 15 nm. The broadband nature of the cavity eliminates the need for implementing tuning mechanisms typically required to achieve QD-cavity resonance, thus relaxing fabrication constraints. Ultimately, this QD-cavity architecture represents a significant stride towards developing solid-state quantum emitters generating near-ideal single-photon states at GHz-level repetition rates.

quant-ph

Nonlinear Optical Microscopy of Semiconductor Metal-Nanocavities

We use second and third harmonic generation microscopy to investigate the nonlinear optical response of GaAs nanocavities embedded in a gold film and compare them to bare GaAs nanocavities. Our results reveal that the surrounding metallic environment significantly modifies both the intensity and spatial distribution of the nonlinear signals. When the harmonic wavelength is spectrally detuned from the nanocavity resonance, the effects due to the metallic environment start suppressing the SHG contrast. Numerical simulations confirm that at a 1060 nm pump wavelength, the SHG produced at 530 nm is suppressed due to the dominant plasmonic response of gold. Meanwhile, the THG produced at 353 nm, which coincides with the nanocavity resonance, enables high contrast imaging. Furthermore, by shifting the pump to 710 nm, aligning SHG at 356 nm with the nanocavity resonance, we recover strong SHG contrast, demonstrating a pathway to enhanced imaging of metal-semiconductor heterostructures.

physics.optics