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arXiv:2309.06734

Reversible tuning of nanowire quantum dot to atomic transitions

Rubayet Al Maruf, Sreesh Venuturumilli, Divya Bharadwaj, Anderson, Paul, Jiawei Qiu, Yujia Yuan, Mohd Zeeshan, Behrooz Semnani, Philip J. Poole, Dan Dalacu, Kevin J. Resch, Michael E. Reimer, Michal Bajcsy

Published Sep 13, 2023• 2 citations
arXivHTMLPDF

Abstract

Quantum dots embedded in semiconductor photonic nanowires (NW-QDs) can deterministically produce single-photons and entangled photon pairs at high repetition rates. These photons can be efficiently coupled from the photonic nanowire into free space or optical fibers thanks to the sharp tip of the nanowire, which provides impedance matching. However, precise control of the NW-QD emission frequency in a way that is reversible, does not degrade the properties of the emitted photons, and can be used independently for individual NW-QDs on the same chip has so far remained a challenge. Resolving this issue is crucial for applications when interfacing the photons with quantum systems that require MHz to sub-GHz precision, such as atomic ensembles acting as memories in a quantum network. Here, we demonstrate a reversible tuning method that can tune the emission frequency of a NW-QD by more than 300 GHz with sub-GHz precision. We achieve this through gas condensation that is then partially reversed with localized laser ablation. This process finely adjusts stress applied to the quantum dots, thereby tuning their emission frequency. We validate the precision and stability of this method by tuning the frequency of the emitted single-photons across an atomic resonance to probe its absorption and dispersion. We observed up to 80\% absorption of the single-photons from NW-QD in hot caesium vapour at the D1-line resonances and a 75-fold decrease in group velocity associated with the hyperfine transitions of the D1-line ground states. We observed no discernible effects in the second-order autocorrelation function, lifetime, or linewidth of the NW-QD emission for up to 300 GHz of tuning and we saw minimal effects on the fine structure splitting of the NW-QD when tuning up to 100 GHz.

DOI
10.48550/arxiv.2309.06734

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Quantum dots embedded in semiconductor photonic nanowires (NW-QDs) can deterministically produce single-photons and entangled photon pairs at high repetition rates. These photons can be efficiently coupled from the photonic nanowire into free space or optical fibers thanks to the sharp tip of the nanowire, which provides impedance matching. However, precise control of the NW-QD emission frequency in a way that is reversible, does not degrade the properties of the emitted photons, and can be used independently for individual NW-QDs on the same chip has so far remained a challenge. Resolving this issue is crucial for applications when interfacing the photons with quantum systems that require MHz to sub-GHz precision, such as atomic ensembles acting as memories in a quantum network. Here, we demonstrate a reversible tuning method that can tune the emission frequency of a NW-QD by more than 300 GHz with sub-GHz precision. We achieve this through gas condensation that is then partially reversed with localized laser ablation. This process finely adjusts stress applied to the quantum dots, thereby tuning their emission frequency. We validate the precision and stability of this method by tuning the frequency of the emitted single-photons across an atomic resonance to probe its absorption and dispersion. We observed up to 80% absorption of the single-photons from NW-QD in hot caesium vapour at the D1-line resonances and a 75-fold decrease in group velocity associated with the hyperfine transitions of the D1-line ground states. We observed no discernible effects in the second-order autocorrelation function, lifetime, or linewidth of the NW-QD emission for up to 300 GHz of tuning and we saw minimal effects on the fine structure splitting of the NW-QD when tuning up to 100 GHz.
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Abstract Hybrid quantum technologies aim to combine diverse quantum systems, mirroring classical computers' integration of electronic, photonic, magnetic, and mechanical components. Quantum dots in semiconductor nanowires emit high-purity, deterministic single photons with high repetition, while atomic ensembles offer photon storage and strong optical nonlinearities controllable by single photons. To interface quantum dots with atomic ensembles successfully, precise optical frequency matching of these two platforms is crucial. We demonstrate a simple, precise, reversible, broad-range, and local method for controlling the emission frequency of individual quantum dots embedded in tapered semiconductor nanowires. We then interface the quantum dots with an atomic ensemble via single-photons matched to hyperfine transitions and slow-light regions of the cesium D1-line. Our approach allows linking atomic and solid-state quantum systems and can potentially also be applied to other types of nanowire-embedded solid-state emitters, as well as for creating devices based on multiple solid-state emitters tuned to produce indistinguishable photons.
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Semiconductor quantum dots (QDs) are a leading platform for realising bright, wavelength-tunable sources of single and entangled photon pairs for photonic quantum technologies. Site-selected nanowire quantum dots (NWQDs) are a promising platform for fabricating such photonic devices in a scalable manner. However, implementing additional structures around the photonic nanowire while maintaining its vertical growth geometry has remained a challenge. In this work, we develop a deterministic pick-and-place technique to conduct a vertical-to-vertical transfer of NWQDs from the growth substrate to arbitrary templates. Using this transfer technique, we enhance the photon extraction efficiency to 75% by implementing a bottom gold mirror and tune the emission wavelength by 3.6 GHz via implementing electrostatic gates around the QD. Importantly, we measure low-multiphoton probability (g^(2)(0) = 0.002) and high indistinguishability (>80% for +/-100 ps) of the QD emission after the transfer process, yielding high-quality devices. These results demonstrate the repeatability and versatility of the developed transfer technique, which is an enabling step towards scalable single and entangled photon sources.
Abstract Hybrid quantum interfaces that combine the fast, deterministic single-photon emission of semiconductor quantum dots (QDs) with the long-lived quantum memories of atomic vapors represent a promising route towards scalable quantum networks and distributed quantum computing. However, the realization of such interfaces is fundamentally limited by the stringent spectral matching required between the narrow optical transitions of atomic systems and the intrinsically variable emission of QDs. Moreover, achieving bright QD emission requires integration into an efficient light-collecting structure. In this work, we present a systematic investigation of three tuning mechanisms for cavity-enhanced QDs embedded in micropillar cavities: thermal tuning, in situ laser processing, and nitrogen gas deposition. We experimentally evaluated the applicability of each method and characterized their tuning ranges and precisions. All three methods enable reliable and precise wavelength shifts, even for QDs in larger micropillars. These results provide practical strategies for achieving spectral resonance between QD emitters and atomic vapor lines, paving the way for tunable solid-state-atomic hybrid platforms for photon storage, synchronization, and interfacing in hybrid quantum systems.