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Matteo Pennacchietti

Publications and source records attributed to Matteo Pennacchietti.

3 recordsLinked to original sources

Deterministic nanofabrication for engineering nanowire quantum dot devices

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.

cond-mat.mes-hall

Observation and Control of the Magnetic Photogalvanic Effect from Strongly Bound Excitons

Photogalvanic effects arising from the quantum geometry of noncentrosymmetric materials are promising for next-generation light-harvesting devices that do not require a built-in electric field. Recent theories predict photogalvanic currents generated in magnetic systems with spin-dependent symmetry breaking as well as by bound exciton states, allowing for potential magnetic field control of the photoresponse and enhanced detection of deep sub-gap signals, respectively. We demonstrate the magnetic photogalvanic effect in a bilayer CrI3 tunnel junction with both magnetic field switching and electric field tuning of interlayer symmetry. By controlling for the polarization and energy of light illumination, we disentangle the shift and injection current contributions and find that the peak response occurs under resonant excitation of strongly bound excitons in CrI3. Our results can be captured within a many-body framework of the photogalvanic effect, while our devices function as tunable, multispectral helicity- and polarization-sensitive detectors that highlight the potential of 2D magnets for future optoelectronic applications.

cond-mat.mtrl-sci

Oscillating photonic Bell state from a semiconductor quantum dot for quantum key distribution

An on-demand source of bright entangled photon pairs is desirable for quantum key distribution (QKD) and quantum repeaters. The leading candidate to generate entangled photon pairs is based on spontaneous parametric down-conversion (SPDC) in a non-linear crystal. However, there exists a fundamental trade-off between entanglement fidelity and efficiency in SPDC sources due to multiphoton emission at high brightness, which limits the pair extraction efficiency to 0.1% when operating at near-unity fidelity. Quantum dots in photonic nanostructures can in principle overcome this trade-off; however, the quantum dots that have achieved entanglement fidelities on par with SPDC sources (99%) have poor pair extraction efficiencies of 0.01%. Here, we demonstrate a 65-fold increase in the pair extraction efficiency compared to quantum dots with equivalent peak fidelity from an InAsP quantum dot in a photonic nanowire waveguide. We measure a raw peak concurrence and fidelity of 95.3% $\pm$ 0.5% and 97.5% $\pm$ 0.8%, respectively. Finally, we show that an oscillating two-photon Bell state generated by a semiconductor quantum dot can be utilized to establish a secure key for QKD, alleviating the need to remove the quantum dot energy splitting of the intermediate exciton states in the biexciton-exciton cascade.

quant-ph