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Stephen R. Harrigan

Publications and source records attributed to Stephen R. Harrigan.

4 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↗

Stable electroluminescence in ambipolar dopant-free lateral p-n junctions

Dopant-free lateral p-n junctions in the GaAs/AlGaAs material system have attracted interest due to their potential use in quantum optoelectronics (e.g., optical quantum computers or quantum repeaters) and ease of integration with other components, such as single electron pumps and spin qubits. A major obstacle to integration has been unwanted charge accumulation at the p-n junction gap that suppresses light emission, either due to enhanced non-radiative recombination or inhibition of p-n current. Typically, samples must frequently be warmed to room temperature to dissipate this built-up charge and restore light emission in a subsequent cooldown. Here, we introduce a practical gate voltage protocol that clears this parasitic charge accumulation, in-situ at low temperature, enabling the indefinite cryogenic operation of devices. This reset protocol enabled the optical characterization of stable, bright, dopant-free lateral p-n junctions with electroluminescence linewidths among the narrowest (< 1 meV; < 0.5 nm) reported in this type of device. It also enabled the unambiguous identification of the ground state of neutral free excitons (heavy and light holes), as well as charged excitons (trions). The free exciton emission energies for both photoluminescence and electroluminescence are found to be nearly identical (within 0.2 meV or 0.1 nm). The binding and dissociation energies for free and charged excitons are reported. A free exciton lifetime of 237 ps was measured by time-resolved electroluminescence, compared to 419 ps with time-resolved photoluminescence.

cond-mat.mes-hall↗

Geometry-dependent two-photon absorption followed by free-carrier absorption in AlGaAs waveguides

Nonlinear absorption can limit the efficiency of nonlinear optical devices. However, it can also be exploited for optical limiting or switching applications. Thus, characterization of nonlinear absorption in photonic devices is imperative. This work used the nonlinear transmittance technique to measure the two-photon absorption coefficients ($α_2$) of AlGaAs waveguides in the strip-loaded, nanowire, and half-core geometries in the wavelength range from $1480$ to $1560~\text{nm}$. The highest $α_2$ values of $2.4$, $2.3$, and $1.1~\text{cm}/\text{GW}$ were measured at $1480~\text{nm}$ for a $0.8$-nm-wide half-core, $0.6$-nm-wide nanowire, and $0.9$-nm-wide strip-loaded waveguides, respectively, with $α_2$ decreasing with increasing wavelength. The free-carrier absorption cross-section was also estimated from the nonlinear transmittance data to be around $2.2\times10^{-16}~\text{cm}^2$ for all three geometries. Our results contribute to a better understanding of the nonlinear absorption in heterostructure waveguides of different cross-sectional geometries. We discuss how the electric field distribution in the different layers of a heterostructure can lead to geometry-dependent effective two-photon absorption coefficients. More specifically, we pinpoint the third-order nonlinear confinement factor as a design parameter to estimate the strength of the effective nonlinear absorption, in addition to tailoring the bandgap energy by varying material composition.

physics.optics↗

Tunable Four-Wave Mixing in AlGaAs Waveguides of Three Different Geometries

The AlGaAs material platform has been intensively used to develop nonlinear photonic devices on-a-chip, thanks to its superior nonlinear optical properties. We propose a new AlGaAs waveguide geometry, called half-core etched, which represents a compromise between two previously studied geometries, namely the nanowire and strip-loaded waveguides, combining their best qualities. We performed tunable four-wave mixing (FWM) experiments in all three of these geometries in the telecommunications C-band (wavelengths around 1550 nm), with a pulsed pump beam and a continuous-wave (CW) signal beam. The maximum FWM peak efficiencies achieved in the nanowire, strip-loaded and half-core geometries were about -5 dB, -8 dB and -9 dB, respectively. These values are among the highest reported in AlGaAs waveguides. The signal-to-idler conversion ranges were also remarkable: 161 nm for the strip-loaded and half-core waveguides and 152 nm for the nanowire. Based on our findings, we conclude that the half-core geometry is an alternative approach to the nanowire geometry, which has been earlier deemed the most efficient geometry, to perform wavelength conversion in the spectral region above the half-bandgap. Moreover, we show that the half-core geometry exhibits fewer issues associated with multiphoton absorption than the nanowire geometry.

physics.optics↗