We study experimentally and theoretically the in-plane magnetic field dependence of the coupling between dots forming a vertically stacked double dot molecule. The InAsP molecule is grown epitaxially in an InP nanowire and interrogated optically at millikelvin temperatures. The strength of interdot tunneling, leading to the formation of the bonding-antibonding pair of molecular orbitals, is investigated by adjusting the sample geometry. For specific geometries, we show that the interdot coupling can be controlled in-situ using a magnetic field-mediated redistribution of interdot coupling strengths. This is an important milestone in the development of qubits required in future quantum information technologies.

We analyze experimentally and theoretically the transport spectra of a gated lateral GaAs double quantum dot containing two holes. The strong spin-orbit interaction present in the hole subband lifts the Pauli spin blockade and allows to map out the complete spectra of the two-hole system. By performing measurements in both source-drain voltage directions, at different detunings and magnetic fields, we carry out quantitative fitting to a Hubbard two-site model accounting for the tunnel coupling to the leads and the spin-flip relaxation process. We extract the singlet-triplet gap and the magnetic field corresponding to the singlet-triplet transition in the double-hole ground state. Additionally, at the singlet-triplet transition we find a resonant enhancement (in the blockaded direction) and suppression of current (in the conduction direction). The current enhancement stems from the multiple resonance of two-hole levels, opening several conduction channels at once. The current suppression arises from the quantum interference of spin-conserving and spin-flipping tunneling processes.

We present a compact, fibre-coupled single photon source using gradient-index (GRIN) lenses and an InAsP semiconductor quantum dot embedded within an InP photonic nanowire waveguide. A GRIN lens assembly is used to collect photons close to the tip of the nanowire, coupling the light immediately into a single mode optical fibre. The system provides a stable, high brightness source of fibre-coupled single photons. Using pulsed excitation, we demonstrate on-demand operation with a single photon purity of 98.5% when exciting at saturation in a device with a source-fibre collection efficiency of 35% and an overall single photon collection efficiency of 10%. We also demonstrate "plug and play" operation using room temperature photoluminescence from the InP nanowire for room temperature alignment.

Birefringence in optical fibers poses a challenge to controllably delivering polarized light. Strain-induced birefringence caused by bends in the fiber, vibrations, or a large temperature gradient can significantly alter the polarization, making it particularly difficult to deliver polarization states to low-temperature environments by fiber. In this paper, we investigate the transmission of polarized light through a fiber and discuss a method we have developed for delivering arbitrarily polarized light to the base stage of a dilution refrigerator using a standard optical fiber. We have created a compact, cryogenic optical system to identify the polarization of the delivered light, while room-temperature waveplates and a mathematical fiber model are used to fully characterize and compensate for the fiber's birefringent effects. We show here that we are able to deliver horizontal, vertical, diagonal, anti-diagonal, right circular, and left circular polarization states to milli-Kelvin temperatures, with state fidelities of greater than 0.96 being achieved in all cases. Additionally, we demonstrate that we can deliver randomly selected elliptical states through a standard fiber to the refrigerator. This opens up new opportunities for fiber-based optical experiments using polarized light, such as quantum information experiments using quantum states encoded in the polarization of single photons.