We present a coupled pair approach for studying few-body physics in harmonically trapped ultracold gases. The method is applied to a two-component Fermi system of $N$ particles. A stochastically variational gaussian expansion method is applied, focus
ing on optimization of the two-body correlations present in the strongly interacting, or unitary, limit. The groundstate energy of the four-, six- and eight-body problem with equal spin populations is calculated with high accuracy and minimal computational effort. We also calculate the structural properties of these systems and discuss their implication for the many-body ultracold gas and other few-body calculations.
We present vortex solutions for the homogeneous two-dimensional Bose-Einstein condensate featuring dipolar atomic interactions, mapped out as a function of the dipolar interaction strength (relative to the contact interactions) and polarization direc
tion. Stable vortex solutions arise in the regimes where the fully homogeneous system is stable to the phonon or roton instabilities. Close to these instabilities, the vortex profile differs significantly from that of a vortex in a nondipolar quantum gas, developing, for example, density ripples and an anisotropic core. Meanwhile, the vortex itself generates a mesoscopic dipolar potential which, at distance, scales as 1/r^2 and has an angular dependence which mimics the microscopic dipolar interaction.
The confluence of quantum physics and biology is driving a new generation of quantum-based sensing and imaging technology capable of harnessing the power of quantum effects to provide tools to understand the fundamental processes of life. One of the
most promising systems in this area is the nitrogen-vacancy centre in diamond - a natural spin qubit which remarkably has all the right attributes for nanoscale sensing in ambient biological conditions. Typically the nitrogen-vacancy qubits are fixed in tightly controlled/isolated experimental conditions. In this work quantum control principles of nitrogen-vacancy magnetometry are developed for a randomly diffusing diamond nanocrystal. We find that the accumulation of geometric phases, due to the rotation of the nanodiamond plays a crucial role in the application of a diffusing nanodiamond as a bio-label and magnetometer. Specifically, we show that a freely diffusing nanodiamond can offer real-time information about local magnetic fields and its own rotational behaviour, beyond continuous optically detected magnetic resonance monitoring, in parallel with operation as a fluorescent biomarker.
