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Synthetic dimensions provide a powerful approach for simulating condensed matter physics in cold atoms and photonics, whereby a set of discrete degrees of freedom are coupled together and re-interpreted as lattice sites along an artificial spatial dimension. However, atomic experimental realisations have been limited so far by the number of artificial lattice sites that can be feasibly coupled along the synthetic dimension. Here, we experimentally realise for the first time a very long and controllable synthetic dimension of atomic harmonic trap states. To create this, we couple trap states by dynamically modulating the trapping potential of the atomic cloud with patterned light. By controlling the detuning between the frequency of the driving potential and the trapping frequency, we implement a controllable force in the synthetic dimension. This induces Bloch oscillations in which atoms move periodically up and down tens of atomic trap states. We experimentally observe the key characteristics of this behaviour in the real space dynamics of the cloud, and verify our observations with numerical simulations and semiclassical theory. This experiment provides an intuitive approach for the manipulation and control of highly-excited trap states, and sets the stage for the future exploration of topological physics in higher dimensions.

We report on the realization and characterisation of optical potentials for ultracold atoms using a superluminescent diode. The light emitted by this class of diodes is characterised by high spatial coherence but low temporal coherence. On the one hand, this implies that it follows Gaussian propagation similar to lasers, allowing for high intensities and well-collimated beams. On the other, it significantly reduces those interference effects that lead to severe distortions in imaging. By using a high-resolution optical setup, we produce patterned optical potentials with a digital micromirror device and demonstrate that the quality of the patterns produced by our superluminescent diode is consistently and substantially higher than those produced by our laser. We show that the resulting optical potentials can be used to arrange the atoms in arbitrary structures and manipulate them dynamically. Our results can open new opportunities in the fields of quantum simulations and atomtronics.

We propose an approach to position measurements based on the hypothesis that the action of a position detector on a quantum system can be effectively described by a dissipative disordered potential. We show that such kind of potential is able, via the dissipation-induced Anderson localization, to contemporary localize the wavefunction of the system and to dissipate information to modes bounded to the detector. By imposing a diabaticity condition we demonstrate that the dissipative dynamics between the modes of the system leads to a localized energy exchange between the detector and the rest of the environment -the "click" of the detector- thus providing a complete deterministic description of a position measurement. We finally numerically demonstrate that our approach is consistent with the Born probability rule.

We study the thermodynamic properties of a 2D array of coupled one-dimensional Bose gases. The system is realized with ultracold bosonic atoms loaded in the potential tubes of a two-dimensional optical lattice. For negligible coupling strength, each tube is an independent weakly interacting 1D Bose gas featuring Tomonaga Luttinger liquid behavior. By decreasing the lattice depth, we increase the coupling strength between the 1D gases and allow for the phase transition into a 3D condensate. We extract the phase diagram for such a system and compare our results with theoretical predictions. Due to the high effective mass across the periodic potential and the increased 1D interaction strength, the phase transition is shifted to large positive values of the chemical potential. Our results are prototypical to a variety of low-dimensional systems, where the coupling between the subsystems is realized in a higher spatial dimension such as coupled spin chains in magnetic insulators., Comment: 5 pages, 5 pictures, final version, Phys. Rev. Lett. in print (2014)

We investigate the thermodynamics of one-dimensional Bose gases in the strongly correlated regime. To this end, we prepare ensembles of independent 1D Bose gases in a two-dimensional optical lattice and perform high-resolution in situ imaging of the column-integrated density distribution. Using an inverse Abel transformation we derive effective one-dimensional line-density profiles and compare them to exact theoretical models. The high resolution allows for a direct thermometry of the trapped ensembles. The knowledge about the temperature enables us to extract thermodynamic equations of state such as the phase-space density, the entropy per particle and the local pair correlation function., Comment: 4 pages, 5 figures

We measure the temporal pair correlation function $g^{(2)}(\tau)$ of a trapped gas of bosons above and below the critical temperature for Bose-Einstein condensation. The measurement is performed {\it in situ} using a local, time-resolved single-atom sensitive probing technique. Third and fourth order correlation functions are also extracted. We develop a theoretical model and compare it with our experimental data, finding good quantitative agreement and highlighting the role of interactions. Our results promote temporal correlations as new observables to study the dynamics of ultracold quantum gases.