With the advent of spatially resolved fluorescence imaging in quantum gas microscopes, it is now possible to directly image glassy phases and probe the local effects of disorder in a highly controllable setup. Here we present numerical calculations using a spatially resolved local mean-field theory, show that it captures the essential physics of the disordered system, and use it to simulate the density distributions seen in single-shot fluorescence microscopy. From these simulated images we extract local properties of the phases which are measurable by a quantum gas microscope and show that unambiguous detection of the Bose glass is possible. In particular, we show that experimental determination of the Edwards-Anderson order parameter is possible in a strongly correlated quantum system using existing experiments. We also suggest modifications to the experiments which will allow further properties of the Bose glass to be measured.
With the advent of spatially resolved fluorescence imaging in quantum gas microscopes, it is now possible to directly image glassy phases and probe the local effects of disorder in a highly controllable setup. Here we present numerical calculations using a spatially resolved local mean-field theory, show that it captures the essential physics of the disordered system, and use it to simulate the density distributions seen in single-shot fluorescence microscopy. From these simulated images we extract local properties of the phases which are measurable by a quantum gas microscope and show that unambiguous detection of the Bose glass is possible. In particular, we show that experimental determination of the Edwards-Anderson order parameter is possible in a strongly correlated quantum system using existing experiments. We also suggest modifications to the experiments which will allow further properties of the Bose glass to be measured.
With the advent of spatially resolved fluorescence imaging in quantum gas microscopes (see e.g. [1]), it is now possible to directly image glassy phases and probe the local effects of disorder in a highly controllable setup. Here we present numerical calculations using a spatially resolved local mean-field theory, show that it captures the essential physics of the disordered system, and use it to simulate the density distributions seen in single-shot fluorescence microscopy [2]. From these simulated images we extract local properties of the phases which are measurable by a quantum gas microscope and show that unambiguous detection of the Bose glass is possible. In particular, we show that experimental determination of the Edwards-Anderson order parameter is possible in a strongly correlated quantum system using existing experiments. We also suggest modifications to the experiments by using spatial light modulators (see [3] and references therein) to tailor the lattice, which will allow further properties of the Bose glass to be measured. References: [1] E Haller, et al., "Single-atom imaging of fermions in a quantum-gas microscope" Nature Physics 11, 738 (2015) [2] S J Thomson, et al., "Measuring the Edwards-Anderson order parameter of the Bose glass: A quantum gas microscope approach" Phys. Rev. A 94, 051601(R) (2016) [3] F Buccheri, et al., "Holographic optical traps for atom-based topological Kondo devices" New J. Phys. 18, 075012 (2016)
Disordered potentials fundamentally affect transport and coherence in quantum systems, giving rise to a Bose-glass phase in interacting bosonic systems—an insulating yet compressible phase lacking long-range coherence. Directly measuring a reduced coherence length of the Bose glass has been a outstanding challenge. We address this by employing Talbot interferometry combined with single-atom-resolved detection in a quantum-gas microscope. Using ultracold bosonic atoms in a two-dimensional lattice with site-resolved, reproducible disorder, we identify the Bose-glass phase through density distributions and particle-number fluctuations, quantified via the Edwards-Anderson parameter, and through the visibility of interference patterns after time of flight. By driving the system across the Bose-glass phase, we further observe signatures of nonergodic dynamics. Our studies provide a starting point to further explore disordered systems in and out of equilibrium, and are relevant for understanding the dynamics and stability of disordered and glasslike quantum states in solid-state systems.
This thesis contains four studies of the effects of disorder and randomness on strongly correlated quantum phases of matter. Starting with an itinerant ferromagnet, I first use an order-by-disorder approach to show that adding quenched charged disorder to the model generates new quantum fluctuations in the vicinity of the quantum critical point which lead to the formation of a novel magnetic phase known as a helical glass. Switching to bosons, I then employ a momentum-shell renormalisation group analysis of disordered lattice gases of bosons where I show that disorder breaks ergodicity in a non-trivial way, leading to unexpected glassy freezing effects. This work was carried out in the context of ultracold atomic gases, however the same physics can be realised in dimerised quantum antiferromagnets. By mapping the antiferromagnetic model onto a hard-core lattice gas of bosons, I go on to show the importance of the non-ergodic effects to the thermodynamics of the model and find evidence for an unusual glassy phase known as a Mott glass not previously thought to exist in this model. Finally, I use a mean-field numerical approach to simulate current generation quantum gas microscopes and demonstrate the feasibility of a novel measurement scheme designed to measure the Edwards-Anderson order parameter, a quantity which describes the degree of ergodicity breaking and which has never before been experimentally measured in any strongly correlated quantum system. Together, these works show that the addition of disorder into strongly interacting quantum systems can lead to qualitatively new behaviour, triggering the formation of new phases and new physics, rather than simply leading to small quantitative changes to the physics of the clean system. They provide new insights into the underlying physics of the models and make direct connection with experimental systems which can be used to test the results presented here.
The question of how the low-energy properties of disordered quantum systems may be connected to exotic localization phenomena at high energy is a key open question in the context of quantum glasses and many-body localization. In the preceding Letter [L. Villa, S. J. Thomson, and L. Sanchez-Palencia, preceding Letter, Phys. Rev. A 104, L021301 (2021)] we have shown that key features of the excitation spectrum of a disordered system can be efficiently probed from out-of-equilibrium dynamics following a quantum quench, providing distinctive signatures of the various phases. Here we extend this work by providing a more-in-depth study of the behavior of the quench spectral functions associated with different observables and investigating an extended parameter regime. We provide a detailed introduction to quench spectroscopy for disordered systems and show how spectral properties can be probed using both local operators and two-point correlation functions. We benchmark the technique using the one-dimensional Bose-Hubbard model in the presence of a random external potential, focusing on the low-lying excitations, and demonstrate that quench spectroscopy can distinguish the Mott insulator, superfluid, and Bose glass phases. We then explicitly reconstruct the zero-temperature phase diagram of the disordered Bose-Hubbard at fixed filling using two independent methods, experimentally accessible via both time-of-flight imaging and quantum gas microscopy, respectively, and demonstrate that quench spectroscopy can give valuable insights into the distribution of rare regions within disordered systems.
We investigate the thermodynamic properties of a dilute Bose gas in a correlated random potential using exact path integral Monte Carlo methods. The study is carried out in continuous space and disorder is produced in the simulations by a three-dimensional (3D) speckle pattern with tunable intensity and correlation length. We calculate the shift of the superfluid transition temperature due to disorder and we highlight the role of quantum localization by comparing the critical chemical potential with the classical percolation threshold. The equation of state of the gas is determined in the regime of strong disorder, where superfluidity is suppressed and the normal phase exists down to very low temperatures. We find a T 2 dependence of the energy in agreement with the expected behavior in the Bose glass phase. We also discuss the major role played by the disorder correlation length and we make contact with a Hartree–Fock mean-field approach that holds if the correlation length is very large. The density profiles are analyzed as a function of temperature and interaction strength. Effects of localization and the depletion of the order parameter are emphasized in the comparison between local condensate and total density. At very low temperature, we find that the energy and the particle distribution of the gas are very well described by the T =0 Gross–Pitaevskii theory, even in the regime of very strong disorder.
We numerically investigate the two-dimensional Bose-Hubbard model with local onsite disorder, where the competition between disorder and short-range interactions leads to the emergence of a Bose glass (BG) phase between the Mott insulator (MI) and superfluid (SF) phases. In order to analyze the inhomogeneous system we employ real-space bosonic dynamical mean-field theory (RBDMFT) and perform an ensemble average over disorder realizations. To distinguish the MI from the BG phase, we compare the Edwards-Anderson order parameter and the compressibility with the energy-gap condition. To identify the insulator to SF transition, we apply a percolation analysis to the condensate order parameter. In qualitative accordance with the theorem of inclusions we always find an intermediate BG phase between the SF and MI. However, the quantitative comparison indicates significant deviations between the MI to BG phase boundary expected in the thermodynamic limit and the one obtained for a finite system size. Additionally, RBMDFT is capable of reliably calculating spectral information throughout the phase diagram. Analyzing the spectral function reveals evidence for analytically predicted damped localized modes in the dispersion relation in the strong-coupling regime.