We investigate the dynamics of Rydberg electrons excited from the ground state of ultracold atoms trapped in an optical lattice. We first consider a lattice comprising an array of double-well potentials, where each double well is occupied by two ultracold atoms. We demonstrate the existence of molecular states with equilibrium distances of the order of experimentally attainable interwell spacings and binding energies of the order of ${10}^{3}\phantom{\rule{0.3em}{0ex}}\mathrm{GHz}$. We also consider the situation whereby ground-state atoms trapped in an optical lattice are collectively excited to Rydberg levels, such that the charge-density distributions of neighboring atoms overlap. We compute the hopping rate and interaction matrix elements between highly excited electrons separated by distances comparable to typical lattice spacings. Such systems have tunable interaction parameters and a temperature $\ensuremath{\sim}{10}^{4}$ times smaller than the Fermi temperature, making them potentially attractive for the study and simulation of strongly correlated electronic systems.
We investigate the dynamics of Rydberg electrons excited from the ground state of ultracold atoms trapped in an optical lattice. We first consider a lattice comprising an array of double-well potentials, where each double well is occupied by two ultracold atoms. We demonstrate the existence of molecular states with equilibrium distances of the order of experimentally attainable interwell spacings and binding energies of the order of 103GHz. We also consider the situation whereby ground-state atoms trapped in an optical lattice are collectively excited to Rydberg levels, such that the charge-density distributions of neighboring atoms overlap. We compute the hopping rate and interaction matrix elements between highly excited electrons separated by distances comparable to typical lattice spacings. Such systems have tunable interaction parameters and a temperature \ensuremath∼104 times smaller than the Fermi temperature, making them potentially attractive for the study and simulation of strongly correlated electronic systems.
Optical lattices make it possible to trap and coherently control large ensembles of ultracold atoms. They provide the possibility to create lattice potentials that mimic the structure of solid-state systems, and to control these potentials dynamically. In this thesis, we study how dynamical manipulations of the lattice geometry can be used to perform different tasks, ranging from quantum information processing to the creation of diatomic molecules. We first examine the dynamical properties of ultracold atoms trapped in a lattice whose periodicity is dynamically doubled. We derive a model describing the dynamics of the atoms during this process, and compute the different interaction parameters of this model. We investigate different ways of using this lattice manipulation to optimise the initialisation time of a Mott-insulating state with one atom per site, and provide a scaling law related to the interaction parameters of the system. We go on to show that entangling operations between the spin of adjacent atoms are realisable with optical lattices forming arrays of double-well potentials. We study the creation of a lattice containing a spin-encoded Bell-pair in each double-well, and show that resilient, highly-entangled many-body states are realisable using lattice manipulations. We show that the creation of cluster-like states encoded on Bell-pairs can be achieved using these systems, and we provide measurement networks that allow the execution of quantum algorithms while maintaining intact the resilience of the system. Finally, we investigate the possibility to create a diatomic molecular state and simulate Fermi systems via the excitation to Rydberg levels of ground-state atoms trapped in optical lattices. We develop a method based on symbolical manipulations to compute the interaction parameters between highly-excited electrons, and evaluate them for different electronic configurations. We use these parameters to investigate the existence of diatomic molecular states with equilibrium distances comparable to typical lattice spacings. Considering the possibility to excite atoms trapped in an optical lattice to Rydberg levels such that the electronic cloud of neighbouring atoms overlap, we propose a model describing their interactions and compute its parameters. If such systems were realised, they would allow the simulation of Fermi systems at a temperature much below the Fermi temperature, thus enabling the observation of quantum phenomena hitherto inaccessible with current technology.
Rydberg-dressed ground state atoms are atoms with an electron off-resonantly excited to a very high energy state, i.e., a state of high principal quantum number n ≫ 1. This thesis investigates the quantum dynamics of interacting Rydberg-dressed ground state atoms trapped in several multi-well potential traps. Rydberg atoms are atoms with exaggerated properties. One of their most interesting properties is that they exhibit a strong and long-ranged interaction that can be tuned leading to a variety of different quantum behaviours. My work focuses on studying the effects of these interacting atoms when loaded in multi-well potential traps. Generally, multi-well systems are considered as the simplest example of a finite optical lattice structure. For this reason, this thesis covers three research topics that examine the effects of long-range interaction on Rydberg-dressed atoms trapped in several potential confinements. I begin, in the introduction, by discussing the theoretical background of relevance to this work. It starts with presenting the physics of Bose-Einstein condensate. Then, the fundamentals of the interaction between two-level atom and light are analytically studied. This study has the purpose of understanding both; the dressed interacting atoms and optical lattices. The definition, characteristics, and the nature of the interaction between Rydberg atoms are analysed afterwards. The second chapter examines the dynamics of an ensemble of interacting Rydberg- dressed atoms trapped in static, i.e., time-independent, multi-well potentials using a mean-field theoretical approach. I choose one-dimensional double- and triple-well in addition to a two-dimensional quadruple-well potentials. The time-dependent non-linear Gross-Pitaevskii equation is used to numerically explore the ensemble’s quantum dynamics. Solving the dynamical differential equations along with tuning the strength of the applied long-range interaction shows that the behaviour of non-interacting Rydberg-dressed atoms does not differ conceptually according to the geometry of the trapping potential. However, this changes when the interactions are switched on where the shape of the confinement leads to interesting outcomes especially in the non-linear interacting limit, such as macroscopic quantum self-trapping. After investigating an ensemble of interacting Rydberg-dressed atoms in static multi-well potential traps, the second research topic examines the dynamical evolution of these atoms when loaded in a finite optical lattice using the extended Bose-Hubbard model. In this chapter, the atoms ensemble is assumed to be in a superfluid state where I investigate both, the order parameter when the Rydberg excitation laser is applied and the interference pattern of the condensates in different dimensions. The study shows the emerging long-range interactions lead to a rapid collapse of the superfluid order parameter and in general allow only for partial revivals. In addition, the interference experiments can directly reveal the interaction between Rydberg-dressed atoms. In the fourth chapter, the dynamics of Rydberg-dressed atoms trapped in a dynamical, i.e., time-dependent, potential confinement is presented. The dynamical trap is constructed such that it begins as a harmonic oscillator and ends as a double- well potential. The analysis investigates an ensemble of contact-interacting atoms via the time-dependent non-linear GP equation.
The subnanoscale size of typical diatomic molecules hinders direct optical access to their constituents. Rydberg macrodimers-bound states of two highly excited Rydberg atoms-feature interatomic distances easily exceeding optical wavelengths. We report the direct microscopic observation and detailed characterization of such molecules in a gas of ultracold rubidium atoms in an optical lattice. The bond length of about 0.7 micrometers, comparable to the size of small bacteria, matches the diagonal distance of the lattice. By exciting pairs in the initial two-dimensional atom array, we resolved more than 50 vibrational resonances. Using our spatially resolved detection, we observed the macrodimers by correlated atom loss and demonstrated control of the molecular alignment by the choice of the vibrational state. Our results allow for rigorous testing of Rydberg interaction potentials and highlight the potential of quantum gas microscopy for molecular physics.
Ultracold atoms in optical lattices provide a versatile platform for studying many-body physics in a defect-free system with tunable parameters. For the analog quantum simulation of the Fermi-Hubbard model, fermionic atoms take on the role of the valence electrons and optical lattices provide the periodic potential in place of the solid-state crystal. The dynamics in the system are described by the tunneling amplitude t between neighboring lattice sites and the interaction energy U of two particles occupying the same lattice site. With the depth of the optical lattices and an external magnetic field, both parameters can be tuned to access a wide range of regimes. Two superimposed lattices with different lattice periods form an optical superlattice, where the most common configuration is a bichromatic superlattice with lattice periods different by a factor of two. Depending on the lattice depths and the relative phase of the lattices, the bichromatic superlattice potential ranges from an array of weakly-coupled double wells to a continuous lattice potential with a staggered energy offset. We developed a calibration technique for measuring the depth of an optical lattice with local resolution. The band structure of the optical lattice is probed by modulating the lattice depth and exciting the atoms to higher bands. However, compared to resolving the band occupations in a time-of-flight measurement, we further excite the atoms to an untrapped band to deplete the optical lattice along equipotential lines where the modulation frequency is resonant with the local band transitions. From the profile of the lattice depth, we obtain the calibration factor for the power regulation, the waist of the underlying lattice beams and the position of the lattice axis. This technique combines several calibration measurements, thereby reducing the measurement time and enabling an automation of the lattice alignment. For the bichromatic superlattice we realized an active stabilization of the superlattice phase that enables long-term measurements with a precise control over the superlattice phase. The instability of the superlattice phase is a result of the different refractive indices for the two lattices in air and the optical elements along the optical path. Using environmental sensors, we monitor the temperature, the pressure, and the relative humidity to apply the expected correction to the superlattice phase. The stabilized superlattice phase enabled the investigation of Floquet-driven double wells by modulating the energy offset through the superlattice phase. We used a near-resonant driving frequency with respect to the interaction energy to enhance the pair-tunneling amplitude in doubly-occupied double wells compared to static double wells and compared to the tunneling amplitude in singly-occupied double wells.
We study the ground state properties of ultracold fermions trapped in a one-dimensional double-well optical lattice by using the density-matrix renormalization group method. The system is described by an extended Hubbard model with alternating hopping integrals and an external harmonic confining potential. We clarify the characteristic features of the metal–insulator phase transition originating from the double-well structure of the lattices. Several different types of insulating regions coexist when the number of atoms at each site is an integer or a half integer. We found that each insulating phase except for a band insulator exhibits rather large local density fluctuations, reflecting the strong dimerization of atoms within the unit cells of double-well lattices. The phase characteristics are elucidated in detail by investigating the profiles of the local density of atoms, the local density (spin) fluctuations, the double-occupancy probability and the spatially extended sp in correlations.
The past three decades have seen extraordinary progress in the manipulation of neutral atoms with laser light, to the point where it is now routine to trap and cool both individual atoms and entire atomic clouds to temperatures of only a few tens of nanoKelvin in a controlled and repeatable fashion. In this thesis we study several applications of Rydberg atoms – atoms with an electron in a highly excited state – within such ultracold atomic systems. Due to their highly-excited electron, Rydberg atoms have a number of exaggerated properties: in addition to being physically large, they have long radiative lifetimes, and interact strongly both with one another and with applied external fields. Rydberg atoms consequently find many interesting applications within ultracold atomic physics. We begin this thesis by analysing the way in which a rubidium atom prepared in an excited Rydberg state decays to the ground state. Using quantum defect theory to model the wavefunction of the excited electron, we compute branching ratios for the various decay channels that lead out of the Rydberg states of rubidium. By using these results to carry out detailed simulations of the radiative cascade process, we show that the dynamics of spontaneous emission from Rydberg states cannot be adequately described by a truncated atomic level structure. We then investigate the stability of ultra-large diatomic molecules formed by pairs of Rydberg atoms. Using quantum defect theory to model the electronic wavefunctions, we apply molecular integral techniques to calculate the equilibrium distance and binding energy of these molecular Rydberg states. Our results indicate that these Ryberg macro-dimers are predicted to show a potential minimum, with equilibrium distances of up to several hundred nanometres. In the second half of this thesis, we present a new method of symbolically evaluating functions of matrices. This method, which we term the method of path-sums, has applications to the simulation of strongly-correlated many-body Rydberg systems, and is based on the combination of a mapping between matrix multiplications and walks on weighted directed graphs with a universal result on the structure of such walks. After presenting and proving this universal graph theoretic result, we develop the path-sum approach to matrix functions. We discuss the application of path-sums to the simulation of strongly-correlated many-body quantum systems, and indicate future directions for the method.