We theoretically investigate the spin structure of weakly bound diatomic van der Waals molecules formed by two identical bosonic alkali atoms. Our studies were performed using known Born-Oppenheimer potentials while developing a reduced interaction potential model. Such reduced potential models are currently a key for solving certain classes of few-body problems of atoms as they decrease the numerical burden on the computation. Although the reduced potentials are significantly shallower than actual Born-Oppenheimer potentials, they still capture the main properties of the near-threshold bound states, including their spin structure, and the scattering states over a broad range of magnetic fields. At zero magnetic field, we find that the variation in spin structure across different alkali species originates from the interplay between electronic spin exchange and hyperfine interactions. To characterize this competition we introduce a single parameter that is a function of the singlet and triplet scattering lengths, the atomic hyperfine splitting constant, and the molecular binding energy. We show that this parameter can be used to classify the spin structure of vdW molecules for each atomic species.
We theoretically investigate the spin structure of weakly bound diatomic van der Waals molecules formed by two identical bosonic alkali atoms. Our studies were performed using known Born-Oppenheimer potentials while developing a reduced interaction potential model. Such reduced potential models are currently a key for solving certain classes of few-body problems of atoms as they decrease the numerical burden on the computation. Although the reduced potentials are significantly shallower than actual Born-Oppenheimer potentials, they still capture the main properties of the near-threshold bound states, including their spin structure, and the scattering states over a broad range of magnetic fields. At zero magnetic field, we find that the variation in spin structure across different alkali species originates from the interplay between electronic spin exchange and hyperfine interactions. To characterize this competition we introduce a single parameter that is a function of the singlet and triplet scattering lengths, the atomic hyperfine splitting constant, and the molecular binding energy. We show that this parameter can be used to classify the spin structure of vdW molecules for each atomic species.
By applying a magnetic field across a trapped ultracold gas of alkali metal atoms, it is possible to alter the binding energies of near threshold molecular states. The proximity of molecular states to the scattering threshold has a strong effect on the threshold scattering characteristics. Because of this the magnetic field strength can be used to control low energy scattering within the gas. This resonant phenomena is referred to as a magnetically tuneable Feshbach resonance. This thesis looks at these and related phenomena in the context of trapped potassium atoms. First, we perform coupled-channels calculations in order to characterise a group of previously unreported Feshbach resonances, occurring in a host of different collision channels. Next, we compare these characterisations to empirical data, and more simplified models. Second, a detailed investigation into the photodissociation of weakly bound Feshbach molecules is carried out. This allows us to gain new insights into the structure of the exit channel interaction. We make semi-classical arguments which enable experimentalists to directly measure the height of potential barriers. We also perform detailed numerical calculations which, in conjunction with experimental data, allow us to develop a fine-tuned potential model for the exit state. Third, we model weakly bound triatomic states and their impact on near threshold scattering. Then, we discuss the use of three body recombination as a tool for observing Efimov states. Furthermore, we model the three body recombination rate using a simplified two channel model. Finally we suggest a method intended to provide the basis for numerical calculations using realistic Born-Oppenheimer potentials. It could also be used to analytically study near threshold three body physics.
We show that, for ultracold neutral bosonic atoms held in a three-dimensional periodic potential or optical lattice, a Hubbard model with dominant, attractive three-body interactions can be generated. In fact, we derive that the effect of pairwise interactions can be made small or zero starting from the realization that collisions occur at the zero-point energy of an optical lattice site and the strength of the interactions is energy dependent from effective-range contributions. We determine the strength of the two- and three-body interactions for scattering from van der Waals potentials and near Fano-Feshbach resonances. For van der Waals potentials, which for example describe scattering of alkaline-earth atoms, we find that the pairwise interaction can only be turned off for species with a small negative scattering length, leaving the 88Sr isotope a possible candidate. Interestingly, for collisional magnetic Feshbach resonances this restriction does not apply and there often exist magnetic fields where the two-body interaction is small. We illustrate this result for several known narrow resonances between alkali-metal atoms as well as chromium atoms. Finally, we compare the size of the three-body interaction with hopping rates and describe limits due to three-body recombination.
Ultracold bialkali polar molecules play a leading part at the frontline of quantum physics. They recently attract a lot of attention in the field of ultracold quantum chemistry, quantum many-body physics and quantum simulations. The key for their success is the rich internal level structure with rotational and vibrational degrees of freedom and their large electric dipole moments. Still, only a handful of molecular species are available at ultracold temperatures until now, although it is highly desirable to produce new molecular species to further expand the range of applications. Besides direct laser cooling methods for molecules, the assembly of heteronuclear ground-state molecules from ultracold atomic mixtures is the most promising approach for the creation of polar molecules. It includes the formation of weakly bound Feshbach molecules from the diatomic mixture and the subsequent two-photon stimulated Raman adiabatic passage (STIRAP) transfer to the rovibrational ground state. This creation strategy has been successfully demonstrated for the first time in the pioneering experiments at JILA with ultracold 40K87Rb molecules. Since then, only a few more molecular species from different alkali atoms have been created, namely 6Li23Na, 23Na40K, 23Na87Rb and 87Rb133Cs. In this thesis, I report the successful creation of a new species of ultracold polar ground-state molecules: 23Na39K. Starting from an ultracold mixture of bosonic 23Na and 39K atoms, weakly bound molecules are created. For this purpose, a Feshbach resonance in a high angular momentum scattering channel is chosen, experimentally identified and characterized. Close to this resonance the weakly bound Feshbach molecules are formed using resonant radio frequency radiation. For the two-photon ground-state transfer, a unique, highly specialized two-color laser system is designed and realized. It is used for one- and two-photon spectroscopy to identify the relevant transitions for the ground-state transfer. Based on the obtained data, a local model of the singlet-triplet mixed excited state manifolds is developed, with which the hyperfine structure and the magnetic field dependence is predicted with high accuracy. According to these findings, a suitable pathway to a single hyperfine ground state is chosen considering selection rules and experimental conditions such as laser polarization and beam alignment. To precisely determine the two-photon resonance condition for STIRAP, electromagnetically induced transparency measurements are performed. The ground-state transfer is then performed using STIRAP. The experimental findings regarding the STIRAP are successfully supported theoretically by a model based on a five-level master equation. The pure molecular gas shows evidence for two-body dominated loss mechanisms, such as sticky four-body collisions. The molecule-atom mixture of 23Na39K+39K reveals an unexpectedly low loss rate coefficient although sticky three-body collisions are assumed to occur. This behavior demands further investigations regarding different hyperfine collisional chan-nels and magnetic field regions.
By analyzing the measured spin-relaxation transients of 129Xe nuclear spins and alkali-metal-atomic spins in mixtures of alkali-metal-atom vapors, Xe gas, and larger amounts of N2 gas, we have determined the three-body formation rates and the spin-transfer probabilities for alkali- metal--noble-gas van der Waals molecules. Three parameters, in addition to the spin quantum numbers of the alkali-metal and noble-gas nuclei, are needed to predict the spin-transfer rates. These parameters, which we have determined from experimental measurements, are x=\ensuremath{\gamma}N/\ensuremath{\alpha}, the ratio of the spin-rotation interaction \ensuremath{\gamma}N to the spin-exchange interaction \ensuremath{\alpha}; p0, the third-body pressure for which the molecular breakup rate ${\ensuremath{\tau}}^{\mathrm{\ensuremath{-}}1}$ is equal to the spin-rotation frequency \ensuremath{\gamma}N/h; and Z, the three-body rate constant for forming van der Waals molecules.
We introduce a coupled-channel method for elastic three-body scattering in systems of identical bosonic alkali-metal atoms. The approach relies on the numerically exact two-body off-the-energy-shell transition matrix, constructed from realistic multichannel molecular interaction potentials that support many bound states. By rigorously accounting for this off-shell structure, the method captures both the short-range physics as well as multichannel couplings characteristic of alkali-metal potentials without resorting to model pseudopotentials. The central output is the complex three-body scattering hypervolume—the three-body analog of the two-body scattering length—which we obtain with controlled and verifiable numerical accuracy. As a realistic benchmark, we apply our framework to spin-polarized potassium-39, performing full coupled-channel three-body scattering calculations and extracting the hypervolume over experimentally relevant conditions. The method is general and transferable to other atomic species and interaction models featuring deep molecular potentials with an arbitrarily large number of bound states.
We construct a simple model to calculate the trimer bound state energy ET(n) and three-body recombination rate K30 of three identical bosons with van der Waals interaction without using any two- or three-body fitting parameter. Using this simple model, we investigate the influence of the van der Waals finite-range effect on ET(n) and K30. Our calculation shows that the finite-range effect leads to the ground trimer state energy ET(0) not crossing the atom-dimer threshold, and the scaled three-body recombination rate K30/a4 deviating from the universal three-body theory. The results of our simple model agree within a few percent with other theoretical works with van der Waals interaction and also the experimental data.