We study the use of an optical Feshbach resonance to modify the
p-wave interaction between ultracold polarized
171Yb spin-
1/2 fermions. A laser exciting two colliding atoms to the
1S0+3P1 channel can be detuned near a purely-long-range excited molecular bound state. Such an exotic molecule has an inner turning point far from the chemical binding region, and thus, three-body recombination in the Feshbach resonance will be highly suppressed in contrast to that typically seen in a ground-state
p-wave magnetic Feshbach resonance. We calculate the excited molecular bound-state spectrum using a multichannel integration of the Schr\"odinger equation, including an external perturbation by a magnetic field. From the multichannel wave functions, we calculate the Feshbach resonance properties, including the modification of the elastic
p-wave scattering volume and inelastic spontaneous scattering rate. The use of magnetic fields and selection rules for polarized light yields a highly controllable system. We apply this control to propose a toy model for three-color superfluidity in an optical lattice for spin-polarized
171Yb, where the three colors correspond to the three spatial orbitals of the first excited
p band. We calculate the conditions under which tunneling and on-site interactions are comparable, at which point quantum critical behavior is possible.
We report control of the scattering wave function by an optical Feshbach resonance effect using ytterbium atoms. The narrow intercombination line (1S0-3P1) is used for efficient control as proposed by Ciuryło et al. [Phys. Rev. A 71, 030701(R) (2005)10.1103/PhysRevA.71.030701]. The manipulation of the scattering wave function is monitored with the change of a photoassociation rate caused by another laser. The optical Feshbach resonance is especially efficient for isotopes with large negative scattering lengths such as 172Yb, and we have confirmed that the scattering phase shift divided by the wave number, which gives the scattering length in the zero energy limit, is changed by about 30 nm.
Ultracold neutral atoms in optical lattices are rich systems for the investigation of many-body physics as well as for the implementation of quantum information processing. While traditionally alkali atoms were used for this research, in recent years alkaline-earth-like atoms have attracted considerable interest. This is due to their more complex but tractable internal structure and easily accessible transitions. Furthermore, alkaline-earth-like atoms have extremely narrow
1S→3P intercombination transitions, which lend themselves for the implementation of next generation atomic clocks. In this dissertation, I show that exquisite control of alkaline-earth-like atoms can be reached with optical methods, and elucidate ways to use this controllability to further different aspects of research, mainly quantum information processing. Additionally, the control of alkaline-earth-like atoms is very interesting in many-body physics and the improvement of atomic clocks. Since heating usually degrades the performance of quantum gates, recooling of qubits is a necessity for the implementation of large scale quantum computers. Laser cooling has advantages over the usually used sympathetic cooling, given that it requires no additional atoms, which have to be controlled separately. However, for qubits stored in hyperfine states, as usually done in alkali atoms, laser cooling leads to optical pumping and therefore to loss of coherence. On the other hand, in the ground state, the nuclear spin of alkaline-earth-like atoms is decoupled from the electronic degrees of freedom. As I show in this dissertation, this allows for the storage of quantum information in the nuclear spin and laser cooling on the electronic degrees of freedom. The recooling protocol suggested here consists of two steps: resolved sideband cooling on the extremely narrow
1S0→3P0 clock transition and subsequent quenching on the much shorter lived
1P1 state. A magnetic field is used to overcome the hyperfine interaction in this excited state and thus ensures decoupling of the nuclear spin degrees of freedom during the quenching. The application of this magnetic field also allows for photon scattering on the
1P1 state, while preserving the nuclear spin, e. g. for electronic qubit detection. The manipulation of the scattering properties of neutral atoms is an important aspect of quantum control. In contrast to alkali atoms, whose broad linewidths cause large losses, this can be done with purely optical methods via the implementation of an optical Feshbach resonance for alkaline-earth-like atoms. Here, the scattering length resulting from the application of an optical Feshbach resonance on the
1S0→3P1 intercombination line, including hyperfine interaction and rotation is calculated for
171Yb. Due to their different parities, the p-wave scattering length can be controlled independently from the s-wave scattering length, thus allowing for unprecedented control over the scattering properties of neutral atoms. Furthermore, I also show how optical Feshbach resonances in alkaline-earth-like atoms can be used together with the underlying quantum symmetry to implement collisional gates between nuclear-spin qubits over comparatively long ranges.
Ultracold gases of fermionic alkaline-earth(-like) atoms are hopeful candidates for the quantum simulation of many-body physics induced by magnetic impurities (e.g., the Kondo physics), because there are spin-exchange interactions (SEIs) between two atoms in the electronic ground (
1S0) and metastable (
3P) state, respectively. Nevertheless, this SEI cannot be tuned via magnetic Feshbach resonance. In this paper, we propose three methods to control the SEI between one atom in the
1S0 state and another atom in the
3P2 states or $^{3}\mathrm{P}_{2}\text{\ensuremath{-}}^{3}\mathrm{P}_{0}$ dressed states, with one or two laser beams. These methods are based on the spin-dependent ac-Stark shifts of the
3P2 states or the $^{3}\mathrm{P}_{2}\text{\ensuremath{-}}^{3}\mathrm{P}_{0}$ Raman coupling. We show that due to the structure of alkaline-earth (like) atoms, the heating effects induced by the laser beams of our methods are very weak. For instance, for ultracold Yb atoms, ac-Stark-shift difference of variant spin states of the
3P2(F=3/2) level, or the strength of the $^{3}\mathrm{P}_{2}\text{\ensuremath{-}}^{3}\mathrm{P}_{0}$ Raman coupling, could be of the order of $(2\ensuremath{\pi})\phantom{\rule{0.28em}{0ex}}\mathrm{MHz}$, while the heating rate (photon scattering rate) is only of the order of Hz. As a result, the Feshbach resonances, with which one can efficiently control the SEI by changing the laser intensity, may be induced by the laser beams with a low-enough heating rate, even if the scattering lengths of the bare interatomic interaction are so small that they are comparable with the length scale associated with the van der Waals interaction.
It is possible to tune the scattering length for the collision of ultracold ground-state alkaline-earth-metal atoms using an optical Feshbach resonance. This is achieved with a laser far detuned from an excited molecular level near the frequency of the atomic intercombination transition. Simple resonant-scattering theory, illustrated by the example of , allows an estimate of the magnitude of the effect. Unlike alkali metal species, large changes of the scattering length are possible while atom loss remains small, because of the very narrow linewidth of the molecular photoassociation transition. This raises prospects for control of atomic interactions for a system without magnetically tunable Feshbach resonance levels.
The properties of bosonic ytterbium photoassociation spectra near the intercombination transition ${^{1}S}_{0}\ensuremath{-}{^{3}P}_{1}$ are studied theoretically at ultralow temperatures. We demonstrate how the shapes and intensities of rotational components of optical Feshbach resonances are affected by mass tuning of the scattering properties of the two colliding ground-state atoms. Particular attention is given to the relationship between the magnitude of the scattering length and the occurrence of shape resonances in higher partial waves of the van der Waals system. We develop a mass-scaled model of the excited-state potential that represents the experimental data for different isotopes. The shape of the rotational photoassociation spectrum for various bosonic Yb isotopes can be qualitatively different.