Die Arbeit beschäftigt sich mit der Dynamik von Gasen aus hoch angeregten Atomen. Es wird sowohl die Erzeugung von Rydberggasen, als auch ihre Dynamik nach der Laser-Anregung betrachtet. Zur Beschreibung des Anregungsprozesses wird ein quasi-klassischer Zugang verwendet. Er basiert auf der adiabatischen Eliminierung von Kohärenzen aus der vollen Quanten-Beschreibung und führt auf eine klassische Mastergleichung. Diese Näherung ist gerade für typische experimentelle Situationen durchführbar. Die klassische Mastergleichung kann durch ein simples Monte-Carlo-Verfahren für Systeme aus zehntausenden von Teilchen unter voller Berücksichtigung der Rydberg-Rydberg-Wechselwirkung gelöst werden. Mit Hilfe des Monte-Carlo-Verfahrens wird die Anregung von Rydbergatomen in einem ultrakalten Gas untersucht. Die in Experimenten gefundene Anregungsblockade wird durch die Methode gut beschrieben. Bei der Anregung von Rydbergatomen aus einem optischen Gitter wird sogar eine Anregungsverstärkung - eine Antiblockade - vorhergesagt. Die Antiblockade in einem Gitter erlaubt eine Charakterisierung räumlicher Korrelationen der Rydbergatome allein durch die Messung ihrer Dichte. Sie ist robust gegenüber Gitterfehlstellen und sollte mit heutigen experimentellen Techniken nachweisbar sein. Für die Anregung im ungeordneten Gas wird gezeigt, dass sich die räumlichen Korrelationen der Rydbergatome indirekt in den Momenten der Häufigkeitsverteilung angeregter Atome widerspiegeln. Durch die Untersuchung der Fluktuationen in der Zahl angeregter Atome lassen sich die Unterschiede in den Paarkorrelationsfunktionen bei Blockade und Antiblockade im Gas messen. Ein Vergleich mit experimentellen Daten zeigt eine qualitativ gute Übereinstimmung. Für die Dynamik des Rydberggases nach dem Abschalten der Anregungslaser ist der Fall besonders interessant, dass Atome in unterschiedlichen Rydbergzuständen resonant ihre Anregungsenergie austauschen können. In der Arbeit wird argumentiert, dass sich der räumliche Transfer von Anregungsenergie in Rydbergsystemen ohne störende Umgebungseinflüsse gezielt untersuchen lässt. Mit Hilfe der Frenkelschen Exziton-Theorie wird der Energietransfer entlang einer eindimensionalen Anordnung von Rydbergatomen untersucht. Zusätzlich wird dargelegt, dass die exzitonische Anregung auch mechanische Kräfte auf die Rydbergatome induziert. Diese werden mit Hilfe einer quanten-klassischen Methode analysiert. Der Zusammenhang der auftretenden Kräfte mit den Symmetrien der exzitonischen Eigenfunktionen wird aufgezeigt. In einer eindimensionalen Anordnung von Rydbergatomen wird ein adiabatischer Energietransfer vorhergesagt, der an die Bewegung der Atome gebunden ist. Er läuft vollständig auf einer einzigen adiabatischen Potentialfläche ab. Dieser Transport ist langsam genug, um mit heutigen experimentellen Methoden im Prinzip orts- und zeitaufgelöst abgebildet zu werden.

Ultracold neutron (UCN) projection imaging is demonstrated using a boron-coated back-illuminated CCD camera and the Los Alamos UCN source. Each neutron is recorded through the capture reactions with10B. By direct detection at least one of the byproducts α, 7Li and γ (electron recoils) derived from the neutron capture and reduction of thermal noise of the scientific CCD camera, a signal-to-noise improvement on the order of 104 over the indirect detection has been achieved. Sub-pixel position resolution of a few microns is confirmed for individual UCN events. Projection imaging of test objects shows a spatial resolution less than 100μm by an integrated UCN flux one the order of 106 cm−2. The bCCD can be used to build UCN detectors with an area on the order of 1 m2. The combination of micrometer scale spatial resolution, low readout noise of a few electrons, and large area makes bCCD suitable for quantum science of UCN.

京都大学 / 0048 / 新制・課程博士 / 博士(理学) / 甲第17973号 / 理博第3917号 / 新制||理||1565(附属図書館) / 80817 / 京都大学大学院理学研究科物理学・宇宙物理学専攻 / (主査)教授 高橋 義朗, 教授 田中 耕一郎, 教授 石田 憲二 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DGAM

京都大学 / 0048 / 新制・課程博士 / 博士(理学) / 甲第20163号 / 理博第4248号 / 新制||理||1611(附属図書館) / 京都大学大学院理学研究科物理学・宇宙物理学専攻 / (主査)教授 川上 則雄, 教授 高橋 義朗, 准教授 柳瀬 陽一 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DFAM

京都大学 / 0048 / 新制・課程博士 / 博士(理学) / 甲第20892号 / 理博第4344号 / 新制||理||1624(附属図書館) / 京都大学大学院理学研究科物理学・宇宙物理学専攻 / (主査)教授 高橋 義朗, 教授 川上 則雄, 教授 田中 耕一郎 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DFAM

付記する学位プログラム名: 京都大学卓越大学院プログラム「先端光・電子デバイス創成学」 / 京都大学 / 新制・課程博士 / 博士(理学) / 甲第24402号 / 理博第4901号 / 新制||理||1700(附属図書館) / 京都大学大学院理学研究科物理学・宇宙物理学専攻 / (主査)教授 川上 則雄, 教授 佐々 真一, 教授 高橋 義朗 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DFAM

We use an interferometric method for measuring the plasma density in a laser-induced plasma as a function of time. Any changes in the density within 5 ns of generation is due plasma expansion and not recombination. The analytic solution for plasma expansion derived for ultracold Neutral Plasmas describes the expansion of our laser produced Neon plasma of densities up to approximately 40 Torr. A model for the utlracold neutral plasmas, in comparison with measurements of our plasmas, can be used to extract an electron temperature. Currently our plasmas have shown to have an electron temperature of approximately 44 eV.

Ultracold neutral plasmas are created by photoionizing laser-cooled atoms in a magneto-optical trap (MOT). Due to their large electrical potential energies and comparatively small kinetic energies, ultracold plasmas fall into a regime of plasma systems which are called “strongly coupled.” A priority in the field of ultracold plasmas is to generate plasmas with higher values of the strong coupling parameter Γ, which is given as the ratio of the nearest-neighbor Coulomb potential energy to the average kinetic energy. The equilibrium strong coupling in ultracold plasmas is limited by the ultrafast relaxation of the ions due to spatial disorder in the initial system. This heating mechanism is called “disorder-induced heating” (DIH) and it limits the ion strong coupling in ultracold plasmas to order unity. This thesis describes experiments that explore ways to generate higher values of the strong coupling parameter in an ultracold neutral calcium plasma.One way to increase Γ is to mitigate the effects of DIH using electron screening. This thesis describes an experiment in which the initial electron temperature was systematically changed to determine the effect that electron screening has on the ion thermalization. At lower initial electron temperatures, corresponding to a higher degree of electron shielding, it was found that the screening slows the ion thermalization and reduces the equilibrium ion temperature by as much as a factor of two. However, electron screening also reduces the ion interaction strength by the same amount, which has the net effect of leaving the effective Γ unchanged.Another method for increasing the strong coupling of an ultracold plasma is to excite the plasma ions to a higher ionization state. Simulations predict that doubly ionizing the plasma ions can increase the strong coupling in an ultracold plasma by as much as a factor of 4, with the maximum value of Γ depending on the timing of the second ionization relative to the DIH process. This thesis describes an experiment designed to test these predictions in a Ca2+ plasma. Measurements of the change in the Ca+ ion temperature as a function of the timing of the second ionization pulses were made using laser-induced fluorescence. Results of these measurements show that the heating of the Ca+ ions due to the second ionization depends on the timing of the second ionization pulses, as predicted by MD simulations.

The immaculate control of atoms and molecules with light is the defining trait of modern experiments in ultracold physics. The rich internal degrees of freedom afforded by molecules enrich the toolbox of precision spectroscopy for fundamental physics, and hold great promise for applications in quantum simulation and quantum information science. A vibrational molecular lattice clock with systematic fractional uncertainty at the 14th decimal place is demonstrated for the first time, matching the performance of the earliest optical atomic clocks. Van der Waals dimers of strontium are created at ultracold temperatures and levitated by an optical standing wave, whose wavelength is finely tuned to preserve the delicate molecular vibrational coherence. Guided by quantum chemistry theory refined by highly accurate frequency-comb-assisted laser spectroscopy, record-long Rabi oscillations were demonstrated between vibrational molecular states that span the entire depth of the ground molecular potential. Enabled by the narrow molecular clock linewidth, hertz-level frequency shifts were resolved, facilitating the first characterization of molecular hyperpolarizability in this context. In a parallel effort, deeply bound strontium dimers are coherently created using the technique of stimulated Raman adiabatic passage. Ultracold collisions of alkaline-earth metal molecules in the absolute ground state are studied for the first time, revealing inelastic losses at the universal rate. This thesis reports one of the most accurate measurement of a molecule's vibrational transition frequency to date, which may potentially serve as a secondary representation of the SI unit of time in the terahertz (THz) band where standards are scarce. The prototypical molecular clock lays the important groundwork for future explorations into THz metrology, quantum chemistry, and fundamental interactions at atomic length scales.

We are developing theoretical and computational methods to study two related three-body processes in ultracold quantum gases: three-body resonances and three-body recombination. Three-body recombination causes the ultracold gas to heat up and atoms to leave the trap where they are confined. Therefore, it is an undesirable effect in the process of forming ultracold quantum gases. Metastable three-body states (resonances) are formed in the ultracold gas. When decaying they also give additional kinetic energy to the gas, that leads to the heating too. In addition, a reliable method to obtain three-body resonances would be useful in a number of problems in other fields of physics, for example, in models of metastable nuclei or to study dissociative recombination of H3 +. Our project consists of employing computer modeling to develop a method to obtain three-body resonances. The method uses a novel two-step diagonalization approach to solve the three-body Schrödinger equation. The approach employs the SVD method of Tolstikhin et al. coupled with a complex absorbing potential. We tested this method on a model system of three identical bosons with nucleon mass and compared it to the results of a previous study. This model can be employed to understand the 3He nucleus . We found one three-body bound state and four resonances. We are also studying Efimov resonances using a 4He-based model. In a system of identical spinless bosons, Efimov states are a series of loosely bound three-body states which begin to appear as the energy of the two-body bound state approaches zero . Although they were predicted 35 years ago, recent evidence of Efimov states found by Kraemer et al. in a gas of ultracold Cs atoms has sparked great interest by theorists and experimentalists. Efimov resonances are a kind of pre-dissociated Efimov trimer. To search for Efimov resonances we tune the diatom interaction potential, V(r): V(r) → λV(r) as Esry et al. did . We calculated the first two values of λ for which there is a "condensation" (infinite number) of Efimov states. They are λEfimov1 = 0.9765 and λEfimov2 = 6.834. We performed calculations for λ = 2.4, but found no evidence of Efimov resonances. For future work we plan to work with λ ≈ 4 and λ ≈ λEfimov2 where we might see d-wave and higher l-wave Efimov resonances. There is also a many-body project that forms part of this thesis and consists of a direct diagonalization of the Bogolyubov Hamiltonian, which describes elementary excitations of a gas of bosons interacting through a pairwise interaction. We would like to reproduce the corresponding energy spectrum. So far we have performed several convergence tests, but have not observed the desired energy spectrum. We show preliminary results.