We report on the stable effective trapping of cold rubidium atoms by a method for a single optical trap in the near-optical resonant regime. An optical trap with the near-optical resonance condition consists of not only the dipole but also the radiative forces, while a trap using a far-off resonance dominates only the dipole force. We measure the spatial behaviors of the center-of-mass positions and the loading efficiencies of the trapped atoms in the near-optical resonant trap, by changing the detuning over the range of $\ensuremath{-}0.373$ to $\ensuremath{-}2.23$ THz from the ${\mathrm{D}}_{2}$ resonance. The time dependence of the spatial behavior in the trap indicates that the suitable positions for stably holding atoms are altered because the equilibrium condition between the optical dipole and the radiative forces depends on the trap laser detuning. The stable position, which is not a primary position of focus in the Gaussian beam optics, depends only on the laser detuning due to the change in the radiative force, while it is independent of the change in the laser intensity, which results in a balance between the radiative and dipole forces.
We report on the stable effective trapping of cold rubidium atoms by a method for a single optical trap in the near-optical resonant regime. An optical trap with the near-optical resonance condition consists of not only the dipole but also the radiative forces, while a trap using a far-off resonance dominates only the dipole force. We measure the spatial behaviors of the center-of-mass positions and the loading efficiencies of the trapped atoms in the near-optical resonant trap, by changing the detuning over the range of \ensuremath−0.373 to \ensuremath−2.23 THz from the D2 resonance. The time dependence of the spatial behavior in the trap indicates that the suitable positions for stably holding atoms are altered because the equilibrium condition between the optical dipole and the radiative forces depends on the trap laser detuning. The stable position, which is not a primary position of focus in the Gaussian beam optics, depends only on the laser detuning due to the change in the radiative force, while it is independent of the change in the laser intensity, which results in a balance between the radiative and dipole forces.
This dissertation reports on the design, construction, and investigation of a pulsed optical dipole force trap which uses laser light to confine ultracold rubidium (Rb) atoms. Because the laser frequency is detuned far from the atomic resonance frequency, the optical dipole force trap is also called a "far-off-resonance trap" (FORT). The use of pulsed laser light to create an optical trap may find application in expanding the number of atomic species which can be confined. The experiments reported here are principally aimed, however, at understanding the physics of pulsed FORT dynamics in anticipation of using the free electron laser (FEL) at Jefferson Lab (Jlab) to construct a FORT. The Jlab FEL will provide a tunable, high power laser light source enabling the realization of spatially large and/or energetically deep traps which are not presently accessible with table-top laser sources. Here, a mode-locked Nd:YAG laser is used as a pulsed laser source. Since the conservative optical dipole force trap does not cool Rb atoms, ultracold atoms must be loaded into the FORT. The optical dipole force trap is formed at the focus of a Gaussian, 1.06 μm Nd:YAG laser beam which is located at the center of a high vacuum chamber and superimposed onto the center of a pre-cooled Rb atom cloud that has been previously accumulated in a magneto-optic trap (MOT). The performance of the pulsed FORT is compared to a continuous wave mode (cw) FORT which is built using the same laser beam; the operation of the two kinds of FORTs can be switched easily without disturbing the experimental alignment. The dependencies of FORT loading efficiency to FORT and MOT parameters such as FORT laser power, loading time, storage/holding time, detuning of the primary MOT laser frequency, and repump laser intensity are investigated. There are about 1.5×107 ultracold rubidium atoms in the MOT. At 7 Watts FORT laser power, about 8% of the atoms are loaded successfully into the cw FORT and about 5% into the pulsed FORT under similar, but not identical, conditions. In most respects both the cw and pulsed FORTs show comparable behavior. The behavior of both FORTs depends strongly on FORT laser power. As expected, at higher power, more atoms can be loaded into the FORT. Both FORTs also depend on the loading time and holding time.
Experiments are performed on loading cold atoms into a far-off resonance optical dipole trap that is spatially separated from the laser-cooling region. The atoms are delivered using a far-off resonant optical dipole guide and enter the trap through a switchable blue-detuned light sheet or ``trap door.'' This scheme provides a means to transfer atoms from a dissipative to a non-dissipative trap without a significant loss of phase-space density. We study the dynamics of atoms within the trap and measure their lifetime. Preliminary results on multiple loading are presented. As the technique does not rely on near-resonant light, the atom number limit characteristic of laser-cooling experiments can, in principle, be exceeded.
This thesis reports on the design, setup, and operation of a new atom trap apparatus, which is developed to confine few rubidium atoms in ultrahigh vacuum by means of taylored and dynamically variable light potentials (dipole traps), thus making the atoms available for spectroscopy and controlled manipulations. To maintain low background pressure, atoms of a vapour cell are transferred into a cold atomic beam by laser cooling techniques, and accumulated by a magneto-optic trap (MOT) in a separate part of the vacuum system. The laser cooled atoms are then transferred into dipole traps made of focused far-off-resonant laser fields in single or crossed-beam geometry, which are superimposed with the center of the MOT. Gaussian as well as hollow Laguerre-Gaussian (LG01) beam profiles are used with red-detuned and blue-detuned light. Microfabricated dielectric phase objects allow the efficient and robust mode conversion of Gaussian into Laguerre-Gaussian laser beams. Trap geometries can easily be changed due to the highly flexible experimental setup. The dipole trap laser beams have powers up to several hundred milliwatts and are focused to around 10 m. At a detuning of several tens of nanometers from the atomic resonance, the resulting traps are a few millikelvin deep, and the trapped atoms exhibit motional frequencies near 30 kHz, trap light scattering rates of a few hundred photons per second per atom, and storage times of several seconds. The number of dipole-trapped atoms ranges from more than ten thousand to below ten. The dipole-trapped atoms are detected either by a photon counting system with efficient straylight discrimination, or by recapture into the MOT, which is imaged onto a sensitive photodiode and a CCD-camera. Due to the strong AC-Stark shift imposed by the high-intensity trapping light, energy-selective resonant excitation and detection of the stored atoms is possible. The measured energy distribution is consistent with a harmonic potential shape and allows for the determination of temperatures and heating rates. From initial measurements, the thermal energy is found to be about 10 % of the trap depth. Using a crossed-beam geometry with red-detuned laser light, efficient transfer of atoms between the beams is observed. Optimum transfer occurs when the two beams cross at a radial offset, which can qualitatively be understood when the particle energy and geometrical properties of the two-beam trapping potential are considered. Numerical simulations reproduce the general features of the measured transfer efficiency vs. radial beam offset. This experiment is a first step towards dynamically variable potentials. Atoms have been radially confined in a blue-detuned hollow beam, and their decay time has been determined. This configuration is currently extended to a three-dimensionally confining blue-detuned dipole trap. For advanced laser cooling, state manipulation and spectroscopy of trapped atoms, a system of two diode lasers has been set up which are phase-coherently locked with a difference frequency near 6.834 GHz, to drive Raman transitions between the hyperfine-split ground states of 87Rb atoms. Resonances of such a transition have been recorded in a buffer gas loaded rubidium vapour cell with linewidths below 100 Hz.
The interaction of light with atoms and molecules is of fundamental interest in many branches of science. In atomic physics, this interaction can be used to cool and spatially confine (trap) atoms. These traps can be used as the starting point for other experiments, but the dynamics of the cooling and trapping processes is itself of interest. In order to better understand the physics of trapping atoms in an optical dipole force trap, we have conducted a series of spectroscopic measurements of ultracold rubidium atoms in such a trap. The trap was created at the focus of a Nd:YAG laser beam with wavelength 1064nm and nearly Gaussian spatial mode. For rubidium, the trap light is red-detuned and the atoms are confined to the highest intensity in the beam. In order to probe the atoms confined in the trap, we have performed spectroscopy on the 5S1/2 → 5P3/2 transition. Because the polarizability of the ground and excited states is not the same at the trap wavelength, the spectra exhibit both a shift and inhomogeneous broadening. We have investigated the spectra for both linear and circular polarized traps. We also studied the application of a second laser to couple the excited state (5P3/2) to another higher excited state (5D5/2) to reduce the inhomogeneous broadening of the 5S1/2 → 5P 3/2 transition. Finally, two-photon spectroscopy was performed on atoms in the dipole force trap and compared to spectra taken in a magneto optical trap (MOT). Autler-Townes splitting was clearly observed in the MOT and appears to have been observed in the dipole force trap also.
We demonstrate a robust method for the efficient optically levitated loading of ultracold Cs atoms in a crossed dipole trap. When preparing a large number of atomic samples, a large-volume crossed dipole trap is required to form a shallow but very efficient loading potential. The scattering force coming from a red near-off-resonance laser is utilized to precisely compensate for the destructive gravitational force of the atoms, making it a promising method for loading and trapping ∼ atoms in a pure optical trap. The optimum levitation laser intensity is ∼177 W cm −2 with a detuning of −25.0 GHz. The dependence of the variation in the number of atoms loaded and trapped in the optically levitated dipole trap on the intensity and detuning of the levitated laser is in good agreement with theoretical predictions.
The theory of an atom dipole trap composed of a focused, far red-detuned, trapping laser beam, and a pair of red-detuned, counterpropagating, cooling beams is developed for the simplest realistic multilevel dipole interaction scheme based on a model of a (3+5)-level atom. The description of atomic motion in the trap is based on the quantum kinetic equations for the atomic density matrix and the reduced quasiclassical kinetic equation for atomic distribution function. It is shown that when the detuning of the trapping field is much larger than the detuning of the cooling field, and with low saturation, the one-photon absorption (emission) processes responsible for the trapping potential can be well separated from the two-photon processes responsible for sub-Doppler cooling atoms in the trap. Two conditions are derived that are necessary and sufficient for stable atomic trapping. The conditions show that stable atomic trapping in the optical dipole trap can be achieved when the trapping field has no effect on the two-photon cooling process and when the cooling field does not change the structure of the trapping potential but changes only the numerical value of the trapping potential well. It is concluded that the separation of the trapping and cooling processes in a pure optical dipole trap allows one to cool trapped atoms down to a minimum temperature close to the recoil temperature, keeping simultaneously a deep potential well.