Polarization Limits in K-Rb Spin-Exchange Mixtures

We present measurements of the optical absorption of K vapor at 795 nm due to the presence of high pressure He gas. The results set a limit on the polarization attainable in hybrid spin-exchange optical pumping of He-3

Consequences of Zeeman Degeneracy for van der Waals Blockade between Rydberg Atoms

We analyze the effects of Zeeman degeneracies on the long-range interactions between like Rydberg atoms, with particular emphasis on applications to quantum information processing using van der Waals blockade. We present a general analysis of how degeneracies affect the primary error sources in blockade experiments, emphasizing that blockade errors are sensitive primarily to the weakest possible atom-atom interactions between the degenerate states, not the mean interaction strength. We present explicit calculations of the van der Waals potentials in the limit where the fine-structure interaction is large compared to the atom-atom interactions. The results are presented for all potential angular momentum channels invoving s, p, and d states. For most channels there are one or more combinations of Zeeman levels that have extremely small dipole-dipole interactions and are therefore poor candidates for effective blockade experiments. Channels with promising properties are identified and discussed. We also present numerical calculations of Rb and Cs dipole matrix elements and relevant energy levels using quantum defect theory, allowing for convenient quantitative estimates of the van der Waals interactions to be made for principal quantum numbers up to 100. Finally, we combine the blockade and van der Waals results to quantitatively analyze the angular distribution of the blockade shift and its consequence for angular momentum channels and geometries of particular interest for blockade experiments with Rb.Comment: 16 figure

A Synchronous Spin-Exchange Optically Pumped NMR-Gyroscope

Inertial navigation systems generally consist of timing, acceleration, and orientation measurement units. Although much progress has been made towards developing primary timing sources such as atomic clocks, acceleration and orientation measurement units often require calibration. Nuclear Magnetic Resonance (NMR) gyroscopes, which rely on continuous measurement of the simultaneous Larmor precession of two co-located polarized noble gases, can be configured to have scale factors that depend to first order only on fundamental constants. The noble gases are polarized by spin-exchange collisions with co-located optically pumped alkali-metal atoms. The alkali-metal atoms are also used to detect the phase of precession of the polarized noble gas nuclei. Here we present a version of an NMR gyroscope designed to suppress systematic errors from the alkali-metal atoms. We demonstrate rotation rate angle random walk (ARW) sensitivity of 16 $\mu \text{Hz}/\sqrt{\text{Hz}}$ and bias instability of $\sim$800 nHz

Optical Magnetometer Array for Fetal Magnetocardiography

We describe an array of spin-exchange relaxation free optical magnetometers designed for detection of fetal magnetocardiography (fMCG) signals. The individual magnetometers are configured with a small volume with intense optical pumping, surrounded by a large pump-free region. Spin-polarized atoms that diffuse out of the optical pumping region precess in the ambient magnetic field and are detected by a probe laser. Four such magnetometers, at the corners of a 7 cm square, are configured for gradiometry by feeding back the output of one magnetometer to a field coil to null uniform magnetic field noise at frequencies up to 200 Hz. Using this array, we present the first measurements of fMCG signals using an atomic magnetometer

Zeros of Rydberg-Rydberg Foster Interactions

Rydberg states of atoms are of great current interest for quantum manipulation of mesoscopic samples of atoms. Long-range Rydberg-Rydberg interactions can inhibit multiple excitations of atoms under the appropriate conditions. These interactions are strongest when resonant collisional processes give rise to long-range C_3/R^3 interactions. We show in this paper that even under resonant conditions C_3 often vanishes so that care is required to realize full dipole blockade in micron-sized atom samples.Comment: 10 pages, 4 figures, submitted to J. Phys.

Formation and dynamics of van der Waals molecules in buffer-gas traps

We show that weakly bound He-containing van der Waals molecules can be produced and magnetically trapped in buffer-gas cooling experiments, and provide a general model for the formation and dynamics of these molecules. Our analysis shows that, at typical experimental parameters, thermodynamics favors the formation of van der Waals complexes composed of a helium atom bound to most open-shell atoms and molecules, and that complex formation occurs quickly enough to ensure chemical equilibrium. For molecular pairs composed of a He atom and an S-state atom, the molecular spin is stable during formation, dissociation, and collisions, and thus these molecules can be magnetically trapped. Collisional spin relaxation is too slow to affect trap lifetimes. However, 3He-containing complexes can change spin due to adiabatic crossings between trapped and untrapped Zeeman states, mediated by the anisotropic hyperfine interaction, causing trap loss. We provide a detailed model for Ag3He molecules, using ab initio calculation of Ag–He interaction potentials and spin interactions, quantum scattering theory, and direct Monte Carlo simulations to describe formation and spin relaxation in this system. The calculated rate of spin-change agrees quantitatively with experimental observations, providing indirect evidence for molecular formation in buffer-gas-cooled magnetic traps. Finally, we discuss the possibilities for spectroscopic detection of these complexes, including a calculation of expected spectra for Ag3He, and report on our spectroscopic search for Ag3He, which produced a null result.Astronom

Formation and dynamics of van der Waals molecules in buffer-gas traps

We show that weakly bound He-containing van der Waals molecules can be produced and magnetically trapped in buffer-gas cooling experiments, and provide a general model for the formation and dynamics of these molecules. Our analysis shows that, at typical experimental parameters, thermodynamics favors the formation of van der Waals complexes composed of a helium atom bound to most open-shell atoms and molecules, and that complex formation occurs quickly enough to ensure chemical equilibrium. For molecular pairs composed of a He atom and an S-state atom, the molecular spin is stable during formation, dissociation, and collisions, and thus these molecules can be magnetically trapped. Collisional spin relaxations are too slow to affect trap lifetimes. However, helium-3-containing complexes can change spin due to adiabatic crossings between trapped and untrapped Zeeman states, mediated by the anisotropic hyperfine interaction, causing trap loss. We provide a detailed model for Ag3He molecules, using ab initio calculation of Ag-He interaction potentials and spin interactions, quantum scattering theory, and direct Monte Carlo simulations to describe formation and spin relaxation in this system. The calculated rate of spin-change agrees quantitatively with experimental observations, providing indirect evidence for molecular formation in buffer-gas-cooled magnetic traps.Comment: 20 pages, 13 figure