Benjamin Stuhl

2D Magneto-Optical Trapping of Diatomic Molecules

We demonstrate one- and two-dimensional transverse laser cooling and magneto-optical trapping of the polar molecule yttrium (II) oxide (YO). In a 1D magneto-optical trap (MOT), we characterize the magneto-optical trapping force and decrease the transverse temperature by an order of magnitude, from 25 to 2 mK, limited by interaction time. In a 2D MOT, we enhance the intensity of the YO beam and reduce the transverse temperature in both transverse directions. The approach demonstrated here can be applied to many molecular species and can also be extended to 3D.

Visualizing edge states with an atomic Bose gas in the quantum Hall regime

Visualizing edge states in atomic systems Visualizing edge states in atomic systems Simulating the solid state using ultracold atoms is an appealing research approach. In solids, however, the charged electrons are susceptible to an external magnetic field, which curves their trajectories and makes them skip along the edge of the sample. To observe this phenomenon with cold atoms requires an artificial magnetic field to have a similar effect on the neutral atoms (see the Perspective by Celi and Tarruell). Stuhl et al. obtained skipping orbits with bosonic atoms using a lattice that consisted of an array of atoms in one direction and three internal atomic spin states in the other. In a complementary experiment, Mancini et al. observed similar physics with fermionic atoms. Science, this issue pp. 1514 and 1510; see also p. 1450 Skipping orbits of neutral bosonic rubidium-87 atoms are imaged after an artificial magnetic field is induced in a synthetic lattice. [Also see Perspective by Celi and Tarruell] Bringing ultracold atomic gases into the quantum Hall regime is challenging. We engineered an effective magnetic field in a two-dimensional lattice with an elongated-strip geometry, consisting of the sites of an optical lattice in the long direction and of three internal atomic spin states in the short direction. We imaged the localized states of atomic Bose-Einstein condensates in this strip; via excitation dynamics, we further observed both the skipping orbits of excited atoms traveling down the system’s edges, analogous to edge magnetoplasmons in two-dimensional electron systems, and a dynamical Hall effect for bulk excitations. Our technique involves minimal heating, which will be important for spectroscopic measurements of the Hofstadter butterfly and realizations of Laughlin’s charge pump.

Magnetoelectrostatic Trapping of Ground State OH Molecules

We report magnetic confinement of neutral, ground state OH at a density of approximately 3 x 10(3) cm(-3) and temperature of approximately 30 mK. An adjustable electric field sufficiently large to polarize the OH is superimposed on the trap in various geometries, making an overall potential arising from both Zeeman and Stark effects. An effective molecular Hamiltonian is constructed, with Monte Carlo simulations accurately modeling the observed single-molecule dynamics in various trap configurations. Magnetic trapping of cold polar molecules under adjustable electric fields may enable study of low energy dipolar interactions.

Evaporative cooling of the dipolar hydroxyl radical

Atomic physics was revolutionized by the development of forced evaporative cooling, which led directly to the observation of Bose–Einstein condensation, quantum-degenerate Fermi gases and ultracold optical lattice simulations of condensed-matter phenomena. More recently, substantial progress has been made in the production of cold molecular gases. Their permanent electric dipole moment is expected to generate systems with varied and controllable phases, dynamics and chemistry. However, although advances have been made in both direct cooling and cold-association techniques, evaporative cooling has not been achieved so far. This is due to unfavourable ratios of elastic to inelastic scattering and impractically slow thermalization rates in the available trapped species. Here we report the observation of microwave-forced evaporative cooling of neutral hydroxyl (OH•) molecules loaded from a Stark-decelerated beam into an extremely high-gradient magnetic quadrupole trap. We demonstrate cooling by at least one order of magnitude in temperature, and a corresponding increase in phase-space density by three orders of magnitude, limited only by the low-temperature sensitivity of our spectroscopic thermometry technique. With evaporative cooling and a sufficiently large initial population, much colder temperatures are possible; even a quantum-degenerate gas of this dipolar radical (or anything else it can sympathetically cool) may be within reach.

Molecular beam collisions with a magnetically trapped target.

Cold, neutral hydroxyl radicals are Stark decelerated and confined within a magnetic trap consisting of two permanent ring magnets. The OH molecules are trapped in the ro-vibrational ground state at a density of ∼10 cm−3 and temperature of 70 mK. Collisions between the trapped OH sample and supersonic beams of atomic He and molecular D2 are observed and absolute collision cross sections measured. The He–OH and D2–OH center-of-mass collision energies are tuned from 60 cm−1 to 230 cm−1 and 145 cm−1 to 510 cm−1, respectively, yielding evidence of reduced He–OH inelastic cross sections at energies below 84 cm−1, the OH ground rotational level spacing.

Cold heteromolecular dipolar collisions

Cold molecules promise to reveal a rich set of novel collision dynamics in the low-energy regime. By combining for the first time the techniques of Stark deceleration, magnetic trapping, and cryogenic buffer gas cooling, we present the first experimental observation of cold collisions between two different species of state-selected neutral polar molecules. This has enabled an absolute measurement of the total trap loss cross sections between OH and ND(3) at a mean collision energy of 3.6 cm(-1) (5 K). Due to the dipolar interaction, the total cross section increases upon application of an external polarizing electric field. Cross sections computed from ab initio potential energy surfaces are in agreement with the measured value at zero external electric field. The theory presented here represents the first such analysis of collisions between a (2)Π radical and a closed-shell polyatomic molecule.

Cold State-Selected Molecular Collisions and Reactions

Over the past decade, and particularly the past five years, a quiet revolution has been building at the border between atomic physics and experimental quantum chemistry. The rapid development of techniques for producing cold and even ultracold molecules without a perturbing rare-gas cluster shell is now enabling the study of chemical reactions and scattering at the quantum scattering limit with only a few partial waves contributing to the incident channel. Moreover, the ability to perform these experiments with nonthermal distributions comprising one or a few specific states enables the observation and even full control of state-to-state collision rates in this computation-friendly regime: This is perhaps the most elementary study possible of scattering and reaction dynamics.

Mitigation of loss within a molecular Stark decelerator

Abstract.The transverse motion inside a Stark decelerator plays a large role in the total efficiency of deceleration. We differentiate between two separate regimes of molecule loss during the slowing process. The first mechanism involves distributed loss due to coupling of transverse and longitudinal motion, while the second is a result of the rapid decrease of the molecular velocity within the final few stages. In this work, we describe these effects and present means for overcoming them. Solutions based on modified switching time sequences with the existing decelerator geometry lead to a large gain of stable molecules in the intermediate velocity regime, but fail to address the loss at very low final velocities. We propose a new decelerator design, the quadrupole-guiding decelerator, which eliminates distributed loss due to transverse/longitudinal couplings throughout the slowing process and also exhibits gain over normal deceleration to the lowest velocities.

Microwave state transfer and adiabatic dynamics of magnetically trapped polar molecules

Cold and ultracold polar molecules with nonzero electronic angular momentum are of great interest for studies in quantum chemistry and control, investigations of novel quantum systems, and precision measurement. However, in mixed electric and magnetic fields, these molecules are generically subject to a large set of avoided crossings among their Zeeman sublevels; in magnetic traps, these crossings lead to distorted potentials and trap loss from electric bias fields. We have characterized these crossings in OH by microwave-transferring trapped OH molecules from the upper |f; M = +3/2> parity state to the lower |e; +3/2> state and observing their trap dynamics under an applied electric bias field. Our observations are very well described by a simple Landau-Zener model, yielding insight to the rich spectra and dynamics of polar radicals in mixed external fields.

Feshbach enhanced s-wave scattering of fermions: direct observation with optimized absorption imaging

We directly measured the normalized s-wave scattering cross-section of ultracold 40K atoms across a magnetic-field Feshbach resonance by colliding pairs of degenerate Fermi gases (DFGs) and imaging the scattered atoms. We extracted the scattered fraction for a range of bias magnetic fields, and measured the resonance location to be B0 = 20.206(15) mT with width Δ = 1.0(5) mT. To optimize the signal-to-noise ratio of atom number in scattering images, we developed techniques to interpret absorption images in a regime where recoil induced detuning corrections are significant. These imaging techniques are generally applicable to experiments with lighter alkalis that would benefit from maximizing signal-to-noise ratio on atom number counting at the expense of spatial imaging resolution.