Ramsey-type microwave spectroscopy on CO (a3Πa^3\Pi)

Using a Ramsey-type setup, the lambda-doublet transition in the $J=1,\, \Omega=1$ level of the $a^3\Pi$ state of CO was measured to be 394 064 870(10) Hz. In our molecular beam apparatus, a beam of metastable CO is prepared in a single quantum level by expanding CO into vacuum and exciting the molecules using a narrow-band UV laser system. After passing two microwave zones that are separated by 50 cm, the molecules are state-selectively deflected and detected 1 meter downstream on a position sensitive detector. In order to keep the molecules in a single $m_J^B$ level, a magnetic bias field is applied. We find the field-free transition frequency by taking the average of the $m_J^B = +1 \rightarrow m_J^B = +1$ and $m_J^B = -1 \rightarrow m_J^B = -1$ transitions, which have an almost equal but opposite Zeeman shift. The accuracy of this proof-of-principle experiment is a factor of 100 more accurate than the previous best value obtained for this transition

Stark deceleration of CaF molecules in strong- and weak-field seeking states

We report the Stark deceleration of CaF molecules in the strong-field seeking ground state and in a weak-field seeking component of a rotationally-excited state. We use two types of decelerator, a conventional Stark decelerator for the weak-field seekers, and an alternating gradient decelerator for the strong-field seekers, and we compare their relative merits. We also consider the application of laser cooling to increase the phase-space density of decelerated molecules.Comment: 10 pages, 8 figure

Field-linked States of Ultracold Polar Molecules

We explore the character of a novel set of ``field-linked'' states that were predicted in [A. V. Avdeenkov and J. L. Bohn, Phys. Rev. Lett. 90, 043006 (2003)]. These states exist at ultralow temperatures in the presence of an electrostatic field, and their properties are strongly dependent on the field's strength. We clarify the nature of these quasi-bound states by constructing their wave functions and determining their approximate quantum numbers. As the properties of field-linked states are strongly defined by anisotropic dipolar and Stark interactions, we construct adiabatic surfaces as functions of both the intermolecular distance and the angle that the intermolecular axis makes with the electric field. Within an adiabatic approximation we solve the 2-D Schrodinger equation to find bound states, whose energies correlate well with resonance features found in fully-converged multichannel scattering calculations

Trapping molecules on a chip in traveling potential wells

A microstructured array of over 1200 electrodes on a substrate has been configured to generate an array of local minima of electric field strength with a periodicity of $120 \mu$m about $25 \mu$m above the substrate. By applying sinusoidally varying potentials to the electrodes, these minima can be made to move smoothly along the array. Polar molecules in low field seeking quantum states can be trapped in these traveling potential wells. This is experimentally demonstrated by transporting metastable CO molecules in 30 mK deep wells that move at constant velocities above the substrate.Comment: 4 pages, 3 figure

Slowing heavy, ground-state molecules using an alternating gradient decelerator

Cold supersonic beams of molecules can be slowed down using a switched sequence of electrostatic field gradients. The energy to be removed is proportional to the mass of the molecules. Here we report deceleration of YbF, which is 7 times heavier than any molecule previously decelerated. We use an alternating gradient structure to decelerate and focus the molecules in their ground state. We show that the decelerator exhibits the axial and transverse stability required to bring these molecules to rest. Our work significantly extends the range of molecules amenable to this powerful method of cooling and trapping.Comment: 4 pages, 5 figure

Multiple packets of neutral molecules revolving for over a mile

The level of control that one has over neutral molecules in beams dictates their possible applications. Here we experimentally demonstrate that state-selected, neutral molecules can be kept together in a few mm long packet for a distance of over one mile. This is accomplished in a circular arrangement of 40 straight electrostatic hexapoles through which the molecules propagate over 1000 times. Up to 19 packets of molecules have simultaneously been stored in this ring structure. This brings the realization of a molecular low-energy collider within reach

A continuous source of translationally cold dipolar molecules

The Stark interaction of polar molecules with an inhomogeneous electric field is exploited to select slow molecules from a room-temperature reservoir and guide them into an ultrahigh vacuum chamber. A linear electrostatic quadrupole with a curved section selects molecules with small transverse and longitudinal velocities. The source is tested with formaldehyde (H2CO) and deuterated ammonia (ND3). With H2CO a continuous flux is measured of approximately 10^9/s and a longitudinal temperature of a few K. The data are compared with the result of a Monte Carlo simulation.Comment: 4 pages, 4 figures v2: small changes in the abstract, text and references. Figures 1 & 2 regenerated to prevent errors in the pd

Nonlinear dynamics in an alternating gradient guide for neutral particles

Neutral particles can be guided and focussed using electric field gradients that focus in one transverse direction and defocus in the other, alternating between the two directions. Such a guide is suitable for transporting particles that are attracted to strong electric fields, which cannot be guided using static fields. Particles are only transmitted if their initial positions and transverse speeds lie within the guide's phase space acceptance. Nonlinear forces are always present in the guide and can severely reduce this acceptance. We consider the effects of the two most important nonlinear forces, a term in the force that is cubic in the off-axis displacement, and a nonlinear term which couples together the two transverse motions. We use approximate analytical techniques, along with numerical methods, to calculate the influence of these nonlinear forces on the particle trajectories and on the phase space acceptance. The cubic term alters the focussing and defocussing powers, leading either to an increase or a decrease of the acceptance depending on its sign. We find an approximate analytical result for the phase space acceptance including this cubic term. Using a perturbation method we show how the coupling term leads to slow changes in the amplitudes of the transverse oscillations. This term reduces the acceptance when it reduces the focussing power, but has little influence when it increases that power. It is not possible to eliminate both nonlinear terms, but one can be made small at the expense of the other. We show how to choose the guide parameters so that the acceptance is optimized.Comment: 31 pages, 12 figure

Superfluid pairing in a polarized dipolar Fermi gas

We calculate the critical temperature of a superfluid phase transition in a polarized Fermi gas of dipolar particles. In this case the order parameter is anisotropic and has a nontrivial energy dependence. Cooper pairs do not have a definite value of the angular momentum and are coherent superpositions of all odd angular momenta. Our results describe prospects for achieving the superfluid transition in single-component gases of fermionic polar molecules.Comment: 12 pages, 2 figure

Deterministic delivery of externally cold and precisely positioned single molecular ions

We present the preparation and deterministic delivery of a selectable number of externally cold molecular ions. A laser cooled ensemble of Mg^+ ions subsequently confined in several linear Paul traps inter-connected via a quadrupole guide serves as a cold bath for a single or up to a few hundred molecular ions. Sympathetic cooling embeds the molecular ions in the crystalline structure. MgH^+ ions, that serve as a model system for a large variety of other possible molecular ions, are cooled down close to the Doppler limit and are positioned with an accuracy of one micrometer. After the production process, severely compromising the vacuum conditions, the molecular ion is efficiently transfered into nearly background-free environment. The transfer of a molecular ion between different traps as well as the control of the molecular ions in the traps is demonstrated. Schemes, optimized for the transfer of a specific number of ions, are realized and their efficiencies are evaluated. This versatile source applicable for broad charge-to-mass ratios of externally cold and precisely positioned molecular ions can serve as a container-free target preparation device well suited for diffraction or spectroscopic measurements on individual molecular ions at high repetition rates (kHz).Comment: 11 pages, 8 figure