Linking Ultracold Polar Molecules

We predict that pairs of polar molecules can be weakly bound together in an ultracold environment, provided that a dc electric field is present. The field that links the molecules together also strongly influences the basic properties of the resulting dimer, such as its binding energy and predissociation lifetime. Because of their long-range character these dimers will be useful in disentangling cold collision dynamics of polar molecules. As an example, we estimate the microwave photoassociation yield for OH-OH cold collisions.Comment: 4 pages 2 figure

Feshbach spectroscopy and analysis of the interaction potentials of ultracold sodium

We have studied magnetic Feshbach resonances in an ultracold sample of Na prepared in the absolute hyperfine ground state. We report on the observation of three s-, eight d-, and three g-wave Feshbach resonances, including a more precise determination of two known s-wave resonances, and one s-wave resonance at a magnetic field exceeding 200mT. Using a coupled-channels calculation we have improved the sodium ground-state potentials by taking into account these new experimental data, and derived values for the scattering lengths. In addition, a description of the molecular states leading to the Feshbach resonances in terms of the asymptotic-bound-state model is presented.Comment: 11 pages, 4 figure

Novel technique for the CO₂ laser fabrication of optical devices with sub-micrometer ablation depth precision

We present novel techniques for the processing of fibre end face and cladding surfaces using a 9.6 µm CO2 laser. We investigate the effects of pulse duration on process parameters

Creation and manipulation of Feshbach resonances with radio-frequency radiation

We present a simple technique for studying collisions of ultracold atoms in the presence of a magnetic field and radio-frequency radiation (rf). Resonant control of scattering properties can be achieved by using rf to couple a colliding pair of atoms to a bound state. We show, using the example of 6Li, that in some ranges of rf frequency and magnetic field this can be done without giving rise to losses. We also show that halo molecules of large spatial extent require much less rf power than deeply bound states. Another way to exert resonant control is with a set of rf-coupled bound states, linked to the colliding pair through the molecular interactions that give rise to magnetically tunable Feshbach resonances. This was recently demonstrated for 87Rb [Kaufman et al., Phys. Rev. A 80:050701(R), 2009]. We examine the underlying atomic and molecular physics which made this possible. Lastly, we consider the control that may be exerted over atomic collisions by placing atoms in superpositions of Zeeman states, and suggest that it could be useful where small changes in scattering length are required. We suggest other species for which rf and magnetic field control could together provide a useful tuning mechanism.Comment: 21 pages, 8 figures, submitted to New Journal of Physic

Photoassociation spectroscopy of cold alkaline earth atoms near the intercombination line

The properties of photoassociation (PA) spectra near the intercombination line (the weak transition between $^{1}S_{0}$ and $^{3}P_{1}$ states) of group II atoms are theoretically investigated. As an example we have carried out a calculation for Calcium atoms colliding at ultra low temperatures of 1 mK, 1 $\mu$K, and 1 nK. Unlike in most current photoassociation spectroscopy the Doppler effect can significantly affect the shape of the investigated lines. Spectra are obtained using Ca--Ca and Ca--Ca$^*$ short-range {\it ab initio} potentials and long-range van der Waals and resonance dipole potentials. The similar van der Waals coefficients of ground $^{1}S_{0} + ^{1}S_{0}$ and excited $^{1}S_{0} + ^{3}P_{1}$ states cause the PA to differ greatly from those of strong, allowed transitions with resonant dipole interactions. The density of spectral lines is lower, the Condon points are at relatively short range, and the reflection approximation for the Franck-Condon factors is not applicable, and the spontaneous decay to bound ground-state molecules is efficient. Finally, the possibility of efficient production of cold molecules is discussed

Acrylamides with hydrolytically labile carbonate ester side chains as versatile building blocks for well-defined block copolymer micelles via RAFT polymerization

En route towards improved delivery systems for targeted chemotherapy, we propose a straightforward approach for the hydrophobic modification of the acrylamide N-(2-Hydroxyethyl) acrylamide (HEAm). An ethyl or benzyl group was introduced via a hydrolytically sensitive carbonate ester yielding HEAm-EC and HEAm-BC, respectively. Block copolymers of HEAm, respectively PEG and HEAm-EC or HEAm-BC were successfully synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization, obtaining a library of well-defined block copolymers with different degrees of polymerization (DP). To further explore the versatility of our approach in terms of polymer synthesis, self-assembly, drug solubilization and in vitro cell interaction, polyethylene glycol (PEG) and polyHEAm as hydrophilic polymer blocks were compared. The block copolymers formed micellar nanoparticles (10-100 nm) in PBS and could efficiently solubilize hydrophobic dyes and anti-cancer drugs. Benzyl carbonate ester side chains increased micellar stability and drug loading capacity. Moreover, PEG as hydrophilic block showed in comparison to HEAm more promising results concerning both colloidal stability and drug loading capacity. Confocal microscopy showed that the micelles could efficiently deliver a hydrophobic dye inside the cells. Finally, we also demonstrated efficient formulation of the anti-cancer drug paclitaxel with an in vitro cancer cell killing performance comparable or even better than the two commercial PTX nano-formulations Abraxane and Genexol-PM at equal drug dose. In conclusion, modification of HEAm through carbonate linkages offers a versatile platform for the design of degradable polymers with potential for biomedical applications

Atom-molecule equilibration in a degenerate Fermi gas with resonant interactions

We present a nonequilibrium kinetic theory describing atom-molecule population dynamics in a two-component Fermi gas with a Feshbach resonance. Key collision integrals emerge that govern the relaxation of the atom-molecule mixture to chemical and thermal equilibrium. Our focus is on the pseudogap regime where molecules form above the superfluid transition temperature. In this regime, we formulate a simple model for the atom-molecule population dynamics. The model predicts the saturation of molecule formation that has been observed in recent experiments, and indicates that a dramatic enhancement of the atom-molecule conversion efficiency occurs at low temperatures.Comment: Updated manuscript on July 5, 2004. Four pages with three embedded figure

Prediction of Feshbach resonances from three input parameters

We have developed a model of Feshbach resonances in gases of ultracold alkali metal atoms using the ideas of multichannel quantum defect theory. Our model requires just three parameters describing the interactions - the singlet and triplet scattering lengths, and the long range van der Waals coefficient - in addition to known atomic properties. Without using any further details of the interactions, our approach can accurately predict the locations of resonances. It can also be used to find the singlet and triplet scattering lengths from measured resonance data. We apply our technique to $^{6}$Li--$^{40}$K and $^{40}$K--$^{87}$Rb scattering, obtaining good agreement with experimental results, and with the more computationally intensive coupled channels technique.Comment: 5 pages, 2 figures, revised versio

Tree-body loss of of trapped ultracold 87^{87}Rb atoms due to a Feshbach resonance

The loss of ultracold trapped atoms in the vicinity of a Feshbach resonance is treated as a two-stage reaction, using the Breit-Wigner theory. The first stage is the formation of a resonant diatomic molecule, and the second one is its deactivation by inelastic collisions with other atoms. This model is applied to the analysis of recent experiments on $^{87}$Rb, leading to an estimated value of $7\times 10^{-11}$ cm$^{3}/$s for the deactivation rate coefficient.Comment: LaTeX, 4 pages with 1 figures, uses REVTeX4, uses improved experimental dat

Microscopic theory of atom-molecule oscillations in a Bose-Einstein condensate

In a recent experiment at JILA [E.A. Donley et al., Nature (London) 417, 529 (2002)] an initially pure condensate of Rb-85 atoms was exposed to a specially designed time dependent magnetic field pulse in the vicinity of a Feshbach resonance. The production of new components of the gas as well as their oscillatory behavior have been reported. We apply a microscopic theory of the gas to identify these components and determine their physical properties. Our time dependent studies allow us to explain the observed dynamic evolution of all fractions, and to identify the physical relevance of the pulse shape. Based on ab initio predictions, our theory strongly supports the view that the experiments have produced a molecular condensate.Comment: 18 pages, 20 figure