Depolarisation cooling of an atomic cloud

We propose a cooling scheme based on depolarisation of a polarised cloud of trapped atoms. Similar to adiabatic demagnetisation, we suggest to use the coupling between the internal spin reservoir of the cloud and the external kinetic reservoir via dipolar relaxation to reduce the temperature of the cloud. By optical pumping one can cool the spin reservoir and force the cooling process. In case of a trapped gas of dipolar chromium atoms, we show that this cooling technique can be performed continuously and used to approach the critical phase space density for BECComment: 8 pages, 5 figure

Expansion dynamics of a dipolar Bose-Einstein condensate

Our recent measurements on the expansion of a chromium dipolar condensate after release from an optical trapping potential are in good agreement with an exact solution of the hydrodynamic equations for dipolar Bose gases. We report here the theoretical method used to interpret the measurement data as well as more details of the experiment and its analysis. The theory reported here is a tool for the investigation of different dynamical situations in time-dependent harmonic traps.Comment: 12 pages. Submitted to PR

Observation of Feshbach resonances in an ultracold gas of 52{}^{52}Cr

We have observed Feshbach resonances in elastic collisions between ultracold ${}^{52}$Cr atoms. This is the first observation of collisional Feshbach resonances in an atomic species with more than one valence electron. The zero nuclear spin of ${}^{52}$Cr and thus the absence of a Fermi-contact interaction leads to regularly-spaced resonance sequences. By comparing resonance positions with multi-channel scattering calculations we determine the s-wave scattering length of the lowest $^{2S+1}\Sigma_{g}^{+}$ potentials to be \unit[112(14)]{a_0}, \unit[58(6)]{a_0} and -\unit[7(20)]{a_0} for S=6, 4, and 2, respectively, where a_{0}=\unit[0.0529]{nm}.Comment: 4 pages, 2 figures, 1 tabl

Rydberg trimers and excited dimers bound by internal quantum reflection

Quantum reflection is a pure wave phenomena that predicts reflection of a particle at a changing potential for cases where complete transmission occurs classically. For a chemical bond, we find that this effect can lead to non-classical vibrational turning points and bound states at extremely large interatomic distances. Only recently has the existence of such ultralong-range Rydberg molecules been demonstrated experimentally. Here, we identify a broad range of molecular lines, most of which are shown to originate from two different novel sources: a single-photon associated triatomic molecule formed by a Rydberg atom and two ground state atoms and a series of excited dimer states that are bound by a so far unexplored mechanism based on internal quantum reflection at a steep potential drop. The properties of the Rydberg molecules identified in this work qualify them as prototypes for a new type of chemistry at ultracold temperatures.Comment: 6 pages, 3 figures, 1 tabl

Observation of dipole-dipole interaction in a degenerate quantum gas

We have investigated the expansion of a Bose-Einstein condensate (BEC) of strongly magnetic chromium atoms. The long-range and anisotropic magnetic dipole-dipole interaction leads to an anisotropic deformation of the expanding Cr-BEC which depends on the orientation of the atomic dipole moments. Our measurements are consistent with the theory of dipolar quantum gases and show that a Cr-BEC is an excellent model system to study dipolar interactions in such gases.Comment: 4 pages, 2 figure

Separation and Characterization of Respirable Amphibole Fibers from Libby, Montana

The vermiculite mine in Libby, Montana, was in operation for over 70 yr and was contaminated with asbestos-like amphibole fibers. The mining, processing, and shipping of this vermiculite led to significant fiber inhalation exposure throughout the community, and residents of Libby have developed numerous pulmonary diseases such as lung cancer and mesothelioma. The present study describes the separation of Libby 6-mix into respirable and nonrespirable size fractions by means of aqueous elutriation. The elutriator, designed to separate fibers with aerodynamic diameters smaller than 2.5 μm (respirable) from larger fibers, used an upward flow rate of 3.4 × 10−4 cm s−1. The resultant respirable fraction constituted only 13% of the raw Libby 6-mix mass, and less than 2% of the fibers in the elutriated fraction had aerodynamic diameters exceeding 2.5 μm. Surface area of the elutriated fibers was 5.3 m−2 g−1, compared to 0.53 m−2 g−1 for the raw fibers. There were no detectable differences in chemical composition between the larger and smaller fibers. Such harvesting of respirable fractions will allow toxicological studies to be conducted within a controlled laboratory setting, utilizing fiber sizes that may more accurately simulate historical exposure of Libby residents’ lungs. Importantly, this work describes a method that allows the use of material enriched in more uniform respirable material than raw Libby 6-mix, making comparisons with other known fiber preparations more valid on a mass basis

Neural network variational Monte Carlo for positronic chemistry

Quantum chemical calculations of the ground-state properties of positron-molecule complexes are challenging. The main difficulty lies in employing an appropriate basis set for representing the coalescence between electrons and a positron. Here, we tackle this problem with the recently developed Fermionic neural network (FermiNet) wavefunction, which does not depend on a basis set. We find that FermiNet produces highly accurate, in some cases state-of-the-art, ground-state energies across a range of atoms and small molecules with a wide variety of qualitatively distinct positron binding characteristics. We calculate the binding energy of the challenging non-polar benzene molecule, finding good agreement with the experimental value, and obtain annihilation rates which compare favourably with those obtained with explicitly correlated Gaussian wavefunctions. Our results demonstrate a generic advantage of neural network wavefunction-based methods and broaden their applicability to systems beyond the standard molecular Hamiltonian.Comment: 14 pages, 3 figure