de Haas-van Alphen study of the Fermi surfaces of superconducting LiFeP and LiFeAs

We report a de Haas-van Alphen oscillation study of the 111 iron pnictide superconductors LiFeAs with T(c) ≈ 18 K and LiFeP with T(c) ≈ 5 K. We find that for both compounds the Fermi surface topology is in good agreement with density functional band-structure calculations and has almost nested electron and hole bands. The effective masses generally show significant enhancement, up to ~3 for LiFeP and ~5 for LiFeAs. However, one hole Fermi surface in LiFeP shows a very small enhancement, as compared with its other sheets. This difference probably results from k-dependent coupling to spin fluctuations and may be the origin of the different nodal and nodeless superconducting gap structures in LiFeP and LiFeAs, respectively.     

Producing translationally cold, ground-state CO molecules

Carbon monoxide molecules in their electronic, vibrational, and rotational ground state are highly attractive for trapping experiments. The optical or ac electric traps that can be envisioned for these molecules will be very shallow, however, with depths in the sub-milliKelvin range. Here, we outline that the required samples of translationally cold CO (X(1)Σ(+), v' = 0, N' = 0) molecules can be produced after Stark deceleration of a beam of laser-prepared metastable CO (a(3)Π(1)) molecules followed by optical transfer of the metastable species to the ground state via perturbed levels in the A(1)Π state. The optical transfer scheme is experimentally demonstrated and the radiative lifetimes and the electric dipole moments of the intermediate levels are determined.     

Rotational-state-specific guiding of large molecules

A beam of polar molecules can be focused and transported through an ac electric quadrupole guide. At a given ac frequency, the transmission of the guide depends on the mass-to-dipole-moment (m/μ) ratio of the molecular quantum state. Here we present a detailed characterization of the m/μ selector, using a pulsed beam of benzonitrile (C(6)H(5)CN) molecules in combination with rotational quantum state resolved detection. The arrival time distribution as well as the transverse velocity distribution of the molecules exiting the selector are measured as a function of ac frequency. The μ/Δμ resolution of the selector can be controlled by the applied ac waveforms and a value of up to 20 can be obtained with the present setup. This is sufficient to exclusively transmit benzonitrile molecules in quantum states with the same m/μ value as the absolute ground state. The operation characteristics of the m/μ selector are in quantitative agreement with the outcome of trajectory simulations.     

Optimal navigation of a smart active particle: directional and distance sensing

The European Physical Journal E - This work aims at finding optimal navigation policies for thin, deformable microswimmers that progress in a viscous fluid by propagating a sinusoidal undulation...