A recent time-of-flight (TOF) expansion experiment with polarized fermionic erbium atoms measured a Fermi surface deformation from a sphere to an ellipsoid due to dipole-dipole interaction, thus confirming previous theoretical predictions. Here we perform a systematic study of the ground-state properties and TOF dynamics for trapped dipolar Fermi gases from the collisionless to the hydrodynamic regime at zero temperature. To this end we solve analytically the underlying BoltzmannVlasov equation within the relaxation-time approximation in the vicinity of equilibrium by using a suitable rescaling of the equilibrium distribution. The resulting ordinary differential equations for the respective scaling parameters are then solved numerically for experimentally realistic parameters and relaxation times that correspond to the collisionless, collisional, and hydrodynamic regime. The equations for the collisional regime are first solved in the approximation of a fixed relaxation time, and then this approach is extended to include a self-consistent determination of the relaxation time. The presented analytical and numerical results are relevant for a detailed quantitative understanding of ongoing experiments and the design of future experiments with ultracold fermionic dipolar atoms and molecules. In particular, the obtained results are relevant for systems with strong dipole-dipole interaction, which turn out to affect significantly the aspect ratios during the TOF expansion.

Many-body dipolar effects in Fermi gases are quite subtle as they energetically compete with the large kinetic energy at and below the Fermi surface (FS). Recently it was experimentally observed in a sample of erbium atoms that its FS is deformed from a sphere to an ellipsoid due to the presence of the anisotropic and long-range dipole-dipole interaction Aikawa et al (2014 Science 345 1484). Moreover, it was suggested that, when the dipoles are rotated by means of an external field, the FS follows their rotation, thereby keeping the major axis of the momentum-space ellipsoid parallel to the dipoles. Here we generalise a previous Hartree-Fock mean-field theory to systems confined in an elongated triaxial trap with an arbitrary orientation of the dipoles relative to the trap. With this we study for the first time the effects of the dipoles' arbitrary orientation on the ground-state properties of the system. Furthermore, taking into account the geometry of the system, we show how the ellipsoidal FS deformation can be reconstructed, assuming ballistic expansion, from the experimentally measurable real-space aspect ratio after a free expansion. We compare our theoretical results with new experimental data measured with erbium Fermi gas for various trap parameters and dipole orientations. The observed remarkable agreement demonstrates the ability of our model to capture the full angular dependence of the FS deformation. Moreover, for systems with even higher dipole moment, our theory predicts an additional unexpected effect: the FS does not simply follow rigidly the orientation of the dipoles, but softens showing a change in the aspect ratio depending on the dipoles' orientation relative to the trap geometry, as well as on the trap anisotropy itself. Our theory provides the basis for understanding and interpreting phenomena in which the investigated physics depends on the underlying structure of the FS, such as fermionic pairing and superfluidity.

A recent experimental realization of quantum degenerate gas of 40 K 87 Rb molecules opens up prospects of exploring strong dipolar Fermi gases and many-body phenomena arising in that regime. Here we derive a mean-field variational approach based on the Wigner function for the description of ground-state properties of such systems. We show that the stability of dipolar fermions in a general harmonic trap is universal as it only depends on the trap aspect ratios and the dipoles' orientation. We calculate the species-independent stability diagram and the deformation of the Fermi surface (FS) for polarized molecules, whose electric dipoles are oriented along a preferential direction. Compared to atomic magnetic species, the stability of a molecular electric system turns out to strongly depend on its geometry and the FS deformation significantly increases. arXiv:1902.09518v2 [cond-mat.quant-gas]