The laser cooling and trapping of ultracold neutral dysprosium has been demonstrated recently using the broad, open, 421-nm cycling transition. Narrow-line magneto-optical trapping of Dy on longer wavelength transitions would enable the preparation of ultracold Dy samples suitable for loading optical dipole traps and subsequent evaporative cooling. We have identified the closed 741-nm cycling transition as a candidate for the narrow-line cooling of Dy. We present experimental data on the isotope shifts, the hyperfine constants A and B, and the decay rate of the 741-nm transition. In addition, we report a measurement of the 421-nm transition's linewidth, which agrees with previous measurements. We summarize the laser-cooling characteristics of these transitions as well as other narrow cycling transitions that may prove useful for cooling Dy.
We study the decay of a dense, ultracold sample of weakly bound DyK dimers stored in an optical dipole trap. Our bosonic dimers are composed of the fermionic isotopes Dy 161 and K 40 , which is of particular interest for experiments related to pairing and superfluidity in fermionic systems with mass imbalance. We have realized dipole traps with near-infrared laser light in four different wavelength regions between 1050 and 2002 nm . We have identified trap-light-induced processes as the overall dominant source of losses, except for wavelengths around 2000 nm , where light-induced losses appeared to be much weaker. In a trap near 1550 nm , we found a plateau of minimal light-induced losses, and by carefully tuning the wavelength we reached conditions where losses from inelastic collisions between the trapped dimers became observable. For very weakly bound dimers close to the center of a magnetically tuned Feshbach resonance, we demonstrate the Pauli suppression of collisional losses by about an order of magnitude.
Open-shell lanthanide atoms, and dysprosium in particular, combine a large ground-state angular momentum with dense electronic spectra, making their dynamical polarizability strongly dependent on wavelength and internal state, and therefore challenging to calculate and characterize experimentally. This issue has become especially relevant with the recent development of single-atom trapping of dysprosium in optical-tweezer arrays, where precise knowledge of the polarizability is needed to design optimized trapping architectures. Here, we exploit the strong spin-dependent light shift near the J′=J−1 intercombination line at 530.306 nm to determine the background scalar and vector polarizabilities of 162Dy in its ground state near this wavelength. Our measurements quantitatively agree with atomic-structure calculations and provide new insight into the contributions of nearby transitions in a spectral region relevant to emerging dysprosium tweezer platforms.