Prof Dieter Jaksch

Abstract:

We study an impurity atom trapped by an anharmonic potential, immersed within a cold atomic Fermi gas with attractive interactions that realizes the crossover from a Bardeen-Cooper-Schrieffer (BCS) superfluid to a Bose-Einstein condensate (BEC). Considering the qubit comprising the lowest two vibrational energy eigenstates of the impurity, we demonstrate that its dynamics probes the equilibrium density fluctuations encoded in the dynamic structure factor of the superfluid. Observing the impurity's evolution is thus shown to facilitate nondestructive measurements of the superfluid order parameter and the contact between collective and single-particle excitation spectra. Our setup constitutes a novel model of an open quantum system interacting with a thermal reservoir, the latter supporting both bosonic and fermionic excitations that are also coupled to each other.

Abstract:

Estimating the temperature of a cold quantum system is difficult. Usually, one measures a wellunderstood thermal state and uses that prior knowledge to infer its temperature. In contrast, we introduce a method of thermometry that assumes minimal knowledge of the state of a system and is potentially non-destructive. Our method uses a universal temperature-dependence of the quench dynamics of an initially thermal system coupled to a qubit probe that follows from the Tasaki-Crooks theorem for non-equilibrium work distributions. We provide examples for a cold-atom system, in which our thermometry protocol may retain accuracy and precision at subnanokelvin temperatures.

Abstract:

We use midinfrared pulses with stable carrier-envelope phase offset to drive molecular vibrations in the charge transfer salt ET-F_{2}TCNQ, a prototypical one-dimensional Mott insulator. We find that the Mott gap, which is probed resonantly with 10 fs laser pulses, oscillates with the pump field. This observation reveals that molecular excitations can coherently perturb the electronic on-site interactions (Hubbard U) by changing the local orbital wave function. The gap oscillates at twice the frequency of the vibrational mode, indicating that the molecular distortions couple quadratically to the local charge density.