Probing BCS pairing and quasiparticle formation in ultracold gases by Rydberg atom spectroscopy
Emilio Ramos Rodríguez, Marcel Gievers, Richard Schmidt
TL;DR
This work proposes using a heavy Rydberg impurity as a local spectroscopic sensor to probe BCS pairing in ultracold two-component Fermi gases. By extending the functional determinant approach to anomalous (BCS) baths and computing the absorption spectrum from the Ramsey signal, the authors show that dimer and trimer bound-state peaks encode the superconducting gap $\Delta$, revealing whether Cooper pairs are broken or trapped intact. The analysis also demonstrates suppression of the orthogonality catastrophe by the gap, leading to a well-defined quasiparticle peak and a Bogoliubov two-branch spectrum, with peak shifts directly measuring $\Delta$ locally. This method provides high spatial and temporal resolution for mapping pairing properties in strongly correlated matter and can be extended to finite temperature, imbalanced mixtures, or mobile impurities.
Abstract
Locally probing pairing in fermionic superfluids, ranging from micro- to macroscopic scales, has been a long-standing challenge. Here, we investigate a new approach that uses Rydberg impurities as a spectroscopic sensor of the surrounding strongly correlated state of ultracold paired fermions. The extended wavefunction of the Rydberg electron induces a finite-range potential that can bind atoms from the BCS medium, forming molecular states. As a consequence, the optical absorption spectrum of the impurity encodes key many-body properties. Using the functional determinant approach, we provide a direct measure of the superfluid gap through frequency shifts of dimer and trimer peaks. The spectra also reveal whether the Cooper pairs are broken or trapped intact. For static Rydberg atoms, we relate this signature of pairing to the suppression of the orthogonality catastrophe due to the superconducting gap resulting in the formation of well-defined polaron quasiparticles. Our work establishes Rydberg atom spectroscopy as a powerful local probe of strongly correlated matter.
