Measuring the Casimir-Polder interaction of Rydberg atoms by vapour cell spectroscopy
Résumé
The modification of quantum fluctuations by a surface of finite reflectivity shifts the energy levels of atoms and changes their radiative properties (Casimir-Polder effect). At nanometric distances away from a surface (near field), the Casimir-Polder energy shift is given by −C3/z3 (where C3 is the van der Waals coefficient and z is the atom-surface distance) corresponding to the interaction of the fluctuating atomic dipole with its surface induced image. Near field Rydberg-surface interactions are of fundamental interest because the atomic size, scaling as n∗2 (where n∗ is the principle quantum number corrected by the quantum defect), is no longer negligible compared to the atom-surface separation, z. In this case, the dipole approximation, (−C3/z3 law of interaction), is no longer valid and higher-order terms, corresponding to the interaction of the fluctuation quadrupole with its own image, need to be taken into account. Quadrupole interaction terms in the atom-surface interaction manifest themselves with a novel distance dependence of z5 that has not been experimentally investigated yet1. Casimir-Polder experiments were first performed with low-lying Rydberg states (n= 10-14), demonstrating the −C3/z3 law of interaction2. Nevertheless, more recent experiments with high-lying rubidium Rydbergs (n=32-43)3 were not in agreement with Casimir-Polder theory thus highlighting the need for further experimental studies.
Domaines
Physique Quantique [quant-ph]Origine | Fichiers produits par l'(les) auteur(s) |
---|