RESUMO
By measuring the transmission of near-resonant light through an atomic vapor confined in a nanocell we demonstrate a mesoscopic optical response arising from the nonlocality induced by the motion of atoms with a phase coherence length larger than the cell thickness. Whereas conventional dispersion theory-where the local atomic response is simply convolved by the Maxwell-Boltzmann velocity distribution-is unable to reproduce the measured spectra, a model including a nonlocal, size-dependent susceptibility is found to be in excellent agreement with the measurements. This result improves our understanding of light-matter interaction in the mesoscopic regime and has implications for applications where mesoscopic effects may degrade or enhance the performance of miniaturized atomic sensors.
RESUMO
We report on the fabrication of an all-glass vapor cell with a thickness varying linearly between (exactly) 0 and â¼1 µm. The cell is made in Borofloat glass that allows state-of-the-art super polish roughness, a full optical bonding assembling and easy filling with alkali vapors. We detail the challenging manufacture steps and present experimental spectra resulting from fluorescence and transmission spectroscopy of the cesium D1 line. The very small surface roughness of 1 Å rms is promising to investigate the atom-surface interaction or to minimize parasite stray light.
RESUMO
We measure the near-resonant transmission of light through a dense medium of potassium vapor confined in a cell with nanometer thickness in order to investigate the origin and validity of the collective Lamb shift. A complete model including the multiple reflections in the nanocell reproduces accurately the observed line shape. It allows the extraction of a density-dependent shift and width of the bulk atomic medium resonance, deconvolved from the cavity effect. We observe an additional, unexpected dependence of the shift with the thickness of the medium. This extra dependence demands further experimental and theoretical investigations.
