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Register a new userResolution-enhanced quantitative spectroscopy of atomic vapor in optical nanocells based on second-derivative processing of spectra
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We present a method for recovery of narrow homogeneous spectral features out of broad inhomogeneous overlapped profile based on second-derivative processing of the absorption spectra of alkali metal atomic vapor nanocells. The method is shown to preserve the frequency positions and amplitudes of spectral transitions, thus being applicable for quantitative spectroscopy. The proposed technique was successfully applied and tested for: measurements of hyperfine splitting and atomic transition probabilities; development of an atomic frequency reference; determination of isotopic abundance; study of atom-surface interaction; and determination of magnetic field-induced modification of atomic transitions frequency and probability. The obtained experimental results are fully consistent with theoretical modeling.
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We investigate an integrated optical chip immersed in atomic vapor providing several waveguide geometries for spectroscopy applications. The narrow-band transmission through a silicon nitride waveguide and interferometer is altered when the guided light is coupled to a vapor of rubidium atoms via the evanescent tail of the waveguide mode. We use grating couplers to couple between the waveguide mode and the radiating wave, which allow for addressing arbitrary coupling positions on the chip surface. The evanescent atom-light interaction can be numerically simulated and shows excellent agreement with our experimental data. This work demonstrates a next step towards miniaturization and integration of alkali atom spectroscopy and provides a platform for further fundamental studies of complex waveguide structures.
Traditionally, measuring the center-of-mass (c.m.) velocity of an atomic ensemble relies on measuring the Doppler shift of the absorption spectrum of single atoms in the ensemble. Mapping out the velocity distribution of the ensemble is indispensable when determining the c.m. velocity using this technique. As a result, highly sensitive measurements require preparation of an ensemble with a narrow Doppler width. Here, we use a dispersive measurement of light passing through a moving room temperature atomic vapor cell to determine the velocity of the cell in a single shot with a short-term sensitivity of 5.5 $mu$m s$^{-1}$ Hz$^{-1/2}$. The dispersion of the medium is enhanced by creating quantum interference through an auxiliary transition for the probe light under electromagnetically induced transparency condition. In contrast to measurement of single atoms, this method is based on the collective motion of atoms and can sense the c.m. velocity of an ensemble without knowing its velocity distribution. Our results improve the previous measurements by 3 orders of magnitude and can be used to design a compact motional sensor based on thermal atoms.
By measuring the transmission of near-resonant light through an atomic vapor confined in a nano-cell we demonstrate a mesoscopic optical response arising from the non-locality 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 non-local, 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.
We describe a simple strontium vapor cell for laser spectroscopy experiments. Strontium vapor is produced using an electrically heated commercial dispenser source. The sealed cell operates at room temperature, and without a buffer gas or vacuum pump. The cell was characterised using laser spectroscopy, and was found to offer stable and robust operation, with an estimated lifetime of >10,000 hours. By changing the dispenser, this technique can be readily extended to other alkali and alkaline earth elements.
Nonlinear magneto-optical (NMO) resonances occurring for near-zero magnetic field are studied in Rb vapor using light-noise spectroscopy. With a balanced detection polarimeter, we observe high contrast variations of the noise power (at fixed analysis frequency) carried by diode laser light resonant with the 5S$_{1/2}(F=2) to 5$P$_{1/2}(F=1) $ transition of $^{87}$Rb and transmitted through a rubidium vapor cell, as a function of magnetic field $B$. A symmetric resonance doublet of anti-correlated noise is observed for orthogonal polarizations around $B=0 $ as a manifestation of ground state coherence. We also observe sideband noise resonances when the magnetic field produces an atomic Larmor precession at a frequency corresponding to one half of the analysis frequency. The resonances on the light fluctuations are the consequence of phase to amplitude noise conversion owing to nonlinear coherence effects in the response of the atomic medium to the fluctuating field. A theoretical model (derived from linearized Bloch equations) is presented that reproduces the main qualitative features of the experimental signals under simple assumptions.
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