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Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE

Atomic sources controlled by light: main features and applications

Andrea Bogi, A. Burchianti, C. de Mauro, Silvia Gozzini, A. Lucchesini, C. Marinelli, E. Mariotti, Luca Marmugi, L. Moi

Published Oct 8, 2010• 1 citation

Abstract

We present in this paper recent results on Light - Induced Atom Desorption (LIAD) in sealed and open coated cells. LIAD is defined via the description of an experiment on rubidium atoms stored in a dry - film coated cell, where a few milliwatts of even non coherent and non resonant light are able to increase the alkali atomic density for more than one order of magnitude. Modeling of the effect is given. New features become relevant in the case of LIAD in porous glasses: in fact, although the photodesorption efficiency per unit area in bare glass is much lower, photoatomic sources can be prepared, due to the huge inner surface of porous samples. We applied LIAD from organic coatings to the stabilization of alkali densities out of equilibrium: sodium case is here discussed. Finally, we report on fully original, preliminary measurements of rubidium Magneto - Optical Trap loading via LIAD from a dry - film coated cell.

DOI: 10.1117/12.885326

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We present in this paper recent results on Light - Induced Atom Desorption (LIAD) in sealed and open coated cells. LIAD is defined via the description of an experiment on rubidium atoms stored in a dry - film coated cell, where a few milliwatts of even non coherent and non resonant light are able to increase the alkali atomic density for more than one order of magnitude. Modeling of the effect is given. New features become relevant in the case of LIAD in porous glasses: in fact, although the photodesorption efficiency per unit area in bare glass is much lower, photoatomic sources can be prepared, due to the huge inner surface of porous samples. We applied LIAD from organic coatings to the stabilization of alkali densities out of equilibrium: sodium case is here discussed. Finally, we report on fully original, preliminary measurements of rubidium Magneto - Optical Trap loading via LIAD from a dry - film coated cell.

We review some recent studies on light-induced atomic desorption (LIAD) from dielectric surfaces. Alkali-metal atoms adsorbed either on organic films or on porous glass are released into the vapor phase under illumination. The measurements were performed in Pyrex resonance cells either coated with siloxane films or containing a porous glass sample. In both cases, the experimental results show that LIAD can be used to produce atomic densities suitable for most atomic physics experiments. Moreover, we find that photoinduced effects, correlated with LIAD, produce reversible formation and evaporation of alkali-metal clusters in porous glass. These processes depend on the light frequency, making the porous glass transmittance controllable by light.

We report the first experimental evidence of nonthermal light induced atomic desorption (LIAD) from octadecyltrichlorosilane dry film. The experiment has been made with Rb confined in a coated cell kept at room temperature. A detailed study of the main features of LIAD effect has been made by varying intensity and wavelength of desorbing light. A discussion about the differences and similarities with other organic films that were studied first is reported. This result is important as it expands the list of materials showing such an effect and increases the possibilities to get suitable light controlled atomic sources for spectroscopy and applications. In particular, we plan to exploit this feature in a Fr magneto-optical trap apparatus.

Light-induced atomic desorption (LIAD) is a non-thermal process in which atoms adsorbed at a surface are released under illumination. It is applied mostly to implementing optical dispensers in the cases when high atomic density at low temperature is needed – for example, for loading atomic devices as atomic magnetometers, atomic clocks, magneto-optical traps and their miniaturization. However, as the desorption depends on the atom-surface interaction, it can also be used for optical characterization and manipulation of alkali metal nanoparticles. The paper describes an experimental investigation of the shape of the transmission spectra and their dependence on the illuminating blue-light power in PDMS coated cells prepared with two different concentrations of PDMS in ether. A comparison is conducted with the LIAD effect in SC-77 coated and in uncoated cells. All measurements are performed on the Rb D2 line in vacuum. The potential is discussed for application of these dependences to analyzing the quality of the coating surface and its optimization.

We report some preliminary results on experimental investigation of the potential of Light Induced Atomic Desorption (LIAD) applications for density control in antirelaxation coated cells and coherent spectroscopy. LIAD is a non-thermal process whereby atoms adsorbed on a surface are released under illumination. It is applied mostly to implementing optical atomic dispensers in the cases when high atomic density at low temperature is needed - for example, for loading atomic devices as atomic magnetometers, atomic clocks, atomic traps and their miniaturization. An advantage of the light control is that it is faster than the temperature control. More than an order of increase of the density with LIAD is obtained. Some peculiarities in the 780 nm absorption and fluorescence spectra registered in dense Rb vapor are registered. The absorption and fluorescence spectra in Rb vapors controlled by temperature and LIAD are compared.

Atomic-vapor density change due to light induced atomic desorption (LIAD) is studied in paraffin-coated rubidium, cesium, sodium, and potassium cells. In the present experiment, low-intensity probe light is used to obtain an absorption spectrum and measure the vapor density, while light from an argon-ion laser, array of light emitting diodes, or discharge lamp is used for desorption. Potassium is found to exhibit significantly weaker LIAD from paraffin compared to Rb and Cs, and we were unable to observe LIAD with sodium. A simple LIAD model is applied to describe the observed vapor-density dynamics, and the role of the cell's stem is explored through the use of cells with lockable stems. Stabilization of Cs vapor density above its equilibrium value over

25\phantom{\rule{0.3em}{0ex}}\mathrm{min}

is demonstrated. The results of this work could be used to assess the use of LIAD for vapor-density control in magnetometers, clocks, and gyroscopes utilizing coated cells.