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Journal of Physics Conference Series

Light-induced atomic desorption in cells with different PDMS coatings

S. Tsvetkov, S. Gateva, Marian A. Taslakov, E. Mariotti, S. Cartaleva

Published May 15, 2014• 5 citations
Publisher

Abstract

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.

DOI
10.1088/1742-6596/514/1/012030

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Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE•Oct 8, 2010•1 citation
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.
An investigation of the influence of light-induced atomic desorption (LIAD) on the transmission spectra from point of view of LIAD application for miniaturization of magneto-optical sensors and anti-relaxation coatings diagnostics is reported. With reduction of the dimensions of the cells, the amplitude of the signals decreases and it can be compensated by increasing the atomic density with temperature using special high temperature anti-relaxation coatings, or by LIAD. LIAD is a non-thermal process in which atoms adsorbed at a surface are released under illumination. It is investigated in various papers and has different applications - vapor density stabilization, MOT loading, surface nanostructuring etc. In this work the dependence of the shape of the absorption spectra on the laser power and blue light power is measured and analysis of the influence of different factors is done. All measurements are performed on the Rb D2 line in 3 different vacuum cells (uncoated, paraffin coated and SC-77 coated) with a 460 nm light emitting diode illumination. The good knowledge of the factors influencing the alkali atom spectra will be useful not only for the development of new alloptical sensors, but for study atom-dielectric surface interactions and development of new all-optical methods for surface and coating diagnostics.
The dynamics of Light-Induced Atomic Desorption (LIAD) in 6 cells with different coatings (PDMS coated cells prepared with two different concentrations of PDMS in ether, SC-77, PCHS, DCDMS, OTS) is investigated. The rates of desorption and adsorption of the Rb atoms when the illuminating light is switched ON and OFF and their dependence on the illuminating blue-light power are measured. The influence of the homogeneity of illumination for increasing the desorption and adsorption rates is evaluated. The results are interesting for the better understanding of LIAD and its dynamics and for the development of new optoelectronic elements, LIAD-loaded atomic devices and their miniaturization, and new methods for surface and coating diagnostics.
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.
This work is devoted to a systematic study of the effect of Light-Induced Atomic Desorption (LIAD). LIAD is a non-heating process in which atoms adsorbed on a surface are desorbed by illumination with non-resonant light. The aim of the dissertation is an experimental study of the LIAD process, its influence on the spectra of alkali atoms in optical cells without and with Anti-Relaxation Coating (ARC) and the possibilities of LIAD for optical characterization of ARC, as well as in high resolution spectroscopy. For the first time, the LIAD process under homogeneous illumination was investigated experimentally, whereby the efficiency of the LIAD was significantly increased even for a cell without ARC, the dynamic characteristics are obtained with a better signal to noise ratio and repeatability, and the desorption and adsorption processes are faster. LIAD effect in cells with different ARC coatings has shown that each coating has different desorption and adsorption rates and the results obtained show the possibility of applying the method for optical characterization of ARC. An experimental study of the number of collisions without atomic spin depolarization in cells with different ARCs and the impact of LIAD was performed, as well as various parameters such as laser intensity and cell temperature were investigated.
We studied the light-induced atomic desorption (LIAD) at different geometries and homogeneities of cell illumination. An original system for homogeneous illumination of the cells was developed and the Rb D2 line absorption spectra in several uncoated and coated cells were compared without illumination, with single-side illumination and with homogeneous illumination. The transmission as a function of the illumination intensity and the tuning direction was measured. The absorption coefficients with and without illumination of the stem were compared. The system developed for homogeneous illumination increases the efficiency of the LIAD, enables the investigation of LIAD without lateral diffusion, prevents cluster formation and reduces the influence of the stem. A good knowledge of the factors influencing the alkali atom spectra will be useful not only for the development of new LIAD-loaded atomic devices and their miniaturization, but also for the study of atom-dielectric surface interactions and the development of new all-optical methods for surface and coating diagnostics.
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.