We present an experimental study of light-induced atomic desorption (LIAD) of Rb atoms from porous alumina. The well defined geometry of the nano-structured alumina allows a description of the LIAD process at the microscopic level.
We present a study of light-induced atom desorption (LIAD) of an alkali-metal atom (Rb) in porous alumina. We observe the variation due to LIAD of the rubidium density in a vapor cell as a function of illumination time, intensity, and wavelength. The simple and regular structure of the alumina pores allows a description of the atomic diffusion in the porous medium in which the diffusion constant only depends on the known pore geometry and the atomic sticking time to the pore wall. A simple one-dimensional theoretical model is presented which reproduces the essential features of the observed signals. Fitting of the model to the experimental data gives access to the diffusion constant and consequently the atom-wall sticking time and its dependence on light intensity and wavelength. The nonmonotonic dependence of the LIAD yield on the illumination light frequency is indicative of the existence of Rb clusters in the porous medium.
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.