We present here the first evidence of photodesorption induced by low-intensity non-resonant light from an yttrium thin foil, which works as a neutralizer for Rb and Fr ions beam. Neutral atoms are suddenly ejected from the metal surface in a pulsed regime upon illumination with a broadband flash light and then released in the free volume of a pyrex cells. Here atoms are captured by a Magneto-Optical Trap (MOT), which is effectively loaded by the photodesorption. Loading times of the order of the flash rise time are measured. Desorption is also obtained in the continuous regime, by exploiting CW visible illumination of the metallic neutralizer surface. We demonstrate that at lower CW light intensities vacuum conditions are not perturbed by the photodesorption and hence the MOT dynamics remains unaffected, while the trap population increases thanks to the incoming desorbed atoms flux. Even with the Y foil at room temperature and hence with no trapped atoms, upon visible illumination, the number of trapped atoms reaches 10(5). The experimental data are then analyzed by means of an analytical rate equation model, which allows the analysis of this phenomenon and its dynamics and allows the determination of critical experimental parameters and the test of the procedure in the framework of radioactive Francium trapping. In this view, together with an extensive investigation of the phenomenon with (85)Rb, the first demonstration of the photodesorption-aided loading of a (210)Fr MOT is shown.
Nowadays, the use of lasers has become commonplace in everyday life, and laser protection has become an important field of scientific investigation, as well as a security issue. In this context, optical limiters are receiving increasing attention. This work focuses on the identification of the significant parameters affecting optical limiting properties of aqueous suspensions of pristine single-wall carbon nanohorns. The study is carried out on the spectral range, spanning from ultraviolet to near-infrared (355, 532 and 1064 nm). Optical nonlinear properties are systematically investigated as a function of nanohorn morphology, concentration, dimensions of aggregates, sample preparation procedure, nanostructure oxidation and the presence and concentration of surfactants to identify the role of each parameter in the nonlinear optical behavior of colloids. The size and morphology of individual nanoparticles were identified to primarily determine optical limiting. A cluster size effect was also demonstrated, showing more effective optical limiting in larger aggregates. Most importantly, we describe an original approach to identify the dominant nonlinear mechanism. This method requires simple transmittance measurements and a fitting procedure. In our suspensions, nonlinearity was identified to be of electronic origin at a 532 nm wavelength, while at 355 nm, it was found in the generation of bubbles.
We present a setup devoted to the study of adsorption and desorption processes of alkali atoms after deposition on a 300 nm thick porous alumina substrate in an Ultra High Vacuum chamber. Rubidium atoms, delivered by a dispenser source, enter the 20-30 nm diameter pores, diffuse in and stick to their walls. A 1 W power laser is used in order to induce detachment and take the atoms back in the vapor phase in a very tight confinement region. The desorbed atoms coming out the sample can be monitored via both a resonant optical detection and an electronic amplifier after ionization. The desorbing laser is also able to promote the formation of Rubidium nanoparticles, as the high Rb vapor density in the pores favors aggregation around nucleation point defects. In this way, the apparatus allows for the study of the fundamental processes related to atom – surface interactions in presence of light as well as of several promising application to nanomaterials.
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