Computational design of multi-states monomolecular device using molecular hydrogen and C20 isomers

Аннотация

We perform detailed calculations for the interaction of molecular hydrogen with C₂₀isomers in the framework of density functional theory method. The adsorption of H₂ outside the C₂₀-e isomer with parallel orientation with respect to the plane of the hexagon is found to be the most stable adsorption configuration. Thus this might have potential for the hydrogen storing. We have also investigated the number and the position of adsorption sites in the pentagon for the parallel configurations of the H₂/C₂₀ systems. We find two stable configurations of the molecule for the C₂₀-bowl isomer that have a small difference in energy. Thus, surprisingly, despite their apparent simplicity these H₂/C₂₀-bowl systems are shown to exhibit the flip-flop motion by a small current pulse. Hence, it might be a candidate for multi-states monomolecular device. Convenient experimental techniques such as field emission microscopy are proposed to test these predictions.