Hydrogen sorption by nanostructures at low temperatures (Review article)

Abstract

The features of hydrogen sorption by a wide range of nanostructures — fullerite C60, carbon nanotubes, graphene structures, nanodispersed carbon, including Pd-containing nanoclusters, ordered silicon-oxide-based nanostructures (the MCM-41 family) and silicon-oxide aerogel — have been reviewed. Special attention is given to the sorption characteristics of carbon nanostructures that have been exposed to various modifying treatments (oxidation, gamma-ray irradiation in gas atmosphere, action of pulsed high frequency gas discharge). Two mechanisms of physical low-temperature sorption of hydrogen have been revealed to predominate in such nanostructures in different temperature intervals. At the lowest temperatures (8–12 K), the sorption can actually proceed without thermal activation: it is realized through the tunnel motion of hydrogen molecules along the nanostructure surfaces. The periodic structure of the potential relief, allowed by the surface frame of carbon and silicon-oxide nanostructures, along the rather low interpit barriers are beneficial for the formation of low-dimensional (including quantum) hydrogen-molecule systems practically without thermally activated diffusion. In such nanostructures, the hydrogen diffusion coefficients are actually independent of temperature at 8–12 K. At higher temperatures (12–295 K), a thermally activated mechanism of hydrogen diffusion prevails. The periodic structure of fullerite C60 contains periodic interstitial cavities, separated by rather low potential barriers. Their sizes are sufficient to accommodate impurity hydrogen molecules and, thus, allow diffusion processes, which can also have a tunnel nature. It is shown that gamma-irradiation and high-frequency gas discharge processing increase markedly the quantity of hydrogen strongly bonded to carbon nanostructures.