Nanoconfinement in activated mesoporous carbon of calcium borohydride for improved reversible hydrogen storage.

Mesoporous carbon frameworks were synthesized using the soft-template method. Ca(BH(4))(2) was incorporated into activated mesoporous carbon by the incipient wetness method. The activation of mesoporous carbon was necessary to optimize the surface area and pore size. Thermal programmed absorption measurements showed that the confinement of this borohydride into carbon nanoscaffolds improved its reversible capacity (relative to the reactive portion) and performance of hydrogen storage compared to unsupported borohydride. Hydrogen release from the supported hydride started at a temperature as low as 100 °C and the dehydrogenation rate was fast compared to the bulk borohydride. In addition, the hydrogen pressure necessary to regenerate the borohydride from the dehydrogenation products was reduced.

Improvement of dehydrogenation kinetics of LiBH(4) dispersed on modified multi-walled carbon nanotubes.

The dehydrogenation kinetics of LiBH(4) dispersed on multi-walled carbon nanotubes (MWCNTs) by the solvent infiltration technique has been studied. Commercial MWCNTs were ball-milled for different milling times in order to increase the specific surface area (SSA) as measured by the BET technique. Thermal programmed desorption measurements have been performed using a Sievert's apparatus on samples with different SSA of MWCNTs and different LiBH(4) to MWCNT ratio. Pressure composition isotherms (PCI) have been obtained at different temperatures in order to estimate the DeltaH and DeltaS of dehydrogenation. It has been observed that the dispersion of LiBH(4) on MWCNTs leads to a lower dehydrogenation temperature compared to pure LiBH(4). Moreover, the dehydrogenation temperature further decreases with increasing MWCNT surface area. An interpretation of the kinetic effect is proposed.