A hydrogen storage composite material includes: a graphene oxide framework provided as a porous structure and having an average pore diameter of 1 to 2 nm; and the graphene oxide framework is impregnated with a metal hydride, the graphene oxide framework comprises: a graphene oxide; and a linker connecting the graphene oxide.

A method for preparing a magnesium-based hydrogen storage material, includes: a Mg—Ce—Ni family amorphous alloy is prepared by a rapid cooling process; the amorphous alloy is pulverized, so as to obtain a amorphous powder; the amorphous alloy is activated, so as to obtain a MgH.sub.2—Mg.sub.2NiH.sub.4—CeH.sub.2.73 family nanocrystalline composite; the abovementioned composite is carried out a hydrogen absorption and desorption cycle, then the composite is placed in a pure Ar atmosphere for passivation, finally, the passivated composite is oxidized, so as to obtain a MgH.sub.2—Mg.sub.2NiH.sub.4—CeH.sub.2.73—CeO.sub.2 family nanocrystalline composite.

A method and a system is provided for obtaining solid-state hydrogen storage and release in materials with at least theoretical loaded hydrogen densities of 11 wt % or greater that can deliver hydrogen and be recharged at moderate temperatures enabling incorporation into hydrogen storage systems suitable for transportation applications. These materials comprise ternary boride materials comprising certain light transition metals and alkaline or alkaline earth metals, and ideally have no or very little phase separation. A process of making these materials is also provided.

Disclosed is a method for preparing a reduced graphene oxide-magnesium nanocrystal composite. The method includes contacting graphene oxide with a first reducing agent to prepare a reduced graphene oxide, and co-reducing the reduced graphene oxide and a precursor of magnesium in the presence of a second reducing agent to prepare a reduced graphene oxide-magnesium nanocrystal composite, wherein by adjusting the amount of the first reducing agent in contact with the graphene oxide, the size of the magnesium nanocrystals in the composite may be controlled.

The present invention concerns a hydrogen store comprising a hydrogenable material, and a method for producing a hydrogen store.

A hydrogen storage composition, a hydrogen storage container and a method for producing the hydrogen storage container are provided. The hydrogen storage composition includes a thermally-conductive material, a hydrogen storage material, and optionally a granular elastic material. The hydrogen storage container includes a canister body and the hydrogen storage composition. After the hydrogen storage composition is placed into a canister body, a vacuum environment within the canister body is created, and a first weight of the canister body is recorded. Then, hydrogen gas is charged into the canister body, and a second weight of the canister body is recorded. Then, a hydrogen storage amount is calculated according to the first weight and the second weight. If the hydrogen storage amount reaches the predetermined value, the hydrogen storage container is produced.

Provided is a core/shell composite that includes a core portion containing a heat resistant material selected from an inorganic oxide, a ceramic, a mineral and the like and having rigidity, and at least one layer of shell portion containing a hydrogen absorbing/desorbing metal covering the entire or a part of the core portion. The heat resistant material contained in the core portion has a melting point higher than the highest melting point among the hydrogen absorbing/desorbing metal contained in the shell portion. In a method for producing the core/shell composite, the core portion is covered with the shell portion by deposition in the absence of oxygen.

This disclosure relates to novel metal hydrides, processes for their preparation, and their use in hydrogen storage applications.

The present invention relates to a composite material for hydrogen storage based on metal hydrides and to a method of operating a hydrogen storage system based on metal hydrides capable of releasing and absorbing hydrogen. Such hydrogen storage systems based on metal hydrides may be applicable as a fuel source for a fuel cell. The composite material for hydrogen storage comprises a powder or pellets of a hydride and a phase changing material (PCM), wherein the PCM is an encapsulated phase changing material (EPCM) which is homogeneously dispersed within the powder or pellets of the hydride.

A provided ammonia synthesis catalyst is a composite catalyst including: a catalyst exhibiting catalytic activity for synthesis of ammonia; and a support supporting the catalyst. The support includes a hydrogen storage material. The hydrogen storage material is, for example, a hydrogen storage metal. The hydrogen storage metal is, for example, a hydrogen storage alloy. The hydrogen storage alloy is, for example, a solid solution. The hydrogen storage alloy is, for example, a Ti—Mn-based alloy. The catalyst includes, for example, a transition metal. The transition metal is, for example, at least one selected from the group consisting of Ru, Co, Ni, Fe, Mn, V, and Ti.