Set forth herein are compositions comprising A.(LiBH.sub.4).B.(LiX).C.(LiNH.sub.2), wherein X is fluorine, bromine, chloride, iodine, or a combination thereof, and wherein 0.1≤A≤3, 0.1≤B≤4, and 0≤C≤9 that are suitable for use as solid electrolyte separators in lithium electrochemical devices. Also set forth herein are methods of making A.(LiBH.sub.4).B.(LiX).C.(LiNH.sub.2) compositions. Also disclosed herein are electrochemical devices which incorporate A.(LiBH.sub.4).B.(LiX).C.(LiNH.sub.2) compositions and other materials.

The present invention relates to a method for producing tetrahydridoborate salts with high efficiency at low cost. The method for the production of metal borohydride salts according to the present invention comprises the steps of providing an anhydrous metal borate salt and milling the anhydrous metal borate salt in the presence of a metal material based on magnesium or magnesium alloys in a hydrogen atmosphere at a temperature and for a time sufficient to produce the metal borohydride salt. In another embodiment of the invention, the method for the production of metal borohydride salts according to the present invention comprises the steps of providing an hydrated metal borate salt and milling the hydrated metal borate salt in the presence of a metal material based on magnesium or magnesium alloys in an inert gas atmosphere at a temperature and for a time sufficient to produce the metal borohydride salts. In a still further embodiment of the invention, the metal material based on magnesium or magnesium alloys is a secondary magnesium material, preferably a Class 2, Class 3, or Class 6 secondary magnesium material.

The present invention relates to a method for producing tetrahydridoborate salts with high efficiency at low cost. The method for the production of metal borohydride salts according to the present invention comprises the steps of providing an anhydrous metal borate salt and milling the anhydrous metal borate salt in the presence of a metal material based on magnesium or magnesium alloys in a hydrogen atmosphere at a temperature and for a time sufficient to produce the metal borohydride salt. In another embodiment of the invention, the method for the production of metal borohydride salts according to the present invention comprises the steps of providing an hydrated metal borate salt and milling the hydrated metal borate salt in the presence of a metal material based on magnesium or magnesium alloys in an inert gas atmosphere at a temperature and for a time sufficient to produce the metal borohydride salts. In a still further embodiment of the invention, the metal material based on magnesium or magnesium alloys is a secondary magnesium material, preferably a Class 2, Class 3, or Class 6 secondary magnesium material.

A method for producing a tetrahydroborate is disclosed. The method includes a plasma treatment step of exposing a borate to a hydrogen plasma. The method also includes that the plasma treatment is performed using hydrogen plasma generated by microwave or RF excitation, and the plasma treatment is performed while heating the borate at a temperature between 40° C. and 300° C.

An allotrope-specific reagent includes a hydride molecule in complex with a specified elemental allotrope. The elemental allotrope included in the complex substantially retains a specified allotropic structure of the bulk element. For example, the reagent can contain a specified allotrope of carbon, such as amorphous carbon, diamond, or graphite. The allotrope-specific reagent can be useful for the synthesis of allotropic nanoparticles. A method for synthesizing the allotrope-specific reagent includes a step of ball-milling a mixture that includes a bulk hydride molecule, such as lithium borohydride powder, and a powder of a specified elemental allotrope.

An allotrope-specific reagent includes a hydride molecule in complex with a specified elemental allotrope. The elemental allotrope included in the complex substantially retains a specified allotropic structure of the bulk element. For example, the reagent can contain a specified allotrope of carbon, such as amorphous carbon, diamond, or graphite. The allotrope-specific reagent can be useful for the synthesis of allotropic nanoparticles. A method for synthesizing the allotrope-specific reagent includes a step of ball-milling a mixture that includes a bulk hydride molecule, such as lithium borohydride powder, and a powder of a specified elemental allotrope.

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.

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.

A device for producing a tetrahydroborate, the device including a reaction chamber inside which a hydrogen plasma is generated, a sample stage which is provided in the reaction chamber and on which a borate is placed, and a hydrogen ion shielding member which is provided to cover at least some of the borate to be placed.

A device for producing a tetrahydroborate, the device including a reaction chamber inside which a hydrogen plasma is generated, a sample stage which is provided in the reaction chamber and on which a borate is placed, and a hydrogen ion shielding member which is provided to cover at least some of the borate to be placed.