The Master Key to the Problem of Reversible Chemical Hydrogen Storage is 12 kJ (mol H2)-1

31 May 2021, Version 11
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

This article unveils on basis of the ideal gas law, the atomic conception of matter and classic equilibrium thermodynamics the ideal final regularity of reversible hydrogen mass transfer. This result allows to clarify problems of metal hydride chemistry which otherwise are impossible to understand e.g. why the substitution of 4 mol % Na by K in Ti-doped NaAlH4 raises the reversible hydrogen capacity by 42 % at no substantial change to thermodynamic reaction parameters or how the dopants take effect in (Rb/K)-co-doped Mg(NH2)2/2LiH; both cases are discussed in this context. This ideal final regularity is a hitherto missed out superposition of physical chemistry fundamentals and defines the maximum specific energy at distinct conditions: directly for two-phase hydrogen storage methods and indirectly for electrochemical systems due to the normative role of hydrogen electrode potentials.

Keywords

Reversible Hydrogen Storage Capacity
Equilibrium thermodynamics
Hydrogen Energy Storage
hydrogen storage issues
Metal Hydrides Reaction
hydrogen storage materials
metal hydrides

Supplementary materials

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V11 12article ESI Figure2
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V11 12article ESI to Figure1
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V11 12article ESI Discussion Mg-Li-N-H and Ti NaK-Al-H systems
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