Abstract
Hydrogen storage technology plays an important role on the development of hydrogen fuel cell and lithium aluminum hydride is a powerful candidate for solid-state hydrogen storage materials. However, the high stability and slow dehydrogenation kinetics of LiAlH4 hinder its application. In this paper, the two-step thermal decomposition properties of LiAlH4 with and without Fe–Fe2O3 catalysts are investigated. According to the master plots, the model of mample power law (Pn) and nucleation and growth (An) are the optimal mechanism functions for the two-step decomposition of LiAlH4, respectively. After doping catalysts, the activation energies decrease significantly. The theoretical and optimized kinetic method are consistent with each other on activation energy. And the latter can also yield other kinetic parameters for a more comprehensive kinetic modelling of LiAlH4 decomposition. Furthermore, Fe–Al2O3 and Fe–Al intermetallics generated during dehydrogenation might significantly improve the hydrogen release properties of LiAlH4.
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