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New Insight on the Hydrogen Absorption Evolution of the Mg–Fe–H System under Equilibrium Conditions
oleh: Julián Puszkiel, M. Victoria Castro Riglos, José M. Ramallo-López, Martin Mizrahi, Thomas Gemming, Claudio Pistidda, Pierre Arneodo Larochette, José Bellosta von Colbe, Thomas Klassen, Martin Dornheim, Fabiana Gennari
| Format: | Article |
|---|---|
| Diterbitkan: | MDPI AG 2018-11-01 |
Deskripsi
Mg<sub>2</sub>FeH<sub>6</sub> is regarded as potential hydrogen and thermochemical storage medium due to its high volumetric hydrogen (150 kg/m<sup>3</sup>) and energy (0.49 kWh/L) densities. In this work, the mechanism of formation of Mg<sub>2</sub>FeH<sub>6</sub> under equilibrium conditions is thoroughly investigated applying volumetric measurements, X-ray diffraction (XRD), X-ray absorption near edge structure (XANES), and the combination of scanning transmission electron microscopy (STEM) with energy-dispersive X-ray spectroscopy (EDS) and high-resolution transmission electron microscopy (HR-TEM). Starting from a 2Mg:Fe stoichiometric powder ratio, thorough characterizations of samples taken at different states upon hydrogenation under equilibrium conditions confirm that the formation mechanism of Mg<sub>2</sub>FeH<sub>6</sub> occurs from elemental Mg and Fe by columnar nucleation of the complex hydride at boundaries of the Fe seeds. The formation of MgH<sub>2</sub> is enhanced by the presence of Fe. However, MgH<sub>2</sub> does not take part as intermediate for the formation of Mg<sub>2</sub>FeH<sub>6</sub> and acts as solid-solid diffusion barrier which hinders the complete formation of Mg<sub>2</sub>FeH<sub>6</sub>. This work provides novel insight about the formation mechanism of Mg<sub>2</sub>FeH<sub>6</sub>.