Atoms and Nanoparticles of Transition Metals as Catalysts for Hydrogen Desorption from Magnesium Hydride
The hydrogen desorption kinetics of composite materials made of magnesium hydride with transition metal additives (TM: Nb, Fe, and Zr) was studied by several experimental techniques showing that (i) a few TM at.% concentrations catalyse the H2 desorption process, (ii) the H2 desorption kinetics resu...
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Series: | Journal of Nanomaterials |
Online Access: | http://dx.doi.org/10.1155/2011/865969 |
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doaj-bf14f468628246c19b3afa3a14fcba8f2020-11-24T22:56:14ZengHindawi LimitedJournal of Nanomaterials1687-41101687-41292011-01-01201110.1155/2011/865969865969Atoms and Nanoparticles of Transition Metals as Catalysts for Hydrogen Desorption from Magnesium HydrideN. Bazzanella0R. Checchetto1A. Miotello2Dipartimento di Fisica Università degli Studi di Trento, 38123 Povo, ItalyDipartimento di Fisica Università degli Studi di Trento, 38123 Povo, ItalyDipartimento di Fisica Università degli Studi di Trento, 38123 Povo, ItalyThe hydrogen desorption kinetics of composite materials made of magnesium hydride with transition metal additives (TM: Nb, Fe, and Zr) was studied by several experimental techniques showing that (i) a few TM at.% concentrations catalyse the H2 desorption process, (ii) the H2 desorption kinetics results stabilized after a few H2 sorption cycles when TM atoms aggregate by forming nanoclusters; (iii) the catalytic process occurs also at TM concentration as low as 0.06 at.% when TM atoms clustering is negligible, and (iv) mixed Fe and Zr additives produce faster H2 desorption kinetics than single additive. The improved H2 desorption kinetics of the composite materials can be explained by assuming that the interfaces between the MgH2 matrix and the TM nanoclusters act as heterogeneous sites for the nucleation of the Mg phase in the MgH2 matrix and promote the formation of fast diffusion channels for H migrating atoms.http://dx.doi.org/10.1155/2011/865969 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
N. Bazzanella R. Checchetto A. Miotello |
spellingShingle |
N. Bazzanella R. Checchetto A. Miotello Atoms and Nanoparticles of Transition Metals as Catalysts for Hydrogen Desorption from Magnesium Hydride Journal of Nanomaterials |
author_facet |
N. Bazzanella R. Checchetto A. Miotello |
author_sort |
N. Bazzanella |
title |
Atoms and Nanoparticles of Transition Metals as Catalysts for Hydrogen Desorption from Magnesium Hydride |
title_short |
Atoms and Nanoparticles of Transition Metals as Catalysts for Hydrogen Desorption from Magnesium Hydride |
title_full |
Atoms and Nanoparticles of Transition Metals as Catalysts for Hydrogen Desorption from Magnesium Hydride |
title_fullStr |
Atoms and Nanoparticles of Transition Metals as Catalysts for Hydrogen Desorption from Magnesium Hydride |
title_full_unstemmed |
Atoms and Nanoparticles of Transition Metals as Catalysts for Hydrogen Desorption from Magnesium Hydride |
title_sort |
atoms and nanoparticles of transition metals as catalysts for hydrogen desorption from magnesium hydride |
publisher |
Hindawi Limited |
series |
Journal of Nanomaterials |
issn |
1687-4110 1687-4129 |
publishDate |
2011-01-01 |
description |
The hydrogen desorption kinetics of composite materials made of magnesium hydride with transition metal additives (TM: Nb, Fe, and Zr) was studied by several experimental techniques showing that (i) a few TM at.% concentrations catalyse the H2 desorption process, (ii) the H2 desorption kinetics results stabilized after a few H2 sorption cycles when TM atoms aggregate by forming nanoclusters; (iii) the catalytic process occurs also at TM concentration as low as 0.06 at.% when TM atoms clustering is negligible, and (iv) mixed Fe and Zr additives produce faster H2 desorption kinetics than single additive. The improved H2 desorption kinetics of the composite materials can be explained by assuming that the interfaces between the MgH2 matrix and the TM nanoclusters act as heterogeneous sites for the nucleation of the Mg phase in the MgH2 matrix and promote the formation of fast diffusion channels for H migrating atoms. |
url |
http://dx.doi.org/10.1155/2011/865969 |
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