Magnetized/charged MgH2-based hydrogen storage materials

We propose two methods to facilitate the Mg-H bond cleavage of magnesium hydride Mg H2. We found via density functional calculations that Mn (or Fe), when inserted between two Mg H2, exhibits a much higher catalytic activity than the other 3d transition metal elements because of the induced spin pol...

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Main Authors: Tsuda, Muneyuki, Diño, Wilson Agerico, Kasai, Hideaki, Nakanishi, Hiroshi
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Published: Animo Repository 2005
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Online Access:https://animorepository.dlsu.edu.ph/faculty_research/3267
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Institution: De La Salle University
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spelling oai:animorepository.dlsu.edu.ph:faculty_research-42282022-05-12T07:44:40Z Magnetized/charged MgH2-based hydrogen storage materials Tsuda, Muneyuki Diño, Wilson Agerico Kasai, Hideaki Nakanishi, Hiroshi We propose two methods to facilitate the Mg-H bond cleavage of magnesium hydride Mg H2. We found via density functional calculations that Mn (or Fe), when inserted between two Mg H2, exhibits a much higher catalytic activity than the other 3d transition metal elements because of the induced spin polarization of the Mg H2. We also found that an ionized Mg H2 (Mg H2+) has considerably softer Mg-H bonds. We can thus significantly reduce the H2 desorption temperatures from Mg H2 to practical levels, ~400 K, by forming an alloy hydride with Mn (or Fe), and/or ionizing the Mg H2. © 2005 American Institute of Physics. 2005-05-23T07:00:00Z text https://animorepository.dlsu.edu.ph/faculty_research/3267 Faculty Research Work Animo Repository Magnesium Hydrides Physics
institution De La Salle University
building De La Salle University Library
continent Asia
country Philippines
Philippines
content_provider De La Salle University Library
collection DLSU Institutional Repository
topic Magnesium
Hydrides
Physics
spellingShingle Magnesium
Hydrides
Physics
Tsuda, Muneyuki
Diño, Wilson Agerico
Kasai, Hideaki
Nakanishi, Hiroshi
Magnetized/charged MgH2-based hydrogen storage materials
description We propose two methods to facilitate the Mg-H bond cleavage of magnesium hydride Mg H2. We found via density functional calculations that Mn (or Fe), when inserted between two Mg H2, exhibits a much higher catalytic activity than the other 3d transition metal elements because of the induced spin polarization of the Mg H2. We also found that an ionized Mg H2 (Mg H2+) has considerably softer Mg-H bonds. We can thus significantly reduce the H2 desorption temperatures from Mg H2 to practical levels, ~400 K, by forming an alloy hydride with Mn (or Fe), and/or ionizing the Mg H2. © 2005 American Institute of Physics.
format text
author Tsuda, Muneyuki
Diño, Wilson Agerico
Kasai, Hideaki
Nakanishi, Hiroshi
author_facet Tsuda, Muneyuki
Diño, Wilson Agerico
Kasai, Hideaki
Nakanishi, Hiroshi
author_sort Tsuda, Muneyuki
title Magnetized/charged MgH2-based hydrogen storage materials
title_short Magnetized/charged MgH2-based hydrogen storage materials
title_full Magnetized/charged MgH2-based hydrogen storage materials
title_fullStr Magnetized/charged MgH2-based hydrogen storage materials
title_full_unstemmed Magnetized/charged MgH2-based hydrogen storage materials
title_sort magnetized/charged mgh2-based hydrogen storage materials
publisher Animo Repository
publishDate 2005
url https://animorepository.dlsu.edu.ph/faculty_research/3267
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