Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (8/8 displayed)

  • 2023Hydrogen Absorption Reactions of Hydrogen Storage Alloy LaNi5 under High Pressure32citations
  • 2022Magnesium- and intermetallic alloys-based hydrides for energy storage : modelling, synthesis and properties78citations
  • 2022Magnesium- and intermetallic alloys-based hydrides for energy storage: modelling, synthesis and properties ; ENEngelskEnglishMagnesium- and intermetallic alloys-based hydrides for energy storage: modelling, synthesis and properties78citations
  • 2022Magnesium- and intermetallic alloys-based hydrides for energy storage: modelling, synthesis and properties78citations
  • 2020Pseudo-ternary LiBH4-LiCl-P2S5 system as structurally disordered bulk electrolyte for all-solid-state lithium batteries28citations
  • 2020Materials for hydrogen-based energy storage – past, recent progress and future outlook742citations
  • 2020Pseudo-ternary LiBH 4 ·LiCl·P 2 S 5 system as structurally disordered bulk electrolyte for all-solid-state lithium batteries28citations
  • 2003Hydrogen diffusion in metallic and nanostructured materials28citations

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Saitoh, Hiroyuki
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Co-Authors (by relevance)

  • Nakahira, Yuki
  • Saitoh, Hiroyuki
  • Obana, Kazuki
  • Takagi, Shigeyuki
  • Ito, Junya
  • Utsumi, Reina
  • Cuevas, Fermin
  • Latroche, Michel
  • Sørby, Magnus Helgerud
  • Høgset, Astrid Bygdås
  • Hauback, Bjørn
  • Wind, Julia
  • Ruud, Amund
  • Zhang, Junxian
  • Nygård, Magnus Moe
  • Fichtner, Maximilian
  • Fjellvåg, Helmer
  • Kim, Sangryun
  • El-Kharbachi, Abdelouahab
  • Høgset, Astrid
  • El Kharbachi, Abdelouahab
  • Sørby, Magnus
  • Fjellvag, Helmer
  • Nygård, Magnus
  • Hauback, Bjorn
  • Stanik, E.
  • Majer, Günter
  • Eberle, Ulrich
  • Kimmerle, F.
OrganizationsLocationPeople

article

Hydrogen Absorption Reactions of Hydrogen Storage Alloy LaNi5 under High Pressure

  • Nakahira, Yuki
  • Saitoh, Hiroyuki
  • Obana, Kazuki
  • Takagi, Shigeyuki
  • Ito, Junya
  • Orimo, Shin-Ichi
  • Utsumi, Reina
Abstract

<jats:p>Hydrogen can be stored in the interstitial sites of the lattices of intermetallic compounds. To date, intermetallic compound LaNi5 or related LaNi5-based alloys are known to be practical hydrogen storage materials owing to their higher volumetric hydrogen densities, making them a compact hydrogen storage method and allowing stable reversible hydrogen absorption and desorption reactions to take place at room temperature below 1.0 MPa. By contrast, gravimetric hydrogen density is required for key improvements (e.g., gravimetric hydrogen density of LaNi5: 1.38 mass%). Although hydrogen storage materials have typically been evaluated for their hydrogen storage properties below 10 MPa, reactions between hydrogen and materials can be facilitated above 1 GPa because the chemical potential of hydrogen dramatically increases at a higher pressure. This indicates that high-pressure experiments above 1 GPa could clarify the latent hydrogen absorption reactions below 10 MPa and potentially explore new hydride phases. In this study, we investigated the hydrogen absorption reaction of LaNi5 above 1 GPa at room temperature to understand their potential hydrogen storage capacities. The high-pressure experiments on LaNi5 with and without an internal hydrogen source (BH3NH3) were performed using a multi-anvil-type high-pressure apparatus, and the reactions were observed using in situ synchrotron radiation X-ray diffraction with an energy dispersive method. The results showed that 2.07 mass% hydrogen was absorbed by LaNi5 at 6 GPa. Considering the unit cell volume expansion, the estimated hydrogen storage capacity could be 1.5 times higher than that obtained from hydrogen absorption reaction below 1.0 MPa at 303 K. Thus, 33% of the available interstitial sites in LaNi5 remained unoccupied by hydrogen atoms under conventional conditions. Although the hydrogen-absorbed LaNi5Hx (x &lt; 9) was maintained below 573 K at 10 GPa, LaNi5Hx began decomposing into NiH, and the formation of a new phase was observed at 873 K and 10 GPa. The new phase was indexed to a hexagonal or trigonal unit cell with a ≈ 4.44 Å and c ≈ 8.44 Å. Further, the newly-formed phase was speculated to be a new hydride phase because the Bragg peak positions and unit cell parameters were inconsistent with those reported for the La-Ni intermetallic compounds and La-Ni hydride phases.</jats:p>

Topics
  • density
  • impedance spectroscopy
  • compound
  • phase
  • experiment
  • Hydrogen
  • intermetallic
  • interstitial
  • synchrotron radiation X-ray diffraction