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Article: Effect of nitride additives on Li-N-H hydrogen storage system

TitleEffect of nitride additives on Li-N-H hydrogen storage system
Authors
KeywordsHydrogen storage
Amide
Solid state reaction
Nitride
Issue Date2011
Citation
International Journal of Hydrogen Energy, 2011, v. 36, n. 13, p. 7920-7926 How to Cite?
AbstractSolid state reaction between LiNH2and LiH potentially offers a practical pathway for hydrogen supply to fuel cell powered vehicles, particularly if the reaction kinetics can be further improved. Here we performed a comparative study of the effects of selected micron and nano-sized nitrides using temperature programmed desorption, mass spectrometry, X-ray diffraction and infrared spectroscopy. It was found that both micron and nano-sized BN and TiN act as effective catalysts within the system. While an increase in the concentration of TiN reduces dehydrogenation temperature, the opposite was observed for BN catalyst. Employment of both nano and micron-sized BN catalysts resulted in an almost similar dehydrogenation temperature; but dehydrogenation temperature was decreased about 20 °C by switching from micron to nano-sized TiN. The catalytic effects of the additives were proposed to be an improvement of surface reactivity and diffusion enhancement across the interface of the reactants. However, the role of BN and TiN are different in the way that TiN is likely to improve the surface reactivity of LiNH2,while BN mainly enhances diffusion across the interface of the reactants. Our findings also indicate that TiCl3behaves like TiN, as a catalyst in Li-N-H system. © 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights.
Persistent Identifierhttp://hdl.handle.net/10722/262945
ISSN
2023 Impact Factor: 8.1
2023 SCImago Journal Rankings: 1.513
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorNayebossadri, Shahrouz-
dc.contributor.authorAguey-Zinsou, Kondo Francois-
dc.contributor.authorGuo, Z. Xiao-
dc.date.accessioned2018-10-08T09:28:54Z-
dc.date.available2018-10-08T09:28:54Z-
dc.date.issued2011-
dc.identifier.citationInternational Journal of Hydrogen Energy, 2011, v. 36, n. 13, p. 7920-7926-
dc.identifier.issn0360-3199-
dc.identifier.urihttp://hdl.handle.net/10722/262945-
dc.description.abstractSolid state reaction between LiNH2and LiH potentially offers a practical pathway for hydrogen supply to fuel cell powered vehicles, particularly if the reaction kinetics can be further improved. Here we performed a comparative study of the effects of selected micron and nano-sized nitrides using temperature programmed desorption, mass spectrometry, X-ray diffraction and infrared spectroscopy. It was found that both micron and nano-sized BN and TiN act as effective catalysts within the system. While an increase in the concentration of TiN reduces dehydrogenation temperature, the opposite was observed for BN catalyst. Employment of both nano and micron-sized BN catalysts resulted in an almost similar dehydrogenation temperature; but dehydrogenation temperature was decreased about 20 °C by switching from micron to nano-sized TiN. The catalytic effects of the additives were proposed to be an improvement of surface reactivity and diffusion enhancement across the interface of the reactants. However, the role of BN and TiN are different in the way that TiN is likely to improve the surface reactivity of LiNH2,while BN mainly enhances diffusion across the interface of the reactants. Our findings also indicate that TiCl3behaves like TiN, as a catalyst in Li-N-H system. © 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights.-
dc.languageeng-
dc.relation.ispartofInternational Journal of Hydrogen Energy-
dc.subjectHydrogen storage-
dc.subjectAmide-
dc.subjectSolid state reaction-
dc.subjectNitride-
dc.titleEffect of nitride additives on Li-N-H hydrogen storage system-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.ijhydene.2011.01.088-
dc.identifier.scopuseid_2-s2.0-79957613655-
dc.identifier.volume36-
dc.identifier.issue13-
dc.identifier.spage7920-
dc.identifier.epage7926-
dc.identifier.isiWOS:000292123900070-
dc.identifier.issnl0360-3199-

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