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dc.contributor.authorLei Wang
dc.contributor.authorQuadir, Md Zakaria
dc.contributor.authorKondo-Francois Aguey-Zinsou
dc.date.accessioned2017-01-30T14:33:15Z
dc.date.available2017-01-30T14:33:15Z
dc.date.created2016-10-26T19:30:22Z
dc.date.issued2016
dc.identifier.citationLei Wang and Quadir, M.Z. and Kondo-Francois Aguey-Zinsou 2016. Direct and reversible hydrogen storage of lithium hydride (LiH) nanoconfined in high surface area graphite. International Journal of Hydrogen Energy. 41 (40): pp. 18088-18094.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/39361
dc.identifier.doi10.1016/j.ijhydene.2016.07.073
dc.description.abstract

LiH has great potential as a high capacity hydrogen storage material (12 wt.%), however its thermodynamic stability has so far precluded practical application. Temperatures near 700 °C are required for hydrogen release and uptake. Herein, we report on a novel method to realise hydrogen uptake and release under milder temperature conditions without using any catalyst or alloying. Through nanoconfinement within the pores (2–20 nm) of high surface area graphite (HSAG) LiH displayed remarkable hydrogen storage properties and was able to release 1.9 wt.% of hydrogen from 200 °C. Reversibility was also achieved under the moderate conditions of 300 °C and 6 MPa hydrogen pressure. This demonstrates that the properties of LiH are particle size dependent and thus leads to new possibilities to realise the potential of LiH as a practical high capacity hydrogen storage material.

dc.publisherElsevier Ltd
dc.titleDirect and reversible hydrogen storage of lithium hydride (LiH) nanoconfined in high surface area graphite
dc.typeJournal Article
dcterms.source.volume41
dcterms.source.startPage18088
dcterms.source.endPage18094
dcterms.source.issn1879-3487
dcterms.source.titleInternational Journal of Hydrogen Energy
curtin.departmentJohn de Laeter CoE in Mass Spectrometry
curtin.accessStatusFulltext not available


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