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dc.contributor.authorYang, J.
dc.contributor.authorBeaumont, P.
dc.contributor.authorHumphries, Terry
dc.contributor.authorJensen, C.
dc.contributor.authorLi, X.
dc.date.accessioned2017-01-30T11:03:11Z
dc.date.available2017-01-30T11:03:11Z
dc.date.created2015-12-10T04:26:07Z
dc.date.issued2015
dc.identifier.citationYang, J. and Beaumont, P. and Humphries, T. and Jensen, C. and Li, X. 2015. Efficient synthesis of an aluminum amidoborane ammoniate. Energies. 8 (9): pp. 9107-9116.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/7897
dc.identifier.doi10.3390/en8099107
dc.description.abstract

A novel species of metal amidoborane ammoniate, [Al(NH2BH3)6 3-][Al(NH3)6 3+] has been successfully synthesized in up to 95% via the one-step reaction of AlH3·OEt2 with liquid NH3BH3·nNH3 (n = 1~6) at 0 °C. This solution based reaction method provides an alternative pathway to the traditional mechano-chemical ball milling methods, avoiding possible decomposition. MAS 27Al NMR spectroscopy confirms the formulation of the compound as an Al(NH2BH3)6 3- complex anion and an Al(NH3)6 3+ cation. Initial dehydrogenation studies of this aluminum based M-N-B-H compound demonstrate that hydrogen is released at temperatures as low as 65 °C, totaling ~8.6 equivalents of H2 (10.3 wt %) upon heating to 105 °C. This method of synthesis offers a promising route towards the large scale production of metal amidoborane ammoniate moieties.

dc.titleEfficient synthesis of an aluminum amidoborane ammoniate
dc.typeJournal Article
dcterms.source.volume8
dcterms.source.number9
dcterms.source.startPage9107
dcterms.source.endPage9116
dcterms.source.titleEnergies
curtin.note

This open access article is distributed under the Creative Commons license http://creativecommons.org/licenses/by/4.0/

curtin.departmentDepartment of Physics and Astronomy
curtin.accessStatusOpen access


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