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Please use this identifier to cite or link to this item: https://doi.org/10.1039/b719420j
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dc.titleCobalt-catalyzed hydrogen desorption from the LiNH2-LiBH 4 system
dc.contributor.authorTang, W.S.
dc.contributor.authorWu, G.
dc.contributor.authorLiu, T.
dc.contributor.authorWee, A.T.S.
dc.contributor.authorYong, C.K.
dc.contributor.authorXiong, Z.
dc.contributor.authorHor, A.T.S.
dc.contributor.authorChen, P.
dc.date.accessioned2014-10-16T08:22:59Z
dc.date.available2014-10-16T08:22:59Z
dc.date.issued2008
dc.identifier.citationTang, W.S., Wu, G., Liu, T., Wee, A.T.S., Yong, C.K., Xiong, Z., Hor, A.T.S., Chen, P. (2008). Cobalt-catalyzed hydrogen desorption from the LiNH2-LiBH 4 system. Dalton Transactions (18) : 2395-2399. ScholarBank@NUS Repository. https://doi.org/10.1039/b719420j
dc.identifier.issn14779226
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93320
dc.description.abstractA doping of 5 wt% CoCl2 considerably decreases the dehydrogenation temperature of a mixture of LiNH2 and LiBH 4. More that 8 wt% of hydrogen can be released at ca. 155 °C. X-Ray absorption near edge structure (XANES) spectroscopy indicated the formation of metallic Co after ball milling CoCl2 with LiNH 2 and LiBH4. Extended X-ray absorption fine structure (EXAFS) spectroscopy measurements revealed that Co particles have poor crystallinity and are finely dispersed in the sample, which could lead to a high catalytic efficiency. © The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/b719420j
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentPHYSICS
dc.description.doi10.1039/b719420j
dc.description.sourcetitleDalton Transactions
dc.description.issue18
dc.description.page2395-2399
dc.identifier.isiut000255599000006
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