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Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/23718
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dc.contributor.authorPukazhselvan, D.pt
dc.contributor.authorNasani, N.pt
dc.contributor.authorYang, T.pt
dc.contributor.authorRamasamy, D.pt
dc.contributor.authorShaula, A.pt
dc.contributor.authorFagg, D. P.pt
dc.date.accessioned2018-06-29T16:19:15Z-
dc.date.issued2018-
dc.identifier.issn0169-4332pt
dc.identifier.urihttp://hdl.handle.net/10773/23718-
dc.description.abstractThe present work deals with a comparative study of Mg2TiO4, MgTiO3 and titania additives incorporated MgH2. Hydrogen storage measurements suggest that all these additives improve the hydrogen desorption/absorption performance of MgH2. X-ray diffraction (XRD) and X ray photoelectron spectroscopy (XPS) studies highlight that rock salt phases consisting of highly reduced Ti exist in the samples. These results reiterate that in-situ formation of chemically reduced Ti containing active species is a critical step in the catalysis of TiO2/Mg2TiO4/MgTiO3 additives loaded MgH2.pt
dc.language.isoengpt
dc.publisherElsevierpt
dc.relationFCT-PTDC/CTM-ENE/6319/2014pt
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F88756%2F2012/PTpt
dc.relationIF/01344/2014/CP1222/CT0001pt
dc.rightsrestrictedAccesspor
dc.subjectTernary oxidespt
dc.subjectHydrogen storagept
dc.subjectCatalytic activitypt
dc.titleChemically transformed additive phases in Mg2TiO4 and MgTiO3 loaded hydrogen storage system MgH2pt
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.titleApplied Surface Sciencept
dc.date.embargo10000-01-01-
dc.identifier.doi10.1016/j.apsusc.2018.04.052pt
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