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dc.contributor.authorRavnsbaek, Dorthe B.-
dc.contributor.authorLey, Morten B.-
dc.contributor.authorLee, Young-Su-
dc.contributor.authorHagemann, Hans-
dc.contributor.authorD'Anna, Vincenza-
dc.contributor.authorCho, Young Whan-
dc.contributor.authorFilinchuk, Yaroslav-
dc.contributor.authorJensen, Torben R.-
dc.date.accessioned2024-01-20T15:01:25Z-
dc.date.available2024-01-20T15:01:25Z-
dc.date.created2021-09-05-
dc.date.issued2012-05-
dc.identifier.issn0360-3199-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/129302-
dc.description.abstractA new sodium-yttrium borohydride-chloride, NaY(BH4)(2)Cl-2, is obtained by a combination of mechanochemical synthesis and annealing of NaBH4-YCl3 mixtures and is characterized by in-situ synchrotron radiation X-ray powder diffraction, density functional theory, thermal analysis and vibrational spectroscopy. Several simultaneous and coupled reactions occur during the synthesis, also yielding Na3YCl6 and Na(BH4)(1-x)Cl-x besides the title compound. The polymeric pseudo-orthorhombic crystal structure of NaY(BH4)(2)Cl-2 (space group P2/c) is built of edge- and corner-sharing octahedral coordination polyhedra of yttrium (4Cl + 2BH(4)) and sodium (2Cl + 4BH(4)). The structure is isomorphous to the high temperature polymorph of NaYCl4. The BH4 units in NaY(BH4)(2)Cl-2 are located only on the larger of the two independent anion sites in NaYCl4. Density functional theory optimization of the experimental structure suggests that the BH4 units act as eta(3)-ligands (face-sharing) towards yttrium and eta(1)-ligands (corner-sharing) towards sodium. Raman spectroscopy confirms this BH4 configuration. NaY(BH4)(2)Cl-2 decomposes at similar to 300 degrees C under formation of Na3YCl6, while the latter compound at higher temperatures reacts with Na(BH4)(1-x)Cl-x to form NaCl and possibly amorphous products. The reactions are associated with mass losses of 2.62 and 3.78 wt% for the NaBH4-YCl3 (3:1) and (4:1) samples, respectively. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectCRYSTALLOGRAPHY BEAMLINE-
dc.subjectCRYSTAL-STRUCTURES-
dc.subjectTERNARY CHLORIDES-
dc.subjectPOLYMORPHISM-
dc.subjectY(BH4)(3)-
dc.subjectSTORAGE-
dc.subjectLIBH4-
dc.subjectDECOMPOSITION-
dc.subjectBEHAVIOR-
dc.subjectHYDRIDES-
dc.titleA mixed-cation mixed-anion borohydride NaY(BH4)(2)Cl-2-
dc.typeArticle-
dc.identifier.doi10.1016/j.ijhydene.2012.02.130-
dc.description.journalClass1-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v.37, no.10, pp.8428 - 8438-
dc.citation.titleINTERNATIONAL JOURNAL OF HYDROGEN ENERGY-
dc.citation.volume37-
dc.citation.number10-
dc.citation.startPage8428-
dc.citation.endPage8438-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000305040400036-
dc.identifier.scopusid2-s2.0-84860364608-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryElectrochemistry-
dc.relation.journalWebOfScienceCategoryEnergy & Fuels-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaElectrochemistry-
dc.relation.journalResearchAreaEnergy & Fuels-
dc.type.docTypeArticle-
dc.subject.keywordPlusCRYSTALLOGRAPHY BEAMLINE-
dc.subject.keywordPlusCRYSTAL-STRUCTURES-
dc.subject.keywordPlusTERNARY CHLORIDES-
dc.subject.keywordPlusPOLYMORPHISM-
dc.subject.keywordPlusY(BH4)(3)-
dc.subject.keywordPlusSTORAGE-
dc.subject.keywordPlusLIBH4-
dc.subject.keywordPlusDECOMPOSITION-
dc.subject.keywordPlusBEHAVIOR-
dc.subject.keywordPlusHYDRIDES-
dc.subject.keywordAuthorHydrides-
dc.subject.keywordAuthorX-ray diffraction-
dc.subject.keywordAuthorSolid state structure-
dc.subject.keywordAuthorSolid phase synthesis-
dc.subject.keywordAuthorTransition metal-
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