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dc.contributor.authorFaisal, Mohammad-
dc.contributor.authorKim, June-Hyung-
dc.contributor.authorCho, Young Whan-
dc.contributor.authorJang, Jae-il-
dc.contributor.authorSuh, Jin-Yoo-
dc.contributor.authorShim, Jae-Hyeok-
dc.contributor.authorLee, Young-Su-
dc.date.accessioned2024-01-19T14:01:08Z-
dc.date.available2024-01-19T14:01:08Z-
dc.date.created2022-01-10-
dc.date.issued2021-09-
dc.identifier.issn1996-1944-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/116511-
dc.description.abstractTitanium iron (TiFe) alloy is a room-temperature hydrogen-storage material, and it absorbs hydrogen via a two-step process to form TiFeH and then TiFeH2. The effect of V addition in TiFe alloy was recently elucidated. The V substitution for Ti sublattice lowers P-2/P-1 ratio, where P-1 and P-2 are the equilibrium plateau pressure for TiFe/TiFeH and TiFeH/TiFeH2, respectively, and thus restricts the two-step hydrogenation within a narrow pressure range. The focus of the present investigation was to optimize the V content such that maximum usable storage capacity can be achieved for the target pressure range: 1 MPa for absorption and 0.1 MPa for desorption. The effect of V substitution at selective Ti or Fe sublattices was closely analyzed, and the alloy composition Ti46Fe47.5V6.5 displayed the best performance with ca. 1.5 wt.% of usable capacity within the target pressure range. At the same time, another issue in TiFe-based alloys, which is a difficulty in activation at room temperature, was solved by Ce addition. It was shown that 3 wt.% Ce dispersion in TiFe alloy imparted to it easy room-temperature (RT) activation properties.-
dc.languageEnglish-
dc.publisherMDPI-
dc.subjectHYDROGEN STORAGE PROPERTIES-
dc.subjectPHASE-EQUILIBRIA-
dc.subjectFE-
dc.subjectMN-
dc.subjectZR-
dc.subjectMICROSTRUCTURE-
dc.subjectCE-
dc.subjectCO-
dc.subjectCR-
dc.titleDesign of V-Substituted TiFe-Based Alloy for Target Pressure Range and Easy Activation-
dc.typeArticle-
dc.identifier.doi10.3390/ma14174829-
dc.description.journalClass1-
dc.identifier.bibliographicCitationMATERIALS, v.14, no.17-
dc.citation.titleMATERIALS-
dc.citation.volume14-
dc.citation.number17-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000694370200001-
dc.identifier.scopusid2-s2.0-85114008554-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryMetallurgy & Metallurgical Engineering-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.relation.journalWebOfScienceCategoryPhysics, Condensed Matter-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaMetallurgy & Metallurgical Engineering-
dc.relation.journalResearchAreaPhysics-
dc.type.docTypeArticle-
dc.subject.keywordPlusHYDROGEN STORAGE PROPERTIES-
dc.subject.keywordPlusPHASE-EQUILIBRIA-
dc.subject.keywordPlusFE-
dc.subject.keywordPlusMN-
dc.subject.keywordPlusZR-
dc.subject.keywordPlusMICROSTRUCTURE-
dc.subject.keywordPlusCE-
dc.subject.keywordPlusCO-
dc.subject.keywordPlusCR-
dc.subject.keywordAuthorhydrogen storage-
dc.subject.keywordAuthorTiFe alloy-
dc.subject.keywordAuthorequilibrium pressure-
dc.subject.keywordAuthoractivation-
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