Magnetic hysteresis and strong ferromagnetic coupling of sulfur-bridged Dy ions in clusterfullerene Dy2S@C82

dc.bibliographicCitation.firstPage3521eng
dc.bibliographicCitation.issue19eng
dc.bibliographicCitation.lastPage3532eng
dc.bibliographicCitation.volume7eng
dc.contributor.authorKrylov, Denis
dc.contributor.authorVelkos, Georgios
dc.contributor.authorChen, Chia-Hsiang
dc.contributor.authorBüchner, Bernd
dc.contributor.authorKostanyan, Aram
dc.contributor.authorGreber, Thomas
dc.contributor.authorAvdoshenko, Stanislav M.
dc.contributor.authorPopov, Alexey A.
dc.date.accessioned2021-08-23T11:55:08Z
dc.date.available2021-08-23T11:55:08Z
dc.date.issued2020
dc.description.abstractTwo isomers of metallofullerene Dy2S@C82 with sulfur-bridged Dy ions exhibit broad magnetic hysteresis with sharp steps at sub-Kelvin temperature. Analysis of the level crossing events for different orientations of a magnetic field showed that even in powder samples, the hysteresis steps caused by quantum tunneling of magnetization can provide precise information on the strength of intramolecular Dy⋯Dy interactions. A comparison of different methods to determine the energy difference between ferromagnetic and antiferromagnetic states showed that sub-Kelvin hysteresis gives the most robust and reliable values. The ground state in Dy2S@C82 has ferromagnetic coupling of Dy magnetic moments, whereas the state with antiferromagnetic coupling in Cs and C3v cage isomers is 10.7 and 5.1 cm-1 higher, respectively. The value for the Cs isomer is among the highest found in metallofullerenes and is considerably larger than that reported in non-fullerene dinuclear molecular magnets. Magnetization relaxation times measured in zero magnetic field at sub-Kelvin temperatures tend to level off near 900 and 3200 s in Cs and C3v isomers. These times correspond to the quantum tunneling relaxation mechanism, in which the whole magnetic moment of the Dy2S@C82 molecule flips at once as a single entity. © the Partner Organisations.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/6573
dc.identifier.urihttps://doi.org/10.34657/5620
dc.language.isoengeng
dc.publisherCambridge : RSCeng
dc.relation.doihttps://doi.org/10.1039/d0qi00771d
dc.relation.essn2052-1553
dc.relation.ispartofseriesInorganic Chemistry Frontiers 7 (2020), Nr. 19eng
dc.relation.issn2052-1545
dc.rights.licenseCC BY 3.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/eng
dc.subjectAntiferromagnetismeng
dc.subjectElectron tunnelingeng
dc.subjectFerromagnetic materialseng
dc.subjectFerromagnetismeng
dc.subjectFullereneseng
dc.subjectGround stateeng
dc.subjectMagnetic fieldseng
dc.subjectMagnetic hysteresiseng
dc.subjectMagnetic momentseng
dc.subjectMagnetizationeng
dc.subjectPlants (botany)eng
dc.subjectSulfureng
dc.subjectAntiferromagnetic couplingeng
dc.subjectFerromagnetic and anti-ferromagneticeng
dc.subjectFerromagnetic couplingeng
dc.subjectKelvin temperatureseng
dc.subjectMagnetization relaxationeng
dc.subjectQuantum tunneling of magnetizationeng
dc.subjectRelaxation mechanismeng
dc.subjectZero magnetic fieldseng
dc.subjectIsomerseng
dc.subject.ddc540eng
dc.titleMagnetic hysteresis and strong ferromagnetic coupling of sulfur-bridged Dy ions in clusterfullerene Dy2S@C82eng
dc.typearticleeng
dc.typeTexteng
dcterms.bibliographicCitation.journalTitleInorganic Chemistry Frontierseng
tib.accessRightsopenAccesseng
wgl.contributorIFWDeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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