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dc.contributor.authorChen, Jen_US
dc.contributor.authorHuang, DJen_US
dc.contributor.authorTanaka, Aen_US
dc.contributor.authorChang, CFen_US
dc.contributor.authorChung, SCen_US
dc.contributor.authorWu, WBen_US
dc.contributor.authorChen, CTen_US
dc.date.accessioned2019-04-03T06:37:36Z-
dc.date.available2019-04-03T06:37:36Z-
dc.date.issued2004-02-01en_US
dc.identifier.issn2469-9950en_US
dc.identifier.urihttp://dx.doi.org/10.1103/PhysRevB.69.085107en_US
dc.identifier.urihttp://hdl.handle.net/11536/27046-
dc.description.abstractMeasurements of magnetic circular dichroism in Fe 2p resonant photoemission and calculations based on a full-multiplet cluster model reveal the parameters of the electronic structure of Fe3O4. We obtained on-site Coulomb energy U-dd of 3d electrons, charge-transfer energy Delta which is defined as the energy required to transfer an electron from O 2p to Fe 3d, and the hybridization strength between Fe 3d and O 2p at different Fe ion sites of Fe3O4 by analyzing the data of magnetic circular dichroism. The charge-transfer energy of Fe3+ ions was found to be significantly smaller than that of Fe2+ ions. We determined the energy positions of the low-lying multiplets of each Fe ion site. These energy positions for Fe3+ ion sites are 1.5-2.5 eV higher than those obtained from band-structure calculations. Our calculations also show that the photoemission spectral weight in binding energy bigger than 10 eV is substantial, in contrast to the results of band-structure calculations. Our findings conclude that Fe3O4 is a system with strong electron-electron interactions.en_US
dc.language.isoen_USen_US
dc.titleMagnetic circular dichroism in Fe 2p resonant photoemission of magnetiteen_US
dc.typeArticleen_US
dc.identifier.doi10.1103/PhysRevB.69.085107en_US
dc.identifier.journalPHYSICAL REVIEW Ben_US
dc.citation.volume69en_US
dc.citation.issue8en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000220185100024en_US
dc.citation.woscount52en_US
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