dc.contributor.author
Hermanns, Christian Felix
dc.contributor.author
Bernien, Matthias
dc.contributor.author
Krüger, Alex
dc.contributor.author
Walter, Waldemar
dc.contributor.author
Chang, Yin-Ming
dc.contributor.author
Weschke, Eugen
dc.contributor.author
Kuch, Wolfgang
dc.date.accessioned
2018-06-08T04:07:24Z
dc.date.available
2014-02-07T14:11:51.110Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/16608
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-20789
dc.description.abstract
Using x-ray magnetic circular dichroism, we show that Co porphyrin molecules
adsorbed on graphenecovered Ni surfaces possess a huge in-plane (IP) orbital
magnetic moment of the Co ions, despite their fourfold coordination, even
comparable in size to the spin moment. Both are antiferromagnetically coupled
to the Ni spins, leading to IP magnetization at zero external magnetic field.
Adsorption of carbon monoxide on top of the molecules reduces the Co orbital
moment by (77 ± 6)%. This is attributed to the change of the crystal field by
the chemical stimulus which determines, together with the spin-orbit coupling
(SOC), the orbital moment. Thermal desorption of the CO fully restores the
initial electronic and magnetic properties.
de
dc.rights.uri
http://publish.aps.org/authors/transfer-of-copyright-agreement
dc.subject.ddc
500 Naturwissenschaften und Mathematik::530 Physik
dc.title
Huge magnetically coupled orbital moments of Co porphyrin molecules and their
control by CO adsorption
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Physical Review B. - 88 (2013), 10, 6 S.
dc.identifier.sepid
32484
dcterms.bibliographicCitation.doi
10.1103/PhysRevB.88.104420
dcterms.bibliographicCitation.url
http://dx.doi.org/10.1103/PhysRevB.88.104420
refubium.affiliation
Physik
de
refubium.mycore.fudocsId
FUDOCS_document_000000019571
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000003027
dcterms.accessRights.openaire
open access