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Metamagnetic transition and a loss of magnetic hysteresis caused by electron trapping in monolayers of single-molecule magnet Tb$_{2}$@C$_{79}$N

Koutsouflakis, Emmanouil; Krylov, Denis; Bachellier, Nicolas; Sostina, Daria 1; Dubrovin, Vasilii; Liu, Fupin; Spree, Lukas; Velkos, Georgios; Schimmel, Sebastian; Wang, Yaofeng; Büchner, Bernd; Westerström, Rasmus; Bulbucan, Claudiu; Kirkpatrick, Kyle; Muntwiler, Matthias; Dreiser, Jan; Greber, Thomas; Avdoshenko, Stas M.; Dorn, Harry; ... mehr

Abstract:

Realization of stable spin states in surface-supported magnetic molecules is crucial for their applications in molecular spintronics, memory storage or quantum information processing. In this work, we studied the surface magnetism of dimetallo-azafullerene Tb$_{2}$@C$_{79}$N, showing a broad magnetic hysteresis in a bulk form. Surprisingly, monolayers of Tb$_{2}$@C$_{79}$N exhibited a completely different behavior, with the prevalence of a ground state with antiferromagnetic coupling at low magnetic field and a metamagnetic transition in the magnetic field of 2.5–4 T. Monolayers of Tb$_{2}$@C$_{79}$N were deposited onto Cu(111) and Au(111) by evaporation in ultra-high vacuum conditions, and their topography and electronic structure were characterized by scanning tunneling microscopy and spectroscopy (STM/STS). X-ray photoelectron spectroscopy (XPS), in combination with DFT studies, revealed that the nitrogen atom of the azafullerene cage tends to avoid metallic surfaces. Magnetic properties of the (sub)monolayers were then studied by X-ray magnetic circular dichroism (XMCD) at the Tb-M$_{4,5}$ absorption edge. While in bulk powder samples Tb$_{2}$@C$_{79}$N behaves as a single-molecule magnet with ferromagnetically coupled magnetic moments and blocking of magnetization at 28 K, its monolayers exhibited a different ground state with antiferromagnetic coupling of Tb magnetic moments. ... mehr


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Originalveröffentlichung
DOI: 10.1039/d1nr08475e
Scopus
Zitationen: 5
Dimensions
Zitationen: 6
Zugehörige Institution(en) am KIT Physikalisches Institut (PHI)
Publikationstyp Zeitschriftenaufsatz
Publikationsdatum 14.07.2022
Sprache Englisch
Identifikator ISSN: 2040-3364, 2040-3372
KITopen-ID: 1000154632
Erschienen in Nanoscale
Verlag Royal Society of Chemistry (RSC)
Band 14
Heft 27
Seiten 9877–9892
Vorab online veröffentlicht am 28.06.2022
Nachgewiesen in Dimensions
Web of Science
Scopus
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