| Literature DB >> 33717832 |
Chia-Hsiang Chen1,2, Lukas Spree1, Emmanouil Koutsouflakis1, Denis S Krylov1,3, Fupin Liu1, Ariane Brandenburg1, Georgios Velkos1, Sebastian Schimmel1, Stanislav M Avdoshenko1, Alexander Fedorov1,4, Eugen Weschke4, Fadi Choueikani5, Philippe Ohresser5, Jan Dreiser6, Bernd Büchner1, Alexey A Popov1.
Abstract
Tremendous progress in the development of single molecule magnets (SMMs) raises the question of their device integration. On this route, understanding the properties of low-dimensional assemblies of SMMs, in particular in contact with electrodes, is a necessary but difficult step. Here, it is shown that fullerene SMM self-assembled on metal substrate from solution retains magnetic hysteresis up to 10 K. Fullerene-SMM DySc2N@C80 and Dy2ScN@C80 are derivatized to introduce a thioacetate group, which is used to graft SMMs on gold. Magnetic properties of grafted SMMs are studied by X-ray magnetic circular dichroism and compared to the films of nonderivatized fullerenes prepared by sublimation. In self-assembled films, the magnetic moments of the Dy ions are preferentially aligned parallel to the surface, which is different from the disordered orientation of endohedral clusters in nonfunctionalized fullerenes. Whereas chemical derivatization reduces the blocking temperature of magnetization and narrows the hysteresis of Dy2ScN@C80, for DySc2N@C80 equally broad hysteresis is observed as in the fullerene multilayer. Magnetic bistability in the DySc2N@C80 grafted on gold is sustained up to 10 K. This study demonstrates that self-assembly of fullerene-SMM derivatives offers a facile solution-based procedure for the preparation of functional magnetic sub-monolayers with excellent SMM performance.Entities:
Keywords: XMCD; fullerenes; magnetic hysteresis; self‐assembled monolayers; single‐molecule magnets
Year: 2021 PMID: 33717832 PMCID: PMC7927621 DOI: 10.1002/advs.202000777
Source DB: PubMed Journal: Adv Sci (Weinh) ISSN: 2198-3844 Impact factor: 16.806