Author
Listed:
- Fupin Liu
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
- Georgios Velkos
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
- Denis S. Krylov
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
- Lukas Spree
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
- Michal Zalibera
(Slovak University of Technology)
- Rajyavardhan Ray
(Leibniz Institute for Solid State and Materials Research (IFW Dresden)
Dresden Center for Computational Materials Science (DCMS), TU Dresden)
- Nataliya A. Samoylova
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
- Chia-Hsiang Chen
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
- Marco Rosenkranz
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
- Sandra Schiemenz
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
- Frank Ziegs
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
- Konstantin Nenkov
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
- Aram Kostanyan
(Physik-Institut der Universität Zürich)
- Thomas Greber
(Physik-Institut der Universität Zürich)
- Anja U. B. Wolter
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
- Manuel Richter
(Leibniz Institute for Solid State and Materials Research (IFW Dresden)
Dresden Center for Computational Materials Science (DCMS), TU Dresden)
- Bernd Büchner
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
- Stanislav M. Avdoshenko
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
- Alexey A. Popov
(Leibniz Institute for Solid State and Materials Research (IFW Dresden))
Abstract
Engineering intramolecular exchange interactions between magnetic metal atoms is a ubiquitous strategy for designing molecular magnets. For lanthanides, the localized nature of 4f electrons usually results in weak exchange coupling. Mediating magnetic interactions between lanthanide ions via radical bridges is a fruitful strategy towards stronger coupling. In this work we explore the limiting case when the role of a radical bridge is played by a single unpaired electron. We synthesize an array of air-stable Ln2@C80(CH2Ph) dimetallofullerenes (Ln2 = Y2, Gd2, Tb2, Dy2, Ho2, Er2, TbY, TbGd) featuring a covalent lanthanide-lanthanide bond. The lanthanide spins are glued together by very strong exchange interactions between 4f moments and a single electron residing on the metal–metal bonding orbital. Tb2@C80(CH2Ph) shows a gigantic coercivity of 8.2 Tesla at 5 K and a high 100-s blocking temperature of magnetization of 25.2 K. The Ln-Ln bonding orbital in Ln2@C80(CH2Ph) is redox active, enabling electrochemical tuning of the magnetism.
Suggested Citation
Fupin Liu & Georgios Velkos & Denis S. Krylov & Lukas Spree & Michal Zalibera & Rajyavardhan Ray & Nataliya A. Samoylova & Chia-Hsiang Chen & Marco Rosenkranz & Sandra Schiemenz & Frank Ziegs & Konsta, 2019.
"Air-stable redox-active nanomagnets with lanthanide spins radical-bridged by a metal–metal bond,"
Nature Communications, Nature, vol. 10(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-08513-6
DOI: 10.1038/s41467-019-08513-6
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