| Literature DB >> 31873288 |
Alexander Köbke1, Florian Gutzeit2, Fynn Röhricht2, Alexander Schlimm3, Jan Grunwald3, Felix Tuczek3, Michał Studniarek4, Danilo Longo5, Fadi Choueikani5, Edwige Otero5, Philippe Ohresser5, Sebastian Rohlf1,6, Sven Johannsen1, Florian Diekmann1,6, Kai Rossnagel1,6,7, Alexander Weismann1, Torben Jasper-Toennies1, Christian Näther3, Rainer Herges8, Richard Berndt1, Manuel Gruber9.
Abstract
Molecular spin switches are attractive candidates for controlling the spin polarization developing at the interface between molecules and magnetic metal surfaces1,2, which is relevant for molecular spintronics devices3-5. However, so far, intrinsic spin switches such as spin-crossover complexes have suffered from fragmentation or loss of functionality following adsorption on metal surfaces, with rare exceptions6-9. Robust metal-organic platforms, on the other hand, rely on external axial ligands to induce spin switching10-14. Here we integrate a spin switching functionality into robust complexes, relying on the mechanical movement of an axial ligand strapped to the porphyrin ring. Reversible interlocked switching of spin and coordination, induced by electron injection, is demonstrated on Ag(111) for this class of compounds. The stability of the two spin and coordination states of the molecules exceeds days at 4 K. The potential applications of this switching concept go beyond the spin functionality, and may turn out to be useful for controlling the catalytic activity of surfaces15.Entities:
Year: 2019 PMID: 31873288 DOI: 10.1038/s41565-019-0594-8
Source DB: PubMed Journal: Nat Nanotechnol ISSN: 1748-3387 Impact factor: 39.213