Controlling spins in adsorbed molecules by a chemical switch
Christian Wäckerlin,
Dorota Chylarecka,
Armin Kleibert,
Kathrin Müller,
Cristian Iacovita,
Frithjof Nolting,
Thomas A. Jung () and
Nirmalya Ballav ()
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Christian Wäckerlin: Laboratory for Micro- and Nanotechnology, Paul Scherrer Institut
Dorota Chylarecka: Laboratory for Micro- and Nanotechnology, Paul Scherrer Institut
Armin Kleibert: Swiss Light Source, Paul Scherrer Institut
Kathrin Müller: Laboratory for Micro- and Nanotechnology, Paul Scherrer Institut
Cristian Iacovita: University of Basel
Frithjof Nolting: Swiss Light Source, Paul Scherrer Institut
Thomas A. Jung: Laboratory for Micro- and Nanotechnology, Paul Scherrer Institut
Nirmalya Ballav: Laboratory for Micro- and Nanotechnology, Paul Scherrer Institut
Nature Communications, 2010, vol. 1, issue 1, 1-7
Abstract:
Abstract The development of chemical systems with switchable molecular spins could lead to the architecture of materials with controllable magnetic or spintronic properties. Here, we present conclusive evidence that the spin of an organometallic molecule coupled to a ferromagnetic substrate can be switched between magnetic off and on states by a chemical stimulus. This is achieved by nitric oxide (NO) functioning as an axial ligand of cobalt(II)tetraphenylporphyrin (CoTPP) ferromagnetically coupled to nickel thin-film (Ni(001)). On NO addition, the coordination sphere of Co2+ is modified and a NO–CoTPP nitrosyl complex is formed, which corresponds to an off state of the Co spin. Thermal dissociation of NO from the nitrosyl complex restores the on state of the Co spin. The NO-induced reversible off–on switching of surface-adsorbed molecular spins observed here is attributed to a spin trans effect.
Date: 2010
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:1:y:2010:i:1:d:10.1038_ncomms1057
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DOI: 10.1038/ncomms1057
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