Esat T., Lechtenberg B., Deilmann T., Wagner C., Krüger P., Temirov R., Rohlfing M., Anders F., Tautz F.
Forschungsartikel (Zeitschrift) | Peer reviewedThe magnetic properties of nanostructures that consist of a small number of atoms or molecules are typically determined by magnetic exchange interactions. Here, we show that non-magnetic, chemical interactions can have a similarly decisive effect if spin-moment-carrying orbitals extend in space and therefore allow the direct coupling of magnetic properties to wavefunction overlap and the formation of bonding and antibonding orbitals. We demonstrate this for a dimer of metal-molecule complexes on the Au(111) surface. A changing wavefunction overlap between the two monomers drives the surface-adsorbed dimer through a quantum phase transition from an underscreened triplet to a singlet ground state, with one configuration being located extremely close to a quantum critical point.
Krüger, Peter | Professur für Festkörpertheorie (Prof. Rohlfing) |
Rohlfing, Michael | Professur für Festkörpertheorie (Prof. Rohlfing) |