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The electroluminescence of a polythiophene wire suspended between a metallic surface and the tip of a scanning tunneling microscope is reported. Under positive sample voltage, the spectral and voltage dependencies of the emitted light are consistent with the fluorescence of the wire junction mediated by localized plasmons. This emission is strongly attenuated for the opposite polarity. Both emission mechanism and polarity dependence are similar to what occurs in organic light emitting diodes (OLED) but at the level of a single molecular wire.

Structural and electronic properties of oligothiophene nano-wires and rings synthesized on a Au(111) surface are investigated by scanning tunneling microscopy. The spectroscopic data of the linear and cyclic oligomers show remarkable differences which, to a first approximation, can be accounted by considering electronic states confinement to one-dimensional (1D) boxes having respectively fixed and periodic boundary conditions. A more detailed analysis shows that polythiophene must be treated as a ribbon (i.e. having an effective width) rather than a purely 1D structure. A fascinating consequence is that the molecular nano-rings act as whispering gallery mode resonators for electrons, opening the way for new applications in quantum-electronics., Comment: 4 pages with 4 figures, To be published in Physical Review Letters

We have studied the repercussion of the molecular adsorption mechanism on the electronic properties of the interface between model nonmagnetic or magnetic metallic surfaces and metallo-organic phthalocyanines molecules (Pcs). Our intertwined x-ray absorption spectroscopy experiments and computational studies reveal that manganese Pc (MnPc) is physisorbed onto a Cu(001) surface and retains the electronic properties of a free molecule. On the other hand, MnPc is chemisorbed onto Co(001), leading to a dominant direct exchange interaction between the Mn molecular site and the Co substrate. By promoting an interfacial spin-polarized conduction state on the molecule, these interactions reveal an important lever to tailor the spintronic properties of hybrid organic-metallic interfaces.