Reversible switching of Kondo resonance in a single-molecule junction

The control of the Kondo effect is of great interest in single-molecule junction due to its potential applications in spin based electronics. Here, we demonstrate that the Kondo effect is reversibly switched on and off in an iron phthalocyanine (FePc) single-molecule junction by using a superconducting Nb tip. In a scanning tunneling microscope-based Nb-insulator-FePc-Au junction, we achieve a reversible switching between the Kondo dip and inelastic electronic tunneling spectra by simply adjusting the tip-sample distance to tune the tunnel coupling at low temperature. Further approaching the tip leads to the picking up of the molecule to the tip apex, which transfers the geometry of the single-molecule junction into a Nb-FePc-insulator-Au type. As the molecule forms an effective magnetic impurity embedded into the superconducting ground states of the Nb tip, the out-gap Kondo dip switched to an in-gap Yu-Shiba-Rusinov state. Our results open up a new route for manipulating the Kondo effect within a single-molecule junction.

Automated summary

The study demonstrates that the Kondo effect in an iron phthalocyanine single-molecule junction can be reversibly switched on and off using a superconducting Nb tip, by adjusting the tip-sample distance to tune the tunnel coupling at low temperature. Approaching the tip leads to the picking up of the molecule to the tip apex, transferring the geometry of the single-molecule junction into a Nb-FePc-insulator-Au type. The molecule forms an effective magnetic impurity embedded into the superconducting ground states of the Nb tip, switching the out-gap Kondo dip to an in-gap Yu-Shiba-Rusinov state.