The surface diffusion of individual molecules is of paramount importance in self-assembly processes and catalytic processes. However, the fundamental understanding of molecule diffusion peculiarities considering conformations and adsorption sites remain poorly known at the atomic scale. Here, we probe the 4'-(4-tolyl)-2,2':6',2″-terpyridine adsorbed on the Au(111) herringbone structure combining scanning tunneling microscopy and atomic force microscopy. Molecules are controllably translated by electrons excitations over the reconstruction, except at elbows acting as pinning centers. Experimental data supported by theoretical calculations show the formation of coordination bonds between the molecule and Au atoms of the surface. Using force spectroscopy, we quantify local variation of the surface potential and the lateral force required to move the molecule. We found an elevation of the diffusion barrier at elbows of the reconstruction of ∼100 meV compared to the rest of the surface.

Abstract. The performances of the new ScientaOmicron LT-UHV 4-STM microscope have been certified by a series of state-of-art STM experiments on an Au(1 1 1) surface at 4.3 K. During the STM operation of the 4 STM scanners (independently or in parallel with an inter tip apex front to front distance down to a few tens of nanometers), a ΔZ stability of about 2 pm per STM was demonstrated. With this LT-UHV 4-STM stability, single Au atom manipulation experiments were performed on Au(1 1 1) by recording the pulling, sliding and pushing manipulation signals per scanner. Jump to contact experiments lead to perfectly linear low voltage I-V characteristics on a contacted single Au ad-atom with no need of averaging successive I-V's. Our results show how this new instrument is exactly 4 times a very precise single tip LT-UHV-STM. Two tips surface conductance measurements were performed on Au(1 1 1) using a lock-in technique in a floating sample mode of operation to capture the Au(1 1 1) surface states via two STM tips dI/dV characteristics.