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We report on a transition in a monolayer of  C  60  molecules deposited on a WO 2 /W(110) substrate. The transition from a static state, where the molecules are rigidly bound to the surface by a coordination bond, to a state where the molecules are loosely bound to the surface by van der Waals force and rotate continuously, has been studied using scanning tunnelling microscopy (STM). The separation between the molecules and the surface increases by 1.2 Å across the transition. The transition from the static state into the rotating state takes place at 259  K . The energy of the spinning state with respect to the lowest energy state, having a single coordinated bond, can be obtained from the statistics of the molecules switching. The binding energy of the molecule in the spinning state can be easily altered by changing the polarity of the bias voltage applied between the STM tip and the surface. The binding energy decreases by 80  meV  when the bias polarity of the sample changes from positive to negative with respect to the tip. The results are consistent with the Coulomb blockade model: when electrons travel from the surface to the  C  60  molecule, and then to the tip; charge accumulates on the molecule due to the Coulomb blockade. This increases the electrostatic interaction between the molecule’s charge and a corresponding image charge generated on the metallic surface.

Control of binding of C60 molecules to the substrate by Coulomb blockade