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Towards an understanding of friction at electrodes on the atomic scale

Subject Area Physical Chemistry of Molecules, Liquids and Interfaces, Biophysical Chemistry
Physical Chemistry of Solids and Surfaces, Material Characterisation
Term from 2016 to 2023
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 288879147
 
Final Report Year 2025

Final Report Abstract

Friction is one of the most important origins of energetic losses. In this project we studied atomic scale friction using lateral force microscopy for various systems (copper, silver and iodine monolayers as well as a lipid bilayer, both in aqueous and aprotic electrolytes) as function of potential on a Au(111) single crystal surface. We routinely obtained atomic resolution; for low normal loads we reproduced structures reported before obtained e.g. by STM. For higher normal loads, structures often changed to that of the metallic under-layer indicating a penetration of the tip at least through the outermost layer. In general, friction (or the friction coefficient) is low at high potentials where no metallic layer is adsorbed, or at very low potentials where the metallic adlayer is so strongly adsorbed that the layer cannot be penetrated by the tip. Penetration of the tip through a layer leads to a large increase in friction, demonstrating that the frictional energy dissipation under those conditions is mainly due the displacement/desorption of the adsorbate during the tip scan. Steps in force separation curves clearly indicated displacement of solvent and dissolved ions from the surface or compression of the lipid layer. Displacement of the strongly adsorbed atoms was not possible under static conditions without scanning, obviously a shear force is necessary.

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