Measurement of Surface Diffusion at the Electrochemical Interface by In Situ Linear Optical Diffraction.

A new in situ method for measuring the surface diffusion rates of adsorbates on electrode surfaces in electrolyte solution is presented. The method is based on the generation of a periodic spatial modulation of the adsorbate coverage via interfering laser pulses and subsequent monitoring of the diffusion-induced decay of this pattern using the optical diffraction signal of a second laser. Proof-of-principle measurements of the surface diffusion of adsorbed sulfur on Pt(111) electrodes in 0.1 M H2SO4 indicate potential- and coverage-dependent diffusion constants that are significantly higher than those of sulfur on Pt(111) under vacuum conditions.

Influence of coverage on adsorbate diffusion measurements at electrode surfaces by in situ linear optical diffraction.

In situ linear optical diffraction is a new method for studies of surface mass transport in electrochemical environments that is based on the equilibration of coverage gratings in an adlayer on the electrode surface. We, here, discuss the temporal evolution of the diffraction intensity on the basis of experimental data for sulfur adsorbates on Pt(111) electrodes in 0.1M H2SO4 and simulations of the time-dependent diffusion profiles. At low and medium sulfur coverage, the decay of the signal exhibits two time scales, which can be explained by the influence of coverage-dependent diffusion rates on the evolution of gratings with large coverage modulation. At high coverage, a further ultra-slow decay process or even a complete termination of the decay is observed, which we attribute to the presence of high-density, ordered, adlayer phases with low sulfur mobility. These results provide insight into the approaches required for extracting quantitative surface transport rates from linear optical diffraction measurements.