Repulsive interactions induced by specific adsorption: Anomalous step diffusivity and inadequacy of nearest-neighbor Ising model

Al-Shakran, Mohammad; Ibach, Harald; Beltramo, Guillermo; Kibler, Ludwig A.; Giesen, Margret; Jacob, Timo

doi:10.1016/j.susc.2016.03.021

Journal Article

FZJ-2017-02398

Repulsive interactions induced by specific adsorption: Anomalous step diffusivity and inadequacy of nearest-neighbor Ising model

Al-Shakran, M. ; Kibler, L. A. ; Jacob, T. ; Ibach, H.FZJ* ; Beltramo, G.FZJ* ; Giesen, M. (Corresponding author)FZJ*

2016
Elsevier Amsterdam

Surface science 651, 84 - 93 (2016) [10.1016/j.susc.2016.03.021]

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Please use a persistent id in citations: doi:10.1016/j.susc.2016.03.021

Abstract: This is Part I of two closely related papers, where we show that the specific adsorption of anions leads to a failure of the nearest-neighbor Ising model to describe island perimeter curvatures on Au(100) electrodes in dilute KBr, HCl and H2SO4 electrolytes and the therewith derived step diffusivity vs. step orientation. This result has major consequences for theoretical studies aiming at the understanding of growth, diffusion and degradation phenomena. Part I focuses on the experimental data.As shown theoretically in detail in Part II (doi:10.1016/j.susc.2016.03.022), a set of nearest-neighbor and next-nearest-neighbor interaction energies (ϵNN, ϵNNN) can uniquely be derived from the diffusivity of steps along 〈100〉 and 〈110〉. We find strong repulsive next-nearest neighbor (NNN) interaction in KBr and HCl, whereas NNN interaction is negligibly for H2SO4. The NNN repulsive interaction energy ϵNNN therefore correlates positively with the Gibbs adsorption energy of the anions. We find furthermore that ϵNNN increases with increasing Br− and Cl− coverage.The results for ϵNN and ϵNNN are quantitatively consistent with the coverage dependence of the step line tension. We thereby establish a sound experimental base for theoretical studies on the energetics of steps in the presence of specific adsorption.

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