Two-Step Adsorption of PtCl62– Complexes at a Charged Langmuir Monolayer: Role of Hydration and Ion Correlations

Abstract

Anion exchange at positively charged interfaces plays an important role in a variety of physical and chemical processes. However, the molecular scale details of these processes, especially with heavy and large anionic complexes, are not well-understood. We studied the adsorption of $PtCl_6^{2-}$ anionic complexes to floating DPTAP monolayers in the presence of excess $Cl^-$ as a function of the bulk chlorometalate concentration. In situ x-ray scattering and fluorescence measurements, which are element and depth sensitive, show that the chlorometalate ions only adsorb in the diffuse layer at lower concentrations, while they adsorb predominantly in the Stern layer at higher concentrations. The response of DPTAP molecules to the adsorbed ions is determined independently by grazing incidence x-ray diffraction, and supports this picture. Molecular dynamics simulations further elucidate the nanoscale structure of the interfacial complexes. The results suggest that ion hydration and ion-ion correlations play a key role in the competitive adsorption process.