Capturing Structural Transitions in Surfactant Adsorption Isotherms at Solid/Solution Interfaces

Although adsorption isotherms of surfactants are critical in determining the relationship between interfacial properties and structures of surfactants, providing quantitative predictions of the isotherms remains challenging. This is especially true for adsorption at hard interfaces such as on two-dimensional (2D) layered materials or on nanoparticles where simulation techniques developed for fluid-fluid interfaces that dynamically change surface properties by adjusting unit cells do not apply. In this work, we predict nonideal adsorption at a solid-solution interface with a molecular thermodynamic theory (MTT) model that utilizes molecular dynamics (MD) simulations for the determination of free-energy parameters in the MTT. Furthermore, the MD/MTT model provides atomistic insights into the nonideal behavior of surfactants by capturing structural phases of the surfactants at the interface. Our approach captures structural transitions from the ideal state at low concentrations and then to the critical surface aggregation concentration (CSAC) and finally through the critical micelle concentration (CMC). We validate our model against the original MTT model by comparing predicted adsorption isotherms of a simplified surfactant system from both approaches. We further substantiate the applicability of our model in complex systems by providing adsorption isotherms in an aqueous sodium dodecyl sulfate (SDS)-graphene system, in good agreement with the experimental observations of the CSAC for the same system.