Understanding the electrochemical double layer at the hematite/water interface: A first principles molecular dynamics study.

Using first principles molecular dynamics simulations, we probe the electrochemical double layer formed at the interface between the hematite surface and water. We consider two terminations of the (001) surface, viz., the fully hydroxylated (OH) and the stoichiometric (FeO3Fe) termination. We explicitly incorporate the counterions (Na+ and F−) in the solution, and model both specific and nonspecific adsorption of F− ions. We find that F− ions prefer to bind directly to the Fe ions (specific adsorption), with a substantial energy gain (0.75 eV/ion). We investigate the effect of the interface and the counterions on the dipole of individual water molecules. We find significant deviations of +0.2/−0.15 D for dipoles of the first solvation shell water molecules of F−/Na+ ions, respectively. Additionally, the hydration layers at the interface show an enhancement in the dipole moment resulting from stronger hydrogen bonding interactions between the water molecules and surface charged species. Furthermore, we analyze the electrostatic potential profile at the solid/liquid interface as a function of the kind of counterion present in the double layer and compute the capacitance of the compact (Helmholtz) layer. We find that our results (40.3 ± 3.5 μF/cm2 for the OH termination and 51 ± 5 μF/cm2 for the FeO3Fe termination) compare favorably with values reported by potentiometric titration based experimental studies (10–100 μF/cm2). [ABSTRACT FROM AUTHOR]