Characteristics of mono-, di-, and trivalent cations in electric double layers: a molecular dynamic investigation

Abstract

Ionic behaviors, including ion distributions and hydration characteristics at solid-liquid interfaces, are important research interests in many important applications, such as electric double-layer capacitors and water lubrication. Here, we systematically investigated the concentration distributions, hydration numbers, and screening properties of Li+, Na+, K+, Ca2+, Mg2+, and La3+ ions inside electric double layers (EDLs) at various charge densities. For the surface charge density weaker than -0.16 C m-2, monovalent cations mainly accumulate in the outer Helmholtz plane (OHP). As the charge density magnitude increases, monovalent cations start to dehydrate and migrate to the inner Helmholtz plane (IHP), following the order of K+, Na+, and Li+. This size-dependent behavior arises from the lower hydration energy of larger ions. While for the di- and trivalent ions, no obvious IHP appears. Based on ion distributions, the screening effect of counterions on surface charges is evaluated by analyzing the net charge distributions. As the charge density changes from 0 to -0.32 C m-2, due to the stronger accumulation of cations in EDLs, the location of the neutral plane changes from ~1.2 to ~0.4 nm. When the charge density reaches a threshold, excessive accumulation of cations can induce charge inversion. The threshold value and the maximum reversed charge are found to correlate with the ion size, cation valence, and concentration.