Limitations of charge efficiency in capacitive deionization processes III: The behavior of surface oxidized activated carbon electrodes

In previous papers we reported on attempts to improve the performance of water desalination using capacitive de-ionization (CDI) processes by understanding the ions transport and adsorption/desorption behavior of activated carbon electrodes as a function of the applied potential. We also investigated the charge efficiency in CDI processes of brackish water in symmetrical cells containing identical highly porous activated carbon electrodes. In this work, we study the influence of oxygen-containing surface groups on activated carbon electrodes on the adsorption/desorption behavior of ions in brackish water. A special methodology was developed in order to estimate the charge efficiency of CDI processes which include the ability to prepare various kinds of activated carbon electrodes (ACEs) with controlled porosity and surface groups, measuring the PZC (potential of zero charge) of ACE in solutions and simultaneous adsorption and desorption of ions into/from them. The presence of polar, oxygen containing surface groups on ACE does not affect the electroadsorption behavior of Na+ and Cl− ions into porous carbons whose average pore size is greater than 0.58 nm, apart of considerably changing the PZC. This results in a shift of the entire curves of ion adsorption vs. potential. The possible use of ACE with oxidized surfaces in CDI processes is discussed.