Overview: the Janus-nature of molecular CO₂ in charge adjustment at wet surfaces.

Abstract

Molecular CO₂ readily dissolves in aqueous electrolyte solutions and partially dissociating to form carbonic acid. The decharging effects of the dissociation products mediated by the ensuing pH-shift and the additional salinity are well established. However, the effects of dissolved molecular CO₂ have not been studied systematically. We summarize recent and novel investigations on the role of CO₂ regarding charge control at surfaces submersed in aqueous electrolytes. In our electrokinetic and conductometric measurements on representative surfaces, we took special care to control and monitor the electrolyte composition <i>in situ</i>. We discriminate the effects of molecular and dissociated CO₂<i>via</i> control experiments using HCl. Depending on the surface under investigation and the charging mechanisms involved, we find that molecular CO₂ assists either charging, de-charging and/or recharging. This contrasting charge regulating behaviour reveals the Janus nature of dissolved molecular CO₂ with respect to charge control at wet surfaces. In our complementary molecular dynamics simulations, Q4 silica and 9% ionized Q3 silica surfaces are studied as hydrophobic/hydrophilic, respectively charged/uncharged, analogues, as well as uncharged Q3 silica and molecularly rough Isoleucin-coated quartz surfaces. In all cases, we find that the charge-neutral CO₂ molecule physisorbs in a thin diffusive layer close to the surface, which leads to pronounced re-structuring of the electric double layer. Based on this result, we suggest to interpret the experimentally observed Janus nature of molecular CO₂ in terms of a local decrease of the dielectric permittivity. This in turn leads to a local strengthening of electrostatic interactions dominating the double layer structure next to charged surfaces. Specifically, we propose that CO₂ induces a dielectric charge regulation for weakly acidic surface groups, assists the incorporation of OH^- into the H-bond network at smooth inert surfaces, and induces significant ion-correlations promoting co-ion binding. Overall, we demonstrate that molecular CO₂ allows for a controlled charge-adjustment in opposing directions. We anticipate that our findings on the one hand provide substantial challenges for analytical or numerical modelling as well as for controlled experimental work, but on the other hand bear important practical implications for applications ranging from desalination to bio-membranes.