By considering a water capillary bridge confined between two flat surfaces, we investigate the thermodynamics of the triple line delimiting this solid–liquid–vapor system when supplemented in carbon dioxide. In more detail, by means of atom-scale simulations, we show that carbon dioxide accumulates at the solid walls and, preferably, at the triple lines where it plays the role of a line active agent. The line tension of the triple line, which is quantitatively assessed using an original mechanical route, is shown to be driven by the line excess concentrations of the solute (carbon dioxide) and solvent (water). Solute accumulation at the lines decreases the negative line tension (i.e., more negative) while solvent depletion from the lines has the opposite effect. Such an unprecedented quantitative assessment of gas-induced line tension modifications shows that the absolute value of the negative line tension increases upon increasing the carbon dioxide partial pressure. As a striking example, for hydrophilic surfaces, the line tension is found to increase by more than an order of magnitude when the carbon dioxide pressure exceeds 3 MPa. By considering the coupling between line and surface effects induced by gaseous adsorption, we hypothesize from the observed gas concentration-dependent line tension a nontrivial impact on heterogeneous nucleation of nanometric critical nuclei.
The influence of droplet size on line tension
