The equilibrium surface tension of anionic surfactant n-decyl sulfate (DS-) for various monovalent (alkali) counterions was investigated. It was found that surface activity of surface chemically pure DS- significantly increases with decreasing hydrated size of the counterion. We describe our experimental results in terms of the previously developed adsorption model, which assumes that the counterions may penetrate the Stern layer where the surfactant headgroups are adsorbed. The headgroups and counterions have a finite size that leads to the surface exclusion effects in the adsorption isotherm. The model is improved by explicitly taking into account the electric interactions between adsorbed ions in the adsorbed layer. We obtain a good correlation between the relative counterion size in the Stern layer, the measure of the area excluded by the adsorbed counterions, and the effective radius of the hydrated counterion in the solution. The limiting areas per molecule at the critical micelle concentration for the adsorbed decyl sulfate for various counterions are in good agreement with those measured by neutron scattering.