The ion and polymer content of polyelectrolyte multilayers constructed via layer-by-layer deposition have been directly probed using radioanalytical methods. Multilayers were fabricated using salt-containing or salt-free solutions. Charges on polyions quantitatively balance each other. As-deposited multilayers contain no salt ions within a limit of detection of a few ppm. All excess charge, which is reversed on each deposition step, resides at the surface. Surface charge controls the amount of polymer deposited and represents, on average, one-half of the charge within a single molecular layer. Internal charge can be regulated following deposition if one of the polyelectrolytes employed is redox-active, such as a polyviologen. Under electrochemical reduction, bulk charge compensation in a polyviologen/poly(styrene sulfonate) multilayer is preserved mainly by cation influx. Residual salt ions accumulate as conformational changes occur during repeated electrochemical cycling. When a thermally labile precursor to poly(p-phenylene vinylene) is incorporated as polycation, salt cation uptake is observed when positive charge is thermally eliminated from the multilayer. Evidence for disruption of this structure is observed when the charge density on one of the constituents approaches zero. For typical deposition times, usually up to 1 h, polymer deposition is kinetically irreversible, and the top layer is not stripped from the surface on exposure to its oppositely charged counterpart. These results provide further confirmation of extensive interpenetration and disorder as well as limited mobility within polyelectrolyte multilayers.