Plasma-anodic experiments on the oxidation of silver electrodes were performed in an inductively coupled chlorine plasma in the temperature range between 50 and 180°C. Pure chlorine plasmas with gas pressures on the order of 1 mbar were employed. The growth rate of the silver chloride films was strongly enhanced in the plasma compared to thermal conditions, and it could be controlled effectively by applying an external electric potential under both galvanostatic and potentiostatic conditions. An analysis of the growth kinetics of the silver halide film shows that the growth rate is limited by the electron flux across the product film in the thermal experiment and across the plasma in the plasma-anodic experiment. It is experimentally shown that the thickness of the product layer is proportional to the electrical charge passed through the plasma-electrochemical cell Ag/AgCl/plasma/carbon. Current densities across the product layer were in the order of 1 mA/cm 2 . The enhancement of the growth rate is smaller than predicted by Faraday's law, indicating either electronic leakage currents or anode sputtering.Gaseous low-temperature plasmas exhibit nonzero electrical conductivity, and they are used as fluid conductors and highly reactive media in a number of technical applications. Most of these industrial applications employ plasmas in the chemical modification of solid surfaces. Studying ion-conducting crystals, their transport properties, and application, we decided to investigate whether gaseous plasmas can also be used in a quasi-electrochemical approach to control reactions between solid electrolytes and the gas phase.In electrochemistry a plasma can be regarded as a fluid mixed conductor with low ionic conductivity but high electronic conductivity, i.e., with a small ionic transference number, but the analogy to conventional liquid or solid electrolytes is not straightforward. Extended space-charge regions exist at the boundaries of any nonequilibrium plasma as a consequence of ambipolar diffusion of charged plasma species from the plasma bulk to the plasma wall. These kinetically driven space-charge regions ͑diffusion potentials͒ lead to strongly nonlinear transport properties of the plasma as a whole. Correspondingly, the possible use of gaseous plasmas in either liquid or solid-state electrochemistry is not yet well investigated, and applications in electrochemistry are rare. In addition, plasmas usually contain a variety of excited atomic and molecular species which complicate the theoretical modeling on the microscopic scale.Besides some historical experiments with glow discharges and aequeous electrolytes more than a hundred years ago, 1 only recently a few electrochemical experiments were performed using electrodeless radio frequency ͑rf͒ or W discharges. Focusing on solid-state electrochemistry, experiments with halogen-containing plasmas were reported by Uchimoto and Ogumi et al.,2,3 Escoffier et al.,4,5 and by this group of the authors. 6-9 To our knowledge no other experimental studies on plasma elec...