In the era of molecular devices and nanotechnology, precise control over electron-transfer processes is strongly desired. However, redox reactions are usually characterized by reaction equilibrium constants strongly departing from unity. This leads to strong favoring of either reactants or products and does not permit subtle control of transferred charge (doping).Here we propose, based on theoretical studies for periodic systems, how charge transfer between reactants could be finely manipulated in the epitaxially grown system composed of extremely strong oxidizer, reducing agent, and an inert separator-the key factor of control.Electron transfer reactions, together with acid-base ones, constitute the most important types of elemental processes in chemistry. One unique feature of redox reactions is that their equilibrium constants strongly depart from unity. For example, for a model one-electron reaction where the standard redox potentials, E 0 , for the two involved redox pairs differ by a mere 0.1 V, the reaction equilibrium constant, K [Eq. (1)] K eq ¼ expðDE 0 F=RTÞ ð1Þ