A new paradigm for nonlinear doping-controlled ion transport in soft condensed matter is
presented, where the mobility of a minority “probe” ion is controlled by majority “salt” ion. The class of
materials to which this paradigm applies is represented by ultrathin films of polyelectrolyte complexes, or
multilayers. Intersite hopping of probe ions of charge ν occurs only when the charge of the destination site,
produced by clustering of monovalent salt ions, is at least −ν, conserving electroneutrality. Salt ions are
reversibly “doped” into the multilayer under the influence of external salt concentration. In situ ATR-FTIR
reveals that the doping level, y, is proportional to salt concentration. Because hopping requires coincidence,
or clustering, of salt, a strongly nonlinear dependence of flux, J, on salt concentration is observed: J ∼
[NaCl]ν ∼ yν. This scaling was reproduced both by Monte Carlo simulations of ion hopping and by continuum
probability expressions. The theory also predicts the observed scaling, though it underestimates the
magnitude, of the strong selectivity of multilayers for ions of different charge