Reverse electrodialysis (RED) is a promising technology to extract sustainable salinity gradient energy. However, the RED technology has not reached its full potential due to membrane efficiency and fouling and the complex interplay between ionic flows and fluidic configurations. We investigate renewable power generation by harnessing salinity gradient energy during reverse electrodialysis using a lab-scaled fluidic cell, consisting of two reservoirs separated by a nanoporous ion exchange membrane, under various flow rates (qf) and salt-concentration difference (Δc). The current-voltage (I-V) characteristics of the single RED unit reveals a linear dependence, similar to an electrochemical cell. The experimental results show that the change of inflow velocity has an insignificant impact on the I-V data for a wide range of flow rates explored (0.01–1 mL/min), corresponding to a low-Peclet number regime. Both the maximum RED power density (Pc,m) and open-circuit voltage (ϕ0) increase with increasing Δc. On the one hand, the RED cell’s internal resistance (Rc) empirically reveals a power-law dependence of Rc∝Δc−α. On the other hand, the open-circuit voltage shows a logarithmic relationship of ϕ0=BlnΔc+β. These experimental results are consistent with those by a nonlinear numerical simulation considering a single charged nanochannel, suggesting that parallelization of charged nano-capillaries might be a good upscaling model for a nanoporous membrane for RED applications
