Low porosity, high areal-capacity Prussian blue analogue electrodes enhance salt removal and thermodynamic efficiency in symmetric Faradaic deionization with automated fluid control

Prussian blue analogues (PBAs) show great potential for low-energy Faradaic deionization (FDI) with reversible Na-ion capacity approaching 5 M in the solid-state. However, past continuous-flow demonstrations using PBAs in FDI were unable to desalinate brackish water to potable levels using single-pass architectures. Here, we show that recirculation of effluent from a symmetric cation intercalation desalination cell into brine/diluate reservoirs enables salt removal exceeding 80% at thermodynamic efficiency as high as 80% when cycled with 100 mM NaCl influent and when controlled by a low-volume, automated fluid circuit. This exceptional performance is achieved using a novel heated, alkaline wet phase inversion process that modulates colloidal forces to increase carbon black aggregation within electrode slurries to solidify crack-free, high areal-capacity PBA electrodes that are calendered to minimize cell impedance and electrode porosity. The results obtained demonstrate the need for co-design of auxiliary fluid-control systems together with electrode materials to advance FDI beyond brackish salinity.

Automated summary

Recirculating effluent from a symmetric cation intercalation desalination cell into brine/diluate reservoirs can achieve high salt removal rates and efficiency. This exceptional performance is achieved through a novel heated, alkaline wet phase inversion process that modulates colloidal forces to increase carbon black aggregation within electrode slurries, resulting in crack-free, high areal-capacity PBA electrodes that are calendered to minimize cell impedance and electrode porosity.