Sustainably-produced hydrogen is currently intensively investigated as an energy carrier to replace fossil fuels. We here characterize an emerging electrochemical cell termed a desalination fuel cell (DFC) that can continuously generate electricity and desalinate water while using hydrogen and oxygen gases as inputs. We investigated two operational modes, a near-neutral pH operation with H2, O2, and feedwater inputs (H2|O2), and a pH-gradient mode with H2, O2, feedwater, acid, and base inputs (H2 + B|O2 + A). We show that our cell can desalinate water with 30 g/L of salt content to near-zero salt concentration, while generating an enormous amount of electricity of up to 8.6 kW h per m3 of treated water when operated in the pH-gradient mode and up to about 1 kW h per m3 for the near-neutral mode. We quantify the thermodynamic energy efficiency of our device in both operational modes, showing that significantly higher efficiency is achievable in the pH-gradient mode, with up to 95.6%. Further, we present results elucidating the key bottlenecks in the DFC process, showing that the cell current and voltage are limited in the near-neutral pH operation due to a lack of H+ to serve as a reactant, and further reinforce the deleterious effect of halide poisoning on the cathode Pt catalyst and cell open circuit voltage. Such findings demonstrate that new fuel cell catalyst materials, tailored for environments associated with water treatment, can unlock yet-improved performance.
Keywords: desalination fuel cell; electrode catalyst; energy conversion; hydrogen fuel cell; thermodynamic energy efficiency; water desalination.