Enhanced Desalination Performance Using Phosphate Buffer-Mediated Redox Reactions of Manganese Oxide Electrodes in a Multichannel System

Water desalination mediated by electrochemical reactions to directly capture and release salt at electrode materials offers a low-voltage method for producing freshwater. Developing new system designs has allowed electrode materials to maximize their capacity for salt separation, especially when a multichannel system is used to introduce a separate electrode rinse solution. Here, we show that the use of an additive can provide a new strategy for improving electrode capacity and, hence desalination performance, which so far has been limited to increasing the electrolyte concentration. A custom-built, 2/2-channel flow cell divided by two cation exchange membranes and an anion exchange membrane was fed with 50 mM NaCl as the feed (two inner channels) and 0.5 M NaCl containing up to 0.1 M phosphate as the electrode rinse (two outer channels). Using manganese oxide electrodes with phosphate buffer-mediated redox reactions exhibited an improved desalination capacity of 68.0 +/- 5.2 mg g(-1) (0.55 mA cm(-2)) and a rate of 5.6 +/- 1.3 mg g(-1) min(-1) (0.96 mA cm(-2)). The improvement was attributed to the buffer that served as a proton donor for promoting the H+ insertion reaction of amorphous or poorly crystalline MnO2. Additionally, the buffering capacity against acidification and the creation of insoluble manganese phosphate on the electrode surface prevented the dissolution of Mn2+, which could otherwise occur at the anode due to a decrease in the local pH upon H+ deinsertion. Thus, the use of manganese oxide electrodes coupled with phosphate provides a new strategy of increasing electrode capacity for water desalination.