- Marin, Daniela H;
- Perryman, Joseph T;
- Hubert, McKenzie A;
- Lindquist, Grace A;
- Chen, Lihaokun;
- Aleman, Ashton M;
- Kamat, Gaurav A;
- Niemann, Valerie A;
- Stevens, Michaela Burke;
- Regmi, Yagya N;
- Boettcher, Shannon W;
- Nielander, Adam C;
- Jaramillo, Thomas F
Generation of H2 and O2 from untreated water sources represents a promising alternative to ultrapure water required in contemporary proton exchange membrane-based electrolysis. Bipolar membrane-based devices, often used in electrodialysis and CO2 electrolysis, facilitate impure water electrolysis via the simultaneous mediation of ion transport and enforcement of advantageous microenvironments. Herein, we report their application in direct seawater electrolysis; we show that upon introduction of ionic species such as Na+ and Cl− from seawater, bipolar membrane electrolyzers limit the oxidation of Cl− to corrosive OCl− at the anode to a Faradaic efficiency (FE) of 0.005%, while proton exchange membrane electrolyzers under comparable operating conditions exhibit up to 10% FE to Cl− oxidation. The effective mitigation of Cl− oxidation by bipolar membrane electrolyzers underpins their ability to enable longer-term seawater electrolysis than proton exchange membrane assemblies by a factor of 140, suggesting a path to durable seawater electrolysis.