- Xie, Ke;
- Miao, Rui;
- Ozden, Adnan;
- Liu, Shijie;
- Chen, Zhu;
- Dinh, Cao-Thang;
- Huang, Jianan;
- Xu, Qiucheng;
- Gabardo, Christine;
- Lee, Geonhui;
- Edwards, Jonathan;
- OBrien, Colin;
- Boettcher, Shannon;
- Sinton, David;
- Sargent, Edward
In alkaline and neutral MEA CO2 electrolyzers, CO2 rapidly converts to (bi)carbonate, imposing a significant energy penalty arising from separating CO2 from the anode gas outlets. Here we report a CO2 electrolyzer uses a bipolar membrane (BPM) to convert (bi)carbonate back to CO2, preventing crossover; and that surpasses the single-pass utilization (SPU) limit (25% for multi-carbon products, C2+) suffered by previous neutral-media electrolyzers. We employ a stationary unbuffered catholyte layer between BPM and cathode to promote C2+ products while ensuring that (bi)carbonate is converted back, in situ, to CO2 near the cathode. We develop a model that enables the design of the catholyte layer, finding that limiting the diffusion path length of reverted CO2 to ~10 μm balances the CO2 diffusion flux with the regeneration rate. We report a single-pass CO2 utilization of 78%, which lowers the energy associated with downstream separation of CO2 by 10× compared with past systems.