| Literature DB >> 35750665 |
Ke Xie1, Rui Kai Miao2, Adnan Ozden2, Shijie Liu2, Zhu Chen1, Cao-Thang Dinh3, Jianan Erick Huang1, Qiucheng Xu4, Christine M Gabardo2, Geonhui Lee1, Jonathan P Edwards2, Colin P O'Brien2, Shannon W Boettcher4, David Sinton5, Edward H Sargent6.
Abstract
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.Entities:
Year: 2022 PMID: 35750665 PMCID: PMC9232613 DOI: 10.1038/s41467-022-31295-3
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 17.694