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Operando cathode activation with alkali metal cations for high current density operation of water-fed zero-gap carbon dioxide electrolyzers

Continuous-flow electrolyzers allow CO(2) reduction at industrially relevant rates, but long-term operation is still challenging. One reason for this is the formation of precipitates in the porous cathode from the alkaline electrolyte and the CO(2) feed. Here we show that while precipitate formation...

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Detalles Bibliográficos
Autores principales: Endrődi, B., Samu, A., Kecsenovity, E., Halmágyi, T., Sebők, D., Janáky, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7610664/
https://www.ncbi.nlm.nih.gov/pubmed/33898057
http://dx.doi.org/10.1038/s41560-021-00813-w
Descripción
Sumario:Continuous-flow electrolyzers allow CO(2) reduction at industrially relevant rates, but long-term operation is still challenging. One reason for this is the formation of precipitates in the porous cathode from the alkaline electrolyte and the CO(2) feed. Here we show that while precipitate formation is detrimental for the long-term stability, the presence of alkali metal cations at the cathode improves performance. To overcome this contradiction, we develop an operando activation and regeneration process, where the cathode of a zero-gap electrolyzer cell is periodically infused with alkali cation-containing solutions. This enables deionized water-fed electrolyzers to operate at a CO(2) reduction rate matching that of those using alkaline electrolytes (CO partial current density of 420 ± 50 mA cm(−2) for over 200 hours). We deconvolute the complex effects of activation and validate the concept with five different electrolytes and three different commercial membranes. Finally, we demonstrate the scalability of this approach on a multi-cell electrolyzer stack, with a 100 cm(2) / cell active area.