4.8 Article

Electroosmotic flow steers neutral products and enables concentrated ethanol electroproduction from CO2

期刊

JOULE
卷 5, 期 10, 页码 2742-2753

出版社

CELL PRESS
DOI: 10.1016/j.joule.2021.08.013

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资金

  1. Natural Sciences and Engineering Research Council (NSERC)
  2. Government of Ontario, through the Ontario Research Fund
  3. Suncor Energy
  4. NSERC Alliance grant program
  5. NSERC
  6. Hatch
  7. Government of Ontario

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By reversing the direction of ion and electroosmotic transport with a porous proton exchange layer, both convective and diffusive routes of ethanol loss are blocked, resulting in less than 1% ethanol crossover to the anode and achieving an ethanol concentration of 13.1 wt % directly from the cathode outlet.
Electrochemical reduction of carbon dioxide (CO2RR) converts intermittent renewable energy into high energy density fuels, such as ethanol. Membrane electrode assembly (MEA) electrolyzers are particularly well-suited for CO2-to-ethanol conversion in view of their low ohmic resistance and high stability. However, over 75% of the ethanol produced at the cathode migrates through the membrane where it is diluted by the anolyte and may be oxidized. The ethanol concentration that results is two orders of magnitude below the 10 wt % standard set by the incumbent industrial process, fermentation. Here, we reverse the direction of ion and electroosmotic transport by means of a porous proton exchange layer, thereby blocking both the convective and diffusive routes of ethanol loss. With this strategy, we eliminate ethanol crossover to the anode (< 1%) and achieve an ethanol concentration of 13.1 wt % directly from the cathode outlet.

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