4.8 Article

Vapor-Fed Cathode Microbial Electrolysis Cells with Closely Spaced Electrodes Enables Greatly Improved Performance

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 56, Issue 2, Pages 1211-1220

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.1c06769

Keywords

hydrogen generation; microbial electrolysis cell; vapor-fed cathode; anion exchange membrane; pH control

Funding

  1. Department of Energy [DE-EE0009623]
  2. Penn State University

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The study developed a vapor-fed MEC design to enhance hydroxide ion transport to the anode without using a liquid catholyte, achieving record-high current density and H2 production rate. This innovative approach demonstrated higher and more stable performance compared to liquid-fed cathodes.
Hydrogen can be electrochemically produced in microbial electrolysis cells (MECs) by current generated from bacterial anodes with a small added voltage. MECs typically use a liquid catholyte containing a buffer or salts. However, anions in these catholytes result in charge being balanced predominantly by ions other than hydroxide or protons, leading to anode acidification. To enhance only hydroxide ion transport to the anode, we developed a novel vapor-fed MEC configuration lacking a catholyte with closely spaced electrodes and an anion exchange membrane to limit the acidification. This MEC design produced a record-high sustained current density of 43.1 +/- 0.6 A/m(2) and a H-2 production rate of 72 +/- 2 LH2/L-d (cell voltage of 0.79 +/- 0.00 V). There was minimal impact on MEC performance of increased acetate concentrations, solution conductivity, or anolyte buffer capacity at applied voltages up to 1.1 V, as shown by a nearly constant internal resistance of only 6.8 +/- 0.3 m Omega m(2). At applied external voltages >1.1 V, the buffer capacity impacted performance, with current densities increasing from 28.5 +/- 0.6 A/m(2) (20 mM phosphate buffer solution (PBS)) to 51 +/- 1 A/m(2) (100 mM PBS). These results show that a vapor-fed MEC can produce higher and more stable performance than liquid-fed cathodes by enhancing transport of hydroxide ions to the anode.

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