Issue 18, 2020

In situ electrochemical H2 production for efficient and stable power-to-gas electromethanogenesis

Abstract

Bioelectrochemical power-to-gas presents a promising technology for long-term storage of excess renewable energy in the form of methane. The transition of the technology from laboratory to applied scale is currently challenged by low volumetric production rates, energy losses at the cathode, as well as the unknown physiology of the microbes in an electrochemical reactor. Here, we introduce a stable electromethanogenesis system based on efficient in situ hydrogen production by non-precious-metal catalysts and effective hydrogen uptake by the methanogenic microorganisms. Using NiMo-cathodes and pure cultures of hydrogenotrophic Methanococcus maripaludis, our system achieved an unprecedented volumetric methane production rate from CO2 of 1.4 L methane per L per day. The system performed stably for over 4 weeks with columbic efficiencies steadily above 90%. A physiological analysis of cells in the electromethanogenic reactor revealed robustly-growing cells with nearly identical protein expression patterns to gas-fed controls. Local pH fluctuations at the surface of cathode and cation exchange membrane resulted in a small but noticeable fraction of cell lysis. Our data collectively indicate that physiologically uncompromised cells of a pure methanogenic culture can perform methanogenesis robustly at high specific rate in a biocompatible electromethanogenic reactor using inexpensive, earth-abundant cathode materials.

Graphical abstract: In situ electrochemical H2 production for efficient and stable power-to-gas electromethanogenesis

Associated articles

Supplementary files

Article information

Article type
Paper
Submitted
03 Jun 2020
Accepted
02 Sep 2020
First published
02 Sep 2020

Green Chem., 2020,22, 6194-6203

In situ electrochemical H2 production for efficient and stable power-to-gas electromethanogenesis

F. Kracke, J. S. Deutzmann, W. Gu and A. M. Spormann, Green Chem., 2020, 22, 6194 DOI: 10.1039/D0GC01894E

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