Enhancing Microbial Electrosynthesis of Acetate and Butyrate from CO2 Reduction Involving Engineered Clostridium ljungdahlii with a Nickel-Phosphide-Modified Electrode

Abstract

Microbial electrosynthesis (MES) is an emerging technology through which autotrophic microorganisms can directly uptake electrons or indirectly uptake electrons through H2 in the cathode for reducing CO2 to chemicals. In this study, the performance of MES with engineered Clostridium ljungdahlii was improved by electrochemically depositing a nickel phosphide (Ni–P) catalyst on the cathode. The acetate production rate of MES with 15 cycles was 0.17 g L–1 day–1, which was 1.7 times higher than that of MES without the catalyst. The corresponding butyrate production rate was remarkably enhanced at 0.1 g L–1 day–1, which was 2.5 times higher than that of MES without the catalyst. Electrochemical studies, scanning electron microscopy, and confocal scanning laser microscopy showed that Ni–P could accelerate the release of hydrogen and promote biofilm formation. These results also implied that more H2 evolution could provide more reducing power for butyrate production in the presence of Ni–P. This study attempted to provide effective strategies for the accumulation of C4 products in MES.