posted on 2025-03-24, 07:47authored byShofu MATSUDA, Yuta YOSHIDA, Minoru UMEDA
<div>CH<sub>4</sub> production by CO<sub>2</sub> reduction using a membrane electrode assembly containing a Pt/C electrocatalyst was recently demonstrated. Because this CO<sub>2</sub> reduction reaction occurs at approximately its theoretical electrode potential, it is possible to generate electric power as an H<sub>2</sub>-CO<sub>2</sub> fuel cell by the reduction reaction occurring in combination with the H<sub>2</sub> oxidation reaction. However, the CH<sub>4</sub>-generation reaction deactivated in a short time (∼5 min) due to the influence of the CO adsorbed on the Pt surface (CO<sub>ads</sub>) as a reaction intermediate. In this study, we investigated the CO<sub>2</sub> reduction using a Pt<sub>0.5</sub>Ru<sub>0.5</sub>/C electrocatalyst in order to realize a continuous CH<sub>4</sub> production. As a result, steady CH<sub>4</sub> generation for more than 15 min with a faradaic efficiency of 12.0 % was observed at 0.22 V vs. RHE under a 4 vol% CO<sub>2</sub> atmosphere. In other words, an improved continuous CH<sub>4</sub> production was achieved by employing a Pt<sub>0.5</sub>Ru<sub>0.5</sub>/C electrocatalyst instead of Pt/C, and their faradaic efficiencies were equivalent. This result was obtained because the adsorption energy of CO<sub>ads</sub> decreased due to the alloying of Pt and Ru based on the changes in the onset potential of the CH<sub>4</sub> production. In addition, power generation as an H<sub>2</sub>-CO<sub>2</sub> polymer electrolyte fuel cell was observed while converting CO<sub>2</sub> to CH<sub>4</sub>.</div>
Funding
CO2 reduction for a life-supporting O2 recycling during space exploration by applying fuel cell system