Enhancing Long-Term Durability of Electrochemical Reactors Producing Formate from CO 2 and Water Designed for Integration with Solar Cells

• Published in: ACS omega Vol. 9; no. 10; pp. 11646 - 11657
• Main Authors: Kato, Naohiko, Kawai, Yasuaki, Nojiri, Natsumi, Shiozawa, Masahito, Kikuzawa, Yoshihiro, Suzuki, Nobuaki, Kosaka, Satoru, Kato, Yuichi, Seki, Juntaro, Hamaguchi, Tsuyoshi, Takeda, Yasuhiko
• Format: Journal Article
• Language: English
• Published: United States 12-03-2024
• ISSN: 2470-1343; 2470-1343
• DOI: 10.1021/acsomega.3c08911

Artificial photosynthetic cells producing organic matter from CO
and water have been extensively studied for carbon neutrality, and the research trend is currently transitioning from proof of concept using small-sized cells to large-scale demonstrations for practical applications. We previously demonstrated a 1 m
size cell in which an electrochemical (EC) reactor featuring a ruthenium (Ru)-complex polymer (RuCP) cathode catalyst was integrated with photovoltaic cells. In this study, we tackled the remaining issue to improve the long-term durability of cathode electrodes used in the EC reactors, demonstrating high Faradaic efficiencies exceeding 80% and around 60% electricity-to-chemical energy-conversion efficiencies of a 75 cm
sized EC reactor after continuous operation for 3000 h under practical conditions. Introduction of a pyrrole derivative containing an amino group in the RuCP coupled with UV-ozone treatment to create carboxyl groups on the carbon supports effectively reduced the detachment of the RuCP catalyst by forming a strong amide linkage. A newly developed chemically resistant graphite adhesive prevented the carbon supports from peeling off of the conductive substrates. In addition, highly durable anodes composed of IrO
-TaO
/Pt-metal oxide/Ti were adopted. Even though the EC reactor was installed at an inclined angle of 30°, which is approximately the optimal angle for receiving more solar energy, the crossover reactions were sufficiently suppressed because the porous separator film impeded the transfer of oxygen gas bubbles from the anode to the cathode. The intermittent operation improved the energy-conversion efficiency because the accumulated bubbles were removed at night.