Unlocking the Potential for Methanol Synthesis via Electrochemical CO2 Reduction Using CoPc-Based Molecular Catalysts

• Published in: ACS nano Vol. 18; no. 33; pp. 21623 - 21632
• Main Authors: Yao, Libo, Ding, Jie, Cai, Xinhai, Liu, Lingyue, Singh, Nirala, McCrory, Charles C. L., Liu, Bin
• Format: Journal Article
• Language: English
• Published: American Chemical Society 20.08.2024
• Subjects: methanol synthesis; electrochemical CO2 reduction; cobalt phthalocyanine; binding strength; molecular modification
• ISSN: 1936-0851; 1936-086X; 1936-086X
• DOI: 10.1021/acsnano.4c07613

The electrochemical CO2 reduction reaction (CO2RR) to produce methanol (CH3OH) is an attractive yet challenging approach due to a lack of selective electrocatalysts. An immobilized cobalt phthalocyanine (CoPc) molecular catalyst has emerged as a promising electrocatalyst for CH3OH synthesis, demonstrating decent activity and selectivity through a CO2–CO–CH3OH cascade reaction. However, CoPc’s performance is limited by its weak binding strength toward the CO intermediate. Recent advancements in molecular modification aimed at enhancing CO intermediate binding have shown great promise in improving CO2-to-CH3OH performance. In this Perspective, we discuss the competitive binding mechanism between CO2 and CO that hinders CH3OH formation and summarize effective molecular modification strategies that can enhance both the binding of the CO intermediate and the conversion of the CO2-to-CH3OH activity. Finally, we offer future perspectives on optimization strategies to inspire further research efforts to fully unlock the potential for methanol synthesis via the CO2RR using molecular catalysts.