Amphiphilic Cobalt Phthalocyanine Boosts Carbon Dioxide Reduction

Due to the easy accessibility, chemical stability, and structural tunability of the macrocyclic skeleton, cobalt phthalocyanines immobilized on carbon supports offer an ideal research model for advanced electrochemical carbon dioxide reduction reaction (eCO₂ RR). In this work, an amphiphilic cobalt phthalocyanine (TC-CoPc) is loaded on multiwalled carbon nanotubes to reveal the roles of hydrophilic/hydrophobic properties on catalytic efficiency. Surprisingly, the resultant electrode exhibits a CO Faradaic efficiency (FE_CO ) of 95% for CO₂ RR with turnover frequency (TOF) of 29.4 s^-1 at an overpotential of 0.585 V over long-term electrolysis in a H-type cell. In the membrane electrode assembly (MEA) device, the boosted transport of water vapor to the catalyst layer slows down carbonate crystallization and enhances the stability of the electrode, with FE_CO value of >99% over 27 h at -0.25 A, representing the best selectivity and stability among reported molecular catalysts in MEA devices. The amphiphilic cobalt phthalocyanine, which decreases interfacial charge and mass transfer resistance and maintains effective contact between active sites and the electrolyte, highlights the exceptional CO₂ conversion from a molecular perspective.