The electrochemical reduction of CO2 to CO using renewable electricity offers a compelling pathway for greenhouse gas recycling. The two-electron, two-proton process is particularly attractive due to its operational simplicity and scalability, with copper- and silver-based nanomaterials being the most widely studied catalysts as the field approaches industrial maturity. However, achieving the necessary efficiency and stability for practical applications remains a significant challenge. Recently, molecular catalysts immobilized on conductive surfaces with carbon-based inks have emerged as highly tunable hybrid systems capable of remarkable selectivity. In this work, we report that a straightforward cobalt phthalocyanine complex, simply modified with a single trimethylammonium group, delivers outstanding CO2-to-CO conversion rates and selectivity, reaching a Faradaic efficiency of 93% at a total current density of 700 mA/cm2 (jCO = 650 mA/cm2) at neutral pH. Notably, CO selectivity above 90% was sustained for over 42 h at 150 mA/cm2, illustrating the potential of simply designed molecular catalysts for large-scale applications.

This study reports the first cobalt-catalysed C–H functionalization of furfural derivatives, demonstrating distinct reactivities based on the substrate. Furfurylimines enable selective C5–H alkenylati...