Catalyst Aggregation Matters for Immobilized Molecular CO₂RR Electrocatalysts

Abstract

Here, we detail how the catalytic behavior of immobilized molecular electrocatalysts for the CO₂ reduction reaction (CO₂RR) can be impacted by catalyst aggregation. <i>Operando</i> Raman spectroscopy was used to study the CO₂RR mediated by a layer of cobalt phthalocyanine (CoPc) immobilized on the cathode of an electrochemical flow reactor. We demonstrate that during electrolysis, the oxidation state of CoPc in the catalyst layer is dependent upon the degree of catalyst aggregation. Our data indicate that immobilized molecular catalysts must be dispersed on conductive supports to mitigate the formation of aggregates and produce meaningful performance data. We leveraged insights from this mechanistic study to engineer an improved CO-forming immobilized molecular catalyst─cobalt octaethoxyphthalocyanine (EtO₈-CoPc)─that exhibited high selectivity (FE_CO ≥ 95%), high partial current density (<i>J</i>_CO ≥ 300 mA/cm²), and high durability (ΔFE_CO < 0.1%/h at 150 mA/cm²) in a flow cell. This work demonstrates how to accurately identify CO₂RR active species of molecular catalysts using <i>operando</i> Raman spectroscopy and how to use this information to implement improved molecular electrocatalysts into flow cells. This work also shows that the active site of CoPc during CO₂RR catalysis in a flow cell is the metal center.