Porphyrin Aggregation under Homogeneous Conditions Inhibits Electrocatalysis: A Case Study on CO2 Reduction

• Published in: ACS central science 2024-06, Vol.10 (6), p.1251-1261
• Main Authors: Branch, Kaitlin L., Johnson, Erin R., Nichols, Eva M.
• Format: Article
• Language: English
• Subjects: Aggregates; Carbon dioxide; Catalysts; Chemical reduction; Clean energy; Dimethylformamide; Electrocatalysis; Electrocatalysts; Electrolytes; Heavy metals; Ligands; Light scattering; Nonaqueous electrolytes; Porphyrins; Reaction kinetics; Redox properties; Spectroscopy; Spectrum analysis; Structure-function relationships
• ISSN: 2374-7943; 2374-7951
• DOI: 10.1021/acscentsci.4c00121

Metalloporphyrins are widely used as homogeneous electrocatalysts for transformations relevant to clean energy and sustainable organic synthesis. Metalloporphyrins are well-known to aggregate due to π–π stacking, but surprisingly, the influence of aggregation on homogeneous electrocatalytic performance has not been investigated previously. Herein, we present three structurally related iron meso-phenylporphyrins whose aggregation properties are different in commonly used N,N-dimethylformamide (DMF) electrolyte. Both spectroscopy and light scattering provide evidence of extensive porphyrin aggregation under conventional electrocatalytic conditions. Using the electrocatalytic reduction of CO2 to CO as a test reaction, cyclic voltammetry reveals an inverse dependence of the kinetics on the catalyst concentration. The inhibition extends to bulk performance, where up to 75% of the catalyst at 1 mM is inactive compared to at 0.25 mM. We additionally report how aggregation is perturbed by organic additives, axial ligands, and redox state. Periodic boundary calculations provide additional insights into aggregate stability as a function of metalloporphyrin structure. Finally, we generalize the aggregation phenomenon by surveying metalloporphyrins with different metals and substituents. This study demonstrates that homogeneous metalloporphyrins can aggregate severely in well-solubilizing organic electrolytes, that aggregation can be easily modulated through experimental conditions, and that the extent of aggregation must be considered for accurate catalytic benchmarking.