Cooperative Electrocatalytic O 2 Reduction Involving Co(salophen) with p-Hydroquinone as an Electron-Proton Transfer Mediator

The molecular cobalt complex, Co(salophen), and para-hydroquinone (H Q) serve as effective cocatalysts for the electrochemical reduction of O to water. Mechanistic studies reveal redox cooperativity between Co(salophen) and H Q. H Q serves as an electron-proton transfer mediator (EPTM) that enables electrochemical O reduction at higher potentials and with faster rates than is observed with Co(salophen) alone. Replacement of H Q with the higher-potential EPTM, 2-chloro-H Q, allows for faster O reduction rates at higher applied potential. These results demonstrate a unique strategy to achieve improved performance with molecular electrocatalyst systems.