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Manipulating Intermetallic Charge Transfer for Switchable External Stimulus-Enhanced Water Oxidation Electrocatalysis

   Chalil Oglou, Ramadan; Ulusoy Ghobadi, Turkan Gamze; Hegner, Franziska Simone; Galan-Mascaros, Jose Ramon; Lopez, Nuria; Ozbay, Ekmel; Karadas, Ferdi

Electrocatalytic processes involving the oxygen evolution reaction (OER) present a kinetic bottleneck due to the existence of linear-scaling relationships, which bind the energies of the different intermediates in the mechanism limiting optimization. Here, we offer a way to break these scaling relationships and enhance the electrocatalytic activity of a Co-Fe Prussian blue modified electrode in OER by applying external stimuli. Improvements of & AP;11 % and & AP;57 % were achieved under magnetic field (0.2 T) and light irradiation (100 mW cm(-2)), respectively, when working at fixed overpotential, & eta;=0.6 V at pH 7. The observed enhancements strongly tie in with the intermetallic charge transfer (IMCT) intensity between Fe and Co sites. Density Functional Theory simulations suggest that tuning the IMCT can lead to a change of the OER mechanism to an external stimuli-sensitive spin crossover-based pathway, which opens the way for switchable electrocatalytic devices.

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