Abstract

The cobalt–phosphate amorphous oxyhydroxide water-splitting catalyst, CoPi, is widely investigated because of its reactivity and self-repair analogous to the oxygen-evolving catalyst in Photosystem II. CoPi films show optical absorption features analogous to those seen more generally in transition metal oxides and oxygen-evolving catalysts. Possible photocatalytic properties of CoPi have, up until now, not been considered. Herein, we report on the finding of wavelength-dependent photo-electrochemical responses in CoPi. Red light excitation (623 nm) into a manifold of charge transfer and d–d electronic transitions was seen to produce photoanodic current responses that enhance OER, while blue light excitation (415 nm) within the ligand-to-metal charge-transfer transition was found to produce photocathodic responses that inhibit OER and oxidative repair. These results demonstrate intrinsic wavelength-dependent photo-electrochemistry in CoPi and opportunities to use light-excited states in CoPi, and potentially other transition metal oxides, to enhance OER and to track reaction mechanisms using light-triggered, pump–probe techniques.

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