Instability of Cobalt-Substituted Polyoxometalates during the Oxygen Evolution Reaction: An Operando X-ray Absorption Spectroscopy Study

Complexes of cobalt(II) stabilized by lacunary polyoxometalates (CoPOMs) are highly discussed water oxidation catalysts (WOC). While their activity and stability in the oxygen evolution reaction (OER) have been widely explored, there is still no consensus between those claiming that CoPOMs are active and stable OER catalysts and those suggesting that they rather act as precatalysts, which degrade into OER-active heterogeneous CoO_x catalysts. In this work, we use operando X-ray absorption spectroscopy along with electrochemical methods (cyclic voltammetry, chronoamperometry) to assess the activity and stability of [Co₉(H₂O)₆(OH)₃(HPO₄)₂(PW₉O₃₄)₃]^16– (Co₉POM) under chemical and electrochemical operating conditions. First, we demonstrate that Co₉POM dissolved in a phosphate buffer quickly degrades during an electrochemical OER, leaving a Co(III)/Co(II)-containing layer on the electrode surface that acts as a heterogeneous OER catalyst. This degradation is detected using both the post mortem and operando X-ray absorption near-edge structure and extended X-ray absorption fine structure. Then, the electrochemical OER is studied in the presence of 2,2′-bipyridine, which is used to eliminate Co²⁺ aqua-complexes resulting from Co₉POM dissociation equilibrium. Yet, this does not avoid the formation of a Co-containing precipitate, albeit of a different composition. Finally, to differentiate between degradation associated with the catalytic cycle itself and the one provoked by local pH changes in the vicinity of the electrode during the OER, the Co₉POM is studied as a homogeneous WOC with NaClO as a chemical oxidant. An irreversible loss of Co from the Co₉POM is detected after the addition of two NaClO equivalents per Co ion. These combined insights provide clear operando evidence of Co₉POM instability under either electrochemical OER or chemical WOC operating conditions.

B. Rotonnelli, Be. Lassalle-Kaiser, A. Bonnefont, S. Renaudineau, D. Garnier, A. Proust, F. Bournel, J.-J. Gallet, T. Asset, and E. Savinova

J. Phys. Chem. C 2024, 128, 19, 7968–7976; https://doi.org/10.1021/acs.jpcc.4c01265