Controlled formation of CoOOH/Co(III)-MOF active phase for boosting electrocatalytic alkaline water oxidation

Surface reconstituted metal-organic frameworks (MOFs) offer appealing properties for electrocatalysis due to their unique structural and compositional advantages. In this work, a controlled potential-induced reconstruction of a two-dimensional cobalt metal-organic framework for boosting oxygen evolution reaction in alkaline media is reported. The current MOF is shown to undergo a partial structural transformation that generates a heterogeneous system, where the original MOF coexists with an oxyhydroxide phase. In fact, the potential-induced stabilization of Co(III) metal centers in the MOF is crucial for delaying its full degradation in alkaline media. This partial retention of the Co(III)MOF phase in the so-derived heterogeneous catalyst has been demonstrated to be decisive for boosting the alkaline electrocatalytic oxygen evolution reaction (OER), displaying superior OER activity in terms of both thermodynamic and kinetic merits compared to the benchmark IrO 2 and RuO 2 electrocatalysts and the prototypical cobalt (oxy)hydroxides, with a Tafel slope of 52 mV dec −1 and a turnover frequency (TOF) of 6.8 s −1 at 450 mV. Remarkably, the generated final product is stable, exhibiting high robustness and long durability for long-term OER electrolysis. This work provides new insight into the impact of the reconstruction of a MOF for alkaline OER under typical electrochemical conditions, which ultimately benefits the rational design of MOF-based catalysts with high electrocatalytic activity for oxidation reactions. • Controlled in-situ reconstruction of Co-MOF by anodic polarization in basic media. • As-generated product consists of a CoOOH/Co(III)-MOF heterogeneous system. • Promotion of Co(III) metal centres decisive for slowing down the MOF phase degradation. • As-formed catalyst exhibits outstanding electrocatalytic OER activity and stability. • Revealed synergy between the two phases for boosting for electrocatalytic OER.