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Cobalt imidazolate frameworks are classical electrocatalysts for the oxygen evolution reaction (OER) but suffer from the relatively low activity. Here, a non-3d metal modulation strategy is presented for enhancing the OER activity of cobalt imidazolate frameworks. Two isomorphous frameworks [Co₄ (MO₄ )(eim)₆ ] (M=Mo or W, Heim=2-ethylimidazole) having Co(eim)₃ (MO₄ ) units and high water stabilities were designed and synthesized. In different neutral media, the Mo-modulated framework coated on a glassy carbon electrode shows the best OER performances (1 mA cm⁻² at an overpotential of 210 mV in CO₂ -saturated 0.5 m KHCO₃ electrolyte and 2/10/22 mA cm⁻² at overpotential of 388/490/570 mV in phosphate buffer solution) among non-precious metal catalysts and even outperforms RuO₂ . Spectroscopic measurements and computational simulations revealed that the non-3d metals modulate the electronic structure of Co for optimum reactant/product adsorption and tailor the energy of rate-determining step to a more moderate value.
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Xu et al. (2018) studied this question.
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