Abstract

Seawater splitting requires highly active and stable electrocatalysts to sustain electrolysis without chloride corrosion, especially for the anode. Herein, a boron (B) doped MnFe2O4 spinel-type electrocatalyst with a heterostructure was derived from MnFe-MOF-74 precursor and applied for seawater electrolysis. It is found that the introduction of B species can effectively optimize the electronic configuration of MnFe2O4 with the promoted electron transfer ability between neighboring O to FeOh, thereby significantly reducing the energy barrier of the electron transfer and boosting the reaction process. As expected, in the real seawater environment, it required a low overpotential of 330 mV for oxygen evolution reaction (OER) to drive a current density of 100 mA cm−2 at 60 ℃, and exhibited high stability for over 200-h continuing test without producing hypochlorite and corrosion. This work provides a new strategy for enhancing the intrinsic activity of spinel-type oxides in seawater splitting.

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