PO6 geometric configuration unit enhanced electrocatalytic performance of Co3O4 in acidic oxygen evolution

J Colloid Interface Sci. 2023 Jul:641:329-337. doi: 10.1016/j.jcis.2023.03.036. Epub 2023 Mar 13.

Abstract

It is challenging to develop high-efficient and stable nonprecious metal-based electrocatalyst for oxygen evolution reaction (OER) in acid for proton exchange membrane (PEM) water splitting. Herein, P atoms were introduced into the lattice of spinel Co3O4 (P-Co3O4) to replace with octahedral coordinated Co3+ via a hydrothermal process following a thermal treatment. The formation of PO6 geometric configuration unit in Co3O4 can trigger electron rearrangement around Co ions, which resulted in the high-active Co2+ site on the surface, significantly decreasing the energy barrier of rate-determining step for OER. Moreover, the weaker covalency of the Co 3d-O 2p bond and higher formation energy of oxygen vacancy around Co2+ in P-Co3O4 inhibited the participation of lattice oxygen during OER process, enabling that P-Co3O4 can work stably in acidic media. The obtained P-Co3O4 afforded satisfying stability over 30 h in a PEM electrolysis device with an overpotential of 400 mV@10 mA/cm2 in 0.1 M HClO4.

Keywords: Co(3)O(4); Non-precious electrocatalyst; Oxygen evolution reaction in acid; PO(6) geometric configuration unit.