The
oxygen evolution reaction (OER) is an electrochemical process
that involves the spin-dependent conversion of singlet OH–/H2O to triplet O2. However, the sluggish dynamics
associated with this reaction severely limits its efficiency in electrochemical
water splitting. Fortunately, the utilization of a magnetic field
can significantly enhance the spin selectivity and accelerate reaction
kinetics. Herein, we report a unique strategy to regulate the spin
polarization of NiFe layered double hydroxide (NiFe-LDH) by harnessing
an internal magnetic field induced by a built-in magnetic core. The
exchange bias effect between the magnetic core and NiFe-LDH can selectively
remove electrons with opposite magnetic moments, thereby reducing
magnetoresistances and minimizing spin scattering during electron
transport. Benefiting from this bias effect, the obtained catalyst
exhibits excellent OER performance with a low overpotential of 196
mV at a current density of 30 mA cm–2. Furthermore,
density functional theory (DFT) calculations further confirm that
the exchange bias effect can increase the hybrid strength of Fe-3d
and O-2p orbitals while decreasing the adsorption energy of the reactant
intermediates, thus accelerating the generation of paramagnetic oxygen.