Regulating the Spin State of Fe^III Enhances the Magnetic Effect of the Molecular Catalysis Mechanism

Abstract

Aqueous-phase oxygen evolution reaction (OER) is the bottleneck of water splitting. The formation of the O-O bond involves the generation of paramagnetic oxygen molecules from the diamagnetic hydroxides. The spin configurations might play an important role in aqueous-phase molecular electrocatalysis. However, spintronic electrocatalysis is almost an uncultivated land for the exploration of the oxygen molecular catalysis process. Herein, we present a novel magnetic Fe^III site spin-splitting strategy, wherein the electronic structure and spin states of the Fe^III sites are effectively induced and optimized by the Jahn-Teller effect of Cu²⁺. The theoretical calculations and operando attenuated total reflectance-infrared Fourier transform infrared (ATR FT-IR) reveal the facilitation for the O-O bond formation, which accelerates the production of O₂ from OH^- and improves the OER activity. The Cu₁-Ni₆Fe₂-LDH catalyst exhibits a low overpotential of 210 mV at 10 mA cm^-2 and a low Tafel slope (33.7 mV dec^-1), better than those of the initial Cu₀-Ni₆Fe₂-LDHs (278 mV, 101.6 mV dec^-1). With the Cu²⁺ regulation, we have realized the transformation of NiFe-LDHs from ferrimagnets to ferromagnets and showcase that the OER performance of Cu-NiFe-LDHs significantly increases compared with that of NiFe-LDHs under the effect of a magnetic field for the first time. The magnetic-field-assisted Cu₁-Ni₆Fe₂-LDHs provide an ultralow overpotential of 180 mV at 10 mA cm^-2, which is currently one of the best OER performances. The combination of the magnetic field and spin configuration provides new principles for the development of high-performance catalysts and understandings of the catalytic mechanism from the spintronic level.