the sluggish kinetics of oxygen evolution reaction (OER) for water splitting still hinders the wide application of this technology. Ru-and Ir-based oxides are highly active catalysts for OER, nevertheless, the scarcity and cost of Ru and Ir largely constrains the broad deployment of hydrogen production utilities. [4][5][6] To this end, transition metal oxide (TMO) electrocatalysts have been extensively investigated due to their earth-abundant and outstanding OER performance. [7][8][9][10] It is remarkable that spinel oxides present stunning catalytic performance for OER in alkaline electrolytes, benefitting from the coexistence of tetrahedral (T d ) and octahedral (O h ) transition-metal cation sites in TMOs, whereas such a complex structure with multiple sites also brings a great challenge on precise identification toward active sites for OER. [11][12][13][14] The tailoring of catalytic active sites for spinel oxides is of importance on the design of highly efficient electrocatalysts for OER, but the active sites of spinel oxides for OER are still elusive. [11,[15][16][17][18] For example, it is reported that the high OER activity of ZnCo 2 O 4 relies on the amounts of Co 3+ on the O h sites. [19] However, on the contrary, it also has been found that the Zn 2+ at T d sites is contributed Magnetic field enhanced electrocatalysis has recently emerged as a promising strategy for the development of a viable and sustainable hydrogen economy via water oxidation. Generally, the effects of magnetic field enhanced electrocatalysis are complex including magnetothermal, magnetohydrodynamic and spin selectivity effects. However, the exploration of magnetic field effect on the structure regulation of electrocatalyst is still unclear whereas is also essential for underpinning the mechanism of magnetic enhancement on the electrocatalytic oxygen evolution reaction (OER) process. Here, it is identified that in a mixed NiFe 2 O 4 (NFO), a large magnetic field can force the Ni 2+ cations to migrate from the octahedral (O h ) sites to tetrahedral (T d ) sites. As a result, the magnetized NFO electrocatalyst (NFO-M) shows a two-fold higher current density than that of the pristine NFO in alkaline electrolytes. The OER enhancement of NFO is also observed at 1 T (NFO@1T) under an operando magnetic field. Our first-principles calculations further confirm the mechanism of magnetic field driven structure regulation and resultant OER enhancement. These findings provide a strategy of manipulating tetrahedral units of spinel oxides by a magnetic field on boosting OER performance.