Developing efficient bifunctional catalysts for nonprecious metal-based oxygen reduction (ORR) and oxygen evolution (OER) is crucial to enhance the practical application of zinc−air batteries. The study harnessed electrostatic forces to anchor the nanoflower-like NiCo 2 O 4 onto graphene oxide, mitigating the poor inherent conductivity in NiCo 2 O 4 as a transition metal oxide and preventing excessive agglomeration of the nanoflower-like structures during catalysis. Consequently, the resulting composite, NiCo 2 O 4 -GO/C, exhibited notably superior ORR and OER catalytic performance compared to pure nanoflower-like NiCo 2 O 4 . Notably, it excelled in OER catalytic activity of the OER relative to the precious metal RuO 2 . As a bifunctional catalyst for ORR and OER, NiCo 2 O 4 -GO/C displayed a potential difference of 0.88 V between the ORR half-wave potential and the OER potential at 10 mA•cm −2 , significantly lower than the 1.08 V observed for pure flower-like NiCo 2 O 4 and comparable to the 0.88 V exhibited by precious metal catalysts Pt/C + RuO 2 . The NiCo 2 O 4 -GO/C-based zinc−air battery demonstrated a discharge capacity of 817.3 mA h•g −1 , surpassing that of precious metalbased zinc−air batteries. Moreover, charge−discharge cycling tests indicated the superior stability of the NiCo 2 O 4 -GO/C-based zinc−air battery compared to its precious metal-based counterparts.