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The rational control of the active site of metal-organic frameworks (MOFs) derived nanomaterials is essential to build efficient bifunctional oxygen reduction/evolution reaction (ORR/OER) catalysts. Accordingly, through designing and constructing a Co3O4-Co heterostructure embedded in Co, N co-doped carbon polyhedra derived (Co3O4-Co@NC) from the in-situ compositions of ZIF-67 and cobalt nanocrystals synthesized by the strategy of in-situ NaBH4 reduction, the dual-active site (Co3O4-Co and Co-Nx) is synchronously realized in a MOFs derived nanomaterials. The formed Co3O4-Co@NC shows excellent bifunctional electrocatalytic activity with ultra-small potential gap (ΔE = Ej=10 (OER) - E1/2 (ORR)) of 0.72 V, which surpasses the commercial Pt/C and RuO2 catalysts. The theory calculation results reveal that the excellent bifunctional electrocatalytic activity can be attributed to the charge redistribution of Co of Co-Nx induced by the synergistic effects of well-tuned active sites of Co3O4-Co nanoparticle and Co-Nx, thus optimizing the rate-determining step of the desorption of O2* intermediate in ORR and OH* intermediate in OER. The rechargeable Zn-air batteries with our bifunctional catalysts exhibit superior performance as well as high cycling stability. This simple-effective optimization strategy offers prospects for tuning the active site of MOF derived bifunctional catalyst in electrochemical energy devices.
The authors acknowledge support from the National Natural Science Foundation of China (No. 21875039), Minjiang Professorship (XRC-1677), Fujian province’s high level innovative and entrepreneurial talents (No. 50012709), the Open Project Program of the State Key Laboratory of Photocatalysis on Energy and Environment (No. SKLPEE-201814), Fuzhou University.