Metal-organic framework-derived core-shell-structured nitrogen-doped CoCx/FeCo@C hybrid supported by reduced graphene oxide sheets as high performance bifunctional electrocatalysts for ORR and OER

• DOI: 10.1016/j.jcat.2019.02.005
• Publication Date: 2019-02-14T07:31:44Z
• Authors: Hengyi Fang; Taizhong Huang; Yue Sun; Baotao Kang; Dong Liang; Shuo Yao; Jiemei Yu; M. Mayilvel Dinesh; Si Wu; Jin Yong Lee; Shun Mao
• Keywords: 02 engineering and technology; 0210 nano-technology; 7. Clean energy

Abstract Metal-organic framework derived materials have a great promise as non-precious metal-based electrocatalysts for large-scale applications of energy storage and transition devices with low-cost and high efficiency. Here, we report a high performance core-shell-structured nitrogen-doped CoCx/FeCo@C/reduced graphene oxide (rGO) hybrid, which is derived from Fe-doped Co3[Co(CN)6]2 MOFs, as bifunctional catalysts for both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Structure characterizations show that the carbon shell of CoCx/FeCo and graphene support are bonded to each other, which offer a large surface area and stable anchoring sites for the CoCx/FeCo. Electrochemical tests show that N-doped CoCx/FeCo@C/rGO hybrid exhibits superior onset potential (1.0183 V vs RHE), half-wave potential (0.9653 V vs RHE), peak current intensity (0.9233 mA/cm−2) and long-term durability for ORR than those of Pt/C (onset potential, half-wave potential and peak current intensity are 1.0174 V and 0.9213 V, 0.8233 mA/cm−2, respectively) in 0.1 M KOH electrolyte. The overpotential of the hybrid for OER is only ∼390 mV at a current intensity of 10 mA/cm−2, which is close to that of the RuO2. The excellent electrocatalytic properties of this hybrid make it a great potential to be substitute for precious-based catalysts for ORR and OER in fuel cells and water splitting.